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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">GqBgsZmqs4ShL4MgvNzHYTG</article-id>
      <article-id pub-id-type="other">00012</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v2">S0066-782X2010000100012</article-id>
      <article-id pub-id-type="publisher-id" specific-use="scielo-v1">S0066-782X(10)09400112</article-id>
      <article-id pub-id-type="doi">10.1590/S0066-782X2010000100012</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Artigos Originais</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>M&#233;todos para identificar o limiar anaer&#243;bio em indiv&#237;duos com diabete tipo 2 e em indiv&#237;duos n&#227;o-diab&#233;ticos</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Sim&#245;es</surname>
            <given-names>Herbert G.</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Moreira</surname>
            <given-names>S&#233;rgio R.</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Moffatt</surname>
            <given-names>Robert J.</given-names>
          </name>
          <xref ref-type="aff" rid="aff02"/>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Campbell</surname>
            <given-names>Carmen S. G.</given-names>
          </name>
          <xref ref-type="aff" rid="aff01"/>
        </contrib>
      </contrib-group>
      <aff id="aff02">
        <addr-line>
          <named-content content-type="city">Tallahassee</named-content>
          <named-content content-type="state"/>
        </addr-line>
        <institution content-type="orgname">Florida State University</institution>
        <country country="US">United States</country>
      </aff>
      <aff id="aff01">
        <addr-line>
          <named-content content-type="city">Bras&#237;lia</named-content>
          <named-content content-type="state">Distrito Federal</named-content>
        </addr-line>
        <institution content-type="orgname">Universidade Cat&#243;lica de Bras&#237;lia</institution>
        <country country="BR">Brazil</country>
      </aff>
      <pub-date date-type="collection" publication-format="electronic">
        <month>01</month>
        <year>2010</year>
      </pub-date>
      <volume>94</volume>
      <issue>1</issue>
      <fpage>71</fpage>
      <lpage>78</lpage>
      <history>
        <date date-type="accepted">
          <day>08</day>
          <month>11</month>
          <year>2008</year>
        </date>
        <date date-type="rev-recd">
          <day>03</day>
          <month>11</month>
          <year>2008</year>
        </date>
        <date date-type="received">
          <day>16</day>
          <month>06</month>
          <year>2008</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/4.0/" xml:lang="en">
          <license-p>This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.</license-p>
        </license>
      </permissions>
      <abstract>
        <p>FUNDAMENTO: Apesar de o limiar anaer&#243;bio (LAn) ser utilizado na avalia&#231;&#227;o funcional de diferentes popula&#231;&#245;es, estudos comparando m&#233;todos para sua identifica&#231;&#227;o em diab&#233;ticos tipo-2 tem sido pouco realizados. OBJETIVO: Comparar protocolos de identifica&#231;&#227;o do LAn em indiv&#237;duos diab&#233;ticos tipo 2 e em n&#227;o-diab&#233;ticos, e analisar respostas relacionadas ao equil&#237;brio &#225;cido-b&#225;sico em intensidades relativas ao LAn. M&#201;TODOS: Diab&#233;ticos tipo 2 (n=10; 54,5&#177;9,5 anos; 30,1&#177;5,0 kg/m&#178;) e jovens n&#227;o-diab&#233;ticos (n=10; 36,6&#177;12,8 anos; 23,9&#177;5,0 kg/m&#178;) realizaram teste incremental (TI) em ciclo erg&#244;metro. O aumento desproporcional no equivalente ventilat&#243;rio de oxig&#234;nio (VE/VO2) e lactatemia ([lac]) identificaram intensidades (Watts-W) correspondentes aos limiares ventilat&#243;rio (LV) e de lactato (LL), respectivamente. A intensidade correspondente &#224; menor glicemia ([glic]) foi considerada limiar glic&#234;mico individual (LGI). O LAn tamb&#233;m foi determinado por ajuste polinomial das raz&#245;es VE/Watts (LV VE/W) e [lac]/Watts (LL[lac]/W), as quais identificaram intensidades acima das quais um aumento desproporcional na VE e [lac] ocorreram. RESULTADOS: N&#227;o foram observadas diferen&#231;as entre LL, LV, LG, LL[lac]/W e LV VE/W em diab&#233;ticos (85,0&#177;32,1; 88,0&#177;31,7; 86,0&#177;33,8; 82,0&#177;20,9 e 90,2&#177;22,2W) e n&#227;o-diab&#233;ticos (139,0&#177;39,0; 133,0&#177;42,7; 140,8&#177;36,4; 122,7&#177;44,3 e 133,0&#177;39,1W). Contudo os valores de LAn diferiram significativamente entre grupos (p&lt;0.001). A t&#233;cnica de Bland-Altman confirmou concord&#226;ncia entre os protocolos. Redu&#231;&#245;es significativas no pH e pCO2 em paralelo a um aumento na [lac], pO2 e VE foram observadas em intensidades supra limiares. CONCLUS&#195;O: Os protocolos apresentaram, para ambos os grupos estudados, concord&#226;ncia na identifica&#231;&#227;o do LAn, que se mostrou como uma intensidade de exerc&#237;cio acima da qual ocorre perda de equil&#237;brio &#225;cido-b&#225;sico.</p>
      </abstract>
      <kwd-group xml:lang="pt" kwd-group-type="author-generated">
        <kwd>Limiar anaer&#243;bio</kwd>
        <kwd>protocolos cl&#237;nicos</kwd>
        <kwd>glicemia</kwd>
        <kwd>equil&#237;brio &#225;cido b&#225;sico</kwd>
      </kwd-group>
      <pub-date publication-format="electronic" date-type="pub">
        <day>22</day>
        <month>09</month>
        <year>2010</year>
      </pub-date>
    </article-meta>
  </front>
  <body>
    <p>ARTIGO ORIGINAL </p>
    <p> FISIOLOGIA</p>
    <p>
      <bold>M&#233;todos para identificar o limiar anaer&#243;bio em indiv&#237;duos com diabete tipo 2 e em indiv&#237;duos n&#227;o-diab&#233;ticos</bold>
    </p>
    <p>
      <bold>Herbert G. Sim&#245;es<sup>I</sup>; S&#233;rgio R. Moreira<sup>II</sup>; Robert J. Moffatt<sup>II</sup>; Carmen S. G. Campbell<sup>I</sup></bold>
    </p>
    <p><sup>I</sup>Universidade Cat&#243;lica de Bras&#237;lia (UCB), Bras&#237;lia DF - Brasil </p>
    <p><sup>II</sup>Florida State University (FSU), Tallahassee FL - EUA</p>
    <p>
      <xref ref-type="corresp" rid="back">Correspond&#234;ncia</xref>
    </p>
    <p>
      <bold>RESUMO</bold>
    </p>
    <p><bold>FUNDAMENTO: </bold> Apesar de o limiar anaer&#243;bio (LAn) ser utilizado na avalia&#231;&#227;o funcional de diferentes popula&#231;&#245;es, estudos comparando m&#233;todos para sua identifica&#231;&#227;o em diab&#233;ticos tipo-2 tem sido pouco realizados. </p>
    <p><bold>OBJETIVO: </bold> Comparar protocolos de identifica&#231;&#227;o do LAn em indiv&#237;duos diab&#233;ticos tipo 2 e em n&#227;o-diab&#233;ticos, e analisar respostas relacionadas ao equil&#237;brio &#225;cido-b&#225;sico em intensidades relativas ao LAn. </p>
    <p><bold>M&#201;TODOS: </bold> Diab&#233;ticos tipo 2 (n=10; 54,5&#177;9,5 anos; 30,1&#177;5,0 kg/m<sup>2</sup>) e jovens n&#227;o-diab&#233;ticos (n=10; 36,6&#177;12,8 anos; 23,9&#177;5,0 kg/m<sup>2</sup>) realizaram teste incremental (TI) em ciclo erg&#244;metro. O aumento desproporcional no equivalente ventilat&#243;rio de oxig&#234;nio (VE/VO<sub>2</sub>) e lactatemia ([lac]) identificaram intensidades (Watts-W) correspondentes aos limiares ventilat&#243;rio (LV) e de lactato (LL), respectivamente. A intensidade correspondente &#224; menor glicemia ([glic]) foi considerada limiar glic&#234;mico individual (LGI). O LAn tamb&#233;m foi determinado por ajuste polinomial das raz&#245;es VE/Watts (LV<sub>VE/W</sub>) e [lac]/Watts (LL<sub>[lac]/W</sub>), as quais identificaram intensidades acima das quais um aumento desproporcional na VE e [lac] ocorreram. </p>
    <p><bold>RESULTADOS: </bold> N&#227;o foram observadas diferen&#231;as entre LL, LV, LG, LL<sub>[lac]/W</sub> e LV<sub>VE/W</sub> em diab&#233;ticos (85,0&#177;32,1; 88,0&#177;31,7; 86,0&#177;33,8; 82,0&#177;20,9 e 90,2&#177;22,2W) e n&#227;o-diab&#233;ticos (139,0&#177;39,0; 133,0&#177;42,7; 140,8&#177;36,4; 122,7&#177;44,3 e 133,0&#177;39,1W). Contudo os valores de LAn diferiram significativamente entre grupos (p&lt;0.001). A t&#233;cnica de Bland-Altman confirmou concord&#226;ncia entre os protocolos. Redu&#231;&#245;es significativas no pH e pCO<sub>2</sub> em paralelo a um aumento na [lac], pO<sub>2</sub> e VE foram observadas em intensidades supra limiares. </p>
    <p><bold>CONCLUS&#195;O: </bold> Os protocolos apresentaram, para ambos os grupos estudados, concord&#226;ncia na identifica&#231;&#227;o do LAn, que se mostrou como uma intensidade de exerc&#237;cio acima da qual ocorre perda de equil&#237;brio &#225;cido-b&#225;sico.</p>
    <p><bold>Palavras-chave: </bold> Limiar anaer&#243;bio, protocolos cl&#237;nicos, glicemia, equil&#237;brio &#225;cido b&#225;sico.</p>
    <p>
      <bold>Introdu&#231;&#227;o</bold>
    </p>
    <p>O limiar anaer&#243;bio (LAn) reflete uma intensidade de exerc&#237;cio acima da qual um aumento desproporcional na glicemia, lactato sangu&#237;neo ([lac]) e ventila&#231;&#227;o (VE) &#233; observado em paralelo com a diminui&#231;&#227;o do pH<sup>1,2</sup>.</p>
    <p>A determina&#231;&#227;o invasiva do LAn a partir das respostas de [lac] (limiar de lactato - LL) tem sido considerada o padr&#227;o-ouro para avaliar a capacidade aer&#243;bia<sup>3-5</sup>, enquanto a identifica&#231;&#227;o do LAn a partir das respostas de VE (limiar ventilat&#243;rio - LV) apresenta vantagens devido &#224; sua natureza n&#227;o-invasiva e tem sido recomendada para prescri&#231;&#227;o de exerc&#237;cios para popula&#231;&#245;es especiais<sup>5-8</sup>, incluindo diab&#233;ticos<sup>7,9-14</sup>. Entretanto, a determina&#231;&#227;o do LV requer equipamentos caros e as medidas s&#227;o muito dependentes dos m&#233;todos de calibra&#231;&#227;o antes do teste. Al&#233;m disso, geralmente dois ou mais especialistas em fisiologia do exerc&#237;cio experientes s&#227;o frequentemente necess&#225;rios para identificar a intensidade &#224; qual o LAn ocorre<sup>15,16</sup>. Por outro lado, o modelo matem&#225;tico das respostas da VE aos testes incrementais atrav&#233;s de fun&#231;&#227;o polinomial aumentam a acur&#225;cia da identifica&#231;&#227;o do LAn.</p>
