<?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>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>S1688-04202005000300004</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Factores asociados con enfermedad valvular aórtica en pacientes con falla renal]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[TAVELLA]]></surname>
<given-names><![CDATA[NORBERTO]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[VENTURA]]></surname>
<given-names><![CDATA[JOSé]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[ROMERO]]></surname>
<given-names><![CDATA[CARLOS]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[PETRAGLIA]]></surname>
<given-names><![CDATA[ALICIA]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[BáEZ]]></surname>
<given-names><![CDATA[ÁLVARO]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[MUñOZ]]></surname>
<given-names><![CDATA[LEóN]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[OLASCOAGA]]></surname>
<given-names><![CDATA[ALICIA]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[ALALLóN]]></surname>
<given-names><![CDATA[WALTER]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Hospital de Clínicas Departamento de Cardiología ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A02">
<institution><![CDATA[,Servicio de Asistencia Renal Integral  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A03">
<institution><![CDATA[,Hospital de Clínicas. Departamento de Laboratorio Clínico ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>11</month>
<year>2005</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>11</month>
<year>2005</year>
</pub-date>
<volume>20</volume>
<numero>3</numero>
<fpage>150</fpage>
<lpage>157</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_arttext&amp;pid=S1688-04202005000300004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_abstract&amp;pid=S1688-04202005000300004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_pdf&amp;pid=S1688-04202005000300004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN La frecuencia de estenosis valvular aórtica en pacientes con falla renal es mayor que en la población general, lo que sugiere la presencia de mecanismos patogénicos acelerados o diferentes. En 135 pacientes con falla renal en tratamiento dialítico estudiamos las prevalencias de fibrosis y estenosis valvular aórtica y los factores presuntamente asociados con ella. Los datos clínicos y de laboratorio se obtuvieron de los registros de diálisis, en todos se hizo un ecocardiograma Doppler y se calculó el gradiente transvalvular aórtico y el índice de masa ventricular izquierda (IMVI). En 116 pacientes dosificamos colesterol total (CT), triglicéridos, HDL-colesterol, apolipoproteína A1 y B y lipoproteína (a); se calculó el LDL-colesterol, relación CT/HDL-colesterol, y el índice apo B/apo A1. La frecuencia de fibrosis (72%) y estenosis (6%) valvular aórtica fue más del doble que la conocida en la población general. El análisis multivariado mostró una asociación independiente de la patología valvular aórtica con la edad (p<0,0005), diabetes mellitus (p=0,013) y tiempo en diálisis (p=0,013). Concentraciones de CT mayores de 200 mg/dL se asociaron con patología valvular aórtica (p<0,004). La valvulopatía no mostró asociación con tabaquismo, hipertensión arterial o alteraciones fosfo-cálcicas. Comparadas con las normales, las válvulas con fibrosis tuvieron mayor valor de velocidad máxima (p<0,01), gradiente transvalvular (p=0,005) e IMVI (p=0,005). La alta frecuencia de enfermedad valvular aórtica en diálisis sugiere que los pacientes con falla renal presentan factores que favorecen su aparición; los cuatro factores independientes que identificamos: edad, diabetes mellitus, tiempo en diálisis e hipercolesterolemia se asocian también tradicionalmente con la aterosclerosis. Los aumentos de gradiente transvalvular y de IMVI en la fibrosis valvular aórtica señalan la presencia de alteraciones funcionales y morfológicas en etapas previas a la estenosis aórtica.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[SUMMARY The prevalence of aortic valve stenosis in renal failure patients is higher than the observed in general population, suggesting accelerated or different pathogenic mechanisms. We studied the prevalence of aortic valve fibrosis and stenosis in 135 renal failure patients on maintenance dialysis, and the possible associated factors. Clinical and laboratory data were collected from dialysis registers; a cardiac echo-Doppler study was performed in all patients and the aortic transvalvular gradient and left ventricle mass index were calculated (LVMI). We measured total cholesterol (TC), triglycerides, HDL-cholesterol, apolipoprotein A1 and B and lipoprotein (a) in 116 patients; LDL-cholesterol, TC/HDL-cholesterol, and apo B/apo A1 ratio were calculated. The frequencies of aortic valve fibrosis (72%) and stenosis (6%) were more than double than in general population. An independent association of aortic valve disease with age (p<0,0005), diabetes mellitus (p=0,013), and time on dialysis (vintage) (p=0,013), was demonstrated by multivariate analysis. TC concentrations higher than 200 mg/dL were associated with aortic valve disease (p<0,004). There was no association with smoking, hypertension or phospho-calcium alterations. Compared to normal, fibrotic valves had higher values of maximal velocity (p<0,01), transvalvular gradient (p=0,005) and LVMI (p=0,005). The high prevalence of aortic valve disease in dialysis patients suggests that renal failure is a predisposing condition; the four independent factors that we recognized: age, diabetes mellitus, time on dialysis and hypercholesterolemia, are also traditionally associated with atherosclerosis. Higher transvalvular gradients and LVMI values suggest the presence of functional and morphologic alterations prior to aortic stenosis.