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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">5WyCbryWbx6MSKDQg74dD7H</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2012000400010</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(12)09800410</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2012005000021</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigos Originais</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Variabilidade da frequ&#234;ncia card&#237;aca em pacientes com Distrofia Miot&#244;nica tipo 1</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Fregonezi</surname>
            <given-names>Guilherme</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ara&#250;jo</surname>
            <given-names>Thaise</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Dourado Junior</surname>
            <given-names>Mario Emilio</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ferezini</surname>
            <given-names>Joceline</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Silva</surname>
            <given-names>Ester</given-names>
          </name>
          <xref ref-type="aff" rid="aff03"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Resqueti</surname>
            <given-names>Vanessa</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
      </contrib-group>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="city">Natal</named-content>
          <named-content content-type="state">Rio Grande do Norte</named-content>
        </addr-line>
        <institution content-type="orgname">Universidade Federal do Rio Grande do Norte</institution>
        <institution content-type="orgdiv1">Centro de Ci&#234;ncias da Sa&#250;de </institution>
        <institution content-type="orgdiv2">Departamento de Fisioterapia</institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff03">
        <addr-line>
          <named-content content-type="city">Piracicaba</named-content>
          <named-content content-type="state">S&#227;o Paulo</named-content>
        </addr-line>
        <institution content-type="orgname">Universidade Metodista de Piracicaba</institution>
        <institution content-type="orgdiv1">Laborat&#243;rio de Doen&#231;as Cardiovasculares </institution>
        <country country="BR">Brazil</country>
      </aff>
      <aff id="aff02">
        <addr-line>
          <named-content content-type="city">Natal</named-content>
          <named-content content-type="state">Rio Grande do Norte</named-content>
        </addr-line>
        <institution content-type="orgname">Universidade Federal do Rio Grande do Norte</institution>
        <institution content-type="orgdiv1">Hospital Onofre Lopes </institution>
        <institution content-type="orgdiv2">Cl&#237;nica das Doen&#231;as Neuromusculares</institution>
        <country country="BR">Brazil</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>04</month>
        <year>2012</year>
      </pub-date>
      <volume>98</volume>
      <issue>4</issue>
      <fpage>353</fpage>
      <lpage>361</lpage>
      <history>
        <date date-type="received">
          <day>04</day>
          <month>07</month>
          <year>2011</year>
        </date>
        <date date-type="accepted">
          <day>10</day>
          <month>10</month>
          <year>2011</year>
        </date>
        <date date-type="rev-recd">
          <day>10</day>
          <month>10</month>
          <year>2011</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 envolvimento card&#237;aco &#233; comum em pacientes com Distrofia Miot&#244;nica (DM). A Variabilidade da Frequ&#234;ncia Card&#237;aca (VFC) &#233; uma t&#233;cnica simples e confi&#225;vel que pode ser &#250;til para estudar a influ&#234;ncia do sistema nervoso auton&#244;mico sobre o cora&#231;&#227;o. OBJETIVO: Estudar a variabilidade da frequ&#234;ncia card&#237;aca em pacientes com DM tipo 1. M&#201;TODOS: Estudamos a VFC durante registros de 5 minutos em pacientes com DM em um grupo controle saud&#225;vel. Analisamos os dom&#237;nios da frequ&#234;ncia (BF e AF) em unidades normalizadas (un) e balan&#231;o simp&#225;tico-vagal, na posi&#231;&#227;o sentada e em dec&#250;bito dorsal. RESULTADOS: Dezessete pacientes (10 homens e 7 mulheres) e dezessete indiv&#237;duos pareados saud&#225;veis (10 homens e 7 mulheres) foram estudados. As modula&#231;&#245;es simp&#225;tica e parassimp&#225;tica do cora&#231;&#227;o elevadas em pacientes do sexo masculino com DM da posi&#231;&#227;o em dec&#250;bito dorsal para a posi&#231;&#227;o sentada em 19% da AFun e a raz&#227;o BF/AF aumentaram 42,3%. Na posi&#231;&#227;o sentada, os pacientes do sexo masculino com DM apresentaram balan&#231;os simp&#225;tico-vagal significativamente mais elevados em 50,9% em compara&#231;&#227;o com indiv&#237;duos controles saud&#225;veis. A VFC foi influenciada tanto pelo sexo quanto pela enfermidade apresentada. O sexo influenciou a AFun na posi&#231;&#227;o em dec&#250;bito dorsal, enquanto a raz&#227;o BF/AF e AFun foi afetada em ambas as posi&#231;&#245;es. An&#225;lises post hoc mostraram que o sexo afeta significativamente pacientes com DM e indiv&#237;duos saud&#225;veis de diferentes maneiras (p &lt; 0,01). O dom&#237;nio de baixa frequ&#234;ncia na posi&#231;&#227;o sentada (AFun) foi significativamente influenciado pela enfermidade. CONCLUS&#195;O: Os resultados deste estudo sugerem que o est&#237;mulo simp&#225;tico em pacientes de meia-idade do sexo masculino com DM que n&#227;o est&#225; gravemente comprometido e apresenta dura&#231;&#227;o moderada da doen&#231;a parece ser maior do que em indiv&#237;duos saud&#225;veis pareados.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>Frequ&#234;ncia card&#237;aca</kwd>
        <kwd>distrofia miot&#244;nica</kwd>
        <kwd>an&#225;lise espectral</kwd>
        <kwd>sistema nervoso aut&#244;nomo</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>08</day>
        <month>03</month>
        <year>2012</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>
      <bold>Variabilidade da frequ&#234;ncia card&#237;aca em pacientes com Distrofia Miot&#244;nica tipo 1</bold>
    </p>
    <p>
      <bold>Guilherme Fregonezi<sup>I</sup>; Thaise Ara&#250;jo<sup>I</sup>; Mario Emilio Dourado Junior<sup>II</sup>; Joceline Ferezini<sup>I</sup>; Ester Silva<sup>III</sup>; Vanessa Resqueti<sup>I</sup></bold>
    </p>
    <p><sup>I</sup>Laborat&#243;rio de Fisioterapia Pneumocardiovascular - Departamento de Fisioterapia - Centro de Ci&#234;ncias da Sa&#250;de - Universidade Federal do Rio Grande do Norte, Natal, RN </p>
    <p><sup>II</sup>Cl&#237;nica das Doen&#231;as Neuromusculares - Hospital Onofre Lopes - Universidade Federal do Rio Grande do Norte, Natal, RN </p>
    <p><sup>III</sup>Laborat&#243;rio de Doen&#231;as Cardiovasculares - Universidade Metodista de Piracicaba, Piracicaba, SP, Brasil</p>
    <p>
      <xref ref-type="corresp" rid="back">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p><bold>FUNDAMENTO:</bold> O envolvimento card&#237;aco &#233; comum em pacientes com Distrofia Miot&#244;nica (DM). A Variabilidade da Frequ&#234;ncia Card&#237;aca (VFC) &#233; uma t&#233;cnica simples e confi&#225;vel que pode ser &#250;til para estudar a influ&#234;ncia do sistema nervoso auton&#244;mico sobre o cora&#231;&#227;o. </p>
    <p><bold>OBJETIVO:</bold> Estudar a variabilidade da frequ&#234;ncia card&#237;aca em pacientes com DM tipo 1. </p>
    <p><bold>M&#201;TODOS:</bold> Estudamos a VFC durante registros de 5 minutos em pacientes com DM em um grupo controle saud&#225;vel. Analisamos os dom&#237;nios da frequ&#234;ncia (BF e AF) em unidades normalizadas (un) e balan&#231;o simp&#225;tico-vagal, na posi&#231;&#227;o sentada e em dec&#250;bito dorsal. </p>
    <p><bold>RESULTADOS:</bold> Dezessete pacientes (10 homens e 7 mulheres) e dezessete indiv&#237;duos pareados saud&#225;veis (10 homens e 7 mulheres) foram estudados. As modula&#231;&#245;es simp&#225;tica e parassimp&#225;tica do cora&#231;&#227;o elevadas em pacientes do sexo masculino com DM da posi&#231;&#227;o em dec&#250;bito dorsal para a posi&#231;&#227;o sentada em 19% da AFun e a raz&#227;o BF/AF aumentaram 42,3%. Na posi&#231;&#227;o sentada, os pacientes do sexo masculino com DM apresentaram balan&#231;os simp&#225;tico-vagal significativamente mais elevados em 50,9% em compara&#231;&#227;o com indiv&#237;duos controles saud&#225;veis. A VFC foi influenciada tanto pelo sexo quanto pela enfermidade apresentada. O sexo influenciou a AFun na posi&#231;&#227;o em dec&#250;bito dorsal, enquanto a raz&#227;o BF/AF e AFun foi afetada em ambas as posi&#231;&#245;es. An&#225;lises post hoc mostraram que o sexo afeta significativamente pacientes com DM e indiv&#237;duos saud&#225;veis de diferentes maneiras (p &lt; 0,01). O dom&#237;nio de baixa frequ&#234;ncia na posi&#231;&#227;o sentada (AFun) foi significativamente influenciado pela enfermidade. </p>
    <p><bold>CONCLUS&#195;O:</bold> Os resultados deste estudo sugerem que o est&#237;mulo simp&#225;tico em pacientes de meia-idade do sexo masculino com DM que n&#227;o est&#225; gravemente comprometido e apresenta dura&#231;&#227;o moderada da doen&#231;a parece ser maior do que em indiv&#237;duos saud&#225;veis pareados.</p>
    <p><bold>Palavras-chave:</bold> Frequ&#234;ncia card&#237;aca, distrofia miot&#244;nica, an&#225;lise espectral, sistema nervoso aut&#244;nomo.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>A Distrofia Miot&#244;nica (DM) &#233; a forma mais frequente de distrofia muscular em adultos<sup>1,2</sup>. As manifesta&#231;&#245;es cl&#237;nicas da DM s&#227;o miotonia, fraqueza muscular, anormalidades card&#237;acas, catarata, dist&#250;rbios end&#243;crinos e do trato digestivo, dist&#250;rbios do sono e calv&#237;cie<sup>3-5</sup>. Problemas card&#237;acos experimentados por pacientes com DM s&#227;o bem conhecidos<sup>1,6</sup>. A maioria dos pacientes &#233; assintom&#225;tica; no entanto, altera&#231;&#245;es na fisiologia card&#237;aca s&#227;o comuns, como observado em eletrocardiogramas<sup>6</sup>. As manifesta&#231;&#245;es cl&#237;nicas incluem atraso na condu&#231;&#227;o, dist&#250;rbios do ritmo e doen&#231;a do mioc&#225;rdio. Altera&#231;&#245;es eletrocardiogr&#225;ficas indicam anormalidades na condu&#231;&#227;o intraventricular e atrioventricular, fibrila&#231;&#227;o atrial e arritmias ventriculares. Dados histopatol&#243;gicos mostram fibrose no sistema de condu&#231;&#227;o e no n&#243; sinoatrial associado &#224; hipertrofia dos mi&#243;citos<sup>7</sup>. Pacientes com comprometimentos musculoesquel&#233;ticos maiores possuem idade mais avan&#231;ada e problemas do cora&#231;&#227;o com mais frequ&#234;ncia<sup>8</sup>.</p>
    <p>O sistema nervoso auton&#244;mico desempenha um papel crucial na modula&#231;&#227;o da Frequ&#234;ncia Card&#237;aca (FC). Uma diminui&#231;&#227;o em sua variabilidade &#233; um preditor de morbidade e mortalidade<sup>9,10</sup>. Pesquisas anteriores descobriram que as mulheres saud&#225;veis apresentavam maior domin&#226;ncia vagal sobre a FC, o que parece dar conta de sua melhor cardioprote&#231;&#227;o em rela&#231;&#227;o aos homens, embora essas diferen&#231;as diminuam com a idade<sup>11</sup>. O estudo da Variabilidade da Frequ&#234;ncia Card&#237;aca (VFC) tem, portanto, sido proposto como um m&#233;todo simples, barato e n&#227;o invasivo, que fornece informa&#231;&#245;es sobre a integridade neurocardial. Uma s&#233;rie de investiga&#231;&#245;es sobre a fun&#231;&#227;o global do sistema nervoso auton&#244;mico em pacientes com DM mostra que a presen&#231;a de neuropatia auton&#244;mica &#233; altamente improv&#225;vel<sup>1,12,13</sup>. No entanto, estudos sobre a modula&#231;&#227;o auton&#244;mica da FC em pacientes com DM t&#234;m obtido resultados conflitantes<sup>14-18</sup>.</p>
    <p>O presente estudo teve como objetivo avaliar as poss&#237;veis diferen&#231;as na modula&#231;&#227;o auton&#244;mica da FC entre os sexos para os pacientes com DM e indiv&#237;duos saud&#225;veis em diferentes posi&#231;&#245;es corporais e a influ&#234;ncia da intera&#231;&#227;o entre sexo e doen&#231;a na modula&#231;&#227;o auton&#244;mica da FC em diferentes posi&#231;&#245;es corporais.</p>
    <p>
      <bold>M&#233;todos</bold>
    </p>
    <p>
      <bold>Indiv&#237;duos</bold>
    </p>
