<?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>0120-5633</journal-id>
<journal-title><![CDATA[Revista Colombiana de Cardiología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Colomb. Cardiol.]]></abbrev-journal-title>
<issn>0120-5633</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Colombiana de Cardiologia. Oficina de Publicaciones]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0120-56332015000100004</article-id>
<article-id pub-id-type="doi">10.1016/j.rccar.2015.02.001</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Guía de práctica clínica para la prevención, detección temprana, diagnóstico, tratamiento y seguimiento de las dislipidemias: tratamiento farmacológico con estatinas]]></article-title>
<article-title xml:lang="en"><![CDATA[Clinical practice guidelines for prevention, early detection, diagnose, treatment and follow-up of dyslipidemias: farmacological treatment with statins]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Múñoz]]></surname>
<given-names><![CDATA[Oscar]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[García]]></surname>
<given-names><![CDATA[Ángel A]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Fernández]]></surname>
<given-names><![CDATA[Daniel G.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Higuera]]></surname>
<given-names><![CDATA[Angélica M.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ruiz]]></surname>
<given-names><![CDATA[álvaro J.]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Aschner]]></surname>
<given-names><![CDATA[Pablo]]></given-names>
</name>
<xref ref-type="aff" rid="A04"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Toro]]></surname>
<given-names><![CDATA[Juan M.]]></given-names>
</name>
<xref ref-type="aff" rid="A05"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Arteaga]]></surname>
<given-names><![CDATA[Juan M.]]></given-names>
</name>
<xref ref-type="aff" rid="A06"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Merchán]]></surname>
<given-names><![CDATA[Alonso]]></given-names>
</name>
<xref ref-type="aff" rid="A07"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sánchez Vallejo]]></surname>
<given-names><![CDATA[Gregorio]]></given-names>
</name>
<xref ref-type="aff" rid="A08"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Villalba]]></surname>
<given-names><![CDATA[Yadira]]></given-names>
</name>
<xref ref-type="aff" rid="A09"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Pontificia Universidad Javeriana  ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Pontificia Universidad Javeriana  ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Pontificia Universidad Javeriana  ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A04">
<institution><![CDATA[,Pontificia Universidad Javeriana  ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A05">
<institution><![CDATA[,Universidad de Antioquia  ]]></institution>
<addr-line><![CDATA[ Antioquia]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A06">
<institution><![CDATA[,Universidad Nacional de Colombia  ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A07">
<institution><![CDATA[,Fundación Clínica Shaio  ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A08">
<institution><![CDATA[,Hospital Departamental Universitario del Quindío San Juan de Dios  ]]></institution>
<addr-line><![CDATA[ Quindío]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A09">
<institution><![CDATA[,Universidad de Cartagena  ]]></institution>
<addr-line><![CDATA[Cartagena ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>01</day>
<month>01</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epub">
<day>01</day>
<month>01</month>
<year>2015</year>
</pub-date>
<volume>22</volume>
<numero>1</numero>
<fpage>14</fpage>
<lpage>21</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0120-56332015000100004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0120-56332015000100004&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0120-56332015000100004&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Objetivo: Evaluar el impacto del tratamiento con estatinas sobre la incidencia y la recurrencia de los eventos cardiovasculares y los cerebrovasculares (prevención primaria y secundaria), los niveles de las fracciones lipídicas y la incidencia de efectos secundarios (el cáncer y la diabetes mellitus) en personas con hipercolesterolemia. Métodos: Se elaboró una guía de práctica clínica siguiendo los lineamientos de la guía metodológica del Ministerio de Salud y Protección Social para recolectar de forma sistemática la evidencia científica y formular las recomendaciones utilizando la metodología GRADE. Resultados: Se evidenció un efecto benéfico del tratamiento farmacológico con estatinas tanto en población de prevención primaria como en prevención secundaria, logrando reducciones clínica y estadísticamente significativas en la mortalidad y en los eventos cardiovasculares y cerebrovasculares. Adicionalmente, el tratamiento intensivo con estatinas mostró mayor reducción en los eventos cardiovasculares y cerebrovasculares ateroscleróticos al compararlo con el tratamiento de intensidad moderada. No se encontraron diferencias significativas en el riesgo de desarrollar cáncer al comparar estatinas frente a placebo pero sí se encontró un incremento de nueve por ciento en el riesgo de presentar diabetes mellitus asociado al tratamiento con estatinas. Conclusiones: Se formulan recomendaciones a favor del uso de estatinas como primera línea de tratamiento de hipercolesterolemia, y se establecen criterios para definir la intensidad de la terapia (alta o moderada respuesta) según el riesgo cardiovascular a 10 años, el nivel de colesterol LDL (cLDL), la edad y los antecedentes personales y los familiares.