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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">h8F4H53z5xPhcq3tDcfLcKg</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2013002900012</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(13)10100300012</article-id>
      <article-id pub-id-type="doi">10.5935/abc.20130174</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Comunica&#231;&#227;o Breve</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Preval&#234;ncia de dislipidemia em popula&#231;&#227;o infantil com cardiopatia cong&#234;nita</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Fuenmayor</surname>
            <given-names>Gabriela</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Redondo</surname>
            <given-names>Ana Carolina Costa</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Shiraishi</surname>
            <given-names>Karen Saori</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Souza</surname>
            <given-names>Rogerio</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Elias</surname>
            <given-names>Patr&#237;cia Figueiredo</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Jatene</surname>
            <given-names>Ieda Biscegli</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="city">S&#227;o Paulo</named-content>
          <named-content content-type="state"/>
        </addr-line>
        <institution content-type="orgname">Hospital do Cora&#231;&#227;o</institution>
        <institution content-type="orgdiv1">Associa&#231;&#227;o do Sanat&#243;rio S&#237;rio </institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff02">
        <addr-line>
          <named-content content-type="city">S&#227;o Paulo</named-content>
          <named-content content-type="state">S&#227;o Paulo</named-content>
        </addr-line>
        <institution content-type="orgname">Universidade de S&#227;o Paulo</institution>
        <institution content-type="orgdiv1">Faculdade de Medicina </institution>
        <institution content-type="orgdiv2">Hospital das Cl&#237;nicas</institution>
        <country country="BR">Brazil</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>09</month>
        <year>2013</year>
      </pub-date>
      <volume>101</volume>
      <issue>3</issue>
      <fpage>273</fpage>
      <lpage>276</lpage>
      <history>
        <date date-type="received">
          <day>06</day>
          <month>03</month>
          <year>2013</year>
        </date>
        <date date-type="accepted">
          <day>07</day>
          <month>06</month>
          <year>2013</year>
        </date>
        <date date-type="rev-recd">
          <day>04</day>
          <month>06</month>
          <year>2013</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>A dislipidemia &#233; um dos grandes fatores de risco associados a doen&#231;as cardiovasculares. Poucos s&#227;o os dados relacionados ao impacto da cardiopatia cong&#234;nita na preval&#234;ncia da dislipidemia na popula&#231;&#227;o pedi&#225;trica. O objetivo deste estudo foi avaliar o perfil lip&#237;dico de crian&#231;as portadoras de cardiopatia cong&#234;nita seguidas em um centro de refer&#234;ncia. Foram inclu&#237;dos 52 pacientes pedi&#225;tricos que tiveram perfil lip&#237;dico, metab&#243;lico e cl&#237;nico determinados entre janeiro de 2011 e julho de 2012. Com m&#233;dia de idade de 10,4 &#177; 2,8 anos e predomin&#226;ncia do sexo masculino (1,38:1), nossa popula&#231;&#227;o apresentou 53,8% de pacientes com aumento no colesterol total e 13,4% (IC 95% de 6,6-25,2%) de crian&#231;as que tamb&#233;m apresentavam LDL &gt; 130 mg/dL, caracterizando dislipidemia. Dos pacientes com dislipidemia, s&#243; doisforam classificados como obesos. Conclu&#237;mos que a presen&#231;a de cardiopatia cong&#234;nita n&#227;o confere risco aumentado associado &#224; presen&#231;a de dislipidemia, devendo o rastreamento nessa popula&#231;&#227;o seguir as mesmas diretrizes da popula&#231;&#227;o pedi&#225;trica normal, as quaistamb&#233;m independem do estado nutricional da crian&#231;a.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>Dislipidemias</kwd>
