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de la serie llevaba THAP&#46; En la <a class="elsevierStyleCrossRef" href="#tbl0005">tabla 1</a> se describen las caracter&#237;sticas basales de los pacientes&#46; En el 79&#44;1&#37; de los casos el iPCSK9 de inicio fue evolocumab&#46; Solo 3 pacientes &#40;7&#44;1&#37;&#41; tuvieron que retirar el f&#225;rmaco por intolerancia&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">En la <a class="elsevierStyleCrossRef" href="#tbl0010">tabla 2</a> se describen los resultados anal&#237;ticos antes y despu&#233;s del inicio de iPCSK9&#46; El cLDL previo al inicio de iPCSK9 fue de 120<span class="elsevierStyleHsp" style=""></span>mg&#47;dl &#40;102-154&#41;&#46; El tratamiento con iPCSK9 permiti&#243; reducciones significativas del colesterol total &#40;CT&#41;&#44; del cLDL y de los TG&#44; siendo la de cLDL del 61&#37;&#46; Esto permiti&#243; que el 59&#37; de la serie alcanzaran su objetivo recomendado de cLDL&#46; Se vio una diferencia significativa en la reducci&#243;n de cLDL conseguida con iPCSK9 entre los pacientes que llevaban o no estatina previamente&#44; siendo mayor la reducci&#243;n en aquellos pacientes en tratamiento con estatina &#40;66&#37; frente al 48&#37;&#41;&#46; No observamos diferencias significativas en la funci&#243;n renal o en los niveles de albuminuria&#46;</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">En este estudio hemos observado una reducci&#243;n significativa del cLDL similar a lo observado en los ensayos cl&#237;nicos con dichos f&#225;rmacos&#44; incluyendo poblaci&#243;n renal<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">2&#44;5&#44;6</span></a>&#46; Esto ha permitido que un amplio porcentaje de pacientes de alto&#47;muy alto RCV que previamente no hab&#237;an alcanzado su objetivo de cLDL con la terapia convencional lo consigan&#46; Estudios similares en vida real han sido publicados en nuestro pa&#237;s&#44; con resultados comparables&#46; En los estudios RETOSS-NEFRO<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> y RETOSS-CARDIO<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> se comparte la experiencia con evolocumab desde unidades de Cardiolog&#237;a y Nefrolog&#237;a en Espa&#241;a&#46; La reducci&#243;n de cLDL en ambos estudios se sit&#250;a en torno al 60&#37;&#44; similar a nuestros datos&#46; En otro estudio acerca de la experiencia en un hospital terciario<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a>&#44; se consiguieron reducciones en torno al 55&#37;&#46; En estos trabajos tambi&#233;n se ha observado una muy buena tolerancia al f&#225;rmaco&#44; con peque&#241;os porcentajes de discontinuaci&#243;n&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">En nuestro trabajo hemos analizado la reducci&#243;n de cLDL seg&#250;n el paciente estuviera tomando o no estatina previamente&#44; observando resultados m&#225;s potentes en los pacientes con estatina&#46; Esto puede poner de manifiesto el efecto sin&#233;rgico sobre las v&#237;as metab&#243;licas de las terapias en combinaci&#243;n<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">4</span></a>&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Aunque no hemos analizado en este trabajo otros par&#225;metros lip&#237;dicos que no son de pr&#225;ctica cl&#237;nica habitual&#44; los iPCSK9 han mostrado reducir la lipoprote&#237;na<span class="elsevierStyleHsp" style=""></span>&#40;a&#41; entre otras part&#237;culas aterog&#233;nicas y tener impacto sobre la concentraci&#243;n y tama&#241;o de las lipopart&#237;culas&#44; lo que es de especial inter&#233;s en el paciente renal&#44; ya que el tratamiento hipolipemiante cl&#225;sico v&#237;a oral no ha mostrado mucho beneficio en la ERC avanzada&#44; pudiendo ser la falta de eficacia de las estatinas y de ezetimiba sobre par&#225;metros lip&#237;dicos no medidos habitualmente o el tama&#241;o de las lipopart&#237;culas&#44; especialmente alterado en la poblaci&#243;n renal&#44; una de las razones<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a>&#46; Teniendo en cuenta el beneficio visto con evolocumab en diferentes estadios de ERC<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a>&#44; son necesarios futuros estudios que analicen el impacto de los iPCSK9 sobre todos estos par&#225;metros lip&#237;dicos y su impacto pron&#243;stico&#44; especialmente en la poblaci&#243;n renal&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Financiaci&#243;n</span><p id="par0045" class="elsevierStylePara elsevierViewall">Este estudio no ha recibido ning&#250;n tipo de financiaci&#243;n&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflicto de intereses</span><p id="par0050" class="elsevierStylePara elsevierViewall">V&#46; Escudero ha recibido honorarios por conferencias de Sanofi y Amgen&#46; C&#46; Castro ha recibido honorarios por conferencias de Amgen&#46; El resto de autores no declaran ning&#250;n tipo de conflicto de intereses&#46;</p></span></span>"
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Carta al Director
Experiencia con inhibidores PCSK9 desde una consulta de Nefrología
Experience with PCSK9 inhibitors from a Nephrology unit
Verónica Escudero Quesada
Autor para correspondencia
veesque@gmail.com

Autor para correspondencia.