    <p>Adicionalmente, tem sido demonstrado que durante o teste incremental (TI), a glicemia ([glic]) apresenta diminui&#231;&#227;o at&#233; que o LAn seja atingido, e a intensidade de exerc&#237;cio acima da qual a [glic] come&#231;a a aumentar &#233; definida como Limiar Glic&#234;mico Individual (LGI)<sup>17</sup>. O LGI parece demarcar uma intensidade de exerc&#237;cio acima da qual a produ&#231;&#227;o de glicose supera sua capta&#231;&#227;o, e que n&#227;o difere do LV e do LL identificados em indiv&#237;duos jovens saud&#225;veis<sup>2</sup>. O diabete tipo 2 tem sido associado ao ac&#250;mulo de gordura no m&#250;sculo esquel&#233;tico, o que inibe a sinaliza&#231;&#227;o da insulina e dessa forma diminui a transloca&#231;&#227;o do GLUT-4, resultando em hiperglicemia<sup>18</sup>. Assim, um m&#233;todo mais pr&#225;tico de identifica&#231;&#227;o do LAn (por exemplo LGI) e/ou um procedimento n&#227;o-invasivo e menos dispendioso (por ex., LV identificado atrav&#233;s da raz&#227;o VE/carga de trabalho (VE/W)) seria &#250;til para a prescri&#231;&#227;o de exerc&#237;cios a fim de evitar o ac&#250;mulo de gordura no m&#250;sculo esquel&#233;tico e controlar a glicemia em indiv&#237;duos com diabete tipo 2 e em indiv&#237;duos n&#227;o-diab&#233;ticos.</p>
    <p>Entretanto, a identifica&#231;&#227;o do LAn a partir das respostas da glicemia, bem como a utiliza&#231;&#227;o de uma determina&#231;&#227;o n&#227;o-invasiva e simples por meio da an&#225;lise das respostas da raz&#227;o VE/carga de trabalho, ainda n&#227;o foram investigadas em portadores de diabete tipo 2.</p>
    <p>O presente estudo comparou as rela&#231;&#245;es entre o LAn identificado atrav&#233;s da [glic] e o LAn identificado por outros m&#233;todos (por ex., LL e LV) em indiv&#237;duos com diabete tipo 2 e em indiv&#237;duos mais jovens n&#227;o-diab&#233;ticos. Adicionalmente, a possibilidade de determinar o LV e o LL ao aplicar uma fun&#231;&#227;o polinomial de segundo grau nas respostas das raz&#245;es VE/carga de trabalho e [lac]/carga de trabalho ([lac]/W) durante o teste incremental na bicicleta ergom&#233;trica foi analisada. Os resultados foram comparados &#224; outros m&#233;todos de determina&#231;&#227;o do LAn, e respostas do pH, press&#227;o parcial de oxig&#234;nio (pO<sub>2</sub>) e de di&#243;xido de carbono (pCO<sub>2</sub>) em rela&#231;&#227;o &#224;s intensidades de LAn identificadas foram analisadas para esclarecer o significado do LAn identificado atrav&#233;s da [glic] e das raz&#245;es (VE/W) e ([lac]/W).</p>
    <p>
      <bold>M&#233;todos</bold>
    </p>
    <p>
      <bold>Indiv&#237;duos</bold>
    </p>
    <p>O Comit&#234; de &#201;tica para Pesquisa em Seres Humanos da Universidade aprovou os m&#233;todos utilizados nesta investiga&#231;&#227;o. Ap&#243;s assinarem o Termo de Consentimento Livre e Esclarecido, 12 indiv&#237;duos sedent&#225;rios com diabete tipo 2 e 10 indiv&#237;duos n&#227;o-diab&#233;ticos fisicamente ativos foram volunt&#225;rios do presente estudo. Os dados de apenas 10 dos 12 indiv&#237;duos diab&#233;ticos s&#227;o apresentados, pois em 2 deles n&#227;o foi poss&#237;vel identificar todos os par&#226;metros de interesse. As caracter&#237;sticas descritivas dos participantes est&#227;o apresentadas na <xref ref-type="table" rid="t01">Tabela 1</xref>. Os indiv&#237;duos n&#227;o-diab&#233;ticos participavam de programas de treinamento de car&#225;ter recreacional h&#225; pelo menos dois anos (por ex., ciclismo e treinamento resistido), consistindo em pelo menos 20 minutos de exerc&#237;cios 3 vezes por semana regularmente, enquanto os participantes diab&#233;ticos eram sedent&#225;rios. Al&#233;m disso, os diab&#233;ticos mantiveram o tratamento hipoglicemiante oral (por ex. sulfonilur&#233;ias, biguanidas, inibidores de alfa-glucosidase) durante o estudo.</p>
    <p content-type="asset">
      <table-wrap id="t01">
        <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gt01.jpg"/></table-wrap>
    </p>
    <p>
      <bold>Procedimentos</bold>
    </p>
    <p>A coleta de dados foi realizada no Laborat&#243;rio de Fisiologia do Exerc&#237;cio da Universidade Cat&#243;lica de Bras&#237;lia e na <italic>Florida State University.</italic> Os participantes foram previamente submetidos &#224; um exame cardiovascular, incluindo um eletrocardiograma de repouso e medidas da press&#227;o arterial (Microlife, Inglaterra). Os indiv&#237;duos com complica&#231;&#245;es cardiovasculares, neurol&#243;gicas e ortop&#233;dicas foram exclu&#237;dos da participa&#231;&#227;o no estudo. Os indiv&#237;duos selecionados realizaram um teste incremental em bicicleta ergom&#233;trica eletromagn&#233;tica (Lode Excalibur, Pa&#237;ses Baixos) ap&#243;s uma noite em jejum entre 8:30 e 9:30 horas da manh&#227; em uma sala a uma temperatura de 22-23&#176; C, 665 mmHg de press&#227;o barom&#233;trica e 50% de umidade.</p>
    <p>
      <bold>Teste Incremental (TI)</bold>
    </p>
    <p>Um TI foi aplicado para identificar o LL, o LV, o LGI e o VO<sub>2max</sub>. Para isso, antes do in&#237;cio do TI era realizado aquecimento de um minuto pedalando a 0 Watts (W) com carga entre 15 e 50 W, e incrementos de 15-25 W a cada 3-min, dependendo das caracter&#237;sticas do participante (se diab&#233;tico ou saud&#225;vel, fisicamente ativo ou sedent&#225;rio etc). Para a maioria dos participantes (incluindo todos os diab&#233;ticos) o teste foi iniciado com 15 W e incrementos de 15 W a cada est&#225;gio de 3 minutos. O teste foi interrompido devido &#224; exaust&#227;o volunt&#225;ria ou se qualquer anormalidade eletrocardiogr&#225;fica fosse observada. Adicionalmente, os crit&#233;rios para interrup&#231;&#227;o do teste inclu&#237;ram um aumento exagerado na press&#227;o arterial sist&#243;lica (PAS), press&#227;o arterial diast&#243;lica (PAD) acima de 115 mmHg, al&#233;m da incapacidade de aumentar o pulso de oxig&#234;nio em paralelo ao aumento na carga de trabalho e/ou uma raz&#227;o de troca respirat&#243;ria (RER) acima de 1,15<sup>7,19</sup>.</p>
    <p>
      <bold>An&#225;lise ventilat&#243;ria</bold>
    </p>
    <p>Gases expirados foram mensurados de forma cont&#237;nua usando-se um sistema Parvomedics MMS-2400 (<italic>Florida State University</italic>) ou o sistema <italic>Cortex Metalyzer</italic> 3B (Universidade Cat&#243;lica de Bras&#237;lia). A calibra&#231;&#227;o dos equipamentos de an&#225;lise gasosa era realizada antes de cada teste. Os resultados obtidos dos &#250;ltimos 20 segundos de cada est&#225;gio foram considerados para a identifica&#231;&#227;o da ventila&#231;&#227;o minuto (VE), consumo de oxig&#234;nio (VO<sub>2</sub>), produ&#231;&#227;o de di&#243;xido de carbono (VCO<sub>2</sub>), raz&#227;o de troca respirat&#243;ria (RER) e LV. O maior VO<sub>2</sub> obtido na exaust&#227;o volunt&#225;ria era considerado o VO<sub>2pico.</sub></p>
    <p>
      <bold>Coleta de sangue e an&#225;lises laboratoriais</bold>
    </p>
    <p>Durante os &#250;ltimos 10 segundos de cada est&#225;gio, uma amostra de 25 &#956;l de sangue era coletada do l&#243;bulo da orelha, usando microcapilares heparinizados e calibrados para mensura&#231;&#245;es de [lac] e [glic] de todos os participantes. Uma amostra de 75 &#956;l de sangue tamb&#233;m foi coletada em 5 indiv&#237;duos n&#227;o-diab&#233;ticos em repouso, no meio do teste incremental (geralmente no final dos est&#225;gios 3 a 5; por volta do LAn) e imediatamente na conclus&#227;o do teste.</p>
    <p>Os 25 &#956;l foram transferidos para tubos de Eppendorf contendo 50 &#956;l de fluoreto de s&#243;dio (NaF) a 1%. O [lac] e a [glic] foram determinados em cada amostra em duplicata usando-se um analisador de lactato e glicose sangu&#237;neos (Yellow Springs 2700S). Os resultados de [lac] e [glic] foram corrigidos pelo volume da amostra de sangue dentro do tubo de Eppendorf e s&#227;o apresentados em mM. A pO<sub>2</sub> e pCO<sub>2</sub> (mmHg), o Excesso de Base - EB (mM) e o pH foram medidos na amostra de 75 &#956;l utilizando o sistema AVL (<italic>Blood Gas Analyser</italic> - OMNI 3 <italic>Modular Analyzer</italic>, AVL <italic>Scientific Corporation, Roswell</italic>, GA).</p>
    <p>
      <bold>Identifica&#231;&#227;o do Limiar Anaer&#243;bio</bold>
    </p>
    <p>O LL foi considerado como o ponto de inflex&#227;o da curva de [lac], enquanto o LGI foi determinado pela cin&#233;tica da [glic], sendo definido como a intensidade de exerc&#237;cio em que a [glic] come&#231;ava a aumentar durante o TI<sup>17</sup>. O LV foi identificado por dois pesquisadores independentes, considerando-se um aumento na raz&#227;o VE/VO<sub>2</sub> sem um aumento paralelo na raz&#227;o VE/VCO<sub>2.</sub><sup>1,20</sup> (<xref ref-type="fig" rid="f1">Figura 1</xref>), e na impossibilidade de se identificar o LV por esta t&#233;cnica, o mesmo era identificado considerando-se o ponto de quebra na rela&#231;&#227;o VCO<sub>2</sub>-VO<sub>2</sub>.</p>
    <fig id="f1">
      <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf01.jpg"/></fig>
    <p>Al&#233;m disso, a raz&#227;o VE/W e [lac]/W foram plotadas <italic>versus</italic> a carga de trabalho para cada participante durante o TI. Sobre os resultados foi aplicada fun&#231;&#227;o polinomial de segundo grau e a equa&#231;&#227;o originada foi derivada a fim de determinar uma intensidade de exerc&#237;cio acima da qual ocorria um aumento desproporcional da VE e do [lac] em rela&#231;&#227;o &#224; carga de trabalho. A identifica&#231;&#227;o do LAn atrav&#233;s dessas abordagens matem&#225;ticas foi chamada respectivamente de LV<sub>VE/W</sub> e LL<sub>[lac]/W</sub>. A identifica&#231;&#227;o do LV<sub>VE/W</sub> e LL<sub>[lac]/W</sub> para um &#250;nico participante diab&#233;tico &#233; mostrada na <xref ref-type="fig" rid="f2">Figura 2 (A-B)</xref>.</p>
    <fig id="f2">
      <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf02.jpg"/></fig>
    <p>
      <bold>Tratamento estat&#237;stico e procedimentos para compara&#231;&#227;o</bold>
    </p>
    <p>Os dados s&#227;o apresentados como m&#233;dias e desvios-padr&#227;o (DP). Os resultados m&#233;dios do TI para todos os participantes s&#227;o apresentados no "In&#237;cio" (primeiro est&#225;gio do teste incremental), M1 (ponto m&#233;dio entre o primeiro est&#225;gio e o LAn), LAn (cargas de trabalho do LV, LGI e LL), M2 (ponto m&#233;dio entre o LAn e o &#250;ltimo est&#225;gio/exaust&#227;o) e o "final" (&#250;ltimo est&#225;gio/momento de exaust&#227;o). Compara&#231;&#245;es entre as intensidades de LAn identificado por diferentes m&#233;todos foram realizadas atrav&#233;s de An&#225;lise de Vari&#226;ncia, com <italic>post-hoc</italic> de Tuckey-Kraemer. Teste t-student para amostras n&#227;o pareadas foi aplicado para compara&#231;&#245;es entre vari&#225;veis correspondentes de ambos os grupos. As rela&#231;&#245;es entre as vari&#225;veis foram determinadas atrav&#233;s da correla&#231;&#227;o de Pearson. Adicionalmente, a concord&#226;ncia entre a intensidade do LAn identificada pelo lactato sangu&#237;neo, que foi estabelecida como o padr&#227;o-ouro, e o LAn identificado atrav&#233;s de outros m&#233;todos no presente estudo foi avaliada pela t&#233;cnica de Bland e Altman<sup>21</sup>. O n&#237;vel de signific&#226;ncia estabelecido foi p&lt;0,05.</p>