    <p>Os pacientes diagnosticados com DM pelo neurologista de um hospital universit&#225;rio e grupos controles saud&#225;veis pareados foram convidados a participar do estudo. Pacientes com hist&#243;rico de doen&#231;as respirat&#243;rias ou doen&#231;a card&#237;aca, hipertens&#227;o, diabete melito, doen&#231;a tromboemb&#243;lica, doen&#231;as da tireoide, derrame, depress&#227;o, tabagismo ou alcoolismo foram exclu&#237;dos. Nenhum indiv&#237;duo tomava medica&#231;&#227;o anti-hipertensiva, antiarr&#237;tmicos ou outros f&#225;rmacos que possam afetar o controle auton&#244;mico da FC. Nenhum dos indiv&#237;duos encontrava-se em tratamento de fisioterapia ou participava de qualquer programa regular de exerc&#237;cios aer&#243;bicos. Os pacientes n&#227;o apresentavam outras doen&#231;as que pudessem influenciar o sistema nervoso auton&#244;mico, nem qualquer dist&#250;rbio de condu&#231;&#227;o ao eletrocardiograma anterior (ECG). O grupo controle era composto por volunt&#225;rios saud&#225;veis recrutados na comunidade acad&#234;mica por meio de an&#250;ncio. Os controles foram pareados por sexo, altura e peso, bem como n&#227;o usavam nenhuma medica&#231;&#227;o e foram julgados saud&#225;veis de acordo com anamnese e exame f&#237;sico. Todos os participantes assinaram um termo de consentimento informado e o estudo foi aprovado pelo Comit&#234; de &#201;tica do hospital (protocolo n&#250;mero 151/07) e est&#225; em conformidade com os Princ&#237;pios da Declara&#231;&#227;o de Helsinki<sup>19</sup>.</p>
    <p>
      <bold>Classifica&#231;&#227;o cl&#237;nica de comprometimento muscular</bold>
    </p>
    <p>Todos os pacientes foram categorizados em cinco graus de comprometimento, utilizando a Escala de Acometimento Muscular (MIRS) de acordo com a progress&#227;o distal a proximal da caracter&#237;stica do envolvimento muscular perif&#233;rico da MD: Grau 1 - aus&#234;ncia de sinais cl&#237;nicos de comprometimento muscular; grau 2 - sinais m&#237;nimos, tais como miotonia e fraqueza facial, ptose palpebral e/ou fraqueza proximal leve ou moderada; grau 3 - fraqueza distal sem comprometimento proximal; grau 4 - fraqueza proximal leve ou moderada; grau 5 - fraqueza proximal grave com o paciente confinado a uma cadeira de rodas<sup>20</sup>.</p>
    <p>
      <bold>Avalia&#231;&#227;o da variabilidade da frequ&#234;ncia card&#237;aca</bold>
    </p>
    <p>Os participantes foram avaliados pela manh&#227; para evitar diferen&#231;as causadas por altera&#231;&#245;es circadianas. A temperatura do laborat&#243;rio foi mantida entre 22 &#176;C e 24 &#176;C e a umidade relativa do ar entre 50% e 60%. Os pacientes foram informados sobre o protocolo, instru&#237;dos a abster-se de estimulantes ou bebidas alco&#243;licas nas 24 horas anteriores ao teste e a ingerir uma refei&#231;&#227;o leve pelo menos duas horas antes da avalia&#231;&#227;o.</p>
    <p>No dia do teste, os pacientes foram questionados e examinados em rela&#231;&#227;o ao seu bem-estar geral, uma boa noite de sono (7-8 horas) e cumprimento das instru&#231;&#245;es. Depois de um per&#237;odo de descanso de 20 minutos, a press&#227;o arterial sist&#234;mica (Missouri-Mikato, SP, Brasil) e o pulso radial (Nonin Medical, MN, EUA) foram medidos para determinar se as condi&#231;&#245;es basais eram adequadas para o teste.</p>
    <p>Para obter dados de FC, os volunt&#225;rios foram monitorados em dec&#250;bito dorsal por 15 minutos usando um monitor Polar S810i&#174; (Polar Electro Oy&#174;, Finl&#226;ndia) ap&#243;s 5 minutos de estabiliza&#231;&#227;o do sinal. O monitor Polar S810i&#174; &#233; um dispositivo pr&#225;tico e confi&#225;vel para monitorar a FC batimento a batimento para a an&#225;lise da VFC; o equipamento capta intervalos RR por meio de dois eletrodos adesivos. Os eletrodos foram colocados sobre a pele, sobre o ap&#234;ndice xifoide e sobre a linha axilar m&#233;dia ao n&#237;vel do ap&#234;ndice xifoide. Os dados obtidos pelo monitor Polar foram transferidos para o computador usando uma interface com um dispositivo de infravermelho para a emiss&#227;o do sinal. Esse sistema detecta a despolariza&#231;&#227;o ventricular, correspondente &#224; onda R do ECG, com uma taxa de amostragem de 500 Hz e uma resolu&#231;&#227;o temporal de 1 milissegundo<sup>21</sup>, validado por Loimaala e cols.<sup>22</sup>. A interface infravermelha foi colocada a uma dist&#226;ncia m&#225;xima de 8 polegadas e em um &#226;ngulo de 15&#176; em rela&#231;&#227;o ao Polar S810i&#174;<sup>20</sup>. Os sinais de FC foram processados para calcular os valores da VFC utilizando um programa espec&#237;fico MatLab<sup>&#174;</sup> (Math Works, USA), que calcula os valores da VFC com base nos intervalos RR obtidos no dispositivo. A VFC foi avaliada nos dom&#237;nios de tempo e frequ&#234;ncia, utilizando a regi&#227;o de maior estabilidade para rastrear os intervalos RR, tendo em vista que foram observados no m&#237;nimo 256 batimentos consecutivos. Os dom&#237;nios de frequ&#234;ncia foram analisados pela transformada r&#225;pida de Fourier aplicada em uma &#250;nica janela, ap&#243;s a subtra&#231;&#227;o linear da tend&#234;ncia em intervalos R-R previamente selecionados. A an&#225;lise no dom&#237;nio da frequ&#234;ncia foi realizada utilizando faixas de frequ&#234;ncia baixa (BF: 0,04 a 0,15 Hz) e alta (AF: 0,15-0,4 Hz) de pot&#234;ncia total em unidades normalizadas (<italic>un</italic>) e uma raz&#227;o BF/AF. A faixa AF &#233; modulada pelos sistemas simp&#225;tico e parassimp&#225;tico nervoso e a banda de AF est&#225; relacionada ao controle vagal card&#237;aco<sup>23</sup>.</p>
    <p>
      <bold>An&#225;lise estat&#237;stica</bold>
    </p>
    <p>Os participantes foram caracterizados por meio da estat&#237;stica descritiva, obtendo-se as m&#233;dias e desvios padr&#227;o da idade, &#205;ndice de Massa Corporal (IMC) e intervalo de tempo desde o diagn&#243;stico. A distribui&#231;&#227;o normal dos dados foi verificada por meio do teste de caminhada de Shapiro. O teste <italic>t</italic> pareado foi aplicado para comparar os dados da VFC intragrupos. ANOVA bifatorial foi utilizado em pacientes com DM e o grupo controle para determinar a influ&#234;ncia da doen&#231;a e o sexo sobre a variabilidade da frequ&#234;ncia card&#237;aca. Os resultados foram considerados estatisticamente significativos para p &lt; 0,05. O programa <italic>GraphPad Prism</italic><sup>&#174;</sup> foi utilizado para as an&#225;lises.</p>
    <p>
      <bold>Resultados</bold>
    </p>
    <p>Vinte e seis pacientes foram convidados para fazer parte do estudo. Tr&#234;s foram exclu&#237;dos por hist&#243;rico pr&#233;vio da doen&#231;a e quatro se recusaram a participar por falta de interesse. A amostra final era composta de 17 pacientes (10 homens e 7 mulheres) e 17 indiv&#237;duos saud&#225;veis pareados (10 homens e 7 mulheres). Conforme demonstrado na <xref ref-type="table" rid="aop02012_portt01">tabela 1</xref>, n&#227;o foram encontradas diferen&#231;as entre as caracter&#237;sticas antropom&#233;tricas entre os dois grupos.</p>
    <p content-type="asset">
      <table-wrap id="aop02012_portt01">
        <graphic xlink:href="1678-4170-abc-98-04-0353-00021-gt01.jpg"/></table-wrap>
    </p>
    <p>
      <bold>Caracter&#237;sticas cl&#237;nicas em pacientes com DM</bold>
    </p>
    <p>Entre os indiv&#237;duos com DM, pacientes do sexo masculino demonstraram mais tempo desde o diagn&#243;stico do que pacientes do sexo feminino e, portanto, encontravam-se em um est&#225;gio mais avan&#231;ado da doen&#231;a, de acordo com a classifica&#231;&#227;o cl&#237;nica de comprometimento muscular. Quase todos os pacientes do sexo masculino apresentavam comprometimento muscular perif&#233;rica ligeiro a moderado (sinais m&#237;nimos ou fraqueza distal), enquanto a maioria das mulheres foi classificada como grau 3 (<xref ref-type="table" rid="aop02012_portt02">tab. 2</xref>). Nenhum dos participantes era dependente de cadeira de roda e todos eram capazes de executar atividades normais do dia a dia.</p>
    <p content-type="asset">
      <table-wrap id="aop02012_portt02">
        <graphic xlink:href="1678-4170-abc-98-04-0353-00021-gt02.jpg"/></table-wrap>
    </p>
    <p>
      <bold>Variabilidade da frequ&#234;ncia card&#237;aca: diferen&#231;as de g&#234;nero entre os pacientes com DM</bold>
    </p>
    <p>Diferen&#231;as significativas interg&#234;nero foram encontradas nos pacientes com DM na posi&#231;&#227;o sentada. Os valores de BF/AF e BF<italic>un</italic> foram 73% e 25% maiores entre os homens, respectivamente, enquanto os valores de AF<italic>un</italic> foram 51,2% maiores em mulheres (<xref ref-type="table" rid="aop02012_portt03">tab. 3</xref>). A raz&#227;o BF/AF foi maior em homens nas posi&#231;&#245;es dec&#250;bito dorsal e na sentada. Mudan&#231;as significativas tamb&#233;m foram observadas a partir da posi&#231;&#227;o em dec&#250;bito dorsal para a posi&#231;&#227;o sentada em pacientes do sexo masculino, com uma diminui&#231;&#227;o de 19% nos valores de AF<italic>un</italic>, aumento de 19% em BF<italic>un</italic> e aumento de 42,3% na raz&#227;o BF/AF (<xref ref-type="table" rid="aop02012_portt03">tab. 3</xref>).</p>
    <p content-type="asset">
      <table-wrap id="aop02012_portt03">
        <graphic xlink:href="1678-4170-abc-98-04-0353-00021-gt03.jpg"/></table-wrap>
    </p>
    <p>
      <bold>Variabilidade da frequ&#234;ncia card&#237;aca: diferen&#231;as de g&#234;nero em indiv&#237;duos saud&#225;veis</bold>
    </p>
    <p>Conforme a <xref ref-type="table" rid="aop02012_portt04">tabela 4</xref>, o grupo controle n&#227;o apresentou diferen&#231;as entre g&#234;nero e durante as mudan&#231;as na posi&#231;&#227;o corporal de dec&#250;bito dorsal para a posi&#231;&#227;o sentada. Os valores de AF<italic>un</italic> na posi&#231;&#227;o dec&#250;bito dorsal foi 22,8% maior para as mulheres em rela&#231;&#227;o aos homens. Mudan&#231;as na posi&#231;&#227;o corporal de dec&#250;bito dorsal para a posi&#231;&#227;o sentada reduziram os valores AF<italic>un</italic> em 30,8% entre as mulheres saud&#225;veis. A raz&#227;o BF/AF aumentou para homens e mulheres durante as mudan&#231;as na posi&#231;&#227;o corporal em 50% e 132%, respectivamente.</p>
    <p content-type="asset">
      <table-wrap id="aop02012_portt04">
        <graphic xlink:href="1678-4170-abc-98-04-0353-00021-gt04.jpg"/></table-wrap>
    </p>
    <p>
      <bold>Influ&#234;ncia do sexo e da doen&#231;a sobre a VFC em indiv&#237;duos saud&#225;veis e pacientes com DM</bold>
    </p>
    <p>Na posi&#231;&#227;o sentada, os pacientes do sexo masculino com DM apresentavam balan&#231;os simp&#225;tico-vagais significativamente elevados em compara&#231;&#227;o com indiv&#237;duos controle saud&#225;veis, em 50,9% (<xref ref-type="table" rid="aop02012_portt05">Tab. 5</xref>). A influ&#234;ncia do sexo e da doen&#231;a sobre a VFC em indiv&#237;duos saud&#225;veis e pacientes com DM &#233; ilustrada nas <xref ref-type="fig" rid="aop02012_portf01">figuras 1</xref> e <xref ref-type="fig" rid="aop02012_portf02">2</xref> e demonstrado nas <xref ref-type="table" rid="aop02012_portt05">tabelas 5</xref> e <xref ref-type="table" rid="aop02012_portt06">6</xref>. Ao considerar as influ&#234;ncias da doen&#231;a e do g&#234;nero na VFC em pacientes com DM e indiv&#237;duos saud&#225;veis, observou-se significativa influ&#234;ncia de g&#234;nero sobre a raz&#227;o BF/AF, AF<italic>un</italic> na posi&#231;&#227;o sentada e em dec&#250;bito dorsal e BF<italic>un</italic> em dec&#250;bito dorsal. An&#225;lises <italic>post hoc</italic> mostram que o g&#234;nero impacta significativamente pacientes com DM e indiv&#237;duos saud&#225;veis de diferentes maneiras (p &lt; 0,01). O dom&#237;nio de baixa frequ&#234;ncia na posi&#231;&#227;o sentada, BF<italic>un</italic>, foi significativamente influenciado pela doen&#231;a.</p>
    <p content-type="asset">
      <table-wrap id="aop02012_portt05">
        <graphic xlink:href="1678-4170-abc-98-04-0353-00021-gt05.jpg"/></table-wrap>
    </p>
    <p content-type="asset">
      <fig id="aop02012_portf01">
        <graphic xlink:href="1678-4170-abc-98-04-0353-00021-gf01.jpg"/></fig>
    </p>
    <p content-type="asset">
      <fig id="aop02012_portf02">
        <graphic xlink:href="1678-4170-abc-98-04-0353-00021-gf02.jpg"/></fig>
    </p>
    <p content-type="asset">
      <table-wrap id="aop02012_portt06">
        <graphic xlink:href="1678-4170-abc-98-04-0353-00021-gt06.jpg"/></table-wrap>
    </p>
    <p>
      <bold>Discuss&#227;o</bold>
    </p>