        <kwd>Crian&#231;a</kwd>
        <kwd>Cardiopatias Cong&#234;nitas</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>20</day>
        <month>09</month>
        <year>2013</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>
      <bold>COMUNICA&#199;&#195;O BREVE</bold>
    </p>
    <p>
      <bold>Preval&#234;ncia de dislipidemia em popula&#231;&#227;o infantil com cardiopatia cong&#234;nita</bold>
    </p>
    <p>
      <bold>Gabriela Fuenmayor<sup>I</sup>; Ana Carolina Costa Redondo<sup>I</sup>; Karen Saori Shiraishi<sup>I</sup>; Rogerio Souza<sup>I,II</sup>; Patr&#237;cia Figueiredo Elias<sup>I</sup>; Ieda Biscegli Jatene<sup>I</sup></bold>
    </p>
    <p><sup>I</sup>Hospital do Cora&#231;&#227;o - Associa&#231;&#227;o do Sanat&#243;rio S&#237;rio, S&#227;o Paulo, SP - Brasil </p>
    <p><sup>II</sup>Instituto do Cora&#231;&#227;o, Hospital das Cl&#237;nicas da Faculdade de Medicina da Universidade de S&#227;o Paulo, S&#227;o Paulo, SP - Brasil</p>
    <p>
      <xref ref-type="corresp" rid="enda">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p>A dislipidemia &#233; um dos grandes fatores de risco associados a doen&#231;as cardiovasculares. Poucos s&#227;o os dados relacionados ao impacto da cardiopatia cong&#234;nita na preval&#234;ncia da dislipidemia na popula&#231;&#227;o pedi&#225;trica. O objetivo deste estudo foi avaliar o perfil lip&#237;dico de crian&#231;as portadoras de cardiopatia cong&#234;nita seguidas em um centro de refer&#234;ncia. Foram inclu&#237;dos 52 pacientes pedi&#225;tricos que tiveram perfil lip&#237;dico, metab&#243;lico e cl&#237;nico determinados entre janeiro de 2011 e julho de 2012. Com m&#233;dia de idade de 10,4 &#177; 2,8 anos e predomin&#226;ncia do sexo masculino (1,38:1), nossa popula&#231;&#227;o apresentou 53,8% de pacientes com aumento no colesterol total e 13,4% (IC 95% de 6,6-25,2%) de crian&#231;as que tamb&#233;m apresentavam LDL <underline>&gt;</underline> 130 mg/dL, caracterizando dislipidemia. Dos pacientes com dislipidemia, s&#243; doisforam classificados como obesos. Conclu&#237;mos que a presen&#231;a de cardiopatia cong&#234;nita n&#227;o confere risco aumentado associado &#224; presen&#231;a de dislipidemia, devendo o rastreamento nessa popula&#231;&#227;o seguir as mesmas diretrizes da popula&#231;&#227;o pedi&#225;trica normal, as quaistamb&#233;m independem do estado nutricional da crian&#231;a.</p>
    <p><bold>Palavras-chave:</bold> Dislipidemias / epidemiologia; Crian&#231;a; Cardiopatias Cong&#234;nitas.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>A doen&#231;a cardiovascular (DCV) &#233; a maior causa de morbimortalidade, tanto em pa&#237;ses desenvolvidos quanto em pa&#237;ses em desenvolvimento, sendo respons&#225;vel por 31,8% das causas de &#243;bito em adultos no Brasil<sup>1</sup>. S&#227;o v&#225;rios os fatores de risco associados ao desenvolvimento das doen&#231;as cardiovasculares, como tabagismo, obesidade e dislipidemia<sup>2</sup>. Especificamente, a dislipidemia constitui o maior fator de impacto no desenvolvimento da doen&#231;a ateroscler&#243;tica, em particular a presen&#231;a de concentra&#231;&#245;es aumentadas de lipoprote&#237;na de baixa densidade (LDL)<sup>2</sup>.</p>
    <p>A aterosclerose e a doen&#231;a cardiovascular t&#234;m sua origem na inf&#226;ncia e apresentam evolu&#231;&#227;o lenta e subcl&#237;nica, refor&#231;ando portanto a import&#226;ncia de a&#231;&#245;es preventivas para o seu controle. Na popula&#231;&#227;o pedi&#225;trica, a preval&#234;ncia de n&#237;veis s&#233;ricos elevados de LDL, por exemplo, situa-se em 6-13%<sup>3-5</sup>. Existem v&#225;rias condi&#231;&#245;es cl&#237;nicas que podem levar a taxas ainda mais altas, como diabetes melito e insufici&#234;ncia renal cr&#244;nica<sup>6</sup>. Embora as cardiopatias cong&#234;nitas possam estar relacionadas com ativa&#231;&#227;o do eixo neuro-hormonal e com diferentes fen&#244;menos inflamat&#243;rios<sup>7</sup>, pouco se sabe sobre seu impacto na preval&#234;ncia de altera&#231;&#245;es no metabolismo lip&#237;dico. O objetivo deste estudo foi avaliar a preval&#234;ncia de dislipidemia em um centro de refer&#234;ncia em cardiopatias cong&#234;nitas.</p>