    <p>
      <bold>Resultados</bold>
    </p>
    <p>O LAn estabelecido pelas respostas ventilat&#243;ria, [lac] e [glic], bem como atrav&#233;s das raz&#245;es LV<sub>VE/W</sub> e LL<sub>[lac]/W</sub>, foi identificado para ambos os grupos, mas o LGI n&#227;o p&#244;de ser identificado em dois participantes diab&#233;ticos. No geral, 5 a 8 est&#225;gios foram necess&#225;rios para concluir o TI para a maioria dos indiv&#237;duos. As m&#233;dias (<underline>+</underline>DP) da VE, [lac], [glic], raz&#245;es LV<sub>VE/W</sub> e LL<sub>[lac]/W</sub> nas mesmas intensidades relativas s&#227;o apresentadas para os participantes diab&#233;ticos e os n&#227;o-diab&#233;ticos (<xref ref-type="fig" rid="f03">Figura 3 A-E</xref>). Adicionalmente, as concentra&#231;&#245;es m&#233;dias de [lac] e [glic] sangu&#237;neos, pH, EB, pO<sub>2</sub> e pCO<sub>2</sub> em repouso e durante o teste incremental s&#227;o apresentadas na <xref ref-type="fig" rid="f4">Figura 4 (A-D)</xref>. Ap&#243;s alcan&#231;ar o LAn, as respostas da [glic] e pO<sub>2</sub> foram similares &#224;s respostas do [lac], enquanto o pH, EB e pCO<sub>2</sub> responderam inversamente ao [lac], VE e &#224;s raz&#245;es LV<sub>VE/W</sub> e LL<sub>[lac]/W</sub> (<xref ref-type="fig" rid="f03">Figuras 3</xref> e <xref ref-type="fig" rid="f4">4</xref>). A despeito das diferen&#231;as entre os grupos apresentadas nas <xref ref-type="table" rid="t01">Tabelas 1</xref> e <xref ref-type="table" rid="t02">2</xref>, nenhuma diferen&#231;a foi observada dentro dos grupos para carga de trabalho, consumo de oxig&#234;nio e frequ&#234;ncia card&#237;aca em rela&#231;&#227;o ao LL, LV, LGI, LV<sub>VE/W</sub>, LL<sub>[lac]/W</sub> (p&gt;0,05). Adicionalmente, as vari&#225;veis apresentaram uma alta correla&#231;&#227;o entre si (<xref ref-type="table" rid="t3">Tabela 3</xref>) e a t&#233;cnica de Bland e Altman evidenciou uma concord&#226;ncia entre LL e o LAn identificado por outros m&#233;todos (<xref ref-type="fig" rid="f05">Figura 5</xref>).</p>
    <p content-type="asset">
      <fig id="f03">
        <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf03.jpg"/></fig>
    </p>
    <p content-type="asset">
      <table-wrap id="t02">
        <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gt02.jpg"/></table-wrap>
    </p>
    <p content-type="asset">
      <fig id="f05">
        <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf04.jpg"/></fig>
    </p>
    <fig id="f4">
      <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf05.jpg"/></fig>
    <table-wrap id="t3">
      <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gt03.jpg"/></table-wrap>
    <p>
      <bold>Discuss&#227;o</bold>
    </p>
    <p>O presente estudo comparou m&#233;todos para identificar o LAn em indiv&#237;duos com diabete tipo 2 e indiv&#237;duos mais jovens, n&#227;o-diab&#233;ticos. Esta escolha de compara&#231;&#227;o entre indiv&#237;duos com diabete tipo 2 e indiv&#237;duos mais jovens saud&#225;veis e fisicamente ativos foi devido ao fato de, como esperado, esses grupos diferirem em termos de composi&#231;&#227;o corporal e aptid&#227;o f&#237;sica em rela&#231;&#227;o aos resultados do VO<sub>2</sub>pico e LAn. Mesmo assim, os protocolos estudados foram consistentes dentro dos grupos, independente de suas caracter&#237;sticas. Portanto, nossos principais achados foram que o LGI foi identificado em indiv&#237;duos com diabete tipo 2 de forma similar aos indiv&#237;duos n&#227;o-diab&#233;ticos (<xref ref-type="fig" rid="f2">Figuras 2 a-b</xref> e <xref ref-type="fig" rid="f03">Figura 3</xref>), apesar das diferen&#231;as entre grupos em rela&#231;&#227;o &#224;s suas caracter&#237;sticas f&#237;sicas e estado de sa&#250;de. Foi demonstrado em ambos os grupos que o LAn pode ser identificado com sucesso durante um teste incremental em cicloergon&#244;metro empregando as respostas das raz&#245;es VE/carga de trabalho e [lac]/carga de trabalho por meio de uma fun&#231;&#227;o polinomial de segundo grau sem diferen&#231;as quando comparados a outros m&#233;todos (<xref ref-type="table" rid="t02">Tabela 2</xref>). Al&#233;m disso, os diferentes m&#233;todos para identificar o LAn no presente estudo apresentaram alta correla&#231;&#227;o entre si e a t&#233;cnica de Bland e Altman demonstrou uma concord&#226;ncia entre o LL e outros m&#233;todos para identificar o LAn em indiv&#237;duos diab&#233;ticos e n&#227;o-diab&#233;ticos (<xref ref-type="table" rid="t3">Tabela 3</xref>; <xref ref-type="fig" rid="f05">Figura 5</xref>). Em concord&#226;ncia com nossos estudos anteriores envolvendo indiv&#237;duos jovens e fisicamente ativos<sup>2</sup>, o presente estudo mostrou n&#227;o haver equil&#237;brio &#225;cido-base em intensidades acima dos limiares identificados durante o teste incremental (<xref ref-type="fig" rid="f4">Figura 4</xref>), sugerindo que os protocolos estudados s&#227;o v&#225;lidos para a identifica&#231;&#227;o de intensidades nas quais o equil&#237;brio &#225;cido-base pode ser mantido durante o exerc&#237;cio. Apesar da menor aptid&#227;o f&#237;sica dos indiv&#237;duos diab&#233;ticos no presente estudo, os limiares foram observados entre 60 e 71%VO<sub>2 max</sub> para ambos os grupos (<xref ref-type="table" rid="t01">Tabela 1</xref> e <xref ref-type="table" rid="t02">2</xref>). Considerados juntos, nossos achados refor&#231;am a validade dos presentes m&#233;todos para identificar o LAn como uma intensidade de exerc&#237;cio acima da qual ambos a acidose metab&#243;lica e a eleva&#231;&#227;o da [glic] ocorrem.</p>
    <p>Sugerimos que o LGI possa demarcar uma transi&#231;&#227;o da predomin&#226;ncia da capta&#231;&#227;o da [glic] para a produ&#231;&#227;o da [glic] estimulada pelas catecolaminas e glucagon durante exerc&#237;cios de alta intensidade<sup>22</sup>. O LGI foi determinado em 83,3% (10/12) dos participantes diab&#233;ticos enquanto todos os participantes n&#227;o-diab&#233;ticos tiveram seu LGI identificado no presente estudo. A n&#227;o-identifica&#231;&#227;o do LGI em alguns participantes diab&#233;ticos foi causada por dist&#250;rbios metab&#243;lico-hormonais ou por efeito de agentes hipoglicemiantes, cuja utiliza&#231;&#227;o n&#227;o foi interrompida durante o estudo. Entretanto, nossos resultados indicam que a intensidade do exerc&#237;cio que pode causar um aumento da [glic] foi similarmente identificada pelas respostas do lactato sangu&#237;neo ou ventilat&#243;ria (<xref ref-type="table" rid="t02">Tabela 2</xref>), o que por sua vez pode ter aplica&#231;&#245;es cl&#237;nicas no controle da glicemia do diabete tipo 2. Considerando que os indiv&#237;duos com diabete tipo 2 podem ter problemas com a coagula&#231;&#227;o sangu&#237;nea e recupera&#231;&#227;o de dano tecidual, a utiliza&#231;&#227;o do LV parece ser atraente devido &#224; sua natureza n&#227;o-invasiva, por&#233;m o seu custo &#233; elevado. Nossos dados demonstraram que a raz&#227;o VE/carga de trabalho atrav&#233;s de uma fun&#231;&#227;o polinomial resulta em uma equa&#231;&#227;o de segundo grau que pode ser derivada e aplicada a fim de se identificar em qual intensidade ocorre um aumento desproporcional da VE e portanto o LV ocorre (<xref ref-type="fig" rid="f2">Figura 2</xref>). O modelo da fun&#231;&#227;o polinomial da raz&#227;o VE/carga de trabalho resulta em uma curva em U similar &#224; raz&#227;o [lac]/carga de trabalho em ambos os grupos. Este m&#233;todo permite a identifica&#231;&#227;o do LAn sem an&#225;lises de O<sub>2</sub> e CO<sub>2</sub> ou interpreta&#231;&#227;o de dois ou mais especialistas. Al&#233;m disso, sendo n&#227;o-invasiva, ela &#233; independente da qualquer valor especifico de ventila&#231;&#227;o, mas ao inv&#233;s disso, dependente de seu comportamento.</p>
    <p>A resist&#234;ncia &#224; insulina tem sido associada com ac&#250;mulo de gordura no m&#250;sculo<sup>18</sup>. A identifica&#231;&#227;o do LAn a partir da glicemia e das respostas VE/carga de trabalho s&#227;o m&#233;todos simples que podem identificar as intensidades ideais de exerc&#237;cio para o controle da glicemia em portadores de diabete tipo 2. Enquanto o exerc&#237;cio agudo na intensidade do LGI pode melhorar o perfil da glicemia, cronicamente ele evitaria o ac&#250;mulo da gordura no m&#250;sculo e assim, melhoraria a sensibilidade &#224; insulina de tais pacientes. Entretanto, estudos futuros devem investigar ambos os efeitos agudo e cr&#244;nico do exerc&#237;cio realizado em intensidades relacionadas ao LAn em indiv&#237;duos portadores de diabete tipo 2.</p>
    <p>Conclu&#237;mos que, similarmente a indiv&#237;duos n&#227;o-diab&#233;ticos, o LAn pode ser identificado de forma precisa em indiv&#237;duos com diabete tipo 2 durante o teste incremental em cicloerg&#244;metro, por meio das respostas de glicemia, bem como atrav&#233;s da aplica&#231;&#227;o de uma fun&#231;&#227;o polinomial de segundo grau na rela&#231;&#227;o VE/carga de trabalho. Al&#233;m disso, os resultados obtidos pela aplica&#231;&#227;o dos m&#233;todos propostos para identificar o LAn n&#227;o diferiram uns dos outros e parecem indicar uma intensidade de exerc&#237;cio acima da qual a glicemia &#233; aumentada e o equil&#237;brio &#225;cido-base &#233; perdido.</p>
    <p>
      <bold>Agradecimentos</bold>
    </p>
    <p>Os autores agradecem ao CNPq (proc. <italic>475575/2004-0)</italic> e SIGEP/UCB pelo apoio financeiro. Al&#233;m disso, nossos agradecimentos ao Dr. Ricardo Jac&#243; de Oliveira por sua colabora&#231;&#227;o e ao LAFIT-UCB pela assist&#234;ncia t&#233;cnica.</p>
    <p>
      <bold>Potencial Conflito de Interesses</bold>
    </p>
    <p>Declaro n&#227;o haver conflito de interesses pertinentes.</p>
    <p>
      <bold>Fontes de Financiamento</bold>
    </p>
    <p>O presente estudo foi financiado pelo Cnpq.</p>
    <p>
      <bold>Vincula&#231;&#227;o Acad&#234;mica</bold>
    </p>
    <p>Este artigo &#233; parte de tese de Mestrado e Doutorado de S&#233;rgio R. Moreira, Gabrielle do Valle e Herbert G. Sim&#245;es, pela Universidade Cat&#243;lica de Bras&#237;lia, Universidade Estadual da Fl&#243;rida e Universidade Federal de S&#227;o Carlos.</p>
    <p>
      <fn id="back" fn-type="corresp">
        <p>Correspond&#234;ncia:</p>
        <p> Herbert G. Sim&#245;es </p>
        <p> Universidade Cat&#243;lica de Bras&#237;lia - UCB </p>
        <p> EPTC, QS07, LT1 s/n. Bloco G Sala 116 </p>
        <p> 72030-170 &#193;guas Claras, Bras&#237;lia, DF - Brasil </p>
        <p> E-mail: </p>
        <p>
          <email xlink:href="hgsimoes@gmail.com">hgsimoes@gmail.com</email>
        </p>
      </fn>
    </p>
    <p>Artigo recebido em 16/09/08; revisado recebido em 03/11/08; aceito em 03/11/08.</p>
  </body>
  <back>
