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  <front>
    <journal-meta>
      <journal-id journal-id-type="nlm-ta">Arq Bras Cardiol</journal-id>
      <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>
    </journal-meta>
    <article-meta>
      <article-id specific-use="scielo-v3" pub-id-type="publisher-id">3zMmZQzLb56PqTrQCb3CQrB</article-id>
      <article-id specific-use="scielo-v2" pub-id-type="publisher-id">S0066-782X2026000103001</article-id>
      <article-id pub-id-type="other">03001</article-id>
      <article-id pub-id-type="doi">10.36660/abc.20250412</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Comunica&#231;&#227;o Breve</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Teste da Esteira e Monitoriza&#231;&#227;o Ambulatorial da Press&#227;o Arterial: Podem Ser Feitos No Mesmo Dia? O Esfor&#231;o Alcan&#231;ado Na Esteira Pode Interferir?</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0002-6723-5758</contrib-id>
          <name>
            <surname>Dourado</surname>
            <given-names>Paulo Magno Martins</given-names>
          </name>
          <role>Concep&#231;&#227;o e desenho da pesquisa</role>
          <role>Obten&#231;&#227;o de dados</role>
          <role>Obten&#231;&#227;o de financiamento</role>
          <role>Revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do</role>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Dourado</surname>
            <given-names>Larissa de Almeida</given-names>
          </name>
          <role>An&#225;lise e interpreta&#231;&#227;o dos dados</role>
          <role>Reda&#231;&#227;o do manuscrito</role>
          <role>Revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do</role>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Silva</surname>
            <given-names>Let&#237;cia Raiane dos Anjos</given-names>
          </name>
          <role>Obten&#231;&#227;o de dados</role>
          <role>An&#225;lise e interpreta&#231;&#227;o dos dados</role>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Oliveira</surname>
            <given-names>Jaciara Gomes de</given-names>
          </name>
          <role>Obten&#231;&#227;o de dados</role>
          <role>An&#225;lise e interpreta&#231;&#227;o dos dados</role>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Matos</surname>
            <given-names>Karolyne de Oliveira</given-names>
          </name>
          <role>Obten&#231;&#227;o de dados</role>
          <role>An&#225;lise e interpreta&#231;&#227;o dos dados</role>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Dourado</surname>
            <given-names>Jo&#227;o Paulo de Almeida</given-names>
          </name>
          <role>An&#225;lise e interpreta&#231;&#227;o dos dados</role>
          <role>Obten&#231;&#227;o de financiamento</role>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Hajjar</surname>
            <given-names>Ludhmila Abrah&#227;o</given-names>
          </name>
          <role>Concep&#231;&#227;o e desenho da pesquisa</role>
          <role>An&#225;lise e interpreta&#231;&#227;o dos dados</role>
          <role>Revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do</role>
          <xref ref-type="aff" rid="aff2">
            <sup>2</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0002-6690-6345</contrib-id>
          <name>
            <surname>Braga</surname>
            <given-names>Pedro Gabriel Senger</given-names>
          </name>
          <role>Concep&#231;&#227;o e desenho da pesquisa</role>
          <role>An&#225;lise e interpreta&#231;&#227;o dos dados</role>
          <role>An&#225;lise estat&#237;stica</role>
          <role>Reda&#231;&#227;o do manuscrito</role>
          <role>Revis&#227;o cr&#237;tica do manuscrito quanto ao conte&#250;do</role>
          <xref ref-type="aff" rid="aff1">
            <sup>1</sup>
          </xref>
          <xref ref-type="aff" rid="aff3">
            <sup>3</sup>
          </xref>
        </contrib>
      </contrib-group>
      <aff id="aff1">
        <label>1</label>
        <institution content-type="orgname">Cl&#237;nica Pr&#243;-Cora&#231;&#227;o</institution>
        <addr-line>
          <named-content content-type="city">S&#227;o Paulo</named-content>
          <named-content content-type="state">SP</named-content>
        </addr-line>
        <country country="BR">Brasil</country>
        <institution content-type="original">Cl&#237;nica Pr&#243;-Cora&#231;&#227;o, S&#227;o Paulo, SP &#8211; Brasil</institution>
      </aff>
      <aff id="aff2">
        <label>2</label>
        <institution content-type="orgdiv2">Hospital das Cl&#237;nicas</institution>
        <institution content-type="orgdiv1">Faculdade de Medicina</institution>
        <institution content-type="orgname">Universidade de S&#227;o Paulo</institution>
        <addr-line>
          <named-content content-type="city">S&#227;o Paulo</named-content>
          <named-content content-type="state">SP</named-content>
        </addr-line>
        <country country="BR">Brasil</country>
        <institution content-type="original">Unidade de Terapia Intensiva do Pronto Atendimento do Hospital das Cl&#237;nicas da Faculdade de Medicina da Universidade de S&#227;o Paulo, S&#227;o Paulo, SP &#8211; Brasil</institution>
      </aff>
      <aff id="aff3">
        <label>3</label>
        <institution content-type="orgdiv2">Hospital das Cl&#237;nicas</institution>
        <institution content-type="orgdiv1">Faculdade de Medicina</institution>
        <institution content-type="orgname">Universidade de S&#227;o Paulo</institution>
        <addr-line>
          <named-content content-type="city">S&#227;o Paulo</named-content>
          <named-content content-type="state">SP</named-content>
        </addr-line>
        <country country="BR">Brasil</country>
        <institution content-type="original">Departamento de Cardio-Oncologia, Instituto do Cora&#231;&#227;o do Hospital das Cl&#237;nicas da Faculdade de Medicina da Universidade de S&#227;o Paulo,S&#227;o Paulo, SP &#8211; Brasil</institution>
      </aff>
      <author-notes>
        <corresp id="c01"><label>Correspond&#234;ncia:</label> Pedro Gabriel Senger Braga Av. Dr. En&#233;as Carvalho de Aguiar, 44. CEP 05403-900, Cerqueira C&#233;sar, S&#227;o Paulo, SP &#8211; Brasil E-mail: <email>pedro.senger@gmail.com</email> </corresp>
        <fn fn-type="coi-statement">
          <label>Potencial conflito de interesse:</label>
          <p>N&#227;o h&#225; conflito com o presente artigo.</p>
        </fn>
        <fn fn-type="edited-by">
          <label>Editor respons&#225;vel pela revis&#227;o:</label>
          <p> Paulo B. Veiga Jardim</p>
        </fn>
      </author-notes>
      <pub-date date-type="pub" publication-format="electronic">
        <day>02</day>
        <month>03</month>
        <year>2026</year>
      </pub-date>
      <pub-date date-type="collection" publication-format="electronic">
        <month>01</month>
        <year>2026</year>
      </pub-date>
      <volume>123</volume>
      <issue>1</issue>
      <elocation-id>e20250412</elocation-id>
      <history>
        <date date-type="received">
          <day>16</day>
          <month>06</month>
          <year>2025</year>
        </date>
        <date>
          <day>29</day>
          <month>07</month>
          <year>2025</year>
        </date>
        <date date-type="accepted">
          <day>23</day>
          <month>10</month>
          <year>2025</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/" xml:lang="pt">
          <license-p>Este &#233; um artigo de acesso aberto distribu&#237;do sob os termos da licen&#231;a de atribui&#231;&#227;o pelo Creative Commons</license-p>
        </license>
      </permissions>
      <abstract>
        <title>Resumo</title>
        <p>O presente estudo tem como objetivo verificar se o teste ergom&#233;trico influencia no exame de monitoriza&#231;&#227;o ambulatorial da press&#227;o arterial (MAPA), nos indiv&#237;duos que os realizam no mesmo dia; e se a intensidade alcan&#231;ada durante o teste pode influenciar nos valores press&#243;ricos obtidos no MAPA. Um total de 190 adultos foram envolvidos no estudo e nas duas an&#225;lises &#8211; realiza&#231;&#227;o dos exames no mesmo dia (n=145) ou em dias diferentes (n=45), e os que alcan&#231;aram valores subm&#225;ximos (n=95) ou m&#225;ximos (n=50) da frequ&#234;ncia card&#237;aca. A realiza&#231;&#227;o do teste ergom&#233;trico e o MAPA no mesmo dia n&#227;o influenciou na press&#227;o arterial m&#225;xima sist&#243;lica na vig&#237;lia (p=0,5307) ou no sono (p=0,7383), na press&#227;o arterial m&#225;xima diast&#243;lica na vig&#237;lia (p=0,2691) ou no sono (p=0,3974), nos valores da press&#227;o sist&#243;lica m&#237;nima na vig&#237;lia (p=0,4615) ou no sono (p=0,5584), e na press&#227;o diast&#243;lica m&#237;nima na vig&#237;lia (p=0,1289) ou no sono (p=0,8075). Quando comparamos a intensidade do esfor&#231;o realizado, os valores da press&#227;o arterial m&#225;xima sist&#243;lica na vig&#237;lia (p=0,1029), no sono (p=0,2149), m&#225;xima diast&#243;lica na vig&#237;lia (p=0,2062) e no sono (p=0,1851), n&#227;o foram diferentes entre os grupos. O mesmo foi observado na m&#237;nima sist&#243;lica na vig&#237;lia (p=0,7964), no sono (p=0,8991), m&#237;nima diast&#243;lica na vig&#237;lia (p=0,8864) e no sono (p=0,4892). N&#227;o houve diferen&#231;a nos valores press&#243;ricos obtidos pelo MAPA entre os indiv&#237;duos que realizaram o teste de esfor&#231;o no mesmo dia e aqueles que o fizeram em dias diferentes. Al&#233;m disso, a intensidade alcan&#231;ada no teste, seja subm&#225;xima ou m&#225;xima, n&#227;o influenciou os resultados do MAPA.</p>
