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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">k8ymwYxyGpcwnBJFPpDzPKS</article-id>
      <article-id pub-id-type="other">00006</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2009000300006</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(09)09200306</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2009000300006</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigos Originais</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>An&#225;lise estrutural e funcional carot&#237;dea em familiares de pacientes com diabete melito tipo 2</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Prado</surname>
            <given-names>S&#244;nia Silva</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ribeiro</surname>
            <given-names>M&#225;rio Luiz</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Cardoso</surname>
            <given-names>Gilberto Perez</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Bousquet-Santos</surname>
            <given-names>Kelb</given-names>
          </name>
          <xref ref-type="aff" rid="aff03"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Velarde</surname>
            <given-names>Luis Guillermo Coca</given-names>
          </name>
          <xref ref-type="aff" rid="aff04"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>N&#243;brega</surname>
            <given-names>Ant&#244;nio Cl&#225;udio Lucas da</given-names>
          </name>
          <xref ref-type="aff" rid="aff03"/>
        </contrib>
      </contrib-group>
      <aff id="aff02">
        <addr-line>
          <named-content content-type="city">Niter&#243;i</named-content>
          <named-content content-type="state">Rio de Janeiro</named-content>
        </addr-line>
        <institution content-type="orgname">Universidade Federal Fluminense</institution>
        <institution content-type="orgdiv1">Departamento de Ci&#234;ncias M&#233;dicas </institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="city">Niter&#243;i</named-content>
          <named-content content-type="state">Rio de Janeiro</named-content>
        </addr-line>
        <institution content-type="orgname">Universidade Federal Fluminense</institution>
        <institution content-type="orgdiv1">Hospital Universit&#225;rio Ant&#244;nio Pedro </institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff03">
        <addr-line>
          <named-content content-type="city">Niter&#243;i</named-content>
          <named-content content-type="state">Rio de Janeiro</named-content>
        </addr-line>
        <institution content-type="orgname">Universidade Federal Fluminense</institution>
        <institution content-type="orgdiv1">Departamento de Fisiologia e Farmacologia </institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff04">
        <addr-line>
          <named-content content-type="city">Niter&#243;i</named-content>
          <named-content content-type="state">Rio de Janeiro</named-content>
        </addr-line>
        <institution content-type="orgname">Universidade Federal Fluminense</institution>
        <institution content-type="orgdiv1">Instituto de Matem&#225;tica </institution>
        <country country="BR">Brazil</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>03</month>
        <year>2009</year>
      </pub-date>
      <volume>92</volume>
      <issue>3</issue>
      <fpage>196</fpage>
      <lpage>202</lpage>
      <history>
        <date date-type="accepted">
          <day>02</day>
          <month>07</month>
          <year>2008</year>
        </date>
        <date date-type="rev-recd">
          <day>22</day>
          <month>06</month>
          <year>2008</year>
        </date>
        <date date-type="received">
          <day>28</day>
          <month>04</month>
          <year>2008</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: O diabete melito tipo 2 (DM2) &#233; a principal causa de morbidade e mortalidade nos pa&#237;ses ocidentais, principalmente de origem cardiovascular. Com base na hist&#243;ria familiar de diabete, mesmo em indiv&#237;duos n&#227;o-diab&#233;ticos, como aumento de risco de doen&#231;a card&#237;aca coronariana, faz-se necess&#225;ria a utiliza&#231;&#227;o de reconhecidos marcadores substitutos de aterosclerose precoce, como as medidas ecogr&#225;ficas carot&#237;deas. OBJETIVO:Comparar tanto caracter&#237;sticas estruturais (espessura m&#233;dio-intimal - EMI) quanto funcionais (medidas de distensibilidade) de art&#233;rias carot&#237;deas dos indiv&#237;duos com hist&#243;ria familiar (HF+) e dos n&#227;o-parentes de portadores de DM2 (HF-), todos sem fatores de risco cardiovasculares reconhecidos. M&#201;TODOS:Trinta e dois indiv&#237;duos (19 HF+ e 13 HF-), com idade entre 21 e 47 anos, de ambos os sexos, foram submetidos a estudo ultra-sonogr&#225;fico de alta resolu&#231;&#227;o das car&#243;tidas (comuns e internas) bilateralmente. Os grupos apresentavam compara&#231;&#227;o (p &gt; 0,05) no que tangia a idade, &#237;ndice de massa corporal (IMC), press&#227;o arterial, glicose e insulina de jejum, leptina e prote&#237;na C reativa (PCR). RESULTADOS:A espessura m&#233;dio-intimal das art&#233;rias car&#243;tidas comuns esquerdas (ACCE) foi estatisticamente mais elevada (p = 0,029) nos HF+ (0,568 &#177; 0,107 mm) que nos HF- (0,477&#177; 0,116 mm). A an&#225;lise de regress&#227;o m&#250;ltipla identificou como prognosticadores independentes da EMI de ACCE a idade, o IMC acima da normalidade, a PCR e o LDL-colesterol. CONCLUS&#195;O:Indiv&#237;duos com hist&#243;ria familiar de DM2, mesmo sem desordens metab&#243;licas laboratoriais detectadas, apresentaram maior espessamento m&#233;dio-intimal em territ&#243;rio carot&#237;deo comum esquerdo que aqueles sem tal parentesco, no entanto n&#227;o houve altera&#231;&#227;o funcional do vaso.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>Art&#233;ria car&#243;tida primitiva</kwd>
        <kwd>diabete melito tipo 2</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>22</day>
        <month>04</month>
        <year>2009</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>ARTIGO ORIGINAL </p>
    <p> DUPLEX-SCAN/ULTRASSONOGRAFIA VASCULAR DOPPLER</p>
    <p>
      <bold>An&#225;lise estrutural e funcional carot&#237;dea em familiares de pacientes com diabete melito tipo 2</bold>
    </p>
    <p>
      <bold>S&#244;nia Silva Prado<sup>I</sup>; M&#225;rio Luiz Ribeiro<sup>I</sup>; Gilberto Perez Cardoso<sup>II</sup>; Kelb Bousquet-Santos<sup>III</sup>; Luis Guillermo Coca Velarde<sup>IV</sup>; Ant&#244;nio Cl&#225;udio Lucas da N&#243;brega<sup>III</sup></bold>
    </p>
    <p><sup>I</sup>Hospital Universit&#225;rio Ant&#244;nio Pedro - UFF; Universidade Federal Fluminense (UFF), Niter&#243;i, RJ - Brasil </p>
    <p><sup>II</sup>Departamento de Ci&#234;ncias M&#233;dicas - UFF; Universidade Federal Fluminense (UFF), Niter&#243;i, RJ - Brasil </p>
    <p><sup>III</sup>Departamento de Fisiologia e Farmacologia - UFF; Universidade Federal Fluminense (UFF), Niter&#243;i, RJ - Brasil </p>
    <p><sup>IV</sup>Instituto de Matem&#225;tica - UFF; Universidade Federal Fluminense (UFF), Niter&#243;i, RJ - Brasil</p>
    <p>
      <xref ref-type="corresp" rid="back">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p><bold>FUNDAMENTO:</bold> O diabete melito tipo 2 (DM2) &#233; a principal causa de morbidade e mortalidade nos pa&#237;ses ocidentais, principalmente de origem cardiovascular. Com base na hist&#243;ria familiar de diabete, mesmo em indiv&#237;duos n&#227;o-diab&#233;ticos, como aumento de risco de doen&#231;a card&#237;aca coronariana, faz-se necess&#225;ria a utiliza&#231;&#227;o de reconhecidos marcadores substitutos de aterosclerose precoce, como as medidas ecogr&#225;ficas carot&#237;deas. </p>
    <p><bold>OBJETIVO:</bold>Comparar tanto caracter&#237;sticas estruturais (espessura m&#233;dio-intimal - EMI) quanto funcionais (medidas de distensibilidade) de art&#233;rias carot&#237;deas dos indiv&#237;duos com hist&#243;ria familiar (HF+) e dos n&#227;o-parentes de portadores de DM2 (HF-), todos sem fatores de risco cardiovasculares reconhecidos. </p>
    <p><bold>M&#201;TODOS:</bold>Trinta e dois indiv&#237;duos (19 HF+ e 13 HF-), com idade entre 21 e 47 anos, de ambos os sexos, foram submetidos a estudo ultra-sonogr&#225;fico de alta resolu&#231;&#227;o das car&#243;tidas (comuns e internas) bilateralmente. Os grupos apresentavam compara&#231;&#227;o (p &gt; 0,05) no que tangia a idade, &#237;ndice de massa corporal (IMC), press&#227;o arterial, glicose e insulina de jejum, leptina e prote&#237;na C reativa (PCR). </p>
    <p><bold>RESULTADOS:</bold>A espessura m&#233;dio-intimal das art&#233;rias car&#243;tidas comuns esquerdas (ACCE) foi estatisticamente mais elevada (p = 0,029) nos HF+ (0,568 &#177; 0,107 mm) que nos HF- (0,477&#177; 0,116 mm). A an&#225;lise de regress&#227;o m&#250;ltipla identificou como prognosticadores independentes da EMI de ACCE a idade, o IMC acima da normalidade, a PCR e o LDL-colesterol. </p>
    <p><bold>CONCLUS&#195;O:</bold>Indiv&#237;duos com hist&#243;ria familiar de DM2, mesmo sem desordens metab&#243;licas laboratoriais detectadas, apresentaram maior espessamento m&#233;dio-intimal em territ&#243;rio carot&#237;deo comum esquerdo que aqueles sem tal parentesco, no entanto n&#227;o houve altera&#231;&#227;o funcional do vaso.</p>
    <p><bold>Palavras-chave: </bold>Art&#233;ria car&#243;tida primitiva/anatomia &amp; histologia, diabete melito tipo 2.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>O diabete melito do tipo2 (DM2), uma enfermidade que est&#225; rapidamente atingindo propor&#231;&#245;es pand&#234;micas, &#233; a principal causa de morbidade e mortalidade nos pa&#237;ses ocidentais<sup>1,2</sup>. A principal etiologia das mortes em portadores de DM2 &#233; de origem cardiovascular, colocando-o, assim, como "risco coronariano equivalente"<sup>1,3</sup>.</p>
    <p>As evid&#234;ncias de aterosclerose j&#225; s&#227;o elevadas antes mesmo do evento cl&#237;nico manifesto, e existem muitos estudos (em portadores ou n&#227;o de DM2), nos &#250;ltimos vinte anos, sobre formas de detec&#231;&#227;o de aterosclerose precoce<sup>4,5</sup>.</p>
    <p>A ultra-sonografia carot&#237;dea de alta resolu&#231;&#227;o, inicialmente descrita por Pignoli e cols.<sup>6</sup> corroborada mais tarde pelo mesmo autor, tem-se mostrado uma ferramenta &#250;til, em tempo real, n&#227;o-invasiva, reprodut&#237;vel, segura e a custo aceit&#225;vel; uma verdadeira janela para a aterosclerose sist&#234;mica<sup>7</sup>. Permite tanto an&#225;lise estrutural (como espessamento m&#233;dio-intimal, j&#225; considerado marcador substituto de doen&#231;a cardiovascular subcl&#237;nica e um forte marcador progn&#243;stico de futuros eventos vasculares) quanto funcional (elasticidade) do vaso<sup>5,7-16</sup>.</p>
    <p>Assim, quando se considera a hist&#243;ria familiar de diabete, mesmo em indiv&#237;duos n&#227;o-diab&#233;ticos e sem os fatores de risco cardiovascular conhecidos, como um aumento <italic>per se</italic> de risco de doen&#231;a card&#237;aca coronariana, a utiliza&#231;&#227;o das medidas ecogr&#225;ficas carot&#237;deas pode tornar-se importante marcador de aterosclerose precoce<sup>17-19</sup>.</p>
    <p>
      <bold>M&#233;todos</bold>
    </p>
    <p>Foram convidados, pela imprensa do Rio de Janeiro e por interm&#233;dio dos pacientes do ambulat&#243;rio de endocrinologia do Hospital Universit&#225;rio Ant&#244;nio Pedro (Huap) com diagn&#243;stico de diabete melito ao prontu&#225;rio, parentes de primeiro e segundo graus destes portadores de diabete melito tipo2 (HF+) e de pacientes-controle (aqueles sem hist&#243;ria familiar de diabete melito tipo 2 - HF-) para entrevista no per&#237;odo de julho de 2004 a janeiro de 2006. Exclu&#237;ram-se indiv&#237;duos com: idade inferior a 18 anos e/ou superior a 50; h&#225;bitos de tabagismo; atividade esportiva competitiva; hist&#243;ria de doen&#231;a cardiovascular, cerebrovascular e/ou de doen&#231;a arterial perif&#233;rica; relato de uso de qualquer terap&#234;utica; e mulheres em fase gestacional. Ante o rigor de sele&#231;&#227;o, obtiveram-se inicialmente 31 volunt&#225;rios HF+ e 15 HF. Destes, 12 HF+ e 2 HF- foram exclu&#237;dos no exame cl&#237;nico inicial, pois apresentavam press&#227;o arterial sist&#243;lica (PAS) &gt; 140 mmHg e/ou press&#227;o arterial diast&#243;lica (PAD) &gt; 90 mmHg e glicemia capilar de jejum &gt; 110 mg/dl. Na an&#225;lise laboratorial, exclu&#237;ram-se aqueles com glicemia de jejum maior ou igual a 110 mg/dl e/ou glicemia ap&#243;s 2 horas de carga oral de 75 g de dextrose (TTOG) maior que 140 mg/dl, colesterol s&#233;rico total &gt; 240 mg/dl e/ou triglicer&#237;deos s&#233;ricos &gt; 150 mg/dl. Os grupos, de ambos os sexos, tiveram a seguinte caracter&#237;stica: 19 HF+, idade variando de 23 a 47 anos (m&#233;dia 37,94); 13 HF-, idade de 21 a 46 anos (m&#233;dia 34).</p>
    <p>Foi obtido consentimento informado de todos os volunt&#225;rios antes de sua admiss&#227;o no estudo. O estudo foi aprovado pelo comit&#234; de &#233;tica em pesquisa do Huap envolvendo seres humanos.</p>