    <p>
      <bold>M&#233;todos</bold>
    </p>
    <p>Foram inclu&#237;dos no estudo pacientes menores de 18 anos, acompanhados no ambulat&#243;rio de cardiopatias cong&#234;nitas do Hospital do Cora&#231;&#227;o, que tiveram perfil lip&#237;dico determinado entre janeiro de 2011 e julho de 2012.</p>
    <p>Foram avaliadas as caracter&#237;sticas cl&#237;nicas (idade, peso, altura, &#237;ndice de massa corp&#243;rea [IMC]), al&#233;m da dosagem s&#233;rica de colesterol total (CT) e fra&#231;&#245;es, triglic&#233;rides, TSH e T4 livre. Os exames laboratoriais foram dosados por meio de coleta de sangue perif&#233;rico no laborat&#243;rio do Hospital do Cora&#231;&#227;o. O m&#233;todo usado para an&#225;lise do lipidograma foi o de eletroforese em gel de agarose e enzim&#225;ticos colorim&#233;tricos (Orto Johnson Modelo Fusion 5.1). O HDL-colesterol foi determinado diretamente, ap&#243;s precipita&#231;&#227;o das outras lipoprote&#237;nas. O LDL-colesterol foi calculado usando a f&#243;rmula de Friedewald<sup>7</sup>.</p>
    <p>Os crit&#233;rios utilizados para classifica&#231;&#227;o laboratorial dos pacientes foram os preconizados pela Sociedade Brasileira de Cardiologia, conforme a I Diretriz de Preven&#231;&#227;o da Aterosclerose na Inf&#226;ncia e na Adolesc&#234;ncia<sup>7</sup>, considerando colesterol total desej&#225;vel quando menor que 150 mg/dL, lim&#237;trofe entre 150-170 mg/dL e aumentado quando maior que 170 mg/dL. Foi considerada dislipidemia a presen&#231;a de n&#237;veis s&#233;ricos de triglicer&#237;deos acima de 150mg/dL e/ou LDL acima de 130 mg/dL<sup>4</sup>.</p>
    <p>A classifica&#231;&#227;o nutricional dos pacientes foi baseada nas tabelas de crescimento da Organiza&#231;&#227;o Mundial da Sa&#250;de<sup>8</sup>, considerando: desnutri&#231;&#227;o com <italic>Z-score</italic>&lt; 2 DS (desvios-padr&#227;o); normal com <italic>Z-score</italic> entre -2 e +1 DS; sobrepeso com <italic>Z-score</italic> entre +1 e +2 DS;obesidade com <italic>Z-score</italic> maior ou igual a 2 DS.</p>
    <p>Os dados cont&#237;nuos foram descritos sob a forma de m&#233;dia e DP, enquanto os dados categ&#243;ricos foram apresentados sob a forma de propor&#231;&#227;o com intervalo de confian&#231;a de 95% quando adequado.</p>
    <p>
      <bold>Resultados</bold>
    </p>
    <p>As caracter&#237;sticas cl&#237;nicas e laboratoriais dos 52 pacientes inclu&#237;dos no estudo encontram-se na <xref ref-type="table" rid="a12tab01">Tabela 1</xref>. Observa-se a m&#233;dia de idade de 10,4 &#177; 2,8 anos, com predomin&#226;ncia do sexo masculino, na propor&#231;&#227;o de 1,38:1. Com rela&#231;&#227;o ao estado nutricional, sete pacientes apresentavam crit&#233;rios de obesidade (13,4% da popula&#231;&#227;o total). Nenhum paciente apresentou altera&#231;&#227;o nos n&#237;veis de glicemia ou de triglic&#233;rides; contudo, dois pacientes estavam em tratamento para hipotireoidismo com reposi&#231;&#227;o oral de horm&#244;nio tireoidiano, mantendo n&#237;veis s&#233;ricos normais, como os demais pacientes.</p>
    <p content-type="asset">
      <table-wrap id="a12tab01">
        <graphic xlink:href="1678-4170-abc-101-03-0273-30174-gt01.jpg"/></table-wrap>
    </p>
    <p>Dos pacientes analisados, 53,8% apresentavam colesterol total (CT) &gt; 150 mg/dL e 13,4% (IC 95% de 6,6-25,2%) tamb&#233;m apresentavam LDL <underline>&gt;</underline> 130 mg/dL, caracterizando dislipidemia. &#201; interessante notar que,entre os pacientes que tinham CT lim&#237;trofe ou normal, nenhum apresentou dosagem de LDL acima de 130 mg/dL, refor&#231;ando a adequa&#231;&#227;o desse n&#237;vel de corte (<xref ref-type="fig" rid="a12gra01">Gr&#225;fico 1A</xref>). Do subgrupo de pacientes com dislipidemia, apenas dois foram classificados como obesos (<xref ref-type="fig" rid="a12gra01">Gr&#225;fico 1B</xref>).</p>