    <p>O presente estudo prop&#245;e avaliar a modula&#231;&#227;o auton&#244;mica interg&#234;nero da FC em pacientes com DM e indiv&#237;duos saud&#225;veis em diferentes posi&#231;&#245;es corporais, bem como a influ&#234;ncia do g&#234;nero e da doen&#231;a e sua intera&#231;&#227;o em ambos os grupos. Os resultados da VFC em pacientes com DM quando comparados os g&#234;neros sugerem uma diferen&#231;a nos valores de BF<italic>un</italic>, AF<italic>un</italic> e raz&#227;o BF/AF, com uma diminui&#231;&#227;o da modula&#231;&#227;o parassimp&#225;tica e aumento da modula&#231;&#227;o simp&#225;tica para os homens avaliados na posi&#231;&#227;o sentada. As modula&#231;&#245;es simp&#225;tica e parassimp&#225;tica do cora&#231;&#227;o, avaliadas pelos valores de BF<italic>un</italic>, balan&#231;o simp&#225;tico-vagal e raz&#227;o BF/AF, aumentam para pacientes do sexo masculino com DM de acordo com mudan&#231;as na posi&#231;&#227;o corporal. Os balan&#231;os simp&#225;tico-vagal apresentam-se significativamente elevados em pacientes do sexo masculino com DM comparados aos controles saud&#225;veis. A VFC foi influenciada tanto pelo sexo quanto pela enfermidade. O sexo influenciou a BF<italic>un</italic> na posi&#231;&#227;o dec&#250;bito dorsal enquanto a raz&#227;o BF/AF e AF<italic>un</italic> foi afetada em ambas as posi&#231;&#245;es. A doen&#231;a influenciou significativamente o dom&#237;nio de baixa frequ&#234;ncia, BF<italic>un</italic>.</p>
    <p>Em contraste com outras pesquisas<sup>14-18</sup>, o presente estudo avalia a VFC durante curtos per&#237;odos na posi&#231;&#227;o sentada e em dec&#250;bito dorsal, al&#233;m de analisar a magnitude das diferen&#231;as de g&#234;nero. Procedimentos metodol&#243;gicos foram estabelecidos com base no fato de que as medi&#231;&#245;es de VFC obtidas com registros de 5 minutos demonstraram boa reprodutibilidade, al&#233;m da rapidez e facilidade de an&#225;lise<sup>24-26</sup>. Al&#233;m disso, as respostas da VFC para altera&#231;&#245;es posturais s&#227;o consideradas um melhor preditor de eventos card&#237;acos<sup>27</sup>. No entanto, a VFC &#233; relativamente simples de se avaliar, embora os resultados possam ser dif&#237;ceis de interpretar<sup>28</sup>. A modula&#231;&#227;o da frequ&#234;ncia card&#237;aca &#233; fortemente influenciada por diversos fatores, incluindo a posi&#231;&#227;o corporal, humor, estresse mental e as condi&#231;&#245;es ambientais<sup>29</sup>. Avalia&#231;&#227;o da VFC tamb&#233;m depende das condi&#231;&#245;es locais, tais como ru&#237;do, temperatura, respira&#231;&#227;o espont&#226;nea e tranquila<sup>30,31</sup>. Como afirmado anteriormente<sup>32</sup>, devido &#224;s diferen&#231;as fisiol&#243;gicas entre homens e mulheres, &#233; essencial comparar as diferen&#231;as interg&#234;nero nos &#237;ndices de VFC. Finalmente, a VFC deve ser analisada considerando os dom&#237;nios de frequ&#234;ncia em unidades normalizadas. Esta &#233; a forma mais recomendada de an&#225;lise, uma vez que representa com precis&#227;o as varia&#231;&#245;es da modula&#231;&#227;o simp&#225;tica e parassimp&#225;tica<sup>23</sup>.</p>
    <p>De acordo com nosso conhecimento, foram publicados cinco estudos anteriores sobre a modula&#231;&#227;o auton&#244;mica da frequ&#234;ncia card&#237;aca em pacientes com DM. Resultados contradit&#243;rios obtidos anteriormente podem ser fruto de diferentes m&#233;todos de an&#225;lise, autorregressivos ou transformada r&#225;pida de Fourier, n&#227;o intercambi&#225;veis<sup>33,34</sup>, bem como diversas posi&#231;&#245;es posturais durante a medi&#231;&#227;o da VFC em cada estudo. Inoue e cols.<sup>14</sup> foram os primeiros autores a investigar a VFC em pacientes com DM tipo 1. Eles analisaram a VFC usando o m&#233;todo autorregressivo em 10 pacientes com DM (4 homens e 6 mulheres) sem dist&#250;rbio de condu&#231;&#227;o card&#237;aca, al&#233;m de 10 controles saud&#225;veis pareados por idade e sexo em repouso em dec&#250;bito dorsal. Os autores descobriram que os valores de BFms<sup>2</sup> e AFms<sup>2</sup> diminu&#237;ram 642% e 452% respectivamente, e que a raz&#227;o BF/AF aumentou 158% em pacientes com DM em rela&#231;&#227;o a indiv&#237;duos saud&#225;veis. O estudo n&#227;o considerou o tempo desde o diagn&#243;stico e o comprometimento muscular. No entanto, os autores afirmam que no momento da investiga&#231;&#227;o todos os pacientes eram capazes de caminhar e realizar suas atividades di&#225;rias sem assist&#234;ncia, correspondendo &#224; classifica&#231;&#227;o 1-4 da escala MIRS. A diferen&#231;a significativa entre pacientes com DM e indiv&#237;duos saud&#225;veis nunca foi confirmada por outros estudos. Flachenecker e cols.<sup>15</sup> investigaram a resposta da fun&#231;&#227;o auton&#244;mica cardiovascular, incluindo a VFC, analisada pelo m&#233;todo r&#225;pido de Fourier, em pacientes com DM tipo 2. No entanto, eles registraram uma redu&#231;&#227;o de 53,7% para BFms<sup>2</sup> em pacientes com DM tipo 2 em compara&#231;&#227;o com volunt&#225;rios saud&#225;veis. Uma pesquisa recente identificou varia&#231;&#245;es significativas em termos de gravidade, tipo e distribui&#231;&#227;o de miotonia el&#233;trica na DM tipo 1 e tipo 2, bem como uma correla&#231;&#227;o entre a fraqueza muscular e miotonia nas duas doen&#231;as<sup>35</sup>. Sendo assim, a compara&#231;&#227;o entre o presente estudo e os resultados obtidos por esses autores &#233; inapropriada. Em um estudo semelhante ao nosso, Di Leo e cols.<sup>17</sup>, investigaram a VFC em pacientes com DM tipo 1 usando o m&#233;todo autorregressivo com diferentes posi&#231;&#245;es corporais. Em 23 pacientes com DM e um grupo controle, eles observaram uma diminui&#231;&#227;o significativa nos valores de BFms<sup>2</sup>, um marcador de atividade simp&#225;tica, para os pacientes com DM em dec&#250;bito dorsal. Os resultados do presente estudo podem ser apenas parcialmente considerados em compara&#231;&#227;o com os nossos. Os autores n&#227;o descreveram caracter&#237;sticas basais do grupo de controle; a an&#225;lise da VFC foi realizada usando o m&#233;todo autorregressivo e o grupo com DM inclu&#237;a homens e mulheres com uma varia&#231;&#227;o substancial na faixa et&#225;ria entre 15 e 51 anos. Esses fatores podem influenciar os resultados, tendo em vista que diferen&#231;as fisiol&#243;gicas s&#227;o estabelecidas pela VFC em homens e mulheres de diferentes idades.</p>
    <p>Outros dois estudos anteriores aplicaram o m&#233;todo r&#225;pido de Fourier para analisar a VFC em pacientes com DM. Em um estudo multic&#234;ntrico, Hardin e cols.<sup>16</sup> avaliaram 289 pacientes com DM em dec&#250;bito dorsal durante curtos per&#237;odos de aquisi&#231;&#227;o da VFC. Eles n&#227;o inclu&#237;ram um grupo controle devido ao fato de que o estudo tem como objetivo avaliar o ECG ambulatorial em uma popula&#231;&#227;o grande e diversificada com DM tipo 1, em que fatores cl&#237;nicos estiveram associados a VFC atrav&#233;s da an&#225;lise de dom&#237;nios de baixa frequ&#234;ncia BFms<sup>2</sup>, AFms<sup>2</sup> e raz&#227;o BF/AF. Al&#233;m disso, dado que a investiga&#231;&#227;o foi realizada em v&#225;rios centros, os dados da VFC mostraram grande variabilidade, com desvio padr&#227;o maior do que a m&#233;dia e superior aos comumente encontrados em estudos da VFC. Esses autores observaram uma diminui&#231;&#227;o na pot&#234;ncia total e predom&#237;nio do est&#237;mulo simp&#225;tico em rela&#231;&#227;o aos valores normais da VFC. Finalmente, Rakocevi&#262;-Stojanovi&#262; e cols.<sup>18</sup> analisaram a VFC de 20 pacientes e 15 controles saud&#225;veis. O estudo n&#227;o descrevia claramente as caracter&#237;sticas dos pacientes e do grupo controle, tais como idade, sexo, tempo de diagn&#243;stico e presen&#231;a de incapacidade maior ou menor. A pot&#234;ncia total caiu 64,6% em pacientes com DM em rela&#231;&#227;o aos controles saud&#225;veis, enquanto os valores de BFms<sup>2</sup>, AFms<sup>2</sup> e raz&#245;es BF/AF n&#227;o estiveram significativamente menores nos pacientes com DM. Os autores conclu&#237;ram que a disfun&#231;&#227;o simp&#225;tica pode ocorrer em pacientes com DM tipo 1.</p>
    <p>O presente estudo se baseia nessa investiga&#231;&#227;o pr&#233;via de v&#225;rias maneiras importantes. Em primeiro lugar, o tempo desde o diagn&#243;stico &#233; extremamente importante para o desenvolvimento de comorbidades em pacientes com DM, n&#227;o tendo sido considerado em nenhum estudo anterior, ao passo que o presente estudo definiu o tempo de diagn&#243;stico para o grupo de pacientes. Em segundo lugar, &#233; importante realizar an&#225;lises da VFC em separado para homens e mulheres, adotando um grupo controle. Em terceiro lugar, usando unidades normalizadas para estudar os dom&#237;nios de frequ&#234;ncia &#233; altamente recomendado, a fim de analisar a influ&#234;ncia da modula&#231;&#227;o auton&#244;mica simp&#225;tica e parassimp&#225;tica do cora&#231;&#227;o. Todos os procedimentos devem ser adotados tendo em conta que n&#227;o existem valores de refer&#234;ncia estabelecidos para a VFC. Por fim, tendo em vista que o estudo da VFC &#233; um assunto de grande interesse em pesquisas cl&#237;nicas e fisiol&#243;gicas, a medi&#231;&#227;o da VFC deve ser obtida sob condi&#231;&#245;es rigorosas para se reduzir os fatores que podem influenciar os resultados. De acordo com dados fornecidos pelos nossos resultados, pode-se estabelecer um ponto de partida na VFC na distrofia miot&#244;nica.</p>
    <p>O presente estudo cont&#233;m diversos pontos fortes; no entanto, a principal limita&#231;&#227;o est&#225; na pequena amostra de participantes e a extrapola&#231;&#227;o dos resultados deve ser feita com cuidado. Um objetivo importante deste trabalho, n&#227;o investigado anteriormente, foi o estudo da modula&#231;&#227;o auton&#244;mica card&#237;aca na DM, considerando pacientes do sexo masculino e feminino e a influ&#234;ncia da mudan&#231;a postural do corpo.</p>
    <p>Os resultados deste estudo sugerem que pacientes em meia-idade com DM do sexo masculino, em est&#225;gio e dura&#231;&#227;o moderada da doen&#231;a, o drive simp&#225;tico parece ser maior que em indiv&#237;duos saud&#225;veis pareados.</p>
    <p>
      <fn id="back" fn-type="corresp">
        <p>Correspond&#234;ncia:</p>
        <p> Guilherme Fregonezi </p>
        <p> Ruas das Algarobas, s/n, apto1402, Torre 2 - Cidade Verde </p>
        <p> 59151-433 - Parnamirim, RN, Brasil </p>
        <p> E-mail: </p>
        <p>
          <email xlink:href="fregonezi@ufrnet.br">fregonezi@ufrnet.br</email>
        </p>
      </fn>
    </p>
    <p>Artigo recebido em 04/07/11 </p>
    <p> Revisado recebido em 10/10/11 </p>
    <p> Aceito em 10/10/11.</p>
  </body>
  <back>
    <ref-list>
      <ref id="B1">
        <mixed-citation>1. Day JW, Roelofs    R, Leroy B, Pech I, Benzow K, Ranum LP. Clinical and genetic characteristics    of a five-generation family with a novel form of myotonic dystrophy (DM2). Neuromuscul    Disord. 1999;9(1):19-27.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy (DM2)</article-title>
          <source>Neuromuscul Disord</source>
          <date>
            <year>1999</year>
          </date>
          <fpage>19</fpage>
          <lpage>27</lpage>
          <issue>1</issue>
          <volume>9</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Day</surname>
              <given-names>JW</given-names>
            </name>
            <name>
              <surname>Roelofs</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Leroy</surname>
              <given-names>B</given-names>
            </name>
            <name>
              <surname>Pech</surname>
              <given-names>I</given-names>
            </name>
            <name>
              <surname>Benzow</surname>
              <given-names>K</given-names>
            </name>
            <name>
              <surname>Ranum</surname>
              <given-names>LP</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B2">
        <mixed-citation>2. Groh WJ, Groh    MR, Shen C, Monckton DG, Bodkin CL, Pascuzzi RM. Survival and CTG repeat expansion    in adults with myotonic dystrophy type 1. Muscle Nerve. 2011;43(5):648-51.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Survival and CTG repeat expansion in adults with myotonic dystrophy type 1</article-title>
          <source>Muscle Nerve</source>
          <date>
            <year>2011</year>
          </date>
          <fpage>648</fpage>
          <lpage>51</lpage>
          <issue>5</issue>
          <volume>43</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Groh</surname>
              <given-names>WJ</given-names>
            </name>
            <name>
              <surname>Groh</surname>
              <given-names>MR</given-names>
            </name>
            <name>
              <surname>Shen</surname>