    <p>&#192; visita inicial, o volunt&#225;rio foi submetido a question&#225;rio padronizado (dados pessoais e antecedentes m&#243;rbido-familiares) e procedeu-se &#224; obten&#231;&#227;o dos valores antropom&#233;tricos - &#237;ndice de massa corporal (IMC), peso/altura<sup>2</sup> (em kg/m<sup>2</sup>), per&#237;metro da cintura (c) e do quadril (q) em cent&#237;metros - em conson&#226;ncia com o International Diabetes Federation (2005), em que a cintura corresponde &#224; m&#237;nima circunfer&#234;ncia entre o ap&#234;ndice xif&#243;ide e o umbigo, e a rela&#231;&#227;o entre eles [c/q] &#233; o &#237;ndice cintura-quadril (ICQ); da glicemia de jejum (de 12 horas) capilar (Accutrend, Roche, Inc.); da press&#227;o arterial sist&#234;mica (PA - fases I e V de Korotkoff), com o indiv&#237;duo na posi&#231;&#227;o sentada, 10 minutos ap&#243;s repouso em ambiente tranq&#252;ilo, com temperatura de cerca de 22&#186; C, utilizando um esfigmoman&#244;metro de merc&#250;rio padr&#227;o, com manguito adequado &#224;s dimens&#245;es do bra&#231;o, posicionado no n&#237;vel do cora&#231;&#227;o; da press&#227;o de pulso (PAS - PAD), em mil&#237;metros de merc&#250;rio.</p>
    <p>&#192; segunda visita, em um &#250;nico centro laboratorial de an&#225;lises cl&#237;nicas, os indiv&#237;duos, ap&#243;s jejum de 12 horas, submeteram-se, por meio de coleta de sangue venoso (veia antecubital), &#224; medida de: glicemia de jejum (G) e TTOG (m&#233;todo automatizado - glicose oxidase/peroxidase, Advia 1650 - <italic>kit</italic> Advia 1650, Bayer, Alemanha), insulina plasm&#225;tica (I) (quimioluminesc&#234;ncia, Immullite, 2000, <italic>kit</italic> DPC, EUA), colesterol total (m&#233;todo enzim&#225;tico automatizado - colesterol oxidase/peroxidase, Advia 1650, <italic>kit</italic> Advia 1650, Bayer, Alemanha), triglicer&#237;deos (m&#233;todo cin&#233;tico enzim&#225;tico automatizado), HDL-colesterol (m&#233;todo enzim&#225;tico automatizado, Advia 1650, <italic>kit</italic> Advia Dasa (m&#233;todo direto, fabrica&#231;&#227;o IN-HOUSE)), LDL-colesterol (calculado pela equa&#231;&#227;o de Friedewald (LDL-colesterol = colesterol total - (HDL-colesterol) + triglicer&#237;deos /5)), PCR-us (turbidimetria - Born, BN II Dade Berhing, <italic>kit</italic> Dade Berhing, EUA) - em que valores inferiores a 0,05, por limita&#231;&#227;o do m&#233;todo, foram considerados iguais a 0,05 - e leptina (radioimunoensaio, manual com Alto Delfio, <italic>kit</italic> IN-HOUSE). A partir da obten&#231;&#227;o dos valores G e I, foi calculado o &#237;ndice de resist&#234;ncia &#224; insulina com a utiliza&#231;&#227;o do modelo matem&#225;tico do Homa-IR ((I* G/22,5)* 0,0555).</p>
    <p>A terceira visita foi realizada no laborat&#243;rio de ecocardiografia do servi&#231;o de cardiologia do Huap, em sala climatizada (22 e 24&#186;C), com aparelho ecogr&#225;fico de alta resolu&#231;&#227;o (Vivid 3 - General Eletric) - capacidade de aferi&#231;&#227;o de at&#233; cent&#233;simo de mil&#237;metros - com transdutor linear 13 MHz, em que todos os estudos foram realizados por um dos dois m&#233;dicos treinados, "cegos" &#224; condi&#231;&#227;o cl&#237;nica dos examinados, atendendo &#224;s especifica&#231;&#245;es das sociedades nacionais de ecocardiografia, com rean&#225;lise das medidas por outro m&#233;dico (diferente do examinador), com todos os dados gravados e estocados em CD-ROM, para subseq&#252;ente processamento <italic>off-line</italic>. Ao estudo carot&#237;deo, bilateral - examinado em posi&#231;&#227;o supina - com preliminar varredura explanat&#243;ria transversa (para acessar a anatomia do mesmo), seguida de an&#225;lise longitudinal (para obten&#231;&#227;o das imagens, em modo B, e medidas), com a cabe&#231;a girada a 45&#186;, para acesso obl&#237;quo anterior, lateral e posterior (sendo, contudo, considerado acesso de an&#225;lise o posterior), para o lado contr&#225;rio &#224; localiza&#231;&#227;o da art&#233;ria a ser estudada, em que a espessura m&#233;dio-intimal (EMI), definida como a dist&#226;ncia entre a borda de destaque l&#250;men-intimal carot&#237;dea e a borda de destaque ecogr&#225;fico m&#233;dio-advent&#237;cia da parede posterior das art&#233;rias carot&#237;deas comum (ACC) e interna (ACI), foi obtida. Os pontos de refer&#234;ncia para mensura&#231;&#227;o da ACC foram: no ponto antes de a ACC se dilatar para sua bifurca&#231;&#227;o (ponto zero), 5 mm distais do ponto 0 (ponto 1), 10 mm distais do ponto 0 (ponto2) e 15 mm distais do ponto 0 (ponto3). Ao n&#237;vel da ACI, as medidas foram: no n&#237;vel do bulbo (ponto 0'), a 2,5 mm proximais do ponto 0' (ponto 1') e a 5 mm proximais do ponto 0' (ponto 2'). As aferi&#231;&#245;es da EMI foram realizadas em conson&#226;ncia com o ponto m&#225;ximo da onda R do eletrocardiograma (ECG) - fase diast&#243;lica - de grava&#231;&#227;o simult&#226;nea ao aparelho de ecografia. Os valores utilizados para an&#225;lise estat&#237;stica foram gerados por &#250;nico examinador e a partir da m&#233;dia das diferentes medidas de cada segmento arterial estudado, ou seja, art&#233;ria car&#243;tida comum esquerda (ACCE), art&#233;ria car&#243;tida comum direita (ACCD), art&#233;ria car&#243;tida interna esquerda (ACIE), art&#233;ria car&#243;tida interna direita (ACID).</p>
    <p>Ap&#243;s a obten&#231;&#227;o da EMI e do raio interadvent&#237;cio (R) [ao corte longitudinal - durante as fases sist&#243;lica (ao final da onda T do ECG) e diast&#243;lica] das art&#233;rias car&#243;tidas comuns, utilizamos as medidas da ACCE (pelo fato de a EMI ser de relev&#226;ncia, em rela&#231;&#227;o aos dois grupos estudados) como fonte de an&#225;lise dos par&#226;metros de distensibilidade arterial, de acordo com as formula&#231;&#245;es, apontadas mais adiante, do <italic>Aric Study</italic> e do <italic>Smart Study</italic><sup>14-16</sup>:</p>
    <p>a) CAS = [D(s) - D(d)]/D(d);</p>
    <p>b) SI = ln [PAS / PAD]/CAS;</p>
    <p>c) CAC = ([Ds-Dd]/Dd / (PAS - PAD);</p>
    <p>d) YEM = (R/EMI) x {[PAS - PAD] / CAS},</p>
    <p>onde CAS = tens&#227;o arterial circunferencial; D(s) = di&#226;metro carot&#237;deo &#224; s&#237;stole; D(d) = di&#226;metro carot&#237;deo &#224; di&#225;stole; SI = &#237;ndice de rigidez arterial carot&#237;deo (ou &#237;ndice &#946;); ln = logaritmo natural; CAC = coeficiente de complac&#234;ncia arterial carot&#237;dea; YEM = m&#243;dulo el&#225;stico de Young.</p>
    <p>Ap&#243;s a consecu&#231;&#227;o dos dados pelos dois examinadores, foi calculado o coeficiente de variabilidade interobservador. Para o estudo da concord&#226;ncia das aferi&#231;&#245;es dos valores de EMI carot&#237;dea (vari&#225;veis num&#233;ricas) entre os dois observadores, nos dois grupos estudados, utilizaram-se a correla&#231;&#227;o de Spearman e o m&#233;todo gr&#225;fico de Brand &amp; Altman.</p>
    <p>Foram utilizados os testes <italic>t</italic> de <italic>Student</italic> e Wilcoxon para compara&#231;&#227;o dos n&#237;veis m&#233;dios de vari&#225;veis num&#233;ricas. Para o estudo da influ&#234;ncia de diversos fatores sobre vari&#225;veis respostas, como ACCD, ACCE, ACID e ACIE, utilizaram-se modelos de regress&#227;o linear m&#250;ltipla, com todas as medidas cl&#237;nicas e laboratoriais como vari&#225;veis independentes em cada um dos modelos. O programa estat&#237;stico utilizado para an&#225;lise foi o S-Plus 6.0, considerando-se <italic>p</italic> significativo quando menor que 0,05 (<italic>p</italic> &lt; 0,05).</p>
    <p>O c&#225;lculo amostral, para o atendimento do objetivo principal do estudo, utilizando como refer&#234;ncia o estudo de Pannacciulli e cols.<sup>17</sup>, que separaram seus volunt&#225;rios de forma semelhante ao nosso interesse (entre HF+ e HF-), na realiza&#231;&#227;o de um teste-t, baseou-se na diferen&#231;a esperada entre as medidas de 0,07 mm, em um desvio padr&#227;o esperado de 0,05 para um poder estat&#237;stico de 0,8 e um valor de <italic>p</italic> de 0,05, encontrando, assim, um valor de 10 indiv&#237;duos em cada grupo<sup>17</sup>.</p>
    <p>
      <bold>Resultados</bold>
    </p>
    <p>Os dados gerais, bioqu&#237;micos e ultra-sonogr&#225;ficos s&#227;o apresentados nas <xref ref-type="table" rid="t1">tabelas 1</xref>, <xref ref-type="table" rid="t2">2</xref> e <xref ref-type="table" rid="t3">3</xref>.</p>
    <table-wrap id="t1">
      <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt01.jpg"/></table-wrap>
    <table-wrap id="t2">
      <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt02.jpg"/></table-wrap>
    <table-wrap id="t3">
      <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt03.jpg"/></table-wrap>
    <p>Os parentes de diab&#233;ticos (HF+) e os controles (HF-) s&#227;o comparados, sem diferen&#231;a significativa, no que tange a idade, sexo, IMC, cintura, quadril, ICQ, press&#227;o arterial sist&#243;lica, PP (press&#227;o de pulso), HDL-colesterol, LDL-colesterol, triglicer&#237;deos, glicemia de jejum, teste de toler&#226;ncia oral &#224; glicose, insulina de jejum, leptina e PRC-us. A EMI de ACCE foi significativamente maior em indiv&#237;duos HF+ em rela&#231;&#227;o aos HF-(<italic>p</italic> &lt; 0,03). H&#225; que ressaltar que, pelo fato de os valores encontrados estarem dentro dos limites de normalidade, pelos m&#233;todos empregados, ocorreu tamb&#233;m diferen&#231;a significativa dos n&#237;veis de HOMA-IR e colesterol total entre os HF+ e os HF-, sendo maior nos primeiros (<italic>p</italic> &lt; 0,05 em ambos), sem, contudo, haver correla&#231;&#227;o entre os n&#237;veis de colesterol e a EMI de ACCE.</p>
    <p>N&#227;o se observou, todavia, diferen&#231;a significativa no que diz respeito a par&#226;metros de distensibilidade arterial carot&#237;dea, entre os HF+ e os HF-, como demonstrado (<xref ref-type="table" rid="t4">tab. 4</xref>) nos coeficientes angulares da an&#225;lise de regress&#227;o (expressos em <italic>p</italic>) entre esses par&#226;metros, em separado, e outras vari&#225;veis. Denotou-se, por&#233;m, positiva correla&#231;&#227;o entre os tr&#234;s par&#226;metros (SI, CAC e YEM) e idade (com <italic>p</italic> &lt; 0,05), com a glicemia de jejum correlacionada ao CAC e ao SI (<italic>p</italic> &lt; 0,05) e &#224; PAS com YEM e CAC (<italic>p</italic> &lt; 0,04). N&#227;o se detectou, contudo, correla&#231;&#227;o de signific&#226;ncia estat&#237;stica entre o raio e as medidas de distensibilidade e de estrutura arterial (<xref ref-type="table" rid="t5">tab. 5</xref>).</p>
    <table-wrap id="t4">
      <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt04.jpg"/></table-wrap>
    <table-wrap id="t5">
      <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt05.jpg"/></table-wrap>
    <p>Os resultados da an&#225;lise de regress&#227;o de EMI de ACCE com outras vari&#225;veis independentes em todos os indiv&#237;duos (<xref ref-type="table" rid="t6">tab. 6</xref>) denotaram correla&#231;&#227;o positiva com IMC (<italic>p</italic> &lt; 0,001), idade (<italic>p</italic> = 0,001), PCR-us (<italic>p</italic> = 0,007), PAD (<italic>p</italic> &lt; 0,05) e fator parente de portador de DM2 (<italic>p</italic> = 0,03).</p>
    <table-wrap id="t6">
      <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt06.jpg"/></table-wrap>
    <p>Em tempo, consideramos cintura alterada aquela que excede os par&#226;metros normais adotados pela International Diabetes Federation, que estabelece, para nosso pa&#237;s, cintura feminina <underline>&lt;</underline> 80 cm e masculina <underline>&lt;</underline> 90 cm, ou e pelo NCEP ATP III (feminina <underline>&lt;</underline> 88 cm e masculina <underline>&lt;</underline> 102 cm).</p>
    <p>No que concerne &#224; correla&#231;&#227;o interobservador, utilizando-se as medidas de ACCE, observou-se que os n&#237;veis aferidos pelos dois observadores foram semelhantes (<italic>p</italic> = 0,2944) e apresentaram uma correla&#231;&#227;o significativa (r = 0,737 e <italic>p</italic> = 0,0109). Para as medidas de ACIE, embora, em m&#233;dia, as aferi&#231;&#245;es entre os observadores tenham sido semelhantes (0,7637), n&#227;o se detectou correla&#231;&#227;o significativa (r = 0,1641 e p = 0,5761).</p>
    <p>
      <bold>Discuss&#227;o</bold>
    </p>
    <p>Este &#233; primeiro estudo com parentes de diab&#233;ticos em que se analisam, em separado, os seguimentos arteriais carot&#237;deos, al&#233;m da associa&#231;&#227;o de avalia&#231;&#227;o dos par&#226;metros estruturais e funcionais da car&#243;tida.</p>
    <p>No que tange &#224; an&#225;lise estrutural carot&#237;dea, observou-se o mesmo achado de maior EMI carot&#237;dea comum em parentes de diab&#233;ticos (tamb&#233;m em adultos jovens), quando comparados aos controles, como no estudo de Pannacciulli e cols.<sup>17</sup>. O nosso estudo, contudo, demonstrou que os valores de EMI e IMC (em ambos os grupos) foram menores do que no estudo referido. A m&#233;dia de EMI foi de 0,840 mm &#177; 0,010 em HF+ e 0,770 mm &#177; 0,001 nos HF- <italic>versus</italic> 0,560 mm &#177; 0,107 em HF+ e 0,477 mm &#177; 0,110 em HF-, este &#250;ltimo em nosso estudo. A m&#233;dia de IMC (kg/m<sup>2</sup>) por eles encontrada foi de 30,0 &#177; 0,500 em HF+ e 29,400 &#177; 0,500 em HF- <italic>versus</italic> 25,040 &#177; 3,240 e 24,240 &#177; 3,660, respectivamente, em nosso estudo. N&#227;o detectamos tamb&#233;m associa&#231;&#227;o com glicemia de jejum e/ou com o TTOG.</p>
