<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>0001-6002</journal-id>
<journal-title><![CDATA[Acta Médica Costarricense]]></journal-title>
<abbrev-journal-title><![CDATA[Acta méd. costarric]]></abbrev-journal-title>
<issn>0001-6002</issn>
<publisher>
<publisher-name><![CDATA[Colegio de Médicos y Cirujanos de Costa Rica]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0001-60022002000200003</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Cáncer gástrico, epidemiología y prevención]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sierra]]></surname>
<given-names><![CDATA[Rafaela]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Universidad de Costa Rica Instituto de Investigaciones en Salud ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2002</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2002</year>
</pub-date>
<volume>44</volume>
<numero>2</numero>
<fpage>55</fpage>
<lpage>61</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_arttext&amp;pid=S0001-60022002000200003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_abstract&amp;pid=S0001-60022002000200003&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.sa.cr/scielo.php?script=sci_pdf&amp;pid=S0001-60022002000200003&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[El cáncer gástrico es una de las neoplasias que produce mayor mortalidad en la población mundial. A pesar de que las tasas de incidencia están disminuyendo, sigue siendo un problema de salud pública. La información y el conocimiento sobre la epidemiología de este tumor es abundante. Aquí se presenta una revisión bibliográfica actualizada sobre los factores de riesgo mejor documentados y aceptados por la comunidad científica: infección por Helicobacter pylori, dieta, susceptibilidad genética y nivel socioeconómico. Además, se analizan formas de enfrentar esta patología, por medio de la prevención (consumo de frutas y verduras) y la detección temprana con Rayos X y marcadores biológicos (pepsinógenos séricos), en poblaciones o grupos identificados como de alto riesgo. Se hace hincapié en las interrogantes y retos que plantean los nuevos conocimientos.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Gastric cancer is one of the tumors with higher worldwide mortality. Although the incidence rate has been declining, it is still a major public health problem still. Epidemiological information and knowledge about this cancer is abundant. This is an up to date review about commonly accepted risk factors: Helicobacter pylori infection, diet, genetic predisposition and socioeconomic status. We also stress the new questions and challenges that recent discoveries about this pathology entail. The ways to tackle this cancer are discussed using X rays and biological markers such as serum pepsinogens in high risk groups or populations.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Cáncer gástrico]]></kwd>
<kwd lng="la"><![CDATA[Helicobacter pylori]]></kwd>
<kwd lng="es"><![CDATA[susceptibilidad genética]]></kwd>
<kwd lng="es"><![CDATA[interleucinas]]></kwd>
<kwd lng="es"><![CDATA[dieta]]></kwd>
<kwd lng="es"><![CDATA[prevención]]></kwd>
<kwd lng="es"><![CDATA[detección temprana]]></kwd>
<kwd lng="es"><![CDATA[pepsinógenos]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  &nbsp;     <br><b><font face="Arial">Revisi&oacute;n</font></b>     <center>     <p><b><font face="Arial">C&aacute;ncer g&aacute;strico, epidemiolog&iacute;a y prevenci&oacute;n</font></b>     <p>    <br>     <p><font face="Arial"><font size=-1>Rafaela Sierra<a NAME="R1"></a></font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#A1">1</a></font></font></sup></center>      <p>    <br><b><font face="Arial"><font size=-1></font></font></b>     <p><b><font face="Arial"><font size=-1>Resumen</font></font></b>     ]]></body>