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Objective: To evaluate the impact of statin therapy on the incidence and recurrence of cardiovascular and cerebrovascular events (primary and secondary prevention), the levels of lipid fractions and the incidence of side effects (cancer and diabetes mellitus) in people with hypercholesterolemia. Methods: A clinical practice guideline was developed following the guidelines of the methodological guidance of the Ministry of Health and Social Protection to systematically collect the evidence and make recommendations using the GRADE methodology. Results: A beneficial effect of pharmacological treatment with statins in both primary prevention and secondary prevention was evident, achieving clinically and statistically significant reductions in mortality and cardiovascular and cerebrovascular events. Additionally, intensive statin therapy showed greater reduction in atherosclerotic cardiovascular and cerebrovascular events as compared to the treatment of moderate intensity. No significant differences in the risk of developing cancer by comparing statins versus placebo were found, but a 9% increase in the risk of diabetes mellitus associated with statin therapy was found. Conclusions: Recommendations for the use of statins as first-line treatment of hypercholesterolemia are formulated, and criteria to define the intensity of therapy (high or moderate response) as cardiovascular risk at 10 years, level of LDL (LDLc), age and personal and family history were established.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Hipercolesterolemia]]></kwd>
<kwd lng="es"><![CDATA[Lípidos]]></kwd>
<kwd lng="es"><![CDATA[Tratamiento]]></kwd>
<kwd lng="es"><![CDATA[Estatinas]]></kwd>
<kwd lng="en"><![CDATA[Hypercholesterolemia]]></kwd>
<kwd lng="en"><![CDATA[Lipid]]></kwd>
<kwd lng="en"><![CDATA[Treatment]]></kwd>
<kwd lng="en"><![CDATA[Statins]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  <font face="verdana" size="2">     <p><a href="http://dx.doi.org/10.1016/j.rccar.2015.02.001" target="_blank">http://dx.doi.org/10.1016/j.rccar.2015.02.001</a></p>     <P align="center"><b><font size="4">Gu&iacute;a de pr&aacute;ctica cl&iacute;nica para la prevenci&oacute;n, detecci&oacute;n temprana, diagn&oacute;stico, tratamiento y seguimiento de las dislipidemias: tratamiento farmacol&oacute;gico con estatinas</font></b></P>     <P align="center"><b><font size="3">Clinical practice guidelines for prevention, early detection, diagnose, treatment and follow-up of dyslipidemias: farmacological treatment with statins</font></b></P>     <P align="center">Oscar M&uacute;&ntilde;oz<SUP>a</SUP>, &Aacute;ngel A. Garc&iacute;a<SUP>b</SUP>, Daniel G. Fern&aacute;ndez<SUP>b</SUP>, Ang&eacute;lica M. Higuera<SUP>b</SUP>, &Aacute;lvaro J. Ruiz<SUP>c</SUP>, Pablo Aschner<SUP>d</SUP>, Juan M. Toro<SUP>e</SUP>, Juan M. Arteaga<SUP>f</SUP>, Alonso Merch&aacute;n<SUP>g</SUP>, Gregorio S&aacute;nchez Vallejo<SUP>h</SUP>, Yadira Villalba<SUP>i</SUP></P>     <P><sup>a</sup>Unidad de Cl&iacute;nica Hospitalaria, Departamento de Epidemiolog&iacute;a Cl&iacute;nica y Bioestad&iacute;stica, Hospital Universitario de San Ignacio, Pontificia Universidad Javeriana, Bogot&aacute;, Colombia    <br>   <sup>b</sup>Unidad de Cardiolog&iacute;a, Departamento de Epidemiolog&iacute;a Cl&iacute;nica y Bioestad&iacute;stica, Hospital Universitario de San Ignacio, Pontificia Universidad Javeriana, Bogot&aacute;, Colombia    <br>   <sup>c</sup>Departamento de Medicina Interna, Departamento de Epidemiolog&iacute;a Cl&iacute;nica y Bioestad&iacute;stica, Pontificia Universidad Javeriana, Bogot&aacute;, Colombia    <br>   <sup>d</sup>Departamento de Medicina Interna, Pontificia Universidad Javeriana, Hospital Universitario San Ignacio, Bogot&aacute;, Colombia    <br>   <sup>e</sup>Departamento de Medicina Interna, Universidad de Antioquia, Hospital Pablo Tob&oacute;n Uribe, Antioquia, Colombia    ]]></body>
<body><![CDATA[<br>   <sup>f</sup>Departamento de Medicina Interna, Universidad Nacional de Colombia, Bogot&aacute;, Colombia    <br>   <sup>g</sup>Sociedad Colombiana de Cardiolog&iacute;a y Cirug&iacute;a Cardiovascular, Fundaci&oacute;n Cl&iacute;nica Shaio, Bogot&aacute;, Colombia    <br>   <sup>h</sup>Departamento de Medicina Interna, Hospital Departamental Universitario del Quind&iacute;o San Juan de Dios, Quind&iacute;o, Colombia    <br>   <sup>i</sup>Departamento de Medicina Interna, Universidad de Cartagena, Cartagena, Colombia</P>     <P>Recibido el 13 de octubre de 2014; Aceptado el 1 de febrero de 2015 </P>     <p>correo electr&oacute;nico:<a href="mailto:angel.garcia@javeriana.edu.co">angel.garcia@javeriana.edu.co</a>(&Aacute;.A. Garc&iacute;a).</p> <hr>     <P><B>Resumen</B></P>     <P><i>Objetivo</i>: Evaluar el impacto del tratamiento con estatinas sobre la incidencia y la recurrencia de los eventos cardiovasculares y los cerebrovasculares (prevenci&oacute;n primaria y secundaria), los niveles de las fracciones lip&iacute;dicas y la incidencia de efectos secundarios (el c&aacute;ncer y la diabetes mellitus) en personas con hipercolesterolemia.</P>     <P><i>M&eacute;todos</i>: Se elabor&oacute; una gu&iacute;a de pr&aacute;ctica cl&iacute;nica siguiendo los lineamientos de la gu&iacute;a metodol&oacute;gica del Ministerio de Salud y Protecci&oacute;n Social para recolectar de forma sistem&aacute;tica la evidencia cient&iacute;fica y formular las recomendaciones utilizando la metodolog&iacute;a GRADE.</P>     <P><i>Resultados</i>: Se evidenci&oacute; un efecto ben&eacute;fico del tratamiento farmacol&oacute;gico con estatinas tanto en poblaci&oacute;n de prevenci&oacute;n primaria como en prevenci&oacute;n secundaria, logrando reducciones cl&iacute;nica y estad&iacute;sticamente significativas en la mortalidad y en los eventos cardiovasculares y cerebrovasculares. Adicionalmente, el tratamiento intensivo con estatinas mostr&oacute; mayor reducci&oacute;n en los eventos cardiovasculares y cerebrovasculares ateroscler&oacute;ticos al compararlo con el tratamiento de intensidad moderada. No se encontraron diferencias significativas en el riesgo de desarrollar c&aacute;ncer al comparar estatinas frente a placebo pero s&iacute; se encontr&oacute; un incremento de nueve por ciento en el riesgo de presentar diabetes mellitus asociado al tratamiento con estatinas.</P>     ]]></body>
