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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">abc</journal-id>
      <journal-title-group>
        <journal-title>Arquivos Brasileiros de Cardiologia</journal-title>
        <abbrev-journal-title abbrev-type="publisher">Arq. Bras. Cardiol.</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="ppub">0066-782X</issn>
      <issn pub-type="epub">1678-4170</issn>
      <publisher>
        <publisher-name>Sociedade Brasileira de Cardiologia - SBC</publisher-name>
        <publisher-loc>S&#227;o Paulo, SP, Brazil</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v3">CrpSzRfV8h6tsnZBDgWN3sb</article-id>
      <article-id pub-id-type="other">00008</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2011000100008</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(11)09600108</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2010005000165</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigos Originais</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Associa&#231;&#227;o entre marcadores inflamat&#243;rios e fatores de risco cardiovascular em mulheres de Kolkata, W.B, &#205;ndia</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Ganguli</surname>
            <given-names>Debdutta</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Das</surname>
            <given-names>Nilanjan</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Saha</surname>
            <given-names>Indranil</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
          <xref ref-type="aff" rid="aff04"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Sanapala</surname>
            <given-names>Krishna Rao</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Chaudhuri</surname>
            <given-names>Debnath</given-names>
          </name>
          <xref ref-type="aff" rid="aff03"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ghosh</surname>
            <given-names>Saurabh</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Dey</surname>
            <given-names>Sanjit</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="city">West Bengal</named-content>
          <named-content content-type="state"/>
        </addr-line>
        <institution content-type="orgname">University of Calcutta</institution>
        <institution content-type="orgdiv1">University College of Science and Technology </institution>
        <institution content-type="orgdiv2">Department of Physiology</institution>
        <country country="IN">India</country>
      </aff>
      <aff id="aff03">
        <addr-line>
          <named-content content-type="city">West Bengal</named-content>
          <named-content content-type="state"/>
        </addr-line>
        <institution content-type="orgname">All India Institute of Hygiene&#160;&amp;&#160;Public Health</institution>
        <institution content-type="orgdiv1">Department of Biochemistry and Nutrition </institution>
        <country country="IN">India</country>
      </aff>
      <aff id="aff04">
        <addr-line>
          <named-content content-type="city">Kolkata</named-content>
        </addr-line>
        <institution content-type="orgname">RG Kar Medical College and Hospital</institution>
        <institution content-type="orgdiv1">Department of Community Medicine </institution>
        <country country="IN">India</country>
      </aff>
      <aff id="aff02">
        <addr-line>
          <named-content content-type="city">Kolkata</named-content>
        </addr-line>
        <institution content-type="orgname">Indian Statistical Institute</institution>
        <institution content-type="orgdiv1">Human Genetics Unit </institution>
        <country country="IN">India</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>01</month>
        <year>2011</year>
      </pub-date>
      <volume>96</volume>
      <issue>1</issue>
      <fpage>38</fpage>
      <lpage>46</lpage>
      <history>
        <date date-type="accepted">
          <day>28</day>
          <month>05</month>
          <year>2010</year>
        </date>
        <date date-type="rev-recd">
          <day>11</day>
          <month>02</month>
          <year>2010</year>
        </date>
        <date date-type="received">
          <day>11</day>
          <month>02</month>
          <year>2010</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/4.0/" xml:lang="en">
          <license-p>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</license-p>
        </license>
      </permissions>
      <abstract>
        <p>FUNDAMENTO: Recentes pesquisas tem se concentrado no uso de biomarcadores inflamat&#243;rios na previs&#227;o de risco cardiovascular. Entretanto, a informa&#231;&#227;o &#233; escassa em rela&#231;&#227;o &#224; associa&#231;&#227;o entre esses marcadores inflamat&#243;rios com outros fatores de risco cardiovasculares em indianos asi&#225;ticos, particularmente em mulheres. OBJETIVO: Explorar a associa&#231;&#227;o entre marcadores inflamat&#243;rios tais como prote&#237;na C-reativa de alta sensibilidade (PCR-as) e contagem de leuc&#243;citos (LEU) e fatores de risco cardiovascular tais como adiposidade geral e central, press&#227;o arterial, vari&#225;veis lip&#237;dicas e lipoproteicas e glicemia de jejum. M&#201;TODOS: Conduzimos uma an&#225;lise transversal de 100 mulheres com idade entre 35-80 anos. As participantes foram selecionadas atrav&#233;s da metodologia de amostragem por cluster, de 12 distritos urbanos selecionadas ao acaso na Corpora&#231;&#227;o Municipal de Kolkata, &#205;ndia. RESULTADOS: A PCR-as apresentou uma associa&#231;&#227;o significante com o &#237;ndice de massa corporal (IMC) (p &lt; 0,001) e circunfer&#234;ncia da cintura (CC) (p = 0,002). Associa&#231;&#245;es significantes inversas foram observadas entre a lipoprote&#237;na de alta densidade colesterol (HDL-c) e ambos marcadores inflamat&#243;rios PCR-as (p = 0,031) e LEU (p = 0,014). A apo-lipoprote&#237;na A1 (Apo A1) tamb&#233;m estava negativamente associada com a PCR-as. A contagem de leuc&#243;citos apresentou uma correla&#231;&#227;o significante com a glicemia de jejum e a raz&#227;o colesterol total (CT) /HDL-C. Usando regress&#227;o log&#237;stica ajustada para idade, IMC (odds ratio/OR, 1,186; intervalo de confian&#231;a/IC, 1,046-1,345; p=0,008) e LEU (OR, 1,045; IC, 1,005-1,087; p=0,027) foram as covariantes significantemente associadas com a PCR-as. CONCLUS&#195;O: No presente estudo, os fatores de risco tais como IMC, CC e HDL-c e Apo-A1 mostraram uma associa&#231;&#227;o significante com PCR-as. A contagem de leuc&#243;citos estava significantemente associada com os n&#237;veis de HDL-c, glicemia de jejum, raz&#227;o CT/HDL-c em mulheres.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>Inflama&#231;&#227;o</kwd>
        <kwd>prote&#237;na C-reativa</kwd>
        <kwd>fatores de risco</kwd>
        <kwd>contagem de leuc&#243;citos</kwd>
        <kwd>adiposidade</kwd>
        <kwd>dislipidemias</kwd>
        <kwd>mulheres</kwd>
        <kwd>&#205;ndia</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>22</day>
        <month>12</month>
        <year>2010</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>
      <bold>Associa&#231;&#227;o entre marcadores inflamat&#243;rios e fatores de risco cardiovascular em mulheres de Kolkata, W.B, &#205;ndia</bold>
    </p>
    <p>
      <bold>Debdutta Ganguli<sup>I</sup>; Nilanjan Das<sup>I</sup>; Indranil Saha<sup>I, IV</sup>; Krishna Rao Sanapala<sup>II</sup>; Debnath Chaudhuri<sup>III</sup>; Saurabh Ghosh<sup>II</sup>; Sanjit Dey<sup>I</sup></bold>
    </p>
    <p><sup>I</sup>Department of Physiology, University College of Science and Technology, University of Calcutta, West Bengal, India </p>
    <p><sup>II</sup>Human Genetics Unit, Indian Statistical Institute, Kolkata, India </p>
    <p><sup>III</sup>Department of Biochemistry and Nutrition, All India Institute of Hygiene and Public Health, West Bengal, India </p>
    <p><sup>IV</sup>Present Address: Department of Community Medicine, RG Kar Medical College and Hospital, Kolkata, India</p>
    <p>
      <xref ref-type="corresp" rid="back">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p><bold>FUNDAMENTO: </bold> Recentes pesquisas tem se concentrado no uso de biomarcadores inflamat&#243;rios na previs&#227;o de risco cardiovascular. Entretanto, a informa&#231;&#227;o &#233; escassa em rela&#231;&#227;o &#224; associa&#231;&#227;o entre esses marcadores inflamat&#243;rios com outros fatores de risco cardiovasculares em indianos asi&#225;ticos, particularmente em mulheres. </p>
    <p><bold>OBJETIVO:</bold> Explorar a associa&#231;&#227;o entre marcadores inflamat&#243;rios tais como prote&#237;na C-reativa de alta sensibilidade (PCR-as) e contagem de leuc&#243;citos (LEU) e fatores de risco cardiovascular tais como adiposidade geral e central, press&#227;o arterial, vari&#225;veis lip&#237;dicas e lipoproteicas e glicemia de jejum. </p>
    <p><bold>M&#201;TODOS: </bold> Conduzimos uma an&#225;lise transversal de 100 mulheres com idade entre 35-80 anos. As participantes foram selecionadas atrav&#233;s da metodologia de amostragem por cluster, de 12 distritos urbanos selecionadas ao acaso na Corpora&#231;&#227;o Municipal de Kolkata, &#205;ndia. </p>
    <p><bold>RESULTADOS: </bold> A PCR-as apresentou uma associa&#231;&#227;o significante com o &#237;ndice de massa corporal (IMC) (p &lt; 0,001) e circunfer&#234;ncia da cintura (CC) (p = 0,002). Associa&#231;&#245;es significantes inversas foram observadas entre a lipoprote&#237;na de alta densidade colesterol (HDL-c) e ambos marcadores inflamat&#243;rios PCR-as (p = 0,031) e LEU (p = 0,014). A apo-lipoprote&#237;na A1 (Apo A1) tamb&#233;m estava negativamente associada com a PCR-as. A contagem de leuc&#243;citos apresentou uma correla&#231;&#227;o significante com a glicemia de jejum e a raz&#227;o colesterol total (CT) /HDL-C. Usando regress&#227;o log&#237;stica ajustada para idade, IMC (odds ratio/OR, 1,186; intervalo de confian&#231;a/IC, 1,046-1,345; p=0,008) e LEU (OR, 1,045; IC, 1,005-1,087; p=0,027) foram as covariantes significantemente associadas com a PCR-as. </p>
    <p><bold>CONCLUS&#195;O: </bold> No presente estudo, os fatores de risco tais como IMC, CC e HDL-c e Apo-A1 mostraram uma associa&#231;&#227;o significante com PCR-as. A contagem de leuc&#243;citos estava significantemente associada com os n&#237;veis de HDL-c, glicemia de jejum, raz&#227;o CT/HDL-c em mulheres.</p>
    <p><bold>Palavras-chave: </bold> Inflama&#231;&#227;o, prote&#237;na C-reativa, fatores de risco, contagem de leuc&#243;citos, adiposidade, dislipidemias, mulheres, &#205;ndia.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>Recentes estudos epidemiol&#243;gicos tem relatado uma forte e consistente associa&#231;&#227;o entre fatores de risco para doen&#231;a cardiovascular (DCV) e inflama&#231;&#227;o<sup>1,2</sup> e esta tem sido identificada como um fator de risco independente para DCV<sup>3,4</sup>. Dos novos marcadores inflamat&#243;rios atualmente sendo investigados, a prote&#237;na C-reativa de alta sensibilidade (PCR-as) e a contagem de leuc&#243;citos ou leucograma (LEU) s&#227;o os mais promissores. Um n&#250;mero de estudos epidemiol&#243;gicos prospectivos tem consistentemente demonstrado que a PCR-as<sup>5,6</sup>, bem como a contagem de leuc&#243;citos<sup>7</sup> podem predizer de forma independente o risco vascular em homens e mulheres aparentemente saud&#225;veis, assintom&#225;ticos para os tradicionais fatores de risco para DCV. Al&#233;m disso, ambos os marcadores<sup>1,2</sup> tamb&#233;m adicionam informa&#231;&#227;o progn&#243;stica em pacientes com sinais cl&#237;nicos de DCV, al&#233;m daquela dispon&#237;vel com base na avalia&#231;&#227;o lip&#237;dica padr&#227;o. Um n&#250;mero substancial de estudos transversais j&#225; estabeleceu o fato de que a PCR-as e a contagem de leuc&#243;citos correlacionam-se de forma significante com componentes da s&#237;ndrome metab&#243;lica<sup>8-10</sup>.</p>
    <p>Na &#205;ndia, os dados s&#227;o escassos em rela&#231;&#227;o &#224; associa&#231;&#227;o desses biomarcadores inflamat&#243;rios com outros fatores de risco para DCV em adultos, particularmente em mulheres. Assim, os objetivos do presente estudo foram investigar a associa&#231;&#227;o entre a PCR-as e a contagem de leuc&#243;citos com fatores de risco tais como &#237;ndice de massa corporal, circunfer&#234;ncia da cintura, raz&#227;o cintura-quadril, press&#227;o arterial, vari&#225;veis lip&#237;dicas e lipoproteicas e glicemia de jejum.</p>
    <p>
      <bold>Materiais e M&#233;todo</bold>
    </p>
    <p>
      <bold>Participantes do estudo</bold>
    </p>
    <p>Selecionamos randomicamente uma popula&#231;&#227;o de 100 mulheres com idade de 35-80 anos a partir de um estudo epidemiol&#243;gico existente sobre avalia&#231;&#227;o de risco cardiovascular, envolvendo 701 mulheres residentes de distritos urbanos que estavam h&#225; 29,8 anos, em m&#233;dia, em Kolkata. O estudo foi realizado de acordo com as recomenda&#231;&#245;es da organiza&#231;&#227;o Mundial da Sa&#250;de (OMS) para estudos utilizando a metodologia de amostragem por cluster<sup>11</sup>, em 12 diferentes distritos de 141 distritos da Corpora&#231;&#227;o Municipal de Kolkata, de acordo com os dados do censo mais recente. Os distritos ou clusters foram inclu&#237;dos no estudo atrav&#233;s de amostragem rand&#244;mica simples sem substitui&#231;&#227;o. De acordo com a estrat&#233;gia de amostragem por cluster, em cada um dos distritos ou clusters, um local perto do centro do distrito era escolhido como o ponto de in&#237;cio e uma dire&#231;&#227;o era selecionada ao acaso. Ent&#227;o os domic&#237;lios eram escolhidos de forma rand&#244;mica ao longo da dire&#231;&#227;o, ap&#243;s a verifica&#231;&#227;o de adequa&#231;&#227;o aos crit&#233;rios de inclus&#227;o - mulheres de 35 anos ou mais, independentemente de seu estado civil, mas n&#227;o gr&#225;vidas. Os crit&#233;rios de exclus&#227;o foram doen&#231;a aguda ou qualquer tratamento para doen&#231;a infecciosa cr&#244;nica ou inflamat&#243;ria, antes ou na &#233;poca da investiga&#231;&#227;o. Indiv&#237;duos n&#227;o dispostos a participar do estudo foram exclu&#237;dos durante a investiga&#231;&#227;o. Indiv&#237;duos que utilizavam aspirina como medica&#231;&#227;o cr&#244;nica tamb&#233;m foram exclu&#237;dos. Nenhum dos indiv&#237;duos relatou estar utilizando medica&#231;&#227;o hipolipemiante. Entre as mulheres eleg&#237;veis, 57 foram identificados como p&#243;s-menopausadas e as restantes 43 mulheres estavam na pr&#233;-menopausa.</p>