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  <sub-article article-type="translation" id="TRen" xml:lang="en">
    <front-stub>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Original Articles</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title xml:lang="en">Methods to identify the anaerobic threshold for type-2 diabetic and non-diabetic subjects</article-title>
      </title-group>
      <abstract xml:lang="en">
        <p>BACKGROUND: In spite of Anaerobic Threshold (AT) to be widely used on exercise evaluation for different populations, there are few studies comparing methods to identify AT for individuals with type-2 diabetes. OBJECTIVE: To compare methods of AT determination on type-2 diabetics (T2D) and non-diabetic (ND) subjects and verify the acid-base balance as related to AT intensity. METHODS: T2D (n=10; 54.5&#177;9.5 yr; 30.1&#177;5.0 kg/m&#178;) and younger ND (n=10; 36.6&#177;12.8 yr; 23.9&#177;5.0 kg/m&#178;) performed an incremental test (IT) on a cycle ergometer. The over-proportional increase in VE/VO2 and blood lactate ([lac]) identified the ventilatory (VT) and lactate thresholds (LT) respectively. The workload corresponding to the lower blood glucose ([gluc]) during test identified the individual glucose threshold (IGT). The AT was also determined by polynomial adjustment of the VE/Workload and [lac]/Workload responses to identify exercise intensities above which an over-proportional increase in VE and [lac] did occur and were named VT VE/W and LT[lac]/W. RESULTS: The workload (Watts-W) corresponding to LT, VT, IGT, LT Lac/W and VT VE/W of diabetics (85.0&#177;32.1; 88.0&#177;31.7; 86.0&#177;33.8; 82.0&#177;20.9 and 90.2&#177;22.2W) and non-diabetics (139.0&#177;39.0; 133.0&#177;42.7; 140.8&#177;36.4; 122.7&#177;44.3 and 133.0&#177;39.1W) differed between groups (p&lt;0.001), but not within groups. Thus it was evidenced an agreement among the studied methods. The pH and pCO2 were significantly decreased in parallel to the increase in [lac], pO2 and VE at supra AT intensities. CONCLUSION: The AT intensities, as determined by different methods both for diabetics and non-diabetic individuals, were in agreement to each other and identified exercise intensities above which the acid-basic balance is disrupted.</p>
      </abstract>
      <kwd-group xml:lang="en">
        <kwd>Anaerobic threshold</kwd>
        <kwd>clinical protocols</kwd>
        <kwd>blood glucose</kwd>
        <kwd>acid-basic equilibrium</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>ORIGINAL ARTICLE</bold>
      </p>
      <p>
        <fn id="top-body2">
          <label>
            <bold>Methods to identify the anaerobic threshold for type-2 diabetic and non-diabetic subjects</bold>
          </label>
          <p>
            <bold>Herbert G. Sim&#245;es<sup>I</sup>; S&#233;rgio R. Moreira<sup>I</sup>; Robert J. Moffatt<sup>II</sup>; Carmen S. G. Campbell<sup>I</sup></bold>
          </p>
        </fn>
      </p>
      <p><sup>I</sup>Universidade Cat&#243;lica de Bras&#237;lia (UCB), Bras&#237;lia DF - Brazil</p>
      <p><sup>II</sup>Florida State University (FSU), Tallahassee FL - EUA</p>
      <p>Mailing address</p>
      <p>
        <bold>ABSTRACT</bold>
      </p>
      <p><bold>BACKGROUND:</bold> In spite of Anaerobic Threshold (AT) to be widely used on exercise evaluation for different populations, there are few studies comparing methods to identify AT for individuals with type-2 diabetes.</p>
      <p><bold>OBJECTIVE: </bold> To compare methods of AT determination on type-2 diabetics (T2D) and non-diabetic (ND) subjects and verify the acid-base balance as related to AT intensity.</p>
      <p><bold>METHODS: </bold> T2D (n=10; 54.5&#177;9.5 yr; 30.1&#177;5.0 kg/m<sup>2</sup>) and younger ND (n=10; 36.6&#177;12.8 yr; 23.9&#177;5.0 kg/m<sup>2</sup>) performed an incremental test (IT) on a cycle ergometer. The over-proportional increase in VE/VO<sub>2</sub> and blood lactate ([lac]) identified the ventilatory (VT) and lactate thresholds (LT) respectively. The workload corresponding to the lower blood glucose ([gluc]) during test identified the individual glucose threshold (IGT). The AT was also determined by polynomial adjustment of the VE/Workload and [lac]/Workload responses to identify exercise intensities above which an over-proportional increase in VE and [lac] did occur and were named VT<sub>VE/W</sub> and LT[<sub>lac]/W</sub>.</p>
      <p><bold>RESULTS: </bold> The workload (Watts-W) corresponding to LT, VT, IGT, LT<sub>Lac/W</sub> and VT<sub>VE/W</sub> of diabetics (85.0&#177;32.1; 88.0&#177;31.7; 86.0&#177;33.8; 82.0&#177;20.9 and 90.2&#177;22.2W) and non-diabetics (139.0&#177;39.0; 133.0&#177;42.7; 140.8&#177;36.4; 122.7&#177;44.3 and 133.0&#177;39.1W) differed between groups (p&lt;0.001), but not within groups. Thus it was evidenced an agreement among the studied methods. The pH and pCO<sub>2</sub> were significantly decreased in parallel to the increase in [lac], pO<sub>2</sub> and VE at supra AT intensities.</p>
      <p><bold>CONCLUSION: </bold> The AT intensities, as determined by different methods both for diabetics and non-diabetic individuals, were in agreement to each other and identified exercise intensities above which the acid-basic balance is disrupted.</p>
      <p><bold>Key-words:</bold> Anaerobic threshold; clinical protocols; blood glucose; acid-basic equilibrium.</p>
      <p>
        <bold>Introduction</bold>
      </p>
      <p>The anaerobic threshold (AT) reflects an exercise intensity above which an over-proportional increase in glycolysis rate, blood lactate ([lac]) and ventilation (VE) is observed paralleled to the pH diminution<sup>1,2</sup>.</p>
      <p>The invasive determination of AT from [lac] responses (lactate threshold - LT) has been considered a gold standard to evaluate aerobic capacity<sup>3-5</sup>, while the AT identification from VE responses (ventilatory threshold - VT) has advantages due its noninvasive nature and has been recommended for exercise prescription for special populations<sup>5-8</sup> including diabetics<sup>7,9-14</sup>. However, the VT determination requires expensive equipment and measurements are quite dependent on calibration methods before testing. Moreover, usually two or more experienced physicians are often needed to identify the intensity at which AT occurs<sup>15,16</sup>. On the other hand, the mathematical modeling of VE responses to incremental tests through polynomial function would increase the accuracy of AT identification.</p>
      <p>Additionally, during the incremental test (IT), the blood glucose ([gluc]) was shown to decrease until AT was reached and the exercise intensity above which the [gluc] recommences to increase was named Individual Glucose Threshold (IGT)<sup>17</sup>. The IGT seems to demarcate an exercise intensity above which blood glucose output overcomes its uptake and it is not different from the VT and LT identified in young health individuals<sup>2</sup>. Type 2 diabetes has been associated to skeletal muscle lipid accumulation, which inhibits insulin signaling and thus decreases GLUT-4 translocation, resulting in hyperglycemia<sup>18</sup>. So, a more practical method for AT identification (e.g. IGT) and/or a non-invasive and less expensive procedure (e.g. VT identified through VE/Workload ratio) would be useful for exercise prescription to prevent skeletal muscle lipid accumulation and to control blood glucose in type 2 diabetics and non-diabetic individuals. However, the AT identification through blood glucose responses, as well as the utilization of a non-invasive and simple AT determination through the modeling of the VE/Workload responses, have not yet been investigated in diabetics.</p>
      <p>The present study compared and established associations between the AT identified through [gluc] and the AT identified by other methods (e.g. LT and VT) on type 2 diabetics and younger non-diabetic counterparts. Moreover, the possibility to determine the VT and LT by applying a second-order polynomial function on the responses of VE/workload and [lac]/workload ratio during incremental test on a cycle ergometer was analyzed. The results were compared to other methods of AT determination and the pH, pO<sub>2</sub> and pCO<sub>2</sub> responses in relation to the identified AT intensities were analyzed to clarify the significance of AT identified through [gluc], VE/Workload and [lac]/Workload ratio.</p>
      <p>
        <bold>Methods</bold>
      </p>
      <p>
        <bold>Subjects</bold>
      </p>
      <p>The University Ethics Committee for Human Research approved the methods used in this study. After completing the written informed consent procedure, 12 sedentary type 2 diabetics and 10 physically-active non-diabetic individuals volunteered for this investigation. Data from 10 of the 12 diabetics are presented, as it was not possible to identify all parameters of interest in 2 of them. Descriptive characteristics of the participants are presented in <xref ref-type="table" rid="en_12t01-body2">Table 1</xref>. The non-diabetic subjects have been involved in recreational training programs for the last 2 years (e.g. cycling and resistance training), consisting of at least 20 minutes of exercise 3 times/week on a regular basis, while the diabetic participants were sedentary. Additionally, the diabetics kept their oral hypoglycemic treatment (e.g. sulphonylureas, biguanides, alpha-glucosidase inhibitors) during the study.</p>
      <p content-type="asset">
        <table-wrap id="en_12t01-body2">
          <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gt01-en.jpg"/></table-wrap>
      </p>
      <p>
        <bold>Procedures</bold>
      </p>
      <p>Data collection was performed at the Exercise Physiology Laboratory of the Catholic University of Bras&#237;lia and at Florida State University. Participants were previously submitted to a cardiovascular examination, including resting electrocardiogram and blood pressure measurements (Microlife, England). Participants with cardiovascular, neurological or orthopedic complications were excluded. The selected subjects performed an incremental exercise test on an electromagnetic cycle ergometer (Lode Excalibur, Netherland) in an overnight fasting state between 8:30 and 9:30 am at a room with a temperature of 22-23&#176; C, 665 mmHg of barometric pressure and 50% of humidity.</p>
      <p>
        <bold>Incremental exercise test (IT)</bold>
      </p>