<body><![CDATA[<P><i>Conclusiones</i>: Se formulan recomendaciones a favor del uso de estatinas como primera l&iacute;nea de tratamiento de hipercolesterolemia, y se establecen criterios para definir la intensidad de la terapia (alta o moderada respuesta) seg&uacute;n el riesgo cardiovascular a 10 a&ntilde;os, el nivel de colesterol LDL (cLDL), la edad y los antecedentes personales y los familiares.</P>     <P><B>Palabras clave</B>: Hipercolesterolemia. L&iacute;pidos. Tratamiento. Estatinas.</P> <hr>     <P><B>Abstract</B></P>     <P><i>Objective</i>: To evaluate the impact of statin therapy on the incidence and recurrence of cardiovascular and cerebrovascular events (primary and secondary prevention), the levels of lipid fractions and the incidence of side effects (cancer and diabetes mellitus) in people with hypercholesterolemia.</P>     <P><i>Methods</i>: A clinical practice guideline was developed following the guidelines of the methodological guidance of the Ministry of Health and Social Protection to systematically collect the evidence and make recommendations using the GRADE methodology.</P>     <P><i>Results</i>: A beneficial effect of pharmacological treatment with statins in both primary prevention and secondary prevention was evident, achieving clinically and statistically significant reductions in mortality and cardiovascular and cerebrovascular events. Additionally, intensive statin therapy showed greater reduction in atherosclerotic cardiovascular and cerebrovascular events as compared to the treatment of moderate intensity. No significant differences in the risk of developing cancer by comparing statins versus placebo were found, but a 9&#37; increase in the risk of diabetes mellitus associated with statin therapy was found.</P>     <P><i>Conclusions</i>: Recommendations for the use of statins as first-line treatment of hypercholesterolemia are formulated, and criteria to define the intensity of therapy (high or moderate response) as cardiovascular risk at 10 years, level of LDL (LDLc), age and personal and family history were established.</P>     <P><B>Keywords</B>:Hypercholesterolemia. Lipid. Treatment. Statins.</P> <hr>     <P><B>Introducci&oacute;n</B></P>     <P>La enfermedad cardiovascular es una de las principales causas de morbilidad y la primera causa de mortalidad a nivel mundial. Dentro del amplio espectro de esta entidad se encuentran la enfermedad ateroscler&oacute;tica y la enfermedad cerebrovascular, con el infarto agudo del miocardio y el ataque cerebrovascular como los que generan la mayor carga de mortalidad<SUP>1</SUP>.</P>     ]]></body>
<body><![CDATA[<P>Los estudios observacionales han mostrado una relaci&oacute;n directamente proporcional entre el riesgo de enfermedad coronaria y las concentraciones s&eacute;ricas de colesterol<SUP>2&ndash;4</SUP>, identificando a la hipercolesterolemia como un factor de riesgo independiente para los eventos cardiovasculares y los cerebrovasculares en personas con o sin historia de enfermedad cardiovascular<SUP>5</SUP>. Por lo cual, la correcci&oacute;n del perfil lip&iacute;dico, especialmente del colesterol de baja densidad (cLDL), constituye un objetivo terap&eacute;utico importante<SUP>1</SUP>.</P>     <P>Las estatinas han sido ampliamente usadas para mejorar la sobrevida y reducir la incidencia de los eventos coronarios y los eventos cerebrovasculares en pacientes con enfermedad cardiovascular, y se constituyen en el grupo farmacol&oacute;gico de primera elecci&oacute;n para la disminuci&oacute;n del cLDL<SUP>6</SUP>.</P>     <P>Aunque inicialmente la terapia con estatinas se enfoc&oacute; en la prevenci&oacute;n secundaria, con el paso del tiempo el tratamiento se ha indicado en pacientes con riesgo cardiovascular progresivamente m&aacute;s bajo, incrementando as&iacute; el n&uacute;mero de personas candidatas a recibir manejo farmacol&oacute;gico con estatinas<SUP>7</SUP>.</P>     <P>Existen m&uacute;ltiples estudios que demuestran el efecto favorable del tratamiento con estatinas en poblaciones de alto riesgo<SUP>8&ndash;19</SUP>, sin embargo, a&uacute;n se discute su beneficio en la reducci&oacute;n del riesgo cardiovascular en personas sin evidencia de enfermedad cardiovascular<SUP>20</SUP>.</P>     <P>Anteriormente las poblaciones de bajo riesgo se defin&iacute;an por la ausencia de enfermedad arterial coronaria, pero se ha reconocido que en estos grupos se incluye tanto a personas con alto riesgo de desarrollar enfermedad coronaria (por ejemplo, aquellos con enfermedad vascular perif&eacute;rica severa) como a personas con riesgo muy bajo (por ejemplo, personas j&oacute;venes, sin enfermedades como la diabetes mellitus o la hipertensi&oacute;n arterial y los niveles de colesterol cLDL &lt; 70 mg/dl). Por lo anterior, actualmente el uso de estatinas est&aacute; basado en el riesgo estimado de presentar un evento ateroscler&oacute;tico y no &uacute;nicamente en la presencia o ausencia de enfermedad coronaria conocida<SUP>21&ndash;23</SUP>.</P>     <P>Los resultados del estudio Jupiter<SUP>24</SUP>, incentivaron el uso de estatinas en personas sin historia de enfermedad coronaria y plantearon la discusi&oacute;n sobre el mayor impacto cl&iacute;nico de las estatinas de alta potencia frente a las de baja potencia. Recientemente, el uso de estatinas en esta poblaci&oacute;n tambi&eacute;n ha sido evaluado por la colaboraci&oacute;n Cholesterol Treatment Trialists&iquest; Collaborators, mostrando una reducci&oacute;n de 21&#37; en el riesgo relativo de eventos vasculares mayores con el uso de estatinas, por cada 1,0 mmol/L (38 mg/dl) de disminuci&oacute;n en el cLDL, independientemente del riesgo basal<SUP>25</SUP>, confirmando la eficacia de las estatinas en prevenci&oacute;n primaria.