    <p>As mulheres deram seu consentimento livre e informado para participar do estudo, que foi aprovado pelo Comit&#234; de &#201;tica Humana do Departamento de Fisiologia Humana da Universidade de Calcult&#225;.</p>
    <p>
      <bold>Question&#225;rio</bold>
    </p>
    <p>Uma entrevista baseada em um question&#225;rio foi utilizada para coletar informa&#231;&#245;es sobre o habito de fumar, uso de tabaco de mascar, consumo de &#225;lcool, hist&#243;rico m&#233;dico familiar e pessoal de hipertens&#227;o, diabete e infarto do mioc&#225;rdio. As participantes foram entrevistadas sobre seu estado menopausal e hist&#243;rico de qualquer interven&#231;&#227;o cir&#250;rgica, como histerectomia. As mulheres foram consideradas pr&#233;-menopausais que haviam tido um ou mais epis&#243;dios de sangramento regulares nos 12 meses anteriores. As mulheres foram consideradas p&#243;s-menopausais se a menstrua&#231;&#227;o houvesse cessado naturalmente ou cirurgicamente (por ex., histerectomia), por pelo menos 12 meses cont&#237;nuos. As participantes tamb&#233;m foram entrevistadas sobre seu hist&#243;rico de dislipidemia, uso corrente de medica&#231;&#227;o anti-hipertensiva ou hipoglic&#234;mica ou medicamentos hipolipemiantes e uso de terapia de reposi&#231;&#227;o hormonal p&#243;s-menopausa. A validade das respostas &#224;s perguntas sobre o uso de medicamentos foi confirmada atrav&#233;s da verifica&#231;&#227;o dos registros m&#233;dicos.</p>
    <p>
      <bold>Medidas antropom&#233;tricas e bioqu&#237;micas</bold>
    </p>
    <p>A altura foi medida com uma precis&#227;o de 0,5 cm, com as participantes descal&#231;as, utilizando um antrop&#244;metro. O peso foi medido com as participantes vestindo roupas leves ap&#243;s a remo&#231;&#227;o dos sapatos, com uma precis&#227;o de 0,1 kg. A circunfer&#234;ncia da cintura (CC) foi medida utilizando uma fita m&#233;trica inel&#225;stica no ponto m&#233;dio entre a &#250;ltima costela e a crista il&#237;aca no plano horizontal. A circunfer&#234;ncia m&#225;xima do quadril (CQ) foi medida horizontalmente ao n&#237;vel da extens&#227;o m&#225;xima dos gl&#250;teos. Para cada medida da circunfer&#234;ncia da cintura e do quadril, duas medidas eram tomadas, com uma precis&#227;o de 0,5 cm. A m&#233;dia das duas medidas mais pr&#243;ximas foi calculada. A raz&#227;o cintura-quadril (RCQ) foi calculada atrav&#233;s da equa&#231;&#227;o padr&#227;o: RCQ = CC (cm)/CQ (cm).</p>
    <p>O IMC foi calculado como peso/altura<sup>2</sup> (kg/m<sup>2</sup>). A press&#227;o arterial foi medida no bra&#231;o direito das participantes na posi&#231;&#227;o sentada, relaxada e com o bra&#231;o apoiado ao n&#237;vel do cora&#231;&#227;o utilizando um esfigmoman&#244;metro de merc&#250;rio padr&#227;o. As press&#245;es sist&#243;lica e diast&#243;lica foram registradas como o inicio do primeiro e quinto sons de Korotkoff, respectivamente. Para cada uma das medidas, foram feitas duas leituras com 5 minutos de intervalo entre elas e a m&#233;dia das duas leituras foi calculada para obter a press&#227;o arterial final. As participantes foram orientadas a evitar o fumo, bebidas cafeinadas e exerc&#237;cio por pelo menos 30 minutos antes da medida da press&#227;o arterial. Foi pedido &#224;s participantes para se manterem em jejum por pelo menos 10 horas antes das amostras serem colhidas na manh&#227; do dia seguinte. A venopun&#231;&#227;o foi realizada por um m&#233;dico treinado com as participantes na posi&#231;&#227;o sentada. A glicemia de jejum foi medida atrav&#233;s do m&#233;todo de glicose-oxidase/peroxidase<sup>12</sup>, colesterol total s&#233;rico foi medido atrav&#233;s do m&#233;todo colesterol oxidase/peroxidase-amidopirina<sup>13</sup> e os triglic&#233;rides (TG) s&#233;ricos foram medidos pelo m&#233;todo glicerol fosfato oxidase/peroxidase-amidopirina<sup>14</sup> utilizando kits de ensaio fornecidos por Randox Laboratories Ltd (Crumlin, Co. Antrim, Reino Unido) em um espectrofot&#244;metro (Bio-rad, Hercules, Calif&#243;rnia, EUA). O HDL-C tamb&#233;m foi determinado pelo mesmo m&#233;todo ap&#243;s precipita&#231;&#227;o de lipoprote&#237;na de muito baixa densidade (VLDL) e a lipoprote&#237;na de baixa densidade (LDL) pelo polietileno-glicol PEG 6000. O LDL-colesterol (LDL-C) foi calculado utilizando-se a f&#243;rmula: LDL-C = colesterol total - HDL-C - (TG/5)<sup>15</sup>. Lipoprote&#237;na (a) (Lp(a)), apolipoprote&#237;na A1 e B foram medidas por m&#233;todo de imunoensaio automatizado turbidim&#233;trico<sup>16,17</sup> com kits de reagentes fornecidos por Randox Laboratories Ltd em um Randox RX Daytona Sistema Autoanalisador (Crumlin, Co. Antrim, Reino Unido).</p>
    <p>
      <bold>Crit&#233;rios de defini&#231;&#245;es e diagn&#243;sticos</bold>
    </p>
    <p>A obesidade foi definida como um IMC &gt; 25 kg/m<sup>2 18</sup>. De acordo com o S&#233;timo Relat&#243;rio do <italic>Joint National Committee</italic> (JNC) sobre Preven&#231;&#227;o, Detec&#231;&#227;o, Avalia&#231;&#227;o e Tratamento da Hipertens&#227;o Arterial<sup>19</sup>, indiv&#237;duos foram considerados hipertensos quando a press&#227;o arterial sist&#243;lica era <underline>&gt;</underline>140 mmHg, a press&#227;o arterial diast&#243;lica era <underline>&gt;</underline> 90 mmHg ou ambos, ou se as participantes estivessem tomando medica&#231;&#227;o anti-hipertensiva. Diabete foi definida como n&#237;veis glic&#234;micos de jejum de 7,0 mmol/l ou mais (<underline>&gt;</underline> 126 mg/dl) ou se estivessem tomando medica&#231;&#227;o para diabete pelos crit&#233;rios estabelecidos pelo Programa Educacional National do Colesterol (NCEP), Painel de Tratamento do Adulto III (ATP III)<sup>20</sup>. Os seguintes pontos de corte foram usados para definir dislipidemia como (i) Hipercolesterolemia: n&#237;vel de colesterol total de 5,18 mmol/l ou mais (<underline>&gt;</underline> 200 mg/dl) (ii) Hipertrigliceridemia: n&#237;veis de triglic&#233;rides de 1,69 mmol/lou mais (<underline>&gt;</underline> 150 mg/dl) (iii) Baixos n&#237;veis de HDL-C: n&#237;veis de HDL-colesterol &lt; 1,03 mmol/l (&lt;40 mg/dl) e (iv) Altos n&#237;veis de LDL-C: N&#237;veis de LDL-colesterol de 3,36 mmol/l ou mais (<underline>&gt;</underline>130 mg/dl) de acordo com os crit&#233;rios diagn&#243;sticos das diretrizes do NCEP, ATP III.</p>
    <p>
      <bold>Medida da PCR-as e leucograma</bold>
    </p>
    <p>As concentra&#231;&#245;es no plasma da PCR-as foram medidas utilizando um ensaio imunoturbidim&#233;trico exaltado com part&#237;culas de l&#225;tex<sup>4</sup>, com kits fornecidos por Spinreact, Santa Coloma, Espanha. O ensaio foi realizado em um sistema auto-analisador (Microlab-300, Merck, Alemanha). De acordo com as instru&#231;&#245;es do fabricante, os coeficientes de varia&#231;&#227;o (CV) intra-ensaio e inter-ensaio para a PCR-as foram 4,3% e 8,4%, respectivamente e o limite m&#237;nimo de detec&#231;&#227;o foi 0,05 mg/l. Os leucogramas foram realizados manualmente com a ajuda do hemocit&#244;metro de Neubauer, sob o microsc&#243;pio, em at&#233; 24 horas ap&#243;s a coleta do sangue por venopuntura<sup>21</sup>. Para manter a uniformidade no processo de contagem, a mesma pessoa treinada foi encarregada durante todo o processo investigativo. O procedimento foi repetido por pelo menos tr&#234;s vezes para cada esp&#233;cime.</p>
    <p>
      <bold>An&#225;lise estat&#237;stica</bold>
    </p>
    <p>Todas as an&#225;lises estat&#237;sticas foram conduzidas em paralelo para PCR-as e leucograma, que foram divididos em respectivos tercis, com base na distribui&#231;&#227;o em 100 participantes do estudo. ANOVA one-way (com compara&#231;&#227;o m&#250;ltipla (<italic>pairwise</italic>) de Tukey) foi utilizado para comparar as m&#233;dias dos grupos para vari&#225;veis cont&#237;nuas pelos tercis; o Teste de Soma de Postos ou Wilcoxon Rank Sum Test foi usado para compara&#231;&#227;o das medianas e o teste &#967;<sup>2</sup> foi usado para comparar propor&#231;&#245;es. Antes dos testes estat&#237;sticos, os dados foram verificados para normalidade. Devido ao fato de a distribui&#231;&#227;o da PCR-as e Lp(a) ser assim&#233;trica, as vari&#225;veis foram transformadas em logaritmo natural pra todas as an&#225;lises. A an&#225;lise de correla&#231;&#227;o de Pearson foi executada para determinar a associa&#231;&#227;o dos marcadores inflamat&#243;rios com fatores de risco cardiovascular. Uma compara&#231;&#227;o entre grupos de mulheres pr&#233; e p&#243;s-menopausa foi realizada com an&#225;lise de covari&#226;ncia (ANCOVA) ap&#243;s ajuste de outras covariantes. Os n&#237;veis s&#233;ricos de PCR-as foram divididos em duas categorias (abaixo e acima), com base no valor mediano da PCR-as considerada como ponto de corte (1,31 mg/l). Modelos de regress&#227;o log&#237;stica n&#227;o-condicionada foram utilizadas para calcular o <italic>odds ratio</italic> (OR), ou raz&#227;o de chances, para avaliar a associa&#231;&#227;o entre a PCR-as e outras vari&#225;veis. Todas as an&#225;lises foram realizadas utilizando-se os softwares SPSS para Windows (vers&#227;o 10.0, Chicago) e MedCalc (vers&#227;o 10.1.6) e valores de p &lt;0,05 foram considerados significantes.</p>
    <p>
      <bold>Resultados</bold>
    </p>
    <p>As preval&#234;ncias de algumas caracter&#237;sticas basais s&#227;o mostradas na <xref ref-type="table" rid="t1">Tabela 1</xref>. A idade m&#233;dia dos sujeitos do estudo era 48,3&#177;9,8 anos. Um total de 35% das mulheres mascava tabaco com freq&#252;&#234;ncia regular ou semanalmente. Nenhuma das participantes relatou fumar cigarros industrializados ou caseiros ou consumir &#225;lcool. A preval&#234;ncia das mulheres p&#243;s-menopausa na popula&#231;&#227;o era de 57.0%, mas nenhuma estava recebendo terapia de reposi&#231;&#227;o hormonal. A preval&#234;ncia geral de obesidade era de 51,5% na popula&#231;&#227;o do estudo, determinado pelo IMC apenas. A preval&#234;ncia da hipertens&#227;o e hist&#243;rico familiar positivo de hipertens&#227;o era de 36,0% e 25,0%, respectivamente. Diabete foi identificada em 12,0% das mulheres e 16,0% dos sujeitos do estudo relataram um hist&#243;rico familiar positivo para diabete. No geral, um total de 3,1% das mulheres apresentou um hist&#243;rico de infarto do mioc&#225;rdio. A Hipercolesterolemia foi observada em 32,0% dos sujeitos. Entretanto, a Hipertrigliceridemia foi observada em 44,0% dos sujeitos e uma porcentagem quase similar (45,0%) apresentava baixos n&#237;veis de HDL-C. Al&#233;m disso, 29,0% das mulheres apresentavam altos n&#237;veis de LDL-C.</p>
    <table-wrap id="t1">
      <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt01.jpg"/></table-wrap>
    <p>A <xref ref-type="table" rid="aop15910t02">Tabela 2</xref> mostra a rela&#231;&#227;o entre os n&#237;veis de PCR-as e v&#225;rias vari&#225;veis de risco entre os sujeitos do estudo. O IMC e a CC eram significantemente mais altos (p= 0,001 e p= 0,021 para IMC e CC, respectivamente) nos tercis crescentes dos n&#237;veis de PCR-as s&#233;rica. As mulheres que apresentavam os tercis mais altos pareciam ter uma tend&#234;ncia &#224; maior incid&#234;ncia de diabete, bem como n&#237;veis maiores de TG e n&#237;veis menores de apolipoprote&#237;na A1, embora as diferen&#231;as n&#227;o tivessem sido significantes.</p>
    <p content-type="asset">
      <table-wrap id="aop15910t02">
        <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt02.jpg"/></table-wrap>
    </p>
    <p>Subsequentemente avaliamos (<xref ref-type="table" rid="aop15910t03">Tabela 3</xref>) a rela&#231;&#227;o entre a contagem dos leuc&#243;citos e outras vari&#225;veis de risco na popula&#231;&#227;o do estudo. A raz&#227;o CT/HDL-C aumentou significantemente (p= 0,007) nos tercis de contagem de leuc&#243;citos, enquanto outras vari&#225;veis, como glicemia de jejum, triglic&#233;rides, HDL-colesterol e apolipoprote&#237;na A1, foram n&#227;o-significantemente mais altas nos tercis superiores. O IMC e a CC foram mais altos nos tercis superiores da contagem de leuc&#243;citos, mas as diferen&#231;as n&#227;o foram estatisticamente significantes. As press&#245;es sist&#243;lica e diast&#243;lica tamb&#233;m foram n&#227;o-significantemente mais altas nos tercis superiores. Mulheres nos tercis superiores apresentavam maior incid&#234;ncia de diabete. O valor m&#233;dio da PCR-as era maior nos tercis crescentes da contagem de leuc&#243;citos, mas n&#227;o apresentava signific&#226;ncia estat&#237;stica.</p>
    <p content-type="asset">
      <table-wrap id="aop15910t03">
        <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt03.jpg"/></table-wrap>
    </p>