<body><![CDATA[<p><font face="Arial"><font size=-1>El c&aacute;ncer g&aacute;strico es una de las neoplasias que produce mayor mortalidad en la poblaci&oacute;n mundial. A pesar de que las tasas de incidencia est&aacute;n disminuyendo, sigue siendo un problema de salud p&uacute;blica. La informaci&oacute;n y el conocimiento sobre la epidemiolog&iacute;a de este tumor es abundante. Aqu&iacute; se presenta una revisi&oacute;n bibliogr&aacute;fica actualizada sobre los factores de riesgo mejor documentados y aceptados por la comunidad cient&iacute;fica: infecci&oacute;n por <i>Helicobacter pylor</i>i, dieta, susceptibilidad gen&eacute;tica y nivel socioecon&oacute;mico. Adem&aacute;s, se analizan formas de enfrentar esta patolog&iacute;a, por medio de la prevenci&oacute;n (consumo de frutas y verduras) y la detecci&oacute;n temprana con Rayos X y marcadores biol&oacute;gicos (pepsin&oacute;genos s&eacute;ricos), en poblaciones o grupos identificados como de alto riesgo. Se hace hincapi&eacute; en las interrogantes y retos que plantean los nuevos conocimientos.</font></font>     <p><b><font face="Arial"><font size=-1>Descriptores</font></font></b>     <p><font face="Arial"><font size=-1>C&aacute;ncer g&aacute;strico, <i>Helicobacter pylor</i>i, susceptibilidad gen&eacute;tica, interleucinas, dieta, prevenci&oacute;n, detecci&oacute;n temprana, pepsin&oacute;genos.</font></font>     <p><i><font face="Arial"><font size=-1>Recibido: 15 de enero, 2002</font></font></i>     <br><i><font face="Arial"><font size=-1>Aceptado para publicaci&oacute;n: 23 de abril, 2002</font></font></i>     <p><font face="Arial"><font size=-1><b>Abreviaturas : </b>PG=Pepsin&oacute;geno; VacA= Citotoxina vacuolizante A ; cagA= gen A asociado a citotoxina.</font></font>     <br>&nbsp;     <p><font face="Arial"><font size=-1>A pesar del descenso continuo de las tasas de incidencia y mortalidad, por c&aacute;ncer g&aacute;strico, este contin&uacute;a siendo la segunda causa de muerte por c&aacute;ncer en el mundo </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#1">1</a></font></font></sup><font face="Arial"><font size=-1>. En el a&ntilde;o 2000 el n&uacute;mero de casos nuevos fue mayor de un mill&oacute;n, dos tercios de los cuales aparecieron en los pa&iacute;ses en desarrollo; ese n&uacute;mero aumenta cada a&ntilde;o debido al envejecimiento de la poblaci&oacute;n. Las tasas m&aacute;s altas se presentan en Jap&oacute;n, China, Corea, pa&iacute;ses del Este de Europa, pa&iacute;ses tropicales de Am&eacute;rica del Sur y Costa Rica. Las tasas m&aacute;s bajas ocurren en la poblaci&oacute;n blanca de los Estados Unidos, Australia y &Aacute;frica </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#1">1-3</a></font></font></sup><font face="Arial"><font size=-1>.</font></font>     <p><font face="Arial"><font size=-1>La supervivencia de los pacientes con c&aacute;ncer g&aacute;strico es muy baja, tanto en los pa&iacute;ses industrializados como en los que est&aacute;n en v&iacute;as de desarrollo, debido a que la mayor&iacute;a de los casos se diagnostican en etapas avanzadas, cuando la probabilidad de curaci&oacute;n es muy reducida </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#4">4</a>,<a href="#5">5</a></font></font></sup><font face="Arial"><font size=-1>. En Jap&oacute;n, las tasas generales de supervivencia son considerablemente mayores gracias a los programas masivos de detecci&oacute;n temprana, lo que permite aplicar el tratamiento oportuno </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#6">6</a>,<a href="#7">7</a></font></font></sup><font face="Arial"><font size=-1>.</font></font>     <p><font face="Arial"><font size=-1>La mayor&iacute;a de los tumores del est&oacute;mago son de origen epitelial (97%), se clasifican como adenocarcinomas y han sido divididos en dos principales tipos: difuso e intestinal.</font></font>     ]]></body>
<body><![CDATA[<p><font face="Arial"><font size=-1>Difieren en su epidemiolog&iacute;a, etiolog&iacute;a, patog&eacute;nesis y comportamiento. El adenocarcinoma de tipo difuso o indiferenciado, produce met&aacute;stasis m&aacute;s temprano, se presenta por igual en toda la poblaci&oacute;n, es m&aacute;s frecuente en poblaciones j&oacute;venes que el intestinal y est&aacute; m&aacute;s relacionado con factores gen&eacute;ticos </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#8">8-10</a></font></font></sup><font face="Arial"><font size=-1>.</font></font>     <p><font face="Arial"><font size=-1>El adenocarcinoma de tipo intestinal es bien diferenciado, de crecimiento expansivo y es prevalente en poblaciones de alto riesgo de c&aacute;ncer g&aacute;strico y en hombres de mayor edad.