      <p>An IT was applied to identify the LT, the VT, the IGT and the VO<sub>2</sub>max. A 1-min warm-up while pedaling at 0 Watts was performed before starting with a workload of 15 to 50 Watts. Then the workload was increased every 3-mins by 15-25 Watts according to the participant's life style and physical fitness. For most participants (including all diabetics) the test initiated at 15 Watts with increments of 15 Watts at each 3-min stage. Work was terminated due to voluntary exhaustion or if any electrocardiographic abnormality was observed. Also, criteria for stopping the test included reaching an over-proportional increase in systolic blood pressure (SBP) and/or a diastolic blood pressure (DBP) over 115 mmHg, a failure to increase the oxygen pulse paralleled to the increase in the workload and/or a respiratory exchange ratio over 1.15<sup>7,19</sup>.</p>
      <p>
        <bold>Ventilatory measurement</bold>
      </p>
      <p>Respiratory gas was measured continuously using either a Parvomedics MMS-2400 system (Florida State University) or the Cortex Metalyzer 3B system (Catholic University of Brasilia). Both the gas calibration and a flow meter calibration took place before every test. The results obtained from the last 20 seconds of each stage were considered for the identification of the minute ventilation (VE), oxygen consumption (VO<sub>2</sub>), carbon dioxide production (VCO<sub>2</sub>), respiratory exchange ratio (RER) and VT. The highest VO<sub>2</sub> obtained at the voluntary exhaustion was considered VO<sub>2peak.</sub></p>
      <p>
        <bold>Blood collection and laboratory analyses</bold>
      </p>
      <p>During the last 10-sec of each stage, a 25-&#956;l sample was collected from the ear lobe using heparinized and calibrated microcapillaries for [lac] and [gluc] measurements for all participants. A 75-&#956;l sample of blood was also collected from 5 non-diabetics at rest, in the middle of the incremental test (usually at the end of stages 3 to 5; around the AT) and immediately at the conclusion of the test.</p>
      <p>The 25ul were transferred into Eppendorf tubes containing 50&#956;l of Sodium Fluoride (NaF) 1%. The [lac] and [gluc] were determined from each sample in duplicate by using a blood lactate and glucose analyzer (Yellow Springs 2700S). The [lac] and [gluc] results were corrected by the volume of the blood sampled within the Eppendorf tubes and are presented in mM. The pO<sub>2</sub> and pCO<sub>2</sub> (mmHg), the Base Excess - BE (mM) and pH were measured at the 75-&#956;l sample using the AVL system (Blood Gas Analyzer - OMNI 3 Modular Analyzer, AVL Scientific Corporation, Roswell, GA).</p>
      <p>
        <bold>Anaerobic threshold identification</bold>
      </p>
      <p>The LT was identified by the [lac] breakpoint, while the IGT was determined by [gluc] kinetics and was defined as the exercise intensity at which the [gluc] began to increase during the IT<sup>17</sup>. The VT was identified by two independent researchers, considering an increase in the VE/VO<sub>2</sub> without a parallel increase in the VE/VCO<sub>2</sub><sup>1,20</sup>. If the VT could not be identified by VE/VO<sub>2</sub> and VE/VCO<sub>2</sub> responses, the VT was identified considering the breakpoint in the VCO<sub>2</sub>-VO<sub>2</sub> relationship (<xref ref-type="fig" rid="f1-body2">Figure 1</xref>).</p>
      <fig id="f1-body2">
        <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf01-en.jpg"/></fig>
      <p>In addition, the VE/workload and the [lac]/workload ratios were plotted against the workload for each participant during IT. The results were modeled through a second-order polynomial function and the originated equation was derived in order to determine an exercise intensity above which an over-proportional increase in both VE and [lac] in relation to workload did occur. The AT identification though these mathematical approaches were named respectively VT<sub>VE/W</sub> and LT<sub>[lac]/W</sub>. The identification of the VT<sub>VE/W</sub> and LT<sub>[lac]/W</sub> for a single diabetic participant is presented in <xref ref-type="fig" rid="f2-body2">Figure 2 (a-b)</xref>.</p>
      <fig id="f2-body2">
        <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf02-en.jpg"/></fig>
      <p>
        <bold>Statistical treatment and procedures for comparison</bold>
      </p>
      <p>Data are presented as mean and standard deviation (SD). The mean results of IT for all participants are presented at the "1<sup>st</sup> stage" (first stage of incremental test - "Beg"), "Mid1" (midpoint between 1<sup>st</sup> stage and AT), "TRANS" (either the VT, IGT or LT workloads), "Mid2" (midpoint between the AT and the last stage/exhaustion) and the "End" (last stage/exhaustion moment). Comparison between AT identified by different methods was performed by one-way ANOVA with the Tukey-Kramer as a post hoc. A unpaired t-tes was applied for comparisons between groups for correspondent variables .The associations among variables were determined by Pearson's moment correlation. Also, the agreement between AT intensity identified by blood lactate, which was set as the gold standard, and the AT identified by other methods in the present study were assessed by the Bland and Altman technique<sup>21</sup>. The level of significance was set at P&lt;0.05.</p>
      <p>
        <bold>Results</bold>
      </p>
      <p>The AT by ventilatory, [lac] and [gluc] responses as well as through the VE/Workload and [lac]/Workload ratios was identified for both groups, but the IGT could not be identified in two diabetic participants. In general, five to eight stages were necessary to conclude the IT for most of the subjects. The mean (<underline>+</underline>SD) VE, [lac], [gluc], VE/Workload and [lac]/Workload at the same relative intensities are presented for non-diabetic and diabetic participants (<xref ref-type="fig" rid="en_12f03-body2">Figure 3 A-E</xref>). Also, the mean blood lactate and glucose, pH, BE, pO<sub>2</sub> and pCO<sub>2</sub> at rest and during the incremental test are presented in <xref ref-type="fig" rid="en_12f04-body2">Figure 4 (A-D)</xref>. After reaching the AT, the [gluc] and pO<sub>2</sub> responses were similar to [lac] responses, while the pH, BE and pCO<sub>2</sub> responded inversely to the [lac], VE, VE/Workload and [lac]/Workload ratios (<xref ref-type="fig" rid="en_12f03-body2">Figures 3</xref> and <xref ref-type="fig" rid="en_12f04-body2">4</xref>). In spite of the differences between groups as presented in <xref ref-type="table" rid="en_12t01-body2">Tables 1</xref> and <xref ref-type="table" rid="en_12t02-body2">2</xref>, no differences were observed within groups for the workload, oxygen consumption and heart rate as related to the LT, VT, IGT, VT<sub>VE/W</sub>, LTv<sub>[lac]/W</sub> (p&gt;0.05). Also, variables were highly correlated with each other (<xref ref-type="table" rid="t3-body2">Table 3</xref>) and the Bland and Altman technique evidenced an agreement between LT and the AT identified by other methods (<xref ref-type="fig" rid="en_12f05-body2">Figure 5</xref>).</p>
      <p content-type="asset">
        <fig id="en_12f03-body2">
          <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf03-en.jpg"/></fig>
      </p>
      <p content-type="asset">
        <fig id="en_12f04-body2">
          <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf04-en.jpg"/></fig>
      </p>
      <p content-type="asset">
        <table-wrap id="en_12t02-body2">
          <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gt02-en.jpg"/></table-wrap>
      </p>
      <p content-type="asset">
        <fig id="en_12f05-body2">
          <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf05-en.jpg"/></fig>
      </p>
      <table-wrap id="t3-body2">
        <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gt03-en.jpg"/></table-wrap>
      <p>
        <bold>Discussion</bold>
      </p>
      <p>This study compared methods to identify the AT on type-2 diabetics and younger non-diabetic subjects. This choice of comparison between type-2 diabetics and younger health and physically active subjects was that, as expected, these groups were different in terms of body composition and physical fitness as related to the VO<sub>2</sub>peak and AT results. Even so, the studied protocols were consistent within groups regardless of their characteristics. So, our main findings were that the IGT was identified in diabetics similarly to non-diabetic subjects (<xref ref-type="fig" rid="f2-body2">Figures 2a-b</xref> and <xref ref-type="fig" rid="en_12f03-body2">Figure 3</xref>), in spite of the differences between groups regarding their physical characteristics and health status. It was demonstrated for both groups that AT may be successfully identified during an incremental test on a cycle ergometer by modeling the responses of VE/workload and [lac]/workload ratios through a second-order polynomial function with no differences when compared to other methods (<xref ref-type="table" rid="en_12t02-body2">Table 2</xref>). Also, different methods used to identify the AT in the present study showed high correlation to each other and the Bland and Altman technique showed an agreement between the LT and other methods to identify the AT, both for diabetics and non-diabetic subjects (<xref ref-type="table" rid="t3-body2">Table 3</xref>; <xref ref-type="fig" rid="en_12f05-body2">Figure 5</xref>). In support of our earlier studies with young physical active subjects<sup>2</sup> the present study showed that the acid-base balance was disrupted during incremental exercise at intensities above the identified thresholds (<xref ref-type="fig" rid="en_12f04-body2">Figure 4</xref>), suggesting that the studied protocols are robust to identify intensities at which the acid-base balance may be kept during exercise. In spite of the lower aerobic fitness of diabetics in the present study, the thresholds of VO<sub>2</sub>peak were observed at around 68-70% for both groups (<xref ref-type="table" rid="en_12t01-body2">Table 1</xref>). Taken together, our findings reinforce the validity of the present methods to identify AT as an exercise intensity above which both metabolic acidosis and [gluc] elevation occur.</p>
      <p>We speculate that the IGT demarcates a transition from the predominance of [gluc] uptake to [gluc] output, stimulated by catecholamines and glucagon during high intensity exercises<sup>22</sup>. The IGT was determined in 83.3% (10 of the 12) of the diabetic participants, while all non-diabetics had their IGT identified in the present study. The reason for the non-identification of IGT in some diabetics would be due to secondary metabolic/hormonal disturbances or the effect of hypoglycemic agents on [gluc]. However, our results indicated that the exercise intensity that may elicits a [gluc] increase was similarly identified by either blood lactate and ventilatory responses (<xref ref-type="table" rid="en_12t02-body2">Table 2</xref>), which in turn may have clinical applications in blood glucose control and type-2 diabetes management. Since diabetic subjects may have problems both with blood coagulation and recovery from tissue damage, VT utilization seems to be attractive due its non-invasive nature.</p>