      </abstract>
      <kwd-group xml:lang="pt">
        <title>Palavras-chave:</title>
        <kwd>Palavras-chave: Press&#227;o Arterial</kwd>
        <kwd>Teste de Esfor&#231;o</kwd>
        <kwd>Monitoriza&#231;&#227;o Ambulatorial da Press&#227;o Arterial</kwd>
      </kwd-group>
      <funding-group>
        <award-group>
          <funding-source>Minist&#233;rio da Educa&#231;&#227;o</funding-source>
        </award-group>
        <award-group>
          <funding-source>Funda&#231;&#227;o Coordena&#231;&#227;o de Aperfei&#231;oamento de Pessoal de N&#237;vel Superior</funding-source>
          <award-id>88887.102383/2025-00</award-id>
        </award-group>
        <funding-statement>PGSB: Ao Minist&#233;rio da Educa&#231;&#227;o &#8211; MEC/Funda&#231;&#227;o Coordena&#231;&#227;o de Aperfei&#231;oamento de Pessoal de N&#237;vel Superior &#8211; CAPES &#8211; n&#250;mero do processo: 88887.102383/2025-00.</funding-statement>
      </funding-group>
      <counts>
        <fig-count count="2"/>
        <table-count count="6"/>
        <equation-count count="0"/>
        <ref-count count="9"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <sec sec-type="intro">
      <title>Introdu&#231;&#227;o</title>
      <p>O exame de monitoriza&#231;&#227;o ambulatorial da press&#227;o arterial (MAPA) &#233; considerado padr&#227;o ouro para o diagn&#243;stico da hipertens&#227;o arterial sist&#234;mica (HAS), e tamb&#233;m para o acompanhamento do tratamento farmacol&#243;gico. Em compara&#231;&#227;o &#224; press&#227;o arterial (PA) de consult&#243;rio, o MAPA tem maior poder preditivo e sensibilidade, para an&#225;lise do desfecho referente a doen&#231;a cardiovascular &#8211; eventos coronarianos fatais e n&#227;o fatais e acidente vascular encef&#225;lico &#8211; e &#224;s les&#245;es de &#243;rg&#227;o-alvo.<sup><xref ref-type="bibr" rid="B1">1</xref>,<xref ref-type="bibr" rid="B2">2</xref></sup> Comumente, na avalia&#231;&#227;o de rotina cardiol&#243;gica, o paciente realiza o teste ergom&#233;trico em esteira, e em caso de sintomas ou uma resposta press&#243;rica exacerbada ao esfor&#231;o, realiza, no mesmo dia, ou pr&#243;ximo &#224;quela data, o MAPA.</p>
      <p>A pr&#225;tica de exerc&#237;cio aer&#243;bio promove a redu&#231;&#227;o da PA, tanto a PA sist&#243;lica (PAS) quanto a PA diast&#243;lica (PAD), e esse efeito pode durar por at&#233; 24 horas ap&#243;s o esfor&#231;o.<sup><xref ref-type="bibr" rid="B3">3</xref>-<xref ref-type="bibr" rid="B6">6</xref></sup> Por outro lado, n&#227;o sabemos se um est&#237;mulo de exerc&#237;cio f&#237;sico, curto (&lt;10 minutos), m&#225;ximo ou subm&#225;ximo, pode promover a redu&#231;&#227;o na press&#227;o arterial durante a investiga&#231;&#227;o da hipertens&#227;o arterial. Portanto, o presente estudo tem como objetivo: 1) verificar se a realiza&#231;&#227;o do esfor&#231;o f&#237;sico pode influenciar no exame de MAPA, nos indiv&#237;duos que fazem ambos os exames no mesmo dia; e 2) dos que fazem no mesmo dia, se a intensidade alcan&#231;ada durante o esfor&#231;o do teste ergom&#233;trico, pode impactar nos valores press&#243;ricos obtidos no MAPA.</p>
    </sec>
    <sec sec-type="methods">
      <title>M&#233;todos</title>
      <sec>
        <title>Casu&#237;stica</title>
        <p>Para o presente estudo, foi realizada a coleta de uma amostra por conveni&#234;ncia, com base nos pacientes atendidos no servi&#231;o ambulatorial da Cl&#237;nica Pr&#243;-Cora&#231;&#227;o. Os crit&#233;rios de inclus&#227;o foram: realiza&#231;&#227;o de teste ergom&#233;trico com intensidade ao menos subm&#225;xima (&#8805;85% da frequ&#234;ncia card&#237;aca m&#225;xima para a idade); realiza&#231;&#227;o do MAPA e do teste ergom&#233;trico no mesmo dia ou, no m&#225;ximo, na mesma semana. Para a interpreta&#231;&#227;o do MAPA, foi necess&#225;rio que pelo menos 80% das leituras fossem v&#225;lidas, a fim de que o exame fosse considerado satisfat&#243;rio.</p>
        <p>Por outro lado, os crit&#233;rios de exclus&#227;o inclu&#237;ram: uso de medicamentos anti-hipertensivos; PAS &#8805;180 mmHg ou PAD &#8805;110 mmHg antes do teste ergom&#233;trico; eletrocardiograma ileg&#237;vel ou com sinais positivos de isquemia do mioc&#225;rdio. Tamb&#233;m foram exclu&#237;dos indiv&#237;duos fisicamente ativos, trabalhadores noturnos, tabagistas e aqueles com hist&#243;rico de evento cardiovascular pr&#233;vio. Os participantes foram orientados a n&#227;o consumir bebidas alco&#243;licas e a se abster de esfor&#231;o f&#237;sico durante o per&#237;odo de monitoramento com o MAPA.</p>
        <p>A partir desses dados, foram realizadas duas an&#225;lises: 1) compara&#231;&#227;o entre indiv&#237;duos que realizaram o teste ergom&#233;trico e o MAPA no mesmo dia ou em dias diferentes, desde que dentro da mesma semana; 2) entre os que realizaram ambos os exames no mesmo dia, foram criados dois grupos: aqueles que atingiram esfor&#231;o subm&#225;ximo (&#8805;85% da frequ&#234;ncia card&#237;aca m&#225;xima para a idade) e aqueles que atingiram esfor&#231;o m&#225;ximo (&#8805;95% da frequ&#234;ncia card&#237;aca m&#225;xima). O estudo foi aprovado pelo Comit&#234; de &#201;tica do Hospital das Cl&#237;nicas da Faculdade de Medicina da Universidade de S&#227;o Paulo, e todos os participantes assinaram o Termo de Consentimento Livre e Esclarecido. Este estudo est&#225; registrado na plataforma Clinical Trials (NCT05987891).</p>
      </sec>
      <sec>
        <title>Teste ergom&#233;trico em esteira</title>
        <p>As vari&#225;veis iniciais como a PA e a frequ&#234;ncia card&#237;aca (FC) foram coletadas em repouso, na esteira, com o participante na posi&#231;&#227;o em p&#233; e com os eletrodos posicionados no t&#243;rax (Inbramed<sup>&#174;</sup>, Porto Alegre, Brazil). A PAS e a PAD foram avaliadas pelo m&#233;todo auscultat&#243;rio. Todos os aparelhos passam anualmente por manuten&#231;&#245;es preventivas, garantindo a qualidade do dado analisado. A FC, PAS e PAD foram avaliadas no repouso e no pico de esfor&#231;o. O pico do exerc&#237;cio foi definido pela incapacidade do participante de continuar realizando esfor&#231;o naquela carga, referindo exaust&#227;o volunt&#225;ria, induzindo o avaliador a parar o teste e introduzir a fase de recupera&#231;&#227;o na esteira. Os protocolos realizados na esteira foram: Bruce e Ellestad. Os exames foram analisados e laudados pelos mesmos cardiologistas, excluindo os testes positivos para isquemia mioc&#225;rdica (PMMD, LAD e JPAD).</p>
      </sec>
      <sec>
        <title>Monitoriza&#231;&#227;o ambulatorial da press&#227;o arterial</title>
        <p>A monitoriza&#231;&#227;o ambulatorial da PA foi feita pelos aparelhos da empresa Cardios (S&#227;o Paulo, Brasil), que s&#227;o devidamente calibrados semestralmente. A coloca&#231;&#227;o do MAPA foi feita pelas enfermeiras devidamente treinadas (LRAS, JGO e KOM). O MAPA tem como objetivo registrar de forma cont&#237;nua os n&#237;veis press&#243;ricos ao longo de 24 horas, durante as atividades habituais e o per&#237;odo de sono. O procedimento consiste na coloca&#231;&#227;o de um manguito de press&#227;o ajustado ao bra&#231;o do paciente, conectado a um gravador eletr&#244;nico port&#225;til. Este dispositivo foi programado para inflar automaticamente e realizar medi&#231;&#245;es da press&#227;o arterial em intervalos regulares, geralmente a cada 15 minutos durante o dia e a cada 30 minutos durante a noite. Os dados obtidos foram armazenados na mem&#243;ria interna do aparelho para posterior an&#225;lise.</p>