              <given-names>C</given-names>
            </name>
            <name>
              <surname>Monckton</surname>
              <given-names>DG</given-names>
            </name>
            <name>
              <surname>Bodkin</surname>
              <given-names>CL</given-names>
            </name>
            <name>
              <surname>Pascuzzi</surname>
              <given-names>RM</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B3">
        <mixed-citation>3. Bouhour F, Bost    M, Vial C. Maladie de steinert. Presse Med. 2007;36(6 Pt 2):965-71.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Maladie de steinert</article-title>
          <source>Presse Med</source>
          <date>
            <year>2007</year>
          </date>
          <fpage>965</fpage>
          <lpage>71</lpage>
          <issue>6</issue>
          <volume>36</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Bouhour</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Bost</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Vial</surname>
              <given-names>C</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B4">
        <mixed-citation>4. Romigi A, Izzi    F, Pisani V, Placidi F, Pisani LR, Marciani MG, et al. Sleep disorders in adult-onset    myotonic dystrophy type 1: a controlled polysomnographic study. Eur J Neurol.    2011;18(9):1139-45.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Sleep disorders in adult-onset myotonic dystrophy type 1: a controlled polysomnographic study</article-title>
          <source>Eur J Neurol</source>
          <date>
            <year>2011</year>
          </date>
          <fpage>1139</fpage>
          <lpage>45</lpage>
          <issue>9</issue>
          <volume>18</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Romigi</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Izzi</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Pisani</surname>
              <given-names>V</given-names>
            </name>
            <name>
              <surname>Placidi</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Pisani</surname>
              <given-names>LR</given-names>
            </name>
            <name>
              <surname>Marciani</surname>
              <given-names>MG</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B5">
        <mixed-citation>5. Palmer PM, Neel    AT, Sprouls G, Morrison L. Swallow characteristics in patients with oculopharyngeal    muscular dystrophy. J Speech Lang Hear Res. 2010;53(6):1567-78.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Swallow characteristics in patients with oculopharyngeal muscular dystrophy</article-title>
          <source>J Speech Lang Hear Res</source>
          <date>
            <year>2010</year>
          </date>
          <fpage>1567</fpage>
          <lpage>78</lpage>
          <issue>6</issue>
          <volume>53</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Palmer</surname>
              <given-names>PM</given-names>
            </name>
            <name>
              <surname>Neel</surname>
              <given-names>AT</given-names>
            </name>
            <name>
              <surname>Sprouls</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Morrison</surname>
              <given-names>L</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B6">
        <mixed-citation>6. McNally E M,    Sparano D. Mechanisms and management of the heart in myotonic dystrophy. Heart.    2011;97(13):1094-100.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Mechanisms and management of the heart in myotonic dystrophy</article-title>
          <source>Heart</source>
          <date>
            <year>2011</year>
          </date>
          <fpage>1094</fpage>
          <lpage>100</lpage>
          <issue>13</issue>
          <volume>97</volume>
          <person-group person-group-type="author">
            <name>
              <surname>McNally E</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Sparano</surname>
              <given-names>D</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B7">
        <mixed-citation>7. Groh WJ, Groh    MR, Saha C, Kincaid JC, Simmons Z, Ciofaloni E, et al. Electrocardiographic    abnormalities and sudden death in myotonic dystrophy type 1. N Engl J Med. 2008;358(25):2688-97.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Electrocardiographic abnormalities and sudden death in myotonic dystrophy type 1</article-title>
          <source>N Engl J Med</source>
          <date>
            <year>2008</year>
          </date>
          <fpage>2688</fpage>
          <lpage>97</lpage>
          <issue>25</issue>
          <volume>358</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Groh</surname>
              <given-names>WJ</given-names>
            </name>
            <name>
              <surname>Groh</surname>
              <given-names>MR</given-names>
            </name>
            <name>
              <surname>Saha</surname>
              <given-names>C</given-names>
            </name>
            <name>
              <surname>Kincaid</surname>
              <given-names>JC</given-names>
            </name>
            <name>
              <surname>Simmons</surname>
              <given-names>Z</given-names>
            </name>
            <name>
              <surname>Ciofaloni</surname>
              <given-names>E</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B8">
        <mixed-citation>8. Pelargonio G,    Dello Russo A, Sanna T, De Martino G, Bellocci F. Myotonic dystrophy and the    heart. Heart. 2002;88(6):665-70.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Myotonic dystrophy and the heart</article-title>
          <source>Heart</source>
          <date>
            <year>2002</year>
          </date>
          <fpage>665</fpage>
          <lpage>70</lpage>
          <issue>6</issue>
          <volume>88</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Pelargonio</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Dello Russo</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Sanna</surname>
              <given-names>T</given-names>
            </name>
            <name>
              <surname>De Martino</surname>
              <given-names>G</given-names>
            </name>
            <name>
              <surname>Bellocci</surname>
              <given-names>F</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B9">
        <mixed-citation>9. Tsuji H, Larson    MG, Venditti FJ Jr, Manders ES, Evans JC, Feldman CL, et al. Impact of reduced    heart rate variability on risk for cardiac events. The Framingham Heart Study.    Circulation. 1996;94(11):2850-5.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Impact of reduced heart rate variability on risk for cardiac events: The Framingham Heart Study</article-title>
          <source>Circulation</source>
          <date>
            <year>1996</year>
          </date>
          <fpage>2850</fpage>
          <lpage>5</lpage>
          <issue>11</issue>
          <volume>94</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Tsuji</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Larson</surname>
              <given-names>MG</given-names>
            </name>
            <name>
              <surname>Venditti FJ</surname>
              <given-names>Jr</given-names>
            </name>
            <name>
              <surname>Manders</surname>
              <given-names>ES</given-names>
            </name>
            <name>
              <surname>Evans</surname>
              <given-names>JC</given-names>
            </name>
            <name>
              <surname>Feldman</surname>
              <given-names>CL</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B10">
        <mixed-citation>10. Stein PK, Kleiger    RE. Insights from the study of heart rate variability. Annu Rev Med. 1999;50:249-61.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Insights from the study of heart rate variability</article-title>
          <source>Annu Rev Med</source>
          <date>
            <year>1999</year>
          </date>
          <fpage>249</fpage>
          <lpage>61</lpage>
          <volume>50</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Stein</surname>
              <given-names>PK</given-names>
            </name>
            <name>
              <surname>Kleiger</surname>
              <given-names>RE</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B11">
        <mixed-citation>11. Hoikkala H,    Haapalahti P, Viitasalo M, Vaananen H, Sovijarvi AR, Ylikorkala O, et al. Association    between vasomotor hot flashes and heart rate variability in recently postmenopausal    women. Menopause. 2010;17(2):315-20.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Association between vasomotor hot flashes and heart rate variability in recently postmenopausal women</article-title>
          <source>Menopause</source>
          <date>
            <year>2010</year>
          </date>
          <fpage>315</fpage>
          <lpage>20</lpage>
          <issue>2</issue>
          <volume>17</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Hoikkala</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Haapalahti</surname>
              <given-names>P</given-names>
            </name>
            <name>
              <surname>Viitasalo</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Vaananen</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Sovijarvi</surname>
              <given-names>AR</given-names>
            </name>
            <name>
              <surname>Ylikorkala</surname>
              <given-names>O</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B12">
        <mixed-citation>12. Olofsson BO,    Niklasson U, Forsberg H, Bjerle P, Anderson S, Henriksson A. Assessment of autonomic    nerve function in myotonic dystrophy. J Auton Nerv Syst. 1990;29(3):187-92.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Assessment of autonomic nerve function in myotonic dystrophy</article-title>
          <source>J Auton Nerv Syst</source>
          <date>
            <year>1990</year>
          </date>
          <fpage>187</fpage>
          <lpage>92</lpage>
          <issue>3</issue>
          <volume>29</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Olofsson</surname>
              <given-names>BO</given-names>
            </name>
            <name>
              <surname>Niklasson</surname>
              <given-names>U</given-names>
            </name>
            <name>
              <surname>Forsberg</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Bjerle</surname>
              <given-names>P</given-names>
            </name>
            <name>
              <surname>Anderson</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Henriksson</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B13">
        <mixed-citation>13. den Heijer    JC, van Dijk JG, Bollen WL, Bos JE, Wintzen AR. Assessment of autonomic function    in myotonic dystrophy. J Neurol Neurosurg Psychiatry. 1991;54(6):531-4.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Assessment of autonomic function in myotonic dystrophy</article-title>
          <source>J Neurol Neurosurg Psychiatry</source>
          <date>
            <year>1991</year>
          </date>
          <fpage>531</fpage>
          <lpage>4</lpage>
          <issue>6</issue>
          <volume>54</volume>
          <person-group person-group-type="author">
            <name>
              <surname>den Heijer</surname>
              <given-names>JC</given-names>
            </name>
            <name>
              <surname>van Dijk</surname>
              <given-names>JG</given-names>
            </name>
            <name>
              <surname>Bollen</surname>
              <given-names>WL</given-names>
            </name>
            <name>
              <surname>Bos</surname>
              <given-names>JE</given-names>
            </name>
            <name>
              <surname>Wintzen</surname>
              <given-names>AR</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B14">
        <mixed-citation>14. Inoue K, Ogata    H, Matsui M, Hayano J, Miyake S, Kumashiro M, et al. Assessment of autonomic    function in myotonic dystrophy by spectral analysis of heart-rate variability.    J Auton Nerv Syst. 1995;55(1-2):131-4.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Assessment of autonomic function in myotonic dystrophy by spectral analysis of heart-rate variability</article-title>
          <source>J Auton Nerv Syst</source>
          <date>
            <year>1995</year>
