<?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>1130-1473</journal-id>
<journal-title><![CDATA[Neurocirugía]]></journal-title>
<abbrev-journal-title><![CDATA[Neurocirugía]]></abbrev-journal-title>
<issn>1130-1473</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Española de Neurocirugía]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1130-14732011000100001</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Dianas quirúrgicas en el tratamiento de enfermedades psiquiátricas: Desde el movimiento a las emociones]]></article-title>
<article-title xml:lang="en"><![CDATA[Surgical targets in Psychiatric disorders: From movement to emotions]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Guridi]]></surname>
<given-names><![CDATA[J.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Aldave]]></surname>
<given-names><![CDATA[G.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Clínica Universidad de Navarra Servicio de Neurocirugía ]]></institution>
<addr-line><![CDATA[Pamplona ]]></addr-line>
<country>España</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>02</month>
<year>2011</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>02</month>
<year>2011</year>
</pub-date>
<volume>22</volume>
<numero>1</numero>
<fpage>5</fpage>
<lpage>22</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_arttext&amp;pid=S1130-14732011000100001&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_abstract&amp;pid=S1130-14732011000100001&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_pdf&amp;pid=S1130-14732011000100001&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[La estimulación cerebral profunda para las enfermedades psiquiátricas que son refractarias a los distintos tratamientos convencionales, se está realizando actualmente debido en gran parte a los conocimientos adquiridos en la cirugía para los trastornos del movimiento, sobre todo la enfermedad de Parkinson (EP). La depresión, los trastornos obsesivo-compulsivos (TOC) y el síndrome de Gilles de la Tourette son problemas córtico-estriato-tálamo-corticales relacionados con los circuitos límbicos de los ganglios basales. En esta revisión se analizan las distintas dianas quirúrgicas para las diferentes patologías neuro-psiquiátricas. Para el TOC actualmente existen dos dianas, el complejo estriado ventral (VS)-núcleo accumbens (Nacc) y el núcleo subtalámico (NST). Para la depresión refractaria, el área subgenual (área 25 de Brodmann) y el VS/Nacc. Para el Tourette, el ventralis oralis interno y centromediano parafascicularis (Voi, CM/Pf) del tálamo y el globo pálido interno (GPi). En la actualidad no existe una única diana específica en cualquiera de las patologías, ya que los resultados clínicos tras la estimulación pueden considerarse similares. Por otro lado, una misma diana quirúrgica puede mejorar diferentes patologías.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Deep brain stimulation (DBS) for psychiatric disorders refractory to conventional treatments are currently been performed based in the knowledgment obtained in the motor disorder surgery and mainly in Parkinson's disease. Depression, obsessive-compulsive disorder (OCD) and Tourette syndrome, all of them are cortico-striato-thalamo-cortical pathological process involved in the limbic loop of the basal ganglia. This review describes the different targets in these pathological neuro-psychiatric disorders. For OCD there are currently two targets, ventral striatum (VS) Accumbens nucleus (Nacc) and the subthalamic nucleus (STN). In refractory depression the subgenual area (25 Brodmann area) and VS/Nacc. For Tourette syndrome the ventralis oralis internus and centromedianum/parafascicularis of the thalamus (Voi and CM/Pf) and the internal part of the globus pallidus (GPi). Currently there are no specific surgical target for each pathological disorder because clinical results reported are very similar after stimulation surgery. In other point, a selected surgical target also may improve different pathologies.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Estimulación cerebral profunda]]></kwd>
<kwd lng="es"><![CDATA[Enfermedad de Parkinson]]></kwd>
<kwd lng="es"><![CDATA[Trastorno obsesivo-compulsivo]]></kwd>
<kwd lng="es"><![CDATA[Gilles de la Tourette]]></kwd>
<kwd lng="es"><![CDATA[Depresión]]></kwd>
<kwd lng="en"><![CDATA[Deep brain stimulation]]></kwd>
<kwd lng="en"><![CDATA[Parkinson's disease]]></kwd>
<kwd lng="en"><![CDATA[Obsessive-compulsive disorder]]></kwd>
<kwd lng="en"><![CDATA[Tourette syndrome]]></kwd>
<kwd lng="en"><![CDATA[Depression]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p>&nbsp;</p>     <p>&nbsp;</p>     <p><a name="top"></a><font face="Verdana" size="4"><b>Dianas quir&uacute;rgicas en el tratamiento de enfermedades psiqui&aacute;tricas. Desde el movimiento a las emociones</b></font></p>     <p><font face="Verdana" size="4"><b>Surgical targets in Psychiatric disorders. From movement to emotions</b></font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>J. Guridi y G. Aldave</b></font></p>     <p><font face="Verdana" size="2">Servicio de Neurocirug&iacute;a. Cl&iacute;nica Universidad de Navarra. Pamplona. Espa&ntilde;a.</font></p>     <p><font face="Verdana" size="2"><a href="#bajo">Dirección para correspondencia</a></font></p>     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p>&nbsp;</p> <hr size="1">     <p><font face="Verdana" size="2"><b>RESUMEN</b></font></p>     <p><font face="Verdana" size="2">La estimulaci&oacute;n cerebral profunda para las enfermedades psiqui&aacute;tricas que son refractarias a los distintos tratamientos convencionales, se est&aacute; realizando actualmente debido en gran parte a los conocimientos adquiridos en la cirug&iacute;a para los trastornos del movimiento, sobre todo la enfermedad de Parkinson (EP). La depresi&oacute;n, los trastornos obsesivo-compulsivos (TOC) y el s&iacute;ndrome de Gilles de la Tourette son problemas c&oacute;rtico-estriato-t&aacute;lamo-corticales relacionados con los circuitos l&iacute;mbicos de los ganglios basales.    <br>En esta revisi&oacute;n se analizan las distintas dianas quir&uacute;rgicas para las diferentes patolog&iacute;as neuro-psiqui&aacute;tricas. Para el TOC actualmente existen dos dianas, el complejo estriado ventral (VS)-n&uacute;cleo accumbens (Nacc) y el n&uacute;cleo subtal&aacute;mico (NST). Para la depresi&oacute;n refractaria, el &aacute;rea subgenual (&aacute;rea 25 de Brodmann) y el VS/Nacc. Para el Tourette, el ventralis oralis interno y centromediano parafascicularis (Voi, CM/Pf) del t&aacute;lamo y el globo p&aacute;lido interno (GPi). En la actualidad no existe una &uacute;nica diana espec&iacute;fica en cualquiera de las patolog&iacute;as, ya que los resultados cl&iacute;nicos tras la estimulaci&oacute;n pueden considerarse similares. Por otro lado, una misma diana quir&uacute;rgica puede mejorar diferentes patolog&iacute;as.</font></p>     <p><font face="Verdana" size="2"><b>Palabras clave:</b> Estimulaci&oacute;n cerebral profunda. Enfermedad de Parkinson. Trastorno obsesivo-compulsivo. Gilles de la Tourette. Depresi&oacute;n.</font></p> <hr size="1">     <p><font face="Verdana" size="2"><b>SUMMARY</b></font></p>     <p><font face="Verdana" size="2">Deep brain stimulation (DBS) for psychiatric disorders refractory to conventional treatments are currently been performed based in the knowledgment obtained in the motor disorder surgery and mainly in Parkinson's disease. Depression, obsessive-compulsive disorder (OCD) and Tourette syndrome, all of them are cortico-striato-thalamo-cortical pathological process involved in the limbic loop of the basal ganglia.    <br>This review describes the different targets in these pathological neuro-psychiatric disorders. For OCD there are currently two targets, ventral striatum (VS) Accumbens nucleus (Nacc) and the subthalamic nucleus (STN). In refractory depression the subgenual area (25 Brodmann area) and VS/Nacc. For Tourette syndrome the ventralis oralis internus and centromedianum/parafascicularis of the thalamus (Voi and CM/Pf) and the internal part of the globus pallidus (GPi). Currently there are no specific surgical target for each pathological disorder because clinical results reported are very similar after stimulation surgery. In other point, a selected surgical target also may improve different pathologies.</font></p>     <p><font face="Verdana" size="2"><b>Key words:</b> Deep brain stimulation. Parkinson's disease. Obsessive-compulsive disorder. Tourette syndrome. Depression.</font></p> <hr size="1">     <p>&nbsp;</p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2"><b>Introducci&oacute;n</b></font></p>     <p><font face="Verdana" size="2">El tratamiento quir&uacute;rgico de los problemas psiqui&aacute;tricos ha venido realiz&aacute;ndose desde los albores de la cirug&iacute;a con estereotaxia<sup>23,105</sup>. Sin embargo, durante a&ntilde;os la cirug&iacute;a de dichos trastornos dej&oacute; de practicarse, en gran parte debido a lo indiscriminado de su realizaci&oacute;n, lo que llev&oacute; a un descr&eacute;dito de dichas t&eacute;cnicas y a su pr&aacute;ctica desaparici&oacute;n. Tambi&eacute;n la aparici&oacute;n de los neurol&eacute;pticos ha podido beneficiar a muchos pacientes, por lo que la cirug&iacute;a para los trastornos psiqui&aacute;tricos se redujo considerablemente. Sin embargo, actualmente con la mejora en t&eacute;cnicas de imagen, disminuci&oacute;n de los riesgos quir&uacute;rgicos de la cirug&iacute;a funcional y la aparici&oacute;n de t&eacute;cnicas de estimulaci&oacute;n en este campo quir&uacute;rgico, todo ello ha conllevado la reintroducci&oacute;n de la cirug&iacute;a en las enfermedades psiqui&aacute;tricas refractarias a los diferentes tratamientos convencionales<sup>69</sup>.</font></p>     <p><font face="Verdana" size="2">La cirug&iacute;a realizada desde hace varios a&ntilde;os en patolog&iacute;a de los trastornos del movimiento, tanto enfermedad de Parkinson (EP), diston&iacute;a como temblor, han llevado a incrementar el conocimiento tanto anat&oacute;mico como fisiopatol&oacute;gico sobre la organizaci&oacute;n funcional de los ganglios basales (GB) en los distintos procesos patol&oacute;gicos. Esto en gran medida se debe a los estudios realizados en primates y desde los cuales hemos podido comprender el funcionamiento de los GB en condiciones de hipercinesia e hipocinesia creando un modelo de funcionamiento. As&iacute; la lesi&oacute;n del n&uacute;cleo subtal&aacute;mico (NST) en animales y en humanos induce una corea/balismo (estado hipercin&eacute;tico), o bien la introducci&oacute;n de un t&oacute;xico como el MPTP (1-metyl-4 fenil-1,2,3,6 tetrahidropiridina) en primates conlleva un cuadro parkinsoniano con temblor, rigidez y lentitud similar a la EP en humanos (condici&oacute;n hipocin&eacute;tica)<sup>18,24,27</sup>. En ambos modelos, el NST juega un papel capital, ya que en el primero, su hipoactividad inducir&iacute;a las disquinesias debido a una hiperactividad del eje t&aacute;lamo-cortical<sup>24</sup>. En la condici&oacute;n parkinsoniana, ser&iacute;a la hiperactividad del NST la que conllevar&iacute;a una hiperactividad inhibitoria desde el globo p&aacute;lido interno (GPi) sobre el t&aacute;lamo favoreciendo la acinesia en el modelo de GB<sup>18,27</sup>. De esta manera, la hiperactividad de la proyecci&oacute;n NST-GPi es capital para entender el funcionamiento de los GB en el EP. En consecuencia, la lesi&oacute;n tanto por t&eacute;cnicas qu&iacute;micas como por radiofrecuencia, o la inhibici&oacute;n del NST por t&eacute;cnicas de estimulaci&oacute;n, conlleva a un beneficio de los animales, tanto del temblor como la rigidez y la lentitud<sup>10,16,17,46</sup>.</font></p>     <p><font face="Verdana" size="2">La creaci&oacute;n de este modelo de funcionamiento por un lado y la aparici&oacute;n de t&eacute;cnicas de estimulaci&oacute;n cerebral (deep brain stimulation: DBS) sin tener que lesionar estructuras profundas, as&iacute; como el buen resultado quir&uacute;rgico en este tipo de patolog&iacute;a de los trastornos del movimiento sobre todo en la enfermedad de Parkinson, ha llevado a introducir la cirug&iacute;a de estimulaci&oacute;n en los pacientes con trastornos psiqui&aacute;tricos que son refractarios a las diferentes terapias convencionales. Es por tanto desde la experiencia quir&uacute;rgica en los trastornos motores, desde donde partimos para abordar las distintas patolog&iacute;as neuro-psiqui&aacute;tricas. Adem&aacute;s, como veremos en la revisi&oacute;n, ambos campos, est&aacute;n muy relacionados entre s&iacute;, ya que las mismas estructuras anat&oacute;micas relacionadas con los problemas motores tambi&eacute;n lo est&aacute;n con las &aacute;reas cognitivas y l&iacute;mbicas que regulan las emociones.</font></p>     <p><font face="Verdana" size="2">La introducci&oacute;n de t&eacute;cnicas de estimulaci&oacute;n en el campo de la psiquiatr&iacute;a no es nueva ya que los primeros pacientes fueron referidos hace a&ntilde;os, tanto en el trastorno obsesivo-compulsivo como en pacientes con Gilles de la Tourette<sup>84,110</sup>. En esta revisi&oacute;n analizamos las diferentes dianas quir&uacute;rgicas que est&aacute;n apareciendo para tratar pacientes con enfermedades psiqui&aacute;tricas, as&iacute; como la disfunci&oacute;n de los circuitos c&oacute;rtico-estriato-t&aacute;lamo-cortical que conllevan las alteraciones del comportamiento y de las emociones en los trastornos obsesivo-compulsivos, s&iacute;ndrome de Tourette y la depresi&oacute;n refractaria. Tambi&eacute;n revisaremos los signos no motores relacionados con la EP y tratados con estimulaci&oacute;n del NST.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>Anatom&iacute;a del circuito l&iacute;mbico</b></font></p>     <p><font face="Verdana" size="2">Es bien conocido, basado en el modelo cl&aacute;sico de funcionamiento de los GB que toda la informaci&oacute;n cortical es procesada a trav&eacute;s de circuitos segregados del estriado que proyecta sobre el globo p&aacute;lido hacia el t&aacute;lamo y nuevamente a la corteza<sup>5,27,89</sup>. Esto ha dado soporte anat&oacute;mico a que existan subdivisiones dentro de los GB como regiones motoras, asociativas y l&iacute;mbicas. Las proyecciones sensitivo-motoras procesar&iacute;an la informaci&oacute;n motora, los territorios asociativos la informaci&oacute;n cognitiva y los l&iacute;mbicos la informaci&oacute;n emocional dentro de los GB.