        <p>Durante o per&#237;odo de monitoriza&#231;&#227;o, o paciente foi orientado a manter suas atividades habituais, evitando apenas esfor&#231;o f&#237;sico intenso e exposi&#231;&#227;o &#224; &#225;gua, a fim de n&#227;o danificar o equipamento. Foi solicitado ao paciente para que registre, em um di&#225;rio espec&#237;fico, os hor&#225;rios de sono, alimenta&#231;&#227;o, atividades f&#237;sicas e sintomas, para correla&#231;&#227;o com os valores obtidos. Ap&#243;s 24 horas, o dispositivo foi removido e os dados foram transferidos para um software espec&#237;fico de an&#225;lise, que gera gr&#225;ficos e relat&#243;rios contendo os valores m&#233;dios da PA nas 24 horas.</p>
      </sec>
      <sec>
        <title>An&#225;lise estat&#237;stica</title>
        <p>O teste de normalidade e Kolmogorov-Smirnov foi realizado para verificar a distribui&#231;&#227;o dos dados. As an&#225;lises estat&#237;sticas foram feitas pelo teste t de Student, quando o dado era normal, ou Mann-Whitney, quando a distribui&#231;&#227;o do dado n&#227;o era normal. Foi considerado estat&#237;stica se p&lt;0,05. Os dados foram expressos em m&#233;dia &#177; desvio padr&#227;o. Foi utilizado o programa GraphPad Prism, vers&#227;o 5.0.</p>
      </sec>
    </sec>
    <sec sec-type="results">
      <title>Resultados</title>
      <p>Dos indiv&#237;duos eleg&#237;veis para o estudo durante o per&#237;odo de coleta, 18 foram exclu&#237;dos por estarem com a PAS &#8805; 180 mmHg e/ou PAD &#8805; 110 mmHg antes do teste ergom&#233;trico e seis se recusaram a participar. Ap&#243;s o teste ergom&#233;trico, 83 indiv&#237;duos n&#227;o atingiram ao menos a FC subm&#225;xima para a idade e 14 tiveram o eletrocardiograma incapaz de ser interpretado, ou ent&#227;o, positivo para isquemia mioc&#225;rdica (<xref ref-type="fig" rid="f01">Figura 1</xref>). Assim, 190 pacientes foram inclu&#237;dos na an&#225;lise final do estudo, conforme apresentado na <xref ref-type="table" rid="t1">Tabela 1</xref>.</p>
      <p>
        <fig id="f01">
          <label>Figura 1</label>
          <caption>
            <title>&#8211; Fluxograma de pacientes. PAS: press&#227;o arterial sist&#243;lica; PAD: press&#227;o arterial diast&#243;lica.</title>
          </caption>
          <graphic xlink:href="1678-4170-abc-123-01-e20250412-50412-gf01.tif"/></fig>
      </p>
      <p>
        <table-wrap id="t1">
          <label>Tabela 1</label>
          <caption>
            <title>&#8211; Caracter&#237;sticas antropom&#233;tricas e do teste ergom&#233;trico da amostra estudada</title>
          </caption>
          <table frame="hsides" rules="groups">
            <colgroup>
              <col/>
              <col/>
            </colgroup>
            <thead>
              <tr>
                <th align="left">Vari&#225;vel</th>
                <th>Amostra (n=190)</th>
              </tr>
            </thead>
            <tbody>
              <tr>
                <td>Sexo (F/M)</td>
                <td align="center">88/102</td>
              </tr>
              <tr>
                <td>Idade (anos)</td>
                <td align="center">53 &#177; 13</td>
              </tr>
              <tr>
                <td>Peso (kg)</td>
                <td align="center">84,7 &#177; 18,3</td>
              </tr>
              <tr>
                <td>Altura (m)</td>
                <td align="center">1,70 &#177; 0,10</td>
              </tr>
              <tr>
                <td>IMC (kg/m<sup>2</sup>)</td>
                <td align="center">29,2 &#177; 5,1</td>
              </tr>
              <tr>
                <td colspan="2">
                  <bold>Teste ergom&#233;trico</bold>
                </td>
              </tr>
              <tr>
                <td>
                  <bold>Frequ&#234;ncia card&#237;aca (bpm)</bold>
                </td>
                <td> </td>
              </tr>
              <tr>
                <td>Repouso</td>
                <td align="center">77 &#177; 15</td>
              </tr>
              <tr>
                <td>M&#225;xima</td>
                <td align="center">154 &#177; 21</td>
              </tr>
              <tr>
                <td>
                  <bold>Press&#227;o arterial (mmHg)</bold>
                </td>
                <td> </td>
              </tr>
              <tr>
                <td>Sist&#243;lica Repouso</td>
                <td align="center">131 &#177; 12</td>
              </tr>
              <tr>
                <td>Sist&#243;lica M&#225;xima</td>
                <td align="center">161 &#177; 17</td>
              </tr>
              <tr>
                <td>Diast&#243;lica Repouso</td>
                <td align="center">82 &#177; 4</td>
              </tr>
              <tr>
                <td>Diast&#243;lica M&#225;xima</td>
                <td align="center">83 &#177; 7</td>
              </tr>
              <tr>
                <td>Tempo de teste (segundos)</td>
                <td align="center">333 &#177; 98</td>
              </tr>
            </tbody>
          </table>
          <table-wrap-foot>
            <fn id="TFN1">
              <p>IMC: &#237;ndice de massa corp&#243;rea; bpm: batimentos por minuto.</p>
            </fn>
          </table-wrap-foot>
        </table-wrap>
      </p>
      <p>A compara&#231;&#227;o entre a realiza&#231;&#227;o do MAPA e do teste ergom&#233;trico no mesmo dia ou em dias diferentes est&#225; apresentada na <xref ref-type="table" rid="t2">Tabela 2</xref>. N&#227;o houve diferen&#231;a na PAS m&#225;xima durante a vig&#237;lia (p = 0,5307) e durante o sono (p = 0,7383), assim como na PAD m&#225;xima na vig&#237;lia (p = 0,2691) e no sono (p = 0,3974). Os valores de PAS m&#237;nima na vig&#237;lia (p = 0,4615) e no sono (p = 0,5584), bem como os de PAD m&#237;nima na vig&#237;lia (p = 0,1289) e no sono (p = 0,8075), tamb&#233;m n&#227;o apresentaram diferen&#231;as significativas entre os grupos estudados.</p>
      <p>
        <table-wrap id="t2">
          <label>Tabela 2</label>
          <caption>
            <title>&#8211; Vari&#225;veis hemodin&#226;micas da monitoriza&#231;&#227;o ambulatorial da press&#227;o arterial em indiv&#237;duos que fizeram o teste da esteira no mesmo dia ou em dias diferentes</title>
          </caption>
          <table frame="hsides" rules="groups">
            <colgroup>
              <col/>
              <col/>
              <col/>
              <col/>
            </colgroup>
            <thead>
              <tr>
                <th align="left">Par&#226;metros/grupos</th>
                <th>Mesmo dia (n=145)</th>
                <th>Dias diferentes (n=45)</th>
                <th>p</th>
              </tr>
              <tr>
                <th align="left" colspan="4">Valores press&#243;ricos (mmHg)</th>
              </tr>
            </thead>
            <tbody>
              <tr>
                <td>M&#225;xima Sist&#243;lica Vig&#237;lia</td>
                <td align="center">152 &#177; 17</td>
                <td align="center">155 &#177; 23</td>
                <td align="center">0,5307</td>
              </tr>
              <tr>
                <td>M&#225;xima Sist&#243;lica Sono</td>
                <td align="center">133 &#177; 16</td>
                <td align="center">134 &#177; 14</td>
                <td align="center">0,7383</td>
              </tr>
              <tr>
                <td>M&#225;xima Diast&#243;lica Vig&#237;lia</td>
                <td align="center">101 &#177; 13</td>
                <td align="center">104 &#177; 15</td>
                <td align="center">0,2691</td>
              </tr>
              <tr>
                <td>M&#225;xima Diast&#243;lica Sono</td>
                <td align="center">87 &#177; 13</td>
                <td align="center">89 &#177; 15</td>
                <td align="center">0,3974</td>
              </tr>
              <tr>
                <td>M&#237;nima Sist&#243;lica Vig&#237;lia</td>
                <td align="center">98 &#177; 13</td>
                <td align="center">100 &#177; 16</td>
                <td align="center">0,4615</td>
              </tr>
              <tr>
                <td>M&#237;nima Sist&#243;lica Sono</td>
                <td align="center">99 &#177; 13</td>
                <td align="center">100 &#177; 16</td>
                <td align="center">0,5584</td>
              </tr>
              <tr>
                <td>M&#237;nima Diast&#243;lica Vig&#237;lia</td>
                <td align="center">59 &#177;10</td>
                <td align="center">56 &#177; 13</td>
                <td align="center">0,1289</td>
              </tr>
              <tr>
                <td>M&#237;nima Diast&#243;lica Sono</td>
                <td align="center">56 &#177; 10</td>
                <td align="center">58 &#177; 13</td>
                <td align="center">0,8075</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </p>