    <p>A ACC (independentemente da associa&#231;&#227;o com doen&#231;a arterial coronariana) demonstra alto grau de reprodutibilidade, em que a manifesta&#231;&#227;o do processo ateroscler&#243;tico &#233; de espessamento difuso por prolifera&#231;&#227;o progressiva de c&#233;lulas musculares lisas e deposi&#231;&#227;o de matriz; um segmento superficial, de paredes retas, que repousa em paralelo &#224; superf&#237;cie da pele, de f&#225;cil an&#225;lise; diferindo da ACI, em que a manifesta&#231;&#227;o se d&#225; por les&#227;o focal ateroscler&#243;tica (ou placas), de localiza&#231;&#227;o profunda no pesco&#231;o, com paredes de origem n&#227;o-paralelas, assim como seu repouso (em rela&#231;&#227;o &#224; superf&#237;cie cervical).</p>
    <p>Em nosso estudo, a correla&#231;&#227;o significativa dos valores obtidos de EMI de ACCE pelos dois observadores refor&#231;a tal reprodutibilidade do m&#233;todo ultra-sonogr&#225;fico na pr&#225;tica cl&#237;nica, em conformidade com estudos pr&#233;vios. Essa correla&#231;&#227;o n&#227;o se aplica aos valores de ACI, refor&#231;ando seu aspecto anat&#244;mico limitante de an&#225;lise.</p>
    <p>Ressalta-se, todavia, que, considerando que a ACCE nasce diretamente do arco a&#243;rtico, com menor estresse de cisalhamento (EC - <italic>shear stress</italic>) - com, tamb&#233;m, associa&#231;&#227;o de DM2 com menor EC da ACC - &#233; o local onde as les&#245;es ateroscler&#243;ticas desenvolvem-se mais precocemente<sup>20-23</sup>.</p>
    <p>Reafirma-se, ainda, em estudo de Balletshofer, a associa&#231;&#227;o entre disfun&#231;&#227;o endotelial e resist&#234;ncia insul&#237;nica em jovens filhos de diab&#233;ticos, independentemente dos cl&#225;ssicos fatores de risco cardiovasculares<sup>24</sup>.</p>
    <p>Em estudos observacionais e cl&#237;nicos, &#224; exce&#231;&#227;o de um &#250;nico de fraca correla&#231;&#227;o, a EMI mostrou-se um marcador de doen&#231;a card&#237;aca vascular subcl&#237;nica, associada com tradicionais fatores de risco de doen&#231;a card&#237;aca coronariana (em conformidade com nossos resultados - a PCR, o LDL-colesterol e a PAD) e carga ateroscler&#243;tica coronariana, sendo preditivo de subseq&#252;entes eventos cardiovasculares e um precoce indicador de aterosclerose, al&#233;m de valioso marcador de risco por an&#225;lise n&#227;o-invasiva<sup>5-7,10-11,14,20-27</sup>.</p>
    <p>No que se relaciona &#224;s propriedades estruturais carot&#237;deas, nenhuma compara&#231;&#227;o com estudos pr&#233;vios, com um mesmo perfil de indiv&#237;duos de an&#225;lise, p&#244;de ser realizada, por n&#227;o se ter encontrado na literatura m&#233;dica. Quando se faz refer&#234;ncia a outra popula&#231;&#227;o de estudo, verifica-se concord&#226;ncia nos achados de correla&#231;&#227;o de SI e CAC com glicemia de jejum, al&#233;m de ratificar que a rigidez arterial n&#227;o &#233; independente dos fatores de risco de eventos vasculares, com rela&#231;&#227;o direta (em nosso estudo apenas no que tange &#224; complac&#234;ncia arterial e ao m&#243;dulo el&#225;stico) com os n&#237;veis de PAS. H&#225; que se salientar que os indiv&#237;duos, dos dois grupos, por n&#243;s analisados n&#227;o apresentavam diferen&#231;as significativas entre eles, no que se relaciona a n&#237;veis de press&#227;o arterial, al&#233;m de possu&#237;rem valores normais (pelos crit&#233;rios do JOINT VII)<sup>28</sup>. Acresce-se, tamb&#233;m, que nossos grupos de estudo (tanto HF+ quanto HF-) n&#227;o possu&#237;am os cl&#225;ssicos fatores de risco cardiovasculares do escore de Framingham e, &#224;s expensas de maiores valores de HOMA-IR e colesterol total (dentro, contudo, dos limites da normalidade), n&#227;o foram suficientes para produzir altera&#231;&#227;o funcional vascular, com n&#237;veis detect&#225;veis de par&#226;metros de distensibilidade inferiores aos outros estudos pertinentes. Reafirma-se, ainda, que a retirada dos maiores valores de HOMA-IR e CT dos HF+, como uma an&#225;lise &#224; parte, manteve a diferen&#231;a significativa dos n&#237;veis de EMI de ACCE entre os grupos estudados, refor&#231;ando, dessa forma, a influ&#234;ncia da hereditariedade.</p>
    <p>Outro componente da aterog&#234;nese, funcionando como freio no desenvolvimento do significante comprometimento do l&#250;men arterial - o remodelamento<sup>29</sup>-, tamb&#233;m n&#227;o foi por n&#243;s detectado (faixa et&#225;ria m&#233;dia inferior a 50 anos?, baixos &#237;ndices m&#233;dios de EMI?), em virtude de n&#227;o ter sido detectada diferen&#231;a significativa das medidas de raio entre os HF+ e os HF-.</p>
    <p>V&#225;rios estudos sugerem fatores gen&#233;ticos como influenciadores da EMI carot&#237;dea, podendo ser esta de maior poder discriminat&#243;rio entre os pacientes de maior e menor risco cardiovascular que a an&#225;lise da distensibilidade arterial, em especial em grupos de parentes de diab&#233;ticos, e a ultra-sonografia &#233; a oportunidade valiosa e pr&#225;tica de estudar a evolu&#231;&#227;o precoce de aterosclerose<sup>30</sup>. Uma nova proposta de marcador de risco cardiovascular, para avalia&#231;&#227;o da suscetibilidade de doen&#231;a card&#237;aca coronariana, considera ainda as limita&#231;&#245;es de todos os escores de risco<sup>26</sup>.</p>
    <p>Existem v&#225;rias limita&#231;&#245;es de nosso estudo. A utiliza&#231;&#227;o de medidas f&#237;sicas para definir doen&#231;a cardiovascular em atividade, al&#233;m de auto-relato de inexist&#234;ncia de sintomas correspondentes (ou seja, indiv&#237;duos aparentemente saud&#225;veis), &#233; uma delas, sendo, todavia, a metodologia utilizada por v&#225;rios estudos relevantes a esse tipo de an&#225;lise<sup>18</sup>. O n&#250;mero pequeno de indiv&#237;duos estudados, o que n&#227;o permitiu a avalia&#231;&#227;o em separado por sexo, preenche os crit&#233;rios de marcador substituto - os tr&#234;s crit&#233;rios de Boissel [mais sens&#237;vel, mais prontamente avali&#225;vel e conveniente (por ser m&#233;todo n&#227;o-invasivo), com comprovada rela&#231;&#227;o causal entre este e o objetivo cl&#237;nico], cujas vantagens v&#227;o desde o menor n&#250;mero de amostra at&#233; a comprova&#231;&#227;o de os objetivos serem mais diretamente associados com o processo da doen&#231;a<sup>8,30</sup>. A ultra-sonografia n&#227;o permite diferenciar processo ateroscler&#243;tico intimal de hipertrofia medial (por efeitos da press&#227;o arterial), o que, a princ&#237;pio, pode ser entendido como limitador do m&#233;todo; h&#225;, por&#233;m, dados que corroboram que a EMI est&#225; em rela&#231;&#227;o mais direta com aterosclerose intimal. Em nosso estudo, a n&#227;o-utiliza&#231;&#227;o de medidas de forma automatizada est&#225; em concord&#226;ncia com outras an&#225;lises recentes, em que a abordagem de car&#225;ter manual, quando bem padronizada por t&#233;cnicos treinados, &#233; t&#227;o boa quanto a obtida de forma automatizada. A an&#225;lise ecogr&#225;fica apenas na parede posterior, diferenciando de alguns estudos pr&#233;vios (com an&#225;lise das duas paredes), foi baseada na considera&#231;&#227;o de reduzirmos risco de nossa acur&#225;cia se inclu&#237;ssemos a parede anterior (n&#227;o permitindo fidedigna separa&#231;&#227;o das medidas &#237;ntima e m&#233;dia, e da utiliza&#231;&#227;o de excesso de ganho para obt&#234;-la). A aferi&#231;&#227;o de n&#237;veis de press&#227;o arterial de modo indireto, via braquial, sabendo-se que a press&#227;o arterial braquial &#233; usualmente de 10% a 15% maior que a da art&#233;ria car&#243;tida comum, baseia-se nos estudos de Borow e Newburger<sup>31</sup> que evidenciaram excelente correla&#231;&#227;o entre a PA obtida de forma invasiva e via press&#227;o braquial<sup>15</sup>. A utiliza&#231;&#227;o de m&#233;todos indiretos de avalia&#231;&#227;o de resist&#234;ncia insul&#237;nica (RI) (insulinemia de jejum, HOMA-IR e TTOG), al&#233;m de marcadores indiretos de RI (IMC, circunfer&#234;ncia abdominal e concentra&#231;&#227;o s&#233;rica de triglicer&#237;deos) e n&#227;o do padr&#227;o-ouro da <italic>American Diabetes Association</italic> - <italic>clamp</italic> euglic&#234;mico hiperinsulin&#234;mico - deu-se pelo fato de, &#224;s expensas deste, fornecer informa&#231;&#227;o mais pura e reprodut&#237;vel sobre a a&#231;&#227;o tecidual da insulina, demanda elevado tempo de realiza&#231;&#227;o, aparelhagem de an&#225;lise instant&#226;nea de n&#237;veis de glicemia, bombas de infus&#227;o e necessidade de pessoal altamente especializado e treinado. At&#233; o momento, todavia, n&#227;o se disp&#245;e de um m&#233;todo de investiga&#231;&#227;o laboratorial que preencha todos os crit&#233;rios para universal aceita&#231;&#227;o e utiliza&#231;&#227;o de an&#225;lise de RI, considerando os m&#233;todos indiretos, como em v&#225;rios estudos, mais pass&#237;veis de utiliza&#231;&#227;o na pr&#225;tica cl&#237;nica<sup>32</sup>. N&#227;o se realizou an&#225;lise por grupo racial ante a miscigena&#231;&#227;o racial de nosso pa&#237;s. A n&#227;o-utiliza&#231;&#227;o de sorteio aleat&#243;rio pode ser um vi&#233;s do estudo, contudo a busca pela elimina&#231;&#227;o de fatores que pudessem obscurecer nossos resultados nos tornou t&#227;o obstinados na procura por "volunt&#225;rios-padr&#245;es".</p>
    <p>Salienta-se ainda que, at&#233; a data de conclus&#227;o do estudo, os valores de refer&#234;ncia de normalidade de EMI foram ratificados pela <italic>American Society of Echocardiography</italic>, datados de 2006, que em muito excediam aos encontrados em nosso estudo<sup>33</sup>. Contudo, o trabalho de Lim e cols.<sup>34</sup>, com 137 indiv&#237;duos "saud&#225;veis", demonstrou-se valores de normalidade de EMI de ACC em conson&#226;ncia, de acordo com a faixa et&#225;ria, com aqueles por n&#243;s encontrados em indiv&#237;duos n&#227;o-parentes de portadores de DM2 (idade entre 35 e 39 anos - 0,49 &#177; 0,06; entre 40 e 49 anos - 0,52 &#177; 0,06 - no estudo de Lim e cols.<sup>34</sup>), colocando, em termos de valores correspondentes, os parentes de portadores de DM2 por n&#243;s estudados em uma faixa et&#225;ria mais velha (de 50 a 59 anos de idade - 0,56&#177;0,08 - no estudo de Lim e cols.<sup>34</sup>), ratificando, talvez, a frase de <italic>sir</italic> William Osler (em 1897): "N&#243;s temos a idade de nossas art&#233;rias"<sup>34</sup>.</p>
    <p>
      <bold>Conclus&#245;es</bold>
    </p>
    <p>Os indiv&#237;duos com hist&#243;ria familiar de DM2, mesmo na aus&#234;ncia de intoler&#226;ncia &#224; glicose e/ou n&#237;veis basais de insulina alterados, apresentaram maiores valores de espessamento m&#233;dio-intimal (EMI) carot&#237;deo (altera&#231;&#227;o estrutural), em especial no territ&#243;rio carot&#237;deo comum esquerdo, quando comparados com um grupo sem tal parentesco, n&#227;o manifestando, todavia, altera&#231;&#227;o funcional do vaso.</p>
    <p>A infer&#234;ncia da predisposi&#231;&#227;o gen&#233;tica ao DM2, provavelmente em associa&#231;&#227;o &#224; resist&#234;ncia insul&#237;nica, sobre os n&#237;veis de EMI carot&#237;deo, em especial no territ&#243;rio carot&#237;deo comum esquerdo, precedendo a altera&#231;&#227;o funcional vascular, necessita de maiores estudos para elucidar tal associa&#231;&#227;o.</p>
    <p>
      <bold>Agradecimentos</bold>
    </p>
    <p>Os autores agradecem a todos os volunt&#225;rios, &#224; equipe m&#233;dica do servi&#231;o de endocrinologia do Huap e ao Laborat&#243;rio Bronstein, sem os quais seria invi&#225;vel a realiza&#231;&#227;o deste estudo.</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 n&#227;o teve fontes de financiamento externas.</p>
    <p>
      <bold>Vincula&#231;&#227;o Acad&#234;mica</bold>
    </p>
    <p>Este artigo &#233; parte de tese de Mestrado de S&#244;nia Silva Prado pela Universidade Federal Fluminense.</p>
    <p>
      <fn id="back" fn-type="corresp">
        <p>Correspond&#234;ncia:</p>
        <p>S&#244;nia Silva Prado </p>
        <p> Rua Santa Clara, 41/201 - Copacabana </p>
        <p> 22041-010 - Rio de Janeiro, RJ - Brasil </p>
        <p> E-mail: </p>
        <p>
          <email xlink:href="ssprado@cardiol.br">ssprado@cardiol.br</email>
        </p>
      </fn>
    </p>