    <p>A prote&#237;na C-reativa de alta sensibilidade (PCR-as) estava significantemente associada com medidas de obesidade como IMC (r=0,373, p&lt;0,001) e CC (r=0,301, p=0,002) ap&#243;s ajuste para idade (<xref ref-type="table" rid="t4">Tabela 4</xref>), enquanto nenhuma correla&#231;&#227;o significante foi observada com a RCQ (r=0,004, p=0,966). Entretanto, a contagem de leuc&#243;citos estava n&#227;o-significantemente associada com o IMC, CC e RCQ ap&#243;s ajuste para idade. A an&#225;lise do coeficiente de correla&#231;&#227;o parcial revelou uma correla&#231;&#227;o negativa significante entre o HDL-c e a PCR-as (r= -0,220, p=0,031) e entre o HDL-C e a contagem de leuc&#243;citos (r= -0,247, p= 0,014). A apolipoprote&#237;na A1 tamb&#233;m estava inversamente associada (r= -0,237, p=0,031) com a PCR-as em mulheres. As associa&#231;&#245;es com a contagem de leuc&#243;citos foram significantes para vari&#225;veis bioqu&#237;micas, tais como glicemia de jejum (r= 0,253, p= 0,011), raz&#227;o CT/HDL-C (r= 0,284, p= 0,004) e PCR-as (r= 0,252, p= 0,012). Como fortes associa&#231;&#245;es foram observadas entre a PCR-as e a medidas de obesidade como o IMC e a CC, n&#243;s ajustamos essas vari&#225;veis junto com idade para o c&#225;lculo de coeficientes de correla&#231;&#227;o parcial entre a PCR-as e outras vari&#225;veis em todos os modelos acima. As associa&#231;&#245;es da contagem de leuc&#243;citos com outras vari&#225;veis foram computados ap&#243;s ajuste para idade.</p>
    <table-wrap id="t4">
      <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt04.jpg"/></table-wrap>
    <p>Uma compara&#231;&#227;o dos n&#237;veis dos marcadores inflamat&#243;rios em mulheres pr&#233;-menopausa e p&#243;s-menopausa &#233; mostrada na <xref ref-type="table" rid="t5">Tabela 5</xref>. Ambos os n&#237;veis de PCR-as e a contagem de leuc&#243;citos n&#227;o diferiram significantemente entre as mulheres na pr&#233; e na p&#243;s-menopausa. As m&#233;dias geom&#233;tricas ajustadas foram 1,68 e 2,66 mg/l respectivamente para PCR-as (aumento de 1,58 vezes com a menopausa). Devido ao fato de a menopausa estar associada com altera&#231;&#245;es nas medidas de obesidade e outros perfis bioqu&#237;micos, ajustamos as m&#233;dias para vari&#225;veis como IMC, CC e HDL-C, al&#233;m da idade.</p>
    <table-wrap id="t5">
      <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt05.jpg"/></table-wrap>
    <p>A an&#225;lise de regress&#227;o log&#237;stica foi conduzida em vari&#225;veis que se correlacionavam significantemente com a PCR-as (<xref ref-type="table" rid="aop15910t06">Tabela 6</xref>). O IMC (OR, 1,186; IC, 1,046-1,345; p=0,008) e CC (OR, 1,045; IC, 1,005-1,087; p=0,027) foram as covariantes que apresentaram uma associa&#231;&#227;o significante e positiva com a PCR-as ap&#243;s o ajuste para idade. Entretanto, nenhuma associa&#231;&#227;o independente foi observada entre o HDL-C e a PCR-as.</p>
    <p content-type="asset">
      <table-wrap id="aop15910t06">
        <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt06.jpg"/></table-wrap>
    </p>
    <p>
      <bold>Discuss&#227;o</bold>
    </p>
    <p>H&#225; um consenso emergente de que a DCV tem uma etiologia multifatorial, incluindo componentes ateroscler&#243;ticos, pr&#243;-tromb&#243;ticos e inflamat&#243;rios. Sendo assim, al&#233;m da avalia&#231;&#227;o dos fatores de risco convencionais, novos marcadores tem sido explorados em estudos observacionais prospectivos na esperan&#231;a de que eles possam melhorar a capacidade de predizer o risco de desenvolvimento de eventos cardiovasculares.</p>
    <p>No presente estudo, encontramos associa&#231;&#245;es significantes entre os n&#237;veis de PCR-as e medidas de adiposidade, como IMC e CC. Esses resultados s&#227;o consistentes com os achados experimentais, sugerindo que o tecido adiposo &#233; uma grande fonte de citoquinas, incluindo IL-6, que &#233; um importante determinante de s&#237;ntese de PCR hep&#225;tica<sup>8,22-24</sup>. Entretanto, em adultos, associa&#231;&#245;es mais fortes entre gordura corporal e valores de PCR tem sido relatadas para mulheres, quando comparadas com homens<sup>25</sup>. O estudo <italic>Third National Health and Nutrition Examination Survey</italic> (NHANES III) realizado nos Estados Unidos, que incluiu homens e mulheres com idade <underline>&gt;</underline>20 anos, revelou que o IMC mais alto est&#225; associado com concentra&#231;&#245;es mais altas de PCR, mesmo em adultos mais jovens<sup>26</sup>. Uma rela&#231;&#227;o significante entre os n&#237;veis de PCR com o IMC tamb&#233;m foi relatada entre homens e mulheres idosos no estudo Cardiovascular Health Study<sup>22</sup> bem como por Mendall e cols.<sup>23</sup>. Lemieux e cols.<sup>27</sup> observaram que apesar do fato da quantidade de gordura corporal (medida como IMC) apresentar a melhor correla&#231;&#227;o com os n&#237;veis de PCR, as maiores concentra&#231;&#245;es de PCR no plasma foram observadas em indiv&#237;duos que apresentavam aumentos paralelos na adiposidade visceral (medida como CC) e gordura total corporal. Apoio adicional &#224; essa observa&#231;&#227;o foi fornecida pelo estudo de Hak e cols.<sup>24</sup>, que relataram que a PCR estava fortemente associada com a CC, mesmo ap&#243;s o ajuste do IMC. A relativa contribui&#231;&#227;o do tecido adiposo intra-abdominal e subcut&#226;neo na gera&#231;&#227;o da PCR ainda n&#227;o &#233; clara. Entretanto, no presente estudo, a CC mostrou uma associa&#231;&#227;o significante com a PCR-as, embora a associa&#231;&#227;o desapare&#231;a ap&#243;s o controle do IMC (dados n&#227;o mostrados). Esse fen&#244;meno pode ser explicado pela forte colinearidade da CC e IMC nos sujeitos do estudo.</p>
    <p>No presente estudo, foi observado que a PCR-as apresentou uma associa&#231;&#227;o inversa com o HDL-C e a apolipoprote&#237;na A-1. Al&#233;m disso, houve uma associa&#231;&#227;o inversa entre a contagem de leuc&#243;citos e os n&#237;veis de HDL-C. Os n&#237;veis de HDL-C consistentemente mostram uma associa&#231;&#227;o inversa com marcadores sist&#234;micos de inflama&#231;&#227;o em v&#225;rios estudos prospectivos<sup>5,24,28</sup>. Um estudo recente por Birjmohun e cols.<sup>29</sup> demonstrou que indiv&#237;duos aparentemente saud&#225;veis com n&#237;veis baixos isolados geneticamente determinados de HDL-C eram mais suscet&#237;veis a teste de sensibilidade com endotoxina de baixa dose em compara&#231;&#227;o com indiv&#237;duos com n&#237;veis normais ou altos de HDL-C. O estudo revelou uma forte associa&#231;&#227;o inversa entre os n&#237;veis de HDL-C e apo A-1 com a resposta dos leuc&#243;citos e n&#237;veis de PCR no plasma, apoiando um efeito antiinflamat&#243;rio do HDL-C. No presente estudo, tem sido mostrado que a associa&#231;&#227;o entre is n&#237;veis de PCR no plasma e valores baixos de HDL-C persiste mesmo ap&#243;s o ajuste para IMC e CC, sugerindo uma associa&#231;&#227;o independente entre essas vari&#225;veis nos indiv&#237;duos. Evid&#234;ncias recentes ap&#243;iam uma s&#233;rie de efeitos anti-aterog&#234;nicos do HDL-C, incluindo efeitos antiinflamat&#243;rios<sup>30</sup>.</p>
    <p>No presente estudo, a contagem de leuc&#243;citos mostrou uma correla&#231;&#227;o positiva significante com os n&#237;veis de PCR-as no plasma e vari&#225;veis como glicemia de jejum e raz&#227;o CT/HDL-C. O estudo transversal ARIC com indiv&#237;duos jovens e de meia-idade<sup>31</sup> mostrou que a contagem de leuc&#243;citos estava associada com os n&#237;veis de insulina e glicemia de jejum em uma an&#225;lise n&#227;o-estratificada por sexo. Um estudo recente na popula&#231;&#227;o asi&#225;tica da &#205;ndia, conduzido por Gokulakrishan e cols.<sup>32</sup> mostrou que a contagem de leuc&#243;citos tinha uma associa&#231;&#227;o positiva com glicemia de jejum e resist&#234;ncia &#224; insulina. Sendo assim, &#233; poss&#237;vel que a inflama&#231;&#227;o e a fun&#231;&#227;o endotelial estejam entre v&#225;rios antecedentes comuns para diabete e doen&#231;a card&#237;aca coronariana<sup>33</sup>. A associa&#231;&#227;o entre concentra&#231;&#245;es de PCR plasm&#225;tica e contagem de leuc&#243;citos tem sido tamb&#233;m consistentemente relatadas em muitos achados cl&#237;nicos<sup>2,34</sup>.</p>
    <p>N&#227;o observamos uma influ&#234;ncia clara do estado menopausal nos n&#237;veis de biomarcadores inflamat&#243;rios. Observa&#231;&#245;es similares foram relatadas pelo estudo de Hak e seu grupo<sup>24</sup> onde os n&#237;veis de PCR ajustados para idade e para a idade e IMC eram levemente mais altos nas mulheres na pr&#233;-menopausa, mas a diferen&#231;a n&#227;o era estatisticamente significante. Em um estudo comparativo de mulheres na pr&#233;-menopausa <italic>vs</italic>. mulheres na p&#243;s-menopausa, conduzido por Sites e cols.<sup>35</sup>, n&#237;veis aumentados de PCR estavam associados com aumento na gordura corporal, mas n&#227;o ao estado menopausal. Entretanto, numerosos testes cl&#237;nicos tem demonstrado que terapias de reposi&#231;&#227;o hormonal ex&#243;gena, bem como os n&#237;veis de horm&#244;nio end&#243;genos est&#227;o associados com aumento nos n&#237;veis de PCR, junto com outros marcadores de inflama&#231;&#227;o, como fibrinog&#234;nio e contagem de leuc&#243;citos, em mulheres na p&#243;s-menopausa<sup>36,37</sup>. Estudos adicionais s&#227;o necess&#225;rios para estudar a associa&#231;&#227;o entre inflama&#231;&#227;o e menopausa.</p>
    <p>A inflama&#231;&#227;o tem um papel fundamental na aterotrombose<sup>38</sup>. A PCR-as, uma medida da inflama&#231;&#227;o, &#233; um mediador bem como um marcador de aterotrombose. Embora v&#225;rios outros marcadores inflamat&#243;rios tenham sido investigados, a PCR-as tem mais estabilidade, precis&#227;o no ensaio, acur&#225;cia e disponibilidade. A PCR-as obteve reconhecimento oficial como teste card&#237;aco do <italic>Centers for Disease Control and Prevention</italic> (Centro de Controle e Preven&#231;&#227;o de Doen&#231;as - CDC) e da <italic>American Heart Association</italic> (AHA)<sup>4</sup>. A utilidade do teste da PCR em pacientes com infarto do mioc&#225;rdio, angina est&#225;vel ou inst&#225;vel, tem sido bem estabelecida<sup>39</sup>. N&#237;veis altos de PCR-as nessas situa&#231;&#245;es cl&#237;nicas identificam pacientes com cargas inflamat&#243;rias mais altas, que apresentam maior risco de eventos isqu&#234;micos futuros. Al&#233;m disso, um n&#237;vel alto de PCR fornece valor progn&#243;stico adicional aos fatores de risco tradicionais. Assim, em um indiv&#237;duo com alto risco, um n&#237;vel elevado de PCR-as deveria alertar o m&#233;dico e o individuo para a necessidade de estabelecer estrat&#233;gias agressivas de diminui&#231;&#227;o de riscos.</p>
    <p>At&#233; o limite de nosso conhecimento, o presente estudo &#233; o primeiro a examinar a associa&#231;&#227;o entre marcadores inflamat&#243;rios sist&#234;micos, tais como a PCR-as e a contagem de leuc&#243;citos e outros fatores de risco cardiovascular em uma amostra baseada na popula&#231;&#227;o geral na &#205;ndia, com foco particularmente nas mulheres. Um ponto forte adicional do estudo foi a qualidade da coleta da amostra e a precis&#227;o na medida na PCR e outros biomarcadores associados. Entretanto, algumas quest&#245;es precisam ser discutidas. Esse estudo foi conduzido em uma popula&#231;&#227;o aparentemente saud&#225;vel com baixa ou nenhuma exposi&#231;&#227;o atual &#224; fatores de DCV clinicamente estabelecida, como infarto do mioc&#225;rdio e fumo, respectivamente. Os fatores acima s&#227;o fortes determinantes dos n&#237;veis de PCR e assim, a escolha de nossa popula&#231;&#227;o facilitou a investiga&#231;&#227;o de confundidores associados com a PCR. Assim, estudos adicionais s&#227;o necess&#225;rios para verificar os achados em situa&#231;&#245;es cl&#237;nicas e epidemiol&#243;gicas nessa popula&#231;&#227;o. Segundo, esse estudo inclui o uso de uma &#250;nica medida de marcadores inflamat&#243;rios, os quais podem n&#227;o refletir de forma acurada o estado inflamat&#243;rio de longo prazo. M&#250;ltiplas medidas com o passar do tempo e altera&#231;&#245;es nessas medidas podem fornecer um mecanismo mais preciso para predizer o risco nos indiv&#237;duos.</p>
    <p>
      <bold>Conclus&#227;o</bold>
    </p>
    <p>Nossos resultados indicam que em uma popula&#231;&#227;o aparentemente saud&#225;vel de mulheres com baixa taxa de fumantes e doen&#231;a cardiovascular clinicamente estabelecida, o IMC e a CC estavam associados com n&#237;veis de biomarcadores sist&#234;micos tais como a PCR-as e a concentra&#231;&#227;o de leuc&#243;citos. Considerando que os mediadores inflamat&#243;rios est&#227;o diretamente envolvidos com a aterog&#234;nese, esses resultados sugerem um importante mecanismo atrav&#233;s do qual a obesidade pode afetar o risco de doen&#231;a cardiovascular. Tamb&#233;m observamos uma importante associa&#231;&#227;o entre marcadores inflamat&#243;rios e vari&#225;veis de lipoprote&#237;nas tais como o HDL-c e a Apo-A1, que foi independente das medidas de adiposidade. Esses achados adicionam a um crescente conjunto de evid&#234;ncias que o HDL-c e a Apo-A1 protegem contra a doen&#231;a cardiovascular atrav&#233;s de mecanismos que se estendem bem al&#233;m de seu envolvimento no transporte de colesterol. Os presentes achados assim refor&#231;am a import&#226;ncia desses biomarcadores inflamat&#243;rios na cria&#231;&#227;o de algoritmos de previs&#227;o de risco cardiovascular junto com as ferramentas de avalia&#231;&#227;o padr&#227;o, especialmente em mulheres.</p>
    <p>
      <bold>Agradecimentos</bold>
    </p>
    <p>Esse trabalho recebeu apoio do Departamento de Ci&#234;ncia e Tecnologia, Governo da &#205;ndia, [Benef&#237;cio n&#186; SSD/WS/059/2004].</p>
    <p>
      <bold>Potencial Conflito de Interesses</bold>
    </p>
    <p>Declaro n&#227;o haver conflito de interesses pertinentes.</p>
    <p>
      <bold>Fontes de Financiamento</bold>
    </p>
    <p>O presente estudo foi financiado pelo Department of Science and Technology Government of India.</p>
    <p>
      <bold>Vincula&#231;&#227;o Acad&#234;mica</bold>
    </p>
    <p>Este artigo &#233; parte de tese de Doutorado de Debdutta Ganguli pela University of Calcuta.</p>