      <p>Ao compararmos a intensidade do esfor&#231;o realizado entre os indiv&#237;duos que realizaram o MAPA e o teste ergom&#233;trico no mesmo dia, observou-se que os valores da press&#227;o arterial sist&#243;lica m&#225;xima durante a vig&#237;lia (p = 0,1029) e durante o sono (p = 0,2149), bem como da press&#227;o arterial diast&#243;lica m&#225;xima na vig&#237;lia (p = 0,2062) e no sono (p = 0,1851), foram semelhantes entre os grupos estudados. O mesmo resultado foi observado para a press&#227;o arterial sist&#243;lica m&#237;nima na vig&#237;lia (p = 0,7964) e no sono (p = 0,8991), assim como para a diast&#243;lica m&#237;nima na vig&#237;lia (p = 0,8864) e no sono (p = 0,4892), conforme demonstrado na <xref ref-type="table" rid="t3">Tabela 3</xref>.</p>
      <p>
        <table-wrap id="t3">
          <label>Tabela 3</label>
          <caption>
            <title>&#8211; Vari&#225;veis hemodin&#226;micas da monitoriza&#231;&#227;o ambulatorial da press&#227;o arterial em indiv&#237;duos que alcan&#231;aram a frequ&#234;ncia card&#237;aca subm&#225;xima e m&#225;xima no teste ergom&#233;trico</title>
          </caption>
          <table frame="hsides" rules="groups">
            <colgroup>
              <col/>
              <col/>
              <col/>
              <col/>
            </colgroup>
            <thead>
              <tr>
                <th align="left">Par&#226;metros/grupos</th>
                <th>Subm&#225;ximo (n=95)</th>
                <th>M&#225;ximo (n=50)</th>
                <th>p</th>
              </tr>
              <tr>
                <th align="left" colspan="4">Valores press&#243;ricos (mmHg)</th>
              </tr>
            </thead>
            <tbody>
              <tr>
                <td>M&#225;xima Sist&#243;lica Vig&#237;lia</td>
                <td align="center">155 &#177; 19</td>
                <td align="center">150 &#177; 15</td>
                <td align="center">0,1029</td>
              </tr>
              <tr>
                <td>M&#225;xima Sist&#243;lica Sono</td>
                <td align="center">134 &#177; 17</td>
                <td align="center">131 &#177; 15</td>
                <td align="center">0,2149</td>
              </tr>
              <tr>
                <td>M&#225;xima Diast&#243;lica Vig&#237;lia</td>
                <td align="center">103 &#177; 12</td>
                <td align="center">100 &#177; 13</td>
                <td align="center">0,2062</td>
              </tr>
              <tr>
                <td>M&#225;xima Diast&#243;lica Sono</td>
                <td align="center">89 &#177; 12</td>
                <td align="center">86 &#177; 14</td>
                <td align="center">0,1851</td>
              </tr>
              <tr>
                <td>M&#237;nima Sist&#243;lica Vig&#237;lia</td>
                <td align="center">98 &#177; 13</td>
                <td align="center">98 &#177; 13</td>
                <td align="center">0,7964</td>
              </tr>
              <tr>
                <td>M&#237;nima Sist&#243;lica Sono</td>
                <td align="center">98 &#177; 13</td>
                <td align="center">98 &#177; 13</td>
                <td align="center">0,8991</td>
              </tr>
              <tr>
                <td>M&#237;nima Diast&#243;lica Vig&#237;lia</td>
                <td align="center">59 &#177; 11</td>
                <td align="center">59 &#177; 11</td>
                <td align="center">0,8864</td>
              </tr>
              <tr>
                <td>M&#237;nima Diast&#243;lica Sono</td>
                <td align="center">57 &#177; 10</td>
                <td align="center">56 &#177; 10</td>
                <td align="center">0,4892</td>
              </tr>
            </tbody>
          </table>
        </table-wrap>
      </p>
      <p>Ap&#243;s a realiza&#231;&#227;o do MAPA, 142 pacientes (75% da amostra) foram diagnosticados com hipertens&#227;o arterial. Al&#233;m disso, dentro da amostra estudada, nenhum dos indiv&#237;duos apresentou resposta hiper-reativa ao esfor&#231;o durante o teste ergom&#233;trico. Foram realizadas an&#225;lises do MAPA considerando diferentes faixas et&#225;rias (&lt;65 anos e &#8805;65 anos) e sexos, conforme apresentado na Tabela 4, no material suplementar. Indiv&#237;duos com idade &#8805;65 anos apresentaram press&#227;o arterial diast&#243;lica durante a vig&#237;lia significativamente menor (103 &#177; 13 vs. 96 &#177; 13 mmHg; p = 0,0015) em compara&#231;&#227;o aos indiv&#237;duos com menos de 65 anos. As demais vari&#225;veis n&#227;o apresentaram diferen&#231;as significativas entre os grupos analisados.</p>
      <p>No que diz respeito ao sexo, o sexo feminino teve menor press&#227;o arterial diast&#243;lica m&#225;xima na vig&#237;lia (104 &#177; 13 vs. 99 &#177; 13; p=0,0053), m&#225;xima diast&#243;lica no sono (91 &#177; 14 vs. 84 &#177; 13mmHg; p=0,0012), m&#237;nima sist&#243;lica na vig&#237;lia (101 &#177; 15 vs. 96 &#177; 12 mmHg; p=0,0064), e por fim, a m&#237;nima diast&#243;lica na vig&#237;lia (60 &#177; 12 vs. 55 &#177; 10 mmHg; p=0,0019), em compara&#231;&#227;o ao sexo masculino. A an&#225;lise isolada do MAPA no mesmo sexo em dias diferentes, ou no mesmo dia do teste ergom&#233;trico, n&#227;o demonstrou diferen&#231;a nas vari&#225;veis estudadas, conforme demonstrado na Tabela 5, do material suplementar.</p>
    </sec>
    <sec sec-type="discussion">
      <title>Discuss&#227;o</title>
      <p>A realiza&#231;&#227;o do teste em esteira no mesmo dia ou em dias diferentes do MAPA n&#227;o influenciou os valores press&#243;ricos na amostra estudada, composta por indiv&#237;duos n&#227;o hipertensos e fisicamente inativos. Esse resultado viabiliza a realiza&#231;&#227;o do teste ergom&#233;trico e do MAPA no mesmo dia, aprimorando a pr&#225;tica cl&#237;nica cardiol&#243;gica, aumentando a reten&#231;&#227;o do paciente no ambiente cl&#237;nico e evitando evas&#245;es e descontinuidade na investiga&#231;&#227;o cl&#237;nica. A hip&#243;tese gerada a partir de um corpo robusto de evid&#234;ncias demonstra que a pr&#225;tica de exerc&#237;cio f&#237;sico aer&#243;bico, de forma aguda, reduz a press&#227;o arterial sist&#243;lica e diast&#243;lica, podendo esse efeito ser dependente da intensidade do exerc&#237;cio.<sup><xref ref-type="bibr" rid="B3">3</xref>-<xref ref-type="bibr" rid="B6">6</xref></sup></p>
      <p>Em pacientes hipertensos tratados, a pr&#225;tica de exerc&#237;cio f&#237;sico reduziu a press&#227;o arterial por at&#233; 24 horas, atingindo valores considerados normais.<sup><xref ref-type="bibr" rid="B6">6</xref></sup> No entanto, no presente estudo, esse efeito n&#227;o foi observado, possivelmente porque a popula&#231;&#227;o era composta por indiv&#237;duos que, embora estivessem em processo de diagn&#243;stico de hipertens&#227;o, ainda n&#227;o estavam em tratamento. Al&#233;m disso, a aus&#234;ncia desse efeito pode estar relacionada ao baixo volume de exerc&#237;cio realizado, com m&#233;dia de cinco minutos e meio de dura&#231;&#227;o, correspondente ao tempo do teste.</p>
      <p>Por outro lado, al&#233;m do teste em esteira, nenhum volunt&#225;rio realizou outro tipo de esfor&#231;o f&#237;sico, n&#227;o houve relato de consumo de &#225;lcool nos di&#225;rios, e a amostra n&#227;o incluiu trabalhadores noturnos, o que poderia ter gerado conflitos nos resultados.</p>
      <p>Ap&#243;s a an&#225;lise isolada por faixa et&#225;ria (&lt;65 anos vs. &#8805;65 anos), como esperado, a FC atingida foi menor no grupo mais velho, devido &#224; redu&#231;&#227;o da fun&#231;&#227;o card&#237;aca promovida pelo envelhecimento.<sup><xref ref-type="bibr" rid="B7">7</xref>,<xref ref-type="bibr" rid="B8">8</xref></sup> Em rela&#231;&#227;o ao sexo masculino, observou-se maiores valores hemodin&#226;micos, bem como maior tempo de teste.<sup><xref ref-type="bibr" rid="B9">9</xref></sup> Esse achado se justifica pela maior capacidade f&#237;sica, consequ&#234;ncia das maiores concentra&#231;&#245;es de testosterona e da maior massa magra.</p>
      <p>As limita&#231;&#245;es do presente estudo incluem a aus&#234;ncia de um grupo de indiv&#237;duos hipertensos e de um grupo com hiper-reatividade ao esfor&#231;o, o que teria permitido compara&#231;&#245;es e aprofundamentos sobre o tema investigado. A escassez de participantes mais idosos, especialmente com idade igual ou superior a 65 anos, tamb&#233;m representa uma limita&#231;&#227;o para an&#225;lises mais detalhadas, sobretudo em uma an&#225;lise secund&#225;rias entre os sexos, que poderia ampliar a discuss&#227;o sobre uma popula&#231;&#227;o predominantemente hipertensa e que demanda cuidados cardiol&#243;gicos espec&#237;ficos.</p>
    </sec>
    <sec sec-type="conclusions">
      <title>Conclus&#227;o</title>