</font></font>     <p><font face="Arial"><font size=-1>Se ha relacionado con factores ambientales. La disminuci&oacute;n de la incidencia de c&aacute;ncer g&aacute;strico se atribuye principalmente a la disminuci&oacute;n del tipo intestinal. Los cambios que preceden a la aparici&oacute;n de este tipo de c&aacute;ncer son la gastritis cr&oacute;nica atr&oacute;fica, la metaplasia y la displasia. El proceso completo tarda por lo menos dos d&eacute;cadas </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#11">11</a>,<a href="#12">12</a></font></font></sup><font face="Arial"><font size=-1>. En todas las etapas de este proceso interact&uacute;an la predisposici&oacute;n gen&eacute;tica, los factores de riesgo y los factores de protecci&oacute;n, facilitando, retrasando o evitando el desarrollo del c&aacute;ncer .</font></font>     <br>&nbsp;     <p><b><font face="Arial"><font size=-1>Factores de riesgo y protecci&oacute;n</font></font></b>     <p><font face="Arial"><font size=-1>La infecci&oacute;n con <i>Helicobacter pylori</i>, especialmente desde edades tempranas, la historia familiar de c&aacute;ncer g&aacute;strico, el bajo nivel socioecon&oacute;mico, la producci&oacute;n end&oacute;gena de nitrosaminas, la alta ingesta de compuestos nitrosados eirritantes y el bajo consumo de frutas y verduras, han sidoasociados con mayor riesgo de padecer c&aacute;ncer g&aacute;strico detipo intestinal. Las variaciones geogr&aacute;ficas en las tasas deincidencia de este tumor, las tendencias temporales decrecientes y las variaciones del riesgo en las poblacionesque emigran, sugieren que existen factores ambientales que cumplen un papel importante en la carcinog&eacute;nesis g&aacute;strica.</font></font>     <br>&nbsp;     <p><b><i><font face="Arial"><font size=-1>Heliocobacter pylori y c&aacute;ncer g&aacute;strico</font></font></i></b>     <p><font face="Arial"><font size=-1>Se reconoce que la infecci&oacute;n con <i>Helicobacter pylori </i>es la principal causa de gastritis cr&oacute;nica, &uacute;lceras p&eacute;pticas y el principal factor de riesgo para el desarrollo de c&aacute;ncer g&aacute;strico. La infecci&oacute;n se adquiere, en la mayor&iacute;a de los casos, en la infancia, y es capaz de permanecer en el hospedero toda la vida. Sin embargo, solo un grupo muy peque&ntilde;o desarrolla c&aacute;ncer g&aacute;strico o &uacute;lceras p&eacute;pticas, mientras que un gran n&uacute;mero de infectados (m&aacute;s del 70%) son asintom&aacute;ticos </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#13">13-17</a></font></font></sup><font face="Arial"><font size=-1>. Los aspectos m&aacute;s relevantes de la infecci&oacute;n son: la inflamaci&oacute;n cr&oacute;nica, la proliferaci&oacute;n celular excesiva y la disminuci&oacute;n de la secreci&oacute;n &aacute;cida, lo cual puede modular el proceso de carcinog&eacute;nesis </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#18">18-20</a></font></font></sup><font face="Arial"><font size=-1>. Surge la pregunta sobre cu&aacute;les son las circunstancias o mecanismos que predisponen al hospedero infectado para que desarrolle las patolog&iacute;as g&aacute;stricas m&aacute;s o menos severas.</font></font>     <p><font face="Arial"><font size=-1>Algunos estudios sugieren la existencia de cepas de <i>H. pylori </i>m&aacute;s virulentas, de acuerdo con algunos fenotipos de lamisma. Las cepas productoras de la toxina VacA y las que poseen el gen cagA, han sido asociadas con mayor riesgo de metaplasia intestinal y c&aacute;ncer g&aacute;strico </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#21">21</a>,<a href="#22">22</a></font></font></sup><font face="Arial"><font size=-1>. Sin embargo, algunas investigaciones encontraron que la fuerza de la asociaci&oacute;n var&iacute;a entre diferentes poblaciones, o no se encuentra asociaci&oacute;n </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#23">23</a>,<a href="#24">24</a></font></font></sup><font face="Arial"><font size=-1>, ni se han podido identificar en la bacteria, los genes o polimorfismos de mayor riesgo para &uacute;lceras o c&aacute;ncer </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#25">25</a>, <a href="#26">26</a></font></font></sup><font face="Arial"><font size=-1>. Actualmente, varios factores de virulencia de la bacteria, est&aacute;n siendo ampliamente investigados.</font></font>     ]]></body>