          </date>
          <fpage>131</fpage>
          <lpage>4</lpage>
          <issue>1-2</issue>
          <volume>55</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Inoue</surname>
              <given-names>K</given-names>
            </name>
            <name>
              <surname>Ogata</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Matsui</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Hayano</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Miyake</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Kumashiro</surname>
              <given-names>M</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B15">
        <mixed-citation>15. Flachenecker    P, Schneider C, Cursiefen S, Ricker K, Toyka KV, Reiners K. Assessment of cardiovascular    autonomic function in myotonic dystrophy tipe 2 (DM2/PROMM). Neuromuscul Disord.    2003;13(4):289-93.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Assessment of cardiovascular autonomic function in myotonic dystrophy tipe 2 (DM2/PROMM)</article-title>
          <source>Neuromuscul Disord</source>
          <date>
            <year>2003</year>
          </date>
          <fpage>289</fpage>
          <lpage>93</lpage>
          <issue>4</issue>
          <volume>13</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Flachenecker</surname>
              <given-names>P</given-names>
            </name>
            <name>
              <surname>Schneider</surname>
              <given-names>C</given-names>
            </name>
            <name>
              <surname>Cursiefen</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Ricker</surname>
              <given-names>K</given-names>
            </name>
            <name>
              <surname>Toyka</surname>
              <given-names>KV</given-names>
            </name>
            <name>
              <surname>Reiners</surname>
              <given-names>K</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B16">
        <mixed-citation>16. Hardin BA,    Lowe MR, Bhakta D, Groh WJ. Heart rate variability declines with increasing    age and CTG repeat length in patients with myotonic dystrophy type 1. Ann Noninvasive    Electrocardiol. 2003;8(3):227-32.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Heart rate variability declines with increasing age and CTG repeat length in patients with myotonic dystrophy type 1</article-title>
          <source>Ann Noninvasive Electrocardiol</source>
          <date>
            <year>2003</year>
          </date>
          <fpage>227</fpage>
          <lpage>32</lpage>
          <issue>3</issue>
          <volume>8</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Hardin</surname>
              <given-names>BA</given-names>
            </name>
            <name>
              <surname>Lowe</surname>
              <given-names>MR</given-names>
            </name>
            <name>
              <surname>Bhakta</surname>
              <given-names>D</given-names>
            </name>
            <name>
              <surname>Groh</surname>
              <given-names>WJ</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B17">
        <mixed-citation>17. Di Leo R, Rodolico    C, De Gregorio C, Recupero A, Cogliatore S, Annesi G, et al. Cardiovascular    autonomic control in myotonic dystrophy type 1: a correlative study with clinical    and genetic data. Neuromuscul Disord. 2004;14(2):136-41.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Cardiovascular autonomic control in myotonic dystrophy type 1: a correlative study with clinical and genetic data</article-title>
          <source>Neuromuscul Disord</source>
          <date>
            <year>2004</year>
          </date>
          <fpage>136</fpage>
          <lpage>41</lpage>
          <issue>2</issue>
          <volume>14</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Di Leo</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Rodolico</surname>
              <given-names>C</given-names>
            </name>
            <name>
              <surname>De Gregorio</surname>
              <given-names>C</given-names>
            </name>
            <name>
              <surname>Recupero</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Cogliatore</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Annesi</surname>
              <given-names>G</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B18">
        <mixed-citation>18. Rakocevi&#262;-Stojanovi&#262;    V, Milovanovi&#262; B, Ivi&#262; N, Ille T, Marjanovic I, Stevic Z, et al. Cardiac    autonomic nervous system in patients with myotonic dystrophy type 1. Acta Myol.    2007;26(2):112-4.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Cardiac autonomic nervous system in patients with myotonic dystrophy type 1</article-title>
          <source>Acta Myol</source>
          <date>
            <year>2007</year>
          </date>
          <fpage>112</fpage>
          <lpage>4</lpage>
          <issue>2</issue>
          <volume>26</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Rakocevi&#262;-Stojanovi&#262;</surname>
              <given-names>V</given-names>
            </name>
            <name>
              <surname>Milovanovi&#262;</surname>
              <given-names>B</given-names>
            </name>
            <name>
              <surname>Ivi&#262;</surname>
              <given-names>N</given-names>
            </name>
            <name>
              <surname>Ille</surname>
              <given-names>T</given-names>
            </name>
            <name>
              <surname>Marjanovic</surname>
              <given-names>I</given-names>
            </name>
            <name>
              <surname>Stevic</surname>
              <given-names>Z</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B19">
        <label>19</label>
        <mixed-citation>19. World Medical Association. Declaration of Helsinki: ethical principals for research involving human subjects. As amended in Tokyo, 2004. Ferney-Voltaire, France: The Association; 2004. [Accessed on 2011 june 26]. Available from: <ext-link ext-link-type="uri" xlink:href="http://www.wma.net/e/ethicsunit/helsinki.htm">http://www.wma.net/e/ethicsunit/helsinki.htm</ext-link></mixed-citation>
        <element-citation publication-type="confproc">
          <source>Declaration of Helsinki: ethical principals for research involving human subjects</source>
          <date>
            <year>2004</year>
          </date>
        </element-citation>
      </ref>
      <ref id="B20">
        <mixed-citation>20. Mathieu J,    Boivin H, Meunier D, Gaudreault M, B&#233;gin P. Assessment of a disease-specific    muscular impairment rating scale in myotonic dystrophy. Neurology. 2001;56(3):336-40.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Assessment of a disease-specific muscular impairment rating scale in myotonic dystrophy</article-title>
          <source>Neurology</source>
          <date>
            <year>2001</year>
          </date>
          <fpage>336</fpage>
          <lpage>40</lpage>
          <issue>3</issue>
          <volume>56</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Mathieu</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Boivin</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Meunier</surname>
              <given-names>D</given-names>
            </name>
            <name>
              <surname>Gaudreault</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>B&#233;gin</surname>
              <given-names>P</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B21">
        <mixed-citation>21. Ruha A, Sallinen    S, Nissila S. A real-time microprocessor QRS detector system with a 1-ms timing    accuracy for the measurement of ambulatory HRV. IEEE Trans Biomed Eng. 1997;44(3):159-67.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>A real-time microprocessor QRS detector system with a 1-ms timing accuracy for the measurement of ambulatory HRV</article-title>
          <source>IEEE Trans Biomed Eng</source>
          <date>
            <year>1997</year>
          </date>
          <fpage>159</fpage>
          <lpage>67</lpage>
          <issue>3</issue>
          <volume>44</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Ruha</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Sallinen</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Nissila</surname>
              <given-names>S</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B22">
        <mixed-citation>22. Loimaala A,    Sievanen H, Laukkanen R, Parkka J, Vuori I, Huikuri H. Accuracy of a novel real-time    microprocessor QRS detector for heart rate variability assessment. Clin Physiol.    1999;19(1):84-8.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Accuracy of a novel real-time microprocessor QRS detector for heart rate variability assessment</article-title>
          <source>Clin Physiol</source>
          <date>
            <year>1999</year>
          </date>
          <fpage>84</fpage>
          <lpage>8</lpage>
          <issue>1</issue>
          <volume>19</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Loimaala</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Sievanen</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Laukkanen</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Parkka</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Vuori</surname>
              <given-names>I</given-names>
            </name>
            <name>
              <surname>Huikuri</surname>
              <given-names>H</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B23">
        <mixed-citation>23. Heart rate    variability: standards of measurement, physiological interpretation, and clinical    use. Task Force of European Society of Cardiology and the North American Society    of Pacing and Electrophysiology. Circulation. 1996;93(5):1043-65.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Heart rate variability: standards of measurement, physiological interpretation, and clinical use. Task Force of European Society of Cardiology and the North American Society of Pacing and Electrophysiology</article-title>
          <source>Circulation</source>
          <date>
            <year>1996</year>
          </date>
          <fpage>1043</fpage>
          <lpage>65</lpage>
          <issue>5</issue>
          <volume>93</volume>
        </element-citation>
      </ref>
      <ref id="B24">
        <mixed-citation>24. Lord SW, Senior    RR, Das M, Whittam AM, Murray A, McComb JM. Low-frequency heart rate variability:    reproducibility in cardiac transplant recipients and normal subjects. Clin Sci.    2001;100(1):43-6.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Low-frequency heart rate variability: reproducibility in cardiac transplant recipients and normal subjects</article-title>
          <source>Clin Sci</source>
          <date>
            <year>2001</year>
          </date>
          <fpage>43</fpage>
          <lpage>6</lpage>
          <issue>1</issue>
          <volume>100</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Lord</surname>
              <given-names>SW</given-names>
            </name>
            <name>
              <surname>Senior</surname>
              <given-names>RR</given-names>
            </name>
            <name>
              <surname>Das</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Whittam</surname>
              <given-names>AM</given-names>
            </name>
            <name>
              <surname>Murray</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>McComb</surname>
              <given-names>JM</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B25">
        <mixed-citation>25. Hojgaard MV,    Holstein-Rathlou NH, Agner E, Kanters JK. Reproducibility of heart rate variability,    blood pressure variability and baroreceptor sensitivity during rest and head-up    tilt. Blood Press Monit. 2005;10(1):19-24.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Reproducibility of heart rate variability, blood pressure variability and baroreceptor sensitivity during rest and head-up tilt</article-title>
          <source>Blood Press Monit</source>
          <date>
            <year>2005</year>
          </date>
          <fpage>19</fpage>
          <lpage>24</lpage>
          <issue>1</issue>
          <volume>10</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Hojgaard</surname>
              <given-names>MV</given-names>
            </name>
            <name>
              <surname>Holstein-Rathlou</surname>
              <given-names>NH</given-names>