</font></p>     <p><font face="Verdana" size="2">Existe evidencia de que la disfunci&oacute;n en el funcionamiento de los GB se muestra por un comportamiento estereotipado con movimientos repetitivos dentro de trastornos del comportamiento, o bien con la aparici&oacute;n de movimientos anormales (disquinesias). Esto se ha podido comprobar en animales de experimentaci&oacute;n en los cuales el bloqueo de diferentes porciones del GPe (globo p&aacute;lido externo) o del estriado dorsal (putamen) con bicuculina (antagonista GABA&eacute;gico) en monos normales, conlleva la aparici&oacute;n de corea o movimientos miocl&oacute;nicos si las inyecciones son realizadas en las porciones motoras de dichas estructuras<sup>35,124</sup>. Mientras que comportamientos de hiperactividad, d&eacute;ficit de atenci&oacute;n con estereotipias o alteraciones en acciones volitivas se apreciar&iacute;an cuando las inyecciones est&aacute;n realizadas en las regiones l&iacute;mbicas del estriado, del GPe o NST (en esta estructura con el agonista GABA&eacute;rgico muscimol)<sup>35,61,124</sup>. Como conclusi&oacute;n, podemos decir que la actuaci&oacute;n sobre diferentes proyecciones anat&oacute;micas funcionalmente distintas de los GB, induce diferentes comportamientos en primates.</font></p>     <p><font face="Verdana" size="2">Toda la informaci&oacute;n emocional o afectiva es transmitida a trav&eacute;s de las porciones l&iacute;mbicas de los GB. As&iacute; el hipocampo, am&iacute;gdala, &aacute;reas l&iacute;mbicas y paral&iacute;mbicas env&iacute;an sus proyecciones al estriado ventral (VS: ventral striatum)<sup>5,89</sup>. Esta estructura, el VS, es capital en las emociones y mecanismos de recompensa y est&aacute; b&aacute;sicamente formada por la porci&oacute;n ventral del caudado y putamen y por el n&uacute;cleo accumbens (NAcc)<sup>47,48,80</sup>. Desde el VS, se env&iacute;an proyecciones sobre el p&aacute;lido ventral (VP), que es considerado como la principal eferencia desde los GB sobre el t&aacute;lamo proyectando sobre el n&uacute;cleo dorso medial (DM), ventral anterior y n&uacute;cleos intralaminares<sup>5</sup>. El n&uacute;cleo DM y los diferentes n&uacute;cleos tal&aacute;micos, cerrar&iacute;an el circuito proyectando sobre el c&oacute;rtex cingular anterior (CCA) (&aacute;rea 24 de Brodmann) y c&oacute;rtex &oacute;rbito frontal (COF) (&aacute;reas 10,11,13,43 de Brodmann)<sup>38</sup>. Las proyecciones t&aacute;lamocorticales pasan por el brazo anterior de la c&aacute;psula interna (CI) en su porci&oacute;n ventral y es la diana de la capsulotom&iacute;a<sup>57</sup>. (<a href="#f1">Figura 1</a>).</font></p>     ]]></body>
<body><![CDATA[<p align="center"><font face="Verdana" size="2"><a name="f1"><img src="/img/revistas/neuro/v22n1/investigacion1_f1.jpg" width="615" height="471"></a>    <br>Figura 1. <i>Esquema de las proyecciones desde el c&oacute;rtex prefrontal a ganglios basales. AB: areas de Bordmann.    <br> DM Tha: dorsomedial del t&aacute;lamo. GPi: globo p&aacute;lido interno. GPe: globo p&aacute;lido externo. NST: n&uacute;cleo subtal&aacute;mico.    <br> VA: n&uacute;cleo anterior del t&aacute;lamo.VP: p&aacute;lido ventral. VS: estriado ventral.</i></font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2">El c&oacute;rtex prefrontal a su vez proyecta sobre todas las estructuras anat&oacute;micas de las cuales recibe aferencias, as&iacute; env&iacute;a proyecciones sobre el DM, n&uacute;cleos intralaminares tal&aacute;micos y sobre los GB como n&uacute;cleo caudado, putamen, GP y el n&uacute;cleo Accumbens (Nacc)<sup>31,38,40</sup>. El c&oacute;rtex medial prefrontal (&aacute;reas 8,9,10,24,25 y 32 de Brodmann) y el COF (&aacute;reas 10,11,13) proyectan sobre el VS, am&iacute;gdala y c&oacute;rtex temporal medial y esto constituye el sustrato anat&oacute;mico del comportamiento emocional, instintivo y de recompensa<sup>38,47,48</sup>. Mientras que el c&oacute;rtex prefrontal lateral, conectar&iacute;a con las porciones laterales del caudado y n&uacute;cleos laterales tal&aacute;micos siendo estructuras anat&oacute;micas relacionadas con el sustrato cognitivo, ejecutivo y del comportamiento. El VS no recibe aferencias motoras, premotoras ni de &aacute;rea motora suplementaria (AMS)<sup>31,38,47,48</sup>. Por lo tanto, el VS y el NAcc son estructuras anat&oacute;micas directamente relacionadas con el c&oacute;rtex prefrontal y por tanto con las emociones y sus comportamientos, as&iacute; como con sus procesos patol&oacute;gicos como puede ocurrir en los trastornos obsesivo-compulsivos (TOC), s&iacute;ndrome de Tourette (ST) y depresi&oacute;n<sup>4</sup>. As&iacute;, todos ellos tienen en com&uacute;n que presentan una anomal&iacute;a a nivel corticoestriado-t&aacute;lamo-cortical.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>Cirug&iacute;a de la EP. Aspectos motores y no motores</b></font></p>     <p><font face="Verdana" size="2">Con los conocimientos actuales, la EP es considerada como una enfermedad neuro-psiqui&aacute;trica y no &uacute;nicamente como un problema motor<sup>3</sup>. Los distintos tratamientos dopamin&eacute;rgicos, as&iacute; como la cirug&iacute;a en las diferentes dianas (GPi y NST) revierten la acinesia, el temblor y rigidez. La estimulaci&oacute;n del NST (DBS-NST) realizada en la regi&oacute;n sensitivo-motora del n&uacute;cleo mejora significativamente los signos capitales de la enfermedad, los signos axiales y las fluctuaciones motoras, como son las disquinesias y bloqueos motores<sup>50,64,87,94,98,114</sup>. La estimulaci&oacute;n inducir&iacute;a una inhibici&oacute;n funcional similar a la lesi&oacute;n, aunque su mecanismo de acci&oacute;n no es del todo conocido. Sin embargo, al ser en NST una estructura peque&ntilde;a (160 mm c&uacute;bicos)<sup>125</sup>, la estimulaci&oacute;n puede alcanzar las regiones l&iacute;mbicas y asociativas del NST, produciendo efectos adversos como man&iacute;a, risa, gritos, conducta agresiva, depresi&oacute;n y trastornos psiqui&aacute;tricos<sup>15,65,67,95,109,123</sup>. Todos estos fen&oacute;menos pueden llevar a tener que disminuir los par&aacute;metros de estimulaci&oacute;n o a cambiar los contactos activos en ocasiones, pudiendo conllevar una reducci&oacute;n del beneficio motor de los pacientes intervenidos.</font></p>     <p><font face="Verdana" size="2">En los &uacute;ltimos a&ntilde;os, en las evaluaciones cl&iacute;nicas de los pacientes con EP, se est&aacute; dando importancia a los aspectos no motores de la misma. Una de las alteraciones del comportamiento que presentan los pacientes es un trastorno en el control de impulsos (ICD) como el juego patol&oacute;gico, compras compulsivas, hipersexualidad, as&iacute; como otros comportamientos compulsivos, como pueden ser el excesivo hobbismo o excesivo uso de internet (punding)<sup>29,72,115,116</sup>. El ICD es un problema poco estudiado y que actualmente comenzamos a conocer pudiendo encontrase hasta en un 14% de los pacientes con EP y en un 17% en los tratados con agonistas dopamin&eacute;rgicos (DA)<sup>29,117,118,120</sup>.</font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">Tambi&eacute;n en este mismo contexto, se han evaluado pacientes tratados con DBS-STN e ICD. Para algunos autores, el beneficio en el ICD tras la cirug&iacute;a podr&iacute;a estar relacionado con la reducci&oacute;n de los dopamin&eacute;rgicos DA<sup>9,62</sup>. Otros autores, por el contrario, han referido la aparici&oacute;n de ICD en pacientes tratados con DBS a pesar de la reducci&oacute;n de agonistas DA<sup>49,72,104</sup>. Por &uacute;ltimo en otros estudios realizados, la estimulaci&oacute;n del n&uacute;cleo subtal&aacute;mico en pacientes j&oacute;venes, aumentar&iacute;a el riesgo de desarrollar ICD y en este contexto, no &uacute;nicamente existir&iacute;a un incremento en presentar un cuadro de impulsividad, sino tambi&eacute;n un  mayor riesgo de suicidio<sup>12,55,98,103,104,119</sup>.