, Jonay Pantoja Pérez, Cristina Castro Alonso, July Vanessa Osma Capera, Alejandro Valero Antón, Asunción Sancho Calabuig
Servicio de Nefrología, Hospital Universitario Dr. Peset, Valencia, España
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que han demostrado la reducci&#243;n del riesgo de enfermedad cardiovascular &#40;ECV&#41; al ser a&#241;adidos al tratamiento con estatina&#44; mediante una disminuci&#243;n potente de los niveles de cLDL<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a>&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">El objetivo de este estudio retrospectivo observacional fue evaluar el perfil de pacientes que iniciaron tratamiento con iPCSK9 &#40;alirocumab o evolocumab&#41;&#44; a&#241;adido a su tratamiento hipolipemiante habitual&#44; al no cumplir el objetivo de cLDL recomendado seg&#250;n su RCV<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a>&#44; desde una consulta de Nefrolog&#237;a&#44; y los cambios anal&#237;ticos logrados con dicho tratamiento&#46; El objetivo de cLDL en alto RCV fue &#60;<span class="elsevierStyleHsp" style=""></span>70<span class="elsevierStyleHsp" style=""></span>mg&#47;dl y en muy alto RCV &#60;<span class="elsevierStyleHsp" style=""></span>55<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#46; El comit&#233; &#233;tico del hospital Dr&#46; Peset aprob&#243; el estudio&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">Definimos tratamiento hipolipemiante de alta potencia &#40;THAP&#41;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">4</span></a> a las estatinas de alta potencia en solitario &#40;atorvastatina 40-80<span class="elsevierStyleHsp" style=""></span>mg&#44; rosuvastatina 20<span class="elsevierStyleHsp" style=""></span>mg&#41; o potencia intermedia &#40;atorvastatina 10-20<span class="elsevierStyleHsp" style=""></span>mg&#44; rosuvastatina 5-10<span class="elsevierStyleHsp" style=""></span>mg&#44; pitavastatina 2-4<span class="elsevierStyleHsp" style=""></span>mg&#41; combinado con ezetimiba&#46; Definimos dislipemia &#40;DL&#41; aterog&#233;nica como la presencia de triglic&#233;ridos &#40;TG&#41; &#62;<span class="elsevierStyleHsp" style=""></span>150<span class="elsevierStyleHsp" style=""></span>mg&#47;dl&#44; junto a colesterol HDL &#40;cHDL&#41; &#60;<span class="elsevierStyleHsp" style=""></span>40<span class="elsevierStyleHsp" style=""></span>mg&#47;dl en hombres&#44; &#60;<span class="elsevierStyleHsp" style=""></span>45<span class="elsevierStyleHsp" style=""></span>mg&#47;dl en mujeres&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Se analizaron 43 pacientes&#44; con una mediana de seguimiento de 12 &#40;7-19&#41; meses&#46; Edad media 65 &#177;<span class="elsevierStyleHsp" style=""></span>12<span class="elsevierStyleHsp" style=""></span>a&#241;os&#44; 58&#44;1&#37; de la serie varones&#46; El 65&#44;1&#37; ten&#237;an ERC&#44; habiendo 5 pacientes trasplantados renales &#40;11&#44;6&#37;&#41;&#46; El 79&#44;1&#37; presentaban antecedentes de ECV&#46; Hab&#237;a 13 pacientes intolerantes a estatinas &#40;30&#44;2&#37;&#41;&#46; El 69&#44;8&#37; llevaban tratamiento con estatinas y el 34&#44;9&#37; con ezetimiba &#40;32&#44;6&#37; de la serie en combinaci&#243;n estatina-ezetimiba&#41;&#46; El 58&#44;1&#37; de la serie llevaba THAP&#46; En la <a class="elsevierStyleCrossRef" href="#tbl0005">tabla 1</a> se describen las caracter&#237;sticas basales de los pacientes&#46; En el 79&#44;1&#37; de los casos el iPCSK9 de inicio fue evolocumab&#46; Solo 3 pacientes &#40;7&#44;1&#37;&#41; tuvieron que retirar el f&#225;rmaco por intolerancia&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">En la <a class="elsevierStyleCrossRef" href="#tbl0010">tabla 2</a> se describen los resultados anal&#237;ticos antes y despu&#233;s del inicio de iPCSK9&#46; El cLDL previo al inicio de iPCSK9 fue de 120<span class="elsevierStyleHsp" style=""></span>mg&#47;dl &#40;102-154&#41;&#46; El tratamiento con iPCSK9 permiti&#243; reducciones significativas del colesterol total &#40;CT&#41;&#44; del cLDL y de los TG&#44; siendo la de cLDL del 61&#37;&#46; Esto permiti&#243; que el 59&#37; de la serie alcanzaran su objetivo recomendado de cLDL&#46; Se vio una diferencia significativa en la reducci&#243;n de cLDL conseguida con iPCSK9 entre los pacientes que llevaban o no estatina previamente&#44; siendo mayor la