</P>     <P>Otros estudios dise&ntilde;ados para determinar la seguridad de las reducciones mayores del colesterol LDL y el impacto sobre los eventos vasculares, comparando esquemas de tratamiento con diferente intensidad, han sugerido mayor beneficio al emplear terapia m&aacute;s intensiva<SUP>26&ndash;30</SUP>.</P>     <P>En la <a href="#t1">tabla 1</a> se presenta la clasificaci&oacute;n de la terapia con estatinas seg&uacute;n su intensidad.</P>     <P align="center"><a name="t1"></a><IMG SRC="img/revistas/rcca/v22n1/v22n1a04t1.jpg"></P>     <P>Teniendo en cuenta estos resultados, es relevante evaluar el impacto cl&iacute;nico del tratamiento con estatinas tanto en la poblaci&oacute;n de prevenci&oacute;n primaria como secundaria, as&iacute; como la intensidad del mismo, para determinar el momento oportuno de inicio de la terapia farmacol&oacute;gica y el esquema que se deba emplear.</P>     ]]></body>
<body><![CDATA[<P>El Ministerio de Salud y Protecci&oacute;n Social ha encargado a la Pontificia Universidad Javeriana y a la Alianza CINETS conformada por las Universidades Javeriana, Nacional y Antioquia el desarrollo de una gu&iacute;a cl&iacute;nica sobre la prevenci&oacute;n, detecci&oacute;n temprana, diagn&oacute;stico, tratamiento y seguimiento de las dislipidemias en la poblaci&oacute;n mayor de 18 a&ntilde;os<B>.</B> El resultado de ese proceso, en lo referente al manejo farmacol&oacute;gico con estatinas en adultos con dislipidemia se presenta de forma resumida en el presente escrito. Cabe resaltar que en este proceso tambi&eacute;n participaron activamente la Asociaci&oacute;n Colombiana de Medicina Interna, la Sociedad Colombiana de Cardiolog&iacute;a, y la Asociaci&oacute;n Colombiana de Endocrinolog&iacute;a.</P>     <P><B>M&eacute;todos</B></P>     <P>El proceso de desarrollo de la gu&iacute;a se describe detalladamente en el manual para desarrollo de gu&iacute;as de pr&aacute;ctica cl&iacute;nica y en la actualizaci&oacute;n de dicha metodolog&iacute;a (disponible en la p&aacute;gina web del Ministerio de Salud y Protecci&oacute;n Social)<SUP>31</SUP>.</P>     <P>Cabe resaltar que dicha metodolog&iacute;a favorece la b&uacute;squeda sistem&aacute;tica de la evidencia cient&iacute;fica (incluyendo tanto las revisiones sistem&aacute;ticas de la literatura como los estudios primarios). As&iacute; mismo, establece una metodolog&iacute;a clara para la selecci&oacute;n de la evidencia que se debe utilizar, evaluando cuidadosamente la calidad de la misma. La versi&oacute;n completa de la gu&iacute;a, en la que se presentan los resultados de todas estas evaluaciones, pueden ser consultados en la p&aacute;gina web del Ministerio de Salud y Protecci&oacute;n Social, as&iacute; como en la p&aacute;gina web de la alianza CINETS.</P>     <P>El grupo metodol&oacute;gico prepar&oacute; un resumen de la evidencia disponible y lo present&oacute; al panel completo durante las reuniones de generaci&oacute;n de recomendaciones. Este panel incluy&oacute; a representantes de las diversas especialidades m&eacute;dicas (cardi&oacute;logos, endocrin&oacute;logos, m&eacute;dicos internistas, m&eacute;dicos de familia, m&eacute;dicos generales) as&iacute; como a otros profesionales de la salud (nutricionistas, terapeutas f&iacute;sicos). Cabe resaltar que durante todo el proceso se cont&oacute; adicionalmente con representantes de los pacientes, que aportaron activamente la generaci&oacute;n de recomendaciones. Todos los integrantes del panel presentaron abiertamente la declaraci&oacute;n de sus conflictos de intereses. Estos documentos est&aacute;n disponibles en la versi&oacute;n completa de la gu&iacute;a.</P>     <P>Durante las reuniones de generaci&oacute;n de recomendaciones se sigui&oacute; la metodolog&iacute;a propuesta por el grupo GRADE, que permite tener en cuenta no solo la calidad de la evidencia disponible, sino consideraciones de los costos, las preferencias de los pacientes y la relaci&oacute;n entre los beneficios y los riesgos de las tecnolog&iacute;as de inter&eacute;s (las pruebas, las estrategias de manejo, las intervenciones, los medicamentos). Las recomendaciones presentadas muestran por tanto la fuerza de la recomendaci&oacute;n (la fuerte o la d&eacute;bil), la direcci&oacute;n de la misma (a favor o en contra de la intervenci&oacute;n) as&iacute; como la calidad de la evidencia que la soporta (muy baja, baja, moderada, alta o consenso de expertos).</P>     <P>La versi&oacute;n final de la gu&iacute;a fue evaluada por pares internacionales, seleccionados por el Ministerio de la Protecci&oacute;n Social, expertos tanto en dislipidemias como en metodolog&iacute;a. Sus aportes fueron tenidos en cuenta por el grupo desarrollador de la gu&iacute;a.</P>     <P><B>Resultados</B></P>     <P>Se condujo una b&uacute;squeda sistem&aacute;tica de la literatura de <I>novo</I> para identificar metaan&aacute;lisis o revisiones sistem&aacute;ticas de la literatura publicadas entre enero de 2008 y julio de 2013, empleando las bases de datos sugeridas en la gu&iacute;a metodol&oacute;gica (MEDLINE, Cochrane, CRD Database). Se identificaron 25 metaan&aacute;lisis que abordan el impacto del tratamiento con estatinas sobre los desenlaces seleccionados (la mortalidad, la angina, el infarto agudo del miocardio, el ataque cerebrovascular, los niveles de las fracciones lip&iacute;dicas, el c&aacute;ncer, la diabetes mellitus)<SUP>1,20,25,32&ndash;53</SUP>. Adicionalmente, por sugerencia de los expertos em&aacute;ticos se incluy&oacute; otro metaan&aacute;lisis<SUP>54</SUP>, que no fue identificado en las b&uacute;squedas realizadas.