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<front>
<journal-meta>
<journal-id>1688-0420</journal-id>
<journal-title><![CDATA[Revista Uruguaya de Cardiología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev.Urug.Cardiol.]]></abbrev-journal-title>
<issn>1688-0420</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Uruguaya de Cardiología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1688-04202005000100007</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Corazón y diabetes]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[LAYERLE]]></surname>
<given-names><![CDATA[BERNARDO]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[VIGNOLO]]></surname>
<given-names><![CDATA[WASHINGTON]]></given-names>
</name>
</contrib>
</contrib-group>
<aff id="A">
<institution><![CDATA[,  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>05</month>
<year>2005</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>05</month>
<year>2005</year>
</pub-date>
<volume>20</volume>
<numero>1</numero>
<fpage>40</fpage>
<lpage>51</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_arttext&amp;pid=S1688-04202005000100007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_abstract&amp;pid=S1688-04202005000100007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_pdf&amp;pid=S1688-04202005000100007&amp;lng=en&amp;nrm=iso"></self-uri></article-meta>
</front><body><![CDATA[      <multicol gutter="18" cols="2"></multicol>     <p align="left"><b><font color="#1f1a17" face="Verdana" size="4">Coraz&oacute;n y diabetes </font> </b></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">DRES. BERNARDO LAYERLE, WASHINGTON VIGNOLO </font></p>          <p><font face="Verdana" size="2">    <br>     </font>     </p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">La diabetes es una enfermedad frecuente: 6% a 10% de la poblaci&oacute;n espa&ntilde;ola y 6,6% de la poblaci&oacute;n de Estados Unidos entre los 20 y 74 a&ntilde;os la padecen <sup><a name="-1"></a>(<a href="#1">1</a>)</sup>. El coraz&oacute;n puede ser afectado de diferentes maneras. La diabetes es un importante factor de riesgo de enfermedad arterial coronaria y de insuficiencia card&iacute;aca; puede adem&aacute;s condicionar la aparici&oacute;n de neuropat&iacute;a auton&oacute;mica. En este cap&iacute;tulo nos ocuparemos &uacute;nicamente del compromiso coronario. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">De acuerdo a la American Diabetes Association <a name="-2"></a><sup>(<a href="#2">2</a>)</sup> y a la Organizaci&oacute;n Mundial de la Salud <sup><a name="-3"></a>(<a href="#3">3</a>)</sup>, la diabetes se define como una enfermedad metab&oacute;lica caracterizada por hiperglucemia: </font></p>      <ul>             <li><font color="#1f1a17" face="Verdana" size="2">Glucemia         en ayunas mayor o igual a 126 mg% (7 mmol/l) cuando se         dosifica en dos oportunidades. </font></li>             <li><font color="#1f1a17" face="Verdana" size="2">Glucemia         dos horas despu&eacute;s de una carga de glucosa de 75 gramos         v&iacute;a oral mayor o igual a 200 mg% (11,1 mmol/l), cuando         se dosifica en dos oportunidades o cuando se asocia a         s&iacute;ntomas sugestivos (poliuria, polidipsia y p&eacute;rdida no         explicada de peso). </font></li>             <li><font color="#1f1a17" face="Verdana" size="2">Glucemia         mayor o igual a 200 mg/dl (11,1 mmol/l) en cualquier         momento del d&iacute;a acompa&ntilde;ada de s&iacute;ntomas de descontrol         metab&oacute;lico. </font></li>         ]]></body>
<body><![CDATA[</ul>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Hay dos grandes tipos de diabetes: </font></p>      <ul>             <li><font color="#1f1a17" face="Verdana" size="2">Diabetes         tipo 1, que se caracteriza por un d&eacute;ficit en la         secreci&oacute;n de insulina por las c&eacute;lulas beta del         p&aacute;ncreas que obliga al aporte ex&oacute;geno de esta hormona         para mantener la vida. </font></li>             <li><font color="#1f1a17" face="Verdana" size="2">Diabetes         tipo 2, que se caracteriza por una alteraci&oacute;n en la         secreci&oacute;n de insulina y una resistencia a la acci&oacute;n         perif&eacute;rica de la hormona. </font></li>         </ul>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Existen situaciones intermedias en las que la glucemia no es normal pero no se llega a valores que definen al sujeto como diab&eacute;tico: </font></p>      <ul>             <li><font color="#1f1a17" face="Verdana" size="2">Glucemia         basal alterada, que de acuerdo a la &uacute;ltima publicaci&oacute;n         del Comit&eacute; de Expertos Internacional para el         Diagn&oacute;stico de la Diabetes <a name="-4"></a><sup>(<a href="#4">4</a>)</sup>, se         define cuando la glucemia presenta niveles entre 100 y         125 mg%. </font></li>             <li><font color="#1f1a17" face="Verdana" size="2">Intolerancia         a la glucosa: glucemia dos horas despu&eacute;s de la         administraci&oacute;n de 75 gramos de glucosa por boca con         valores entre 140 y 199 mg%. </font></li>         </ul>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Por &uacute;ltimo, conviene hacer una breve referencia al s&iacute;ndrome metab&oacute;lico, en cuya base existe una resistencia a la acci&oacute;n insul&iacute;nica e hiperinsulinemia compensadora y que tiene un riesgo vascular y de desarrollo de diabetes tipo 2 francamente aumentado. Este se define de acuerdo al National Cholesterol Education Program (Adult Treatment Panel III) <a name="-5"></a><sup>(<a href="#5">5</a>)</sup>, por la presencia de tres o m&aacute;s de los siguientes criterios cl&iacute;nicos y paracl&iacute;nicos: </font></p>      <ul>             ]]></body>