    <p>Artigo recebido em 28/04/08; revisado recebido em 22/06/08; aceito em 02/07/08.</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">Carotid artery structural and functional evaluation in relatives of type 2 diabetic patients</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>In Western countries type 2 diabetes mellitus (DM2) is the leading cause of morbidity and mortality, particularly from cardiovascular causes. Since a family history of diabetes, even in non-diabetic subjects, is regarded as an increased risk of coronary heart disease, the use of approved surrogate markers of early atherosclerosis, specially of ultrasonic measurements of the carotid arteries, is of vital importance. OBJECTIVE: To analyze the structural properties (intima-media thickness) and functional properties (distensibility measurement) of the carotid arteries in subjects with (FH+) a family history of type 2 diabetes, in comparison to subjects without (FH-) a family history of type 2 diabetes, both groups with no known cardiovascular risk factors. METHODS: 32 individuals (male and female, age range, 21-47 years; 19 FH+, 13 FH-) had their right and left common and internal carotid arteries measured, using high-resolution B-mode ultrasonography. Both groups had similar (p&gt;0.05) age, BMI, blood pressure, and fasting blood glucose and insulin, leptin, and C-reactive protein (CRP) levels. RESULTS: The intima-media thickness (IMT) of the left common carotid artery (LCCA) in the FH+ group (0.568&#177;0.107mm) was statistically greater (p=0.029) than in the FH- group (0.477&#177;0.116mm). Multiple regression analysis identified age, overweight and obesity (determined by BMI), CRP, and LDL-cholesterol levels as independent predictors of the IMT in the LCCA. CONCLUSION: FH+ individuals with no metabolic disorders presented greater IMT of the left common carotid artery (structural alteration) than FH- individuals, but normal vessel function. (Arq Bras Cardiol 2009;92(3): 186-192)</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Carotid artery, common</kwd>
        <kwd>diabetes mellitus type 2</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>ORIGINAL ARTICLE</bold>
      </p>
      <p>
        <fn id="top-body2">
          <label>
            <bold>Carotid artery structural and functional evaluation in relatives of type 2 diabetic patients</bold>
          </label>
          <p>
            <bold>S&#244;nia Silva Prado<sup>I</sup>; M&#225;rio Luiz Ribeiro<sup>I</sup>; Gilberto Perez Cardoso<sup>II</sup>; Kelb Bousquet-Santos<sup>III</sup>; Luis Guillermo Coca Velarde<sup>IV</sup>; Ant&#244;nio Cl&#225;udio Lucas da N&#243;brega<sup>III</sup></bold>
          </p>
        </fn>
      </p>
      <p><sup>I</sup>Hospital Universit&#225;rio Ant&#244;nio Pedro - UFF; Universidade Federal Fluminense (UFF), Niter&#243;i, RJ - Brasil</p>
      <p><sup>II</sup>Departamento de Ci&#234;ncias M&#233;dicas - UFF; Universidade Federal Fluminense (UFF), Niter&#243;i, RJ - Brasil</p>
      <p><sup>III</sup>Departamento de Fisiologia e Farmacologia - UFF; Universidade Federal Fluminense (UFF), Niter&#243;i, RJ - Brasil</p>
      <p><sup>IV</sup>Instituto de Matem&#225;tica - UFF; Universidade Federal Fluminense (UFF), Niter&#243;i, RJ - Brasil</p>
      <p>Mailing address</p>
      <p>
        <bold>SUMMARY</bold>
      </p>
      <p><bold>BACKGROUND: </bold>In Western countries type 2 diabetes mellitus (DM2) is the leading cause of morbidity and mortality, particularly from cardiovascular causes. Since a family history of diabetes, even in non-diabetic subjects, is regarded as an increased risk of coronary heart disease, the use of approved surrogate markers of early atherosclerosis, specially of ultrasonic measurements of the carotid arteries, is of vital importance.</p>
      <p><bold>OBJECTIVE:</bold>To analyze the structural properties (intima-media thickness) and functional properties (distensibility measurement) of the carotid arteries in subjects with (FH+) a family history of type 2 diabetes, in comparison to subjects without (FH-) a family history of type 2 diabetes, both groups with no known cardiovascular risk factors.</p>
      <p><bold>METHODS:</bold>32 individuals (male and female, age range, 21-47 years; 19 FH+, 13 FH-) had their right and left common and internal carotid arteries measured, using high-resolution B-mode ultrasonography. Both groups had similar (P&gt;0.05) age, BMI, blood pressure, and fasting blood glucose and insulin, leptin, and C-reactive protein (CRP) levels.</p>
      <p><bold>RESULTS:</bold>The intima-media thickness (IMT) of the left common carotid artery (LCCA) in the FH+ group (0.568&#177;0.107mm) was statistically greater (p=0.029) than in the FH- group (0.477&#177;0.116mm). Multiple regression analysis identified age, overweight and obesity (determined by BMI), CRP, and LDL-cholesterol levels as independent predictors of the IMT in the LCCA.</p>
      <p><bold>CONCLUSION: </bold>FH+ individuals with no metabolic disorders presented greater IMT of the left common carotid artery (structural alteration) than FH- individuals, but normal vessel function.</p>
      <p><bold>Key words:</bold>Carotid artery, common/anatomy &amp; histology; diabetes mellitus type 2.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>Type 2 diabetes mellitus (DM2), a disease that is rapidly reaching pandemic proportions, is the leading cause of morbidity and mortality in Western countries<sup>1,2</sup>. The main etiology of death in patients with DM2 is cardiovascular. Therefore, DM2 is regarded as a "coronary risk equivalent"<sup>1,3</sup>.</p>
      <p>The presence of atherosclerosis is pronounced even before the clinical event, and much research has been conducted on early detection of atherosclerosis, both in DM2 and non-DM2 patients, over the last two decades<sup>4,5</sup>.</p>
      <p>High resolution carotid ultrasonography, initially described by Pignoli et al<sup>6</sup>, corroborated/ /&#134;later by the same author has proved to be very useful, as a real-time, non-invasive and reproducible method, with negligible risk and at reasonable cost, representing a true window to systemic atherosclerosis<sup>7</sup>. This method allows both structural (for example, intima-media thickness, which is considered a subclinical cardiovascular disease surrogate marker and a strong predictor of future vascular events) and functional (elasticity) vessel analysis<sup>5,7-16</sup>.</p>
      <p>Therefore, since a family history of diabetes, even in non-diabetics subjects with no known cardiovascular risk factors, is regarded as an increased coronary heart disease risk, <italic>per se</italic>, carotid ultrasonic measurements can be an important early atherosclerosis marker. The objective of this study is to analyze the structural and functional properties of the carotid arteries in subjects with and without a family history of type 2 diabetes, both groups with no other known cardiovascular risk factors<sup>17-19</sup>.</p>
      <p>
        <bold>Methods</bold>
      </p>
      <p>Between July 2004 and January 2006, first and second-degree relatives of patients with type 2 diabetes mellitus (FH+) and controls (FH-) - individuals with no family history of type 2 diabetes mellitus - were recruited through an announcement published in Rio de Janeiro newspapers, or through direct invitation by diagnosed DM2 patients of the Endocrinology Outpatient Clinic of Hospital Universit&#225;rio Ant&#244;nio Pedro (HUAP). The following exclusion criteria were used: age &lt; 18 years or &gt; 50 years; smoking habit; competitive physical activities; history of cardiovascular, cerebrovascularand/ or peripheral arterial disease; medication use; and/or pregnancy. Due to the strictness of the selection criteria, only 31 FH+ and 15 FH- volunteers were selected. Out of these, 12 FH+ and 2 FH- volunteers were excluded, at the initial evaluation, due to: systolic blood pressure (SBP) &gt; 140mmHg and/or diastolic blood pressure (DBP) &gt; 90mmHg; capillary fasting glycemia equal to or greater than 110mg/dl; 2-h postchallenge glycemia (OGTT) with 75 g dextrose &gt; 140mg/dl; total plasma cholesterol &gt; 240mg/dL and/or plasma triglycerides &gt; 150mg/dl. Ultimately, there were 19 FH+ volunteers (age range, 23 - 47 years; mean age, 37.94 years) and 13 FH- volunteers (age range, 21 - 46 years; mean age, 34 years), both men and women. All subjects signed a written informed consent to be included on a voluntary basis in the study, in accordance to the HUAP Human Research Ethics Committee Guidelines.</p>
      <p>The protocol required an initial assessment, which consisted of a standard questionnaire (personal data and family health history); anthropometric measurements (body mass index [BMI], calculated as weight in kilograms divided by height in square meters; waist circumference in centimeters [according to the 2005 International Diabetes Federation definition] which corresponds to the minimum circumference below the xiphoid process and above the navel; and waist-hip ratio); capillary fasting (twelve hours) glycemia (ACCUTREND, ROCHE, Inc.); blood pressure measurement (Korotkoff stages I and V), in a sitting position, after a 10-minute rest in a quiet room, at a room temperature of 22&#186;C, using a standard mercury sphigmomanometer, with an appropriate cuff for arm size, at heart level position; and pulse pressure (SBP - DBP) in mmHg.</p>
      <p>On the second assessment, after 12h-fasting, the individuals had a venous blood collection for biochemical analyses conducted in one sole clinical analysis laboratory. The laboratory tests included: fasting glucose (G) and 2h-postload of 75g of dextrose (DEXTROSOL) (automated method - glucose oxidase/peroxidase, ADVIA 1650, ADVIA 1650 BAYER KIT, Germany); plasma insulin (I) (chemiluminescence, DPC IMMULLITE 2000 KIT, USA); total cholesterol (automated enzymatic method - cholesterol oxidase/peroxidase, ADVIA 1650, ADVIA 1650 BAYER KIT, Germany); triglycerides (automated kinetic enzymatic method); HDL-cholesterol (automated enzymatic method, ADVIA 1650, ADVIA DASA KIT [direct method, conducted IN-HOUSE]), LDL-cholesterol (calculated by the Friedewald equation [LDL = Total cholesterol minus HDL minus {Triglycerides &#247; 5}]), CRP-us (turbidimetry - BORN, BN II DADE BERHING, DADE BERHING KIT, USA) - where values lower than 0.05 (due to method limitation) were considered equal to 0.05 - and leptin (radio immune assay, manual with Alto Delfio, IN-HOUSE KIT). The insulin resistance index was calculated from G and I values, using the mathematical model of the HOMA-IR ([G X I/22.5] X 0.0555, the glucose values expressed in mg/dl were transformed into mmol/l).</p>
      <p>The third assessment was conducted in the Echocardiography Laboratory of the Cardiology Service at HUAP, in a climatized room (room temperature between 22 and 24&#186;C), with a high resolution echography machine (VIVID 3 - General Electric, measurement accuracy up to hundredths of millimeters) equipped with a 13MHz linear transducer. All studies were conducted by one of two trained physicians, blinded to the examinees' clinical condition, following the American Society of Echocardiography and the Society of Vascular Medicine and Biology guidelines. A second analysis of the measurements was subsequently performed by the other physician (not the examiner), and all data were recorded and stored in individual CD-Rs, for later off-line processing. As to the bilateral carotid study, the patients were examined in a supine position, and a preliminary transversal plane scanning was performed, to assess the anatomy, followed by a longitudinal scanning (for B-mode imaging and measurements), with the head turned 45&#176;, for anterior oblique, lateral and posterior approaches (using only the posterior approach for measurements), on the opposite side of the artery to be studied. The intima-media thickness (IMT) obtained was defined as the distance between the lumen-intima interface and the media-adventitia interface of the posterior far wall of the common carotid artery (CCA) and internal carotid artery (ICA). The measurement reference points for the CCA were: point 0 (zero), immediately proximal to where the CCA dilates for its bifurcation; point 1, 5mm distal to point 0; point 2, 10mm distal to point 0; and point 3, 15mm distal to point 0. In the ICA, the measurement reference points were: point 0' at the carotid bulb; point 1', 2.5mm proximal to point 0'; and point 2', 5mm proximal to point 0'. The IMT measurements were performed on the R-wave peak of an electrocardiogram (ECG) - diastolic phase - recorded simultaneously to the echosonography. The statistical analysis values used were produced by one sole examiner based on the mean measurement for each studied arterial segment, namely, the left common carotid artery (LCCA), the right common carotid artery (RCCA), the left internal carotid artery (LICA) and the right internal carotid artery (RICA).</p>
      <p>After obtaining the common carotid arteries IMT and the interadventitial radius (R) (at longitudinal approach, during the systolic phase - T wave end, in the ECG - and diastolic phase - R-wave peak, in the ECG), the LCCA measurements were used (as the IMT was relevant in both studied groups) as analysis source for the arterial distensibility parameters, using the following formulas, in consonance with the ARIC Study and corroborating the SMART Study<sup>14-16</sup>:</p>
      <p>a) CAS = [D(s) - D(d)]/D(d);</p>
      <p>b) SI = ln [PAS / PAD]/CAS;</p>
      <p>c) CAC = ([Ds - Dd]/Dd / (PAS - PAD);</p>
      <p>d) YEM = (R/EMI) x {[PAS - PAD] / CAS},</p>