</P>     <P>Para la poblaci&oacute;n de prevenci&oacute;n primaria, al comparar el uso de estatinas frente a placebo se encontr&oacute; una reducci&oacute;n de la mortalidad global de 14&#37; a favor del grupo en tratamiento con estatinas (OR 0,86, IC 95&#37; 0,79; 0,94)<SUP>1</SUP>, as&iacute; como una disminuci&oacute;n de 22&#37;  en el riesgo de presentar ataque cerebrovascular con el uso de estatinas (RR 0,78, IC 95&#37; 0,68; 0,89)<SUP>1</SUP>. Tambi&eacute;n se hall&oacute; una reducci&oacute;n de 37&#37; en el riesgo de presentar infarto agudo del miocardio (RR 0,63, IC 95&#37; 0,50; 0,79)<SUP>20</SUP> y una reducci&oacute;n de 29&#37; en el riesgo de presentar angina inestable en los pacientes tratados con estatinas (RR 0,71 IC 95&#37; 0,55; 0,92)<SUP>20</SUP>. Para el desenlace de niveles de las fracciones lip&iacute;dicas se demostr&oacute; una reducci&oacute;n de 40,53 mg/dl en el colesterol total (DM -40,53 IC 95&#37;   -52,11; -29,33) y de 38,60 mg/dl en el cLDL (DM -38,60, IC 95&#37; -44,77; -32,81)<SUP>1</SUP>. Todas las diferencias resultan cl&iacute;nica y estad&iacute;sticamente significativas.</P>     ]]></body>
<body><![CDATA[<P>Al evaluar el tratamiento con estatinas frente a placebo en la poblaci&oacute;n de prevenci&oacute;n secundaria se encontr&oacute; una asociaci&oacute;n estad&iacute;stica y cl&iacute;nicamente significativa entre el uso de estatinas y reducci&oacute;n de mortalidad, con una disminuci&oacute;n de 18&#37;   en la probabilidad de presentar este desenlace (OR 0,82 IC 95&#37; 0,75; 0,90)<SUP>34</SUP>. Tambi&eacute;n se observ&oacute; una disminuci&oacute;n de 16&#37;   en los eventos de ataque cerebrovascular (RR 0,84 IC 95&#37; 0,76; 0,93) y una reducci&oacute;n de 27&#37; en el riesgo de presentar infarto agudo del miocardio en los pacientes que recibieron tratamiento con estatinas (RR 0,73 IC 95&#37; 0,65; 0,81)<SUP>35</SUP>; en ambos casos los resultados son cl&iacute;nica y estad&iacute;sticamente significativos.</P>     <P>El estudio de la colaboraci&oacute;n Cholesterol Treatment Trialists&iquest; Collaborators<SUP>25</SUP>, evalu&oacute; la eficacia y la seguridad de la disminuci&oacute;n intensiva del cLDL por medio del tratamiento con estatinas. Al comparar terapia intensiva frente a menos intensiva se encontr&oacute; que con una reducci&oacute;n de 38,6 mg/dl en los niveles de cLDL se logra una disminuci&oacute;n del 29&#37; en los eventos de infarto agudo del miocardio no fatal (RR 0,71 IC 95&#37; 0,58; 0,87) y del 26&#37; en los eventos de ataque cerebrovascular (RR 0,74 IC 95&#37; 0,59; 0,92).</P>     <P>Tambi&eacute;n se observ&oacute; que estas reducciones en los eventos vasculares no dependen de la concentraci&oacute;n basal de cLDL, y se logran reducciones significativas en el riesgo de presentar estos eventos en todos los casos en los que se disminuy&oacute; el cLDL con terapia intensiva. Para aquellos con reducci&oacute;n de los niveles de cLDL respecto al valor basal &lt; 38,6 mg/dl se observ&oacute; una disminuci&oacute;n de 29&#37; en los eventos vasculares mayores (RR 0,71 IC 95&#37; 0,52; 0,98); en quienes alcanzaron una reducci&oacute;n del cLDL entre 77,2 y 96,5 mg/dl se observ&oacute; una disminuci&oacute;n de 23&#37; en dichos eventos (RR 0,77; IC 95&#37; 0,64; 0,94) y en quienes alcanzaron una reducci&oacute;n del cLDL &ge; 135,1 mg/dl los eventos disminuyeron 36&#37; (RR 0,64 IC 95&#37; 0,47; 0,86).</P>     <P>No se encontraron diferencias estad&iacute;sticamente significativas en la mortalidad de origen coronario al comparar la terapia intensiva con estatinas frente a la terapia menos intensiva (RR 0,85 IC 95&#37; 0,63; 1,15).</P>     <P>En cuanto a los efectos adversos, al comparar frente a placebo, no se encontr&oacute; asociaci&oacute;n entre el uso de estatinas y riesgo aumentado de desarrollar c&aacute;ncer (OR 0,96, IC 95&#37; 0,91; 1,02)<SUP>54</SUP>. S&iacute; se encontraron diferencias de estad&iacute;stica y cl&iacute;nicamente significativas en la ocurrencia de diabetes mellitus, mostrando 9&#37; m&aacute;s chance de presentar este desenlace (OR 1,09, IC 95&#37; 1,02; 1,16) en aquellos pacientes que estaban recibiendo estatinas.</P>     <P><B>Discusi&oacute;n</B></P>     <P>De acuerdo con la informaci&oacute;n presentada, resulta evidente el efecto ben&eacute;fico del tratamiento farmacol&oacute;gico con estatinas tanto en la poblaci&oacute;n de prevenci&oacute;n primaria como en prevenci&oacute;n secundaria, logrando reducciones cl&iacute;nica y estad&iacute;sticamente significativas en la mortalidad y en los eventos cardiovasculares y los cerebrovasculares (el infarto agudo del miocardio, el ataque cerebrovascular y la angina).</P>     <P>Tambi&eacute;n se encontr&oacute; fuerte evidencia, aportada por la colaboraci&oacute;n Cholesterol Treatment Trialists&iquest; Collaborators<SUP>25</SUP>, a favor del tratamiento intensivo con estatinas, mostrando mayor reducci&oacute;n en los eventos ateroscler&oacute;ticos al compararlo con el tratamiento de intensidad moderada. Adicionalmente, se observ&oacute; que la reducci&oacute;n en el riesgo relativo de los eventos cardiovasculares o los cerebrovasculares es independiente de la concentraci&oacute;n basal de cLDL y que la reducci&oacute;n absoluta en el cLDL se asocia con una reducci&oacute;n proporcional en el riesgo cardiovascular. De tal forma que al definir la intervenci&oacute;n a realizar en el &aacute;mbito cl&iacute;nico, se deber&iacute;a buscar una reducci&oacute;n del cLDL basado en el riesgo cardiovascular calculado a 10 a&ntilde;os para cada paciente y no en la consecuci&oacute;n de metas sobre las cuales no hay evidencia de impacto en prevenci&oacute;n de los eventos cardiovasculares o los cerebrovasculares.