    <p><fig id="a12gra01"/>&#13;
&#160;&#13;
</p>
    <p>
      <fig id="a12gra01a">
        <graphic xlink:href="1678-4170-abc-101-03-0273-30174-gf01.jpg"/></fig>
    </p>
    <p>&#13;
  <fig id="a12gra01xgra1b"/><fig id="a12gra01b"><graphic xlink:href="1678-4170-abc-101-03-0273-30174-gf02.jpg"/></fig></p>
    <p>
      <bold>Discuss&#227;o</bold>
    </p>
    <p>Nosso estudo foi o primeiro a avaliar a preval&#234;ncia de dislipidemia especificamente na popula&#231;&#227;o pedi&#225;trica portadora de cardiopatia cong&#234;nita, evidenciando taxas semelhantes &#224;s encontradas na popula&#231;&#227;o pedi&#225;trica normal. Ao avaliar estudos anteriores que possibilitam o c&#225;lculo do intervalo de confian&#231;a de seus resultados<sup>3,4</sup>, podemos estimar a preval&#234;ncia de eleva&#231;&#227;o de LDL entre 8-15% da popula&#231;&#227;o pedi&#225;trica. Tal intervalo apresenta sobreposi&#231;&#227;o com os dados de nosso estudo (13,4%), sugerindo que a presen&#231;a de cardiopatia cong&#234;nita <italic>per se</italic> n&#227;o caracteriza fator de risco para a eleva&#231;&#227;o de LDL, refor&#231;ando que as diretrizes atuais para preven&#231;&#227;o de aterosclerose devem ser consideradas sem particularidades nesse subgrupo espec&#237;fico.</p>
    <p>A obesidade caracteriza-se como fator de risco importante para o desenvolvimento de doen&#231;as cardiometab&#243;licas, seja diretamente seja por predispor ao aumento de resist&#234;ncia &#224; insulina<sup>4,9</sup>. Contudo, em nosso estudo, apenas dois dos sete pacientes com dislipidemia (28%) apresentavam obesidade, mostrando ser esse um fator importante, mas n&#227;o determinante para o diagn&#243;stico. Na amostra de outros trabalhos feitos no Brasil e internacionalmente, o excesso de peso foi o fator de risco mais fortemente associado &#224; dislipidemia<sup>3-5,9,10</sup>.Todavia, a maior parte dos pacientes portadores de dislipidemia n&#227;o apresenta obesidade como fator de risco, como observado em nosso trabalho, refor&#231;ando que o rastreamento na popula&#231;&#227;o pedi&#225;trica n&#227;o deve ser guiado pela presen&#231;a ou n&#227;o de obesidade ou de outras altera&#231;&#245;es do estado nutricional.</p>
    <p>Nosso estudo apresenta limita&#231;&#245;es que merecem ser ressaltadas, como o tamanho da amostra e seu car&#225;ter retrospectivo. Ainda assim, trata-se do primeiro estudo especificamente conduzido na popula&#231;&#227;o pedi&#225;trica portadora de cardiopatia cong&#234;nita, apresentando intervalo de confian&#231;a bastante superpon&#237;vel com estudos anteriores.</p>
    <p>
      <bold>Conclus&#227;o</bold>
    </p>
    <p>Podemos concluir que a presen&#231;a de cardiopatia cong&#234;nita n&#227;o confere risco aumentado associado &#224; presen&#231;a de dislipidemia, devendo o rastreamento nessa popula&#231;&#227;o seguir as mesmas diretrizes da popula&#231;&#227;o pedi&#225;trica normal, as quais tamb&#233;m independem do estado nutricional da crian&#231;a.</p>
    <p>
      <bold>Contribui&#231;&#227;o dos autores</bold>
    </p>
    <p>Concep&#231;&#227;o e desenho da pesquisa: Fuenmayor G, Redondo ACC, Souza R, Elias PF, Jatene IB; Obten&#231;&#227;o de dados: Fuenmayor G, Elias PF; An&#225;lise e interpreta&#231;&#227;o dos dados, Reda&#231;&#227;o do manuscrito e Revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do intelectual: Fuenmayor G, Shiraishi KS, Souza R, Elias PF, Jatene IB; An&#225;lise estat&#237;stica: Fuenmayor G, Souza R.</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>N&#227;o h&#225; vincula&#231;&#227;o deste estudo a programas de p&#243;s-gradua&#231;&#227;o.</p>
    <p>
      <fn id="enda" fn-type="corresp">
        <label>
          <bold>Correspond&#234;ncia:</bold>
        </label>
        <p> Ieda Biscegli Jatene </p>