<body><![CDATA[<p><font face="Arial"><font size=-1>Por otra parte, investigaciones recientes muestran que los pacientes infectados y que presentan gastritis atr&oacute;fica severa, gastritis predominante en el cuerpo o metaplasia intestinal, tienen mayor riesgo de c&aacute;ncer g&aacute;strico, as&iacute; como tambi&eacute;n aquellas personas con &uacute;lceras g&aacute;stricas o p&oacute;lipos hiperpl&aacute;sicos. Pero no existe ese riesgo entre los pacientes con &uacute;lceras duodenales </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#27">27</a></font></font></sup><font face="Arial"><font size=-1>. Se ha postulado que las enfermedades g&aacute;stricas, asociadas con la infecci&oacute;n por <i>H. pylori </i>se deben principalmente a una inapropiada regulaci&oacute;n de la respuesta inmune y que la respuesta antiinflamatoria contribuye a la patog&eacute;nesis del c&aacute;ncer </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#28">28</a>,<a href="#29">29</a></font></font></sup><font face="Arial"><font size=-1>. El supuesto anterior se debe a que dentro del grupo de personas infectadas por <i>H. pylori</i>, las que presentan determinados polimorfismos del gen IL-1B, que codifica la citoquina inflamatoria interleucina-1&szlig;, tienen mayor riesgo de padecer lesiones precancerosas y c&aacute;ncer g&aacute;strico. Esos polimorfismos, en presencia de <i>H. pylor</i>i, causan sobre expresi&oacute;n de la prote&iacute;na <i>IL - 1</i>&szlig;, lo que produce una disminuci&oacute;n significativa de las secreciones &aacute;cidas del est&oacute;mago </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#30">30</a>,<a href="#31">31</a></font></font></sup><font face="Arial"><font size=-1>, que junto con la hipoclorhidria, crean un ambiente de riesgo de c&aacute;ncer g&aacute;strico </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#32">32-34</a></font></font></sup><font face="Arial"><font size=-1>, que incrementado el da&ntilde;o, permitiendo la acumulaci&oacute;n de bacterias y sus toxinas y de mediadores antiinflamatorios.</font></font>     <p><font face="Arial"><font size=-1>Se sospecha que el resultado final de la infecci&oacute;n est&aacute; determinado por la extensi&oacute;n y severidad de la inflamaci&oacute;n g&aacute;strica (gastritis extensiva al cuerpo, hipoclorhidria y atrofia), la cual depende de interacciones complejas entre la edad en que fue adquirida la infecci&oacute;n, los mecanismos de respuesta inmune del hu&eacute;sped, la virulencia de la bacteria y la dieta </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#13">13</a>,<a href="#25">25</a>,<a href="#27">27</a>,<a href="#29">29</a>,<a href="#34">34</a></font></font></sup><font face="Arial"><font size=-1>.</font></font>     <br>&nbsp;     <p><b><i><font face="Arial"><font size=-1>Historia familiar</font></font></i></b>     <p><font face="Arial"><font size=-1>El riesgo de padecer c&aacute;ncer g&aacute;strico es mayor en personas con una historia familiar positiva de c&aacute;ncer g&aacute;strico</font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#35">35-39</a></font></font></sup><font face="Arial"><font size=-1>. Esta disposici&oacute;n puede ser el resultado de factores gen&eacute;ticos ambientales. Tambi&eacute;n se ha demostrado que la prevalencia de metaplasia intestinal y de gastritis atr&oacute;fica e hipoclorhidria es significativamente mayor en familiares de pacientes con c&aacute;ncer g&aacute;strico, infectados por <i>H. pylori</i>, que en controles tambi&eacute;n infectados </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#40">40</a>,<a href="#41">41</a></font></font></sup><font face="Arial"><font size=-1>. Brenner et al. (2000) encontraron que la infecci&oacute;n por la <i>cepa cagA </i>positiva y una historia familiar de c&aacute;ncer g&aacute;strico, eran factores independientes, y los sujetos que reun&iacute;an esas dos condiciones ten&iacute;an 16 veces m&aacute;s riesgo de padecer este tumor </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#38">38</a></font></font></sup><font face="Arial"><font size=-1>.</font></font>     <p><font face="Arial"><font size=-1>Como se discuti&oacute; antes, la herencia de polimorfismos que disminuyen la secreci&oacute;n &aacute;cida del est&oacute;mago (p.e. <i>IL-1</i>B) , en presencia de <i>H. pylori</i>, podr&iacute;a explicar, en parte, el mayor riesgo de padecer c&aacute;ncer g&aacute;strico en las personas infectadas por esa bacteria y con una historia familiar positiva. Estos ser&iacute;an marcadores &uacute;tiles para identificar individuos con alto riesgo de c&aacute;ncer g&aacute;strico y dirigir los esfuerzos para erradicar la bacteria, o darles seguimiento tendiente a detectar el c&aacute;ncer en etapa temprana.