</P>     <P>Esta intervenci&oacute;n permitir&iacute;a diferenciar el perfil de riesgo de los pacientes y seg&uacute;n esto se definir&iacute;a la intensidad apropiada del tratamiento para lograr una reducci&oacute;n significativa en el riesgo de presentar eventos cardiovasculares ateroscler&oacute;ticos. As&iacute; mismo, en quienes tengan un riesgo cardiovascular bajo (&lt; 10&#37; seg&uacute;n la escala de Framingham ajustada para la poblaci&oacute;n colombiana), habr&iacute;a que considerar la relaci&oacute;n entre riesgos y beneficios para definir el inicio del tratamiento con estatinas en dosis moderada o realizar modificaciones en el estilo de vida.</P>     <P>Respecto a los eventos adversos que fueron evaluados, no se encontraron diferencias significativas en el riesgo de desarrollar c&aacute;ncer al comparar estatinas frente a placebo pero se encontr&oacute; un incremento de 9&#37; en el riesgo de presentar diabetes mellitus asociado con el tratamiento con estatinas. Sin embargo, se encontraron serias limitaciones metodol&oacute;gicas que comprometen la calidad de la evidencia de este &uacute;ltimo desenlace ya que la incidencia de la diabetes no ha sido un desenlace primario en la mayor&iacute;a de los grandes estudios realizados sobre el uso de estatinas y no en todos se realizaron mediciones basales de glucemia. Por otra parte, no se especifica un m&eacute;todo consistente para establecer el diagn&oacute;stico, por lo que pacientes con o sin evidencia bioqu&iacute;mica de diabetes podr&iacute;an ser categorizados como nuevos casos de diabetes y realmente corresponder a casos no diagnosticados previamente. Por tanto, aunque esta ha sido una alternativa para evaluar la incidencia de diabetes mellitus asociada al uso de estatinas, se requiere mayor informaci&oacute;n para analizar la relaci&oacute;n causa-efecto. Y aun si el aumento es real, es de una magnitud claramente inferior al beneficio potencial del tratamiento con estatinas.</P>     ]]></body>
<body><![CDATA[<P>Vale la pena tener en cuenta que durante el proceso de elaboraci&oacute;n de la gu&iacute;a se public&oacute; la versi&oacute;n preliminar de la gu&iacute;a para el tratamiento del colesterol para reducir el riesgo cardiovascular ateroscler&oacute;tico en adultos del Colegio Americano de Cardiolog&iacute;a y de la Asociaci&oacute;n Americana del Coraz&oacute;n (ACC/AHA 2013)<SUP>55</SUP>, se evalu&oacute; su calidad y se consider&oacute; apta para ser incluida como fuente de evidencia.</P>     <P>Esta gu&iacute;a se centra en emplear la intensidad apropiada en la terapia farmacol&oacute;gica con estatinas para reducir el riesgo cardiovascular en quienes m&aacute;s probablemente se beneficien de dicha intervenci&oacute;n. Los autores de esta gu&iacute;a recalcan que las fuentes de evidencia disponibles incluyeron experimentos cl&iacute;nicos controlados que compararon dosis fijas de estatinas frente a placebo o ning&uacute;n tratamiento, y aquellos que compararon dosis fijas de estatinas de intensidad alta frente a estatinas de intensidad moderada. Sin embargo, no se encontraron estudios dise&ntilde;ados para evaluar el impacto del tratamiento con dosis ajustadas de estatinas para lograr metas espec&iacute;ficas de cLDL o colesterol no HDL, por lo cual no hay evidencia que soporte esta intervenci&oacute;n que previamente se hab&iacute;a recomendado en las gu&iacute;as del ATP III<SUP>6</SUP>.</P>     <P>Las gu&iacute;as ACC/AHA 2013<SUP>55</SUP>, recomiendan el inicio de terapia con estatinas en personas con riesgo cardiovascular incrementado, pues son quienes tienen mayor probabilidad de beneficiarse en t&eacute;rminos de la reducci&oacute;n del riesgo cardiovascular, aun al considerar los posibles efectos adversos asociados con esta intervenci&oacute;n. En el caso de prevenci&oacute;n primaria de enfermedad cardiovascular ateroscler&oacute;tica en individuos sin manifestaciones cl&iacute;nicas, el inicio de la terapia con estatinas se determinar&aacute; de acuerdo con el riesgo cardiovascular estimado a 10 a&ntilde;os y en prevenci&oacute;n secundaria, la evidencia soporta el tratamiento de alta intensidad con estatinas para disminuir al m&aacute;ximo los niveles de cLDL.</P>     <P>Estas recomendaciones son consistentes con los resultados hallados tras el proceso de b&uacute;squeda y recolecci&oacute;n sistem&aacute;tica de la evidencia y con las recomendaciones formuladas por el panel de expertos que participaron en la elaboraci&oacute;n de la gu&iacute;a de pr&aacute;ctica cl&iacute;nica para la prevenci&oacute;n, detecci&oacute;n temprana, diagn&oacute;stico, tratamiento y seguimiento de las dislipidemias.</P>     <P><B>Conclusiones</B></P>     <P>A continuaci&oacute;n se presentan las recomendaciones finales de la gu&iacute;a de pr&aacute;ctica cl&iacute;nica para la prevenci&oacute;n, detecci&oacute;n temprana, diagn&oacute;stico, tratamiento y seguimiento de las dislipidemias, en cuanto al tratamiento farmacol&oacute;gico con estatinas. Dichas recomendaciones fueron derivadas de la evidencia presentada y las consideraciones mostradas en la discusi&oacute;n. La informaci&oacute;n completa del proceso para generar las recomendaciones se encuentra en la versi&oacute;n completa de la gu&iacute;a disponible a trav&eacute;s de la p&aacute;gina electr&oacute;nica del Ministerio de Salud y Protecci&oacute;n Social y en la p&aacute;gina electr&oacute;nica de la Alianza CINETS.</P>     <P>Esta misma informaci&oacute;n se presenta a manera de algoritmo en la <a href="#f1">figura 1.</a></P>     <P align="center"><a name="f1"></a><a href="img/revistas/rcca/v22n1/v22n1a04f1.jpg" target="_blank">Figura 1</a></P>     <P><B>Recomendaciones</B></P> <ul>   <ol type="1">         <li>Se recomienda el inicio de terapia con estatinas de alta intensidada<SUP>a</SUP> en:</li>     <UL>           ]]></body>