      <p>A realiza&#231;&#227;o do teste ergom&#233;trico antes do MAPA, ambos realizados no mesmo dia, n&#227;o influenciou os valores press&#243;ricos quando comparados aos indiv&#237;duos que fizeram os exames em dias diferentes. Al&#233;m disso, nos testes de esteira realizados no mesmo dia do MAPA, a intensidade do esfor&#231;o alcan&#231;ado, sendo m&#225;ximo ou subm&#225;ximo, n&#227;o interferiu nos resultados do MAPA.</p>
      <p>Considerando a capacidade do exerc&#237;cio f&#237;sico de promover a redu&#231;&#227;o da press&#227;o arterial, um dos objetivos da investiga&#231;&#227;o foi verificar se esse fen&#244;meno poderia mascarar a hipertens&#227;o em adultos. Esse efeito, no entanto, n&#227;o foi observado, o que est&#225; de acordo com a hip&#243;tese do estudo.</p>
      <p>Portanto, os dados deste estudo fortalecem a pr&#225;tica cl&#237;nica ao demonstrar que o esfor&#231;o f&#237;sico realizado durante o teste ergom&#233;trico, seja subm&#225;ximo ou m&#225;ximo, n&#227;o influencia os resultados do MAPA, permitindo que ambos os exames sejam realizados no mesmo dia.</p>
    </sec>
  </body>
  <back>
    <ack>
      <title>Agradecimentos</title>
      <p>PGSB: Ao Minist&#233;rio da Educa&#231;&#227;o &#8211; MEC/Funda&#231;&#227;o Coordena&#231;&#227;o de Aperfei&#231;oamento de Pessoal de N&#237;vel Superior &#8211; CAPES &#8211; n&#250;mero do processo: 88887.102383/2025-00.</p>
    </ack>
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    <fn-group>
      <fn fn-type="other">
        <label>Vincula&#231;&#227;o acad&#234;mica:</label>
        <p> Este artigo &#233; parte de tese de p&#243;s-doutorado de Pedro Gabriel Senger Braga pelo Hospital das Cl&#237;nicas da Faculdade de Medicina da Universidade de S&#227;o Paulo.</p>
      </fn>
      <fn fn-type="other">
        <label>Aprova&#231;&#227;o &#233;tica e consentimento informado:</label>
        <p> Este estudo foi aprovado pelo Comit&#234; de &#201;tica da Faculdade de Medicina da Universidade de S&#227;o Paulo sob o n&#250;mero de protocolo 6.258.413. Todos os procedimentos envolvidos nesse estudo est&#227;o de acordo com a Declara&#231;&#227;o de Helsinki de 1975, atualizada em 2013. O consentimento informado foi obtido de todos os participantes inclu&#237;dos no estudo.</p>
      </fn>
      <fn fn-type="other">
        <label>Uso de Intelig&#234;ncia Artificial:</label>
        <p> Os autores n&#227;o utilizaram ferramentas de intelig&#234;ncia artificial no desenvolvimento deste trabalho.</p>
      </fn>
      <fn fn-type="data-availability" specific-use="data-available-upon-request">
        <label>Disponibilidade de Dados:</label>
        <p> Todo o conjunto de dados que d&#225; suporte aos resultados deste estudo est&#225; dispon&#237;vel mediante solicita&#231;&#227;o ao autor correspondente (Pedro Gabriel Senger Braga).</p>
      </fn>
      <fn fn-type="financial-disclosure">
        <label>Fontes de financiamento:</label>
        <p> O presente estudo n&#227;o teve fontes de financiamento externas.</p>
      </fn>
    </fn-group>
  </back>
  <sub-article article-type="translation" id="TRen" xml:lang="en">
    <front-stub>
      <article-id pub-id-type="doi">10.36660/abc.20250412i</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Brief Communication</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Treadmill Test and Ambulatory Blood Pressure Monitoring: Can They Be Performed on the Same Day? Can the Effort Reached on the Treadmill Interfere?</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0002-6723-5758</contrib-id>
          <name>
            <surname>Dourado</surname>
            <given-names>Paulo Magno Martins</given-names>
          </name>
          <role>Conception and design of the research</role>
          <role>Acquisition of data</role>
          <role>Obtaining financing</role>
          <role>Critical revision of the manuscript for content</role>
          <xref ref-type="aff" rid="aff1001">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Dourado</surname>
            <given-names>Larissa de Almeida</given-names>
          </name>
          <role>Analysis and interpretation of the data</role>
          <role>Writing of the manuscript</role>
          <role>Critical revision of the manuscript for content</role>
          <xref ref-type="aff" rid="aff1001">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Silva</surname>
            <given-names>Let&#237;cia Raiane dos Anjos</given-names>
          </name>
          <role>Acquisition of data</role>
          <role>Analysis and interpretation of the data</role>
          <xref ref-type="aff" rid="aff1001">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Oliveira</surname>
            <given-names>Jaciara Gomes de</given-names>
          </name>
          <role>Acquisition of data</role>
          <role>Analysis and interpretation of the data</role>
          <xref ref-type="aff" rid="aff1001">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Matos</surname>
            <given-names>Karolyne de Oliveira</given-names>
          </name>
          <role>Acquisition of data</role>
          <role>Analysis and interpretation of the data</role>
          <xref ref-type="aff" rid="aff1001">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Dourado</surname>
            <given-names>Jo&#227;o Paulo de Almeida</given-names>
          </name>
          <role>Analysis and interpretation of the data;</role>
          <role>Obtaining financing</role>
          <xref ref-type="aff" rid="aff1001">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Hajjar</surname>
            <given-names>Ludhmila Abrah&#227;o</given-names>
          </name>
          <role>Conception and design of the research</role>
          <role>Analysis and interpretation of the data</role>
          <role>Critical revision of the manuscript for content</role>
          <xref ref-type="aff" rid="aff2001">
            <sup>2</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid">0000-0002-6690-6345</contrib-id>
          <name>
            <surname>Braga</surname>
            <given-names>Pedro Gabriel Senger</given-names>
          </name>
          <role>Conception and design of the research</role>
          <role>Analysis and interpretation of the data</role>
          <role>Statistical analysis</role>
          <role>Writing of the manuscript</role>
          <role>Critical revision of the manuscript for content</role>
          <xref ref-type="aff" rid="aff1001">
            <sup>1</sup>
          </xref>
          <xref ref-type="aff" rid="aff3001">
            <sup>3</sup>
          </xref>
        </contrib>
      </contrib-group>
      <aff id="aff1001">
        <label>1</label>
        <country country="BR">Brazil</country>
        <institution content-type="original">Cl&#237;nica Pr&#243;-Cora&#231;&#227;o, S&#227;o Paulo, SP &#8211; Brazil</institution>
      </aff>
      <aff id="aff2001">
        <label>2</label>
        <country country="BR">Brazil</country>
        <institution content-type="original">Unidade de Terapia Intensiva do Pronto Atendimento do Hospital das Cl&#237;nicas da Faculdade de Medicina da Universidade de S&#227;o Paulo, S&#227;o Paulo, SP &#8211; Brazil</institution>
      </aff>
      <aff id="aff3001">
        <label>3</label>
        <country country="BR">Brazil</country>
        <institution content-type="original">Departamento de Cardio-Oncologia, Instituto do Cora&#231;&#227;o do Hospital das Cl&#237;nicas da Faculdade de Medicina da Universidade de S&#227;o Paulo,S&#227;o Paulo, SP &#8211; Brazil</institution>
      </aff>
      <author-notes>
        <corresp id="c01001"><label>Mailing Address:</label>Pedro Gabriel Senger Braga Av. Dr. En&#233;as Carvalho de Aguiar, 44. Postal Code 05403-900, Cerqueira C&#233;sar, S&#227;o Paulo, SP &#8211; Brazil E-mail: pedro.senger@gmail.com </corresp>
        <fn fn-type="coi-statement">
          <label>Potential conflict of interest:</label>
          <p> No potential conflict of interest relevant to this article was reported.</p>
        </fn>
        <fn fn-type="edited-by">
          <label>Editor responsible for the review:</label>
          <p> Paulo B. Veiga Jardim</p>
        </fn>
      </author-notes>
      <abstract>
        <title>Abstract</title>