      <p>where CAS corresponds to the circumferential arterial strain; D(s) is the carotid diameter at systole; D(d) is the carotid diameter at diastole; SI is the carotid artery stiffness index (or &#223; index); nl means natural logarithm; SBP is the systolic blood pressure; DBP is the diastolic blood pressure; CAC is the carotid artery compliance coefficient; YEM is Young's elastic modulus and IMT is intima-media thickness.</p>
      <p>After both examiners' data had been obtained, the interobserver variability coefficient was calculated, using Spearman correlation analysis and Brand &amp; Altman graphic method.</p>
      <p>The Student's t-test and the Wilcoxon test were used for comparing the mean levels of the numerical variables. Multiple linear regression, using all the clinical and laboratory measurements as independent variables in each model, was used to study the influence of several factors on the response variables, such as RCCA, LCCA, RICA and LICA. The statistical program used for the analysis was the S-Plus 6.0, considering <italic>P</italic> significant when lower than 0.05 (<italic>p</italic>&lt;0.05).</p>
      <p>The sample size estimation for the main objective of this study was based on the Panacciuli et al<sup>17</sup> study, which separated the volunteers in a similar pattern - DM2 patient relatives (FH+) and controls (FH-). In the performed Student's t-test, the expected difference between the measurements was 0.07, the standard deviation was 0.05, the statistical power was 0.8, the <italic>p</italic> value was 0.05, resulting in 10 individuals for each group<sup>17</sup>.</p>
      <p>
        <bold>Results</bold>
      </p>
      <p>The general, laboratory and ultrasonographic data are shown in <xref ref-type="table" rid="t1-body2">Table 1</xref>, <xref ref-type="table" rid="t2-body2">2</xref> and <xref ref-type="table" rid="t3-body2">3</xref>.</p>
      <table-wrap id="t1-body2">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt01-en.jpg"/></table-wrap>
      <table-wrap id="t2-body2">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt02-en.jpg"/></table-wrap>
      <table-wrap id="t3-body2">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt03-en.jpg"/></table-wrap>
      <p>The HF+ and HF- subjects had no significant difference concerning age, sex, BMI, waist, hip, waist-hip ratio, systolic blood pressure, PP (pulse pressure), HDL-cholesterol, LDL-cholesterol, triglycerides, fasting glycemia, glucose oral tolerance test, fasting insulin, leptin and CRP-us. The LCCE IMT in the FH+ group was significantly greater than in the FH- group (<italic>p</italic>&lt;0.03). Conversely, despite the fact that the values found were within the limits of normality according to the applied methods, there was a significant difference (<italic>p</italic> &lt; 0.05) in the HOMA-IR and the total cholesterol levels between the HF+ group and the HF- group, being greater in the HF+ group, but with no correlation between the cholesterol levels and the LCCA IMT.</p>
      <p>With regard to carotid artery distensibility parameters, no significant difference was observed between the FH+ group and the FH- group, as shown in the angular coefficients of the regression analyses (in <italic>p</italic>) performed between these parameters (in separate) and other variables (<xref ref-type="table" rid="t4-body2">table 4</xref>). However, positive correlations were observed between age and the three indicators of arterial distensibility (SI, CAC and YEM) (<italic>p</italic>&lt;0.05); between fasting glycemia and the values of CAC and SI (<italic>p</italic>&lt;0.05); and between SBP and the values of YEM and CAC (<italic>p</italic>&lt;0.04). However,no correlation of statistical significance was detected between the radius and the distensibility and the artery structural measurements (<xref ref-type="table" rid="t5-body2">table 5</xref>).</p>
      <table-wrap id="t4-body2">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt04-en.jpg"/></table-wrap>
      <table-wrap id="t5-body2">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt05-en.jpg"/></table-wrap>
      <p>The results of the regression analysis between the LCCA IMT and other independent variables in all the individuals (<xref ref-type="table" rid="t6-body2">table 6</xref>) demonstrated a positive correlation with BMI (<italic>p</italic>&lt;0.001), age (<italic>p</italic>=0.001), CRP-us (p=0.007), DBP (p&lt;0.05), and HF+ (p=0.03).</p>
      <table-wrap id="t6-body2">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt06-en.jpg"/></table-wrap>
      <p>Altered waist circumference refers to measurements that exceed normal parameters for Brazil, as defined by International Diabetes Federation (<underline>&lt;</underline>80cm in women, and <underline>&lt;</underline>90cm in men) and by NCEP ATP III (<underline>&lt;</underline>88cm in women, and <underline>&lt;</underline>102cm in men).</p>
      <p>Concerning interobserver correlation, using LCCA measurements, it was observed that the levels measured by the two observers were similar (<italic>p</italic> = 0.294) and presented a significant correlation (r=0.737 and <italic>p</italic>=0.0109). As to LICA measurements, although it was observed that the mean measurements of both observers were also similar (<italic>p</italic>=0.7637), there was no significant correlation (r=0.1641 and <italic>p</italic>=0.5761).</p>
      <p>
        <bold>Discussion</bold>
      </p>
      <p>This is the first study with relatives of diabetic patients in which the carotid arterial segments were separately analyzed, with an evaluation of the carotid arteries structural and functional parameters.</p>
      <p>Concerning the carotid structural analysis, higher values of the common carotid IMT were observed in family members of diabetic patients (including young adults), in comparison to the control group, as in the study conducted by Nicola Pannacciulli et al<sup>17</sup>. Our study, however, demonstrated that the IMT and the BMI values (in both groups) were lower than in the mentioned study. The mean IMT values, in Pannaciulli's study, were 0.840&#177;0.010 mm in the FH+ group, and 0.770&#177;0.001 mm in the FH- group, compared to 0.560&#177;0.107 mm in the FH+ group, and 0.477&#177;0.110 mm in the FH- group, in our study. The mean BMI values (in Kg/m<sup>2</sup>), in Pannaciulli's study, were 30.0&#177;0.500 in the FH+ group, and 29.400&#177;0.500 in the FH- group, compared to 25.040 &#177;3.240, and 24.240 &#177;3.660 kg/m<sup>2</sup>, respectively, in our study. Corroborating the findings from Pannacciulli et al's study, we also found no correlation with fasting glycemia and/or OGTT.</p>
      <p>The CCA assessment, therefore, demonstrates a high degree of reproducibility, since in that segment the atherosclerosis process manifests as a diffuse thickening caused by progressive proliferation of smooth muscle cells and matrix deposition, it is a superficial segment, of straight walls, running parallel to the skin surface, of easy analysis (less time and effort to study), differing from ICA, where the manifestation of the atherosclerosis process occurs by focal atherosclerotic injury (or plaques), it is located deep within the neck, with walls of non-parallel origin in relation to the cervical skin surface. Furthermore, the CCA IMT is strongly, consistently and independently associated with coronary arterial disease.</p>
      <p>In our study, the significant correlation between the LCCA IMT values obtained by both observers confirms the reproducibility of the ultrasound imaging method in clinical practice, when performed by trained professionals, in agreement with previous studies. Nonetheless, such correlation was not observed in the ICA values, confirming the conclusion that its anatomic aspects limit the analysis.</p>
      <p>However, in keeping with other studies, our study considers the LCCA as the earliest atherosclerotic injury site, because the LCCA arises directly from the aortic arch, with lower shear stress (frictional force exerted by the circulating blood column on the intimal surface of the arteries), and DM2 is associated with lower CCA shear stress<sup>20-23</sup>.</p>
      <p>Adipose tissue, a true endocrine organ, produces several peptides (angiotensin, interleukin-6, tumor necrosis factor-alpha, PAI-1, leptin and adiponectin), which affect vascular structure. Interleukin-6 induces hepatic production of CRP, an acute phase protein. In addition to that, a study conducted by Balletshofer et al. observed the association between endothelial dysfunction and insulin-resistance in the young offspring of diabetic parents, regardless of the presence or absence of the classic cardiovascular risk factors<sup>24</sup>.</p>
      <p>In several observational and clinical studies, except one which demonstrated a weak correlation, the IMT has been a marker of subclinical vascular cardiac disease, in association with traditional risk factors for coronary heart disease (according to our findings: CRP, LDL-cholesterol and DBP) and the coronary atheroma load, being a predictor of subsequent cardiovascular events and an early indicator of atherosclerosis, besides being a valuable risk marker in non-invasive assessments<sup>5-7,10-11,14,20-27</sup>.</p>
      <p>With regard to carotid structural properties, no comparison with previous studies with the same group profiles could be conducted because none was found in the medical literature. Nevertheless, with different study groups, the same findings were observed, concerning the correlation between SI and CAC values and fasting glycemia, confirming that arterial stiffness is not independent from the risk factors for vascular events, and has a direct relationship (only regarding arterial compliance and elastic modulus, in our study) with systolic blood pressure levels. It is important to stress that the individuals analyzed in both groups of our study presented no significant differences in blood pressure levels, and both groups had normal blood pressure levels (according to JOINT VII guidelines)<sup>28</sup>. Furthermore, our study groups (both FH+ and FH-) had no classic cardiovascular risk factors, according to the Framingham risk score, and in spite of having greater HOMA-IR and total cholesterol values (although within the normal range), these were not sufficient to produce vascular functional changes, with levels of distensibility parameters lower than those found in other relevant studies. To confirm the importance of the heredity influence, we removed the largest HOMA-IR and total cholesterol values from the FH+ group, and the difference between the LCCA IMT of the two groups remained significant.</p>
      <p>Remodeling, another atherogenesis component that delays significant lumen compromise<sup>29</sup>, was not detected either in the FH+ group or the FH- group. (Mean age range under 50 years? Low mean IMT values?), due to the fact that no significant differences were found in the radius measurement between the FH+ and FH- groups.</p>
      <p>Many studies suggest that genetic factors influence the carotid IMT, which can be more discriminative than the arterial distensibility assessment in distinguishing patients of high and low cardiovascular risk, especially in relatives of diabetic patients. Ultrasonography is a valuable and practical tool for the study of the early evolution of atherosclerosis, transforming us from mere spectators into active inducers of a regression of the atherosclerotic process, even before its first clinical manifestations<sup>30</sup>. It is a proposed cardiovascular risk marker to estimate coronary heart disease susceptibility, since no existing risk score<sup>26</sup> includes altogether obesity, a positive family history of premature coronary heart disease, a family history of diabetes mellitus, sedentary life and/or psychological and economical factors, among others, focusing only on fatal and non-fatal coronary disease, but not ischemic stroke.</p>