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[ESTENOSIS DE LA VáLVULA AóRTICA]]></kwd>
<kwd lng="es"><![CDATA[FIBROSIS]]></kwd>
<kwd lng="es"><![CDATA[FACTORES EPIDEMIOLóGICOS]]></kwd>
<kwd lng="es"><![CDATA[INFORME DE CASO]]></kwd>
<kwd lng="en"><![CDATA[AORTIC VALVE STENOSIS]]></kwd>
<kwd lng="en"><![CDATA[FIBROSIS]]></kwd>
<kwd lng="en"><![CDATA[EPIDEMIOLOGIC FACTORS]]></kwd>
<kwd lng="en"><![CDATA[CASE REPORT]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="left"><font color="#1f1a17" face="Verdana" size="2"><span style="text-transform: uppercase;">ART&iacute;CULO</span> ORIGINAL</font></p>              <p align="left"><font color="#ffffff" face="Verdana" size="2">    <br>  Dres. Norberto Tavella, Jos&eacute; Ventura, Carlos Romero y colaboradores&nbsp;</font></p>              <p align="left"><b><font color="#1f1a17" face="Verdana" size="4">Factores asociados con enfermedad valvular a&oacute;rtica en pacientes con falla renal </font></b></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2"><span style="text-transform: uppercase;"> DRES. NORBERTO TAVELLA <a name="-1"></a></span></font><a href="#1"> <font color="#1f1a17" face="Verdana" size="2"><sup>1</sup></font></a><font color="#1f1a17" face="Verdana" size="2">, JOS&eacute; VENTURA <sup><a name="-2"></a></sup> </font><a href="#2"> <font color="#1f1a17" face="Verdana" size="2"><sup>2</sup></font></a><font color="#1f1a17" face="Verdana" size="2">, CARLOS ROMERO </font><a href="#1"> <font color="#1f1a17" face="Verdana" size="2"><sup>1</sup></font></a><font color="#1f1a17" face="Verdana" size="2">, ALICIA PETRAGLIA </font><a href="#2"><font color="#1f1a17" face="Verdana" size="2"><sup>2</sup></font></a><font color="#1f1a17" face="Verdana" size="2">,     <br>         &Aacute;LVARO B&aacute;EZ </font><a href="#1"> <font color="#1f1a17" face="Verdana" size="2"><sup>1</sup></font></a><font color="#1f1a17" face="Verdana" size="2">, LE&oacute;N MU&ntilde;OZ </font><a href="#1"> <font color="#1f1a17" face="Verdana" size="2"><sup>1</sup></font></a><font color="#1f1a17" face="Verdana" size="2">, ALICIA OLASCOAGA <sup><a name="-3"></a></sup> </font><a href="#3"> <font color="#1f1a17" face="Verdana" size="2"><sup>3</sup></font></a><font color="#1f1a17" face="Verdana" size="2">, WALTER ALALL&oacute;N </font><a href="#3"> <font color="#1f1a17" face="Verdana" size="2"><sup>3</sup></font></a><font color="#1f1a17" face="Verdana" size="2"> </font></p>              <p><font color="#1f1a17" face="Verdana" size="2"><a name="1"></a> <a href="#-1">1</a>. Departamento de Cardiolog&iacute;a. Hospital de Cl&iacute;nicas.    <br>   <a name="2"></a>      <a href="#-2">2</a>. Servicio de Asistencia Renal Integral (SARI).    <br>   <a name="3"></a>      <a href="#-3">3</a>. Departamento de Laboratorio Cl&iacute;nico. Hospital de Cl&iacute;nicas.</font><font face="Verdana" size="2">    <br>         </font>         </p>              ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2"><b>RESUMEN</b> </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">La frecuencia de estenosis valvular a&oacute;rtica en pacientes con falla renal es mayor que en la poblaci&oacute;n general, lo que sugiere la presencia de mecanismos patog&eacute;nicos acelerados o diferentes.    <br>         En 135 pacientes con falla renal en tratamiento dial&iacute;tico estudiamos las prevalencias de fibrosis y estenosis valvular a&oacute;rtica y los factores presuntamente asociados con ella. Los datos cl&iacute;nicos y de laboratorio se obtuvieron de los registros de di&aacute;lisis, en todos se hizo un ecocardiograma Doppler y se calcul&oacute; el gradiente transvalvular a&oacute;rtico y el &iacute;ndice de masa ventricular izquierda (IMVI). En 116 pacientes dosificamos colesterol total (CT), triglic&eacute;ridos, HDL-colesterol, apolipoprote&iacute;na A1 y B y lipoprote&iacute;na (a); se calcul&oacute; el LDL-colesterol, relaci&oacute;n CT/HDL-colesterol, y el &iacute;ndice apo B/apo A1.    <br>         La frecuencia de fibrosis (72%) y estenosis (6%) valvular a&oacute;rtica fue m&aacute;s del doble que la conocida en la poblaci&oacute;n general. El an&aacute;lisis multivariado mostr&oacute; una asociaci&oacute;n independiente de la patolog&iacute;a valvular a&oacute;rtica con la edad (p&lt;0,0005), diabetes mellitus (p=0,013) y tiempo en di&aacute;lisis (p=0,013). Concentraciones de CT mayores de 200 mg/dL se asociaron con patolog&iacute;a valvular a&oacute;rtica (p&lt;0,004). La valvulopat&iacute;a no mostr&oacute; asociaci&oacute;n con tabaquismo, hipertensi&oacute;n arterial o alteraciones fosfo-c&aacute;lcicas. Comparadas con las normales, las v&aacute;lvulas con fibrosis tuvieron mayor valor de velocidad m&aacute;xima (p&lt;0,01), gradiente transvalvular (p=0,005) e IMVI (p=0,005).    <br>         La alta frecuencia de enfermedad valvular a&oacute;rtica en di&aacute;lisis sugiere que los pacientes con falla renal presentan factores que favorecen su aparici&oacute;n; los cuatro factores independientes que identificamos: edad, diabetes mellitus, tiempo en di&aacute;lisis e hipercolesterolemia se asocian tambi&eacute;n tradicionalmente con la aterosclerosis.    <br>         Los aumentos de gradiente transvalvular y de IMVI en la fibrosis valvular a&oacute;rtica se&ntilde;alan la presencia de alteraciones funcionales y morfol&oacute;gicas en etapas previas a la estenosis a&oacute;rtica. </font></p>              <p align="left"><font color="#000000" face="Verdana" size="2">PALABRAS CLAVE:</font><font color="#1f1a17" face="Verdana" size="2">&nbsp;&nbsp;&nbsp;&nbsp;<span style="text-transform: uppercase;">ESTENOSIS DE LA V&aacute;LVULA A&oacute;RTICA    <br>         &nbsp;&nbsp;&nbsp;&nbsp;FIBROSIS    <br>         &nbsp;&nbsp;&nbsp;&nbsp;FACTORES EPIDEMIOL&oacute;GICOS    <br>         &nbsp;&nbsp;&nbsp;&nbsp;INFORME DE CASO</span></font></p>              ]]></body>
<body><![CDATA[<p align="left">&nbsp;</p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2"><b>SUMMARY</b> </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">The prevalence of aortic valve stenosis in renal failure patients is higher than the observed in general population, suggesting accelerated or different pathogenic mechanisms.    <br>         We studied the prevalence of aortic valve fibrosis and stenosis in 135 renal failure patients on maintenance dialysis, and the possible associated factors.    <br>         Clinical and laboratory data were collected from dialysis registers; a cardiac echo-Doppler study was performed in all patients and the aortic transvalvular gradient and left ventricle mass index were calculated (LVMI). We measured total cholesterol (TC), triglycerides, HDL-cholesterol, apolipoprotein A1 and B and lipoprotein (a) in 116 patients; LDL-cholesterol, TC/HDL-cholesterol, and apo B/apo A1 ratio were calculated.    <br>         The frequencies of aortic valve fibrosis (72%) and stenosis (6%) were more than double than in general population. An independent association of aortic valve disease with age (p&lt;0,0005), diabetes mellitus (p=0,013), and time on dialysis (vintage) (p=0,013), was demonstrated by multivariate analysis.     <br>         TC concentrations higher than 200 mg/dL were associated with aortic valve disease (p&lt;0,004). There was no association with smoking, hypertension or phospho-calcium alterations. Compared to normal, fibrotic valves had higher values of maximal velocity (p&lt;0,01), transvalvular gradient (p=0,005) and LVMI (p=0,005). The high prevalence of aortic valve disease in dialysis patients suggests that renal failure is a predisposing condition; the four independent factors that we recognized: age, diabetes mellitus, time on dialysis and hypercholesterolemia, are also traditionally associated with atherosclerosis. Higher transvalvular gradients and LVMI values suggest the presence of functional and morphologic alterations prior to aortic stenosis. </font></p>              <p align="left"><font color="#000000" face="Verdana" size="2">KEY WORDS:&nbsp;&nbsp;&nbsp;&nbsp;AORTIC VALVE STENOSIS</font><font color="#1f1a17" face="Verdana" size="2"> </font> <font color="#000000" face="Verdana" size="2">&nbsp;FIBROSIS    <br>         &nbsp;&nbsp;&nbsp;&nbsp;EPIDEMIOLOGIC FACTORS    <br>         &nbsp;&nbsp;&nbsp;&nbsp;CASE REPORT</font><font color="#1f1a17" face="Verdana" size="2"> </font></p>              ]]></body>
<body><![CDATA[<p align="left">&nbsp;</p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2"><b><span style="text-transform: uppercase;">INTRODUCCI&oacute;N</span></b></font><font face="Verdana" size="2"> </font> </p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">La estenosis a&oacute;rtica calcificada no reum&aacute;tica, asentando en v&aacute;lvulas a&oacute;rticas tric&uacute;spides, constituye actualmente la forma anat&oacute;mica m&aacute;s frecuente de esta enfermedad <sup><a name="1.-"></a><a name="2.-"></a><a name="3.-"></a><a name="4.-"></a>(<a href="#1.">1</a>-<a href="#4.">4</a>)</sup>. Ya no se acepta que se trate de una patolog&iacute;a &ldquo;degenerativa&rdquo; vinculada a la edad, sino que es un proceso activo de naturaleza inflamatoria con una anatom&iacute;a patol&oacute;gica similar a la de la aterosclerosis <a name="5.-"></a><a name="6.-"></a><a name="7.-"></a><a name="8.-"></a><a name="9.-"></a><a name="10.-"></a><a name="11.-"></a><a name="12.-"></a><sup>(<a href="#4.">4</a>-<a href="#12.">12</a>)</sup>. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">La fibrosis valvular a&oacute;rtica (diagnosticada por ecocardiograf&iacute;a) tiene alteraciones anat&oacute;micas iguales a las que se comprueban en la estenosis a&oacute;rtica constituida, por lo que se consideran como diferentes etapas del mismo proceso <sup><a name="13.-"></a>(<a href="#8.">8</a>,<a href="#13.">13</a>)</sup>. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">Se ha<i> </i>identificado la existencia de factores de riesgo para la estenosis a&oacute;rtica similares a los de la aterosclerosis, tales como el sexo masculino, la edad, la hipercolesterolemia, el LDL-colesterol y la lipoprote&iacute;na(a) elevados, el valor bajo de HDL-colesterol, la historia de hipertensi&oacute;n arterial, el tabaquismo y la diabetes<a name="14.-"></a><a name="15.-"></a><a name="16.-"></a><a name="17.-"></a> <sup>(<a href="#14.">14</a>-<a href="#17.">17</a>)</sup>. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">En los pacientes con falla renal la incidencia y prevalencia de estenosis a&oacute;rtica es mayor que en la poblaci&oacute;n normal, lo que sugiere procesos patog&eacute;nicos que pueden ser cualitativa o cuantitativamente diferentes <sup><a name="18.-"></a><a name="19.-"></a><a name="20.-"></a><a name="21.-"></a>(<a href="#18.">18</a>-<a href="#21.">21</a>)</sup>. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">En este trabajo nos propusimos estudiar la frecuencia de estenosis y fibrosis valvular a&oacute;rticas en una poblaci&oacute;n con falla renal y los factores asociados con ellas. </font></p>              <p><font face="Verdana" size="2">    <br>         </font>         </p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2"><b>MATERIAL Y <span style="text-transform: uppercase;"> M&eacute;TODO</span></b></font><font face="Verdana" size="2"> </font> </p>              ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">Se estudiaron todos los pacientes de tres centros de di&aacute;lisis (n=135) de Montevideo, con m&aacute;s de seis meses de tratamiento hemodial&iacute;tico. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">Las caracter&iacute;sticas de la poblaci&oacute;n se muestran en la <a href="#tabla1">tabla 1</a>. Se consideraron diab&eacute;ticos a los pacientes diagnosticados y tratados como tales por el nefr&oacute;logo actuante. </font></p>              <p align="left"><font color="#000000" face="Verdana" size="2">    <br>   </font></p>        <font face="Verdana" size="2">        <a name="tabla1"></a><img style="width: 287px; height: 185px;" alt="" src="/img/revistas/ruc/v20n3/3a04t1.JPG">    <br>        </font>            <p align="left">&nbsp;</p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">DATOS DE LA <span style="text-transform: uppercase;">DI&aacute;LISIS</span></font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">Se obtuvieron datos de los controles cl&iacute;nicos y humorales de los registros m&eacute;dicos. En cada paciente se calcularon los valores medios anuales de la presi&oacute;n arterial sist&oacute;lica (PAS) y diast&oacute;lica (PAD) medidas antes de cada sesi&oacute;n de di&aacute;lisis, el peso corporal antes y despu&eacute;s de cada di&aacute;lisis, azoemia, potasio, calcio y f&oacute;sforo plasm&aacute;ticos, hematocrito y hemoglobina, registrados en el a&ntilde;o anterior al estudio ecocardiogr&aacute;fico. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">El peso seco, considerado como la medida del peso corporal sin exceso de agua, fue el establecido por los nefr&oacute;logos tratantes. Con este valor se calcul&oacute; la sobrehidrataci&oacute;n m&aacute;xima (peso predi&aacute;lisis-peso seco) y la sobrehidrataci&oacute;n residual al fin de la di&aacute;lisis (peso posdi&aacute;lisis-peso seco). El porcentaje de reducci&oacute;n de urea (PRU), obtenido seg&uacute;n la f&oacute;rmula: 1 &ndash; (azoemia posdi&aacute;lisis / azoemia predi&aacute;lisis), se us&oacute; para estimar la eficiencia del tratamiento dial&iacute;tico. La superficie corporal se calcul&oacute; por la f&oacute;rmula de Dubois y Dubois. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">La PAD se defini&oacute; por la fase V de Korotkoff, la presi&oacute;n arterial media (PAM) se calcul&oacute;: PAM = PAD + 1/3 (PAS-PAD). </font></p>              ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">ESTUDIO <span style="text-transform: uppercase;">ECOCARDIOGR&aacute;FICO</span></font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">El ecocardiograma se realiz&oacute; al final de una sesi&oacute;n de di&aacute;lisis para evitar potenciales modificaciones atribuibles a la ganancia de l&iacute;quido entre las di&aacute;lisis. Se obtuvieron cortes est&aacute;ndar paraesternales izquierdos (eje largo y eje corto), cuatro y dos c&aacute;maras desde el &aacute;pex y cuatro c&aacute;maras subcostal, en las modalidades M, bidimensional y Doppler. Las medidas se realizaron seg&uacute;n las recomendaciones de la American Society of Echocardiography <a name="22.-"></a><sup>(<a href="#22.">22</a>)</sup>. Se midi&oacute; la velocidad m&aacute;xima del flujo en la v&aacute;lvula a&oacute;rtica y a partir de ella se calcul&oacute; el gradiente m&aacute;ximo de presi&oacute;n transvalvular. Se registr&oacute; la presi&oacute;n arterial en el momento de la ecograf&iacute;a. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">Para el c&aacute;lculo de masa card&iacute;aca se utiliz&oacute; la f&oacute;rmula de Devereux <a name="23.-"></a><sup>(<a href="#23.">23</a>)</sup>: masa ventricular izquierda (g) = 1,04 (SIVD + DDVI + PPD)<sup>3</sup> &ndash; DDVI<sup>3</sup> &ndash; 13,6, siendo SIVD el espesor del s&eacute;ptum interventricular en di&aacute;stole, DDVI el di&aacute;metro diast&oacute;lico del ventr&iacute;culo izquierdo y PPD la pared posterior del ventr&iacute;culo izquierdo en di&aacute;stole, medidos en cm. El &iacute;ndice de masa se calcul&oacute; dividiendo la masa ventricular izquierda entre la superficie corporal. Se consideraron normales los &iacute;ndices de masa inferiores a 137 g/m<sup> 2</sup> en el hombre y 112 g/m<sup>2</sup> en la mujer. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">En la v&aacute;lvula a&oacute;rtica se estudi&oacute; el<sub> </sub>aspecto ecogr&aacute;fico por modo bidimensional, la velocidad m&aacute;xima de flujo a nivel valvular y el gradiente m&aacute;ximo de presi&oacute;n transvalvular. La v&aacute;lvula fue clasificada como: 1) normal, 2) fibrosada (cuando se observ&oacute; aumento de la ecogenicidad y del espesor sin restricci&oacute;n del movimiento y con una velocidad m&aacute;xima menor de 2,5 m/s), o 3) esten&oacute;tica (por engrosamiento de las valvas con reducci&oacute;n de la apertura sist&oacute;lica y velocidad m&aacute;xima anter&oacute;grada &sup3; 2,5 m/s) <a name="24.-"></a><sup>(<a href="#24.">24</a>)</sup>. Dos ecocardiografistas realizaron los registros que se grabaron en VHS y fueron revisados por otro cardi&oacute;logo (CR) que desconoc&iacute;a los valores del estudio original. Se us&oacute; un ecocardi&oacute;grafo ATL, modelo HDI 3000, con transductor de 2,5 MHz. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">ESTUDIO DEL METABOLISMO <span style="text-transform: uppercase;">LIP&iacute;DICO</span></font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">Se realiz&oacute; en 116 pacientes, a quienes se extrajo sangre luego de 9-12 horas de ayuno, como establece el 2&ordm; Consenso Uruguayo de Dislipidemias <a name="25.-"></a><sup>(<a href="#25.">25</a>)</sup>. Las muestras fueron de sangre venosa separando el suero por centrifugaci&oacute;n, conserv&aacute;ndolo a -20&deg;C hasta su procesamiento en un per&iacute;odo no mayor a 30 d&iacute;as. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">Todas las determinaciones fueron realizadas en un multianalizador BM Hitachi 911, emple&aacute;ndose reactivos, calibradores y controles de la firma Boehringer Manheim. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">A todas las muestras se les realiz&oacute;: </font></p>          <ul>                 <li><font color="#1f1a17" face="Verdana" size="2">dosificaci&oacute;n         de CT por t&eacute;cnica enzim&aacute;tica <a name="26.-"></a><a name="27.-"></a><sup>(<a href="#26.">26</a>,<a href="#27.">27</a>)</sup>; </font></li>                 <li><font color="#1f1a17" face="Verdana" size="2">dosificaci&oacute;n         de triglic&eacute;ridos por t&eacute;cnica enzim&aacute;tica <sup>(<a href="#26.">26</a>,<a href="#27.">27</a>)</sup>; </font></li>                 ]]></body>
<body><![CDATA[<li><font color="#1f1a17" face="Verdana" size="2">dosificaci&oacute;n         de HDL-colesterol por t&eacute;cnica directa con         polietilenglicol <a name="28.-"></a><sup>(<a href="#28.">28</a>)</sup>; </font></li>                 <li><font color="#1f1a17" face="Verdana" size="2">c&aacute;lculo         de LDL-colesterol de acuerdo a la f&oacute;rmula de Friedewald <a name="29.-"></a><sup>(<a href="#29.">29</a>)</sup>; </font></li>                 <li><font color="#1f1a17" face="Verdana" size="2">c&aacute;lculo         de &iacute;ndice CT/HDL-colesterol <a name="30.-"></a><sup>(<a href="#30.">30</a>)</sup>; </font></li>                 <li><font color="#1f1a17" face="Verdana" size="2">dosificaci&oacute;n         de apolipoprote&iacute;na A1 y B por m&eacute;todos         inmuno-turbidim&eacute;tricos <a name="31.-"></a><sup>(<a href="#31.">31</a>)</sup>; </font></li>                 <li><font color="#1f1a17" face="Verdana" size="2">c&aacute;lculo         del &iacute;ndice Apo B/Apo A1; </font></li>                 <li><font color="#1f1a17" face="Verdana" size="2">dosificaci&oacute;n         de lipoprote&iacute;na (a) por t&eacute;cnica inmunoturbidim&eacute;trica <sup>(<a href="#31.">31</a>)</sup>. </font></li>             </ul>              <p align="left"><font color="#1f1a17" face="Verdana" size="2"><span style="text-transform: uppercase;"> M&eacute;TODOS</span> ESTAD&iacute;STICOS </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">Se utilizaron la media y el desv&iacute;o est&aacute;ndar como variables descriptivas y la correlaci&oacute;n de Pearson de primer grado y la regresi&oacute;n lineal m&uacute;ltiple para medir el grado de asociaci&oacute;n entre las variables. Las comparaciones entre los valores se hicieron con el test de t para muestras no pareadas. En todos los