</font></p>     <p><font face="Verdana" size="2">Recientemente se ha publicado que la estimulaci&oacute;n subtal&aacute;mica puede inducir a comportamientos compulsivos, sobre todo cuando existen condiciones de conflicto<sup>36</sup>. Este comportamiento se ha podido apreciar en pacientes con EP en los cuales los tests realizados mostraron una incapacidad para modular sus respuestas al comparar un grupo tratado quir&uacute;rgicamente (n: 17) versus pacientes con medicaci&oacute;n DA (n:15)<sup>36</sup>. Por tanto, podemos concluir que la estimulaci&oacute;n del NST puede conllevar comportamientos impulsivos en algunos pacientes, similares a los de ICD en los pacientes con EP tratados con agonistas DA. Fisiopatol&oacute;gicamente, se tratar&iacute;a de dos mecanismos diferentes en la impulsividad, uno de ellos relacionado con la medicaci&oacute;n dopamin&eacute;rgica, que deriva de los niveles elevados de DA en los receptores D2 estriatales y un segundo mecanismo, ser&iacute;a la estimulaci&oacute;n de la porci&oacute;n l&iacute;mbica del NST, en el cual incluso existe una reducci&oacute;n de DA, pero al ser inhibida la actividad del NST, los pacientes mostrar&iacute;an una impulsividad por la incapacidad para modular decisiones en situaciones de conflicto<sup>36</sup>. Ambas situaciones manifestar&iacute;an un cuadro cl&iacute;nico similar.</font></p>     <p><font face="Verdana" size="2">Estos hallazgos en pacientes tratados quir&uacute;rgicamente en el NST, estar&iacute;an en relaci&oacute;n con estudios realizados previamente en dicha estructura anat&oacute;mica en ratas, induciendo una respuesta anormal en la toma de decisiones tras lesionar el NST<sup>13,14</sup>. Los experimentos mostraron que en animales parkinsonizados tras inyectarles 6-OHDA (hidroxidopamina), la lesi&oacute;n del n&uacute;cleo produc&iacute;a un gran beneficio motor pero aumentaba la respuesta anticipatoria, la conducta perseverativa as&iacute; como el d&eacute;ficit de atenci&oacute;n<sup>14</sup>. En un estudio ulterior, se pudo apreciar que si bien decrec&iacute;a el tiempo de reacci&oacute;n tras la lesi&oacute;n del NST, exist&iacute;a un incremento en las respuestas prematuras llevando a un d&eacute;ficit de comportamiento. Por tanto parece que el NST puede tener un papel en los GB de selecci&oacute;n y de inhibici&oacute;n y que la respuesta anticipatoria conllevar&iacute;a un mayor n&uacute;mero de errores en los animales, pudiendo ser definida como una &quot;disquinesia del comportamiento&quot;<sup>36</sup>. El mismo comportamiento se ha descrito tras estimulaci&oacute;n del NST en los animales intervenidos<sup>25</sup>. La conclusi&oacute;n de dichos estudios, demuestra que la manipulaci&oacute;n, induciendo una inhibici&oacute;n del NST, puede conllevar comportamientos impulsivos<sup>36,108</sup>.</font></p>     <p><font face="Verdana" size="2">Todos estos estudios anat&oacute;micos y cl&iacute;nicos, nos llevan al concepto de que el NST es un potente regulador de los GB en funciones tanto motoras (su lesi&oacute;n o inhibici&oacute;n induce hemicorea/balismo), cognitivas como emocionales (su lesi&oacute;n o inhibici&oacute;n produce conducta impulsiva y anticipatoria) y nos sugiere que juega un importante papel central como modulador en el circuito cortico-estriatot&aacute;lamo-cortical que media los circuitos funcionalmente diferentes como son el motor y el l&iacute;mbico<sup>5,27,88</sup>. El NST por un lado recibe la v&iacute;a hiperdirecta desde el c&oacute;rtex (COF y c&oacute;rtex premotor, AMS y c&oacute;rtex motor primario)<sup>81</sup> y por otro recibe aferencias desde el estriado a trav&eacute;s del GPe, con la misma informaci&oacute;n aunque diferentemente procesada, por lo cual modula la eferencia asociativa y l&iacute;mbica hacia el GPi y SNr (sustancia negra reticulata), los n&uacute;cleos de salida de los GB hacia el t&aacute;lamo<sup>81</sup> (<a href="#f1">Figura 1</a>).</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>Estimulaci&oacute;n cerebral en los trastornos obsesivo-compulsivos</b></font></p>     <p><font face="Verdana" size="2">El trastorno obsesivo-compulsivo (TOC) se caracteriza por la aparici&oacute;n de ideas obsesivas y recurrentes (obsesiones) unidas a actos motores repetitivos (compulsiones) que llevan al paciente a provocar p&eacute;rdidas de tiempo significativas y un bloqueo de cualquier actividad, llegando en ocasiones a incapacitarlo totalmente<sup>106</sup>. La incidencia de esta patolog&iacute;a en la poblaci&oacute;n es del 2%, de los cuales un 30-40% de los pacientes ser&iacute;an refractarios a los distintos tratamientos convencionales<sup>88</sup>.</font></p>     <p><font face="Verdana" size="2">Los estudios funcionales de neuroimagen en el TOC muestran que la medici&oacute;n del flujo sangu&iacute;neo cerebral regional (rCBF) de los pacientes en PET (tomograf&iacute;a por emisi&oacute;n de positrones), al ser comparada con sujetos normales, ha mostrado una hiperactividad en el COF, CCA y estriado<sup>32,91,92</sup>. Dicha actividad estar&iacute;a directamente relacionado con el cuadro cl&iacute;nico, ya que se incrementa durante la provocaci&oacute;n de los s&iacute;ntomas de los pacientes y se reducir&iacute;a con el tratamiento m&eacute;dico<sup>92</sup>. La hiperactividad del COF, estar&iacute;a relacionada con la gravedad del TOC, de esta manera los pacientes con una buena respuesta cl&iacute;nica tras la cirug&iacute;a (DBS en VS/VC) muestran una modulaci&oacute;n de la hiperactividad del COF, &aacute;rea subgenual CCA, estriado, GP y t&aacute;lamo. Esto se ha encontrado en 6 pacientes con TOC tratados quir&uacute;rgicamente, mientras que dicha hiperactividad se manten&iacute;a en los pacientes considerados como refractarios<sup>92</sup>.</font></p>     <p><font face="Verdana" size="2">Nuttin fue el primer neurocirujano que coloc&oacute; un sistema de estimulaci&oacute;n en cuatro pacientes con TOC refractarios a tratamiento m&eacute;dicos, implantando los electrodos en la misma diana donde se realizaba las capsulotom&iacute;as en 1999 (brazo anterior de c&aacute;psula interna en su porci&oacute;n m&aacute;s ventral: CI)<sup>84</sup>. Como hemos visto previamente, por esta zona pasan las proyecciones desde en CM/Pf y n&uacute;cleos intralaminares del t&aacute;lamo hacia el COF y &aacute;reas prefrontales<sup>57,84,85</sup>. Desde entonces, distintos autores han trabajado en esta diana con buenos resultados, ya que se han publicado reducci&oacute;n significativas en las escalas Y-BOCS (Yale Brown Obsessive Compulsive Scale), que es la que mejor eval&uacute;a estos pacientes y se han descrito en el seguimiento, un significativo n&uacute;mero de pacientes con criterios de remisi&oacute;n (<a target="_blank" href="/img/revistas/neuro/v22n1/investigacion1_tabla1.jpg">Tabla 1</a>)<sup>1,40,42,56,85,107</sup>. Tambi&eacute;n los pacientes con TOC con esta diana quir&uacute;rgica mejoran tras la intervenci&oacute;n la depresi&oacute;n, evaluados con la escala de Hamilton y la ansiedad, que son problemas coadyuvantes en esta patolog&iacute;a. Sin embargo, la diana exacta es variable seg&uacute;n los diferentes autores, as&iacute; unos colocan el electrodo en la c&aacute;psula interna (CI)<sup>1,7,84,85</sup> y otros en VS/CI, o bien Nacc/CI, aunque esta estructura formar&iacute;a parte del VS<sup>8,37,41,42,43,44,56,107</sup>. As&iacute;, en algunos estudios cl&iacute;nicos, colocan los contactos de estimulaci&oacute;n dorsales (contactos 2 y 3) en la CI, mientras los m&aacute;s ventrales (contactos 0 y 1) en el VS o bien Nacc, sin llegar a especificar los contactos cl&iacute;nicamente activos en las diferentes publicaciones<sup>8,43,107</sup>.