    <p>
      <fn id="back" fn-type="corresp">
        <p>Correspond&#234;ncia:</p>
        <p> Sanjit Dey </p>
        <p> Department of Physiology </p>
        <p> University College of Science and Technology </p>
        <p> University of Calcutta, 92, APC Road </p>
        <p> Kolkata- 700 009, West Bengal - India </p>
        <p> E-mail: </p>
        <p>
          <email xlink:href="sanjitdey2003@yahoo.com">sanjitdey2003@yahoo.com</email>
        </p>
      </fn>
    </p>
    <p>Artigo recebido em 11/02/10; revisado recebido em 11/02/10; aceito em 28/05/10.</p>
  </body>
  <back>
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  <sub-article article-type="translation" id="TRen" xml:lang="en">
    <front-stub>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Original Articles</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title xml:lang="en">Association between inflammatory markers and cardiovascular risk factors in women from Kolkata, W.B, India</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>BACKGROUND: Recent research has focused on the use of inflammatory biomarkers in the prediction of cardiovascular risk. However, information is scant regarding the association between these inflammatory markers with other cardiovascular risk factors in Asian Indians, particularly in women. OBJECTIVE: To explore the association between inflammatory markers such as high-sensitivity C-reactive protein (hs-CRP) and white blood cell (WBC) count and cardiovascular risk factors such as overall and central adiposity, blood pressure, lipid and lipoprotein variables and fasting glucose. METHODS: We conducted a cross-sectional analysis on 100 women aged 35-80 years. Participants were selected following cluster sampling methodology from 12 different randomly selected urban wards of Kolkata Municipal Corporation. RESULTS: Hs-CRP has a significant association with body mass index (BMI) ( p &lt; 0.001) and waist circumference (WC) (p = 0.002). Significant inverse associations were observed between high-density lipoprotein cholesterol (HDL-C) and both inflammatory markers, hs-CRP (p = 0.031) and WBC count, (p = 0.014). Apolipoprotein A1 (Apo A1) was also negatively associated with hs-CRP. WBC count has significant correlation with fasting glucose and total cholesterol (TC) /HDL-C ratio. Using logistic regression, adjusting for age, BMI (odds ratio/OR, 1.186; confidence interval/CI, 1.046-1.345; p=0.008) and WC (OR, 1.045; CI, 1.005-1.087; p=0.027) were the covariates significantly associated with hs-CRP. CONCLUSION: In the present study, risk factors like BMI, WC, and HDL-C and apo A1 show significant association with hs-CRP. WBC count was significantly correlated with HDL-C, fasting glucose, TC/HDL-C ratio in women.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Inflammation</kwd>
        <kwd>reactive protein C</kwd>
        <kwd>risk factors</kwd>
        <kwd>leukocyte count</kwd>
        <kwd>adiposity</kwd>
        <kwd>dyslipidemias</kwd>
        <kwd>women</kwd>
        <kwd>India</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <fn id="top-body2">
          <label>
            <bold>Association between Inflammatory Markers and Cardiovascular Risk Factors in Women from Kolkata, W.B, India</bold>
          </label>
          <p>
            <bold>Debdutta Ganguli<sup>I</sup>; Nilanjan Das<sup>I</sup>; Indranil Saha<sup>I, IV</sup>; Krishna Rao Sanapala<sup>II</sup>; Debnath Chaudhuri<sup>III</sup>; Saurabh Ghosh<sup>II</sup>; Sanjit Dey<sup>I</sup></bold>
          </p>
        </fn>
      </p>
      <p><sup>I</sup>Department of Physiology, University College of Science and Technology, University of Calcutta, West Bengal, India</p>
      <p><sup>II</sup>Human Genetics Unit, Indian Statistical Institute, Kolkata, India</p>
      <p><sup>III</sup>Department of Biochemistry and Nutrition, All India Institute of Hygiene and Public Health, West Bengal, India</p>
      <p><sup>IV</sup>Present Address: Department of Community Medicine, RG Kar Medical College and Hospital, Kolkata, India</p>
      <p>Mailing address</p>
      <p>
        <bold>ABSTRACT</bold>
      </p>
      <p><bold>BACKGROUND: </bold> Recent research has focused on the use of inflammatory biomarkers in the prediction of cardiovascular risk. However, information is scant regarding the association between these inflammatory markers with other cardiovascular risk factors in Asian Indians, particularly in women.</p>
      <p><bold>OBJECTIVE: </bold> To explore the association between inflammatory markers such as high-sensitivity C-reactive protein (hs-CRP) and white blood cell (WBC) count and cardiovascular risk factors such as overall and central adiposity, blood pressure, lipid and lipoprotein variables and fasting glucose.</p>
      <p><bold>METHODS: </bold> We conducted a cross-sectional analysis on 100 women aged 35-80 years. Participants were selected following cluster sampling methodology from 12 different randomly selected urban wards of Kolkata Municipal Corporation.</p>
      <p><bold>RESULTS: </bold> Hs-CRP has a significant association with body mass index (BMI) (p &lt; 0.001) and waist circumference (WC) (p = 0.002). Significant inverse associations were observed between high-density lipoprotein cholesterol (HDL-C) and both inflammatory markers, hs-CRP (p = 0.031) and WBC count, (p = 0.014). Apolipoprotein A1 (Apo A1) was also negatively associated with hs-CRP. WBC count has significant correlation with fasting glucose and total cholesterol (TC) /HDL-C ratio. Using logistic regression, adjusting for age, BMI (odds ratio/OR, 1.186; confidence interval/CI, 1.046-1.345; p=0.008) and WC (OR, 1.045; CI, 1.005-1.087; p=0.027) were the covariates significantly associated with hs-CRP.</p>
      <p><bold>CONCLUSION: </bold> In the present study, risk factors like BMI, WC, and HDL-C and apo A1 show significant association with hs-CRP. WBC count was significantly correlated with HDL-C, fasting glucose, TC/HDL-C ratio in women.</p>
      <p><bold>Keywords:</bold> Inflammation; reactive protein C; risk factors; leukocyte count; adiposity; dyslipidemias; women: India.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>Recent epidemiological studies have reported a strong and consistent association between cardiovascular disease (CVD) risk factors and inflammation<sup>1,2</sup> and the latter has been identified as an independent risk factor for CVD<sup>3,4</sup>. Of the novel inflammatory markers currently under investigation, hs-CRP and WBC count are the promising ones. A number of prospective epidemiological studies consistently demonstrated that hs-CRP<sup>5,6</sup> as well as WBC count<sup>7</sup> can independently predict vascular risk both in apparently healthy men and women, asymptomatic for traditional risk factors of CVD. In addition, both markers<sup>1,2</sup> also add prognostic information in patients with clinical signs of CVD, beyond that available from standard lipid-screening. A substantial number of cross-sectional studies have already established the fact that hs-CRP and WBC count have been found to significantly correlate with components of metabolic syndrome<sup>8-10</sup>.</p>
      <p>In India, data are scarce regarding the association of these inflammatory biomarkers with other CVD risk factors in adults, particularly among women. Thus the objectives of the present study were to investigate the association between hs-CRP and WBC count with risk factors such as body mass index, waist circumference, waist-hip ratio, blood pressure, lipid and lipoprotein variables and fasting glucose.</p>
      <p>
        <bold>Materials and method</bold>
      </p>
      <p>
        <bold>Study participants</bold>
      </p>
      <p>We randomly selected a population of 100 women aged between 35-80 years from an existing epidemiological study on cardiovascular risk assessment involving 701 women residing at urban wards staying for an average 29.8 years in Kolkata. The study was carried out following the WHO prescribed cluster sampling methodology<sup>11</sup> from 12 different wards out of 141 urban wards of Kolkata Municipal Corporation according to the most recent census data. The wards or clusters were included in the study by simple random sampling without replacement. According to the cluster sampling strategy, in each of the chosen ward or cluster, a location near the center of the ward was taken as the starting point and a random direction was selected. Then the households were chosen randomly along the direction after checking for the compliance with inclusion criteria such as- women aged 35 or above regardless of her marital status, but not pregnant ones. The exclusion criteria were acute illness or any treatment of inflammatory or chronic infectious disease either before or at the time of the investigation. Subjects unwilling to participate in the study were excluded during the survey. Individuals using aspirin as a chronic medication were also excluded. None of the subjects reported taking lipid-lowering medication. Among the eligible subjects, 57 individuals were reported as postmenopausal and the remaining 43 were premenopausal women.</p>
      <p>Subjects submitted their written consent to participate in the study prior to the survey, which was approved by the Human Ethical Committee of Department of Human Physiology, University of Calcutta.</p>
      <p>
        <bold>Questionnaire</bold>
      </p>
      <p>A questionnaire-based interview was used to collect information on smoking habits, use of chewing tobacco, alcohol consumption, personal and family medical history of hypertension, diabetes and myocardial infarction. The participants were interviewed about their menopausal status and history of any surgical intervention, such as hysterectomy. Women were considered pre-menopausal if they had experienced 1 or more regular bleeding episodes in the past 12 months. Women were considered postmenopausal if their menses had ceased naturally or surgically (e.g. hysterectomy) for a period of at least 12 months. The participants were also interviewed about their history of dyslipidemia, current use of anti-hypertensive or hypoglycemic or lipid-lowering drugs and use of postmenopausal hormone therapy. The validity of responses to questions on drug use was confirmed by checking medical records.</p>
      <p>
        <bold>Anthropometric and biochemical measurements</bold>
      </p>
      <p>Height was measured to the nearest 0.5 cm without shoes using an anthropometer. Weight was recorded in light clothing after removal of shoes to the nearest 0.1 kg. WC was measured using a non-stretch measuring tape at the midpoint between the lowest rib and the iliac crest in the horizontal plane. Maximum hip circumference was measured horizontally at the level of the maximum extension of the buttocks. For each of waist and hip circumference, two measurements to the nearest 0.5 cm were recorded. The mean of the two closest measurements was calculated. Waist-hip ratio (WHR) was calculated by the standard equation: WHR = Waist circumference (cm) / Hip circumference (cm).</p>
      <p>BMI was calculated as weight/height<sup>2</sup> (kg/m<sup>2</sup>). Blood pressure was measured on the right arm of participants in a relaxed, sitting position with the arm supported at heart level, using a standard mercury sphygmomanometer. Systolic and diastolic blood pressures were recorded as the onset of the first and fifth Korotkoff phases, respectively. For each of the measurement, two readings 5 minutes apart were taken and the mean of the two readings was calculated to obtain the final blood pressure. Participants were advised to avoid cigarette smoking, caffeinated beverages and exercise for at least 30 minutes before the blood pressure measurement.</p>
      <p>Participants were requested to fast at least 10 hours before the blood samples were collected on next morning. Venipuncture was performed by a trained physician with the participants in a sitting position. Fasting serum glucose was measured by glucose oxidase-peroxidase method<sup>12</sup>, serum total cholesterol was determined by cholesterol oxidase-peroxidase-amidopyrine method<sup>13</sup> and serum triglycerides (TG) were measured by glycerol phosphate oxidase-peroxidase-amidopyrine method<sup>14</sup> using assay kits from Randox Laboratories Ltd (Crumlin, Co. Antrim, United Kingdom) on a spectrophotometer (Bio-rad, Hercules, California, USA). HDL-C was also determined by the same method after precipitation of very low density lipoprotein (VLDL) and low density lipoprotein (LDL) by the polyethylene glycol PEG 6000. LDL- cholesterol (LDL-C) was calculated using the formula: LDL-C = total cholesterol- HDL-C - (TG/5)<sup>15</sup>. Lipoprotein (a) (Lp(a)), apolipoproteins A1 and B were measured by an automated turbidimetric immunoassay<sup>16,17</sup> with reagent kits from Randox Laboratories Ltd on a Randox RX Daytona Autoanalyzer system (Crumlin, Co. Antrim, United Kingdom).</p>
      <p>
        <bold>Definitions and diagnosis criteria</bold>
      </p>
      <p>Obesity was defined as BMI greater than 25 kg/m<sup>2 18</sup>. According to the Seventh Report of the Joint National Committee (JNC) on Prevention, Detection, Evaluation and Treatment of High Blood Pressure<sup>19</sup>, subjects were considered hypertensive if the systolic blood pressure was <underline>&gt;</underline>140 mm of Hg, diastolic blood pressure was <underline>&gt;</underline> 90 mm of Hg or both or they were taking anti-hypertensive medication. Diabetes was defined as fasting serum glucose level of 7.0 mmol/l or more (<underline>&gt;</underline> 126 mg/dl) or on medication for diabetes by the criteria laid down by the National Cholesterol Education Program (NCEP), Adult Treatment Panel III (ATP III)<sup>20</sup>. The following cut-off points were used to define dyslipidemias such as (i) Hypercholesterolemia: total cholesterol level of 5.18 mmol/l or more (<underline>&gt;</underline> 200 mg/dl) (ii) Hypertriglyceridemia: triglyceride level of 1.69 mmol/l or more (<underline>&gt;</underline>150 mg/dl) (iii) Low levels of HDL-C: HDL-cholesterol level less than 1.03 mmol/l (&lt;40 mg/dl) and (iv) High levels of LDL-C: LDL-cholesterol level of 3.36 mmol/l or more (<underline>&gt;</underline> 130 mg/dl) according to the diagnostic criteria of the NCEP, ATP III guidelines.</p>