            </name>
            <name>
              <surname>Agner</surname>
              <given-names>E</given-names>
            </name>
            <name>
              <surname>Kanters</surname>
              <given-names>JK</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B26">
        <mixed-citation>26. Dantas EM,    Gon&#231;alves CP, Silva AB, Rodrigues SL, Ramos MS, Andre&#227;o RV, et    al. Reproducibility of heart rate variability parameters measured in healthy    subjects at rest and after a postural change maneuver. Braz J Med Biol Res.    2010;43(10):982-8.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Reproducibility of heart rate variability parameters measured in healthy subjects at rest and after a postural change maneuver</article-title>
          <source>Braz J Med Biol Res</source>
          <date>
            <year>2010</year>
          </date>
          <fpage>982</fpage>
          <lpage>8</lpage>
          <issue>10</issue>
          <volume>43</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Dantas</surname>
              <given-names>EM</given-names>
            </name>
            <name>
              <surname>Gon&#231;alves</surname>
              <given-names>CP</given-names>
            </name>
            <name>
              <surname>Silva</surname>
              <given-names>AB</given-names>
            </name>
            <name>
              <surname>Rodrigues</surname>
              <given-names>SL</given-names>
            </name>
            <name>
              <surname>Ramos</surname>
              <given-names>MS</given-names>
            </name>
            <name>
              <surname>Andre&#227;o</surname>
              <given-names>RV</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B27">
        <mixed-citation>27. Carnethon MR,    Liao D, Evans GW, Cascio WE, Chambless LE, Rosamond WD, et al. Does the cardiac    autonomic response to postural change predict incident coronary heart disease    and mortality? The Atherosclerosis Risk in Communities Study. Am J Epidemiol.    2002;155(1):48-56.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Does the cardiac autonomic response to postural change predict incident coronary heart disease and mortality?: The Atherosclerosis Risk in Communities Study</article-title>
          <source>Am J Epidemiol</source>
          <date>
            <year>2002</year>
          </date>
          <fpage>48</fpage>
          <lpage>56</lpage>
          <issue>1</issue>
          <volume>155</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Carnethon</surname>
              <given-names>MR</given-names>
            </name>
            <name>
              <surname>Liao</surname>
              <given-names>D</given-names>
            </name>
            <name>
              <surname>Evans</surname>
              <given-names>GW</given-names>
            </name>
            <name>
              <surname>Cascio</surname>
              <given-names>WE</given-names>
            </name>
            <name>
              <surname>Chambless</surname>
              <given-names>LE</given-names>
            </name>
            <name>
              <surname>Rosamond</surname>
              <given-names>WD</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B28">
        <mixed-citation>28. Low PA. Clinical    autonomic disorders. Philadelphia: Lippincott-Raven Publishers; 1997.</mixed-citation>
        <element-citation publication-type="book">
          <source>Clinical autonomic disorders</source>
          <date>
            <year>1997</year>
          </date>
          <person-group person-group-type="author">
            <name>
              <surname>Low</surname>
              <given-names>PA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B29">
        <mixed-citation>29. Ewing DJ, Neilson    JM, Shapiro CM, Stewart JA, Reid W. Twenty four hour heart rate variability:    effects of posture, sleep, and time of day in healthy controls and comparison    with bedside tests of autonomic function in diabetic patients. Br Heart J. 1991;65(5):239-44.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Twenty four hour heart rate variability: effects of posture, sleep, and time of day in healthy controls and comparison with bedside tests of autonomic function in diabetic patients</article-title>
          <source>Br Heart J</source>
          <date>
            <year>1991</year>
          </date>
          <fpage>239</fpage>
          <lpage>44</lpage>
          <issue>5</issue>
          <volume>65</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Ewing</surname>
              <given-names>DJ</given-names>
            </name>
            <name>
              <surname>Neilson</surname>
              <given-names>JM</given-names>
            </name>
            <name>
              <surname>Shapiro</surname>
              <given-names>CM</given-names>
            </name>
            <name>
              <surname>Stewart</surname>
              <given-names>JA</given-names>
            </name>
            <name>
              <surname>Reid</surname>
              <given-names>W</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B30">
        <mixed-citation>30. Pinna GD, Maestri    R, Torunski A, Danilowicz-Szymanowicz L, Szwoch M, La Rovere MT, et al. Heart    rate variability measures: a fresh look at reliability. Clin Sci. 2007;113(3):131-40.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Heart rate variability measures: a fresh look at reliability</article-title>
          <source>Clin Sci</source>
          <date>
            <year>2007</year>
          </date>
          <fpage>131</fpage>
          <lpage>40</lpage>
          <issue>3</issue>
          <volume>113</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Pinna</surname>
              <given-names>GD</given-names>
            </name>
            <name>
              <surname>Maestri</surname>
              <given-names>R</given-names>
            </name>
            <name>
              <surname>Torunski</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Danilowicz-Szymanowicz</surname>
              <given-names>L</given-names>
            </name>
            <name>
              <surname>Szwoch</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>La Rovere</surname>
              <given-names>MT</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B31">
        <mixed-citation>31. Sandercock    GR, Bromley PD, Brodie DA. The reliability of short-term measurements of heart    rate variability. Int J Cardiol. 2005;103(3):238-47.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>The reliability of short-term measurements of heart rate variability</article-title>
          <source>Int J Cardiol</source>
          <date>
            <year>2005</year>
          </date>
          <fpage>238</fpage>
          <lpage>47</lpage>
          <issue>3</issue>
          <volume>103</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Sandercock</surname>
              <given-names>GR</given-names>
            </name>
            <name>
              <surname>Bromley</surname>
              <given-names>PD</given-names>
            </name>
            <name>
              <surname>Brodie</surname>
              <given-names>DA</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B32">
        <mixed-citation>32. Acharya UR,    Kannathal N, Hua LM, Yi LM. Study of heart rate variability signals at sitting    and supine positions. J Body Mov Ther. 2005;9(2):134-41.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Study of heart rate variability signals at sitting and supine positions</article-title>
          <source>J Body Mov Ther</source>
          <date>
            <year>2005</year>
          </date>
          <fpage>134</fpage>
          <lpage>41</lpage>
          <issue>2</issue>
          <volume>9</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Acharya</surname>
              <given-names>UR</given-names>
            </name>
            <name>
              <surname>Kannathal</surname>
              <given-names>N</given-names>
            </name>
            <name>
              <surname>Hua</surname>
              <given-names>LM</given-names>
            </name>
            <name>
              <surname>Yi</surname>
              <given-names>LM</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B33">
        <mixed-citation>33. Chemla D, Young    J, Badilini F, Maison-Blanche P, Affres H, Lecarpentier Y, et al. Comparison    of fast Fourier transform and autoregressive spectral analysis for the study    of heart rate variability in diabetic patients. Int J Cardiol. 2005;104(3):307-13.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Comparison of fast Fourier transform and autoregressive spectral analysis for the study of heart rate variability in diabetic patients</article-title>
          <source>Int J Cardiol</source>
          <date>
            <year>2005</year>
          </date>
          <fpage>307</fpage>
          <lpage>13</lpage>
          <issue>3</issue>
          <volume>104</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Chemla</surname>
              <given-names>D</given-names>
            </name>
            <name>
              <surname>Young</surname>
              <given-names>J</given-names>
            </name>
            <name>
              <surname>Badilini</surname>
              <given-names>F</given-names>
            </name>
            <name>
              <surname>Maison-Blanche</surname>
              <given-names>P</given-names>
            </name>
            <name>
              <surname>Affres</surname>
              <given-names>H</given-names>
            </name>
            <name>
              <surname>Lecarpentier</surname>
              <given-names>Y</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B34">
        <mixed-citation>34. Pichon A, Roulaud    M, Antoine-Jonville S, de Bisschop C, Denjean A. Spectral analysis of heart    rate variability: interchangeability between autoregressive analysis and fast    Fourier transform. J Electrocardiol. 2006;39(1):31-7.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Spectral analysis of heart rate variability: interchangeability between autoregressive analysis and fast Fourier transform</article-title>
          <source>J Electrocardiol</source>
          <date>
            <year>2006</year>
          </date>
          <fpage>31</fpage>
          <lpage>7</lpage>
          <issue>1</issue>
          <volume>39</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Pichon</surname>
              <given-names>A</given-names>
            </name>
            <name>
              <surname>Roulaud</surname>
              <given-names>M</given-names>
            </name>
            <name>
              <surname>Antoine-Jonville</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>de Bisschop</surname>
              <given-names>C</given-names>
            </name>
            <name>
              <surname>Denjean</surname>
              <given-names>A</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
      <ref id="B35">
        <mixed-citation>35. Logigian EL,    Ciafaloni E, Quinn LC, Dilek N, Pandya S, Moscley RT 3rd, et al. Severity, type,    and distribution of myotonic discharges are different in type 1 and type 2 myotonic    dystrophy. Muscle Nerve. 2007;35(4):479-85.</mixed-citation>
        <element-citation publication-type="journal">
          <article-title>Severity, type, and distribution of myotonic discharges are different in type 1 and type 2 myotonic dystrophy</article-title>
          <source>Muscle Nerve</source>
          <date>
            <year>2007</year>
          </date>
          <fpage>479</fpage>
          <lpage>85</lpage>
          <issue>4</issue>
          <volume>35</volume>
          <person-group person-group-type="author">
            <name>
              <surname>Logigian</surname>
              <given-names>EL</given-names>
            </name>
            <name>
              <surname>Ciafaloni</surname>
              <given-names>E</given-names>
            </name>
            <name>
              <surname>Quinn</surname>
              <given-names>LC</given-names>
            </name>
            <name>
              <surname>Dilek</surname>
              <given-names>N</given-names>
            </name>
            <name>
              <surname>Pandya</surname>
              <given-names>S</given-names>
            </name>
            <name>
              <surname>Moscley RT</surname>
              <given-names>3rd</given-names>