      <p>Our data demonstrated that by modeling the VE/workload relationship through polynomial function, the resulting second-order equation may be derived and applied in order to identify at which intensity an over-proportional increase of the VE and thus VT occurs (<xref ref-type="fig" rid="f2-body2">Figure 2</xref>). The polynomial function modeling of the VE/workload results in a U-shaped curve that was similar to [lac]/workload ratio in both groups. This method enables AT identification with no O<sub>2</sub> or CO<sub>2</sub> analyses or interpretation by two or more physicians. Also, in addition to being non-invasive, it is independent from any specific value of ventilation, but dependent on its behavior, instead.</p>
      <p>The insulin resistance has been associated to muscle lipid accumulation<sup>18</sup>. The AT identification from blood glucose and from VE/Workload responses are simple methods that may identify optimal exercise intensities for the management of type 2 diabetes. While acute exercise at IGT intensity would improve the blood glucose profile, chronically it would prevent muscle lipid accumulation and thus, improve the insulin sensitivity of such patients. However, future studies should investigate both the acute and chronic effects of exercise performed at intensities related to AT on type 2 diabetics.</p>
      <p>In summary, we concluded that similarly to non-diabetic subjects, the AT may be accurately identified in type 2 diabetics during incremental test on a cycle ergometer through blood glucose responses, as well as by applying a second-order polynomial function to the VE/workload relationship. Also, the proposed methods to identify the AT did not differ from each other and seem to point out an exercise intensity above which the blood glucose is increased and an acid-base disruption occurs.</p>
      <p>
        <bold>Acknowledgements</bold>
      </p>
      <p>The authors are grateful to CNPq (proc. <italic>475575/2004-0)</italic> and SIGEP/UCB for the financial support. Also, we would like to thank Dr. Ricardo Jaco de Oliveira for the collaboration and LAFIT-UCB for the technical assistance.</p>
      <p>
        <bold>Potential Conflict of Interest</bold>
      </p>
      <p>No potential conflict of interest relevant to this article was reported.</p>
      <p>
        <bold>Sources of Funding</bold>
      </p>
      <p>This study was funded by CAPES.</p>
      <p>
        <bold>Study Association</bold>
      </p>
      <p>This article is part of the thesis of master and doctoral submitted by S&#233;rgio R. Moreira, Gabrielle do Valle e Herbert G. Sim&#245;es, from Universidade Cat&#243;lica de Bras&#237;lia, Universidade Estadual da Fl&#243;rida e Universidade Federal de S&#227;o Carlos.</p>
      <p>
        <bold>References</bold>
      </p>
    </body>
  </sub-article>
  <sub-article article-type="translation" id="TRes" xml:lang="es">
    <front-stub>
      <article-categories/>
      <title-group>
        <article-title xml:lang="es">M&#233;todos para identificar el umbral anaer&#243;bico en individuos con diabetes tipo 2 y en individuos no diab&#233;ticos</article-title>
      </title-group>
      <abstract xml:lang="es">
        <p>FUNDAMENTO: A pesar de que el umbral anaer&#243;bico (UAn) se utiliza en la evaluaci&#243;n funcional de diferentes poblaciones, pocos estudios que comparen m&#233;todos para su identificaci&#243;n en diab&#233;ticos tipo 2 est&#225;n siendo realizados. OBJETIVO: Comparar protocolos de identificaci&#243;n del UAn en individuos diab&#233;ticos tipo 2 y en no diab&#233;ticos, y analizar respuestas relacionadas al equilibrio &#225;cido-base en intensidades relativas al UAn. M&#201;TODOS: Diab&#233;ticos tipo 2 (n=10; 54,5&#177;9,5 a&#241;os; 30,1&#177;5,0 kg/m&#178;) y j&#243;venes no diab&#233;ticos (n=10; 36,6&#177;12,8 a&#241;os; 23,9&#177;5,0 kg/m&#178;) realizaron un test incremental (TI) en ciclo erg&#243;metro. El aumento desproporcionado en el equivalente ventilatorio de ox&#237;geno (VE/VO2) y lactatemia ([lac]) identific&#243; intensidades (Watts-W) correspondientes a los umbrales ventilatorio (UV) y de lactato (UL), respectivamente. La intensidad correspondiente a la menor glucemia ([gluc]) se consider&#243; umbral gluc&#233;mico individual (UGI). El UAn tambi&#233;n fue determinado por ajuste polinomial de las razones VE/Watts (UV VE/W) y [lac]/Watts (UL[lac]/W), las que identificaron intensidades por encima de las cuales ocurriera un aumento desproporcionado en la VE y [lac]. RESULTADOS: No se observaron diferencias entre UL, UV, UG, UL[lac]/W y UV VE/W en diab&#233;ticos (85,0&#177;32,1; 88,0&#177;31,7; 86,0&#177;33,8; 82,0&#177;20,9 y 90,2&#177;22,2W) y no diab&#233;ticos (139,0&#177;39,0; 133,0&#177;42,7; 140,8&#177;36,4; 122,7&#177;44,3 y 133,0&#177;39,1W). Sin embargo, los valores de UAn difirieron significativamente entre los grupos (p&lt;0.001). La t&#233;cnica de Bland-Altman confirm&#243; una concordancia entre los protocolos. En las intensidades sobre los umbrales se observaron reducciones significativas en el pH y pCO2 paralelamente a un aumento en la [lac], pO2 y VE. CONCLUSI&#211;N: Los protocolos presentaron, para ambos grupos estudiados, concordancia en la identificaci&#243;n del UAn, que se mostr&#243; como una intensidad de ejercicio, por encima de la cual ocurre p&#233;rdida de equilibrio &#225;cido-base.</p>
      </abstract>
      <kwd-group xml:lang="es">
        <kwd>Umbral anaer&#243;bico</kwd>
        <kwd>protocolos cl&#237;nicos</kwd>
        <kwd>glucemia</kwd>
        <kwd>equilibrio &#225;cido base</kwd>
      </kwd-group>
    </front-stub>
    <body>
      <p>
        <bold>ART&#205;CULO ORIGINAL</bold>
      </p>
      <p>
        <fn id="top-body3">
          <label>
            <bold>M&#233;todos para identificar el umbral anaer&#243;bico en individuos con diabetes tipo 2 y en individuos no diab&#233;ticos</bold>
          </label>
          <p>
            <bold>Herbert G. Sim&#245;es<sup>I</sup>; S&#233;rgio R. Moreira<sup>I</sup>; Robert J. Moffatt<sup>II</sup>; Carmen S. G. Campbell<sup>I</sup></bold>
          </p>
        </fn>
      </p>
      <p><sup>I</sup>Universidade Cat&#243;lica de Bras&#237;lia (UCB), Bras&#237;lia, DF - Brasil</p>
      <p><sup>II</sup>Florida State University (FSU), Tallahassee FL - EUA</p>
      <p>Correspondencia</p>
      <p>
        <bold>RESUMEN</bold>
      </p>
      <p><bold>FUNDAMENTO:</bold> A pesar de que el umbral anaer&#243;bico (UAn) se utiliza en la evaluaci&#243;n funcional de diferentes poblaciones, pocos estudios que comparen m&#233;todos para su identificaci&#243;n en diab&#233;ticos tipo 2 est&#225;n siendo realizados.</p>
      <p><bold>OBJETIVO: </bold> Comparar protocolos de identificaci&#243;n del UAn en individuos diab&#233;ticos tipo 2 y en no diab&#233;ticos, y analizar respuestas relacionadas al equilibrio &#225;cido-base en intensidades relativas al UAn.</p>
      <p><bold>M&#201;TODOS:</bold> Diab&#233;ticos tipo 2 (n=10; 54,5&#177;9,5 a&#241;os; 30,1&#177;5,0 kg/m<sup>2</sup>) y j&#243;venes no diab&#233;ticos (n=10; 36,6&#177;12,8 a&#241;os; 23,9&#177;5,0 kg/m<sup>2</sup>) realizaron un test incremental (TI) en ciclo erg&#243;metro. El aumento desproporcionado en el equivalente ventilatorio de ox&#237;geno (VE/VO<sub>2</sub>) y lactatemia ([lac]) identific&#243; intensidades (Watts-W) correspondientes a los umbrales ventilatorio (UV) y de lactato (UL), respectivamente. La intensidad correspondiente a la menor glucemia ([gluc]) se consider&#243; umbral gluc&#233;mico individual (UGI). El UAn tambi&#233;n fue determinado por ajuste polinomial de las razones VE/Watts (UV<sub>VE/W</sub>) y [lac]/Watts (UL<sub>[lac]/W</sub>), las que identificaron intensidades por encima de las cuales ocurriera un aumento desproporcionado en la VE y [lac].</p>
      <p><bold>RESULTADOS: </bold> No se observaron diferencias entre UL, UV, UG, UL<sub>[lac]/W</sub> y UV<sub>VE/W</sub> en diab&#233;ticos (85,0&#177;32,1; 88,0&#177;31,7; 86,0&#177;33,8; 82,0&#177;20,9 y 90,2&#177;22,2W) y no diab&#233;ticos (139,0&#177;39,0; 133,0&#177;42,7; 140,8&#177;36,4; 122,7&#177;44,3 y 133,0&#177;39,1W). Sin embargo, los valores de UAn difirieron significativamente entre los grupos (p&lt;0.001). La t&#233;cnica de Bland-Altman confirm&#243; una concordancia entre los protocolos. En las intensidades sobre los umbrales se observaron reducciones significativas en el pH y pCO<sub>2</sub> paralelamente a un aumento en la [lac], pO<sub>2</sub> y VE.</p>
      <p><bold>CONCLUSI&#211;N: </bold> Los protocolos presentaron, para ambos grupos estudiados, concordancia en la identificaci&#243;n del UAn, que se mostr&#243; como una intensidad de ejercicio, por encima de la cual ocurre p&#233;rdida de equilibrio &#225;cido-base. (Arq Bras Cardiol 2010; 94(1) : 67-74)</p>
      <p><bold>Palabras clave: </bold> Umbral anaer&#243;bico, protocolos cl&#237;nicos, glucemia, equilibrio &#225;cido base.</p>
      <p>
        <bold>Introducci&#243;n</bold>
      </p>
      <p>El umbral anaer&#243;bico (UAn) refleja una intensidad de ejercicio por encima de la cual se observa un aumento desproporcionado en la glucemia, lactato sangu&#237;neo ([lac]) y ventilaci&#243;n (VE), paralelamente a la disminuci&#243;n del pH<sup>1,2</sup>.</p>
      <p>La determinaci&#243;n invasiva del UAn a partir de las respuestas de [lac] (umbral de lactato - UL) est&#225; siendo considerada como el patr&#243;n oro para evaluar la capacidad aerobia<sup>3-5</sup>, mientras que la identificaci&#243;n del UAn a partir de las respuestas de VE (umbral ventilatorio - UV) presenta ventajas debido a su naturaleza no invasiva y se viene recomendando a la prescripci&#243;n de ejercicios para poblaciones especiales<sup>5-8</sup>, incluyendo diab&#233;ticos<sup>7,9-14</sup>. Sin embargo, la determinaci&#243;n del UV requiere equipamientos caros y las mediciones son muy dependientes de los m&#233;todos de calibraci&#243;n antes del test. Adem&#225;s, para identificar la intensidad a la cual ocurre el UAn se necesitan generalmente dos o m&#225;s especialistas experimentados en fisiolog&#237;a del ejercicio<sup>15,16</sup>. Por otro lado, el modelo matem&#225;tico de las respuestas de la VE a los test incrementales a trav&#233;s de funci&#243;n polinomial aumentan la exactitud de la identificaci&#243;n del UAn.</p>