</font></font>     <br>&nbsp;     <p><b><i><font face="Arial"><font size=-1>Dieta</font></font></i></b>     <p><font face="Arial"><font size=-1>La conclusi&oacute;n m&aacute;s consistente sobre el v&iacute;nculo entre la dieta y el c&aacute;ncer g&aacute;strico, ha sido que las dietas altas en vegetales frescos y frutas reducen el riesgo de c&aacute;ncer g&aacute;strico </font></font><sup><font face="Arial,Helvetica"><font size=-2>42-45</font></font></sup><font face="Arial"><font size=-1>. Esa asociaci&oacute;n est&aacute; especialmente ligada con el consumo de frutas y verduras que contienen antioxidantes. As&iacute;, la menor ingesta de ese tipo de alimentos o los niveles s&eacute;ricos bajos de</font></font>     <br><font face="Arial"><font size=-1>beta-carotenos, tocoferoles, y vitamina C, est&aacute;n correla-cionados con la aparici&oacute;n del c&aacute;ncer g&aacute;strico </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#46">46-48</a></font></font></sup><font face="Arial"><font size=-1>. Sin embargo, las frutas contienen otras sustancias junto con las mencionadas, que pueden ser, por s&iacute; mismas, relevantes en la prevenci&oacute;n del c&aacute;ncer. Recientemente, varios estudios han encontrado que el consumo de vegetales del g&eacute;nero Allium, especialmente el ajo, disminuyen el riesgo de c&aacute;ncer g&aacute;strico </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#49">49</a>, <a href="#50">50</a></font></font></sup><font face="Arial"><font size=-1>. Pero, el consumo de alimentos salados, ahumados, picantes y aquellos que contienen nitrosaminas esta asociado a un mayor riesgo de padecer ese c&aacute;ncer </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#42">42</a>,<a href="#44">44</a>,<a href="#45">45</a>,<a href="#51">51-53</a></font></font></sup><font face="Arial"><font size=-1>. Algunos autores sostienen la hip&oacute;tesis de que los compuestos N-nitrosos, especialmente las nitrosaminas formadas end&oacute;gena, promueven la carcinog&eacute;nesis g&aacute;strica, mientras que algunos antioxidantes, p.e. el &aacute;cido asc&oacute;rbico, pueden bloquear la preparaci&oacute;n de esos compuestos </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#43">43</a>,<a href="#54">54</a></font></font></sup><font face="Arial"><font size=-1>. Adem&aacute;s, los antioxidantes podr&iacute;an frenar o hacer retroceder las lesiones precancerosas, y evitar que se desarrolle el c&aacute;ncer g&aacute;strico, al reaccionar con los radicales libres o agentes oxidantes. Sin embargo, es necesaria mayor investigaci&oacute;n, para precisar las funciones de los antioxidantes en el complejo proceso carcinog&eacute;nico</font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#12">12</a></font></font></sup><font face="Arial"><font size=-1>.</font></font>     ]]></body>
<body><![CDATA[<br>&nbsp;     <p><b><i><font face="Arial"><font size=-1>Nivel socioecon&oacute;mico</font></font></i></b>     <p><font face="Arial"><font size=-1>Se ha demostrado que la mortalidad por c&aacute;ncer g&aacute;strico est&aacute; estrechamente relacionada con las condiciones socioecon&oacute;micas en los primeros a&ntilde;os de la vida </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#55">55</a></font></font></sup><font face="Arial"><font size=-1>. Esta conclusi&oacute;n es consistente con la mayor prevalencia de infecci&oacute;n con <i>H. pylor</i>i, en la ni&ntilde;ez de poblaciones pobres.</font></font>     <br>&nbsp;     <p><b><font face="Arial"><font size=-1>Prevenci&oacute;n del c&aacute;ncer g&aacute;strico</font></font></b>     <p><font face="Arial"><font size=-1>El c&aacute;ncer g&aacute;strico tiene un mal pron&oacute;stico, en especial porque la mayor&iacute;a de los casos se diagnostican en estad&iacute;os avanzados, cuando la probabilidad de curarse es muy baja. La prevenci&oacute;n primaria de este c&aacute;ncer debe tener en cuenta la promoci&oacute;n del consumo de frutas y verduras frescas, la reducci&oacute;n del consumo de alimentos picantes, salados e irritantes y, en determinados sujetos, la erradicaci&oacute;n de <i>H. pylori</i>.</font></font>     <p><font face="Arial"><font size=-1>La administraci&oacute;n suplementaria de micronutrientes (quimioprevenci&oacute;n), para prevenir el c&aacute;ncer g&aacute;strico y otros c&aacute;nceres, ha sido contradictoria y muy cuestionada </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#56">56 - 60</a></font></font></sup><font face="Arial"><font size=-1>.