        <p>The present study aimed to assess whether the exercise stress test influences the results of ambulatory blood pressure monitoring (ABPM) in individuals who undergo both examinations on the same day, and whether the intensity reached during the test affects the blood pressure values obtained through ABPM. A total of 190 adults participated in the study, which included two analyses: performing the tests on the same day (n=145) versus on different days (n=45) and reaching submaximal (n=95) versus maximal (n=50) heart rate during the exercise stress test. Performing the exercise stress test and ABPM on the same day did not affect maximum systolic blood pressure during wakefulness (p=0.5307) or sleep (p=0.7383), maximum diastolic pressure during wakefulness (p=0.2691) or sleep (p=0.3974), minimum systolic pressure during wakefulness (p=0.4615) or sleep (p=0.5584), or minimum diastolic pressure during wakefulness (p=0.1289) or sleep (p=0.8075). When comparing the intensity of effort reached, there were no differences in maximum systolic pressure during wakefulness (p=0.1029) or sleep (p=0.2149), maximum diastolic pressure during wakefulness (p=0.2062) or sleep (p=0.1851), minimum systolic pressure during wakefulness (p=0.7964) or sleep (p=0.8991), and minimum diastolic pressure during wakefulness (p=0.8864) or sleep (p=0.4892). No differences were found in ABPM blood pressure values between individuals who performed the exercise stress test on the same day and those who did so on different days. Additionally, the intensity reached during the test, whether submaximal or maximal, did not influence ABPM results.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <title>Keywords:</title>
        <kwd>Arterial Pressure</kwd>
        <kwd>Exercise Test</kwd>
        <kwd>Ambulatory Blood Pressure Monitoring</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <sec sec-type="intro">
        <title>Introduction</title>
        <p>Ambulatory blood pressure monitoring (ABPM) is considered the gold standard for diagnosing systemic arterial hypertension (SAH) and for monitoring pharmacological treatment. Compared to office blood pressure (BP) measurements, ABPM offers greater predictive power and sensitivity for assessing cardiovascular outcomes &#8211; such as fatal and non-fatal coronary events and stroke &#8211; as well as target organ damage.<sup><xref ref-type="bibr" rid="B1">1</xref>,<xref ref-type="bibr" rid="B2">2</xref></sup> In routine cardiological evaluations, patients commonly undergo a treadmill exercise test, and if symptoms or an exaggerated blood pressure response to exertion are observed, ABPM is performed on the same day or shortly thereafter.</p>
        <p>Aerobic exercise is known to reduce both systolic BP (SBP) and diastolic BP (DBP), with effects lasting up to 24 hours post-exercise.<sup><xref ref-type="bibr" rid="B3">3</xref>-<xref ref-type="bibr" rid="B6">6</xref></sup> However, it remains unclear whether a brief (&lt;10 minutes), maximal or submaximal physical effort can influence blood pressure readings during hypertension assessment. Therefore, the present study aims to: (1) determine whether physical exertion affects ABPM results in individuals who undergo both tests on the same day; and (2) among those tested on the same day, assess whether the intensity reached during the treadmill test impacts the BP values recorded by ABPM.</p>
      </sec>
      <sec sec-type="methods">
        <title>Methods</title>
        <sec>
          <title>Patients</title>
          <p>For this study, a convenience sample was collected based on patients attending the outpatient service at Cl&#237;nica Pr&#243;-Cora&#231;&#227;o. Inclusion criteria were: performing an exercise stress test with at least submaximal intensity (&#8805;85% of the age-predicted maximum heart rate); undergoing both ABPM and the stress test on the same day or, at most, within the same week. For ABPM interpretation, at least 80% of valid readings were required for the exam to be considered satisfactory.</p>
          <p>Exclusion criteria included: use of antihypertensive medications; SBP &#8805;180 mmHg or DBP &#8805;110 mmHg prior to the stress test; unreadable electrocardiogram or positive signs of myocardial ischemia. Physically active individuals, night-shift workers, smokers, and those with a history of cardiovascular events were also excluded. Participants were instructed to avoid alcohol consumption and refrain from physical exertion during the ABPM monitoring period.</p>
          <p>Based on these data, two analyses were conducted: (1) a comparison between individuals who underwent both the exercise stress test and ABPM on the same day or on different days within the same week; and (2) among those who completed both tests on the same day, participants were divided into two groups&#8212;those who reached submaximal effort (&#8805;85% of age-predicted maximum heart rate) and those who reached maximal effort (&#8805;95% of age-predicted maximum heart rate).</p>
          <p>The study was approved by the Ethics Committee of the Hospital das Cl&#237;nicas, Faculty of Medicine, University of S&#227;o Paulo, and all participants signed an informed consent form. This study is registered on the Clinical Trials platform (NCT05987891).</p>
        </sec>
        <sec>
          <title>Treadmill exercise test</title>
          <p>Initial variables such as BP and heart rate (HR) were collected at rest, with the participant standing on the treadmill and electrodes positioned on the chest (Inbramed<sup>&#174;</sup>, Porto Alegre, Brazil). Systolic (SBP) and diastolic blood pressure (DBP) were assessed using the auscultatory method. All equipment undergoes annual preventive maintenance to ensure data quality. HR, SBP, and DBP were measured at rest and at peak exercise. Peak effort was defined as the participant&#8217;s inability to continue exercising at a given workload due to voluntary exhaustion, prompting the evaluator to stop the test and initiate the recovery phase on the treadmill. The treadmill protocols used were Bruce and Ellestad. All tests were interpreted and reported by the same cardiologists, with those showing positive results for myocardial ischemia (PMMD, LAD, and JPAD) excluded.</p>
        </sec>
        <sec>
          <title>Ambulatory blood pressure monitoring (ABPM)</title>
          <p>Ambulatory blood pressure monitoring was performed using devices from Cardios (S&#227;o Paulo, Brazil), which are calibrated every six months. The ABPM setup was carried out by trained nurses (LRAS, JGO, and KOM). The purpose of ABPM is to continuously record blood pressure levels over a 24-hour period, during both daily activities and sleep. The procedure involves placing a pressure cuff on the patient&#8217;s arm, connected to a portable electronic recorder. This device is programmed to automatically inflate and measure blood pressure at regular intervals &#8211; typically every 15 minutes during the day and every 30 minutes at night. The collected data are stored in the device&#8217;s internal memory for later analysis.</p>
          <p>During the monitoring period, patients were instructed to maintain their usual activities, avoiding only intense physical exertion and exposure to water to prevent damage to the equipment. Patients were also asked to record sleep times, meals, physical activities, and symptoms in a dedicated diary to correlate with the recorded values. After 24 hours, the device was removed and the data were transferred to specialized analysis software, which generates graphs and reports containing the average blood pressure values over the 24-hour period.</p>
        </sec>
        <sec>
          <title>Statistical analysis</title>
          <p>The Kolmogorov-Smirnov test was used to assess data distribution and normality. Statistical analyses were performed using Student&#8217;s t-test for normally distributed data, or the Mann-Whitney test for non-normally distributed data. A p-value &lt; 0.05 was considered statistically significant. Data were expressed as mean &#177; standard deviation. GraphPad Prism software, version 5.0, was used for all analyses.</p>
        </sec>
      </sec>
      <sec sec-type="results">
        <title>Results</title>
        <p>Of the individuals eligible for the study during the data collection period, 18 were excluded due to having SBP &#8805; 180 mmHg and/or DBP &#8805; 110 mmHg prior to the exercise stress test, and six declined to participate. After the stress test, 83 individuals failed to reach at least the age-predicted submaximal heart rate, and 14 had electrocardiograms that were either uninterpretable or showed positive signs of myocardial ischemia (<xref ref-type="fig" rid="f01001">Figure 1</xref>). Thus, 190 patients were included in the final analysis, as shown in <xref ref-type="table" rid="t1001">Table 1</xref>.</p>
        <p>
          <fig id="f01001">
            <label>Figure 1</label>
            <caption>
              <title>&#8211; Flowchart of patients; DBP: diastolic blood pressure; SBP: systolic blood pressure.</title>
            </caption>
            <graphic xlink:href="1678-4170-abc-123-01-e20250412-50412-gf01-en.tif"/></fig>
        </p>
        <p>
          <table-wrap id="t1001">
            <label>Table 1</label>
            <caption>
              <title>&#8211; Anthropometric and exercise stress test characteristics of the study sample</title>