      <p>Our study has several limitations; for example, the use of physical measurements to determine active cardiovascular disease, and the participants' self-reported absence of corresponding symptoms (i.e., all volunteers were apparently healthy individuals). However, this same methodology has been used in many other relevant studies involving this kind of analysis<sup>18</sup>. The small number of studied individuals did not allow a separate evaluation by sex, but that does not limit the importance of the study, since it meets Boissel's three criteria for surrogacy (efficiency and convenience, as a noninvasive method; linkage; and congruency). The advantages of the method range from a lower sample number to the confirmation of a direct association between the measurements and the disease process<sup>8,30</sup>. It is known that ultrasonography does not allow for differentiation between an intimal atherosclerotic process and medial hypertrophy, due to arterial blood pressure effects. At first, this can be viewed as a limitation of the method; however, there are data that corroborate the fact that IMT is more directly related to intimal atherosclerosis than to medial hypertrophy. Although automated measurements have not been used in our study, recent studies have shown that a standardized manual approach, conducted by well-trained technicians, can be as reliable as the automated approach. The echographic analysis has been limited to the far wall, differently from some previous studies which analyzed both near and far arterial walls. This was done because the accuracy would be reduced if the near wall was included, since the method does not allow for differentiation between intima and media measurements, which have been determined using excess gain. The blood pressure levels were assessed by indirect brachial measurements, despite the knowledge that the brachial blood pressure is usually 10 to 15% higher than the common carotid artery blood pressure. This was done based on Borow and Newburger<sup>31</sup> studies, which evidenced an excellent correlation between the systemic blood pressure levels measured by invasive methods and the noninvasive brachial blood pressure measurements<sup>15</sup>. We used indirect methods for evaluating insulin-resistance (IR) - fasting insulinemia, HOMA-IR and oral glucose tolerance test - as well as indirect IR markers - body mass index, abdominal circumference and triglycerides serum concentration - instead of the gold-standard of the American Diabetics Association - hyperinsulinemic euglycemic clamp - because the latter method, in spite of producing purer and more reproducible data on tissue insulin action, requires a long time, instant analysis instruments for measuring blood glucose levels, infusion bombs and highly specialized and trained personnel. Besides, a laboratory investigation method of IR analysis which fulfills all the universally accepted and used criteria is still not available. Therefore, according to many studies, indirect methods are more prone to be used in the clinical practice<sup>32</sup>. No analysis was separately conducted according to race. Brazil is a country of racial miscegenation and, therefore, it is very difficult to separate volunteers by race. We did not use random selection, and this may be viewed as a negative aspect of the study. Nevertheless, all our efforts to eliminate every factor that could have obscured our results turned us into the most obstinate searchers of "ideal volunteers".</p>
      <p>It is noteworthy that, by the conclusion of the study, the normal reference values for intima-media thickness (IMT) had been ratified by The American Society of Echocardiography, in August 2006, and the new values were much higher than those in our findings<sup>33</sup>. Nevertheless, in February 2008, Lim et al<sup>34</sup> conducted a study with 137 healthy participants, and found normal values for the LCC IMT, in agreement with our results, in participants with no DM2 family history (age range, 35-39 years - 0.49&#177;0.06; 40-45 years - 0.52&#177;0.06 - in the Lim et al<sup>34</sup> study) separated according to age group. Those results placed our group of individuals with a family history of DM2 at an older age group (50-59 years - 0.56&#177;0.08 - Lim et al<sup>34</sup> study), reiterating what Sir William Osler declared in 1897: "We are as old as our arteries"<sup>34</sup>.</p>
      <p>
        <bold>Conclusion</bold>
      </p>
      <p>Individuals with a family history of DM2, even those with no glucose-intolerance and/or altered basal insulin levels, presented greater values of carotid intima-media thickness (IMT) (structural change), particularly in the left common carotid territory, when compared to the group with no family history of DM2, although no functional changes were observed in the blood vessels.</p>
      <p>The consequences resulting from a genetic predisposition to DM2, probably associated with insulin resistance, on the carotid IMT values, particularly in the left common carotid territory, preceding the vascular functional alteration, needs to be further investigated in order to elucidate this association.</p>
      <p>
        <bold>Acknowledgments</bold>
      </p>
      <p>The authors would like to thank all volunteers, the medical staff of the Endocrinology Service at HUAP, and the Bronstein Laboratory. Without their assistance, the conduction of this study would not have been possible.</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>There were no external funding sources for this study.</p>
      <p>
        <bold>Study Association</bold>
      </p>
      <p>This article is part of the thesis of Master submitted by S&#244;nia Silva Prado, from <italic>Universidade Federal Fluminense</italic>.</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">Estudio estructural y funcional carot&#237;deo en familiares de pacientes con diabetes mellitus tipo 2</article-title>
      </title-group>
      <abstract xml:lang="es">
        <p>FUNDAMENTO: La diabetes mellitus tipo 2 (DM2) es la principal causa de morbilidad y mortalidad en los pa&#237;ses occidentales, principalmente de origen cardiovascular. Con base en la historia familiar de diabetes - aun en individuos no diab&#233;ticos -, ante el aumento de riesgo de enfermedad cardiaca coronaria, se hace necesaria la utilizaci&#243;n de reconocidos marcadores sustitutos de aterosclerosis precoz, como las mediciones por ecograf&#237;a carot&#237;dea. OBJETIVO: Comparar tanto caracter&#237;sticas estructurales (espesor &#237;ntima-medio - EIM) como funcionales (medidas de distensibilidad) de arterias carot&#237;deas de los individuos con historia familiar (HF+) y de los no parientes de portadores de DM2 (HF-), todos sin factores de riesgo cardiovasculares reconocidos. M&#201;TODOS: Un total de 32 individuos (19 HF+ y 13 HF-), con edad entre 21 y 47 a&#241;os, de ambos sexos, fueron sometidos a estudio ultrasonogr&#225;fico de alta resoluci&#243;n de las car&#243;tidas (comunes e internas) bilateralmente. Los grupos presentaban comparaci&#243;n (P &gt; 0,05) de edad, &#237;ndice de masa corporal (IMC), presi&#243;n arterial, glucosa y insulina de ayuno, leptina y prote&#237;na C reactiva (PCR). RESULTADOS: El espesor &#237;ntima-medio de las arterias car&#243;tidas comunes izquierdas (ACCI) se mostr&#243; estad&#237;sticamente m&#225;s elevado (P = 0,029) en los HF+ (0,568 &#177; 0,107 mm) que en los HF- (0,477&#177; 0,116 mm). El an&#225;lisis de regresi&#243;n m&#250;ltiple identific&#243; como pronosticadores independientes de la EIM de ACCI la edad, el IMC superior al normal, la PCR y el LDL-colesterol. CONCLUSI&#211;N: Individuos con historia familiar de DM2, aun sin des&#243;rdenes metab&#243;licas laboratoriales detectadas, presentaron mayor espesor &#237;ntima-medio en territorio carot&#237;deo com&#250;n izquierdo que pacientes sin tal parentesco. Sin embargo, no hubo alteraci&#243;n funcional de la arteria.</p>
      </abstract>
      <kwd-group xml:lang="es">
        <kwd>Arteria car&#243;tida primitiva</kwd>
        <kwd>diabetes mellitus tipo 2</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>ART&#205;CULO ORIGINAL</bold>
      </p>
      <p>
        <fn id="top-body3">
          <label>
            <bold>Estudio estructural y funcional carot&#237;deo en familiares de pacientes con diabetes mellitus tipo 2</bold>
          </label>
          <p>
            <bold>S&#244;nia Silva Prado<sup>I</sup>; M&#225;rio Luiz RibeiroI; Gilberto Perez Cardoso<sup>II</sup>; Kelb Bousquet-Santos<sup>III</sup>; Luis Guillermo Coca Velarde<sup>IV</sup>; Ant&#244;nio Cl&#225;udio Lucas da N&#243;brega<sup>III</sup></bold>
          </p>
        </fn>
      </p>
      <p><sup>I</sup>Hospital Universit&#225;rio Ant&#244;nio Pedro - Universidade Federal Fluminense (UFF), Niter&#243;i, RJ - Brasil</p>
      <p><sup>II</sup>Departamento de Ci&#234;ncias M&#233;dicas - UFF, Niter&#243;i, RJ - Brasil</p>
      <p><sup>III</sup>Departamento de Fisiologia e Farmacologia - UFF, Niter&#243;i, RJ - Brasil</p>
      <p><sup>IV</sup>Instituto de Matem&#225;tica - UFF; Universidade Federal Fluminense (UFF), Niter&#243;i, RJ - Brasil</p>
      <p>Correspondencia</p>
      <p>
        <bold>RESUMEN</bold>
      </p>
      <p><bold>FUNDAMENTO: </bold>La diabetes mellitus tipo 2 (DM2) es la principal causa de morbilidad y mortalidad en los pa&#237;ses occidentales, principalmente de origen cardiovascular. Con base en la historia familiar de diabetes - aun en individuos no diab&#233;ticos -, ante el aumento de riesgo de enfermedad cardiaca coronaria, se hace necesaria la utilizaci&#243;n de reconocidos marcadores sustitutos de aterosclerosis precoz, como las mediciones por ecograf&#237;a carot&#237;dea.</p>
      <p><bold>OBJETIVO: </bold>Comparar tanto caracter&#237;sticas estructurales (espesor &#237;ntima-medio - EIM) como funcionales (medidas de distensibilidad) de arterias carot&#237;deas de los individuos con historia familiar (HF+) y de los no parientes de portadores de DM2 (HF-), todos sin factores de riesgo cardiovasculares reconocidos.</p>
      <p><bold>M&#201;TODOS: </bold>Un total de 32 individuos (19 HF+ y 13 HF-), con edad entre 21 y 47 a&#241;os, de ambos sexos, fueron sometidos a estudio ultrasonogr&#225;fico de alta resoluci&#243;n de las car&#243;tidas (comunes e internas) bilateralmente. Los grupos presentaban comparaci&#243;n (P &gt; 0,05) de edad, &#237;ndice de masa corporal (IMC), presi&#243;n arterial, glucosa y insulina de ayuno, leptina y prote&#237;na C reactiva (PCR).</p>
      <p><bold>RESULTADOS: </bold>El espesor &#237;ntima-medio de las arterias car&#243;tidas comunes izquierdas (ACCI) se mostr&#243; estad&#237;sticamente m&#225;s elevado (P = 0,029) en los HF+ (0,568 &#177; 0,107 mm) que en los HF- (0,477&#177; 0,116 mm). El an&#225;lisis de regresi&#243;n m&#250;ltiple identific&#243; como pronosticadores independientes de la EIM de ACCI la edad, el IMC superior al normal, la PCR y el LDL-colesterol.</p>
      <p><bold>CONCLUSI&#211;N: </bold>Individuos con historia familiar de DM2, aun sin des&#243;rdenes metab&#243;licas laboratoriales detectadas, presentaron mayor espesor &#237;ntima-medio en territorio carot&#237;deo com&#250;n izquierdo que pacientes sin tal parentesco. Sin embargo, no hubo alteraci&#243;n funcional de la arteria. </p>
      <p><bold>Palabras clave: </bold>Arteria car&#243;tida primitiva/anatom&#237;a &amp; histolog&#237;a, diabetes mellitus tipo 2.</p>
      <p>
        <bold>Introducci&#243;n</bold>
      </p>
      <p>La diabetes mellitus tipo2 (DM2), una enfermedad que alcanza r&#225;pidamente proporciones pand&#233;micas, es la principal causa de morbilidad y mortalidad en los pa&#237;ses occidentales<sup>1,2</sup>. La principal etiolog&#237;a de las muertes en portadores de DM2 es de origen cardiovascular, lo que constituye un "riesgo coronario equivalente"<sup>1,3</sup>.</p>
      <p>Las evidencias de aterosclerosis ya est&#225;n elevadas antes aun del cuadro manifiesto, y hay muchos estudios (en portadores o no de DM2), en los &#250;ltimos 20 a&#241;os, sobre formas de detecci&#243;n de aterosclerosis precoz<sup>4,5</sup>.</p>
      <p>El ultrasonido carot&#237;deo de alta resoluci&#243;n, inicialmente descrito por Pignoli et al<sup>6</sup> y corroborado m&#225;s tarde por el mismo autor, ha se mostrado una herramienta &#250;til, en tiempo real, no-invasiva, reproductible, segura y a un costo aceptable, una verdadera ventana para la aterosclerosis sist&#234;mica<sup>7</sup>. Permite tanto un estudio estructural (como espesor intimo-medio, ya considerado marcador sustituto de enfermedad cardiovascular subcl&#237;nica y un fuerte pronosticador de futuros eventos vasculares) como funcional (elasticidad) del vaso<sup>5,7-16</sup>.</p>
      <p>De esa manera, cuando se toma en consideraci&#243;n la historia familiar de diabetes, aun en individuos no diab&#233;ticos y sin los factores de riesgo cardiovasculares conocidos - como un aumento <italic>per se</italic> de riesgo de enfermedad cardiaca coronaria -, la utilizaci&#243;n de las mediciones ecogr&#225;ficas carot&#237;deas puede convertirse en un importante marcador de aterosclerosis precoz<sup>17-19</sup>.</p>
      <p>
        <bold>M&#233;todos</bold>
      </p>
      <p>Se invitaron, mediante los medios de difusi&#243;n de Rio de Janeiro, y por intermedio de los pacientes del ambulatorio de endocrinolog&#237;a del Hospital Universitario Ant&#244;nio Pedro (Huap) con diagn&#243;stico de diabetes mellitus en la ficha medica, a parientes de primero y segundo grados de portadores de diabetes mellitus tipo2 (HF+) y de pacientes-control (aquellos sin historia familiar de diabetes mellitus tipo 2 - HF-) para entrevista en el periodo de julio de 2004 a enero de 2006. Se excluyeron a los individuos con: edad inferior a los 18 a&#241;os y/o superior a los 50; h&#225;bitos de tabaquismo; actividad deportiva competitiva; historia de enfermedad cardiovascular, cerebrovascular y/o de enfermedad arterial perif&#233;rica; relato de uso de cualquier tratamiento terap&#233;utico; y mujeres en fase gestacional. Ante el rigor de selecci&#243;n, se obtuvieron inicialmente 31 voluntarios HF+ y 15 HF. De esos pacientes, se excluyeron la cantidad de 12 HF+ y 2 HF- en el examen cl&#237;nico inicial, ya que presentaban presi&#243;n arterial sist&#243;lica (PAS) &gt;140 mmHg y/o presi&#243;n arterial diast&#243;lica (PAD) &gt;90 mmHg y glucemia capilar de ayuno &gt;110 mg/dl. En el an&#225;lisis laboratorial, se excluyeron a los individuos con glucemia de ayuno mayor o igual a 110 mg/dl y/o glucemia tras 2 horas de carga oral de 75 g de dextrosa (prueba de tolerancia oral a la glucosa - PTOG) mayor que 140 mg/dl, colesterol s&#233;rico total &gt;240 mg/dl y/o triglic&#233;ridos s&#233;ricos &gt;150 mg/dl. Los grupos, de ambos los sexos, tuvieron la caracter&#237;stica que sigue a continuaci&#243;n: 19 HF+, edad entre 23 y 47 a&#241;os (promedio 37,94 a&#241;os); 13 HF-, edad de 21 a 46 a&#241;os (promedio 34 a&#241;os).</p>