</font></p>     <p><font face="Verdana" size="2">En un estudio de revisi&oacute;n de cuatro centros con experiencia en DBS para TOC en dicha diana quir&uacute;rgica, VS-Nacc, se ha descrito el beneficio progresivo de los pacientes, ya que la gravedad de la enfermedad en las escalas de evaluaci&oacute;n fue reduci&eacute;ndose en las sucesivas revisiones<sup>44</sup>. As&iacute;, a los tres meses tras la cirug&iacute;a, la Y-BOCS disminuy&oacute; una media de 12.5 puntos en la escala (34.0 basal a 21.0 postimplante) y el porcentaje de pacientes que ten&iacute;an criterios de &quot;respondedores&quot; (reducci&oacute;n de un 35% en la escala o mayor) se increment&oacute; de un 28% al mes de la cirug&iacute;a a un 61.5% en la &uacute;ltima revisi&oacute;n<sup>44</sup>. Por otro lado, el cuadro de depresi&oacute;n y de ansiedad de estos pacientes tambi&eacute;n mejora durante el seguimiento de los mismos, existiendo a los 36 meses del implante una reducci&oacute;n del 43.2% en la escala de Hamilton para la depresi&oacute;n y de un 58.7% en la de HARS para la ansiedad. En el mismo trabajo los autores describen que la diana quir&uacute;rgica ha ido acerc&aacute;ndose a la comisura anterior (CA), as&iacute; en los primeros pacientes intervenidos estaba a 15 mm anterior a la misma y los pacientes intervenidos posteriormente en el tiempo, la diana estaba pr&oacute;xima a la CA y m&aacute;s ventral, estimulando VS y NAcc<sup>44</sup>.</font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">Por &uacute;ltimo, recientemente el grupo de la universidad de Colonia ha publicado un estudio doble ciego con estimulaci&oacute;n del NAcc derecho en 10 pacientes<sup>56</sup>. Tras la intervenci&oacute;n y estabilizaci&oacute;n de los mismos, la evaluaci&oacute;n se realiz&oacute; con la estimulaci&oacute;n &quot;on&quot; o bien &quot;off&quot; durante un periodo de tres meses con par&aacute;metros de estimulaci&oacute;n fijos. El estudio ha mostrado una reducci&oacute;n de las escalas de una basal de 32.2 a 27.9 en situaci&oacute;n &quot;on&quot; estimulaci&oacute;n (p: 0.033) y &quot;off&quot; estimulaci&oacute;n de 31.1 en la escala de YBOCS. Seg&uacute;n los autores, tras 12 meses de estimulaci&oacute;n del NAcc derecho, s&oacute;lo uno de los 10 pacientes se consider&oacute; como respuesta total (reducci&oacute;n de la Y-BOCS del 35% o superior) tras un a&ntilde;o de estimulaci&oacute;n cuatro pacientes alcanzaron una respuesta parcial (mejor&iacute;a entre 25-35% con respecto a la basal)<sup>56</sup>. Actualmente los autores, durante el segundo a&ntilde;o de estimulaci&oacute;n, est&aacute;n estudiando la variaci&oacute;n en los par&aacute;metros de estimulaci&oacute;n con una cirug&iacute;a unilateral en cada paciente y su respuesta cl&iacute;nica.</font></p>     <p><font face="Verdana" size="2">Por otro lado, otros autores encontraron que pacientes con EP que tambi&eacute;n ten&iacute;an TOC y que fueron intervenidos con DBS-NST, tras la cirug&iacute;a mejoraron no s&oacute;lo los aspectos motores del Parkinson sino tambi&eacute;n la Y-BOCS<sup>34,74</sup>. Esto llev&oacute; a un estudio aleatorio, doble ciego con la diana en la parte l&iacute;mbica del NST realizado por diferentes centros en Francia. Tras la cirug&iacute;a y estabilizaci&oacute;n de la estimulaci&oacute;n, se eligieron al azar 16/18 pacientes, trat&aacute;ndose en dos fases de 3 meses cada una, para hacer estimulaciones &quot;on&quot; u &quot;off&quot;, separadas por un mes de estimulaci&oacute;n simulada<sup>75</sup>. Se comprob&oacute; que con la estimulaci&oacute;n del NST, la Y-BOCS era significativamente inferior a la estimulaci&oacute;n simulada (28 vs 19). La diana quir&uacute;rgica se situ&oacute; 1 mm medial y 2 mm anterior a la diana para la EP en dicha estructura. El estudio mostr&oacute; 15 efectos adversos serios incluyendo una hemorragia cerebral y 2 infecciones. Entre las complicaciones de esta diana quir&uacute;rgica, la estimulaci&oacute;n en algunos pacientes indujo impulsividad e hipoman&iacute;a similar a los pacientes tratados en la misma diana para EP<sup>75</sup>.</font></p>     <p><font face="Verdana" size="2">Actualmente, una paradoja en este campo es c&oacute;mo la estimulaci&oacute;n del NST en pacientes con EP, puede inducir impulsividad y desinhibici&oacute;n en sus comportamientos, mientras que la misma estructura puede mejorar las obsesiones y compulsiones en los pacientes con TOC. Esto podr&iacute;a indicar que ambos fen&oacute;menos, impulsividad y desinhibici&oacute;n por un lado y obsesiones y compulsiones por otro, pudieran ser opuestos dentro del campo del comportamiento y las emociones.</font></p>     <p><font face="Verdana" size="2">Los par&aacute;metros de estimulaci&oacute;n, en las distintas publicaciones, son muy variables, entre 4-10 voltios, seg&uacute;n los distintos autores<sup>1,8,37,41,43,60,85,107</sup>. As&iacute; Goodman y cols estimularon con 8 voltios y Abelson con 10 voltios en CI, por lo que se debe asumir que el campo de estimulaci&oacute;n es grande y puede alcanzar diferentes estructuras anat&oacute;micas adem&aacute;s de la deseada<sup>1,41</sup>. Anderson y Ahmed son los &uacute;nicos autores que refieren estimulaci&oacute;n con 2 Vols a nivel de CI con buen resultado cl&iacute;nico<sup>7</sup>. Los autores cuya diana fue el NST refieren estimulaciones alrededor de 3 Vols similar a los pacientes con EP<sup>34,73,74</sup>. Los electrodos tambi&eacute;n han variado entre los electrodos modelo 3387 y 3389 (10.5 y 7.5 mm de estimulaci&oacute;n activa; Medtronic) para estimulaci&oacute;n del Nacc/VS/CI o NST. Franzini es el &uacute;nico autor que emple&oacute; el 3389 para Nacc, mientras que todos los autores que fueron al NST emplearon el electrodo 3389<sup>34,37,74</sup> (<a target="_blank" href="/img/revistas/neuro/v22n1/investigacion1_tabla1.jpg">Tabla 1</a>).</font></p>     <p><font face="Verdana" size="2">La experiencia de los trabajos reportados en este campo nos lleva a concluir que existen diferentes dianas quir&uacute;rgicas que pueden llegar a modular la actividad patol&oacute;gica de los circuitos &oacute;rbito-frontal y c&oacute;rtex medial prefrontal a trav&eacute;s de una disrupci&oacute;n o modulaci&oacute;n de sus fibras entre c&oacute;rtex frontal y t&aacute;lamo o bien dentro del propio VS. Ambas dianas, VS/CI y NST, actuar&iacute;an a distintos niveles con resultados cl&iacute;nicos similares. Tambi&eacute;n se ha observado en las revisiones evolutivas, que los pacientes intervenidos mantienen una mejor&iacute;a progresiva, lo que indicar&iacute;a que la modulaci&oacute;n de los circuitos no es inmediata, como ocurre en los trastornos del movimiento, sino que lleva m&aacute;s tiempo en alcanzar el beneficio terap&eacute;utico considerado como &oacute;ptimo.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>S&iacute;ndrome de Gilles de la Tourette</b></font></p>     <p><font face="Verdana" size="2">El s&iacute;ndrome de Gilles de la Tourette (SGT) es una alteraci&oacute;n neuropsiqui&aacute;trica que consiste en la aparici&oacute;n de tics motores tanto faciales, f&oacute;nicos como vocales desde la ni&ntilde;ez. El 96% de los pacientes con el s&iacute;ndrome lo manifiestan antes de los 11 a&ntilde;os de edad<sup>58</sup>. La incidencia de este problema es entre 3-5 casos cada 10.000 habitantes y se trata de una enfermedad autos&oacute;mica dominante con una penetrancia y fenotipo variables. El cuadro cl&iacute;nico del SGT va evolucionando a lo largo de los a&ntilde;os con un incremento de las disquinesias en otras localizaciones como cabeza y extremidades superiores, mientras que en otros pacientes los tics suelen remitir. Por otro lado y en un alto porcentaje de pacientes, existe un cuadro neuropsiqui&aacute;trico como d&eacute;ficit de atenci&oacute;n, hiperactividad y TOC. Este s&iacute;ndrome conocido tanto por psiquiatras como por neur&oacute;logos tiene un sustrato funcional en los GB<sup>4,58</sup>.