            </caption>
            <table frame="hsides" rules="groups">
              <colgroup>
                <col/>
                <col/>
              </colgroup>
              <thead>
                <tr>
                  <th align="left">Variable</th>
                  <th>Sample (n=190)</th>
                </tr>
              </thead>
              <tbody>
                <tr>
                  <td>Sex (F/M)</td>
                  <td align="center">88/102</td>
                </tr>
                <tr>
                  <td>Age (years)</td>
                  <td align="center">53 &#177; 13</td>
                </tr>
                <tr>
                  <td>Weight (kg)</td>
                  <td align="center">84.7 &#177; 18.3</td>
                </tr>
                <tr>
                  <td>Height (m)</td>
                  <td align="center">1.70 &#177; 0.10</td>
                </tr>
                <tr>
                  <td>BMI (kg/m<sup>2</sup>)</td>
                  <td align="center">29.2 &#177; 5.1</td>
                </tr>
                <tr>
                  <td colspan="2">
                    <bold>Exercise stress test</bold>
                  </td>
                </tr>
                <tr>
                  <td>
                    <bold>Heart rate (bpm)</bold>
                  </td>
                  <td> </td>
                </tr>
                <tr>
                  <td>Resting</td>
                  <td align="center">77 &#177; 15</td>
                </tr>
                <tr>
                  <td>Maximum</td>
                  <td align="center">154 &#177; 21</td>
                </tr>
                <tr>
                  <td>
                    <bold>Blood pressure (mmHg)</bold>
                  </td>
                  <td> </td>
                </tr>
                <tr>
                  <td>Resting systolic blood pressure</td>
                  <td align="center">131 &#177; 12</td>
                </tr>
                <tr>
                  <td>Maximum systolic blood pressure</td>
                  <td align="center">161 &#177; 17</td>
                </tr>
                <tr>
                  <td>Resting diastolic blood pressure</td>
                  <td align="center">82 &#177; 4</td>
                </tr>
                <tr>
                  <td>Maximum diastolic blood pressure</td>
                  <td align="center">83 &#177; 7</td>
                </tr>
                <tr>
                  <td>Test duration (seconds)</td>
                  <td align="center">333 &#177; 98</td>
                </tr>
              </tbody>
            </table>
            <table-wrap-foot>
              <fn id="TFN1001">
                <p>BMI: body mass index; bpm: beats per minute.</p>
              </fn>
            </table-wrap-foot>
          </table-wrap>
        </p>
        <p>The comparison between performing ABPM and the exercise stress test on the same day versus on different days is presented in <xref ref-type="table" rid="t2001">Table 2</xref>. No significant differences were observed in maximum SBP during wakefulness (p = 0.5307) or sleep (p = 0.7383), nor in maximum DBP during wakefulness (p = 0.2691) or sleep (p = 0.3974). Similarly, minimum SBP during wakefulness (p = 0.4615) and sleep (p = 0.5584), as well as minimum DBP during wakefulness (p = 0.1289) and sleep (p = 0.8075), did not differ significantly between the groups.</p>
        <p>
          <table-wrap id="t2001">
            <label>Table 2</label>
            <caption>
              <title>&#8211; Hemodynamic variables from ambulatory blood pressure monitoring in individuals who underwent the treadmill test on the same day or on different days</title>
            </caption>
            <table frame="hsides" rules="groups">
              <colgroup>
                <col/>
                <col/>
                <col/>
                <col/>
              </colgroup>
              <thead>
                <tr>
                  <th align="left">Parameters/groups</th>
                  <th>Same day (n=145)</th>
                  <th>Different days (n=45)</th>
                  <th>p</th>
                </tr>
                <tr>
                  <th align="left" colspan="4">Blood pressure values (mmHg)</th>
                </tr>
              </thead>
              <tbody>
                <tr>
                  <td>Maximum systolic pressure during wakefulness</td>
                  <td align="center">152 &#177; 17</td>
                  <td align="center">155 &#177; 23</td>
                  <td align="center">0.5307</td>
                </tr>
                <tr>
                  <td>Maximum systolic pressure during sleep</td>
                  <td align="center">133 &#177; 16</td>
                  <td align="center">134 &#177; 14</td>
                  <td align="center">0.7383</td>
                </tr>
                <tr>
                  <td>Maximum systolic pressure during wakefulness</td>
                  <td align="center">101 &#177; 13</td>
                  <td align="center">104 &#177; 15</td>
                  <td align="center">0.2691</td>
                </tr>
                <tr>
                  <td>Maximum systolic pressure during sleep</td>
                  <td align="center">87 &#177; 13</td>
                  <td align="center">89 &#177; 15</td>
                  <td align="center">0.3974</td>
                </tr>
                <tr>
                  <td>Minimum systolic pressure during wakefulness</td>
                  <td align="center">98 &#177; 13</td>
                  <td align="center">100 &#177; 16</td>
                  <td align="center">0.4615</td>
                </tr>
                <tr>
                  <td>Minimum systolic pressure during sleep</td>
                  <td align="center">99 &#177; 13</td>
                  <td align="center">100 &#177; 16</td>
                  <td align="center">0.5584</td>
                </tr>
                <tr>
                  <td>Maximum systolic pressure during wakefulness</td>
                  <td align="center">59 &#177;10</td>
                  <td align="center">56 &#177; 13</td>
                  <td align="center">0.1289</td>
                </tr>
                <tr>
                  <td>Maximum systolic pressure during sleep</td>
                  <td align="center">56 &#177; 10</td>
                  <td align="center">58 &#177; 13</td>
                  <td align="center">0.8075</td>
                </tr>
              </tbody>
            </table>
          </table-wrap>
        </p>
        <p>When comparing the intensity of physical effort among individuals who underwent both ABPM and the exercise stress test on the same day, no significant differences were observed in systolic blood pressure (SBP) during wakefulness (p = 0.1029) or sleep (p = 0.2149), nor in diastolic blood pressure (DBP) during wakefulness (p = 0.2062) or sleep (p = 0.1851) between the groups. Similar results were found for minimum SBP during wakefulness (p = 0.7964) and sleep (p = 0.8991), as well as for minimum DBP during wakefulness (p = 0.8864) and sleep (p = 0.4892), as shown in <xref ref-type="table" rid="t3001">Table 3</xref>.</p>
        <p>
          <table-wrap id="t3001">
            <label>Table 3</label>
            <caption>
              <title>&#8211; Hemodynamic variables from ambulatory blood pressure monitoring in individuals who reached submaximal and maximal heart rate during the exercise stress test</title>
            </caption>
            <table frame="hsides" rules="groups">
              <colgroup>
                <col/>
                <col/>
                <col/>
                <col/>
              </colgroup>
              <thead>
                <tr>
                  <th align="left">Parameters/groups</th>
                  <th>Submaximal (n=95)</th>
                  <th>Maximum (n=50)</th>
                  <th>p</th>
                </tr>
                <tr>
                  <th align="left" colspan="4">Blood pressure values (mmHg)</th>
                </tr>
              </thead>
              <tbody>
                <tr>
                  <td>Maximum systolic pressure during wakefulness</td>
                  <td align="center">155 &#177; 19</td>
                  <td align="center">150 &#177; 15</td>
                  <td align="center">0.1029</td>
                </tr>
                <tr>
                  <td>Maximum systolic pressure during sleep</td>
                  <td align="center">134 &#177; 17</td>
                  <td align="center">131 &#177; 15</td>
                  <td align="center">0.2149</td>
                </tr>
                <tr>
                  <td>Maximum systolic pressure during wakefulness</td>