      <p>
        <bold>Measurement of hs-CRP and WBC count</bold>
      </p>
      <p>The plasma concentrations of hs-CRP were assayed by a latex-enhanced, immunoturbidimetric assay<sup>4</sup> using a kit from Spinreact, Santa Coloma, Spain. The assay was performed on an autoanalyzer system (Microlab-300, Merck, Germany). According to the manufacturer's instructions, the intra-assay and the inter-assay coefficients of variation (CV) for hs-CRP were 4.3% and 8.4% respectively and the lowest detection limit was 0.05 mg/l. WBC counts were done manually with the help of Neubauer's hemocytometer under the microscope within 24h after venipuncture<sup>21</sup>. For the sake of uniformity in the counting procedure, the same trained person was deputed during the whole investigative process. The procedure was repeated for at least three times for each of the specimens.</p>
      <p>
        <bold>Statistical analysis</bold>
      </p>
      <p>All statistical analyses were conducted in parallel for hs-CRP and WBC counts which were divided into respective tertiles based on the distribution in 100 study participants. One-way ANOVA (with Tukey's pairwise comparisons) was used to compare group means for continuous variables across the tertiles, Wilcoxon's rank-sum test was used for comparison of medians and the &#967;<sup>2</sup> test was used to compare proportions. Before statistical testing, data were checked for normality. Because the distribution of hs-CRP and Lp(a) were skewed, the variables were natural-log-transformed for all analysis. Pearson's correlation analysis was carried out to determine the association of inflammatory markers with cardiovascular risk factors. A between-group comparison of pre- and postmenopausal women was performed with analysis of covariance (ANCOVA) after adjustment of other covariates. Serum hs-CRP levels were divided into two categories (below and above) based on the median value of hs-CRP considered as the cut-off point (1.31 mg/l). Logistic unconditioned regression models were used to calculate odds ratios (OR) to evaluate the association between hs-CRP and other variables. All analyses were performed using Windows-based SPSS statistical package (version 10.0, Chicago) and MedCalc statistical software (version 10.1.6) and p-values &lt;0.05 were considered significant.</p>
      <p>
        <bold>Results</bold>
      </p>
      <p>The prevalence of some baseline characteristics is shown in <xref ref-type="table" rid="t1-body2">Table 1</xref>. The mean age of the study subjects was 48.3&#177;9.8 yrs. A total of 35% of the women chewed tobacco at a regular or weekly frequency. No individual was reported to smoke either cigarettes or beedies or consume alcohol. Prevalence of postmenopausal women in the population was 57.0%, but none of them was found to take any hormone replacement therapy. The overall prevalence of obesity was 51.5% in the study population determined by BMI alone. Prevalence of hypertension and positive family history for hypertension were 36.0% and 25.0%, respectively. Diabetes was observed in 12.0% of women and 16.0% of subjects were reported with positive family history for diabetes. Overall 3.1% women were found with a history of myocardial infarction. Hypercholesterolemia was observed in 32.0% subjects. However, hypertriglyceridemia was observed in 44.0% of subjects and an almost similar percentage (45.0%) was observed for low levels of HDL-C. Furthermore, 29.0% of the women showed high-levels of LDL-C.</p>
      <table-wrap id="t1-body2">
        <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt01-en.jpg"/></table-wrap>
      <p><xref ref-type="table" rid="en_aop15910t02-body2">Table 2</xref> shows the relationship between hs-CRP levels and various risk variables among the study subjects. BMI and waist circumference were each significantly higher (p= 0.001 and p= 0.021 for BMI and WC, respectively) across increasing tertiles of serum hs-CRP levels. Women in higher tertiles of hs-CRP seemed to have a tendency toward higher incidence of diabetes as well as higher triglyceride and lower apolipoprotein A1 levels, although the differences were not statistically significant.</p>
      <p content-type="asset">
        <table-wrap id="en_aop15910t02-body2">
          <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt02-en.jpg"/></table-wrap>
      </p>
      <p>We next examined (<xref ref-type="table" rid="en_aop15910t03-body2">Table 3</xref>) the relationship between WBC count and other risk variables in the study population. TC/HDL-C ratio increased significantly (p= 0.007) across the WBC count tertiles, whereas other variables such as fasting glucose, triglycerides, HDL-cholesterol, apolipoprotein A1 were non-significantly higher among the higher tertiles. BMI and waist circumference were higher in the higher tertiles of WBC count, but the differences were not statistically significant. Both systolic and diastolic blood pressures were also non-significantly higher among the higher tertiles. Women in higher tertiles have higher incidence of diabetes. The mean value of hs-CRP was higher across the tertiles of WBC count but was not statistically significant.</p>
      <p content-type="asset">
        <table-wrap id="en_aop15910t03-body2">
          <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt03-en.jpg"/></table-wrap>
      </p>
      <p>High-sensitivity C-reactive protein (hs-CRP) was significantly associated with measures of obesity such as BMI (r=0.373, p&lt;0.001) and WC (r=0.301, p=0.002) after adjustment for age (<xref ref-type="table" rid="t4-body2">Table 4</xref>), whereas no significant correlation was found with WHR (r=0.004, p=0.966). However, WBC count was non-significantly associated with BMI, WC and WHR after adjustment for age. Analysis of partial correlation coefficient revealed a significant negative correlation between HDL-C and hs-CRP (r= -0.220, p=0.031) and between HDL-C and WBC count (r= -0.247, p=0.014). Apolipoprotein A1 was also inversely associated (r=-0.237, p=0.031) with hs-CRP in women. Associations with WBC count were significant for biochemical variables such as fasting glucose (r=0.253, p=0.011), TC/HDL-C ratio (r=0.284, p=0.004) and hs-CRP (r=0.252, p=0.012). As strong associations were observed between hs-CRP and measures of obesity like BMI and WC, we therefore adjusted these variables along with age for calculating partial correlation coefficients between hs-CRP and other variables in all the above models. Associations of WBC count with other variables were computed after adjustment for age.</p>
      <table-wrap id="t4-body2">
        <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt04-en.jpg"/></table-wrap>
      <p>A comparison of levels of inflammatory markers in premenopausal and menopausal women is shown in <xref ref-type="table" rid="t5-body2">Table 5</xref>. Both hs-CRP and WBC count did not significantly differ between the premenopausal and postmenopausal group. Adjusted geometric means were 1.68 and 2.66 mg/l respectively for hs-CRP (1.58-fold increase with menopause). Because menopause may be associated with changes in measures of obesity and other biochemical profile, we adjusted the means for variables such as BMI, waist circumference and HDL-cholesterol in addition with age.</p>
      <table-wrap id="t5-body2">
        <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt05-en.jpg"/></table-wrap>
      <p>Logistic regression analysis was performed on variables that were significantly correlated with hs-CRP (<xref ref-type="table" rid="en_aop15910t06-body2">Table 6</xref>). BMI (OR, 1.186; CI, 1.046-1.345; p=0.008) and WC (OR, 1.045; CI, 1.005-1.087; p=0.027) were the covariates significantly and positively associated with hs-CRP after adjustment for age. However, no significant independent association was observed between HDL-cholesterol and hs-CRP.</p>
      <p content-type="asset">
        <table-wrap id="en_aop15910t06-body2">
          <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt06-en.jpg"/></table-wrap>
      </p>
      <p>
        <bold>Discussion</bold>
      </p>
      <p>There is an emerging consensus that CVD has a multifactorial etiology, including atherosclerotic, prothrombotic and inflammatory components. Therefore, in addition to the assessment of conventional risk factors, new markers have been explored in prospective observational studies with the hope that they might improve the ability to predict the risk of developing cardiovascular events.</p>
      <p>In the present study, we found significant associations between hs-CRP levels and adiposity measures such as BMI and waist circumference. These results are consistent with the experimental findings suggesting that adipose tissue is a major source of cytokines, including IL-6, which is an important determinant of hepatic CRP synthesis<sup>8,22-24</sup>. However, in adults, stronger associations between body fat and CRP values have been reported for women compared with men<sup>25</sup>. The Third National Health and Nutrition Examination Survey (NHANES III) in United States including both men and women aged <underline>&gt;</underline>20 years, revealed that higher BMI is associated with higher CRP concentrations, even in younger adults<sup>26</sup>. A significant association of CRP levels with BMI was also reported among elderly men and women in the Cardiovascular Health Study<sup>22</sup> as well as by Mendall et al<sup>23</sup>. Lemieux et al<sup>27</sup> observed that despite the fact that the amount of total body fat (measured as BMI) was the best correlate of CRP levels, the highest plasma CRP concentrations were observed among individuals who had concurrent elevations in visceral adiposity (measured as waist circumference) and in total body fatness. Additional support for this observation came from the study by Hak et al<sup>24</sup> where they reported that CRP was strongly correlated with waist circumference even after BMI adjustment. The relative contributions of intra-abdominal and subcutaneous adipose tissue in the generation of CRP remain unclear. However, in the present study, waist circumference showed significant association with hs-CRP, although the association disappeared after controlling for BMI (data not shown). This phenomenon could be explained by the strong collinearity of waist circumference and BMI in the study subjects.</p>
      <p>In the present study it has been observed that hs-CRP has a significant inverse association with HDL-C and apolipoprotein A-1. In addition, there was an inverse association between WBC count and HDL-C. HDL cholesterol has consistently shown an inverse association with systemic markers of inflammation in many prospective studies<sup>5,24,28</sup>. A recent study by Birjmohun et al<sup>29</sup> have demonstrated that apparently healthy individuals with genetically determined isolated low HDL-C levels are more susceptible to low-dose endotoxin challenge in comparison with subjects with normal or high HDL-cholesterol levels. The study revealed a strong inverse association between HDL-C and apo A-1 levels <italic>versus</italic> leukocyte response and plasma CRP levels, supporting an anti-inflammatory effect of HDL-C. In our present investigation, the association between plasma CRP level and low-HDL-C values has been shown to persist even after adjustments for BMI and waist circumference, suggesting an independent association between these variables among the individuals. Recent evidence supports a wide array of antiatherogenic effects by HDL-C, including anti-inflammatory effects<sup>30</sup>.</p>
      <p>In the present investigation, WBC count showed a significant positive correlation with plasma hs-CRP levels and variables such as fasting blood sugar and TC/HDL-C ratio. The ARIC cross-sectional study of young and middle-aged people<sup>31</sup> revealed that WBC count was associated with fasting insulin and blood glucose in an analysis not stratified by gender. A recent study in the Asian Indian population reported by Gokulakrishan et al<sup>32</sup> has shown that leukocyte count was positively associated with fasting plasma glucose and insulin resistance. It is therefore possible that inflammation and endothelial function are among several common antecedents for both diabetes and coronary heart disease<sup>33</sup>. Association between plasma CRP concentrations and WBC count have also been consistently reported in many clinical findings<sup>2,34</sup>.</p>
      <p>We did not find a clear influence of menopausal status on the level of inflammatory biomarkers. Similar observations were reported by Hak and her group<sup>24</sup> where both age and age-and-BMI-adjusted levels of CRP were found slightly higher in postmenopausal than in premenopausal women, but the difference was not statistically significant. In a comparative study of postmenopausal vs. premenopausal women by Sites et al<sup>35</sup>, increased levels of CRP were found to be related to increased body fat, but not to menopausal status. However, numerous clinical trials have demonstrated that exogenous hormone replacement therapies, as well as endogenous hormone levels were associated with increased CRP levels along with other markers of inflammation such as fibrinogen and WBC count in postmenopausal women<sup>36,37</sup>. Further studies are needed to address the association between inflammation and menopause.</p>