      <p>Se obtuvo el formulario de consentimiento informado de todos los voluntarios antes de su ingreso al estudio. El estudio fue aprobado por el Comit&#233; de &#201;tica del Huap, en investigaci&#243;n involucrando seres humanos.</p>
      <p>A la visita inicial, el voluntario fue sometido a un cuestionario estandarizado (datos personales y antecedentes m&#243;rbidos familiares). Despu&#233;s, se hizo la obtenci&#243;n de los valores antropom&#233;tricos: &#237;ndice de masa corporal (IMC); peso/altura<sup>2</sup> (en kg/m<sup>2</sup>); per&#237;metro de la cintura (c<sub>1</sub>) y de la cadera (c<sub>2</sub>) en cent&#237;metros - en consonancia con el International Diabetes Federation (2005), en el que la cintura corresponde a la m&#237;nima circunferencia entre el ap&#233;ndice xifoide y el ombligo. Se calcul&#243; tambi&#233;n la relaci&#243;n entre los per&#237;metros c<sub>1</sub>/c<sub>2</sub>, lleg&#225;ndose al &#237;ndice cintura-cadera (ICC). Seguidamente se midi&#243; la glucemia de ayuno (de 12 horas) capilar (Accutrend, Roche, Inc.). Se midi&#243; la presi&#243;n arterial sist&#233;mica (PA - fases I y V de Korotkoff), con el individuo en la posici&#243;n sentada, 10 minutos tras reposo en ambiente tranquilo, con temperatura de cerca de 22&#186; C, utiliz&#225;ndose un esfigmoman&#243;metro de mercurio est&#225;ndar, con manguito adecuado a las dimensiones del brazo, posicionado en el nivel del coraz&#243;n. La presi&#243;n del pulso (PAS - PAD), se calcul&#243; en mil&#237;metros de mercurio.</p>
      <p>A la segunda visita, en un &#250;nico centro laboratorial de an&#225;lisis cl&#237;nicos, tras ayuno de 12 horas, los individuos fueron sometidos, por medio de colecta de sangre venosa (vena antecubital), a la medici&#243;n de: glucemia de ayuno (G) y PTOG (m&#233;todo automatizado: glucosa oxidasa/peroxidasa, Advia 1650, <italic>kit</italic> Advia 1650, Bayer, Alemania); insulina plasm&#225;tica (I) (quimioluminescencia, Immullite, 2000, <italic>kit</italic> DPC, EUA); colesterol total (m&#233;todo enzim&#225;tico automatizado: colesterol oxidasa/peroxidasa, Advia 1650, <italic>kit</italic> Advia 1650, Bayer, Alemania); triglic&#233;ridos (m&#233;todo cin&#233;tico enzim&#225;tico automatizado); HDL-colesterol (m&#233;todo enzim&#225;tico automatizado, Advia 1650, <italic>kit</italic> Advia Dasa [m&#233;todo directo, fabricaci&#243;n IN-HOUSE]); LDL-colesterol (calculado mediante ecuaci&#243;n de Friedewald [LDL-colesterol = colesterol total - (HDL-colesterol) + triglic&#233;ridos/5]); PCR-us (turbidimetria: Born, BN II Dade Berhing, <italic>kit</italic> Dade Berhing, EUA) - en que valores inferiores a 0,05, por limitaci&#243;n del m&#233;todo, se los consideraron como iguales a 0,05 -; y leptina (radioinmunoensayo, manual con Alto Delfio, <italic>kit</italic> IN-HOUSE). A partir de la obtenci&#243;n de los valores G e I, se calcul&#243; el &#237;ndice de resistencia a la insulina con la utilizaci&#243;n del modelo matem&#225;tico de Homa-IR ((I* G/22,5)* 0,0555).</p>
      <p>La tercera visita tuvo lugar en el laboratorio de ecocardiograf&#237;a del servicio de cardiolog&#237;a del Huap, en sala climatizada (22 y 24&#186;C). Se utiliz&#243; un aparato ecogr&#225;fico de alta resoluci&#243;n (Vivid 3, General Eletric), con capacidad de medici&#243;n de hasta cent&#233;simo de mil&#237;metros y transductor lineal 13 MHz. Todos los estudios fueron realizados por uno de los dos m&#233;dicos entrenados - "ciegos" a la condici&#243;n cl&#237;nica de los examinados.</p>
      <p>Tambi&#233;n atendiendo a las especificaciones de las sociedades nacionales de ecocardiograf&#237;a, rean&#225;lisis de las mediciones fueron realizados por otro m&#233;dico (diferente del examinador), con todos los datos gravados y almacenados en CD-ROM, para subsiguiente procesamiento <italic>off-line</italic>. El estudio carot&#237;deo fue bilateral - examinado en posici&#243;n supina -, con preliminar barrido exploratorio transverso (para acceder su anatom&#237;a), seguido de an&#225;lisis longitudinal (para obtenci&#243;n de las im&#225;genes, en m&#243;dulo B, y las medidas). Se posicion&#243; la cabeza a un &#225;ngulo 45&#186; - para acceso oblicuo anterior, lateral y posterior (se tom&#243; en cuenta como acceso de an&#225;lisis el posterior) -, hacia el lado contrario a la localizaci&#243;n de la arteria a estudiarse. Seguidamente, se obtuvo el espesor &#237;ntima-medio (EIM), definido como la distancia entre el borde de la interfase lumen-&#237;ntima carot&#237;dea y el borde de la interfase media-adventicia, de la pared posterior de las arterias carot&#237;deas com&#250;n (ACC) e interna (ACI).</p>
      <p>Los puntos de referencia para la medici&#243;n de la ACC fueron: en el punto antes de la ACC dilatarse para su bifurcaci&#243;n (punto cero), 5 mm distales del punto 0 (punto 1), 10 mm distales del punto 0 (punto2) y 15 mm distales del punto 0 (punto3). Respecto a la ACI, la medici&#243;n fue: en el nivel del bulbo (punto 0'), a 2,5 mm proximales del punto 0' (ponto 1') y a 5 mm proximales del punto 0' (punto 2'). Las mediciones del EIM se realizaron de acuerdo con el punto m&#225;ximo de la onda R del electrocardiograma (ECG) - fase diast&#243;lica - de grabaci&#243;n simult&#225;nea al aparato de ecograf&#237;a.</p>
      <p>Los valores utilizados para an&#225;lisis estad&#237;stico fueron generados por un &#250;nico examinador y con base en el promedio de las diferentes medidas de cada segmento arterial estudiado. Es decir, arteria car&#243;tida com&#250;n izquierda (ACCI), arteria car&#243;tida com&#250;n derecha (ACCD), arteria car&#243;tida interna izquierda (ACII), arteria car&#243;tida interna derecha (ACID).</p>
      <p>Tras la obtenci&#243;n del EIM y del rayo interadventicio (R) (al corte longitudinal, durante las fases sist&#243;lica, al final de la onda T del ECG, y diast&#243;lica) de las arterias car&#243;tidas comunes, utilizamos las medidas de la ACCI - debido a la relevancia del EIM, con relaci&#243;n a los dos grupos estudiados - como fuente de an&#225;lisis de los par&#225;metros de distensibilidad arterial, de acuerdo con las formulaciones de los estudios Aric y Smart, se&#241;aladas m&#225;s adelante<sup>14-16</sup>:</p>
      <p>a) TAC = [D(s) - D(d)]/D(d);</p>
      <p>b) SI = ln [PAS / PAD]/TAC;</p>
      <p>c) CAC = ([Ds-Dd]/Dd / (PAS - PAD);</p>
      <p>d) YEM = (R/EMI) x {[PAS - PAD] / TAC},</p>
      <p>TAC - tensi&#243;n arterial circunferencial; D(s) - di&#225;metro carot&#237;deo a la s&#237;stole; D(d) = di&#225;metro carot&#237;deo a la di&#225;stole; SI = &#237;ndice de rigidez arterial carot&#237;dea (o &#237;ndice &#946;); ln = logaritmo natural; CAC = coeficiente de complacencia arterial carot&#237;dea; YEM = m&#243;dulo el&#225;stico de Young.</p>
      <p>Luego de la consecuci&#243;n de los datos por dos examinadores, se calcul&#243; el coeficiente de variabilidad interobservador. Para el estudio de la concordancia de las mediciones de los valores de EIM carot&#237;deo (variables num&#233;ricas) entre los dos observadores, en los dos grupos estudiados, se utilizaron la correlaci&#243;n de Spearman y el m&#233;todo gr&#225;fico de Brand &amp; Altman.</p>
      <p>Se utilizaron las pruebas t de Student y Wilcoxon para comparaci&#243;n de los niveles promedios de variables num&#233;ricas. Para el estudio de la influencia de diversos factores sobre variables respuestas, como ACCD, ACCI, ACID y ACII, se utilizaron modelos de regresi&#243;n lineal m&#250;ltiple, con todas las medidas cl&#237;nicas y laboratoriales como variables independientes, en cada uno de los modelos. El programa estad&#237;stico utilizado para an&#225;lisis fue el S-Plus 6.0, con <italic>P</italic> significativo cuando menor que 0,05 (<italic>P</italic> &lt; 0,05).</p>
      <p>A fin de alcanzar el objetivo principal del estudio, y tomando como referencia el estudio de Pannacciulli et al<sup>17</sup> - que agruparon sus voluntarios de forma semejante al nuestro inter&#233;s (entre HF+ y HF-) al realizar una prueba t -, el c&#225;lculo muestral se bas&#243; en la diferencia esperada entre las medidas de 0,07 mm, en una desviaci&#243;n est&#225;ndar esperada de 0,05 para un poder estad&#237;stico de 0,8 y un valor de <italic>P</italic> de 0,05. As&#237;, se pudo llegar al n&#250;mero de 10 individuos en cada grupo<sup>17</sup>.</p>
      <p>
        <bold>Resultados</bold>
      </p>
      <p>Los datos generales, bioqu&#237;micos y de ultrasonido est&#225;n detallados en las <xref ref-type="table" rid="t1-body3">Tablas 1</xref>, <xref ref-type="table" rid="t2-body3">2</xref> y <xref ref-type="table" rid="t3-body3">3</xref>.</p>
      <table-wrap id="t1-body3">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt01-es.jpg"/></table-wrap>
      <table-wrap id="t2-body3">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt02-es.jpg"/></table-wrap>
      <table-wrap id="t3-body3">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt03-es.jpg"/></table-wrap>
      <p>Los parientes de diab&#233;ticos (HF+) y los controles (HF-) se compararon, sin diferencia significativa, en edad, sexo, IMC, cintura, cadera, ICC, presi&#243;n arterial sist&#243;lica, PP (presi&#243;n de pulso), HDL-colesterol, LDL-colesterol, triglic&#233;ridos, glucemia de ayuno, prueba de tolerancia oral a la glucosa, insulina de ayuno, leptina y PRC-us. El EIM de ACCI fue significativamente mayor en individuos HF+ cuando comparados a los HF-(<italic>P</italic> &lt; 0,03). Hay que resaltar que, debido al hecho de los valores encontrados estar dentro de los l&#237;mites de normalidad, y asimismo por los m&#233;todos empleados, ocurri&#243; tambi&#233;n una diferencia significativa de los niveles de HOMA-IR y colesterol total entre los HF+ y los HF-; mostr&#225;ndose mayor en los primeros (<italic>P</italic> &lt; 0,05 en ambos), sin, con todo, haber correlaci&#243;n entre los niveles de colesterol y el EIM de ACCI.</p>
      <p>No se observ&#243;, sin embargo, diferencia significativa respecto a los par&#225;metros de distensibilidad arterial carot&#237;dea, entre los HF+ y los HF-, como se detall&#243; anteriormente (<xref ref-type="table" rid="t4-body3">tab. 4</xref>) en los coeficientes angulares del an&#225;lisis de regresi&#243;n (expresos en <italic>P</italic>) entre esos par&#225;metros, en separado, y otras variables. Por otro lado, se revel&#243; positiva la correlaci&#243;n entre los tres par&#225;metros (SI, CAC e YEM) y la edad (con <italic>P</italic> &lt; 0,05), con la glucemia de ayuno correlacionada al CAC y al SI (<italic>P</italic> &lt; 0,05) y a la PAS con YEM y CAC (<italic>P</italic> &lt; 0,04). No obstante, no se detect&#243; correlaci&#243;n de significancia estad&#237;stica entre el rayo y las medidas de distensibilidad y de la estructura arterial (<xref ref-type="table" rid="t5-body3">tab. 5</xref>).</p>
      <table-wrap id="t4-body3">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt04-es.jpg"/></table-wrap>
      <table-wrap id="t5-body3">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt05-es.jpg"/></table-wrap>
      <p>Los resultados del an&#225;lisis de regresi&#243;n de EIM de ACCI con otras variables independientes en todos los individuos (<xref ref-type="table" rid="t6-body3">tab. 6</xref>) denotaron correlaci&#243;n positiva con IMC (<italic>P</italic> &lt; 0,001), edad (<italic>P</italic> = 0,001), PCR-us (<italic>P</italic> = 0,007), PAD (<italic>P</italic> &lt; 0,05) y factor pariente de portador de DM2 (<italic>P</italic> = 0,03).</p>
      <table-wrap id="t6-body3">
        <graphic xlink:href="1678-4170-abc-92-03-0196-00006-gt06-es.jpg"/></table-wrap>
      <p>En tiempo, consideramos como cintura alterada la que cuyo valor excede los par&#225;metros normales adoptados tanto por International Diabetes Federation, que establece, para Brasil, los valores: cintura femenina <underline>&lt;</underline> 80 cm y masculina <underline>&lt;</underline> 90 cm; como por NCEP ATP III: femenina <underline>&lt;</underline> 88 cm y masculina <underline>&lt;</underline> 102 cm.</p>
      <p>Respecto a la correlaci&#243;n interobservador, utiliz&#225;ndose las mediciones de ACCI, se observ&#243; que los niveles medidos por los dos observadores fueron semejantes (<italic>P</italic> = 0,2944) y presentaron una correlaci&#243;n significativa (r = 0,737 y <italic>P</italic> = 0,0109). Para las mediciones de ACII, adem&#225;s de la semejanza de las mediciones entre los observadores (0,7637), no se detect&#243; correlaci&#243;n significativa (r = 0,1641 y P = 0,5761).</p>
      <p>