                  <td align="center">103 &#177; 12</td>
                  <td align="center">100 &#177; 13</td>
                  <td align="center">0.2062</td>
                </tr>
                <tr>
                  <td>Maximum systolic pressure during sleep</td>
                  <td align="center">89 &#177; 12</td>
                  <td align="center">86 &#177; 14</td>
                  <td align="center">0.1851</td>
                </tr>
                <tr>
                  <td>Minimum systolic pressure during wakefulness</td>
                  <td align="center">98 &#177; 13</td>
                  <td align="center">98 &#177; 13</td>
                  <td align="center">0.7964</td>
                </tr>
                <tr>
                  <td>Minimum systolic pressure during sleep</td>
                  <td align="center">98 &#177; 13</td>
                  <td align="center">98 &#177; 13</td>
                  <td align="center">0.8991</td>
                </tr>
                <tr>
                  <td>Maximum systolic pressure during wakefulness</td>
                  <td align="center">59 &#177; 11</td>
                  <td align="center">59 &#177; 11</td>
                  <td align="center">0.8864</td>
                </tr>
                <tr>
                  <td>Maximum systolic pressure during sleep</td>
                  <td align="center">57 &#177; 10</td>
                  <td align="center">56 &#177; 10</td>
                  <td align="center">0.4892</td>
                </tr>
              </tbody>
            </table>
          </table-wrap>
        </p>
        <p>Following ABPM, 142 patients (75% of the sample) were diagnosed with arterial hypertension. Additionally, none of the participants in the study exhibited a hyper-reactive blood pressure response to exertion during the exercise stress test. ABPM data were also analyzed according to age groups (&lt;65 years and &#8805;65 years) and sex, as presented in Table 4 of the supplementary material. Individuals aged &#8805;65 years showed significantly lower diastolic blood pressure during wakefulness (103 &#177; 13 vs. 96 &#177; 13 mmHg; p = 0.0015) compared to those under 65 years of age. No other variables showed significant differences between the groups analyzed.</p>
        <p>Regarding sex differences, female participants showed lower diastolic blood pressure values compared to males in several parameters: maximum diastolic pressure during wakefulness (104 &#177; 13 vs. 99 &#177; 13 mmHg; p = 0.0053), maximum diastolic pressure during sleep (91 &#177; 14 vs. 84 &#177; 13 mmHg; p = 0.0012), minimum systolic pressure during wakefulness (101 &#177; 15 vs. 96 &#177; 12 mmHg; p = 0.0064), and minimum diastolic pressure during wakefulness (60 &#177; 12 vs. 55 &#177; 10 mmHg; p = 0.0019). The isolated analysis of ABPM within the same sex, comparing different days or the same day as the exercise stress test, did not show significant differences in the variables studied, as presented in Table 5 of the supplementary material.</p>
      </sec>
      <sec sec-type="discussion">
        <title>Discussion</title>
        <p>Performing the treadmill test on the same day or on different days from ABPM did not influence blood pressure values in the studied sample, which consisted of non-hypertensive and physically inactive individuals. This finding supports the feasibility of conducting both the exercise stress test and ABPM on the same day, enhancing cardiological clinical practice by improving patient retention in the clinical setting and reducing dropout and discontinuity in clinical investigation.</p>
        <p>The hypothesis, supported by a robust body of evidence, suggests that acute aerobic physical exercise reduces systolic and diastolic blood pressure, and that this effect may depend on the intensity of the exercise.<sup><xref ref-type="bibr" rid="B3">3</xref>-<xref ref-type="bibr" rid="B6">6</xref></sup></p>
        <p>In treated hypertensive patients, physical exercise has been shown to reduce blood pressure for up to 24 hours, reaching values considered normal.<sup><xref ref-type="bibr" rid="B6">6</xref></sup> However, in the present study, this effect was not observed &#8211; possibly because the population consisted of individuals who, although in the process of being diagnosed with hypertension, were not yet undergoing treatment. Additionally, the absence of this effect may be related to the low volume of exercise performed, with an average duration of five and a half minutes, corresponding to the length of the test.</p>
        <p>Moreover, aside from the treadmill test, no participant engaged in any other form of physical exertion, there were no reports of alcohol consumption in the diaries, and the sample did not include night-shift workers, which could have introduced confounding factors into the results.</p>
        <p>Following the age-based analysis (&lt;65 years vs. &#8805;65 years), as expected, the heart rate achieved was lower in the older group due to the decline in cardiac function associated with aging.<sup><xref ref-type="bibr" rid="B7">7</xref>,<xref ref-type="bibr" rid="B8">8</xref></sup> Regarding male participants, higher hemodynamic values and longer test durations were observed.<sup><xref ref-type="bibr" rid="B9">9</xref></sup> This finding is explained by greater physical capacity, resulting from higher testosterone levels and greater lean muscle mass.</p>
        <p>The limitations of the present study include the absence of a group of hypertensive individuals and a group with hyper-reactivity to physical exertion, which would have allowed for more comprehensive comparisons and deeper exploration of the topic. The limited number of older participants, particularly those aged 65 and above, also restricts more detailed analyses, especially secondary analyses by sex, which could have enriched the discussion around a predominantly hypertensive population that requires specific cardiological care.</p>
      </sec>
      <sec sec-type="conclusions">
        <title>Conclusion</title>
        <p>Performing the exercise stress test prior to ABPM, both conducted on the same day, did not influence blood pressure values when compared to individuals who underwent the tests on different days. Furthermore, in treadmill tests performed on the same day as ABPM, the intensity of effort, whether maximal or submaximal, did not affect the ABPM results.</p>
        <p>Given the ability of physical exercise to reduce blood pressure, one of the objectives of this investigation was to determine whether this phenomenon could mask hypertension in adults. However, this effect was not observed, which aligns with the study&#8217;s hypothesis.</p>
        <p>Therefore, the findings of this study reinforce clinical practice by demonstrating that physical exertion during the exercise stress test, whether submaximal or maximal, does not influence ABPM results, allowing both tests to be performed on the same day.</p>
      </sec>
    </body>
    <back>
      <ack>
        <title>Acknowledgments</title>
        <p>PGSB: To the Ministry of Education &#8211; MEC / Coordination for the Improvement of Higher Education Personnel &#8211; CAPES &#8211; process number: 88887.102383/2025-00.</p>
      </ack>
      <fn-group>
        <fn fn-type="other">
          <label>Study association:</label>
          <p> This article is part of the thesis of post doctoral submitted by Pedro Gabriel Senger Braga, from Hospital das Cl&#237;nicas da Faculdade de Medicina da Universidade de S&#227;o Paulo.</p>
        </fn>
        <fn fn-type="other">
          <label>Ethics approval and consent to participate:</label>
          <p> This study was approved by the Ethics Committee of the Faculdade de Medicina da Universidade de S&#227;o Paulo under the protocol number 6.258.413. All the procedures in this study were in accordance with the 1975 Helsinki Declaration, updated in 2013. Informed consent was obtained from all participants included in the study.</p>
        </fn>
        <fn fn-type="other">
          <label>Use of Artificial Intelligence:</label>
          <p> The authors did not use any artificial intelligence tools in the development of this work.</p>
        </fn>
        <fn fn-type="data-availability" specific-use="data-available-upon-request">
          <label>Data Availability Statement:</label>
          <p> All datasets supporting the results of this study are available upon request from the corresponding author (Pedro Gabriel Senger Braga).</p>
        </fn>
        <fn fn-type="financial-disclosure">
          <label>Sources of funding:</label>
          <p> There were no external funding sources for this study.</p>
        </fn>
      </fn-group>
    </back>
  </sub-article>
</article>