        <p> Rua Des. Eliseu Guilherme, 123, Para&#237;so </p>
        <p> CEP 04004-020, S&#227;o Paulo, SP - Brasil </p>
        <p> E-mail: </p>
        <p>
          <email xlink:href="ijatene@hcor.com.br">ijatene@hcor.com.br</email>
        </p>
      </fn>
    </p>
    <p>Artigo recebido em 06/03/2013; revisado em 04/06/2013; aceito em 07/06/2013.</p>
  </body>
  <back>
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  </back>
  <sub-article article-type="translation" id="TRen" xml:lang="en">
    <front-stub>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Brief Communication</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title xml:lang="en">Prevalence of dyslipidemia in children with congenital heart disease</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>Dyslipidemia is one of the main risk factors associated with cardiovascular diseases. Few data on the impacts of congenital heart diseases are available with regard to the prevalence of dyslipidemia in children. Our study evaluated the lipid profile in children with congenital heart disease at a referral center. From January 2011 to July 2012, 52 pediatric patients had their lipid, metabolic and clinical profiles traced. The mean age was 10.4 &#177; 2.8 years and male/female rate of 1.38:1. Our population had 53.8% patients with high levels of total cholesterol and 13.4% (CI 95 %, from 6.6 to 25.2%) of them also presenting LDL levels &gt; 130 mg/dL, which characterizes dyslipidemia. The group of dyslipidemic patients presented only two obese individuals. Our data show that the presence of congenital heart disease does not lead to higher risk associated with the prevalence of dyslipidemia. Therefore, the screening of this specific population should follow the regular pediatric guidelines, which are also independent of the nutritional status of the children tested.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Dyslipidemia</kwd>
        <kwd>Child</kwd>
        <kwd>Congenital Heart Disease</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>BRIEF COMMUNICATION</bold>
      </p>
      <p>
        <fn id="end-body2">
          <label>
            <bold>Prevalence of dyslipidemia in children with congenital heart disease</bold>
          </label>
          <p>
            <bold>Gabriela Fuenmayor<sup>I</sup>; Ana Carolina Costa Redondo<sup>I</sup>; Karen Saori Shiraishi<sup>I</sup>; Rogerio Souza<sup>I,II</sup>; Patr&#237;cia Figueiredo Elias<sup>I</sup>; Ieda Biscegli Jatene<sup>I</sup></bold>
          </p>
        </fn>
      </p>
      <p><sup>I</sup>Hospital do Cora&#231;&#227;o - Associa&#231;&#227;o do Sanat&#243;rio S&#237;rio, S&#227;o Paulo, SP - Brazil </p>
      <p><sup>II</sup>Instituto do Cora&#231;&#227;o, Hospital das Cl&#237;nicas da Faculdade de Medicina da Universidade de S&#227;o Paulo, S&#227;o Paulo, SP - Brazil</p>
      <p>Mailing Address</p>
      <p>
        <bold>ABSTRACT</bold>
      </p>
      <p>Dyslipidemia is one of the main risk factors associated with cardiovascular diseases. Few data on the impacts of congenital heart diseases are available with regard to the prevalence of dyslipidemia in children. Our study evaluated the lipid profile in children with congenital heart disease at a referral center. From January 2011 to July 2012, 52 pediatric patients had their lipid, metabolic and clinical profiles traced. The mean age was 10.4 &#177; 2.8 years and male/female rate of 1.38:1. Our population had 53.8% patients with high levels of total cholesterol and 13.4% (CI 95 %, from 6.6 to 25.2%) of them also presenting LDL levels <underline>&gt;</underline> 130 mg/dL, which characterizes dyslipidemia. The group of dyslipidemic patients presented only two obese individuals. Our data show that the presence of congenital heart disease does not lead to higher risk associated with the prevalence of dyslipidemia. Therefore, the screening of this specific population should follow the regular pediatric guidelines, which are also independent of the nutritional status of the children tested.</p>