      <p>Adicionalmente, se viene evidenciando que durante el test incremental (TI), la glucemia ([gluc]) disminuye hasta alcanzar el UAn, y la intensidad de ejercicio por encima de la cual la [gluc] comienza a aumentar se define como Umbral Gluc&#233;mico Individual (UGI)<sup>17</sup>. El UGI parece demarcar una intensidad de ejercicio, por encima de la cual la producci&#243;n de glucosa supera su captaci&#243;n, y que no difiere del UV y del UL identificados en individuos j&#243;venes saludables<sup>2</sup>. La diabetes tipo 2 est&#225; siendo asociado a la acumulaci&#243;n de grasa en el m&#250;sculo esquel&#233;tico, lo que inhibe la se&#241;al de insulina y de esta forma disminuye la translocaci&#243;n del GLUT-4, lo cual resulta en hiperglucemia<sup>18</sup>. As&#237;, un m&#233;todo m&#225;s pr&#225;ctico de identificaci&#243;n del UAn (por ejemplo UGI) y/o un procedimiento no invasivo y menos dispendioso (por ej., UV identificado a trav&#233;s de la relaci&#243;n VE/carga de trabajo (VE/W)) seria &#250;til para la prescripci&#243;n de ejercicios a fin de evitar la acumulaci&#243;n de grasa en el m&#250;sculo esquel&#233;tico y controlar la glucemia en individuos con diabetes tipo 2 y en individuos no diab&#233;ticos.</p>
      <p>Entretanto, la identificaci&#243;n del UAn a partir de las respuestas de la glucemia, as&#237; como la utilizaci&#243;n de una determinaci&#243;n no invasiva y simple, mediante el an&#225;lisis de las respuestas de la relaci&#243;n VE/carga de trabajo, a&#250;n no fueron investigadas en portadores de diabetes tipo 2.</p>
      <p>El presente estudio compar&#243; las relaciones entre el UAn identificado a trav&#233;s de la [gluc] y el UAn, identificado por otros m&#233;todos (por ej., UL y UV) en individuos con diabetes tipo 2 y en individuos m&#225;s j&#243;venes no diab&#233;ticos. Adicionalmente, se analiz&#243; la posibilidad de determinar el UV y el UL al aplicar una funci&#243;n polinomial de segundo grado en las respuestas de las razones VE/carga de trabajo y [lac]/carga de trabajo ([lac]/W) durante el test incremental en la bicicleta ergom&#233;trica. Los resultados se compararon con otros m&#233;todos de determinaci&#243;n del UAn, y se analizaron las respuestas del pH, presi&#243;n parcial de ox&#237;geno (pO<sub>2</sub>) y de di&#243;xido de carbono (pCO<sub>2</sub>) en relaci&#243;n a las intensidades de UAn registradas, para esclarecer el significado del UAn identificado a trav&#233;s de la [gluc] y de las razones (VE/W) y ([lac]/W).</p>
      <p>
        <bold>M&#233;todos</bold>
      </p>
      <p>
        <bold>Individuos</bold>
      </p>
      <p>El Comit&#233; de &#201;tica para Investigaci&#243;n en Seres Humanos de la Universidad aprob&#243; los m&#233;todos utilizados en esta investigaci&#243;n. Tras firmar el Formulario de Consentimiento Informado, 12 individuos sedentarios con diabetes tipo 2 y 10 individuos no diab&#233;ticos f&#237;sicamente activos se constituyeron en voluntarios del presente estudio. Se presentan s&#243;lo los datos de 10 de los 12 individuos diab&#233;ticos, pues en 2 de ellos no fue posible identificar todos los par&#225;metros de inter&#233;s. Las caracter&#237;sticas descriptivas de los participantes se presentan en la <xref ref-type="table" rid="es_12t01-body3">Tabla 1</xref>. Los individuos no diab&#233;ticos participaban de programas de entrenamiento de car&#225;cter recreativo hac&#237;a por lo menos dos a&#241;os (por ej., ciclismo y entrenamiento de resistencia), que consist&#237;an en por lo menos 20 minutos de ejercicios 3 veces por semana regularmente, mientras que los participantes diab&#233;ticos eran sedentarios. Adem&#225;s, los diab&#233;ticos mantuvieron el tratamiento hipoglucemiante oral (por ej. sulfonilureas, biguanidas, inhibidores de la alfa-glucosidasa) durante el estudio.</p>
      <p content-type="asset">
        <table-wrap id="es_12t01-body3">
          <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gt01-es.jpg"/></table-wrap>
      </p>
      <p>
        <bold>Procedimientos</bold>
      </p>
      <p>La recolecci&#243;n de datos se realiz&#243; en el Laboratorio de Fisiolog&#237;a del Ejercicio de la Universidad Cat&#243;lica de Brasilia y en la Florida State University. Los participantes fueron sometidos previamente a un examen cardiovascular, que inclu&#237;a un electrocardiograma de reposo y mediciones de la presi&#243;n arterial (Microlife, Inglaterra). Los individuos con complicaciones cardiovasculares, neurol&#243;gicas y ortop&#233;dicas fueron excluidos del estudio. Los individuos seleccionados realizaron un test incremental en bicicleta ergom&#233;trica electromagn&#233;tica (Lode Excalibur, Pa&#237;ses Bajos) luego de una noche de ayuno, entre las 8:30 y las 9:30 de la ma&#241;ana, en una sala a una temperatura de 22-23&#176; C, 665 mmHg de presi&#243;n barom&#233;trica y 50% de humedad.</p>
      <p>
        <bold>Test Incremental (TI)</bold>
      </p>
      <p>Para identificar el UL, el UV, el UGI y el VO<sub>2max</sub> se aplic&#243; un TI. Para ello, antes del inicio del TI se realizaba un precalentamiento de un minuto pedaleando a 0 Watts (W) con una carga entre 15 y 50 W, e incrementos de 15-25 W a cada 3-min, dependiendo de las caracter&#237;sticas del participante (si diab&#233;tico o saludable, f&#237;sicamente activo o sedentario, etc). Para la mayor&#237;a de los participantes (incluyendo todos los diab&#233;ticos) se inici&#243; el test con 15 W e incrementos de 15 W en cada etapa de 3 minutos. Se interrumpi&#243; el test en los casos de agotamiento o de cualquier anormalidad electrocardiogr&#225;fica. Adicionalmente, los criterios para interrupci&#243;n del test incluyeron un aumento exagerado en la presi&#243;n arterial sist&#243;lica (PAS), presi&#243;n arterial diast&#243;lica (PAD) superior a 115 mmHg, adem&#225;s de la incapacidad de aumentar el pulso de ox&#237;geno paralelamente al aumento en la carga de trabajo y/o un cociente de intercambio respiratorio (RER) superior a 1,15<sup>7,19</sup>.</p>
      <p>
        <bold>An&#225;lisis ventilatorio</bold>
      </p>
      <p>Se midieron los gases expirados en forma continua utilizando un sistema Parvomedics MMS-2400 (Florida State University) o el sistema Cortex Metalyzer 3B (Universidad Cat&#243;lica de Brasilia). Antes de cada test se llevaba a cabo la calibraci&#243;n de los equipamientos de an&#225;lisis gaseoso. Para la identificaci&#243;n de la ventilaci&#243;n minuto (VE), consumo de ox&#237;geno (VO<sub>2</sub>), producci&#243;n de di&#243;xido de carbono (VCO<sub>2</sub>), cociente de intercambio respiratorio (RER) y UV se consideraron los resultados obtenidos en los &#250;ltimos 20 segundos de cada etapa. El mayor VO<sub>2</sub> obtenido en el agotamiento voluntario era considerado el VO<sub>2pico</sub>.</p>
      <p>
        <bold>Recolecci&#243;n de sangre y an&#225;lisis de laboratorio</bold>
      </p>
      <p>Durante los &#250;ltimos 10 segundos de cada etapa, se tom&#243; una muestra de 25&#956;l de sangre del l&#243;bulo de la oreja, utilizando microcapilares heparinizados y calibrados para mediciones de [lac] y [gluc] de todos los participantes. Una muestra de 75 &#956;l de sangre se extrajo tambi&#233;n en 5 individuos no diab&#233;ticos en reposo, en medio del test incremental (generalmente al final de las etapas 3 a 5; aproximadamente en el UAn) e inmediatamente a la finalizaci&#243;n del test.</p>
      <p>Los 25&#956;l fueron transferidos a tubos de Eppendorf con 50&#956;l de fluoruro de sodio (NaF) al 1%. El [lac] y la [gluc] se determinaron por duplicado en cada muestra, utilizando un analizador de lactato y glucosa sangu&#237;neos (YeULow Springs 2700S). Los resultados de [lac] y [gluc] fueron corregidos para el volumen de la muestra de sangre dentro del tubo de Eppendorf y se presentaron en mM. La pO<sub>2</sub> y la pCO<sub>2</sub> (mmHg), el Exceso de Base - EB (mM) y el pH fueron medidos en la muestra de 75&#956;l utilizando el sistema AVL (Blood Gas Analyser - OMNI 3 Modular Analyzer, AVL Scientific Corporation, RosweUL, GA).</p>
      <p>
        <bold>Identificaci&#243;n del umbral anaer&#243;bico</bold>
      </p>
      <p>El UL fue considerado como el punto de inflexi&#243;n de la curva de [lac], mientras que el UGI fue determinado por la cin&#233;tica de la [gluc], y definido como la intensidad de ejercicio en que la [gluc] comenzaba a aumentar durante el TI<sup>17</sup>. El UV fue identificado por dos investigadores independientes, consider&#225;ndose un aumento en el cociente VE/VO<sub>2</sub> sin un aumento paralelo en la relaci&#243;n VE/VCO<sub>2.</sub><sup>1,20</sup> (<xref ref-type="fig" rid="f1-body3">Figura 1</xref>), y en la imposibilidad de identificar el UV mediante esta t&#233;cnica, se lo identificaba considerando el punto de quiebra en la relaci&#243;n VCO<sub>2</sub>-VO<sub>2</sub>.</p>
      <fig id="f1-body3">
        <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf01-es.jpg"/></fig>
      <p>Adem&#225;s, fueron trazados los cocientes VE/W y [lac]/W <italic>versus l</italic>a carga de trabajo para cada participante durante el TI. Sobre los resultados se aplic&#243; una funci&#243;n polinomial de segundo grado y la ecuaci&#243;n originada fue derivada a fin de determinar una intensidad de ejercicio por encima de la cual ocurr&#237;a un aumento desproporcionado de la VE y del [lac] en relaci&#243;n a la carga de trabajo. La identificaci&#243;n del UAn a trav&#233;s de esos abordajes matem&#225;ticos fue llamada respectivamente UV<sub>VE/W</sub> y UL<sub>[lac]/W</sub>. La <xref ref-type="fig" rid="f2-body3">Figura 2 (A-B)</xref> muestra la identificaci&#243;n del UV<sub>VE/W</sub> y UL<sub>[lac]/W</sub> para un &#250;nico participante diab&#233;tico.</p>
      <fig id="f2-body3">
        <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf02-es.jpg"/></fig>
      <p>
        <bold>Tratamiento estad&#237;stico y procedimientos para comparaci&#243;n</bold>
      </p>
      <p>Los datos se presentan como promedios y desviaciones est&#225;ndar (DE). Los resultados promedio del TI para todos los participantes se presentan en el "Inicio" (primera etapa del test incremental), M1 (punto medio entre la primera etapa y el UAn), UAn (cargas de trabajo del UV, UGI y UL), M2 (punto medio entre el UAn y la &#250;ltima etapa/agotamiento) y el "final" (&#250;ltima etapa/momento de agotamiento). Se realizaron comparaciones entre las intensidades de UAn identificado por diferentes m&#233;todos, a trav&#233;s del An&#225;lisis de Varianza, con <italic>post-hoc</italic> de Tuckey-Kraemer. El test <italic>t-student</italic> para muestras no apareadas se aplic&#243; para comparaciones entre variables correspondientes de ambos grupos. Las relaciones entre las variables fueron determinadas a trav&#233;s de la correlaci&#243;n de Pearson. Adicionalmente, la concordancia entre la intensidad del UAn identificada por el lactato sangu&#237;neo, que fue establecida como el patr&#243;n oro, y el UAn identificado a trav&#233;s de otros m&#233;todos en el presente estudio fue evaluada mediante la t&#233;cnica de BUAnd y Altman<sup>21</sup>. El nivel de significancia establecido fue p&lt;0,05.</p>