casos se exigi&oacute; un nivel de 5% de significaci&oacute;n. Se utiliz&oacute; el programa SPSS 10.0 para el procesamiento de los datos. </font></p>              <p><font face="Verdana" size="2">&nbsp; </font> </p>              ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2"><b>RESULTADOS</b> </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">La v&aacute;lvula a&oacute;rtica se encontr&oacute; fibrocalcificada en 97 casos (72%), estenosada en 8 (6%) y fue normal en 30 casos (22%). </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">La edad, el tiempo en di&aacute;lisis y la frecuencia de diabetes fueron significativamente mayores entre los pacientes con valvulopat&iacute;a a&oacute;rtica que en el grupo normal (<a href="#tabla2">tabla 2</a>). </font></p>              <p align="left">&nbsp;</p>        <font face="Verdana" size="2">        <a name="tabla2"></a><img style="width: 488px; height: 480px;" alt="" src="/img/revistas/ruc/v20n3/3a04t2.JPG">    <br>          </font>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">La frecuencia de fibrocalcificaci&oacute;n (con o sin estenosis a&oacute;rtica) se asoci&oacute; con edad mayor de 65 a&ntilde;os (p=0,001) (<a href="#tabla3">tabla 3</a>). </font></p>              <p align="left">&nbsp;</p>        <font face="Verdana" size="2">        <a name="tabla3"></a><img style="width: 287px; height: 119px;" alt="" src="/img/revistas/ruc/v20n3/3a04t3.JPG">    <br>        </font>            <p align="left">&nbsp;</p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">Analizando los valores lip&iacute;dicos como variables continuas no hay diferencias entre los dos grupos, pero si consideramos como hipercolesterolemia a los valores iguales o superiores a 200 mg/dL de CT, existe asociaci&oacute;n con la v&aacute;lvula patol&oacute;gica (tablas <a href="#tab4">4</a> y <a href="#tab5">5</a>). </font></p>              ]]></body>
<body><![CDATA[<p align="left"><font color="#000000" face="Verdana" size="2"><a href="/img/revistas/ruc/v20n3/3a04t4.JPG"></a><a name="tab4"></a><img style="width: 576px; height: 257px;" alt="" src="/img/revistas/ruc/v20n3/3a04t4.JPG">    <br>   </font></p>        <font face="Verdana" size="2">            <br>        </font>            <p align="left"><font color="#000000" face="Verdana" size="2"><a href="/img/revistas/ruc/v20n3/3a04t5.JPG"></a><a name="tab5"></a><img style="width: 417px; height: 174px;" alt="" src="/img/revistas/ruc/v20n3/3a04t5.JPG">    <br>   </font></p>        <font face="Verdana" size="2">            <br>        </font>            <p align="left"></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">La velocidad m&aacute;xima del flujo fue significativamente mayor en la v&aacute;lvula fibrosada que en la v&aacute;lvula normal: 1,56&plusmn;0,39 versus 1,37&plusmn;0,33 m/s, p=0,01. La velocidad m&aacute;xima en la v&aacute;lvula esten&oacute;tica fue 2,83&plusmn;0,65 m/s (p=0,0001 comparada con la v&aacute;lvula fibrosada). </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">En correspondencia, el gradiente m&aacute;ximo de presi&oacute;n transvalvular fue m&aacute;s alto en las v&aacute;lvulas fibrosadas que en las normales: 10,4&plusmn;5,3 versus 7,9&plusmn;3,6 mmHg, y mayor aun en las v&aacute;lvulas con estenosis (33,1&plusmn;15,6 mmHg) (<a href="#tab6">tabla 6</a> y <a href="#fig1">figura 1</a>). </font></p>              <p align="left"><font color="#000000" face="Verdana" size="2"><a href="/img/revistas/ruc/v20n3/3a04t6.JPG"></a><span style="text-transform: uppercase;"><a name="tab6"></a><img style="width: 481px; height: 173px;" alt="" src="/img/revistas/ruc/v20n3/3a04t6.JPG">    ]]></body>
<body><![CDATA[<br>   </span></font></p>            <p align="left"><font face="Verdana" size="2"><a name="fig1"></a><img style="width: 470px; height: 265px;" alt="" src="/img/revistas/ruc/v20n3/3a04f1.JPG"></font></p>   <font face="Verdana" size="2">       <br>   </font>       <p align="left"><font color="#1f1a17" face="Verdana" size="2">El IMVI se encontr&oacute; significativamente mayor en los casos con v&aacute;lvula a&oacute;rtica fibrosada que en los casos con v&aacute;lvula normal: 200&plusmn;68 versus 154&plusmn;60 g/m<sup>2</sup>, p=0,01 (<a href="#tab6">tabla 6</a> y <a href="#fig2">figura 2</a>). </font></p>              <p><font face="Verdana" size="2">    <br>         <a name="fig2"></a><img style="width: 412px; height: 266px;" alt="" src="/img/revistas/ruc/v20n3/3a04f2.JPG">    <br>         <b><a href="/img/revistas/ruc/v20n3/3a04f2.JPG"></a></b>    <br>         </font>         </p>              <p align="left">&nbsp;</p>            <p align="left"><font color="#1f1a17" face="Verdana" size="2"><b><span style="text-transform: uppercase;">DISCUSI&oacute;N</span></b></font><font face="Verdana" size="2"> </font> </p>              ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">La prevalencia de estenosis a&oacute;rtica en nuestro grupo de pacientes con falla renal cr&oacute;nica es de 6%, aproximadamente tres veces mayor que la prevalencia informada en otros grupos en poblaci&oacute;n general estudiados con la misma metodolog&iacute;a (2%) <sup>(<a href="#15.">15</a>)</sup>. La prevalencia de fibrosis a&oacute;rtica es de 72% versus 26% en poblaci&oacute;n general. En otra serie con sujetos normales, la prevalencia de estenosis valvular a&oacute;rtica fue de 2,2% <a name="32.