</font></p>     <p><font face="Verdana" size="2">No existen actualmente modelos animales de Tourette que puedan ser estudiados en el laboratorio. Los estudios con RM funcional en pacientes, han mostrado un incremento de la actividad a nivel prefrontal, parietal, temporal y cingular anterior<sup>90</sup>. Aunque la fisiopatolog&iacute;a del SGT no se conoce con exactitud, puede tratarse de un problema de los GB a nivel estriatal y de la funci&oacute;n dopamin&eacute;rgica. La actividad de descarga t&oacute;nica desde esta estructura hacia el GPi estar&iacute;a disminuida, permitiendo movimientos o tics incontrolados hacia el t&aacute;lamo y la corteza, similar al modelo de hipercinesia. Dicha actividad anormal estar&iacute;a en las neuronas estriatales (neuronas espinosas) que responder&iacute;an patol&oacute;gicamente descargando al est&iacute;mulo dopamin&eacute;rgico e induciendo los tics, sin poder inhibir los movimientos (disquinesias) creando una especie de focos aberrantes de descarga sin que actualmente se conozca la fisiopatolog&iacute;a<sup>4</sup> (<a href="#f2">Figura 2</a>). La anomal&iacute;a del estriado, al estar segregado funcionalmente, hace que el cortejo de tics pueda ser variable; bien simples, complejos o compulsiones dependiendo del lugar en que se genere el foco en el estriado.</font></p>     <p align="center"><font face="Verdana" size="2"><a name="f2"><img src="/img/revistas/neuro/v22n1/investigacion1_f2.jpg" width="314" height="317"></a>    ]]></body>
<body><![CDATA[<br>Figura 2. <i>Las neuronas espinosas del estriado (spiny neuron) reciben    <br> aferencias de la corteza cerebral (&aacute;cido glut&aacute;mico como neurotransmisor),    <br>del n&uacute;cleo centro mediano parafascicular (CM/Pf) del t&aacute;lamo (&aacute;cido glut&aacute;mico    <br> como neurotransmisor) y de otros n&uacute;cleos tal&aacute;micos como el ventral anterior    <br>y n&uacute;cleos intralaminares (&aacute;cido glut&aacute;mico como neurotransmisor).    <br>Adem&aacute;s recibe aferencias dopamin&eacute;rgicas desde la SNc (sustancia nigra pars compacta).    <br>La dopamina solo es liberada cuando va a realizarse un movimiento por parte del sujeto.    <br>Existe entre las aferencias glutamat&eacute;rgicas y las dopamin&eacute;rgicas un equilibrio que en    <br>caso de romperse puede generar una patolog&iacute;a. As&iacute; si la dopamina no es capaz de    <br> controlar o inhibir la llegada de aferencias corticales puede inducir la aparici&oacute;n    ]]></body>
<body><![CDATA[<br>de fragmentos de movimiento similares a las disquinesias.</i></font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2">As&iacute; en los tics simples o vocales, existir&iacute;a una actividad anormal a nivel motor, premotor y a nivel cingular y del c&oacute;rtex &oacute;rbito frontal para los tics motores complejos como las compulsiones<sup>4</sup>. Por tanto el SGT se tratar&iacute;a de una desinhibici&oacute;n del circuito cortico-estriado-t&aacute;lamocortical con un origen a nivel estriatal. Esta actividad aberrante mejora o queda suprimida por los antagonistas dopamin&eacute;rgicos y por los inhibidores selectivos de la recaptaci&oacute;n de serotonina<sup>4</sup>.</font></p>     <p><font face="Verdana" size="2">Los tics adem&aacute;s de motores y f&oacute;nicos, pueden ser tambi&eacute;n obsesiones motoras como compulsiones. Las palabras obscenas, coprolalia o ecolalia, son consideradas como un cuadro obsesivo, desde el punto psiqui&aacute;trico, que acompa&ntilde;a a los tics motores dentro del SGT. Debemos de considerar los tics y las obsesiones como disquinesias ya que son fragmentos liberados, motores o cognitivos desde el estriado sobre el t&aacute;lamo<sup>93</sup>. La &uacute;nica diferencia entre los tics y las obsesiones ser&iacute;a el origen en diferente regi&oacute;n dentro del estriado. En este contexto, el GPi puede ser una buena diana quir&uacute;rgica para tratar cualquiera de estas disquinesias, tanto a nivel posteroventral, regi&oacute;n sensitivo-motora, como la anteromedial o regi&oacute;n l&iacute;mbica del GPi.</font></p>     <p><font face="Verdana" size="2">Cuando los tratamientos conservadores fracasan en los pacientes afectos de SGT grave, la estimulaci&oacute;n cerebral puede constituir una alternativa terap&eacute;utica v&aacute;lida. Estos pacientes refractarios a la terapia m&eacute;dica deben ser valorados por neur&oacute;logos y psiquiatras como candidatos a la cirug&iacute;a. Para ello, est&aacute;n publicados unos criterios de inclusi&oacute;n/exclusi&oacute;n tanto m&eacute;dicos como quir&uacute;rgicos para intervenir esta patolog&iacute;a<sup>86</sup>. La evaluaci&oacute;n cl&iacute;nica de los pacientes se realiza con la Yale Global Tic Severity Scale (YGTSS), ya que la escala eval&uacute;a los tics motores, los f&oacute;nicos y la afectaci&oacute;n de los mismos en la vida del paciente, as&iacute; como la gravedad global de los mismos. En 1999, Vanderwalle y cols introdujeron la estimulaci&oacute;n cerebral en tres pacientes que sufr&iacute;an esta patolog&iacute;a, con buena respuesta cl&iacute;nica inicial. La diana quir&uacute;rgica fue el t&aacute;lamo, similar a la diana de las lesiones realizadas por Hassler y Dieckmann en 1970. Los n&uacute;cleos elegidos, seg&uacute;n el art&iacute;culo original fueron el ventral oral interno (Voi) y CM/Pf<sup>53,110</sup>.</font></p>     <p><font face="Verdana" size="2">Diferentes dianas han sido probadas en el SGT desde entonces y unos 60 pacientes han podido ser intervenidos y publicados<sup>11,28,33,66,73,83,100-102,111,113</sup> (<a target="_blank" href="/img/revistas/neuro/v22n1/investigacion1_tabla2.htm">Tabla 2</a>). El GPi, tanto en su porci&oacute;n motora como la anteromedial o l&iacute;mbica y el t&aacute;lamo (CM/Pf y Voi) han sido las m&aacute;s frecuentemente utilizadas. La elecci&oacute;n del GPi se debe a considerar los tics como disquinesias y por tanto un problema exclusivo motor, mientras que en los pacientes con una afectaci&oacute;n psiqui&aacute;trica hay autores que prefieren elegir el t&aacute;lamo como diana quir&uacute;rgica. En ambas dianas, los resultados cl&iacute;nicos han podido ser comparables (66% de mejor&iacute;a en la YGTSS) pero el n&uacute;mero de pacientes intervenidos es bajo como para sacar conclusiones sobre cualquiera de ellas. Los resultados sobre las alteraciones del comportamiento de los pacientes son variables y actualmente no se conoce con exactitud. En los pacientes en los cuales el cuadro psiqui&aacute;trico es el dominante y el motor es menor se ha probado la estimulaci&oacute;n en Nacc/CI similar a los pacientes con TOC, pero son pocos casos y con resultados dispares<sup>22,33,66</sup>.</font></p>     <p><font face="Verdana" size="2">Otros pacientes han sido intervenidos con GPi y CM/ Pf a la vez, aunque no est&aacute; demostrado en las escalas de evaluaci&oacute;n cl&iacute;nica, que la suma de las dos dianas aporte un beneficio nuevo a los pacientes<sup>2,39</sup>. Por tanto, en esta enfermedad la diana quir&uacute;rgica no est&aacute; bien definida y la estimulaci&oacute;n en los mismos circuitos, pero en diferentes puntos, puede producir resultados similares.