      <p>
        <bold>Resultados</bold>
      </p>
      <p>El UAn establecido por las respuestas ventilatoria, [lac] y [gluc], as&#237; como a trav&#233;s de los cocientes UV<sub>VE/W</sub> y UL<sub>[lac]/W</sub>, fue identificado para ambos grupos, pero en dos participantes diab&#233;ticos no pudo ser identificado el UGI. En general, para concluir el TI fueron necesarias 5 a 8 etapas para la mayor&#237;a de los individuos. Los promedios (&#177;DE) de la VE, [lac], [gluc], cocientes UV<sub>VE/W</sub> y UL<sub>[lac]/W</sub> se presentan para los participantes diab&#233;ticos y los no diab&#233;ticos en las mismas intensidades relativas (<xref ref-type="fig" rid="es_12f03-body3">Figura 3 A-E</xref>). En la <xref ref-type="fig" rid="f4-body3">Figura 4 (A-D)</xref> se presentan adicionalmente las concentraciones promedio de [lac] y [gluc] sangu&#237;neos, pH, EB, pO<sub>2</sub> y pCO<sub>2</sub> en reposo y durante el test incremental. Tras alcanzar el UAn, las respuestas de la [gluc] y pO<sub>2</sub> fueron similares a las respuestas del [lac], mientras que el pH, EB y pCO<sub>2</sub> respondieron inversamente al [lac], VE y a los cocientes UV<sub>VE/W</sub> y UL<sub>[lac]/W</sub> (<xref ref-type="fig" rid="es_12f03-body3">Figuras 3</xref> y <xref ref-type="fig" rid="f4-body3">4</xref>). A pesar de las diferencias entre los grupos presentadas en las <xref ref-type="table" rid="es_12t01-body3">Tablas 1</xref> y <xref ref-type="table" rid="es_12t02-body3">2</xref>, no se observ&#243; ninguna diferencia dentro de los grupos para carga de trabajo, consumo de ox&#237;geno y frecuencia cardiaca con relaci&#243;n al UL, UV, UGI, UV<sub>VE/W</sub>, UL<sub>[lac]/W</sub> (p&gt;0,05). Adicionalmente, las variables presentaron una alta correlaci&#243;n entre s&#237; (<xref ref-type="table" rid="t3-body3">Tabla 3</xref>) y la t&#233;cnica de Bland y Altman evidenci&#243; una concordancia entre UL y el UAn identificado por otros m&#233;todos (<xref ref-type="fig" rid="es_12f05-body3">Figura 5</xref>).</p>
      <p content-type="asset">
        <fig id="es_12f03-body3">
          <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf03-es.jpg"/></fig>
      </p>
      <p content-type="asset">
        <table-wrap id="es_12t02-body3">
          <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gt02-es.jpg"/></table-wrap>
      </p>
      <p content-type="asset">
        <fig id="es_12f05-body3">
          <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf04-es.jpg"/></fig>
      </p>
      <fig id="f4-body3">
        <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gf05-es.jpg"/></fig>
      <table-wrap id="t3-body3">
        <graphic xlink:href="1678-4170-abc-94-01-0071-00012-gt03-es.jpg"/></table-wrap>
      <p>
        <bold>Discusi&#243;n</bold>
      </p>
      <p>El presente estudio compar&#243; m&#233;todos para identificar el UAn en individuos con diabetes tipo 2 e individuos m&#225;s j&#243;venes, no diab&#233;ticos. Esta elecci&#243;n de comparar a individuos con diabetes tipo 2 e individuos m&#225;s j&#243;venes saludables y f&#237;sicamente activos se debi&#243; al hecho de que, como se esperaba, estos grupos difieren en t&#233;rminos de composici&#243;n corporal y aptitud f&#237;sica con relaci&#243;n a los resultados del VO<sub>2</sub>pico y UAn. A&#250;n as&#237;, los protocolos estudiados fueron consistentes dentro de los grupos, independientemente de sus caracter&#237;sticas. Por lo tanto, nuestros principales hallazgos fueron que el UGI fue identificado en individuos con diabetes tipo 2 de forma similar a los individuos no diab&#233;ticos (<xref ref-type="fig" rid="f2-body3">Figuras 2</xref> a-b y <xref ref-type="fig" rid="es_12f03-body3">Figura 3</xref>), a pesar de las diferencias entre grupos en relaci&#243;n con sus caracter&#237;sticas f&#237;sicas y estado de salud. Se demostr&#243; en ambos grupos que el UAn puede ser identificado con &#233;xito durante un test incremental en ciclo erg&#243;metro empleando las respuestas de los cocientes VE/carga de trabajo y [lac]/carga de trabajo por medio de una funci&#243;n polinomial de segundo grado sin diferencias si se compara con otros m&#233;todos (<xref ref-type="table" rid="es_12t02-body3">Tabla 2</xref>). Adem&#225;s, los diferentes m&#233;todos para identificar el UAn en el presente estudio mostraron alta correlaci&#243;n entre s&#237; y la t&#233;cnica de Bland y Altman demostr&#243; una concordancia entre el UL y otros m&#233;todos para identificar el UAn en individuos diab&#233;ticos y no diab&#233;ticos (<xref ref-type="table" rid="t3-body3">Tabla 3</xref>; <xref ref-type="fig" rid="es_12f05-body3">Figura 5</xref>). En concordancia con nuestros estudios anteriores que comprend&#237;an individuos j&#243;venes y f&#237;sicamente activos<sup>2</sup>, el presente estudio mostr&#243; que no hay equilibrio &#225;cido-base en intensidades por encima de los umbrales identificados durante el test incremental (<xref ref-type="fig" rid="f4-body3">Figura 4</xref>), lo cual sugiere que los protocolos estudiados son v&#225;lidos para la identificaci&#243;n de intensidades en las que el equilibrio &#225;cido-base puede ser mantenido durante el ejercicio. A pesar de la menor aptitud f&#237;sica de los individuos diab&#233;ticos en el presente estudio, los umbrales fueron observados entre el 60 y el 71%VO<sub>2 max</sub> para ambos grupos (<xref ref-type="table" rid="es_12t01-body3">Tabla 1</xref> y <xref ref-type="table" rid="es_12t02-body3">2</xref>). Considerados juntos, nuestros hallazgos refuerzan la validez de los presentes m&#233;todos para identificar el UAn como una intensidad de ejercicio por encima de la cual aparece tanto la acidosis metab&#243;lica como la elevaci&#243;n de la [gluc].</p>
      <p>Sugerimos que el UGI pueda demarcar una transici&#243;n del predominio de la captaci&#243;n de la [gluc] para la producci&#243;n de la [gluc] estimulada por las catecolaminas y el glucagon durante ejercicios de alta intensidad<sup>22</sup>. El UGI fue determinado en un 83,3% (10/12) de los participantes diab&#233;ticos, mientras que todos los participantes no diab&#233;ticos tuvieron su UGI identificado en el presente estudio. La no identificaci&#243;n del UGI en algunos participantes diab&#233;ticos fue causada por trastornos metab&#243;lico-hormonales o por efecto de agentes hipoglucemiantes, cuya utilizaci&#243;n no fue interrumpida durante el estudio. Sin embargo, nuestros resultados indican que la intensidad del ejercicio que puede causar un aumento de la [gluc] fue identificada en forma similar por las respuestas del lactato sangu&#237;neo o ventilatoria (<xref ref-type="table" rid="es_12t02-body3">Tabla 2</xref>), lo que, a su vez puede tener aplicaciones cl&#237;nicas en el control de la glucemia y de la diabetes tipo 2. Considerando que los individuos con diabetes tipo 2 pueden tener problemas con la coagulaci&#243;n sangu&#237;nea y recuperaci&#243;n de da&#241;o tisular, la utilizaci&#243;n del UV parece ser atrayente debido a su naturaleza no invasiva, aunque su costo es elevado. Nuestros datos demostraron que la relaci&#243;n VE/carga de trabajo a trav&#233;s de una funci&#243;n polinomial resulta en una ecuaci&#243;n de segundo grado que puede ser derivada y aplicada a fin de identificar en qu&#233; intensidad ocurre un aumento desproporcional de la VE y por lo tanto ocurre el UV (<xref ref-type="fig" rid="f2-body3">Figura 2</xref>). El modelo de la funci&#243;n polinomial de la raz&#243;n VE/carga de trabajo resulta en una curva en U similar a la relaci&#243;n [lac]/carga de trabajo en ambos grupos. Este m&#233;todo permite la identificaci&#243;n del UAn sin an&#225;lisis de O<sub>2</sub> y CO<sub>2</sub> o interpretaci&#243;n de dos o m&#225;s especialistas. Adem&#225;s, por ser no invasiva, ella es independiente de cualquier valor espec&#237;fico de ventilaci&#243;n, pero por el contrario, dependiente de su comportamiento.</p>
      <p>La resistencia a la insulina se viene asociando a la acumulaci&#243;n de grasa en el m&#250;sculo<sup>18</sup>. La identificaci&#243;n del UAn a partir de la glucemia y de las respuestas VE/carga de trabajo son m&#233;todos simples que pueden identificar las intensidades ideales de ejercicio para el control de la glucemia en portadores de diabetes tipo 2. Mientras que el ejercicio agudo en la intensidad del UGI puede mejorar el perfil de la glucemia, cr&#243;nicamente evitar&#237;a la acumulaci&#243;n de grasa en el m&#250;sculo y as&#237;, mejorar&#237;a la sensibilidad a la insulina de tales pacientes. Sin embargo, estudios futuros deben investigar ambos efectos, agudo y cr&#243;nico, del ejercicio realizado en intensidades relacionadas al UAn en individuos portadores de diabetes tipo 2.</p>
      <p>Concluimos que, en forma similar a individuos no diab&#233;ticos, el UAn puede ser identificado de forma precisa en individuos con diabetes tipo 2 durante el test incremental en ciclo erg&#243;metro, a trav&#233;s de las respuestas de glucemia, as&#237; como a trav&#233;s de la aplicaci&#243;n de una funci&#243;n polinomial de segundo grado en la relaci&#243;n VE/carga de trabajo. Adem&#225;s, los resultados obtenidos por la aplicaci&#243;n de los m&#233;todos propuestos para identificar el UAn no difirieron unos de otros y parecen indicar una intensidad de ejercicio por encima de la cual la glucemia est&#225; aumentada y se pierde el equilibrio &#225;cido-base.</p>
      <p>
        <bold>Agradecimientos</bold>
      </p>
      <p>Los autores agradecen al CNPq (proc. <italic>475575/2004-0)</italic> y SIGEP/UCB por el apoyo financiero. Adem&#225;s, nuestros agradecimientos al Dr. Ricardo Jac&#243; de Oliveira por su colaboraci&#243;n y al LAFIT-UCB por la asistencia t&#233;cnica.</p>
      <p>
        <bold>Potencial Conflicto de Intereses</bold>
      </p>
      <p>Declaro no haber conflicto de intereses pertinentes.</p>
      <p>
        <bold>Fuentes de Financiaci&#243;n</bold>
      </p>
      <p>El presente estudio fue financiado por el Cnpq.</p>
      <p>
        <bold>Vinculaci&#243;n Acad&#233;mica</bold>
      </p>
      <p>Este art&#237;culo forma parte de la tesis de Mestr&#237;a y Doctorado de S&#233;rgio R. Moreira, Gabrielle do Valle y Herbert G. Sim&#245;es, por la Universidad Cat&#243;lica de Brasilia, Universidad Estadual de Florida y Universidad Federal de S&#227;o Carlos.</p>
      <p>
        <bold>Referencias</bold>
      </p>
    </body>
  </sub-article>
</article>