      <p>Inflammation plays a fundamental role in atherothrombosis<sup>38</sup>. Hs-CRP, a measure of inflammation, is a mediator as well as marker of atherothrombosis. Although a number of other inflammatory markers have been investigated, the 'hs-CRP' level has the most stability, assay precision, accuracy and availability. C-reactive protein has gained official recognition as a cardiac test by the Centers for Disease Control and Prevention (CDC) and the American Heart Association (AHA)<sup>4</sup>. The utility of CRP testing in patients with myocardial infarction, stable or unstable angina has been well established<sup>39</sup>. Elevated hs-CRP levels in these clinical settings identify patients with higher inflammatory burdens who are at higher risk of future ischemic events. In addition, an elevated CRP level provides additional prognostic value to traditional cardiac risk factors. Therefore, in a high-risk individual, an elevated hs-CRP level should even further alert both the physician and the individual to the need for aggressive risk-lowering strategies.</p>
      <p>To the best of our knowledge, the present study is the first to examine the association between systemic inflammatory markers such as hs-CRP and WBC count and other cardiovascular risk factors in a general population-based sample from India and it focuses particularly on women. An additional strength of this study was the quality of sample collection and the precision in the measurement of CRP and other associated biomarkers. However, some issues of our study need to be addressed. This study was conducted in an apparently healthy population with a low or without current exposure to factors like clinically established CVD, such as- myocardial infarction and smoking, respectively. The above factors are strong determinants of CRP levels and therefore the choice of our population facilitates the investigation of confounders associated with CRP. So, additional studies are needed to verify the findings in both epidemiological and clinical settings in this population. Secondly, this study includes the use of a single measurement of inflammatory markers which may not accurately reflect long-term inflammation status. Multiple measurements over time and changes in those measurements may provide a more accurate mechanism for predicting risk in individuals.</p>
      <p>
        <bold>Conclusion</bold>
      </p>
      <p>Our results indicate that in an apparently healthy population of women with a low burden of smoking and clinically established cardiovascular disease, BMI and waist circumference were associated with levels of systemic biomarkers such as- hs-CRP and WBC count. Because inflammatory mediators are directly involved in atherogenesis, these results suggest an important mechanism through which obesity might affect the risk of cardiovascular disease. We also observed a significant association between inflammatory markers and lipoprotein variables such as HDL-C and apo-A1, which was independent from adiposity measures. These findings add to a growing body of evidence that HDL-C and apo-A1 protect against cardiovascular disease by mechanisms that extend well beyond their involvement in cholesterol transport. The present findings thus reinforce the importance of these inflammatory biomarkers for cardiovascular risk prediction algorithms along with the standard screening tools, particularly in women.</p>
      <p>
        <bold>Acknowledgements</bold>
      </p>
      <p>This work was supported by the Department of Science and Technology, Government of India, [Grant Number SSD/WS/059/2004].</p>
      <p>
        <bold>Potential Conflict of Interest</bold>
      </p>
      <p>No potential conflict of interest relevant to this article was reported.</p>
      <p>
        <bold>Sources of Funding</bold>
      </p>
      <p>This study was funded by Department of Science and Technology Government of India.</p>
      <p>
        <bold>Study Association</bold>
      </p>
      <p>This article is part of the thesis of doctoral submitted by Debdutta Ganguli, from University of Calcuta.</p>
      <p>
        <bold>References</bold>
      </p>
    </body>
  </sub-article>
  <sub-article article-type="translation" id="TRes" xml:lang="es">
    <front-stub>
      <article-categories/>
      <title-group>
        <article-title xml:lang="es">Asociaci&#243;n entre marcadores inflamatorios y factores de riesgo cardiovascular en mujeres de Kolkata, W.B, India</article-title>
      </title-group>
      <abstract xml:lang="es">
        <p>FUNDAMENTO: Recientes investigaciones se han concentrado en el uso de biomarcadores inflamatorios en la previsi&#243;n de riesgo cardiovascular. Entre tanto, la informaci&#243;n es escasa en relaci&#243;n a la asociaci&#243;n entre esos marcadores inflamatorios con otros factores de riesgo cardiovasculares en indios asi&#225;ticos, particularmente en mujeres. OBJETIVO: Explorar la asociaci&#243;n entre marcadores inflamatorios tales como prote&#237;na C-reactiva de alta sensibilidad (PCR-as) y recuento de leucocitos (LEU) y factores de riesgo cardiovascular tales como adiposidad general y central, presi&#243;n arterial, variables lip&#237;dicas y lipoproteicas y glucemia de ayuno. M&#201;TODOS: Condujimos un an&#225;lisis transversal de 100 mujeres con edad entre 35-80 a&#241;os. Las participantes fueron seleccionadas a trav&#233;s de la metodolog&#237;a de muestreo por cluster, de 12 distritos urbanos seleccionadas al azar en la Corporaci&#243;n Municipal de Kolkata, India. RESULTADOS: La PCR-as present&#243; una asociaci&#243;n significativa con el &#237;ndice de masa corporal (IMC) (r=0,373, p&lt;0,001) y circunferencia de la cintura (CCI) (r=0,301, p=0,002). Asociaciones significativas inversas fueron observadas entre la lipoprote&#237;na de alta densidad colesterol (HDL-c) y ambos marcadores inflamatorios (r= -0,220, p=0,031 y r= -0,247, p=0,014 para PCR-as y LEU, respectivamente). La apo-lipoprote&#237;na A1 (Apo A1) tambi&#233;n estaba negativamente asociada con la PCR-as (r= -0,237, p=0,031). El recuento de leucocitos present&#243; una correlaci&#243;n significativa con la glucemia de ayuno (r=0,253, p=0,011) y la raz&#243;n colesterol total (CT) /HDL-C (r=0,284, p=0,004). Usando regresi&#243;n log&#237;stica ajustada para edad, IMC (odds ratio/OR, 1,186; intervalo de confianza/IC, 1,046-1,345; p=0,008) y LEU (OR, 1,045; IC, 1,005-1,087; p=0,027) fueron las covariantes significativamente asociadas con la PCR-as. CONCLUSI&#211;N: En el presente estudio, los factores de riesgo tales como IMC, CCI y HDL-c y Apo-A1 mostraron una asociaci&#243;n significativa con PCR-as. El recuento de leucocitos estaba significativamente asociado a los niveles de HDL-c, glucemia de ayuno, raz&#243;n CT/HDL-c en mujeres.</p>
      </abstract>
      <kwd-group xml:lang="es">
        <kwd>Inflamaci&#243;n</kwd>
        <kwd>IMC</kwd>
        <kwd>HDL-C</kwd>
        <kwd>adiposidad</kwd>
        <kwd>prote&#237;na C-reactiva de alta sensibilidad</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>ART&#205;CULO ORIGINAL</p>
      <p> EPIDEMIOLOGIA</p>
      <p>
        <fn id="nota_1-body3">
          <label>
            <bold>Asociaci&#243;n entre marcadores inflamatorios y factores de riesgo cardiovascular en mujeres de Kolkata, W.B, India</bold>
          </label>
          <p>
            <bold>Debdutta Ganguli<sup>I</sup>; Nilanjan Das<sup>I</sup>; Indranil Saha<sup>I,IV</sup>; Krishna Rao Sanapala<sup>II</sup>; Debnath Chaudhuri<sup>III</sup>; Saurabh Ghosh<sup>II</sup>; Sanjit Dey<sup>I</sup></bold>
          </p>
        </fn>
      </p>
      <p><sup>I</sup>Department of Physiology, University College of Science and Technology, University of Calcutta, West Bengal, India</p>
      <p><sup>II</sup>Human Genetics Unit, Indian Statistical Institute, Kolkata, India</p>
      <p><sup>III</sup>Department of Biochemistry and Nutrition, All India Institute of Hygiene and Public Health, West Bengal, India</p>
      <p><sup>IV</sup>Present Address: Department of Community Medicine, RG Kar Medical College and Hospital, Kolkata, India</p>
      <p>Correspondencia</p>
      <p>
        <bold>RESUMEN</bold>
      </p>
      <p><bold>FUNDAMENTO:</bold> Recientes investigaciones se han concentrado en el uso de biomarcadores inflamatorios en la previsi&#243;n de riesgo cardiovascular. Entre tanto, la informaci&#243;n es escasa en relaci&#243;n a la asociaci&#243;n entre esos marcadores inflamatorios con otros factores de riesgo cardiovasculares en indios asi&#225;ticos, particularmente en mujeres.</p>
      <p><bold>OBJETIVO:</bold> Explorar la asociaci&#243;n entre marcadores inflamatorios tales como prote&#237;na C-reactiva de alta sensibilidad (PCR-as) y recuento de leucocitos (LEU) y factores de riesgo cardiovascular tales como adiposidad general y central, presi&#243;n arterial, variables lip&#237;dicas y lipoproteicas y glucemia de ayuno.</p>
      <p><bold>M&#201;TODOS:</bold> Condujimos un an&#225;lisis transversal de 100 mujeres con edad entre 35-80 a&#241;os. Las participantes fueron seleccionadas a trav&#233;s de la metodolog&#237;a de muestreo por cluster, de 12 distritos urbanos seleccionadas al azar en la Corporaci&#243;n Municipal de Kolkata, India.</p>
      <p><bold>RESULTADOS:</bold> La PCR-as present&#243; una asociaci&#243;n significativa con el &#237;ndice de masa corporal (IMC) (r=0,373, p&lt;0,001) y circunferencia de la cintura (CCI) (r=0,301, p=0,002). Asociaciones significativas inversas fueron observadas entre la lipoprote&#237;na de alta densidad colesterol (HDL-c) y ambos marcadores inflamatorios (r= -0,220, p=0,031 y r= -0,247, p=0,014 para PCR-as y LEU, respectivamente). La apo-lipoprote&#237;na A1 (Apo A1) tambi&#233;n estaba negativamente asociada con la PCR-as (r= -0,237, p=0,031). El recuento de leucocitos present&#243; una correlaci&#243;n significativa con la glucemia de ayuno (r=0,253, p=0,011) y la raz&#243;n colesterol total (CT) /HDL-C (r=0,284, p=0,004). Usando regresi&#243;n log&#237;stica ajustada para edad, IMC (odds ratio/OR, 1,186; intervalo de confianza/IC, 1,046-1,345; p=0,008) y LEU (OR, 1,045; IC, 1,005-1,087; p=0,027) fueron las covariantes significativamente asociadas con la PCR-as.</p>
      <p><bold>CONCLUSI&#211;N:</bold> En el presente estudio, los factores de riesgo tales como IMC, CCI y HDL-c y Apo-A1 mostraron una asociaci&#243;n significativa con PCR-as. El recuento de leucocitos estaba significativamente asociado a los niveles de HDL-c, glucemia de ayuno, raz&#243;n CT/HDL-c en mujeres. (Arq Bras Cardiol 2011; 96(1): 38-46)</p>
      <p><bold>Palabras clave:</bold> Inflamaci&#243;n, IMC, HDL-C, adiposidad, prote&#237;na C-reactiva de alta sensibilidad.</p>
      <p>
        <bold>Introducci&#243;n</bold>
      </p>
      <p>Recientes estudios epidemiol&#243;gicos han relatado una fuerte y consistente asociaci&#243;n entre factores de riesgo para enfermedad cardiovascular (ECV) e inflamaci&#243;n<sup>1,2</sup> y esta ha sido identificada como un factor de riesgo independiente para ECV<sup>3,4</sup>. De los nuevos marcadores inflamatorios actualmente investigados, la prote&#237;na C-reactiva de alta sensibilidad (PCR-as) y el recuento de leucocitos o leucograma (LEU) son los m&#225;s promisorios. Un n&#250;mero de estudios epidemiol&#243;gicos prospectivos han demostrado consistentemente que la PCR-as<sup>5,6</sup>, as&#237; como el recuento de leucocitos<sup>7</sup> pueden predecir de forma independiente el riesgo vascular en hombres y mujeres aparentemente sanos, asintom&#225;ticos para los tradicionales factores de riesgo para ECV. Adem&#225;s de eso, ambos marcadores<sup>1,2</sup> tambi&#233;n adicionan informaci&#243;n pron&#243;stica en pacientes con se&#241;ales cl&#237;nicas de ECV, adem&#225;s de aquella disponible con base en la evaluaci&#243;n lip&#237;dica est&#225;ndar. Un n&#250;mero sustancial de estudios transversales ya estableci&#243; el hecho de que la PCR-as y el recuento de leucocitos se correlacionan de forma significativa con componentes del s&#237;ndrome metab&#243;lico <sup>8-10</sup>. </p>
      <p>En la India, los datos son escasos en relaci&#243;n a la asociaci&#243;n de esos biomarcadores inflamatorios con otros factores de riesgo para ECV en adultos, particularmente en mujeres. As&#237;, los objetivos del presente estudio fueron investigar la asociaci&#243;n entre la PCR-as y el recuento de leucocitos con factores de riesgo tales como &#237;ndice de masa corporal, circunferencia de la cintura, raz&#243;n cintura-cadera, presi&#243;n arterial, variables lip&#237;dicas y lipoproteicas y glucemia de ayuno. </p>
      <p>
        <bold>Materiales y M&#233;todo</bold>
      </p>
      <p>
        <bold>Participantes del estudio</bold>
      </p>
      <p>Seleccionamos rand&#243;micamente una poblaci&#243;n de 100 mujeres con edad de 35-80 a&#241;os a partir de un estudio epidemiol&#243;gico existente sobre evaluaci&#243;n de riesgo cardiovascular, envolviendo 701 mujeres residentes (con edad de 35 a&#241;os o m&#225;s) de distritos urbanos que estaban hace 29,8 a&#241;os, en media, en Kolkata. El estudio fue realizado de acuerdo con las recomendaciones de la Organizaci&#243;n Mundial de la Salud (OMS) para estudios utilizando la metodolog&#237;a de muestreo por cluster<sup>11</sup>, en 12 diferentes distritos de 141 distritos de la Corporaci&#243;n Municipal de Kolkata, de acuerdo con los datos del censo m&#225;s reciente. Los distritos o clusters fueron incluidos en el estudio a trav&#233;s de muestreo rand&#243;mico simple sin substituci&#243;n. De acuerdo con la estrategia de muestreo por cluster, en cada uno de los distritos o clusters, un local cerca del centro del distrito era elegido como el punto de inicio y una direcci&#243;n era seleccionada al azar. Entonces los domicilios eran elegidos de forma rand&#243;mica a lo largo de la direcci&#243;n, despu&#233;s de la verificaci&#243;n de adecuaci&#243;n a los criterios de inclusi&#243;n - mujeres de 35 a&#241;os o m&#225;s, independientemente de su estado civil, pero no gr&#225;vidas. Los criterios de exclusi&#243;n fueron enfermedad aguda o cualquier tratamiento para enfermedad infecciosa cr&#243;nica o inflamatoria, antes o en la &#233;poca de la investigaci&#243;n. Individuos no dispuestos a participar del estudio fueron excluidos durante la investigaci&#243;n. Individuos que utilizaban aspirina como medicaci&#243;n cr&#243;nica tambi&#233;n fueron excluidos. Ninguno de los individuos relat&#243; que estaba utilizando medicaci&#243;n hipolipemiante. Entre las mujeres elegibles, 57 fueron identificados como post-menop&#225;usicas y las restantes 43 mujeres estaban en la premenopausia. </p>