            </name>
          </person-group>
        </element-citation>
      </ref>
    </ref-list>
  </back>
  <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">Heart rate variability in Myotonic Dystrophy type 1 patients</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>BACKGROUND: Cardiac involvement is common in myotonic dystrophy (MD) patients. Heart rate variability (HRV) is a simple and reliable technique that can be useful for studying the influence of the autonomic nervous system on the heart. OBJECTIVE: Study heart rate variability in patients with type 1 MD. METHODS: We studied HRV during 5-minute recordings in MD patients and in a healthy control group. We analyzed frequency domains (LF and HF) in normalized units (nu) and sympathovagal balance, in the sitting and supine position. RESULTS: Seventeen patients (10 men and 7 women) and seventeen matched healthy individuals (10 men and 7 women) were studied. Sympathetic and parasympathetic modulations of the heart increased in male MD patients from supine to sitting position in 19% of LFnu and the LF/HF ratio rose by 42.3%. In the sitting position, male MD patients exhibited significantly higher sympathovagal balances in 50.9% compared to healthy control individuals. HRV was influenced by both gender and disease. Gender influenced LFnu in the supine position while the LF/HF ratio and HFnu were affected in both positions. Post hoc analyses showed that gender significantly impacts MD patients and healthy individuals in different ways (p &lt; 0.01). The low frequency domain in the sitting position (LFnu) was significantly influenced by the disease. CONCLUSION: The results of this study suggest that the sympathetic drive in middle-aged male MD patients who are not severely impaired and present moderate disease duration seems to be greater than in healthy matched individuals.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Heart rate</kwd>
        <kwd>myotonic dystrophy</kwd>
        <kwd>spectrum analysis</kwd>
        <kwd>autonomic nervous system</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <fn id="top-body2">
          <label>
            <bold>Heart rate variability in Myotonic Dystrophy type 1 patients</bold>
          </label>
          <p>
            <bold>Guilherme Fregonezi<sup>I</sup>; Thaise Ara&#250;jo<sup>I</sup>; Mario Emilio Dourado Junior<sup>II</sup>; Joceline Ferezini<sup>I</sup>; Ester Silva<sup>III</sup>; Vanessa Resqueti<sup>I</sup></bold>
          </p>
        </fn>
      </p>
      <p><sup>I</sup>Laborat&#243;rio de Fisioterapia Pneumocardiovascular - Departamento de Fisioterapia - Centro de Ci&#234;ncias da Sa&#250;de - Universidade Federal do Rio Grande do Norte, Natal, RN</p>
      <p><sup>II</sup>Cl&#237;nica das Doen&#231;as Neuromusculares - Hospital Onofre Lopes - Universidade Federal do Rio Grande do Norte, Natal, RN</p>
      <p><sup>III</sup>Laborat&#243;rio de Doen&#231;as Cardiovasculares - Universidade Metodista de Piracicaba, Piracicaba, SP, Brazil</p>
      <p>Mailing Address</p>
      <p>
        <bold>ABSTRACT</bold>
      </p>
      <p><bold>BACKGROUND:</bold> Cardiac involvement is common in myotonic dystrophy (MD) patients. Heart rate variability (HRV) is a simple and reliable technique that can be useful for studying the influence of the autonomic nervous system on the heart.</p>
      <p> OBJECTIVE: Study heart rate variability in patients with type 1 MD.</p>
      <p><bold>METHODS:</bold> We studied HRV during 5-minute recordings in MD patients and in a healthy control group. We analyzed frequency domains (LF and HF) in normalized units (nu) and sympathovagal balance, in the sitting and supine position.</p>
      <p><bold>RESULTS:</bold> Seventeen patients (10 men and 7 women) and seventeen matched healthy individuals (10 men and 7 women) were studied. Sympathetic and parasympathetic modulations of the heart increased in male MD patients from supine to sitting position in 19% of LFnu and the LF/HF ratio rose by 42.3%. In the sitting position, male MD patients exhibited significantly higher sympathovagal balances in 50.9% compared to healthy control individuals. HRV was influenced by both gender and disease. Gender influenced LFnu in the supine position while the LF/HF ratio and HFnu were affected in both positions. Post hoc analyses showed that gender significantly impacts MD patients and healthy individuals in different ways (p &lt; 0.01). The low frequency domain in the sitting position (LFnu) was significantly influenced by the disease.</p>
      <p><bold>CONCLUSION:</bold> The results of this study suggest that the sympathetic drive in middle-aged male MD patients who are not severely impaired and present moderate disease duration seems to be greater than in healthy matched individuals.</p>
      <p><bold>Keywords:</bold> Heart rate; myotonic dystrophy; spectrum analysis; autonomic nervous system.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>Myotonic dystrophy (MD) is the most frequent form of muscular dystrophy in adults<sup>1,2</sup>. Clinical manifestations of MD are myotony, muscle weakness, cardiac abnormalities, cataracts, endocrine and digestive tract disturbances; sleep disorders and baldness<sup>3-5</sup>. Heart problems experienced by patients with MD are well known<sup>1,6</sup>. Most patients are asymptomatic; however, alterations in cardiac physiology are common, as observed in electrocardiograms<sup>6</sup>. Clinical manifestations include conduction delay, rhythm disturbances and myocardial disease. Electrocardiographic disorder indicates abnormalities in intraventricular and atrioventricular conduction, atrial fibrillation and ventricular arrhythmias. Histopathology data show fibrosis in the conduction system and in the sinoatrial node associated to myocyte hypertrophy<sup>7</sup>. Patients with greater skeletal muscle impairment are older and experience heart problems more frequently<sup>8</sup>.</p>
      <p>The autonomic nervous system plays a crucial role in heart rate (HR) modulation. A decrease in its variability is a predictor of morbidity and mortality<sup>9,10</sup>. Earlier research found that healthy women showed greater vagal dominance over HR, which seems to account for their enhanced cardioprotection compared to men, although these differences decrease with age<sup>11</sup>. The study of heart rate variability (HRV) has therefore been proposed as a simple, inexpensive and non-invasive method that provides information on neurocardial integrity. A number of investigations on the overall function of the autonomic nervous system in patients with MD show that the presence of autonomic neuropathy is highly unlikely<sup>1,12,13</sup>. However, studies on autonomic modulation of HR in patients with MD have obtained conflicting results<sup>14-18</sup>. The present study aimed to evaluate the possible differences in autonomic modulation of HR between the sexes for patients with MD and healthy individuals in different body positions and the influence of interaction between sex and disease on autonomic modulation of HR in different body positions.</p>
      <p>
        <bold>Methods</bold>
      </p>
      <p>
        <bold>Individuals</bold>
      </p>
      <p>Patients diagnosed with MD by the neurologist of a university hospital and matched healthy control groups were invited to take part in the study. Patients with a history of respiratory or heart disease, hypertension, diabetes mellitus, thromboembolic disease, thyroid disease, stroke, depression, tobacco use or alcoholism were excluded. No individuals took anti-hypertensive drugs, anti-arrhythmic drugs or other medication that could affect the autonomic control of HR. None were undergoing physiotherapy treatment or participating in any regular aerobic exercise program. Patients had no other diseases that could influence the autonomic nervous system and presented no conduction disturbance on previous electrocardiogram (ECG) analyses. The control group consisted of healthy volunteers recruited from the academic community via advertisement. Control individuals were matched for gender, height and weight, did not use any drugs and were judged healthy according to history and physical examination. All participants gave written consent and the study was approved by the hospital's Ethics Committee (protocol number 151/07). The study complies with the Principles of Helsinki declaration<sup>19</sup>.</p>
      <p>
        <bold>Clinical classification of muscular impairment</bold>
      </p>
      <p>All patients were categorized into five degrees of impairment, using the Muscular Impairment Rating Scale (MIRS), in accordance with distal to proximal progression of peripheral muscle involvement characteristic of MD: degree 1 - absence of clinical signs of muscular impairment; degree 2 - minimal signs such as myotony and facial weakness, palpebral ptosis and/or slight or moderate proximal weakness; degree 3 - distal weakness without proximal compromise; degree 4 - slight or moderate proximal weakness; degree 5 - severe proximal weakness, with the patient confined to a wheelchair<sup>20</sup>.</p>
      <p>
        <bold>Assessment of heart rate variability</bold>
      </p>
      <p>Participants were evaluated in the morning to avoid differences caused by circadian changes. Laboratory temperature was maintained between 22&#176;C and 24&#176;C and relative air humidity between 50 and 60%. Patients were informed about the protocol, instructed to abstain from stimulants or alcoholic beverages during the 24 hours preceding the test and to ingest a light meal at least 2h before assessment.</p>
      <p>On the day of the test, patients were questioned and examined as for their overall well being, a good night's sleep (7-8 hours) and compliance with instructions. After a 20-minute rest period, systemic blood pressure (Missouri-Mikato, SP, Brazil) and radial pulse (Nonin Medical, MN, USA) were measured to determine if basal conditions were adequate for the test.</p>
      <p>To obtain HR data, volunteers were monitored in the supine position for 15 minutes using a Polar S810i<sup>&#174;</sup> monitor (Polar Electro Oy<sup>&#174;</sup>, Finland) after 5 minutes of signal stabilization. The Polar S810i<sup>&#174;</sup> monitor is a practical and reliable device to monitor beat-by-beat HR for HRV analysis; the equipment captures R-R intervals through 2 adhesive electrodes. Electrodes were placed on the skin, on top of the xiphoid process and on the middle axillary line at the level of the xiphoid process. Data obtained by the Polar monitor were transferred to the computer using an interface with an infrared device for signal emission. This system detects ventricular depolarization, corresponding to the R wave on the ECG, with a sampling rate of 500 Hz and a temporal resolution of 1 millisecond<sup>21</sup>, validated by Loimaala et al <sup>22</sup>. The infrared interface was placed at a maximum distance of 8 inches and at a 15&#176; angle to the Polar S810i<sup>&#174;20</sup>. HR signals were processed to calculate HRV values using a specific MatLab<sup>&#174;</sup> program (Math Works, USA), which calculates HRV values based on the R-R intervals obtained on the device. HRV was evaluated in both time and frequency domains, using the region of greatest stability in tracing R-R intervals, provided it exhibited at least 256 consecutive beats. Frequency domains were analyzed by fast Fourier transform applied in a single window after linear subtraction of tendency in previously selected R-R intervals. Analysis in the frequency domain was carried out using total power, low (LF: 0.04 to 0.15 Hz) and high (HF: 0.15 to 0.4 Hz) frequency bands in normalized units (<italic>nu</italic>) and an LF/HF ratio. The LF band is modulated by both sympathetic and parasympathetic nervous systems and the HF band is related to cardiac vagal control<sup>23</sup>.</p>
      <p>
        <bold>Statistical analysis</bold>
      </p>
      <p>Participants were characterized using descriptive statistics, obtaining the means and standard deviations of age, body mass index (BMI) and length of time since diagnosis. Normal data distribution was verified by the Shapiro walk test. The paired t- test was applied to compare intra-group HRV data. Ordinary two-way ANOVA was used in MD patients and the control group to determine the influence of disease and gender on heart rate variability. Results were considered statistically significant for <italic>p</italic> &lt; 0.05. The <italic>GraphPad Prism</italic><sup>&#174;</sup> 5.0 program was used for analyses.</p>
      <p>