reducci&#243;n en aquellos pacientes en tratamiento con estatina &#40;66&#37; frente al 48&#37;&#41;&#46; No observamos diferencias significativas en la funci&#243;n renal o en los niveles de albuminuria&#46;</p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">En este estudio hemos observado una reducci&#243;n significativa del cLDL similar a lo observado en los ensayos cl&#237;nicos con dichos f&#225;rmacos&#44; incluyendo poblaci&#243;n renal<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">2&#44;5&#44;6</span></a>&#46; Esto ha permitido que un amplio porcentaje de pacientes de alto&#47;muy alto RCV que previamente no hab&#237;an alcanzado su objetivo de cLDL con la terapia convencional lo consigan&#46; Estudios similares en vida real han sido publicados en nuestro pa&#237;s&#44; con resultados comparables&#46; En los estudios RETOSS-NEFRO<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> y RETOSS-CARDIO<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> se comparte la experiencia con evolocumab desde unidades de Cardiolog&#237;a y Nefrolog&#237;a en Espa&#241;a&#46; La reducci&#243;n de cLDL en ambos estudios se sit&#250;a en torno al 60&#37;&#44; similar a nuestros datos&#46; En otro estudio acerca de la experiencia en un hospital terciario<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a>&#44; se consiguieron reducciones en torno al 55&#37;&#46; En estos trabajos tambi&#233;n se ha observado una muy buena tolerancia al f&#225;rmaco&#44; con peque&#241;os porcentajes de discontinuaci&#243;n&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">En nuestro trabajo hemos analizado la reducci&#243;n de cLDL seg&#250;n el paciente estuviera tomando o no estatina previamente&#44; observando resultados m&#225;s potentes en los pacientes con estatina&#46; Esto puede poner de manifiesto el efecto sin&#233;rgico sobre las v&#237;as metab&#243;licas de las terapias en combinaci&#243;n<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">4</span></a>&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Aunque no hemos analizado en este trabajo otros par&#225;metros lip&#237;dicos que no son de pr&#225;ctica cl&#237;nica habitual&#44; los iPCSK9 han mostrado reducir la lipoprote&#237;na<span class="elsevierStyleHsp" style=""></span>&#40;a&#41; entre otras part&#237;culas aterog&#233;nicas y tener impacto sobre la concentraci&#243;n y tama&#241;o de las lipopart&#237;culas&#44; lo que es de especial inter&#233;s en el paciente renal&#44; ya que el tratamiento hipolipemiante cl&#225;sico v&#237;a oral no ha mostrado mucho beneficio en la ERC avanzada&#44; pudiendo ser la falta de eficacia de las estatinas y de ezetimiba sobre par&#225;metros lip&#237;dicos no medidos habitualmente o el tama&#241;o de las lipopart&#237;culas&#44; especialmente alterado en la poblaci&#243;n renal&#44; una de las razones<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a>&#46; Teniendo en cuenta el beneficio visto con evolocumab en diferentes estadios de ERC<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a>&#44; son necesarios futuros estudios que analicen el impacto de los iPCSK9 sobre todos estos par&#225;metros lip&#237;dicos y su impacto pron&#243;stico&#44; especialmente en la poblaci&#243;n renal&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Financiaci&#243;n</span><p id="par0045" class="elsevierStylePara elsevierViewall">Este estudio no ha recibido ning&#250;n tipo de financiaci&#243;n&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflicto de intereses</span><p id="par0050" class="elsevierStylePara elsevierViewall">V&#46; Escudero ha recibido honorarios por conferencias de Sanofi y Amgen&#46; C&#46; Castro ha recibido honorarios por conferencias de Amgen&#46; El resto de autores no declaran ning&#250;n tipo de conflicto de intereses&#46;</p></span></span>"
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Previo&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">CT &#40;mg&#47;dl&#41;&#44; mediana &#40;RI&#41;&nbsp;\t\t\t\t\t\t\n
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          "es" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Resultados anal&#237;ticos antes y despu&#233;s del tratamiento con iPCSK9</p>"
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ISSN: 02116995
Idioma original: Español
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Idiomas
Nefrología