        <bold>Discusi&#243;n</bold>
      </p>
      <p>Este es el primero estudio con parientes de diab&#233;ticos en el que se analizan, en separado, los seguimientos arteriales carot&#237;deos, adem&#225;s de la asociaci&#243;n de evaluaci&#243;n de los par&#225;metros estructurales y funcionales de la car&#243;tida.</p>
      <p>Con referencia al estudio estructural carot&#237;deo, se pudo observar el mismo cuadro de mayor EIM carot&#237;deo com&#250;n en parientes de diab&#233;ticos (tambi&#233;n en adultos j&#243;venes), cuando comparados a los controles, como revela Pannacciulli et al<sup>17</sup>. Sin embargo, nuestro estudio demostr&#243; que los valores de EIM e IMC (en ambos grupos) fueron menores que en el estudio de Pannacciulli. El promedio de EIM fue de 0,840 mm &#177; 0,010 en HF+ y 0,770 mm &#177; 0,001 en los HF-<italic>versus</italic> 0,560 mm &#177; 0,107 en HF+ y 0,477 mm &#177; 0,110 en HF-, este &#250;ltimo en nuestro estudio. El promedio de IMC (kg/m<sup>2</sup>) por ellos encontrado fue de 30,0 &#177; 0,500 en HF+ y 29,400 &#177; 0,500 en HF- <italic>versus</italic> 25,040 &#177; 3,240 y 24,240 &#177; 3,660, respectivamente, en nuestro estudio. No detectamos tampoco una asociaci&#243;n con glucemia de ayuno y/o con la PTOG.</p>
      <p>La ACC (independientemente de la asociaci&#243;n con la enfermedad arterial coronaria) demuestra un alto grado de reproductibilidad, cuya manifestaci&#243;n del proceso ateroscler&#243;tico se presenta de grosor difuso por proliferaci&#243;n progresiva de c&#233;lulas musculares lisas y deposici&#243;n de matriz; un segmento superficial, de paredes retas, que reposa en paralelo a la superficie de la piel, de f&#225;cil an&#225;lisis. Ello difiere de la ACI, cuya manifestaci&#243;n se muestra por lesi&#243;n focal ateroscler&#243;tica (o placas), de localizaci&#243;n profunda en el cuello, con paredes de origen no paralelas, as&#237; como su reposo (en relaci&#243;n a la superficie cervical).</p>
      <p>En el presente estudio, la correlaci&#243;n significativa de los valores obtenidos de EIM de ACCI por los dos observadores refuerza dicha reproductibilidad del m&#233;todo ultrasonogr&#225;fico en la pr&#225;ctica cl&#237;nica, de acuerdo con los estudios previos. Esa correlaci&#243;n no se aplica a los valores de ACI, lo que refuerza su aspecto anat&#243;mico limitante de an&#225;lisis.</p>
      <p>Al tomarse en cuenta que la ACCI nace directamente del arco a&#243;rtico - con menor estr&#233;s de corte (EC - <italic>shear stress</italic>) y tambi&#233;n asociaci&#243;n de DM2 con menor EC de la ACC - se hace necesario resaltar que <italic>es en arteria car&#243;tida com&#250;n mismo donde</italic> lesiones ateroscler&#243;ticas se desarrollan m&#225;s precozmente<sup>20-23</sup>.</p>
      <p>En estudio de Balletshofer, se reafirma la asociaci&#243;n entre disfunci&#243;n endotelial y resistencia insul&#237;nica en j&#243;venes hijos de diab&#233;ticos, independientemente de los cl&#225;sicos factores de riesgo cardiovasculares<sup>24</sup>.</p>
      <p>En estudios observacionales y cl&#237;nicos, a excepci&#243;n de uno de correlaci&#243;n d&#233;bil, el EIM se mostr&#243; un marcador de enfermedad cardiaca vascular subcl&#237;nica, asociada a tradicionales factores de riesgo tanto de enfermedad cardiaca coronaria (de acuerdo con nuestros resultados: PCR, LDL-colesterol y PAD) como de carga ateroscler&#243;tica coronaria. Fue tambi&#233;n predictivo de subsiguientes cuadros cardiovasculares y un precoz indicador de aterosclerosis, adem&#225;s de un valioso marcador de riesgo por an&#225;lisis no invasiva<sup>5-7,10-11,14,20-27</sup>.</p>
      <p>Respecto a las propiedades estructurales carot&#237;deas, ninguna comparaci&#243;n con estudios previos, con igual perfil de individuos de an&#225;lisis, se pudo realizar a causa de su no existencia en la literatura m&#233;dica. Al hacerse referencia a otra poblaci&#243;n de estudio, se verifica concordancia en los hallazgos de correlaci&#243;n de SI y CAC, con glucemia de ayuno.</p>
      <p>Adem&#225;s de ello, se ratifica que la rigidez arterial no es independiente de los factores de riesgo de cuadros vasculares, con relaci&#243;n directa (en nuestro estudio s&#243;lo respecto a la complacencia arterial y al m&#243;dulo el&#225;stico) con los niveles de PAS. En lo que se refiere a los niveles de presi&#243;n arterial, hay que evidenciarse que los individuos de los dos grupos analizados en nuestro estudio no presentaban diferencias significativas entre ellos, adem&#225;s de presentar valores normales (criterios JOINT VII)<sup>28</sup>.</p>
      <p>Asimismo, hay que a&#241;adir que nuestros grupos de estudio (tanto HF+ como HF-) no presentaban los cl&#225;sicos factores de riesgo cardiovasculares del score de Framingham. Adem&#225;s de ello, por cuenta de mayores valores de HOMA-IR y colesterol total (dentro, con todo, de los l&#237;mites de la normalidad), esos grupos no fueron suficientes para producir alteraci&#243;n funcional vascular, con niveles detectables de par&#225;metros de distensibilidad inferiores a los otros estudios pertinentes. A&#250;n se reafirma que la retirada de los mayores valores de HOMA-IR y CT de los HF+, como un an&#225;lisis aislado, mantuvo la diferencia significativa de los niveles de EIM de ACCI entre los grupos estudiados, lo que refuerza la influencia de las caracter&#237;sticas hereditarias.</p>
      <p>En virtud de no haber sido detectada diferencia significativa de las medidas de rayo entre los HF+ y los HF-, tampoco detectamos otro componente de la aterog&#233;nesis (&#191;grupo de edad promedio inferior a 50 a&#241;os?, &#191;bajos &#237;ndices promedios de EIM?), que desempe&#241;a un rol de freno en el desarrollo del significante compromiso del lumen arterial (remodelaci&#243;n)<sup>29</sup>.</p>
      <p>Varios estudios sugieren factores gen&#233;ticos como influenciadores del EIM carot&#237;deo. &#201;ste puede ser de mayor poder discriminatorio entre los pacientes de mayor y menor riesgo cardiovascular en comparaci&#243;n con el an&#225;lisis de la distensibilidad arterial. Ello sucede espec&#237;ficamente en grupos de parientes de diab&#233;ticos, y el ultrasonido es la importante y pr&#225;ctica oportunidad de estudiar la evoluci&#243;n precoz de aterosclerosis<sup>30</sup>. Una nueva propuesta de marcador de riesgo cardiovascular, para evaluaci&#243;n de la susceptibilidad de enfermedad cardiaca coronaria, considera todav&#237;a las limitaciones de todos los scores de riesgo<sup>26</sup>.</p>
      <p>Hay diversas limitaciones de nuestro estudio. Una de ellas es la utilizaci&#243;n de medidas f&#237;sicas para definirse enfermedad cardiovascular en actividad, adem&#225;s de auto-relato de inexistencia de s&#237;ntomas correspondientes (es decir, individuos aparentemente saludables), aunque sea la metodolog&#237;a utilizada por diversos estudios relevantes para ese tipo de an&#225;lisis<sup>18</sup>. El n&#250;mero peque&#241;o de individuos estudiados, lo que no permiti&#243; la evaluaci&#243;n en separado por sexo, obedece a los criterios de marcador sustituto - los tres criterios de Boissel (m&#225;s sensible, m&#225;s prontamente evaluable y conveniente, por ser m&#233;todo no invasivo, con comprobada relaci&#243;n causal entre este y el objetivo cl&#237;nico) -, cuyas ventajas van desde el menor n&#250;mero de muestra hasta la comprobaci&#243;n de los objetivos ser m&#225;s directamente asociados con el proceso de la enfermedad<sup>8,30</sup>.</p>
      <p>El ultrasonido no permite diferenciar proceso ateroscler&#243;tico intimal de hipertrofia medial (por efectos de la presi&#243;n arterial). Ello se puede entender a principio como limitador del m&#233;todo. Hay, sin embargo, datos que corroboran que el EIM est&#225; en relaci&#243;n m&#225;s directa con la aterosclerosis intimal. En nuestro estudio, la no utilizaci&#243;n de mediciones de forma automatizada est&#225; de acuerdo con otros an&#225;lisis recientes, cuya abordaje de car&#225;cter manual, cuando bien estandarizada por t&#233;cnicos entrenados, se muestra tan buena como la obtenida de forma automatizada.</p>
      <p>La opci&#243;n de realizar un an&#225;lisis ecogr&#225;fico solamente en la pared posterior, difiriendo de algunos estudios previos (con an&#225;lisis de las dos paredes), tuvo como base la posibilidad de reducci&#243;n de nuestra exactitud caso se incluyera la pared anterior. Ello no permitir&#237;a una separaci&#243;n fidedigna de las medidas &#237;ntima y promedio, y de la utilizaci&#243;n de exceso de ganancia para obten&#233;rsela. Tomando en cuenta que la presi&#243;n arterial braquial var&#237;a usualmente del 10% al 15% mayor que la presi&#243;n de la arteria car&#243;tida com&#250;n, la medici&#243;n de los niveles de presi&#243;n arterial de modo indirecto (v&#237;a braquial), tuvo como base los estudios de Borow y Newburger<sup>31</sup>, que evidenciaron una excelente correlaci&#243;n entre la PA obtenida de forma invasiva y por presi&#243;n braquial<sup>15</sup>.</p>
      <p>La utilizaci&#243;n de m&#233;todos indirectos de evaluaci&#243;n de resistencia insul&#237;nica (RI) (insulinemia de ayuno, HOMA-IR y PTOG), adem&#225;s de marcadores indirectos de RI (IMC, circunferencia abdominal y concentraci&#243;n s&#233;rica de triglic&#233;ridos) y no del patr&#243;n-oro de American Diabets Association - <italic>clamp</italic> euglic&#233;mico hiperinsulin&#233;mico - se justifica por suministrar informaci&#243;n m&#225;s pura y reproductible sobre la acci&#243;n tisular de la insulina, demandar elevado tiempo de realizaci&#243;n, aparato de an&#225;lisis instant&#225;nea de niveles de glucemia, bombas de infusi&#243;n y necesidad de personal altamente especializado y entrenado. Sin embargo, hasta el momento no hay disponible un m&#233;todo de investigaci&#243;n laboratorial que obedezca los criterios para universal aceptaci&#243;n y utilizaci&#243;n de an&#225;lisis de RI, tomando en cuenta los m&#233;todos indirectos, como en diversos estudios, m&#225;s pasibles de utilizaci&#243;n en la pr&#225;ctica cl&#237;nica<sup>32</sup>.</p>
      <p>No se realiz&#243; an&#225;lisis por grupo racial ante la miscegenaci&#243;n racial de nuestro pa&#237;s. La no utilizaci&#243;n de sorteo aleatorio puede ser un sesgo del estudio, pero la b&#250;squeda por la eliminaci&#243;n de factores que pudieran oscurecer nuestros resultados nos incentiv&#243; en la b&#250;squeda por "voluntarios-est&#225;ndares".</p>
      <p>Hay que destacarse que, hasta la fecha de conclusi&#243;n del estudio, los valores de referencia de normalidad de EIM fueron ratificados por American Society of Echocardiography, con fecha del a&#241;o 2006, que exced&#237;an bastante a los valores encontrados en nuestro estudio<sup>33</sup>. Sin embargo, el trabajo de Lim et al.<sup>34</sup>, con 137 individuos "saludables", revel&#243; valores de normalidad de EIM de ACC en consonancia, seg&#250;n el grupo de edad, con aquellos encontrados por nosotros en individuos no-parientes de portadores de DM2: edad entre 35 y 39 a&#241;os - 0,49 &#177; 0,06; entre 40 y 49 a&#241;os - 0,52 &#177; 0,06 en el estudio de Lim et al.<sup>34</sup> As&#237;, en t&#233;rminos de valores correspondientes, los parientes de portadores de DM2 estudiados en nuestro trabajo fue ubicado en un grupo de edad m&#225;s avanzada: de 50 a 59 a&#241;os de edad - 0,56&#177;0,08 en el estudio de Lim et al.<sup>34</sup>; ratificando, tal vez, la frase de <italic>sir</italic> William Osler (1897): "<bold>Nosotros tenemos la edad de nuestras arterias</bold>"<sup>34</sup>.</p>
      <p>
        <bold>Conclusi&#243;n</bold>
      </p>
      <p>Los individuos con historia familiar de DM2, aun en la ausencia de intolerancia a la glucosa y/o niveles basales de insulina alterados, presentaron mayores valores de espesor &#237;ntima-medio (EIM) carot&#237;deo (alteraci&#243;n estructural), espec&#237;ficamente en el territorio carot&#237;deo com&#250;n izquierdo, cuando comparados a un grupo sin tal parentesco, no manifestando, sin embargo, alteraci&#243;n del vaso.</p>
      <p>La inferencia de la predisposici&#243;n gen&#233;tica a la DM2, probablemente en asociaci&#243;n a la resistencia insul&#237;nica, sobre los niveles de EIM carot&#237;deo, sobre todo en el territorio carot&#237;deo com&#250;n izquierdo, precediendo la alteraci&#243;n funcional vascular, necesita mayores estudios para elucidar tal asociaci&#243;n.</p>
      <p>
        <bold>Agradecimientos</bold>
      </p>
      <p>Los autores agradecen a todos los voluntarios, al equipo m&#233;dico del servicio de endocrinolog&#237;a del Huap y al Laborat&#243;rio Bronstein, sin los que ser&#237;a inviable la realizaci&#243;n de este estudio.</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>El presente estudio no tuvo fuentes de financiaci&#243;n externas.</p>
      <p>
        <bold>Vinculaci&#243;n Acad&#233;mica</bold>
      </p>
      <p>Este art&#237;culo forma parte de disertaci&#243;n de Maestr&#237;a de S&#244;nia Silva Prado, por la Universidad Federal Fluminense.</p>
      <p>
        <bold>Referencias</bold>
      </p>
    </body>
  </sub-article>
</article>