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>Estimulaci&oacute;n profunda en la depresi&oacute;n</b></font></p>     <p><font face="Verdana" size="2">La depresi&oacute;n es una de las enfermedades m&aacute;s prevalentes actualmente en nuestra sociedad ya que afecta a un 4% de la poblaci&oacute;n general y un 15% de la misma ha tenido depresi&oacute;n alguna vez en su vida<sup>6</sup>. De los pacientes afectos de una depresi&oacute;n mayor o grave, a pesar de los diferentes tratamientos m&eacute;dicos, psicoter&aacute;picos o bien terapia electroconvulsiva (TEC), un 20% de los mismos son considerados como refractarios a los mismos<sup>6,30</sup>. Los pacientes con depresi&oacute;n resistentes eran intervenidos, hasta hace unos a&ntilde;os, con una cirug&iacute;a estereot&aacute;ctica ablativa como la capsulotom&iacute;a, tractotom&iacute;a subcaudada o bien cingulotom&iacute;a. Actualmente se ha iniciado la estimulaci&oacute;n cerebral en esta enfermedad.</font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">La imagen funcional en esta patolog&iacute;a, ha mostrado que los pacientes con tristeza o bien con depresi&oacute;n, presentan una hiperactividad en la regi&oacute;n subgenual (&aacute;rea 25 de Brodmann) y que la misma se revierte en los pacientes tratados por cualquiera de las terapias antes citadas con buena respuesta cl&iacute;nica. Sin embargo, los pacientes considerados como refractarios a cualquier terapia m&eacute;dica, psicoterapia o TEC, mantienen un incremento de la actividad en la regi&oacute;n subgenual<sup>78,99</sup>. La hip&oacute;tesis sobre si la estimulaci&oacute;n cerebral pudiera modular la hiperactividad de esta regi&oacute;n anat&oacute;mica ha sido probada por Lozano y Myberg inicialmente en 6 pacientes, en un estudio abierto, que presentaban criterios de depresi&oacute;n refractaria. La estimulaci&oacute;n de dicha regi&oacute;n se asoci&oacute; con una mejor&iacute;a en 4 de los 6 pacientes intervenidos manteni&eacute;ndose a los 6 meses de la cirug&iacute;a<sup>79</sup>. Todos los pacientes que mejoraron cl&iacute;nicamente, tuvieron una reducci&oacute;n en la actividad subgenual en el PET. Los autores sugirieron que la interupci&oacute;n en el circuito l&iacute;mbico a nivel cortical con la estimulaci&oacute;n, revert&iacute;a los s&iacute;ntomas en pacientes refractarios<sup>79</sup>.</font></p>     <p><font face="Verdana" size="2">El mismo grupo y en una extensi&oacute;n del estudio, public&oacute; un art&iacute;culo basado en 20 pacientes, con observaci&oacute;n cl&iacute;nica a los 6 meses de la cirug&iacute;a, en el cual se pon&iacute;a de manifiesto que el 60% respond&iacute;an a la estimulaci&oacute;n y en el 35% se observ&oacute; una remisi&oacute;n de la enfermedad<sup>71</sup>. Los criterios de respuesta eran si los pacientes alcanzaban un beneficio del 50% o mayor reducci&oacute;n en los 17 items de la escala de Hamilton (Hamilton Rating Scale for depression; HRSD17) y los criterios de remisi&oacute;n eran si la escala llegaba a 7 puntos o inferior. El beneficio postcirug&iacute;a permaneci&oacute; estable durante 12 meses<sup>71</sup>. Sin embargo, no se han encontrado diferencias significativas entre los que respond&iacute;an al tratamiento y los que no respond&iacute;an, tanto en relaci&oacute;n con la colocaci&oacute;n de los electrodos como en los estudios de tractograf&iacute;a en la RM<sup>51,71</sup>.</font></p>     <p><font face="Verdana" size="2">Varios grupos quir&uacute;rgicos han publicado pacientes tratados con estimulaci&oacute;n en diferentes dianas quir&uacute;rgicas. El trabajo cl&iacute;nico con un mayor n&uacute;mero de casos ha sido publicado por Malone y cols con estimulaci&oacute;n del VS/CI en 15 pacientes con depresi&oacute;n refractaria<sup>76</sup>. Se consider&oacute; que un 40% de los pacientes intervenidos hab&iacute;an respondido bien al tratamiento, cuando eran estudiados con la HDRS (Hamilton depresi&oacute;n rating Scale) y que los criterios de remisi&oacute;n se alcanzaron en el 20% de los pacientes a los 6 meses<sup>76</sup>. Los electrodos fueron implantados con los contactos ventrales en el VS y los dorsales en la CI.</font></p>     <p><font face="Verdana" size="2">El NAcc tambi&eacute;n se ha considerado como diana en pacientes con depresi&oacute;n refractaria a tratamientos convencionales. Inicialmente, y en un estudio piloto con tres pacientes, se observ&oacute; un beneficio significativo cuando se aplic&oacute; la escala HDRS y en relaci&oacute;n con las fases de estimulaci&oacute;n &quot;on-off&quot;<sup>97</sup>. Posteriormente el mismo grupo ha publicado 10 pacientes, de los cuales 5 alcanzaron un 50% de reducci&oacute;n de dicha escala. En los pacientes con respuesta cl&iacute;nica, la 18F-2-deoxy-glucosa PET mostr&oacute; que la estimulaci&oacute;n del NAcc reduce el metabolismo de la regi&oacute;n subgenual y regi&oacute;n prefrontal<sup>19</sup>. Seg&uacute;n los autores, el electrodo cuadripolar es introducido con el contacto m&aacute;s distal en el centro del NAcc, el contacto 1 en la parte perif&eacute;rica del mismo n&uacute;cleo y en la regi&oacute;n ventral y dorsal de la c&aacute;psula estar&iacute;an colocados los contactos m&aacute;s dorsales<sup>97</sup>.</font></p>     <p><font face="Verdana" size="2">Sin embargo, desde el an&aacute;lisis anat&oacute;mico y neuroquir&uacute;rgico cuando comparamos las dianas quir&uacute;rgicas de los grupos que realizan estimulaci&oacute;n en el Nacc y los que van al VS podemos considerar que son id&eacute;nticas. El grupo de Schlaepfer y Bewernick elige como diana el Nacc, con las siguientes coordenadas (X: 6-7 mm lateral, Y: 1-2 mm anterior a la comisura anterior (CA); Z: 3-4 mm ventral a la misma), mientras que Malone y cols, van al VS y sus coordenadas son X: 7.5 mm lateral, Y: 1.5 mm anterior a la CA y Z: 4 mm ventral a la misma<sup>19,76,97</sup>. Por lo tanto, podemos consider que la diana estimulada es la misma.</font></p>     <p><font face="Verdana" size="2">En la depresi&oacute;n refractaria, tanto la estimulaci&oacute;n del &aacute;rea subgenual como la regi&oacute;n VS/NAcc/CI obtendr&iacute;an beneficios similares seg&uacute;n las escalas de evaluaci&oacute;n en los pacientes intervenidos, con un 50% de los mismos respondiendo a la misma. Por tanto, la depresi&oacute;n puede ser mejorada quir&uacute;rgicamente desde diferentes dianas, introduciendo cambios en el circuito patol&oacute;gico desde distintos puntos. Por &uacute;ltimo, se debe comentar que los beneficios son progresivos, ya que las escalas de evaluaci&oacute;n contin&uacute;an mejorando durante el seguimiento cl&iacute;nico de los pacientes.</font></p>     <p><font face="Verdana" size="2">Se han publicado otras dianas quir&uacute;rgicas, con un &uacute;nico paciente y como casos cl&iacute;nicos, para la depresi&oacute;n refractaria al tratamiento m&eacute;dico. As&iacute; la estimulaci&oacute;n del ped&uacute;nculo tal&aacute;mico inferior<sup>59</sup>, del GPi en su porci&oacute;n l&iacute;mbica<sup>63</sup> y la hab&eacute;nula<sup>96</sup>, donde los autores refieren voltajes de 10.5 Vols, por lo que la mejor&iacute;a podr&iacute;a deberse a que la estimulaci&oacute;n, con tal voltaje, alcance puntos distantes a la propia diana quir&uacute;rgica, entre ellos la estr&iacute;a medularis  (<a target="_blank" href="/img/revistas/neuro/v22n1/investigacion1_tabla3.jpg">Tabla 3</a>).