-"></a><sup>(<a href="#32.">32</a>)</sup>. En ambas series la prevalencia de fibrosis y<sub> </sub>estenosis valvular a&oacute;rtica aumenta con la edad, tal como sucede en nuestra serie (<a href="#tabla3">tabla 3</a>).Hemos considerado la fibrosis y estenosis valvular a&oacute;rticas como etapas de la misma enfermedad y las agrupamos como opuestas a la v&aacute;lvula normal en un an&aacute;lisis de los factores asociados. Este concepto se basa en los datos histol&oacute;gicos de ambos tipos de v&aacute;lvula y los resultados histoqu&iacute;micos <sup>(<a href="#8.">8</a>-<a href="#13.">13</a>)</sup>. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">Se demostr&oacute; asociaci&oacute;n entre patolog&iacute;a valvular a&oacute;rtica (fibrosis y estenosis) y la edad, el tiempo en di&aacute;lisis y la diabetes mellitus, tres factores estrechamente asociados a la aterosclerosis. La severidad de la aterosclerosis aumenta con la edad, de manera tal que los a&ntilde;osos tienen una carga de placas mayor que los j&oacute;venes <a name="33.-"></a><sup>(<a href="#33.">33</a>)</sup>, por lo que en el contexto cl&iacute;nico es usual considerar a la edad como un suced&aacute;neo de esta enfermedad <a name="34.-"></a><a name="35.-"></a><sup>(<a href="#34.">34</a>,<a href="#35.">35</a>)</sup>. El tiempo en di&aacute;lisis es un representante de la exposici&oacute;n de los pacientes a las condiciones de falla renal cr&oacute;nica no compensadas por esta terap&eacute;utica y que son capaces de elevar de 5 a 50 veces la mortalidad con respecto a la poblaci&oacute;n general <sup><a name="36.-"></a>(<a href="#36.">36</a>)</sup> y los coloca en una escala similar a la de aquellos que han tenido un infarto de miocardio. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">Los pacientes con diabetes 2 tienen un riesgo de morir por causas cardiovasculares equivalente a los pacientes no diab&eacute;ticos que han tenido un infarto de miocardio <a name="37.-"></a><sup>(<a href="#37.">37</a>) </sup>y lo mismo sucede con los ataques cerebrovasculares <a name="38.-"></a><sup>(<a href="#38.">38</a>)</sup>, por lo que en el ATP III se recomienda considerarlos como pacientes con enfermedad arterial coronaria, aun cuando no hayan tenido ning&uacute;n evento cl&iacute;nico <a name="39.-"></a><sup>(<a href="#39.">39</a>)</sup>. Por lo tanto, la asociaci&oacute;n con la edad, el tiempo en di&aacute;lisis y la diabetes, puede interpretarse como una asociaci&oacute;n de la enfermedad valvular a&oacute;rtica con la ateroscler&oacute;tica. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">No se comprob&oacute; en este grupo asociaci&oacute;n con hipertensi&oacute;n arterial y tabaquismo, reconocidos factores de riesgo de aterosclerosis y patolog&iacute;a valvular a&oacute;rtica en la poblaci&oacute;n general. Es posible que otros factores de mucho peso en este grupo de pacientes, tales como la desnutrici&oacute;n, el estado inflamatorio cr&oacute;nico, el estr&eacute;s oxidativo, etc&eacute;tera, sean capaces de borrar el efecto de aquellos factores. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">No se encontraron diferencias significativas de las distintas fracciones lip&iacute;dicas al comparar los pacientes con v&aacute;lvulas normales y los que tienen fibrosis o estenosis a&oacute;rtica. Esto llama la atenci&oacute;n porque en la poblaci&oacute;n general se ha encontrado una diferencia significativa en el nivel de lipoprote&iacute;na (a) y HDL-colesterol entre los normales y quienes tienen la v&aacute;lvula enferma <sup>(<a href="#15.">15</a>)</sup>. En otro estudio realizado por nuestro grupo <sup><a name="40.-"></a>(<a href="#40.">40</a>)</sup> encontramos que los pacientes con falla renal en hemodi&aacute;lisis cr&oacute;nica, comparados con una poblaci&oacute;n normal, ten&iacute;an mayor concentraci&oacute;n de lipoprote&iacute;na (a) y menor de HDL-colesterol. Pensamos que el peso de este factor de riesgo, caracter&iacute;stico de los pacientes en di&aacute;lisis, es de tal magnitud que extingue las diferencias entre los subgrupos. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">En cambio, cuando consideramos la colesterolemia como variable discreta con un valor de corte en 200 mg/dL, a partir del cual se considera que existe hipercolesterolemia, comprobamos diferencias significativas entre los pacientes con v&aacute;lvula sana y los que tienen fibrosis o estenosis a&oacute;rtica. Este resultado coincide con los hallazgos en la poblaci&oacute;n general <sup>(<a href="#15.">15</a>,<a href="#32.">32</a>)</sup> y apoya la hip&oacute;tesis del origen ateroescler&oacute;tico de la valvulopat&iacute;a. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">El HDL-colesterol bajo compromete la funci&oacute;n de transporte del LDL-colesterol desde los tejidos hacia el h&iacute;gado. La mol&eacute;cula de lipoprote&iacute;na (a) tiene un polo aterog&eacute;nico constituido por la apolipoprote&iacute;na B y un polo tromb&oacute;tico constituido por un glucop&eacute;ptido plasmin&oacute;geno-s&iacute;mil; ambos factores podr&iacute;an contribuir a la fibrocalcificaci&oacute;n valvular a&oacute;rtica. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">En este estudio no encontramos una asociaci&oacute;n entre la elevaci&oacute;n del producto fosfo-c&aacute;lcico y de la hormona paratiroidea con la enfermedad de la v&aacute;lvula a&oacute;rtica. Al respecto existen datos contradictorios en la bibliograf&iacute;a. Maher encontr&oacute; esa relaci&oacute;n; en cambio, Straumann no la encuentra <a name="41.-"></a><a name="42.-"></a><sup>(<a href="#41.">41</a>,<a href="#42.">42</a>)</sup>. Una posible explicaci&oacute;n es que los valores de calcio y f&oacute;sforo se encuentran dentro de l&iacute;mites normales. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">Cuando las valvas se mueven sin limitaciones, pero tienen un aspecto engrosado que las diferencia de las normales, se hace el diagn&oacute;stico de fibrosis valvular a&oacute;rtica; si la velocidad m&aacute;xima supera los 2,5 m/s el diagn&oacute;stico es de estenosis valvular a&oacute;rtica <sup>(<a href="#15.">15</a>)</sup>. Este l&iacute;mite, arbitrario aunque &uacute;til desde el punto de vista pr&aacute;ctico, establece un corte en un proceso que es continuo de acuerdo con los hallazgos histol&oacute;gicos e histoqu&iacute;micos. El hallazgo de una velocidad m&aacute;xima mayor que la normal en estos casos representa la repercusi&oacute;n funcional de las alteraciones anat&oacute;micas de la fibrosis a&oacute;rtica. </font></p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2">En base a esta velocidad m&aacute;xima se calcul&oacute; el gradiente de presi&oacute;n entre ventr&iacute;culo izquierdo y aorta, el que result&oacute; ser significativamente mayor en el grupo de los pacientes con fibrosis valvular a&oacute;rtica que en los normales, aunque no tanto como para definir a estos pacientes como portadores de estenosis a&oacute;rtica, de acuerdo con la definici&oacute;n que adoptamos, pero que de todas formas indica la existencia de un obst&aacute;culo al flujo sist&oacute;lico. </font></p>              ]]></body>
<body><![CDATA[<p align="left"><font color="#1f1a17" face="Verdana" size="2">El IMVI es mayor en quienes tienen fibrosis a&oacute;rtica que en los normales. En otro estudio realizado por nosotros sobre la hipertrofia ventricular izquierda analizamos en una regresi&oacute;n lineal m&uacute;ltiple nueve covariables que potencialmente podr&iacute;an afectar el IMVI; encontramos que exist&iacute;an cuatro factores que se asociaban en forma independiente con el IMVI: presi&oacute;n de pulso, nivel de hemoglobina, gradiente de presi&oacute;n transvalvular a&oacute;rtica y sobrehidrataci&oacute;n cr&oacute;nica<a name="43.-"></a> <sup>(<a href="#43.">43</a>)</sup>. Si bien la magnitud del gradiente de presi&oacute;n parece peque&ntilde;a para repercutir en la masa ventricular, es necesario tener en cuenta que estos gradientes, que fueron medidos en reposo, aumentan por los incrementos del gasto card&iacute;aco que ocurren en la actividad diaria. Este hallazgo, que hasta donde sabemos no ha sido comunicado por otros grupos, constituye, desde nuestro punto de vista, la alteraci&oacute;n funcional correspondiente a la alteraci&oacute;n anat&oacute;mica m&iacute;nima y permite considerar a la fibrosis y la estenosis a&oacute;rticas como etapas evolutivas de la misma enfermedad. </font></p>              <p><font face="Verdana" size="2">    <br>         </font>         </p>              <p align="left"><font color="#1f1a17" face="Verdana" size="2"><b><span style="text-transform: uppercase;">BIBLIOGRAF&iacute;A</span></b></font><font face="Verdana" size="2"> </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>Stephan PJ, Henry AC, Hebeler RF, Whiddon L, Roberts WC. </b>Comparison of age, gender, number of aortic valve cusps, concomitant coronary artery bypass grafting and magnitude of left ventricular systemic arterial peak systolic gradient in adults having aortic valve replacement for isolated aortic valve stenosis. Am J Cardiol 1997; 97: 166-72.     </font></p>              <!-- ref --><p align="left"><font color="#1f1a17" face="Verdana" size="2"><a name="2."></a><a href="#2.-">2</a>.&nbsp;&nbsp;&nbsp;&nbsp;<b>Roberts WC, Virmani R. </b>Aschoff bodies at necropsy in valvular heart disease. Evidence from an analysis of 543 patients over 14 years of age that rheumatic heart disease, at least anatomically, is a disease of the mitral valve. Circulation 1978; 57: 803.     </font></p>              <!-- ref --><p align="left"><font color="#000000" face="Verdana" size="2"><a name="3."></a><a href="#3.-">3</a>.&nbsp;&nbsp;&nbsp;&nbsp;<b>Fligner CL, Reichenbach DD. </b>Pathology and etiology of heart disease. En: Valvular Heart Disease. Catherine M. Otto (ed). Philadelphia: Saunders, 1999: 13-43.    </font><font color="#1f1a17" face="Verdana" size="2"> </font></p>              ]]></body>
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