</font></font>     <p><font face="Arial"><font size=-1>Algunas correlaciones encontradas con la suplementaci&oacute;n de antioxidantes, han sido menores que con alimentos, aunque parece que la vitamina C y los beta-carotenos podr&iacute;an tener alg&uacute;n impacto </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#61">61-63</a></font></font></sup><font face="Arial"><font size=-1>.</font></font>     <p><font face="Arial"><font size=-1>En las poblaciones y grupos de alto riesgo deben tomarse medidas audaces, de salud p&uacute;blica, por medio de una "intervenci&oacute;n social", promoviendo y facilitando la disponibilidad y consumo de frutas y verduras ricas en antioxidantes, desde la infancia. Adem&aacute;s, hay evidencia de que mejorando el almacenaje y el transporte de los alimentos, se mantendr&aacute;n mejor su "frescura" y el contenido de antioxidantes, contribuyendo al efecto protector </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#44">44</a></font></font></sup><font face="Arial"><font size=-1>. En poblaciones tropicales con altas tasas de c&aacute;ncer g&aacute;strico, ser&iacute;a f&aacute;cil promover la producci&oacute;n y consumo de frutas y verduras ricas en vitaminas antioxidantes (mangos, c&iacute;tricos, papayas, pejibaye, ayotes, pi&ntilde;as, etc), porque tal tipo de alimentos se produce con facilidad en esas &aacute;reas. Estas intervenciones tendr&iacute;an ventajas adicionales y podr&iacute;an ser beneficiosas, no solo para la prevenci&oacute;n de varios c&aacute;nceres, sino tambi&eacute;n para disminuir el riesgo de enfermedades card&iacute;acas, diabetes y las relacionadas con el sobrepeso.</font></font>     <p><font face="Arial"><font size=-1>Tambi&eacute;n se ha propuesto la erradicaci&oacute;n masiva de <i>H. pylori </i>para prevenir el c&aacute;ncer g&aacute;strico </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#64">64</a></font></font></sup><font face="Arial"><font size=-1>. Sin embargo, aunque combinar antibi&oacute;ticos es una buena soluci&oacute;n para tratar las patolog&iacute;as g&aacute;stricas en algunos individuos infectados por <i>H. pylori</i>, ello no representa una soluci&oacute;n definitiva. La erradicaci&oacute;n masiva de <i>H. pylori </i>para prevenir el c&aacute;ncer g&aacute;strico </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#65">65</a></font></font></sup><font face="Arial"><font size=-1>, es cuestionada por el alto costo, el riesgo de generar cepas resistentes a los antibi&oacute;ticos y por no ofrecer garant&iacute;as de erradicaci&oacute;n definitiva </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#66">66</a>,<a href="#67">67</a></font></font></sup><font face="Arial"><font size=-1>. Adem&aacute;s, no ha sido bien valorado el impacto de la erradicaci&oacute;n en las lesiones precancerosas, y es dif&iacute;cil predecir cu&aacute;ntos c&aacute;nceres se evitar&iacute;an si se erradica <i>H. pylori </i></font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#25">25</a>,<a href="#68">68</a>,<a href="#69">69</a></font></font></sup><font face="Arial"><font size=-1>. Un buen medio preventivo podr&iacute;a ser la vacunaci&oacute;n, que es la pr&aacute;ctica m&eacute;dica m&aacute;s efectiva para controlar una infecci&oacute;n en la escala global. En todo caso, todav&iacute;a no se ha aprobado una vacuna, para los humanos, contra esa bacteria </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#70">70</a></font></font></sup><font face="Arial"><font size=-1>. Mientras aparece una vacuna adecuada, se han elaborado criterios que establecen, seg&uacute;n las diferentes poblaciones, cu&aacute;les son los sujetos que deben recibir tratamiento </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#61">61</a>,<a href="#71">71-75</a></font></font></sup><font face="Arial"><font size=-1>. Adem&aacute;s, los recientes aportes de El-Omar y colaboradores ( 2000 y 2001), en relaci&oacute;n con los polimorfismos gen&eacute;ticos del hospedero con mayor riesgo de desarrollar c&aacute;ncer, podr&iacute;an orientar a&uacute;n m&aacute;s sobre los sujetos infectados que deber&iacute;an recibir tratamiento contra la bacteria </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#31">31</a>,<a href="#41">41</a></font></font></sup><font face="Arial"><font size=-1>.</font></font>     ]]></body>