        <bold>Results</bold>
      </p>
      <p>Twenty-six patients were invited to take a part in the study. Three were excluded due previous disease history and four declined to participate due to lack of interest. The final sample was composed of 17 patients (10 men and 7 women) and 17 matched healthy individuals (10 men and 7 women). As demonstrated in <xref ref-type="table" rid="aop02012_ingt01-body2">table 1</xref>, no differences were found between anthropometric characteristics between the two groups.</p>
      <p content-type="asset">
        <table-wrap id="aop02012_ingt01-body2">
          <graphic xlink:href="1678-4170-abc-98-04-0353-00021-gt01-en.jpg"/></table-wrap>
      </p>
      <p>
        <bold>Clinical characteristics in MD patients</bold>
      </p>
      <p>Among individuals with MD, male patients showed longer time since diagnosis than females and were therefore in a more advanced stage of the disease, according to clinical classification of muscular impairment. Almost all male patients exhibited slight to moderate peripheral muscular impairment (minimal signs or distal weakness), while most women were classified as grade 3 (<xref ref-type="table" rid="aop02012_ingt02-body2">Table 2</xref>). None of the participants were wheelchair-bound and all were capable of executing the activities of daily living.</p>
      <p content-type="asset">
        <table-wrap id="aop02012_ingt02-body2">
          <graphic xlink:href="1678-4170-abc-98-04-0353-00021-gt02-en.jpg"/></table-wrap>
      </p>
      <p>
        <bold>Heart rate variability: gender differences between MD patients</bold>
      </p>
      <p>Significant inter-gender differences were found in MD patients in the sitting position. LF/HF values and LF<italic>nu</italic> were 73% and 25% higher among males respectively, while HF<italic>nu</italic> was 51.2% higher in women (<xref ref-type="table" rid="aop02012_ingt03-body2">Table 3</xref>). The LF/HF ratio was greater in men in the supine and sitting positions. Significant changes also were observed from the supine to the sitting position in male patients, with a 19% decrease in HF<italic>nu</italic>, 19% increase in LF<italic>nu</italic> and 42.3% rise in the LF/HF ratio (<xref ref-type="table" rid="aop02012_ingt03-body2">Table 3</xref>).</p>
      <p content-type="asset">
        <table-wrap id="aop02012_ingt03-body2">
          <graphic xlink:href="1678-4170-abc-98-04-0353-00021-gt03-en.jpg"/></table-wrap>
      </p>
      <p>
        <bold>Heart rate variability: gender differences in healthy individuals</bold>
      </p>
      <p>As per <xref ref-type="table" rid="aop02012_ingt04-body2">table 4</xref>, the control group showed no differences between gender and during changes in body position from supine to sitting. LF<italic>nu</italic> in the supine position was 22.8% higher for women in relation to men. Body position changes from supine to sitting lowered the HF<italic>nu</italic> by 30.8% among healthy females. The LF/HF ratio rose for men and women during changes in body position by 50% and 132%, respectively.</p>
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      <p>
        <bold>Influence of gender and disease on HRV in healthy individuals and MD patients</bold>
      </p>
      <p>In the sitting position, male MD patients presented sympathovagal balances significantly high compared to healthy control individuals in 50.9% (<xref ref-type="table" rid="aop02012_ingt05-body2">Table 5</xref>). Influence of gender and disease on HRV in healthy individuals and MD patients is illustrated in <xref ref-type="fig" rid="aop02012_ingf01-body2">Figure 1</xref> and <xref ref-type="fig" rid="aop02012_ingf02-body2">2</xref> and demonstrated in <xref ref-type="table" rid="aop02012_ingt05-body2">tables 5</xref> and <xref ref-type="table" rid="aop02012_ingt06-body2">6</xref>. Considering influences of disease and gender on HRV in MD patients and healthy individuals, we observed significant gender-influence on the LF/HF ratio, HF<italic>nu</italic> in the sitting and supine position and LF<italic>nu</italic> in the supine position. Post hoc analyses show that gender significantly impacts MD patients and healthy individuals in different ways (p &lt; 0.01). The low frequency domain in the sitting position, LF<italic>nu,</italic> was significantly influenced by the disease.</p>
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      <p>
        <bold>Discussion</bold>
      </p>
      <p>This study proposes to assess inter-gender autonomic modulation of HR in patients with MD and healthy individuals in different body positions, as well as the influence of gender and disease and their interaction in both groups. HRV results in MD patients comparing genders suggest a difference in LF<italic>nu</italic>, HF<italic>nu</italic> and LF/HF ratio, with a decrease in parasympathetic modulation and increase in sympathetic modulation for males assessed in the sitting position. Sympathetic and parasympathetic modulations of the heart evaluated by LF<italic>nu</italic>, sympathovagal balance and LF/HF ratio increase for male MD patients with a change in body position. Sympathovagal balances are significantly high in male MD patients compared to healthy controls. HRV was affected by both gender and disease. Gender influenced LF<italic>nu</italic> in the supine position while the LF/HF ratio and HF<italic>nu</italic> was affected in both positions. Disease significantly influenced low frequency domain, LF<italic>nu.</italic></p>
      <p>In contrast to other research<sup>14-18</sup>, this study assesses HRV during short time periods in sitting and supine positions, in addition to analyzing the magnitude of gender differences. Methodological procedures were based on the fact that HRV measurements obtained with 5-minute recordings demonstrated good reproducibility, as well as being fast and easy to analyze<sup>24-26</sup>. Additionally, HRV responses to postural changes are considered a better predictor of heart events<sup>27</sup>. Nevertheless, HRV is relatively simple to assess, although results can be difficult to interpret<sup>28</sup>. Modulation of heart rate is strongly influenced by several factors, including body position, humor, mental stress and environmental conditions<sup>29</sup>. HRV assessment also depends on local conditions such as noise, temperature, spontaneous and quiet breathing<sup>30,31</sup>. As previously stated<sup>32</sup>, due to physiological differences between males and females, it is essential to compare inter-gender differences in HRV indices. Finally, HRV must be analyzed considering frequency domains in normalized units. This is the most recommended form of analysis since it accurately represents variations of sympathetic and parasympathetic modulation<sup>23</sup>.</p>
      <p>To our knowledge, five previous studies on autonomic modulation of Heart Rate in patients with MD have been published. Discrepant results obtained in the past may be due to different analytical methods, autoregressive or fast Fourier, which were not interchangeable<sup>33,34</sup>, as well as diverse postural positions during HRV measurement in each study. Inoue et al<sup>14</sup> were the first authors to investigate HRV in MD type 1 patients. They analyzed HRV using the autoregressive method in 10 MD patients (4 male and 6 female) without cardiac conduction disturbance, in addition to 10 age and gender-matched healthy controls at rest in the supine position. The authors found that LFms<sup>2</sup> and HFms<sup>2</sup> decreased by 642% and 452% respectively, and that the LF/HF ratio increased 158% in MD patients in relation to healthy individuals. The study did not consider the time since diagnosis and muscle impairment. However, the authors state that at the moment of investigation all patients were capable of walking and performing daily activities without assistance, corresponding to MIRS classification 1 to 4. The significant difference between MD patients and healthy individuals has never been confirmed by other studies. Flachenecker et al<sup>15</sup> investigated the response of cardiovascular autonomic function, including HRV, analyzed by the fast Fourier method, in MD type 2 patients. However, they recorded a reduction of 53.7% for LFms<sup>2</sup> in MD type 2 patients compared to healthy volunteers. Recent research has identified significant variations in severity, type, and distribution of electrical myotony in MD type 1 and MD type 2, as well as a correlation between muscle weakness and myotony in the two disorders<sup>35</sup>. Hence, comparison between this study and the results obtained by these authors is not appropriate. In a study similar to ours, Di Leo et al<sup>17</sup>, investigated HRV in MD type 1 patients using the autoregressive method with different body positions. In 23 MD patients and a control group, they observed a significant decrease in LF<italic>ms</italic><sup>2</sup>, a marker of sympathetic activity, for MD patients in the supine position. The results of this study can only be partially considered for comparison with ours. The authors did not describe baseline characteristics of the control group, HRV analysis was performed using the autoregressive method and the MD group included men and women with a substantial age variation between 15 years and 51 years. These factors may influence results, in that physiological differences are established by HRV in men and women of different ages.</p>
      <p>Other two previous studies applied the fast Fourier method to analyze HRV in patients with MD. In a multicenter study, Hardin et al<sup>16</sup> evaluated 289 MD patients in the supine position during short HRV acquisition periods. They did not include a control group since the study aims were to evaluate ambulatory ECG in a large and diverse population with MD type 1, in which clinical factors were associated to HRV by analyzing low frequency domains LF<italic>ms</italic><sup>2</sup>, HF<italic>ms</italic><sup>2</sup> and LF/HF ratio. Furthermore, the investigation was conducted at several centers. HRV data showed wide variability, with standard deviation greater than the mean and higher than commonly found in HRV studies. These authors observed a decrease in total power and predominance of sympathetic drive compared to normal HRV values. Finally, Rakocevi&#262;-Stojanovi&#262; et al<sup>18</sup> analyzed HRV in twenty patients and fifteen healthy controls. The study does not clearly describe patient and control group characteristics such as age, gender, time since diagnosis and presence of minor or major disability. Total power fell by 64.6% in MD patients in relation to healthy controls, while LF<italic>ms</italic><sup>2</sup>, HF<italic>ms</italic><sup>2</sup> and LF/HF ratios were not significantly lower in MD patients. The authors concluded that sympathetic dysfunction may occur in patients with MD type 1.</p>
      <p>This study builds on this prior investigation in several important ways. Firstly, time since diagnosis is critically important for the development of comorbidities in MD patients and was not considered in any previous studies, whereas this study defined time since diagnosis for the patient group. Secondly, it is important to perform HRV analyses separately for men and women, adopting a control group. Thirdly, using normalized units to study frequency domains is highly recommended in order to analyze the influence of sympathetic and parasympathetic autonomic modulation on the heart. All procedures should be adopted considering that there are no established HRV reference values. Finally, since HRV study is a matter of great interest in clinical and physiological research, HRV measurement must be obtained under rigorous conditions to reduce factors that may influence results. According to data provided by our results, a starting point on HRV in myotony dystrophy type 1 can be established.</p>
      <p>This study contains several strengths; however, the main limitation lies in the small sample of participants and extrapolation of the results should be done carefully. An important objective of this work, not previously investigated, was the study of cardiac autonomic modulation in MD, considering both male and female patients and influence of postural body change.</p>
      <p>The present findings suggest that in middle-aged males, MD patients who are not severely impaired and present a moderate duration of disease, sympathetic drive seems to be greater than in healthy matched individuals.</p>
      <p>
        <bold>References</bold>
      </p>
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