<body><![CDATA[<li><font color="#1f1a17" face="Verdana" size="2">Obesidad         abdominal: circunferencia abdominal mayor a 102 cm en el         hombre y a 88 cm en la mujer. </font></li>             <li><font color="#1f1a17" face="Verdana" size="2">Presi&oacute;n         arterial mayor o igual 130 mm Hg de sist&oacute;lica o 85 de         diast&oacute;lica o ambas. </font></li>             <li><font color="#1f1a17" face="Verdana" size="2">Triglic&eacute;ridos         mayores o iguales a 150 mg/dl. </font></li>             <li><font color="#1f1a17" face="Verdana" size="2">HDL         menor que 40 mg/dl en el hombre y 50 mg/dl en la mujer. </font></li>             <li><font color="#1f1a17" face="Verdana" size="2">Glucemia         basal en ayunas mayor o igual a 110 mg/dl. </font></li>         </ul>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El s&iacute;ndrome metab&oacute;lico afecta a 20% de las personas de edad media y 40% de los a&ntilde;osos en Estados Unidos <sup><a name="-44"></a>(<a href="#44">44</a>)</sup>. En Uruguay, la prevalencia en la poblaci&oacute;n adulta global es de 20% (23% en la poblaci&oacute;n de sexo masculino y 18% en la de sexo femenino), a predominio entre los 50 y 70 a&ntilde;os <sup><a name="-75"></a>(<a href="#75">75</a>)</sup>. Si bien estos pacientes no son diab&eacute;ticos (aunque en la evoluci&oacute;n desarrollan la enfermedad en un porcentaje significativo), presentan igualmente una mortalidad total y cardiovascular que es el doble de la correspondiente a la poblaci&oacute;n general <sup><a name="-45"></a>(<a href="#45">45</a>)</sup>. </font></p>          <p><font face="Verdana" size="2">    <br>     </font>     </p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><b>EPIDEMIOLOG&iacute;A</b> </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">La diabetes se asocia con una alta mortalidad cardiovascular. M&aacute;s de tres de cada cuatro diab&eacute;ticos que fallecen lo hacen por una causa relacionada con la aterosclerosis y en 75% de estos casos por enfermedad coronaria <sup><a name="-6"></a>(<a href="#6">6</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Un estudio de Haffner sobre la poblaci&oacute;n finlandesa <sup><a name="-7"></a>(<a href="#7">7</a>)</sup>, en 1998, encontr&oacute; que el riesgo de muerte de causa vascular de los diab&eacute;ticos era equivalente al de los pacientes no diab&eacute;ticos con infarto previo (15%), y si se trata de un diab&eacute;tico que ya ha sufrido un infarto, el riesgo es unas tres veces mayor al de este &uacute;ltimo grupo (<a href="#figura1">figura 1</a>). </font></p>          <p align="left"><font face="Verdana" size="2"><a name="figura1"></a><img style="border: 1px solid ; width: 400px; height: 333px;" alt="" src="/img/revistas/ruc/v20n1/1a07f1.gif"></font></p>          <p><font face="Verdana" size="2"><b>FIGURA 1. </b>Mortalidad cardiovascular en diab&eacute;ticos y no diab&eacute;ticos con y sin infarto previo en una poblaci&oacute;n finlandesa. </font></p>          <p><font face="Verdana" size="2">    <br>     </font>     </p>          <p><font color="#1f1a17" face="Verdana" size="2">Este trabajo es uno de los fundamentos de la recomendaci&oacute;n del ATP III de considerar a la diabetes como un equivalente de enfermedad arterial coronaria. </font></p>     <multicol gutter="18" cols="2"></multicol>     <p align="left"><font color="#1f1a17" face="Verdana" size="2">El estudio estadounidense ARIC<a name="-8"></a><sup>(<a href="#8">8</a>)</sup> mostr&oacute; tambi&eacute;n que el riesgo de muerte cardiovascular del diab&eacute;tico es sustancialmente mayor que el de las personas no diab&eacute;ticas aunque menor que el del paciente no diab&eacute;tico infartado (<a href="#figura2">figura 2</a>). </font></p>          <p align="left"><font face="Verdana" size="2"><a name="figura2"></a><img style="border: 1px solid ; width: 400px; height: 320px;" alt="" src="/img/revistas/ruc/v20n1/1a07f2.gif"></font></p>          <p align="left"><font face="Verdana" size="2"><b>FIGURA 2. </b>Mortalidad cardiovascular en diab&eacute;ticos y no diab&eacute;ticos con y sin infarto previo en el estudio ARIC.</font></p>          ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">Ocurri&oacute; algo similar con la tasa de eventos coronarios adversos. El riesgo de accidente cerebrovascular fue, en cambio, similar en diab&eacute;ticos sin infarto previo que en no diab&eacute;ticos con infarto previo. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">A pesar de las diferencias con el trabajo de Haffner, ARIC confirma el riesgo vascular aumentado del diab&eacute;tico. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El riesgo de muerte por enfermedad coronaria es aun mayor en las mujeres (cinco a ocho veces mayor que en las mujeres no diab&eacute;ticas) <sup><a name="-9"></a>(<a href="#9">9</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Este mayor riesgo de enfermedad cardiovascular y muerte en los diab&eacute;ticos se deber&iacute;a a la mayor prevalencia de otros factores de riesgo vascular en esta poblaci&oacute;n y al efecto nocivo directo de la diabetes sobre la macro y microvasculatura <a name="-10"></a><a name="-11"></a><sup>(<a href="#10">10</a>,<a href="#11">11</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El riesgo de muerte cardiovascular aumenta progresivamente con el incremento de niveles de tabaquismo, hipertensi&oacute;n arterial o hipercolesterolemia. A su vez, la potenciaci&oacute;n de la diabetes con los otros factores de riesgo es tal que para cada nivel de tabaquismo, dislipemia e hipertensi&oacute;n arterial, el riesgo de mortalidad cardiovascular es dos o tres veces mayor en los diab&eacute;ticos que en los no diab&eacute;ticos <a name="-12"></a><sup>(<a href="#12">12</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Si bien la tasa de eventos y la mortalidad por cardiopat&iacute;a isqu&eacute;mica en la poblaci&oacute;n global est&aacute; disminuyendo, ocurre lo contrario en la poblaci&oacute;n de diab&eacute;ticos <sup><a name="-13"></a>(<a href="#13">13</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Los principales factores que se proponen como responsables de un aumento de la aterosclerosis en los pacientes diab&eacute;ticos son la disfunci&oacute;n endotelial, la dislipemia, la hipercoagulabilidad, la hipobrinolisis, el incrmento de la agregabilidad plaquetaria, el aumento del estr&eacute;s oxidativo y los efectos t&oacute;xicos de la hiperglicemia <a name="-14"></a><sup>(<a href="#14">14</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Los pacientes diab&eacute;ticos tienen mayor probabilidad de experimentar muerte s&uacute;bita o infarto silente que los no diab&eacute;ticos. Tambi&eacute;n tienen mayor n&uacute;mero de vasos afectados y una distribuci&oacute;n m&aacute;s difusa de la enfermedad ateroscler&oacute;tica coronaria as&iacute; como una mayor tasa de reestenosis postangioplastia. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Los pacientes diab&eacute;ticos con cardiopat&iacute;a isqu&eacute;mica tienen mayor porcentaje de disfunci&oacute;n ventricular e insuficiencia card&iacute;aca que los pacientes con cardiopat&iacute;a isqu&eacute;mica sin esta enfermedad <a name="-46"></a><sup>(<a href="#46">46</a>)</sup>. Durante la etapa aguda del infarto de miocardio presentan mayor porcentaje de insuficiencia card&iacute;aca y shock cardiog&eacute;nico con similar extensi&oacute;n de infarto y fracci&oacute;n de eyecci&oacute;n de ventr&iacute;culo izquierdo <sup><a name="-74"></a>(<a href="#74">74</a>)</sup>. </font></p>          <p><font face="Verdana" size="2">    ]]></body>