<body><![CDATA[<LI>Personas con historia de enfermedad cardiovascular ateroscler&oacute;tica<SUP>b</SUP>.</LI>           <li>Personas con nivel de cLDL &gt; 190 mg/dl.</li>           <li>Personas con diabetes mellitus, mayores de 40 a&ntilde;os, que tengan un factor de riesgo cardiovascular asociado<SUP>c</SUP> y cLDL &gt; 70mg/dl</li>           <li>Personas con estimaci&oacute;n de riesgo cardiovascular &gt; 10&#37; a 10 a&ntilde;os, seg&uacute;n la escala de Framingham recalibrada para Colombia.    <br>         <I>Recomendaci&oacute;n</I> fuerte a favor de la intervenci&oacute;n.    <br>         Calidad de la evidencia: &#8853; &#8853; &#8853; &#8853; &#8853;  Alta.</li>         </UL>         <li>Se recomienda el inicio de terapia con estatinas de moderada intensidad<SUP>c</SUP> en:</li>     <ul>           <li>Personas con diabetes mellitus, mayores de 40 a&ntilde;os, con cLDL &gt; 70 mg/dl y sin criterios de terapia intensiva    <br>         <I>Recomendaci&oacute;n</I> fuerte a favor de la intervenci&oacute;n.    ]]></body>
<body><![CDATA[<br>         Calidad de la evidencia: &#8853;&#8853;&#8853;&#8853;&#8854;" Moderada.</li>         </ul>         <li>Se sugiere considerar terapia con estatinas de moderada intensidad en personas que no quedaron incluidas en ninguno de los grupos anteriores y tengan una o m&aacute;s de las siguientes condiciones:</li>     <ul>           <li>Nivel de cLDL &gt; 160 mg/dl.</li>           <li>Historia familiar de eventos cardiovasculares o cerebrovasculares ateroscler&oacute;ticos tempranos en familiares de primer grado de consanguinidad (hombres menores de 55 a&ntilde;os o mujeres menores de 65 a&ntilde;os).</li>         </ul>         <p>Recomendaci&oacute;n d&eacute;bil a favor de la intervenci&oacute;n.    <br>       Calidad de la evidencia: &#8853;&#8853;&#8853;&#8854; Moderada.    <br>       <I>Punto de buena pr&aacute;ctica cl&iacute;nica</I></p>       </ol>   <ul>         ]]></body>
<body><![CDATA[<li>Se deben implementar las estrategias de prevenci&oacute;n primaria de diabetes mellitus definidas para la poblaci&oacute;n general, como parte de la vigilancia cl&iacute;nica de los pacientes que reciben terapia con estatinas.</li>       </ul>     </ul> <HR>     <p><sup>a</sup>En personas con edad mayor de 75 a&ntilde;os podr&aacute; definirse el uso de estatinas de alta o moderada intensidad de acuerdo con el balance de riesgo-beneficio o la preferencia el paciente.    <br>   <sup>b</sup>Se consideran personas con historia de enfermedad cardiovascular ateroscler&oacute;tica a aquellas que hayan presentado eventos coronarios agudos(incluyendo IAM y angina estabel o inestable), ACV, AIT, historia previa de revascularizaci&oacute;n (coronaria o aotro nivel) o enfermedad vascular ateroscler&oacute;tica de miembros inferiores.    <br>   <sup>c</sup>Se consideran factores de riesgo cardiovascular: HTA, Obesidad, tabaquismo</p> <hr>     <P><B>Responsabilidades &eacute;ticas</B></P>     <P><B>Protecci&oacute;n de personas y animales</B>: Los autores declaran que para esta investigaci&oacute;n no se han realizado experimentos en seres humanos ni en animales.</P>     <P><B>Confidencialidad de los datos</B>: Los autores declaran que en este art&iacute;culo no aparecen datos de pacientes.</P>     <P><B>Derecho a la privacidad y consentimiento informado</B>:Los autores declaran que en este art&iacute;culo no aparecen datos de pacientes.</P>     ]]></body>
<body><![CDATA[<P><B>Financiaci&oacute;n</B></P>     <P>El Ministerio de Salud y Protecci&oacute;n Social ha encargado a la Pontificia Universidad Javeriana y a la Alianza CINETS conformada por las Universidades Javeriana, Nacional y Antioquia el desarrollo de una <I>Gu&iacute;a cl&iacute;nica sobre la prevenci&oacute;n, detecci&oacute;n temprana, diagn&oacute;stico, tratamiento y seguimiento de las dislipidemias en la poblaci&oacute;n mayor de 18 a&ntilde;os</I>.</P>     <P><B>Conflicto de intereses</B></P>     <P>Los autores declaran no tener ning&uacute;n conflicto de intereses.</P>     <P><B>Agradecimientos</B></P>     <P>Agradecemos la contribuci&oacute;n de las personas que, en car&aacute;cter de representantes de expertos tem&aacute;ticos, usuarios, poblaci&oacute;n blanco o grupos de inter&eacute;s, asistieron o participaron en las reuniones de socializaci&oacute;n realizadas durante el desarrollo de la presente gu&iacute;a.</P>     <P>Agradecemos la participaci&oacute;n de las instituciones, asociaciones y sociedades cient&iacute;ficas, a trav&eacute;s de sus representantes, por sus aportes y contribuci&oacute;n en los diferentes procesos del desarrollo de la gu&iacute;a:</P> <ul>       <li>Asociaci&oacute;n Colombiana de Medicina Interna (ACMI).</li>       <li>Sociedad Colombiana de Cardiolog&iacute;a y Cirug&iacute;a Cardiovascular.</li>       <li>Asociaci&oacute;n Colombiana de Endocrinolog&iacute;a, Diabetes y Metabolismo.</li>       ]]></body>
<body><![CDATA[<li>Asociaci&oacute;n Colombiana de Fisioterapia (ASCOFI).</li>       <li>Centro Colombiano de Nutrici&oacute;n Integral (CECNI).</li>       <li>Centro Nacional de Investigaci&oacute;n en Evidencia y Tecnolog&iacute;as en Salud (Alianza CINETS).</li>     </ul>     <P>En personas con edad mayor de 75 a&ntilde;os podr&aacute; definirse el uso de estatinas de alta o moderada intensidad de acuerdo con el balance de riesgo-beneficio o la preferencia del paciente.</P>     <P>Se consideran personas con historia de enfermedad cardiovascular ateroscler&oacute;tica a aquellas que hayan presentado eventos coronarios agudos (incluyendo IAM y angina estable o inestable), ACV, AIT, historia previa de revascularizaci&oacute;n (coronaria o a otro nivel) o enfermedad vascular ateroscler&oacute;tica de miembros inferiores.</P>     <P>Se consideran factores de riesgo cardiovascular: HTA, obesidad, tabaquismo.</P>     <P><B>Bibliograf&iacute;a</B></P>     <!-- ref --><P>1. Taylor F., Huffman M.D., Macedo A.F., Moore T.H.M., Burke M., Davey G. Statins for the primary prevention of cardiovascular disease. Cochrane database Syst Rev.2013;1:CD004816.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000121&pid=S0120-5633201500010000400001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     ]]></body>