<body><![CDATA[<p><font face="Arial"><font size=-1>Es importante considerar que para prevenir el c&aacute;ncer g&aacute;strico, posiblemente no ser&aacute; suficiente eliminar un s&oacute;lo factor de riesgo, porque el c&aacute;ncer g&aacute;strico ocurre a trav&eacute;s de un proceso multifactorial y con diferentes estadios. Para elaborar e implementar un programa de prevenci&oacute;n, ser&aacute; necesaria la participaci&oacute;n de un grupo multidisciplinario de cient&iacute;ficos y cl&iacute;nicos que enfrenten el problema de una forma integral.</font></font>     <br>&nbsp;     <p><b><font face="Arial"><font size=-1>Detecci&oacute;n temprana</font></font></b>     <p><font face="Arial"><font size=-1>Los programas de detecci&oacute;n se basan en el supuesto de que el c&aacute;ncer temprano (aquel que est&aacute; circunscrito a la mucosa y submucosa), si no se trata, puede progresar a c&aacute;ncer avanzado, y luego a la muerte del paciente.</font></font>     <p><font face="Arial"><font size=-1>En Jap&oacute;n, donde el c&aacute;ncer g&aacute;strico es un problema importante de salud p&uacute;blica, se han implantado programas masivos de detecci&oacute;n temprana, por medio de fotofluorograf&iacute;a. Los pacientes sospechosos de presentar una lesi&oacute;n cancerosa detectados por Rayos X, se someten a una gastroscop&iacute;a y biopsia. Los casos con c&aacute;ncer se someten a una cirug&iacute;a. Esos programas han tenido un &eacute;xito reconocido ah&iacute; </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#76">76-78</a></font></font></sup><font face="Arial"><font size=-1>, pero, se ha cuestionado la baja especificidad del m&eacute;todo y su costo-efectividad. Es un proceso caro porque requiere de un grupo de m&eacute;dicos y t&eacute;cnicos especializados y de equipos de alta tecnolog&iacute;a </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#79">79-81</a></font></font></sup><font face="Arial"><font size=-1>. Adem&aacute;s, ese sistema debe ser adaptado a las circunstancias socioecon&oacute;micas y culturales de los pa&iacute;ses o grupos donde se trata de instalar </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#82">82</a></font></font></sup><font face="Arial"><font size=-1>. Es importante hacer &eacute;nfasis en la necesidad de que los programas de detecci&oacute;n sean econ&oacute;micos, simples y efectivos </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#83">83</a></font></font></sup><font face="Arial"><font size=-1>, especialmente para pa&iacute;ses pobres, con altas tasas de c&aacute;ncer g&aacute;strico. Algunos han cuestionado si todos los c&aacute;nceres tempranos finalizan en c&aacute;ncer invasor </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#84">84</a></font></font></sup><font face="Arial"><font size=-1>, por lo cual es importante determinar el impacto de los programas de detecci&oacute;n en las tasas de mortalidad por este tipo de c&aacute;ncer.</font></font>     <p><font face="Arial"><font size=-1>Hace poco tiempo, se introdujo en Jap&oacute;n la prueba de pepsin&oacute;genos s&eacute;ricos, se basa en que los niveles de pepsin&oacute;genos I y II (PG I y PG II) en suero reflejan el estadofuncional y morfol&oacute;gico de la mucosa g&aacute;strica </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#85">85</a>,<a href="#86">86</a></font></font></sup><font face="Arial"><font size=-1>. Varios estudios muestran que valores bajos de la raz&oacute;n PGI/PG II significan alto riesgo de gastritis cr&oacute;nica atr&oacute;fica y c&aacute;ncer g&aacute;strico, y la determinaci&oacute;n de estos niveles puede ser usada como un m&eacute;todo de tamizaje para esas patolog&iacute;as</font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#87">87-91</a></font></font></sup><font face="Arial"><font size=-1>. El sistema tiene muchas ventajas, porque es sencillo y barato, aunque antes de usarlo masivamente, se deben determinar, en la poblaci&oacute;n donde se va a emplear, los puntos de corte (cut off ) de los niveles s&eacute;ricos de PGs I y II, que discriminan las diferentes lesiones precancerosas y c&aacute;ncer. Despu&eacute;s ser&iacute;a necesario evaluar el impacto del programa que usa estos marcadores, en las tasas de mortalidad por c&aacute;ncer g&aacute;strico. Se ha demostrado que la sensibilidad de la detecci&oacute;n masiva se incrementa cuando se combinan la determinaci&oacute;n de los niveles de PGs s&eacute;ricos con la serie gastroduodenal de doble contraste </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#80">80</a></font></font></sup><font face="Arial"><font size=-1>. Muchas personas participar&iacute;an con mayor inter&eacute;s, en los programas de detecci&oacute;n, si los resultados de una prueba de sangre indican que son sujetos de alto riesgo de c&aacute;ncer g&aacute;strico </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#92">92</a></font></font></sup><font face="Arial"><font size=-1>. La identificaci&oacute;n de grupos de alto riesgo, por la historia familiar marcadores biol&oacute;gicos, podr&iacute;a disminuir el costo y mejorar la efectividad del m&eacute;todo de detecci&oacute;n de c&aacute;ncer g&aacute;strico.