      <p><bold>Keywords:</bold> Dyslipidemia / Epidemiology, Child, Congenital Heart Disease.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>Cardiovascular diseases (CVD) are the major cause of morbidity and mortality, both in developed and developing countries, accounting for 31.8% of the causes of death in adults in Brazil<sup>1</sup>. There are several risk factors associated with the development of heart diseases, such as smoking, obesity and dyslipidemia.<sup>2</sup> Dyslipidemia is typically spotted as the most significant factor leading to the development of atherosclerotic diseases, mainly the higher concentrations of low-density lipoproteins (LDL)<sup>2</sup>.</p>
      <p>Atherosclerosis and cardiovascular disease begin in childhood and present slow and subclinical evolution, which underscores the importance of preventative efforts for control. In children, the prevalence of high serum levels of LDL range between 6-13%<sup>3-5</sup>. Various clinical conditions may lead to even higher rates, which includes diabetes mellitus and chronic renal failure<sup>6</sup>. Although congenital heart diseases may be associated with neurohormonal activation and different inflammatory phenomena<sup>7</sup>, there is insufficient information on their impact on the prevalence of abnormalities in the lipid metabolism. The purpose of this study is to evaluate the prevalence of dyslipidemia at a referral center relating to congenital heart diseases.</p>
      <p>
        <bold>Methods</bold>
      </p>
      <p>The study included patients under 18 years old, followed up at the outpatient clinic of congenital heart disease of Hospital do Cora&#231;&#227;o, who had their lipid profiles traced from January 2011 to July 2012.</p>
      <p>We evaluated the clinical characteristic (age, weight, height, body mass index [BMI]), in addition to the serum level of total cholesterol (TC) and fractions, triglycerides, TSH and Free T4. Laboratory tests were measured by peripheral blood collection in the laboratory of Hospital do Cora&#231;&#227;o. The method used for analyzing the lipid profile was the agarose gel electrophoresis and enzymatic colorimetric assay (Ortho Johnson Fusion 5.1 Model). The HDL was checked directly after precipitation of other lipoproteins. LDL cholesterol was calculated applying the Friedewald formula<sup>7</sup>.</p>
      <p>The criteria for laboratory classification of patients were those recommended by the Brazilian Society of Cardiology, according to the I Guideline for the Prevention of Atherosclerosis in Childhood and Adolescence<sup>7</sup>, taking into account the desirable total cholesterol when below 150 mg/dL, the neighboring figures between 150-170 mg/dL and the increasing ones when higher than 170 mg/dL. The presence of serum levels of triglycerides above 150 mg/dL and/or LDL above 130 mg/dL<sup>4</sup> was considered dyslipidemia.</p>
      <p>The nutritional classification of the patients was based on the growth tables of the World Health Organization<sup>8</sup>, thus considering: malnutrition with Z-score &lt; 2 SD (standard deviation); normal with Z-score between -2 and +1 DS; overweight with Z-score between +1 and +2 SD; obesity with Z-score higher or equal to 2 SD.</p>
      <p>The continuous data were described as mean and SD, while the categorical data were presented as proportions with confidence interval of 95%, where appropriate.</p>
      <p>
        <bold>Results</bold>
      </p>
      <p><xref ref-type="table" rid="en_a12tab01-body2">Table 1</xref> presents the clinic and laboratory characteristics of the 52 patients included in the study. The mean age was 10.4 &#177; 2.8 years with male predominance, at a rate of 1.38:1. As to the group's nutritional status, seven patients were obese (13.4% of the total population). Not any patient presented abnormality in glucose or triglyceride levels. However, two patients were under hypothyroidism treatment with oral administration of thyroid hormone, keeping the serum levels regular, as in other patients.</p>