<body><![CDATA[<!-- ref --><P>2. Stamler J., Vaccaro O., Neaton J.D., Wentworth D. Diabetes, other risk factors, and 12-yr cardiovascular mortality for men screened in the Multiple Risk Factor Intervention Trial. Diabetes Care.1993;16:434-44.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000123&pid=S0120-5633201500010000400002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>3. Chen Z., Peto R., Collins R., MacMahon S., Lu J., Li W. Serum cholesterol concentration and coronary heart disease in population with low cholesterol concentrations. BMJ.1991;303:276-82.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000125&pid=S0120-5633201500010000400003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>4. Lewington S., Whitlock G., Clarke R., Sherliker P., Emberson J., Halsey J. Blood cholesterol and vascular mortality by age, sex, and blood pressure: a meta-analysis of individual data from 61 prospective studies with 55,000 vascular deaths. Lancet.2007;370:1829-39.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000127&pid=S0120-5633201500010000400004&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>5. Collaborative meta-analysis of 61 studies of vascular risk factors (blood cholesterol, blood pressure, body mass index, diabetes) and cause-specific mortality. Lancet.2007;370:1829-39.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000129&pid=S0120-5633201500010000400005&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>6. Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection. Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report. Circulation.2002;106:3143-421.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000131&pid=S0120-5633201500010000400006&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     ]]></body>
<body><![CDATA[<!-- ref --><P>7. Last A.R., Ference J.D., Falleroni J. Pharmacologic treatment of hyperlipidemia. Am Fam Physician.2011;84:551-8.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000133&pid=S0120-5633201500010000400007&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>8. Baigent C., Keech A., Kearney P.M., Blackwell L., Buck G., Pollicino C. Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90,056 participants in 14 randomised trials of statins. Lancet.2005;366:1267-78.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000135&pid=S0120-5633201500010000400008&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>9. Blauw G.J., Lagaay A.M., Smelt A.H., Westendorp R.G. Stroke, statins, and cholesterol. A meta-analysis of randomized, placebo-controlled, double-blind trials with HMG-CoA reductase inhibitors. Stroke.1997;28:946-50.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000137&pid=S0120-5633201500010000400009&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>10. Briel M., Studer M., Glass T.R., Bucher H.C. Effects of statins on stroke prevention in patients with and without coronary heart disease: a meta-analysis of randomized controlled trials. Am J Med.2004;117:596-606.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000139&pid=S0120-5633201500010000400010&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>11. Cheung B.M.Y., Lauder I.J., Lau C.-P., Kumana C.R. Meta-analysis of large randomized controlled trials to evaluate the impact of statins on cardiovascular outcomes. Br J Clin Pharmacol.2004;57:640-51.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000141&pid=S0120-5633201500010000400011&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     ]]></body>
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<body><![CDATA[<!-- ref --><P>22. Conroy R.M., Py&ouml;r&auml;l&auml; K., Fitzgerald A.P., Sans S., Menotti A., DeBacker G. Estimation of ten year risk of fatal cardio-vascular disease in Europe: the SCORE project. Eur Heart J.2003;24:987-1003.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000163&pid=S0120-5633201500010000400022&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>23. Assmann G., Cullen P., Schulte H. Simple scoring scheme for cal-culating the risk of acute coronary events based on the 10-yearfollow-up of the Prospective Cardiovascular Munster (PROCAM)study. Circulation.2002;105:310-5.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000165&pid=S0120-5633201500010000400023&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>24. Ridker P.M., Danielson E., Fonseca F.A.H., Genest J., Gotto A.M., Kastelein J.J. Rosuvastatin to prevent vascular events in men and women with elevated C-reactive protein. N Engl J Med.2008;359:2195-207.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000167&pid=S0120-5633201500010000400024&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>25. Baigent C., Blackwell L., Emberson J., Holland L.E., Reith C., Bhala N. Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170,000 participants in 26 randomised trials. Lancet.2010;376:1670-81.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000169&pid=S0120-5633201500010000400025&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>     <!-- ref --><P>26. de Lemos J.A., Blazing M.A., Wiviott S.D. Early intensive <I>vs</I> a delayed conservative simvastatin strategy in patients with acute coronary syndromes: phase Z of the A to Z trial. JAMA.2004;292:1307-16.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=000171&pid=S0120-5633201500010000400026&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></P>      ]]></body>
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