      <p>Las mujeres dieron su consentimiento libre e informado para participar del estudio, que fue aprobado por el Comit&#233; de &#201;tica Humana del Departamento de Fisiolog&#237;a Humana de la Universidad de Calcuta. </p>
      <p>
        <bold>Cuestionario</bold>
      </p>
      <p>Una entrevista basada en un cuestionario fue utilizada para colectar informaciones sobre el h&#225;bito de fumar, uso de tabaco de mascar, consumo de alcohol, historial m&#233;dico familiar y personal de hipertensi&#243;n, diabetes e infarto del miocardio. Las participantes fueron entrevistadas sobre su estado menop&#225;usico e historia de cualquier intervenci&#243;n quir&#250;rgica, como histerectom&#237;a. Las mujeres fueron consideradas premenop&#225;usicas que hab&#237;an tenido uno o m&#225;s episodios de sangrado regulares en los 12 meses anteriores. Las mujeres fueron consideradas postmenop&#225;usicas si la menstruaci&#243;n hubiese cesado naturalmente o quir&#250;rgicamente (por ex., histerectom&#237;a), por al menos 12 meses continuos. Las participantes tambi&#233;n fueron entrevistadas sobre su historia de dislipidemia, uso corriente de medicaci&#243;n antihipertensiva o hipoglic&#233;mica o medicamentos hipolipemiantes y uso de terapia de reposici&#243;n hormonal postmenopausia. La validez de las respuestas a las preguntas sobre el uso de medicamentos fue confirmada a trav&#233;s de la verificaci&#243;n de los registros m&#233;dicos. </p>
      <p>
        <bold>Medidas antropom&#233;tricas y bioqu&#237;micas</bold>
      </p>
      <p>La altura fue medida con una precisi&#243;n de 0,5 cm, con las participantes descalzas, utilizando un antrop&#243;metro. El peso fue medido con las participantes vistiendo ropas livianas despu&#233;s de la remoci&#243;n de los zapatos, con una precisi&#243;n de 0,1 kg. La circunferencia de la cintura (CCI) fue medida utilizando una cinta m&#233;trica no el&#225;stica en el punto medio entre la &#250;ltima costilla y la cresta il&#237;aca en el plano horizontal. La circunferencia m&#225;xima de la cadera (CCA) fue medida horizontalmente al nivel de la extensi&#243;n m&#225;xima de los gl&#250;teos. Para cada medida de la circunferencia de la cintura y de la cadera, dos medidas eran tomadas, con una precisi&#243;n de 0,5 cm. La media de las dos medidas m&#225;s pr&#243;ximas fue calculada. La raz&#243;n cintura-cadera (RCC) fue calculada a trav&#233;s de la ecuaci&#243;n est&#225;ndar: RCC = CCI (cm)/CCA (cm).</p>
      <p>El IMC fue calculado como peso/altura<sup>2</sup> (kg/m<sup>2</sup>). La presi&#243;n arterial fue medida en el brazo derecho de las participantes en la posici&#243;n sentada, relajada y con el brazo apoyado al nivel del coraz&#243;n utilizando un esfigmoman&#243;metro de mercurio est&#225;ndar. Las presiones sist&#243;lica y diast&#243;lica fueron registradas como el inicio del primer y quinto sonidos de Korotkoff, respectivamente. Para cada una de las medidas, fueron hechas dos lecturas con 5 minutos de intervalo entre ellas y la media de las dos lecturas fue calculada para obtener la presi&#243;n arterial final. Las participantes fueron orientadas a evitar el tabaco, bebidas cafeinadas y ejercicio por al menos 30 minutos antes de la medida de la presi&#243;n arterial. Fue pedido a las participantes que se mantengan en ayuno por al menos 10 horas antes recoger las muestras la ma&#241;ana del d&#237;a siguiente. La venopunci&#243;n fue realizada por un m&#233;dico entrenado con las participantes en la posici&#243;n sentada. La glucemia de ayuno fue medida a trav&#233;s del m&#233;todo de glucosa-oxidasa/peroxidasa<sup>12</sup>, colesterol total s&#233;rico fue medido a trav&#233;s del m&#233;todo colesterol oxidasa/peroxidasa-amidopirina<sup>13 </sup>y los triglic&#233;ridos (TG) s&#233;ricos fueron medidos por el m&#233;todo glicerol fosfato oxidasa/peroxidasa-amidopirina<sup>14 </sup>utilizando kits de ensayo provistos por Randox Laboratories Ltd (Crumlin, Co. Antrim, Reino Unido) en un espectrofot&#243;metro (Bio-rad, Hercules, California, EUA). El HDL-C tambi&#233;n fue determinado por el mismo m&#233;todo despu&#233;s de precipitaci&#243;n de lipoprote&#237;na de muy baja densidad (VLDL) y la lipoprote&#237;na de baja densidad (LDL) por el polietileno-glicol PEG 6000. El LDL-colesterol (LDL-C) fue calculado utilizando la f&#243;rmula: LDL-C = colesterol total - HDL-C - (TG/5)<sup>15</sup>. Lipoprote&#237;na (a) (Lp(a)), apolipoprote&#237;na A1 y B fueron medidas por m&#233;todo de inmunoensayo automatizado turbidim&#233;trico<sup>16,17</sup> con kits de reactivos provistos por Randox Laboratories Ltd en un Randox RX Daytona Sistema Autoanalizador (Crumlin, Co. Antrim, Reino Unido).</p>
      <p>
        <bold>Criterios de definiciones y diagn&#243;sticos</bold>
      </p>
      <p>La obesidad fue definida como un IMC &gt; 25 kg/m<sup>2 18</sup>. De acuerdo con el S&#233;ptimo Informe del Joint National Committee (JNC) sobre Prevenci&#243;n, Detecci&#243;n, Evaluaci&#243;n y Tratamiento de la Hipertensi&#243;n Arterial<sup>19</sup>, individuos fueron considerados hipertensos cuando la presi&#243;n arterial sist&#243;lica era <underline>&gt;</underline>140 mmHg, la presi&#243;n arterial diast&#243;lica era <underline>&gt;</underline> 90 mmHg o ambos, o si las participantes estuviesen tomando medicaci&#243;n antihipertensiva. Diabetes fue definida como niveles glic&#233;micos de ayuno de 7,0 mmol/l o m&#225;s (<underline>&gt;</underline> 126 mg/dl) o si estuviesen tomando medicaci&#243;n para diabetes por los criterios establecidos por el Programa Educativo Nacional del Colesterol (NCEP), Panel de Tratamiento del Adulto III (ATP III)<sup>20</sup>. Los siguientes puntos de corte fueron usados para definir dislipidemia como (i) Hipercolesterolemia: nivel de colesterol total de 5,18 mmol/l o m&#225;s (<underline>&gt;</underline> 200 mg/dl) (ii) Hipertrigliceridemia: niveles de triglic&#233;ridos de 1,69 mmol/l o m&#225;s (<underline>&gt;</underline> 150 mg/dl) (iii) Bajos niveles de HDL-C: niveles de HDL-colesterol &lt; 1,03 mmol/l (&lt;40 mg/dl) y (iv) Altos niveles de LDL-C: Niveles de LDL-colesterol de 3,36 mmol/l o m&#225;s (<underline>&gt;</underline>130 mg/dl) de acuerdo con los criterios diagn&#243;sticos de las directrices del NCEP, ATP III.</p>
      <p>
        <bold>Medida de la PCR-as y leucograma</bold>
      </p>
      <p>Las concentraciones en el plasma de la PCR-as fueron medidas utilizando un ensayo inmunoturbidim&#233;trico exaltado con part&#237;culas de l&#225;tex<sup>4</sup>, con kits provistos por Spinreact, Santa Coloma, Espa&#241;a. El ensayo fue realizado en un sistema auto-analizador (Microlab-300, Merck, Alemania). De acuerdo con las instrucciones del fabricante, los coeficientes de variaci&#243;n (CV) intraensayo y interensayo para la PCR-as fueron 4,3% y 8,4%, respectivamente y el l&#237;mite m&#237;nimo de detecci&#243;n fue 0,05 mg/l. Los leucogramas fueron realizados manualmente con la ayuda del hemocit&#243;metro de Neubauer, bajo el microscopio, en hasta 24 horas despu&#233;s de la colecta de la sangre por venopunci&#243;n<sup>21</sup>. Para mantener la uniformidad en el proceso de recuento, la misma persona entrenada fue encargada durante todo el proceso investigativo. El procedimiento fue repetido por al menos tres veces para cada esp&#233;cimen. </p>
      <p>
        <bold>An&#225;lisis estad&#237;stico</bold>
      </p>
      <p>Todos los an&#225;lisis estad&#237;sticos fueron conducidos en paralelo para PCR-as y leucograma, que fueron divididos en respectivos terciles, con base en la distribuci&#243;n en 100 participantes del estudio. ANOVA one-way (con comparaci&#243;n m&#250;ltiple (<italic>pairwise</italic>) de Tukey) fue utilizado para comparar las medias de los grupos para variables continuas por los terciles; el Test de Suma de Puestos o Wilcoxon Rank Sum Test fue usado para comparaci&#243;n de las medianas y el test &#967;<sup>2</sup> fue usado para comparar proporciones. Antes de los tests estad&#237;sticos, los datos fueron verificados para normalidad. Debido al hecho de que la distribuci&#243;n de la PCR-as y Lp(a) era asim&#233;trica, las variables fueron transformadas en logaritmo natural para todos los an&#225;lisis. El an&#225;lisis de correlaci&#243;n de Pearson fue ejecutado para determinar la asociaci&#243;n de los marcadores inflamatorios con factores de riesgo cardiovascular. Una comparaci&#243;n entre grupos de mujeres pre y postmenopausia fue realizada con an&#225;lisis de covariancia (ANCOVA) despu&#233;s de ajuste de otras covariantes. Los niveles s&#233;ricos de PCR-as fueron divididos en dos categor&#237;as (abajo y encima), con base en el valor mediano de la PCR-as considerada como punto de corte (1,31 mg/l). Modelos de regresi&#243;n log&#237;stica no condicionada fueron utilizados para calcular el odds ratio (OR), o raz&#243;n de posibilidades, para evaluar la asociaci&#243;n entre la PCR-as y otras variables. Todos los an&#225;lisis fueron realizados utilizando los softwares SPSS para Windows (versi&#243;n 10.0, Chicago) y MedCalc (versi&#243;n 10.1.6) y valores de p &lt; 0,05 fueron considerados significativos. </p>
      <p>
        <bold>Resultados</bold>
      </p>
      <p>Las prevalencias de algunas caracter&#237;sticas basales son mostradas en la <xref ref-type="table" rid="tab1-body3">Tabla 1</xref>. La edad media de los sujetos del estudio era 48,3&#177;9,8 a&#241;os. Un total de 35% de las mujeres mascaba tabaco con frecuencia regular o semanalmente. Ninguna de las participantes relat&#243; fumar cigarros industrializados o caseros o consumir alcohol. La prevalencia de las mujeres postmenopausia en la poblaci&#243;n era de 57.0%, pero ninguna estaba recibiendo terapia de reposici&#243;n hormonal. La prevalencia general de obesidad era de 51,5% en la poblaci&#243;n del estudio, determinado por el IMC apenas. La prevalencia de la hipertensi&#243;n e historia familiar positiva de hipertensi&#243;n era de 36,0% y 25,0%, respectivamente. Diabetes fue identificada en 12,0% de las mujeres y 16,0% de los sujetos del estudio relataron una historia familiar positiva para diabetes. En general, un total de 3,1% de las mujeres present&#243; una historia de infarto de miocardio. Hipercolesterolemia fue observada en 32,0% de los sujetos. Entretanto, hipertrigliceridemia fue observada en 44,0% de los sujetos y un porcentaje casi similar (45,0%) presentaba bajos niveles de HDL-C. Adem&#225;s de eso, 29,0% de las mujeres presentaban altos niveles de LDL-C. </p>
      <table-wrap id="tab1-body3">
        <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt01-es.jpg"/></table-wrap>
      <p>La <xref ref-type="table" rid="es_a08tab02-body3">Tabla 2</xref> muestra la relaci&#243;n entre los niveles de PCR-as y varias variables de riesgo entre los sujetos del estudio. El IMC y la CCI eran significativamente m&#225;s altos (p = 0,001 y p = 0,021 para IMC y CCI, respectivamente) en los terciles crecientes de los niveles de PCR-as s&#233;rica. Las mujeres que presentaban los terciles m&#225;s altos parec&#237;an tener una tendencia a mayor incidencia de diabetes, as&#237; como niveles mayores de TG y niveles menores de apolipoprote&#237;na A1, aunque las diferencias no hubiesen sido significativas. </p>
      <p content-type="asset">
        <table-wrap id="es_a08tab02-body3">
          <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt02-es.jpg"/></table-wrap>
      </p>
      <p>Subsecuentemente evaluamos (<xref ref-type="table" rid="es_a08tab03-body3">Tabla 3</xref>) la relaci&#243;n entre el recuento de los leucocitos y otras variables de riesgo en la poblaci&#243;n del estudio. La raz&#243;n CT/HDL-C aument&#243; significativamente (p= 0,007) en los terciles de recuento de leucocitos, mientras que otras variables, como glucemia de ayuno, triglic&#233;ridos, HDL-colesterol y apolipoprote&#237;na A1, fueron no significativamente m&#225;s altas en los terciles superiores. El IMC y la CCI fueron m&#225;s altos en los terciles superiores del recuento de leucocitos, pero las diferencias no fueron estad&#237;sticamente significativas. Las presiones sist&#243;lica y diast&#243;lica tambi&#233;n fueron no significativamente m&#225;s altas en los terciles superiores. Mujeres en los terciles superiores presentaban mayor incidencia de diabetes. El valor medio de la PCR-as era mayor en los terciles crecientes del recuento de leucocitos, pero no presentaba significancia estad&#237;stica. </p>
      <p content-type="asset">
        <table-wrap id="es_a08tab03-body3">
          <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt03-es.jpg"/></table-wrap>
      </p>