      <p content-type="asset">
        <table-wrap id="en_a12tab01-body2">
          <graphic xlink:href="1678-4170-abc-101-03-0273-30174-gt01-en.jpg"/></table-wrap>
      </p>
      <p>Out of the patients analyzed, 53.8% presented total cholesterol (TC) &gt; 150 mg/dL and 13.4% (CI 95% of 6.6-25.2%) also presented LDL <underline>&gt;</underline> 130 mg/dL, characterizing dyslipidemia. Note that patients presenting neighboring or normal TC did not show LDL levels above 130 mg/dL, which underscores the suitability of this cutoff level (<xref ref-type="fig" rid="en_a12cha01-body2">Chart 1A</xref>). Only two of de subgroup of patients with dyslipidemia were classified as obese (<xref ref-type="fig" rid="en_a12cha01-body2">Chart 1B</xref>).</p>
      <p content-type="html"><fig id="en_a12cha01-body2"><graphic xlink:href="https://minio.scielo.br/documentstore/1678-4170/h8F4H53z5xPhcq3tDcfLcKg/d8e3b1487bb6bace3b0f8999fe5810ea98c8003e.jpg"/><graphic xlink:href="1678-4170-abc-101-03-0273-30174-gf01-en.jpg"/></fig>&#13;
&#160;&#13;
</p>
      <p>
        <bold>Discussion</bold>
      </p>
      <p>This study was the first to evaluate the prevalence of dyslipidemia in children undergoing congenital heart disease, revealing rates similar to those found in normal children. Previous studies that allowed measuring the confidence interval of their results<sup>3,4</sup> helped estimate the prevalence of elevation of LDL in 8-15% of the children in the sample. The said interval overlaps the data revealed by our study (13.4%), suggesting that the presence of congenital heart disease does not stand per se as a risk factor for elevation of LDL, implying that the current guidelines for prevention of atherosclerosis should be considered without consideration to the particularities of this specific subgroup.</p>
      <p>Obesity is characterized as an important risk factor for developing cardiometabolic diseases, whether directly, or because it predisposes patients to increase insulin resistance<sup>4,9</sup>. However, in this study, only two of the seven patients undergoing dyslipidemia (28%) were obese, which implies that this is an important factor, but not decisive for diagnosis. As ascertained in the review of other researches carried out in Brazil and abroad, the overweight was the risk factor which showed the strongest association with dyslipidemia<sup>3-5,9,10</sup>. Nonetheless, most patients with dyslipidemia did not have obesity as a risk factor, as shown in our study, which strengthens the assumption that the analysis of children should not be founded on the presence or not of obesity or other abnormalities of their nutritional status.</p>
      <p>This study has noteworthy limitations, such as the sample size and its retrospective nature. Yet, this is the first research with children undergoing congenital heart disease presenting a confidence interval which is consistent with previous studies.</p>
      <p>
        <bold>Conclusion</bold>
      </p>
      <p>We conclude that the presence of congenital heart disease does not lead to higher risk associated with the prevalence of dyslipidemia. Therefore, the screening of this population should follow the regular pediatric guidelines, which are also independent of their nutritional status.</p>
      <p>
        <bold>Author contributions</bold>
      </p>
      <p>Conception and design of the research: Fuenmayor G, Redondo ACC, Souza R, Elias PF, Jatene IB; Acquisition of data: Fuenmayor G, Elias PF; Analysis and interpretation of the data, Writing of the manuscript and Critical revision of the manuscript for intellectual content: Fuenmayor G, Shiraishi KS, Souza R, Elias PF, Jatene IB; tatistical analysis: Fuenmayor G, Souza R.</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 study is not associated with any post-graduation program.</p>
      <p>
        <bold>References</bold>
      </p>
    </body>
  </sub-article>
</article>