</font></font>     <p><font face="Arial"><font size=-1>En T&aacute;chira, Venezuela, se encontr&oacute; que la detecci&oacute;n temprana de c&aacute;ncer g&aacute;strico, de acuerdo con el modelo japon&eacute;s tradicional, tuvo un efecto protector y disminuy&oacute; la mortalidad por c&aacute;ncer g&aacute;strico, en el grupo tamizado </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#93">93-94</a></font></font></sup><font face="Arial"><font size=-1>.</font></font>     <p><font face="Arial"><font size=-1>Costa Rica es uno de los pa&iacute;ses con mayores tasas de inicidencia y mortalidad por c&aacute;ncer g&aacute;strico. En el per&iacute;odo 1995-2000, se llev&oacute; a cabo un programa piloto de detecci&oacute;n temprana, en una muestra de alto riesgo (Hospital Max Peralta), con la colaboraci&oacute;n de Jap&oacute;n </font></font><sup><font face="Arial,Helvetica"><font size=-2><a href="#95">95</a></font></font></sup><font face="Arial"><font size=-1>. Actualmente, nuestro equipo est&aacute; llevando a cabo un estudio epidemiol&oacute;gico basado en la informaci&oacute;n generada por ese programa. Tambi&eacute;n se est&aacute; evaluando el costo-efectividad del mismo, con el fin de elaborar alternativas para mejorarlo e investigamos marcadores de lesiones g&aacute;stricas precancerosas y c&aacute;ncer (pepsin&oacute;genos s&eacute;ricos I y II) y factores gen&eacute;ticos (polimorfismos de interleucinas), as&iacute; como las diferentes cepas de H. pylori en la poblaci&oacute;n costarricense (Hospital Max Peralta, Hospital Calder&oacute;n Guardia). Se trata de encontrar marcadores biol&oacute;gicos para identificar a los sujetos y grupos con mayor riesgo de c&aacute;ncer g&aacute;strico en el pa&iacute;s, y determinar el m&eacute;todo m&aacute;s adecuado para darles seguimiento o para tratarlos. El objetivo final es encontrar un sistema de detecci&oacute;n adecuado al contexto socioecon&oacute;mico y cultural de Costa Rica, con el fin de disminuir significativamente la mortalidad por ese tumor.</font></font>     <br>&nbsp;     <p><b><font face="Arial"><font size=-1>Agradecimientos</font></font></b>     ]]></body>
<body><![CDATA[<p><font face="Arial"><font size=-1>Agradezco a los Drs. J. Jaramillo, C. A. P&aacute;ez, C. Une, L. Lang y F. Garc&iacute;a, la revisi&oacute;n del art&iacute;culo, y el apoyo de la Vicerrector&iacute;a de Investigaci&oacute;n de la Universidad de Costa Rica, al Programa Epidemiolog&iacute;a de C&aacute;ncer.</font></font>     <p><b><font face="Arial"><font size=-1>Abstract</font></font></b>     <p><font face="Arial"><font size=-1>Gastric cancer is one of the tumors with higher worldwide mortality. Although the incidence rate has been declining, it is still a major public health problem still. Epidemiological information and knowledge about this cancer is abundant. This is an up to date review about commonly accepted risk factors: Helicobacter pylori infection, diet, genetic predisposition and socioeconomic status. We also stress the new questions and challenges that recent discoveries about this pathology entail. The ways to tackle this cancer are discussed using X rays and biological markers such as serum pepsinogens in high risk groups or populations.</font></font>     <br>&nbsp;     <p><b><font face="Arial"><font size=-1>Referencias</font></font></b>     <!-- ref --><p><a NAME="1"></a><font face="Arial"><font size=-1>1. Coleman M.P, Esteve J, Damiecki P, Arslan A, Renard H. Trends in Cancer Incidence and Mortalily. Lyon, 1993: International Agency for Research on Cancer, (IARC/WHO).</font></font>    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=009076&pid=S0001-6002200200020000300001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><!-- ref --><p><a NAME="2"></a><font face="Arial"><font size=-1>2. Parkin DM, Pisani P, Ferlay J. Estimates of the worldwide incidence of 25 major cancers in 1990. 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