      <p>La prote&#237;na C-reactiva de alta sensibilidad (PCR-as) estaba significativamente asociada con medidas de obesidad como IMC (r=0,373, p&lt;0,001) y CCI (r=0,301, p=0,002) despu&#233;s de ajuste para edad (<xref ref-type="table" rid="tab4-body3">Tabla 4</xref>), mientras que ninguna correlaci&#243;n significativa fue observada con la RCC (r=0,004, p=0,966). Entre tanto, el recuento de leucocitos estaba no significativamente asociado con el IMC, CCI y RCC despu&#233;s de ajuste para edad. El an&#225;lisis del coeficiente de correlaci&#243;n parcial revel&#243; una correlaci&#243;n negativa significativa entre el HDL-c y la PCR-as (r= -0,220, p=0,031) y entre el HDL-C y el recuento de leucocitos (r= -0,247, p=0,014). La apolipoprote&#237;na A1 tambi&#233;n estaba inversamente asociada (r=-0,237, p=0,031) con la PCR-as en mujeres. Las asociaciones con el recuento de leucocitos fueron significativas para variables bioqu&#237;micas, tales como glucemia de ayuno (r=0,253, p=0,011), raz&#243;n CT/HDL-C (r=0,284, p=0,004) y PCR-as (r=0,252, p=0,012). Como fuertes asociaciones fueron observadas entre la PCR-as y la medidas de obesidad como el IMC y la CCI, ajustamos esas variables junto con edad para el c&#225;lculo de coeficientes de correlaci&#243;n parcial entre la PCR-as y otras variables en todos los modelos encima. Las asociaciones del recuento de leucocitos con otras variables fueron computadas despu&#233;s de ajuste para edad. </p>
      <table-wrap id="tab4-body3">
        <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt04-es.jpg"/></table-wrap>
      <p>Una comparaci&#243;n de los niveles de los marcadores inflamatorios en mujeres premenopausia y postmenopausia es mostrada en la <xref ref-type="table" rid="tab5-body3">Tabla 5</xref>. Ambos niveles de PCR-as y el recuento de leucocitos no difirieron significativamente entre las mujeres en la pre y postmenopausia. Las medias geom&#233;tricas ajustadas fueron 1,68 y 2,66 mg/l respectivamente para PCR-as (aumento de 1,58 veces con la menopausia). Debido al hecho de que la menopausia est&#225; asociada a alteraciones en las medidas de obesidad y otros perfiles bioqu&#237;micos, ajustamos las medias para variables como IMC, CCI y HDL-C, adem&#225;s de la edad. </p>
      <table-wrap id="tab5-body3">
        <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt05-es.jpg"/></table-wrap>
      <p>El an&#225;lisis de regresi&#243;n log&#237;stica fue conducido en variables que se correlacionaban significativamente con la PCR-as (<xref ref-type="table" rid="es_a08tab06-body3">Tabla 6</xref>). El IMC (OR, 1,186; IC, 1,046-1,345; p=0,008) y CCI (OR, 1,045; IC, 1,005-1,087; p=0,027) fueron las covariantes que presentaron una asociaci&#243;n significativa y positiva con la PCR-as despu&#233;s del ajuste para edad. Entre tanto, ninguna asociaci&#243;n independiente fue observada entre el HDL-C y la PCR-as. </p>
      <p content-type="asset">
        <table-wrap id="es_a08tab06-body3">
          <graphic xlink:href="1678-4170-abc-96-01-0038-00165-gt06-es.jpg"/></table-wrap>
      </p>
      <p>
        <bold>Discusi&#243;n</bold>
      </p>
      <p>Hay un consenso emergente de que la ECV tiene una etiolog&#237;a multifactorial, incluyendo componentes ateroscler&#243;ticos, protromb&#243;ticos e inflamatorios. Siendo as&#237;, adem&#225;s de la evaluaci&#243;n de los factores de riesgo convencionales, nuevos marcadores ha sido explorados en estudios observacionales prospectivos con la esperanza de que puedan mejorar la capacidad de predecir el riesgo de desarrollo de eventos cardiovasculares. </p>
      <p>En el presente estudio, encontramos asociaciones significativas entre los niveles de PCR-as y medidas de adiposidad, como IMC y CCI. Esos resultados son consistentes con los hallazgos experimentales, sugiriendo que el tejido adiposo es una gran fuente de citoquinas, incluyendo IL-6, que es un importante determinante de s&#237;ntesis de PCR hep&#225;tica<sup>8,22-24</sup>. Entre tanto, en adultos, asociaciones m&#225;s fuertes entre grasa corporal y valores de PCR ha sido relatadas para mujeres, cuando fueron comparadas a hombres<sup>25</sup>. El estudio <italic>Third National Health and Nutrition Examination Survey</italic> (NHANES III) realizado en los Estados Unidos, que incluye hombres y mujeres con edad <underline>&gt;</underline> 20 a&#241;os, revel&#243; que el IMC m&#225;s alto est&#225; asociado con concentraciones m&#225;s altas de PCR, aun en adultos m&#225;s j&#243;venes<sup>26</sup>. Una relaci&#243;n significativa entre los niveles de PCR con el IMC tambi&#233;n fue relatada entre hombres y mujeres a&#241;osos en el estudio <italic>Cardiovascular Health Study</italic><sup>22</sup> as&#237; como por Mendall y su group<sup>23</sup>. Lemieux y colegas<sup>27</sup> observaron que a pesar del hecho de que la cantidad de grasa corporal (medida como IMC) presente la mejor correlaci&#243;n con los niveles de PCR, las mayores concentraciones de PCR en el plasma fueron observadas en individuos que presentaban aumentos paralelos en la adiposidad visceral (medida como CCI) y grasa total corporal. Apoyo adicional a esa observaci&#243;n fue provisto por el estudio de Hak y colaboradores<sup>24</sup>, que relataron que la PCR estaba fuertemente asociada con la CCI, aun despu&#233;s del ajuste del IMC. La relativa contribuci&#243;n del tejido adiposo intraabdominal y subcut&#225;neo en la generaci&#243;n de la PCR aun no es clara. Entre tanto, en el presente estudio, la CCI mostr&#243; una asociaci&#243;n significativa con la PCR-as, aunque la asociaci&#243;n desaparezca despu&#233;s del control del IMC (datos no mostrados). Ese fen&#243;meno puede ser explicado por la fuerte colinealidad de la CCI e IMC en los sujetos del estudio. </p>
      <p>En el presente estudio, fue observado que la PCR-as present&#243; una asociaci&#243;n inversa con el HDL-C y la apolipoprote&#237;na LA-1. Adem&#225;s de eso, hubo una asociaci&#243;n inversa entre el recuento de leucocitos y los niveles de HDL-C. Los niveles de HDL-C consistentemente muestran una asociaci&#243;n inversa con marcadores sist&#233;micos de inflamaci&#243;n en varios estudios prospectivos<sup>5, 24, 28</sup>. Un estudio reciente por Birjmohun y colegas<sup>29 </sup>demostr&#243; que individuos aparentemente sanos con niveles bajos aislados gen&#233;ticamente determinados de HDL-C eran m&#225;s susceptibles a test de sensibilidad con endotoxina de baja dosis en comparaci&#243;n con individuos con niveles normales o altos de HDL-C. El estudio revel&#243; una fuerte asociaci&#243;n inversa entre los niveles de HDL-C y apo A-1 con la respuesta de los leucocitos y niveles de PCR en el plasma, apoyando un efecto antiinflamatorio del HDL-C. En el presente estudio, ha sido mostrado que la asociaci&#243;n entre los niveles de PCR en el plasma y valores bajos de HDL-C persiste aun despu&#233;s del ajuste para IMC y CCI, sugiriendo una asociaci&#243;n independiente entre esas variables en los individuos. Evidencias recientes apoyan una serie de efectos antiaterog&#233;nicos del HDL-C, incluyendo efectos antiinflamatorios<sup>30</sup>.</p>
      <p>En el presente estudio, el recuento de leucocitos mostr&#243; una correlaci&#243;n positiva significativa con los niveles de PCR-as en el plasma y variables como glucemia de ayuno y raz&#243;n CT/HDL-C. El estudio transversal ARIC con individuos j&#243;venes y de mediana edad<sup>31</sup> mostr&#243; que el recuento de leucocitos estaba asociado con los niveles de insulina y glucemia de ayuno en un an&#225;lisis no estratificado por sexo. Un estudio reciente en la poblaci&#243;n asi&#225;tica de la India, conducido por Gokulakrishan y colegas<sup>32</sup> mostr&#243; que el recuento de leucocitos ten&#237;a una asociaci&#243;n positiva con glucemia de ayuno y resistencia a la insulina. Siendo as&#237;, es posible que la inflamaci&#243;n y la funci&#243;n endotelial est&#233;n entre varios antecedentes comunes para diabetes y enfermedad card&#237;aca coronaria<sup>33</sup>. La asociaci&#243;n entre concentraciones de PCR plasm&#225;tica y recuento de leucocitos ha sido tambi&#233;n consistentemente relatada en muchos hallazgos cl&#237;nicos<sup>2, 34</sup>. </p>
      <p>No observamos una influencia clara del estado menop&#225;usico en los niveles de biomarcadores inflamatorios. Observaciones similares fueron relatadas por el estudio de Hak y su grupo<sup>24</sup> donde los niveles de PCR ajustados para edad y para la edad y IMC eran levemente m&#225;s altos en las mujeres en la premenopausia, pero la diferencia no era estad&#237;sticamente significativa. En un estudio comparativo de mujeres en la premenopausia <italic>vs</italic> mujeres en la postmenopausia, conducido por Sites et al<sup>35</sup>, niveles aumentados de PCR estaban asociados con aumento en la grasa corporal, pero no al estado menop&#225;usico. Entre tanto, numerosos tests cl&#237;nicos ha demostrado que terapias de reposici&#243;n hormonal ex&#243;gena, as&#237; como los niveles de hormona end&#243;gena est&#225;n asociados con aumento en los niveles de PCR, junto con otros marcadores de inflamaci&#243;n, como fibrin&#243;geno y recuento de leucocitos, en mujeres en la postmenopausia<sup>36,37</sup>. Estudios adicionales son necesarios para estudiar la asociaci&#243;n entre inflamaci&#243;n y menopausia.</p>
      <p>La inflamaci&#243;n tiene un papel fundamental en la aterotrombosis<sup>38</sup>. La PCR-as, una medida de la inflamaci&#243;n, es un mediador as&#237; como un marcador de aterotrombosis. Aunque varios otros marcadores inflamatorios hayan sido investigados, la PCR-as tiene m&#225;s estabilidad, precisi&#243;n en el ensayo y disponibilidad. La PCR-as obtuvo reconocimiento oficial como test card&#237;aco del <italic>Centers for Disease Control and Prevention</italic> (Centro de Control y Prevenci&#243;n de Enfermedades - CDC) y de la <italic>American Heart Association</italic> (AHA) <sup>4</sup>. La utilidad del test de la PCR en pacientes con infarto de miocardio, angina estable o inestable, ha sido bien establecida<sup>39</sup>. Niveles altos de PCR-as en esas situaciones cl&#237;nicas identifican pacientes con cargas inflamatorias m&#225;s altas, que presentan mayor riesgo de eventos isqu&#233;micos futuros. Adem&#225;s de eso, un nivel alto de PCR provee valor pron&#243;stico adicional a los factores de riesgo tradicionales. As&#237;, en un individuo con alto riesgo, un nivel elevado de PCR-as deber&#237;a alertar al m&#233;dico y al individuo sobre la necesidad de establecer estrategias agresivas de disminuci&#243;n de riesgos. </p>
      <p>Hasta el l&#237;mite de nuestro conocimiento, el presente estudio es el primero que examina la asociaci&#243;n entre marcadores inflamatorios sist&#233;micos, tales como la PCR-as y el recuento de leucocitos y otros factores de riesgo cardiovascular en una muestra basada en la poblaci&#243;n general en la India, con foco particularmente en las mujeres. Un punto fuerte adicional del estudio fue la calidad de la colecta de la muestra y la precisi&#243;n en la medida en la PCR y otros biomarcadores asociados. Entre tanto, algunas cuestiones precisan ser discutidas. Ese estudio fue conducido en una poblaci&#243;n aparentemente sana con baja o ninguna exposici&#243;n actual a factores de ECV cl&#237;nicamente establecida, como infarto de miocardio y tabaco, respectivamente. Los factores encima son fuertes determinantes de los niveles de PCR y as&#237;, la elecci&#243;n de nuestra poblaci&#243;n facilit&#243; la investigaci&#243;n de confundidores asociados con la PCR. As&#237;, estudios adicionales son necesarios para verificar los hallazgos en situaciones cl&#237;nicas y epidemiol&#243;gicas en esa poblaci&#243;n. Seg&#250;n, ese estudio incluye el uso de una &#250;nica medida de marcadores inflamatorios, los cuales pueden no reflejar de forma precisa el estado inflamatorio de largo plazo. M&#250;ltiples medidas con el pasar del tiempo y alteraciones en esas medidas pueden proveer un mecanismo m&#225;s preciso para predecir el riesgo en los individuos. </p>
      <p>En conclusi&#243;n, nuestros resultados indican que en una poblaci&#243;n aparentemente sana de mujeres con baja tasa de fumadoras y enfermedad cardiovascular cl&#237;nicamente establecida, el IMC y la CCI estaban asociados con niveles de biomarcadores sist&#233;micos tales como la PCR-as y la concentraci&#243;n de leucocitos. Considerando que los mediadores inflamatorios est&#225;n directamente envueltos con la aterog&#233;nesis, esos resultados sugieren un importante mecanismo a trav&#233;s del cual la obesidad puede afectar el riesgo de enfermedad cardiovascular. Tambi&#233;n observamos una importante asociaci&#243;n entre marcadores inflamatorios y variables de lipoprote&#237;nas tales como el HDL-c y la Apo-A1, que fue independiente de las medidas de adiposidad. Esos hallazgos se agregan a un creciente conjunto de evidencias de que el HDL-c y la Apo-A1 protegen contra la enfermedad cardiovascular a trav&#233;s de mecanismos que se extienden m&#225;s alla de su participaci&#243;n en el transporte de colesterol. Los presentes hallazgos as&#237; refuerzan la importancia de esos biomarcadores inflamatorios en la creaci&#243;n de algoritmos de previsi&#243;n de riesgo cardiovascular junto con las herramientas de evaluaci&#243;n est&#225;ndar, especialmente en mujeres. </p>
      <p>
        <bold>Agradecimientos</bold>
      </p>
      <p>Ese trabajo recibi&#243; apoyo del Departamento de Ciencia y Tecnolog&#237;a, Gobierno de la India, [Beneficio en el SSD/WS/059/2004].</p>
      <p>
        <bold>Potencial Conflicto de Intereses</bold>
      </p>
      <p>Declaro no haber conflicto de intereses pertinentes.</p>
      <p>
        <bold>Fuentes de Financiaci&#243;n</bold>
      </p>
      <p><italic>Department of Science and Technology Government of India</italic> financi&#243; el presente estudio.</p>
      <p>
        <bold>Vinculaci&#243;n Acad&#233;mica</bold>
      </p>
      <p>Este art&#237;culo forma parte de tesis de Doctorado de Debdutta Ganguli, por <italic>University of Calcuta</italic>.</p>
      <p>
        <bold>Referencias</bold>
      </p>
    </body>
  </sub-article>
</article>