<body><![CDATA[<br>     </font>     </p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><b>PREVENCI&Oacute;N DE LA ENFERMEDAD CORONARIA EN DIAB&Eacute;TICOS</b> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">CONTROL DE LA GLUCEMIA </font></p>          <p align="left"><font color="#000000" face="Verdana" size="2">El estudio UKPDS 33 <a name="-15"></a><sup>(<a href="#15">15</a>)</sup> demostr&oacute; en un grupo numeroso de diab&eacute;ticos tipo II seguidos a largo plazo que el control intensivo de las cifras de glucemia ya sea con insulina o con hipoglucemiantes orales disminuy&oacute; significativamente la incidencia de complicaciones microvasculares pero no las macrovasculares (<a href="/img/revistas/ruc/v20n1/1a07f3.gif">figura 3</a>).</font><font color="#1f1a17" face="Verdana" size="2"> </font></p>          <p><font face="Verdana" size="2">    <br>     <b><a href="/img/revistas/ruc/v20n1/1a07f3.gif">FIGURA 3</a>. </b>Efecto del control intensivo de la glucemia sobre distintas complicaciones vinculadas a la diabetes tipo II.</font></p>          <p><font face="Verdana" size="2">&nbsp; </font> </p>     <multicol gutter="18" cols="2"></multicol>     <p align="left"><font color="#000000" face="Verdana" size="2">Si bien hubo una tendencia a la reducci&oacute;n de la tasa de infarto, esta no fue estad&iacute;sticamente significativa. Lo mismo se concluy&oacute; con el estudio DCCT <sup><a name="-16"></a>(<a href="#16">16</a>)</sup> en diab&eacute;ticos tipo 1.</font><font color="#1f1a17" face="Verdana" size="2"> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">La conclusi&oacute;n de los autores del UKPDS fue que el control intensivo de la glucemia reduce las complicaciones de la diabetes, especialmente las microvasculares. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Sin embargo, cuando se estudi&oacute; el efecto del control intensivo de la glucemia con metformina en el grupo de diab&eacute;ticos obesos en el UKPDS 34 <sup><a name="-17"></a>(<a href="#17">17</a>)</sup> se demostr&oacute; una disminuci&oacute;n de infarto no fatal y muerte con respecto al control no intensivo. El resto de los hipoglucemiantes no logr&oacute; demostrar en este subgrupo diferencias estad&iacute;sticamente significativas en estos puntos con respecto al control no intensivo (<a href="/img/revistas/ruc/v20n1/1a07f4.gif">figura 4</a>). </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2">    <br>     <b><a href="/img/revistas/ruc/v20n1/1a07f4.gif">FIGURA 4</a>.</b> Beneficio del control intensivo de la glicemia con metformina en diab&eacute;ticos tipo II obesos.</font></p>          <p align="left"><font face="Verdana" size="2">&nbsp; </font> </p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Tambi&eacute;n se pudo observar una menor tendencia al aumento de peso y una menor tendencia a la hipoglucemia en el grupo tratado con metformina. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Por lo tanto, en diab&eacute;ticos tipo II obesos el control estricto de la glicemia con metformina previene el infarto de miocardio y la muerte. </font></p>     <font size="2"><multicol gutter="18" cols="2"></multicol></font><multicol gutter="18" cols="2"></multicol>      <p align="left"><font color="#1f1a17" face="Verdana" size="2"><b>CONTROL DE LA HIPERTENSI&Oacute;N ARTERIAL</b> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Los hipertensos diab&eacute;ticos tienen mayor morbimortalidad cardiovascular que los hipertensos no diab&eacute;ticos. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El control de la hipertensi&oacute;n arterial es un aspecto esencial en la prevenci&oacute;n de la enfermedad coronaria en el diab&eacute;tico. Dos puntos cr&iacute;ticos son las cifras tensionales deseables en esta poblaci&oacute;n as&iacute; como los f&aacute;rmacos m&aacute;s recomendables para obtenerlas. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">&iquest;QU&Eacute; CIFRAS TENSIONALES DEBE TENER UN DIAB&Eacute;TICO? </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><i>Cifras tensionales diast&oacute;licas</i> </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">El estudio HOT&nbsp;<sup><a name="-18"></a>(<a href="#18">18</a>)</sup> demostr&oacute; que los pacientes diab&eacute;ticos a los que se busc&oacute; disminuir dicha presi&oacute;n arterial (PA) a menos de 80 mmHg presentaron 51% de reducci&oacute;n de los eventos vasculares adversos (infarto y stroke no fatales, muerte cardiovascular) con respecto al grupo en que se trat&oacute; de reducir la PA diast&oacute;lica por debajo de 90 mm Hg. Este resultado fue estad&iacute;sticamente significativo (<a href="#figura5">figura 5</a>). </font></p>          <p align="left"><font face="Verdana" size="2"><a name="figura5"></a><img style="border: 1px solid ; width: 400px; height: 262px;" alt="" src="/img/revistas/ruc/v20n1/1a07f5.gif"></font></p>          <p align="left"><font face="Verdana" size="2"><b>FIGURA 5.</b> Eventos cardiovasculares mayores en diab&eacute;ticos en el estudio HOT.</font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Por lo tanto la, PA diast&oacute;lica recomendada en pacientes diab&eacute;ticos deber&iacute;a ser menor de 80 mm Hg. El Consenso Latinoamericano para Hipertensi&oacute;n Arterial y Diabetes <sup>(<a href="#74">74</a>)</sup> aconseja para pacientes con proteinuria mayor a 1 gramo/d&iacute;a, cifras de presi&oacute;n arterial diast&oacute;lica objetivo aun m&aacute;s bajas, menores de 75 mmHg. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><i>Cifras tensionales sist&oacute;licas</i> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Con respecto a la presi&oacute;n arterial sist&oacute;lica (PAS) la evidencia es menos contundente. El UKPDS 38 <sup><a name="-19"></a>(<a href="#19">19</a>)</sup> demostr&oacute; que la disminuci&oacute;n de la PAS por debajo de 150 mm Hg present&oacute; una disminuci&oacute;n de la mortalidad vinculada a diabetes, y del stroke, con respecto al grupo de control menos estricto (por debajo de 180 mmHg). </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Posteriormente el estudio ABCD <a name="-20"></a><sup>(<a href="#20">20</a>)</sup> logr&oacute; en el grupo de diab&eacute;ticos con cifras de PAS de 132 mmHg promedio, una reducci&oacute;n de la mortalidad (aunque no vascular) y de la microalbuminuria, con respecto al grupo con cifras de PAS promedio de 138 mm Hg. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Finalmente, el UKPDS 36 <sup><a name="-21"></a>(<a href="#21">21</a>)</sup> fue un estudio observacional que mostr&oacute; que a medida que se disminu&iacute;a la PAS disminu&iacute;an progresivamente todas las complicaciones macro y microvasculares sin aparecer un umbral por debajo del cual no existiera beneficio o aparecieran efectos adversos significativos. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Por lo tanto, es opini&oacute;n de expertos que la cifra de PAS objetivo a lograr en los diab&eacute;ticos sea menor de 130 mm Hg. El JNC-7 <sup><a name="-22"></a>(<a href="#22">22</a>)</sup>, la gu&iacute;a de la European Society of Hypertension-European Society of Cardiology <sup><a name="-23"></a>(<a href="#23">23</a>)</sup> y la gu&iacute;a del American College of Physicians <sup><a name="-24"></a><a name="-25"></a>(<a href="#24">24</a>,<a href="#25">25</a>)</sup> y el Consenso Latinoamericano para Hipertensi&oacute;n Arterial y Diabetes <sup>(<a href="#74">74</a>)</sup> concuerdan con estas recomendaciones. En este &uacute;ltimo consenso se recomienda para los pacientes con proteinuria mayor de 1 gramo/d&iacute;a cifras de PAS objetivo menores de 125 mmHg. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Cabe destacar que para lograr este objetivo se necesita usar a menudo varios f&aacute;rmacos. En el UKPDS 38, cuyas cifras objetivo en el grupo de control estricto de la PA fueron altas con respecto a las recomendaciones que acabamos de formular, se requiri&oacute; de m&aacute;s de un f&aacute;rmaco en m&aacute;s de 60% de los pacientes para lograr dichas cifras. Se requiri&oacute; de tres o m&aacute;s f&aacute;rmacos en 29% de los casos y muy pocos pacientes pudieron mantenerse sin ellos. </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">F&Aacute;RMACOS A UTILIZAR </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Pahor y colaboradores <a name="-26"></a><sup>(<a href="#26">26</a>)</sup> publicaron un metaan&aacute;lisis de los estudios que compararon el beneficio de los IECA con respecto a otros f&aacute;rmacos (nisoldipina, amlodipina, betabloqueantes, diur&eacute;ticos) en el control de cifras tensionales de diab&eacute;ticos hipertensos. Se concluy&oacute; que los IECA reduc&iacute;an el infarto no fatal, los eventos cardiovasculares (no el stroke) y la muerte con respecto a los otros f&aacute;rmacos en el conjunto de estudios, salvo en el UKPDS 38 que compar&oacute; captopril versus atenolol sin encontrar diferencias estad&iacute;sticamente significativas entre ambos. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Posteriormente el estudio ALLHAT <a name="-27"></a><sup>(<a href="#27">27</a>)</sup> compar&oacute; el beneficio del uso de clortalidona con respecto a amlodipina y a lisinopril, en el control de pacientes hipertensos, en un seguimiento a largo plazo. En el grupo de diab&eacute;ticos no hubo diferencias estad&iacute;sticamente significativas con respecto a mortalidad y eventos vasculares mayores, y se demostr&oacute; una disminuci&oacute;n del riesgo de desarrollo de insuficiencia card&iacute;aca con clortalidona. </font></p>     <multicol gutter="18" cols="2"></multicol>     <p align="left"><font color="#1f1a17" face="Verdana" size="2">El estudio LIFE <a name="-28"></a><sup>(<a href="#28">28</a>)</sup> demostr&oacute; en el subestudio de diab&eacute;ticos hipertensos con hipertrofia de ventr&iacute;culo izquierdo una disminuci&oacute;n de la mortalidad total y cardiovascular en un seguimiento a cinco a&ntilde;os, con el uso de losart&aacute;n comparado con atenolol. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Algunos IECA e inhibidores de la angiotensina II parecer&iacute;an tener beneficios adicionales independientes del control de la hipertensi&oacute;n arterial. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El estudio HOPE <a name="-29"></a><a name="-30"></a><sup>(<a href="#29">29</a>,<a href="#30">30</a>)</sup> demostr&oacute; en diab&eacute;ticos con otro factor de riesgo vascular adicional que pod&iacute;a ser hipertensi&oacute;n arterial pero bien controlada (sin evidencia cl&iacute;nica de insuficiencia card&iacute;aca), una disminuci&oacute;n de la mortalidad, del infarto no fatal y del stroke, con el uso de ramipril 10 mg/d&iacute;a. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El estudio EUROPA <sup><a name="-31"></a>(<a href="#31">31</a>)</sup> demostr&oacute; en pacientes con cardiopat&iacute;a isqu&eacute;mica estable, sin evidencia cl&iacute;nica de insuficiencia card&iacute;aca, con hipertensi&oacute;n controlada (PA media de 137/82) una disminuci&oacute;n de la morbimortalidad cardiovascular (muerte cardiovascular, infarto de miocardio o paro card&iacute;aco) con el uso del perindopril 8 mg/d&iacute;a. El subestudio del EUROPA en diab&eacute;ticos (PERSUADE) <sup><a name="-32"></a>(<a href="#32">32</a>)</sup> mostr&oacute; similares resultados. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Si bien no es el objetivo de esta revisi&oacute;n, destacamos que tanto los IECA como los bloqueantes de los receptores de angiotensina II tienen beneficios adicionales sobre la glomerulopat&iacute;a diab&eacute;tica <a name="-33"></a><sup>(<a href="#33">33</a>)</sup> y se aconseja en esta enfermedad el uso de IECA en los pacientes diab&eacute;ticos tipo I y de inhibidores de los receptores de angiotensina II en los diab&eacute;ticos tipo II <sup>(<a href="#74">74</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Por &uacute;ltimo, aunque es un objetivo de menor jerarqu&iacute;a que los previos, a nivel metab&oacute;lico el estudio GEMINI <sup><a name="-72"></a>(<a href="#72">72</a>)</sup> demostr&oacute; que el uso de carvedilol se asoci&oacute; a un mejor control metab&oacute;lico a mediano plazo con respecto a metoprolol. Por lo tanto, parecer&iacute;a razonable tener en cuenta esta opci&oacute;n cuando hay que usar un betabloqueante para el control de la hipertensi&oacute;n arterial en un diab&eacute;tico. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">En la elecci&oacute;n de los f&aacute;rmacos antihipertensivos se debe tener en cuenta tambi&eacute;n las situaciones com&oacute;rbidas. Por ejemplo, si el paciente es portador de cardiopat&iacute;a isqu&eacute;mica se debe plantear el uso de betabloqueantes; el hallazgo de microalbuminuria obliga al uso de f&aacute;rmacos inhibidores del sistema RAA (renina angiotensina aldosterona). </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">En conclusi&oacute;n: la asociaci&oacute;n de diabetes e hipertensi&oacute;n arterial aumenta marcadamente el riesgo de eventos cardiovasculares adversos, nefropat&iacute;a y muerte. Este riesgo disminuye al descender las cifras tensionales. Los valores &oacute;ptimos son &lt; 130/80 mmHg (&lt;125/75 si tiene proteinuria &gt; 1 g/d). La evidencia de superioridad o inferioridad de distintas clases de f&aacute;rmacos es m&aacute;s vaga y contradictoria. El tipo de f&aacute;rmacos antihipertensivos debe individualizarse para cada paciente no olvidando las comorbilidades. El uso de m&uacute;ltiples f&aacute;rmacos es habitualmente necesario para lograr las metas propuestas. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">TRATAMIENTO DE LA DISLIPEMIA </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Vijan y colaboradores <a name="-34"></a><sup>(<a href="#34">34</a>)</sup> publicaron un metaan&aacute;lisis de los estudios randomizados que evaluaron reducci&oacute;n de eventos cl&iacute;nicos mayores en diab&eacute;ticos tratados con hipolipemiantes. Se demostr&oacute; amplio beneficio con el uso de estos f&aacute;rmacos tanto en prevenci&oacute;n primaria como en prevenci&oacute;n secundaria. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El metaan&aacute;lisis de seis estudios de prevenci&oacute;n primaria (AFCAPS/TexCAPS; HPS; PROSPER; HHS; ASCOT-LLA; ALLHAT) mostr&oacute; una reducci&oacute;n significativa de 22% del riesgo relativo (RR 0,78; IC 95% 0,67-0,89) y de 3% del riesgo absoluto de eventos cardiovasculares adversos con el uso de hipolipemiantes al cabo de 4,3 a&ntilde;os de tratamiento promedio. Esto implica que tratando 34 pacientes diab&eacute;ticos sin enfermedad vascular conocida se previene un evento cardiovascular mayor. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El metaan&aacute;lisis de ocho estudios de prevenci&oacute;n secundaria (4S; CARE; LIPID; HPS; VA-HIT; Post-CABG; LIPS; PROSPER) con seguimiento promedio de 4,9 a&ntilde;os, demostr&oacute; una reducci&oacute;n significativa del riesgo relativo de eventos vasculares adversos de 24% (RR 0,76; IC 95% 0,59-0,93). El riesgo absoluto disminuy&oacute; 7%, es decir m&aacute;s del doble que en prevenci&oacute;n primaria. Vale mencionar que tratando 13 pacientes diab&eacute;ticos con enfermedad vascular conocida se previene un evento cardiovascular mayor. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">En base a estos resultados el American College of Physicians <sup><a name="-35"></a>(<a href="#35">35</a>)</sup> recomienda la administraci&oacute;n de hipolipemiantes a todos los pacientes diab&eacute;ticos en prevenci&oacute;n primaria y secundaria. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Pero con respecto a los diab&eacute;ticos en prevenci&oacute;n primaria hay autores que los recomiendan en todos los casos mientras que otros se ci&ntilde;en estrictamente a los grupos en los que se demostr&oacute; el mayor beneficio: diab&eacute;ticos con otro factor de riesgo, (mayores de 55 a&ntilde;os, hipertensos, tabaquistas, con hipertrofia ventricular izquierda o LDL &gt; 100 mg/dL) </font></p>          <p><font color="#1f1a17" face="Verdana" size="2">El estudio CARDS <a name="-36"></a><sup>(<a href="#36">36</a>)</sup> (posterior al metaan&aacute;lisis y las recomendaciones citadas) incluy&oacute; 2.838 diab&eacute;ticos tipo II, con edades entre 40 y 75 a&ntilde;os, sin evidencia de enfermedad cardiovascular, pero que adem&aacute;s padec&iacute;an retinopat&iacute;a, albuminuria, hipertensi&oacute;n arterial o tabaquismo. Los niveles de LDL colesterol deb&iacute;an ser menores de 160 mg/ml y los de triglic&eacute;ridos menores de 600 mg/ml. Los pacientes fueron asignados en forma aleatoria a atorvastatina 10 mg o placebo. El seguimiento medio fue de 3,9 a&ntilde;os. Hubo una reducci&oacute;n del riesgo relativo de eventos coronarios agudos, revascularizaci&oacute;n mioc&aacute;rdica o stroke significativa de 37% y una reducci&oacute;n de la mortalidad de 27% en el l&iacute;mite de la significaci&oacute;n estad&iacute;stica. CARDS es el primer estudio de tratamiento con una estatina en prevenci&oacute;n primaria efectuado exclusivamente en diab&eacute;ticos. Sus impactantes resultados no pueden, sin embargo, generalizarse a todos los diab&eacute;ticos en prevenci&oacute;n primaria. No obstante, agregar&iacute;a la retinopat&iacute;a y la albuminuria como una indicaci&oacute;n de estatinas en prevenci&oacute;n primaria de diab&eacute;ticos aun utilizando un criterio conservador. </font></p>     <multicol gutter="18" cols="2"></multicol>     <p align="left"><font color="#1f1a17" face="Verdana" size="2">Los f&aacute;rmacos hipolipemiantes que han demostrado el beneficio mayor son las estatinas, a dosis por lo menos moderadas. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El &uacute;nico f&aacute;rmaco distinto a las estatinas incluido en el metaan&aacute;lisis citado fue el gemfibrozil. El estudio VA-HIT <a name="-37"></a><sup>(<a href="#37">37</a>)</sup> demostr&oacute; que el uso de gemfibrozil en diab&eacute;ticos con enfermedad vascular conocida y portadores de HDL bajo y LDL bajo disminuy&oacute; la tasa de infarto no fatal, pero no la mortalidad. </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">Por lo tanto, consideramos aun en estos casos particulares que lo m&aacute;s razonable es el uso de estatinas que impactaron tambi&eacute;n en la mortalidad. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El LDL objetivo es discutible, la recomendaci&oacute;n del NCEP-ATP III (julio 2004) <sup><a name="-38"></a>(<a href="#38">38</a>)</sup> es de menos de 70 mg/dl para prevenci&oacute;n secundaria y 100 mg/dl para prevenci&oacute;n primaria. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">TRATAMIENTO CON &Aacute;CIDO ACETILSALIC&iacute;LICO (AAS) </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Varios estudios <a name="-39"></a><a name="-40"></a><sup>(<a href="#18">18</a>,<a href="#39">39</a>,<a href="#40">40</a>)</sup> han demostrado beneficio tanto para la prevenci&oacute;n primaria como para la prevenci&oacute;n secundaria de eventos vasculares adversos en diab&eacute;ticos. Un metaan&aacute;lisis del a&ntilde;o 2002 <a name="-41"></a><sup>(<a href="#41">41</a>)</sup>, la mayor&iacute;a de cuyos pacientes correspond&iacute;an a diab&eacute;ticos en prevenci&oacute;n primaria, presentaron una tendencia a la disminuci&oacute;n del riesgo de eventos vasculares mayores y muerte aunque, a diferencia del resto de los pacientes incluidos en el metaan&aacute;lisis, no fue estad&iacute;sticamente significativa. Esto podr&iacute;a explicarse por la p&eacute;rdida del poder estad&iacute;stico que se produce en el an&aacute;lisis de subgrupos. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">La American Diabetes Association <sup><a name="-42"></a>(<a href="#42">42</a>)</sup> recomienda el uso de &aacute;cido acetilsalic&iacute;lico (AAS) en prevenci&oacute;n primaria en diab&eacute;ticos mayores de 40 a&ntilde;os y/o que asocien otros criterios de riesgo como historia familiar de enfermedad vascular, hipertensi&oacute;n arterial, tabaquismo, dislipemia o albuminuria. Tambi&eacute;n recomienda el uso sistem&aacute;tico del AAS en prevenci&oacute;n secundaria. La dosis recomendada es la que ha demostrado beneficio: 75 a 162 mg/d&iacute;a. Por arriba de esta dosis no se ha demostrado mayor beneficio y s&iacute; mayor riesgo de sangrados. </font></p>          <p><font face="Verdana" size="2">    <br>     </font>     </p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><b>ABORDAJE MULTIFACTORIAL DE LA PREVENCI&oacute;N</b> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Como corolario del cap&iacute;tulo de prevenci&oacute;n vascular en el diab&eacute;tico vale la pena mencionar el estudio STENO 2 <a name="-43"></a><sup>(<a href="#43">43</a>)</sup>. &Eacute;ste incluy&oacute; diab&eacute;ticos de alto riesgo con presencia de microalbuminuria (<a href="/img/revistas/ruc/v20n1/1a07f6.gif">figura 6</a>). </font></p>          <p align="left"><font face="Verdana" size="2">    ]]></body>
<body><![CDATA[<br>   </font>   </p>          <p align="left"><font face="Verdana" size="2"><a href="/img/revistas/ruc/v20n1/1a07f6.gif"><b>FIGURA 6</b></a>. STENO 2</font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Se demostr&oacute; con un abordaje multifactorial estricto con dieta, ejercicio y m&uacute;ltiples f&aacute;rmacos (algunos de ellos de uso discutible como las vitaminas), una disminuci&oacute;n de alrededor de 50% de efectos vasculares adversos con respecto al tratamiento convencional. Por lo tanto, para optimizar la prevenci&oacute;n vascular en los diab&eacute;ticos (especialmente los de mayor riesgo), se debe intentar que logren efectuar un cambio de estilo de vida y un tratamiento medicamentoso estricto. </font></p>          <p><font face="Verdana" size="2">    <br>     </font>     </p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><b>CARDIOPAT&Iacute;A ISQU&Eacute;MICA EN EL DIAB&Eacute;TICO</b> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">En t&eacute;rminos generales el tratamiento de la cardiopat&iacute;a isqu&eacute;mica en el diab&eacute;tico es similar al no diab&eacute;tico. Analizaremos a continuaci&oacute;n algunos aspectos que se deben jerarquizar en esta poblaci&oacute;n de pacientes. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">TRATAMIENTO FARMACOL&Oacute;GICO </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Se debe hacer hincapi&eacute; en que el uso de betabloqueantes y de aspirina no s&oacute;lo no est&aacute; contraindicado en pacientes diab&eacute;ticos con cardiopat&iacute;a isqu&eacute;mica estable, sino que, por el contrario, proporciona amplios beneficios en t&eacute;rminos de reducci&oacute;n de morbimortalidad. </font></p>          <p><font color="#1f1a17" face="Verdana" size="2">Est&aacute; demostrado que el uso de AAS no tiene efectos adversos sobre la retinopat&iacute;a diab&eacute;tica<a name="-47"></a><sup>(<a href="#47">47</a>)</sup>. Se debe destacar tambi&eacute;n que, a las dosis recomendadas, el AAS no genera un efecto nocivo significativo a nivel del ri&ntilde;&oacute;n. </font></p>     <multicol gutter="18" cols="2"></multicol>     ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">Es habitual que los m&eacute;dicos teman el enmascaramiento de eventuales hipoglicemias con el uso de betabloqueantes en diab&eacute;ticos. Sin embargo, se ha demostrado que el uso de betabloqueantes a largo plazo en diab&eacute;ticos en prevenci&oacute;n secundaria se asocia a una reducci&oacute;n significativa de la morbimortalidad sin un aumento de las tasas de hospitalizaci&oacute;n por complicaciones vinculadas a la diabetes <a name="-48"></a><sup>(<a href="#48">48</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">INFARTO AGUDO DE MIOCARDIO </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Los diab&eacute;ticos con similar topograf&iacute;a y extensi&oacute;n de infarto agudo de miocardio presentan mayor mortalidad, incidencia de isquemia recurrente e insuficiencia card&iacute;aca que los pacientes no diab&eacute;ticos. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">A continuaci&oacute;n se destacan algunos hechos espec&iacute;ficos en el tratamiento del infarto agudo de miocardio (IAM) en esta poblaci&oacute;n. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><i>Tratamiento fibrinol&iacute;tico</i> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">En los pacientes diab&eacute;ticos el tratamiento fibrinol&iacute;tico en el curso del IAM se asocia con un mayor beneficio relativo en la mortalidad que en los pacientes no diab&eacute;ticos: a un mes se salvan 35 vidas por cada 100 diab&eacute;ticos tratados y 17 por cada 100 pacientes no diab&eacute;ticos tratados <a name="-49"></a><sup>(<a href="#49">49</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Los fibrinol&iacute;ticos no ocasionan un aumento del riesgo de sangrado intraocular en diab&eacute;ticos. Un subestudio del GUSTO 1 demostr&oacute; en 40.899 pacientes con 6.011 diab&eacute;ticos que el uso de fibrinol&iacute;ticos no determin&oacute; un aumento de las hemorragias intraoculares<a name="-50"></a><sup>(<a href="#50">50</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><i>Insulinoterapia</i> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El control estricto de la glucemia en el curso del IAM con insulina cristalina (continuando con insulina cristalina hasta tres meses despu&eacute;s del mismo) demostr&oacute;, en el estudio DIGAMI <a name="-51"></a><sub>(<a href="#51">51</a>)</sub>, una disminuci&oacute;n de la mortalidad del 30% al cabo de un a&ntilde;o con respecto al tratamiento convencional de la diabetes. Por lo tanto, se aconseja un estricto control de la glucemia en el entorno de este evento agudo coronario. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">ANGINA INESTABLE &ndash; IAM NO Q </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2"><i>Inhibidores de la glicoprote&iacute;na IIb-IIIa</i> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Los pacientes diab&eacute;ticos con sindromes coronarios agudos sin supradesnivel del segmento ST tienen mayor beneficio (disminuci&oacute;n de la mortalidad a 30 d&iacute;as) con el uso de inhibidores de la glucoprote&iacute;na IIb-IIIa que los pacientes no diab&eacute;ticos. El beneficio es aun mayor en aquellos diab&eacute;ticos sometidos a angioplastia <a name="-52"></a><sup>(<a href="#52">52</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><i>Revascularizaci&oacute;n</i> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Alrededor de 25% del total de los procedimientos de revascularizaci&oacute;n se realizan en diab&eacute;ticos. La estrategia &oacute;ptima de revascularizaci&oacute;n es discutida. Cualquiera que sea la misma los resultados son peores que en los no diab&eacute;ticos. </font></p>          <p><font color="#1f1a17" face="Verdana" size="2"><i>Angioplastia con bal&oacute;n</i> </font></p>     <multicol gutter="18" cols="2"></multicol>     <p align="left"><font color="#1f1a17" face="Verdana" size="2">La angioplastia con bal&oacute;n en el diab&eacute;tico tiene tasas de &eacute;xito angiogr&aacute;fico inmediato similar a las de los no diab&eacute;ticos. Sin embargo, la mortalidad intrahospitalaria del diab&eacute;tico es el triple. Los resultados cl&iacute;nicos y angiogr&aacute;ficos son tambi&eacute;n peores a largo plazo: 1) las tasas de reestenosis se duplican; 2) hay un marcado aumento en las tasas de infarto de miocardio, necesidad de nueva angioplastia y de cirug&iacute;a de revascularizaci&oacute;n coronaria; y 3) la mortalidad a largo plazo (nueve a&ntilde;os) se duplica <sup><a name="-53"></a><a name="-54"></a>(<a href="#53">53</a>,<a href="#54">54</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><i>Stents</i> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El uso de stents en diab&eacute;ticos disminuye marcadamente la incidencia de reestenosis excepto en vasos de peque&ntilde;o calibre. Van Belle y colaaboradores demostraron una reducci&oacute;n altamente significativa en las tasas de reestenosis binaria angiogr&aacute;fica a seis meses en pacientes diab&eacute;ticos con implante de stent versus angioplastia con bal&oacute;n (62% versus 27%). M&aacute;s importante aun, la tasa de eventos vasculares adversos mayores (muerte, infarto de miocardio o necesidad de nueva revascularizaci&oacute;n) es significativamente menor cuando se utilizan stents (63,1% versus 41,2%) <a name="-55"></a><sup>(<a href="#55">55</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">West y colaboradores identificaron recientemente tres predictores de reestenosis intrastent en diab&eacute;ticos: di&aacute;metro del vaso de referencia, longitud del segmento tratado e &iacute;ndice de masa corporal <a name="-56"></a><sup>(<a href="#56">56</a>)</sup>. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><i>Stents elusores de f&aacute;rmacos</i> </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">La reciente introducci&oacute;n de stents elusores de f&aacute;rmacos mejora aun m&aacute;s los resultados. Pero hay que enfatizar que &eacute;stos siguen siendo peores que en los no diab&eacute;ticos. Dos f&aacute;rmacos han demostrado ser &uacute;tiles para prevenir la reestenosis: la rapamicina (sirolimus) y el paclitaxel. El subestudio de diab&eacute;ticos de SIRIUS <sup><a name="-57"></a>(<a href="#57">57</a>)</sup> demostr&oacute; una notoria reducci&oacute;n en las tasas de reestenosis angiogr&aacute;fica binaria cuando se utiliza el stent Bx velocity elusor de rapamicina que cuando se usa el mismo stent sin f&aacute;rmaco. A destacar que la incidencia de muerte o de infarto de miocardio fue similar con ambos stents. Similares resultados fueron observados en el subgrupo de diab&eacute;ticos de TAXUSIV <a name="-58"></a><sup>(<a href="#58">58</a>)</sup> utilizando stents elusores de paclitaxel. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><i>F&aacute;rmacos asociados a la angioplastia</i> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Los inhibidores de los receptores IIbIIIa son f&aacute;rmacos &uacute;tiles asociados a los procedimientos de revascularizaci&oacute;n percut&aacute;nea sobre todo en pacientes diab&eacute;ticos <sup><a name="-59"></a><a name="-60"></a>(<a href="#59">59</a>,<a href="#60">60</a>)</sup>. Se ha demostrado que estos f&aacute;rmacos reducen en forma marcada y consistente la incidencia de eventos isqu&eacute;micos a 30 d&iacute;as as&iacute; como en la mortalidad a largo plazo. El beneficio de estos f&aacute;rmacos es mayor en diab&eacute;ticos que en no diab&eacute;ticos. Esto ha llevado a la amplia aceptaci&oacute;n del uso de los inhibidores IIb-IIIa para disminuir la mortalidad asociada con los procedimientos de intervenci&oacute;n coronaria percut&aacute;nea en diab&eacute;ticos. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">La introducci&oacute;n de clopidogrel ha cambiado de manera significativa los resultados cl&iacute;nicos postintervenci&oacute;n coronaria percut&aacute;nea. El estudio CREDO <sup><a name="-61"></a>(<a href="#61">61</a>)</sup> mostr&oacute; que el pretratamiento con 300 mg de clopidogrel seis horas antes de un procedimiento de revascularizaci&oacute;n percut&aacute;neo reduce los eventos isqu&eacute;micos periprocedimiento. Adem&aacute;s, el tratamiento a largo plazo (un a&ntilde;o) con este f&aacute;rmaco tambi&eacute;n redujo los eventos cl&iacute;nicos adversos en ese per&iacute;odo. El subgupo de diab&eacute;ticos CREDO mostr&oacute; similares beneficios. ISAR-SWEET <a name="-62"></a><sup>(<a href="#62">62</a>)</sup> estudi&oacute; el efecto de abciximab o placebo en pacientes pretratados con altas dosis de clopidogrel (600 mg) al menos dos horas antes de un procedimiento de revascularizaci&oacute;n percut&aacute;nea. Abciximab no redujo significativamente la tasa de infarto de miocardio o muerte al cabo de un a&ntilde;o de seguimiento aunque s&iacute; redujo la tasa de reestenosis. Estos hallazgos generan controversia, a&uacute;n no resuelta, con respecto a la necesidad o no de asociar inhibidores IIbIIIa a clopidrel en los procedimientos de revascularizaci&oacute;n coronaria percut&aacute;nea en diab&eacute;ticos. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><i>Control glic&eacute;mico</i> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Merece menci&oacute;n especial la conveniencia de un adecuado control glic&eacute;mico cuando se va a efectuar un procedimiento de revascularizaci&oacute;n percut&aacute;nea electivo. Corpus y colaboradores <sup><a name="-64"></a>(<a href="#64">64</a>)</sup> demostraron recientemente que un nivel de hemoglobina glicosilada mayor a 7% es un predictor independiente de la necesidad de una nueva revascularizaci&oacute;n del vaso blanco. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><i>Cirug&iacute;a de revascularizaci&oacute;n coronaria</i> </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">La cirug&iacute;a de revascularizaci&oacute;n coronaria (CRC) tambi&eacute;n tiene peores resultados en diab&eacute;ticos que en no diab&eacute;ticos. La mortalidad es progresivamente mayor a medida que el diab&eacute;tico agrega complicaciones macrovasculares e insuficiencia renal <a name="-65"></a><sup>(<a href="#65">65</a>)</sup>. La cirug&iacute;a se plantea sobre todo en pacientes con enfermedad multivaso. </font></p>          <p><font color="#1f1a17" face="Verdana" size="2">El estudio BARI <sup><a name="-66"></a><a name="-67"></a><a name="-68"></a>(<a href="#66">66</a>-<a href="#68">68</a>)</sup> compar&oacute; los resultados de CRC versus angioplastia con bal&oacute;n en 1.829 pacientes con enfermedad multivaso seguidos durante cinco y luego siete a&ntilde;os. No hubo diferencias de mortalidad entre los pacientes revascularizados quir&uacute;rgicamente o por PCI excepto en el subgrupo de pacientes diab&eacute;ticos (n=323), que tuvo una mortalidad significativamente menor con CRC que con angioplastia con bal&oacute;n. </font></p>     <multicol gutter="18" cols="2"></multicol>     <p align="left"><font color="#1f1a17" face="Verdana" size="2">Los beneficios estuvieron limitados a aquellos individuos a quienes se les coloc&oacute; un puente mamario DA. </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">BARI ha sido criticado por el peque&ntilde;o n&uacute;mero de pacientes diab&eacute;ticos que incluy&oacute; porque el an&aacute;lisis del subgrupo de diab&eacute;ticos no hab&iacute;a sido planeado de antemano, porque las t&eacute;cnicas de revascularizaci&oacute;n percut&aacute;nea no incluyeron stents, porque no se utilizaron inhibidores IIbIIIa y porque la revascularizaci&oacute;n quir&uacute;rgica fue m&aacute;s completa que con PCI. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El registro BARI <a name="-70"></a><sup>(<a href="#70">70</a>)</sup> estudi&oacute; 2.010 pacientes que cumpl&iacute;an con los criterios de inclusi&oacute;n para el estudio randomizado, pero que no aceptaron ser randomizados. El tratamiento fue definido en cada caso por el equipo m&eacute;dico actuante en acuerdo con el paciente. Los diab&eacute;ticos con enfermedad coronaria m&aacute;s extensa recibieron cirug&iacute;a en tanto que aquellos con un perfil angiogr&aacute;fico m&aacute;s favorable fueron tratados con angioplastia. En el registro BARI, en los pacientes diab&eacute;ticos, a diferencia de lo que sucedi&oacute; en el estudio BARI, no hubo diferencias de mortalidad a siete a&ntilde;os entre los pacientes angioplastiados y los sometidos a cirug&iacute;a. Esto sugerir&iacute;a que el buen juicio del binomio m&eacute;dico-paciente podr&iacute;a identificar el m&eacute;todo de revascularizaci&oacute;n m&aacute;s adecuado para cada paciente. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">El estudio ARTS <a name="-71"></a><sup>(<a href="#71">71</a>)</sup> compar&oacute; angioplastia con stent versus CRC en pacientes con enfermedad multivaso. La sobrevida libre de eventos vasculares y cerebrales mayores (muerte, infarto de miocardio, necesidad de nueva revascularizaci&oacute;n o accidente cerebrovascular) fue significativamente mejor con cirug&iacute;a que con PCI tanto en diab&eacute;ticos como en no diab&eacute;ticos. Pero esta diferencia dependi&oacute; exclusivamente de un aumento de la necesidad de nuevos procedimientos de revascularizaci&oacute;n. Los eventos &ldquo;duros&rdquo; (muerte, infarto de miocardio, ACV) no fueron significativamente diferentes en los diab&eacute;ticos sometidos a revascularizaci&oacute;n quir&uacute;rgica o con stent. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">No hay a&uacute;n datos que comparen angioplastia con stent elusores de f&aacute;rmacos versus cirug&iacute;a de revascularizaci&oacute;n mioc&aacute;rdica en pacientes diab&eacute;ticos con enfermedad multivaso. Est&aacute; en curso el estudio FREEDOM que intentar&aacute; resolver este punto. Sin embargo, cuando sus resultados est&eacute;n disponibles probablemente habr&aacute; nuevos stents y nuevas t&eacute;cnicas quir&uacute;rgicas que hagan sus resultados obsoletos. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">A modo de conclusi&oacute;n se podr&iacute;a decir que los diab&eacute;ticos pasibles de revascularizaci&oacute;n por PCI ser&iacute;an aquellos que padecen enfermedad de un vaso, que no son candidatos a la colocaci&oacute;n de un puente mamario DA, que tienen dos o tres lesiones bien discretas sin evidencias de ateromatosis difusa o que tienen contraindicaciones importantes para la cirug&iacute;a. Cuando se realiza PCI en un diab&eacute;tico hay que pensarlo dos veces, usar stents elusores de f&aacute;rmacos, intentar utilizar inhibidores IIb-IIIa (no disponibles en nuestro medio) y maximizar las medidas de prevenci&oacute;n secundaria: control glic&eacute;mico &oacute;ptimo, descenso agresivo del nivel de l&iacute;pidos con estatinas, uso de IECAs. </font></p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2">Como recomendaci&oacute;n final se podr&iacute;a decir que cuando se decide revascularizar a un diab&eacute;tico se debe individualizar el tratamiento al caso concreto, valorar las posibilidades al medio en que se act&uacute;a, y aprovechar el procedimiento de revascularizaci&oacute;n para optimizar las medidas de prevenci&oacute;n. </font></p>          <p><font face="Verdana" size="2">    <br>     </font>     </p>          <p align="left"><font color="#1f1a17" face="Verdana" size="2"><b>BIBLIOGRAF&iacute;A</b> </font></p>          <!-- ref --><p align="left"><font color="#1f1a17" face="Verdana" size="2"><a name="1"></a><a href="#-1">1</a>.&nbsp;&nbsp;&nbsp;&nbsp;<b>Bosch X, Alfonso F, Bermejo J. </b>Diabetes y enfermedad cardiovascular. 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