</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>Discusi&oacute;n</b></font></p>     <p><font face="Verdana" size="2"><i>Por qu&eacute; DBS en lugar de lesiones</i></font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">Basados en la experiencia quir&uacute;rgica previa de los trastornos del movimiento, se est&aacute; abriendo paso la estimulaci&oacute;n cerebral de diferentes estructuras profundas en pacientes con problemas psiqui&aacute;tricos, que son refractarios a los tratamientos convencionales. El porqu&eacute; se prefiere colocar un estimulador a realizar una cirug&iacute;a ablativa es obvio, porque no se realiza una lesi&oacute;n que puede considerarse como irreversible. En la literatura se han publicado buenos resultados con cirug&iacute;a ablativa, similares a los actualmente publicados con estimulaci&oacute;n; as&iacute; capsulotom&iacute;as para TOC o depresi&oacute;nes, pero los resultados adversos, tras las lesiones se han podido minimizar y en un porcentaje importante de pacientes se realizaron m&uacute;ltiples procedimientos<sup>20,23</sup>. Adem&aacute;s las lesiones son bilaterales y esto siempre puede conllevar un riesgo de complicaciones mayor, sobre todo en el lenguaje y de tipo cognitivo en los pacientes intervenidos. Pero esto no ser&iacute;a el principal motivo para preferir actualmente la DBS; la posibilidad de manipular los par&aacute;metros de estimulaci&oacute;n, permite poder modular con diferentes vol&uacute;menes y alcanzar distintas zonas funcionales dentro de una diana. En segundo lugar, con las t&eacute;cnicas de estimulaci&oacute;n tenemos la posibilidad de valoraciones cl&iacute;nicas, cuando el paciente sea estimulado o cuando se suspendan los est&iacute;mulos, lo cual permite realizar estudios doble ciego aleatorios para valorar con una mayor precisi&oacute;n la respuesta cl&iacute;nica de una determinada diana quir&uacute;rgica. Por &uacute;ltimo, comentar que ciertas dianas no se hubieran contemplado si no es por la estimulaci&oacute;n, como la posibilidad de manipular el &aacute;rea subgenual para pacientes con depresi&oacute;n refractaria, ya que en dichas estructuras no se puede realizar una lesi&oacute;n. Tambi&eacute;n la lesi&oacute;n del NST en pacientes con TOC, en la que puede inducirse una corea/ balismo tras la lesi&oacute;n debido a la reducci&oacute;n de la actividad palidal sobre el t&aacute;lamo tampoco hubiera sido contemplada por su alto riesgo quir&uacute;rgico.</font></p>     <p><font face="Verdana" size="2"><i>Mecanismo de acci&oacute;n de la estimulaci&oacute;n</i></font></p>     <p><font face="Verdana" size="2">El mecanismo de acci&oacute;n de la estimulaci&oacute;n no es conocido actualmente. Si el circuito de los GB tiene una actividad neuronal anormal o patol&oacute;gica, la estimulaci&oacute;n puede inducir una disrupci&oacute;n o ruptura de la misma introduciendo un nuevo patr&oacute;n de actividad que inhibir&iacute;a el patol&oacute;gico llevando a una mejora cl&iacute;nica. En las dianas quir&uacute;rgicas, tanto para trastornos del movimiento como para problemas psiqui&aacute;tricos, existen somas neuronales y fibras, por lo que el mecanismo intr&iacute;nseco de acci&oacute;n se desconoce y el mismo puede ser variable dependiendo de la diana quir&uacute;rgica<sup>70</sup>. Conocemos que los axones tienen un umbral m&aacute;s bajo que los somas neuronales y que la estimulaci&oacute;n puede inducir a que sus terminales liberen los neurotransmisores que almacenan, bien excitadores o inhibidores, pudiendo de esta manera alterar el circuito patol&oacute;gico o incluso modulando la corteza cerebral, como puede ocurrir al estimular el NST<sup>45</sup>.</font></p>     <p><font face="Verdana" size="2">No podemos pensar que la estimulaci&oacute;n act&uacute;e de la misma forma en el NST, GPi o Nacc/CI. As&iacute; la estimulaci&oacute;n en primates parkinsonianos con voltajes cl&iacute;nicamente efectivos produce cambios en los patrones de descarga del GPe y del GPi<sup>52</sup> y la estimulaci&oacute;n unilateral del NST en ratas tratadas con 6-OHDA (6-hidroxi-dopamina) induce un incremento de la actividad del &aacute;cido glut&aacute;mico en vez de disminuirlo<sup>21,68,122</sup>. Por tanto, cada diana puede responder de diferente forma a la estimulaci&oacute;n aunque el resultado cl&iacute;nico sea similar.</font></p>     <p><font face="Verdana" size="2">La estimulaci&oacute;n a largo plazo induce cambios pl&aacute;sticos en el circuito de los GB pudiendo llegar a inducir cambios metab&oacute;licos corticales<sup>78,91,92</sup>. Estos cambios pueden no ser inmediatos sino progresivos, por lo que los pacientes pueden mejorar su sintomatolog&iacute;a durante el seguimiento cl&iacute;nico. Esto no ocurre con los pacientes con trastornos del movimiento, en los cuales una vez optimizados los par&aacute;metros de estimulaci&oacute;n la mejor&iacute;a se puede considerar como establecida.</font></p>     <p><font face="Verdana" size="2">Podemos considerar que en los trastornos de los GB de tipo motor, el sistema de estimulaci&oacute;n puede ser m&aacute;s simple, ya que la hiperactividad del circuito NST-GPi/SNr puede ser alterada desde el NST o bien desde el GPi, mejorando cl&iacute;nicamente al reducir o inhibir esta actividad patol&oacute;gica, en este sentido podr&iacute;a tratarse de una cirug&iacute;a predictiva. Sin embargo, esto no ocurre en la patolog&iacute;a psiqui&aacute;trica, donde el circuito l&iacute;mbico puede ser manipulado desde diferentes dianas con resultados similares, e incluso la misma diana quir&uacute;rgica puede mejorar procesos diferentes como la estimulaci&oacute;n del VS/Nacc/CI mejora la depresi&oacute;n y el TOC y la estimulaci&oacute;n del NST mejora la EP y el TOC.</font></p>     <p><font face="Verdana" size="2"><i>Dianas quir&uacute;rgicas en las enfermedades psiqui&aacute;tricas</i></font></p>     <p><font face="Verdana" size="2">Actualmente hay m&aacute;s de 10 dianas quir&uacute;rgicas para las patolog&iacute;as psiqui&aacute;tricas comentadas, ¿c&oacute;mo puede existir algo tan poco espec&iacute;fico y selectivo? Si quitamos los casos concretos publicados como &quot;case report&quot; en los que un &uacute;nico paciente ha sido intervenido, quedar&iacute;an dos dianas para cada entidad cl&iacute;nica. Para el TOC, las dianas ser&iacute;an: VS/Nacc/CI y NST. Para la depresi&oacute;n refractaria ser&iacute;a el &aacute;rea subgenual (&aacute;rea 25 de Brodmann) y la regi&oacute;n VS/NAcc. Para el Guille de la Tourette la diana ser&iacute;a el Voi  y el CM/Pfs del t&aacute;lamo y el GPi<sup>2,19,43,66,71,75,76,79,97,100,107,113</sup>. La actuaci&oacute;n sobre cada una de estas dianas, induce cambios corticales evaluados en PET, as&iacute; en los pacientes con TOC que son intervenidos con buena respuesta cl&iacute;nica, la hiperactividad del COF y del &aacute;rea cingular muestra una reducci&oacute;n<sup>91,92</sup> y los pacientes con depresi&oacute;n con reducci&oacute;n en la escala de Hamilton tienen un hipoactividad del &aacute;rea subgenual<sup>78</sup>. Por lo tanto, el mecanismo de actuaci&oacute;n puede ser la modulaci&oacute;n de la corteza frontal o bien del circuito l&iacute;mbico, desde los GB en sus porciones l&iacute;mbicas en distintos puntos. Esto podr&iacute;a explicar el mecanismo de mejora de estos pacientes desde las distintas dianas  quir&uacute;rgicas.</font></p>     <p><font face="Verdana" size="2">Actualmente no conocemos, por falta de un n&uacute;mero de pacientes adecuado, cu&aacute;l es la diana &oacute;ptima para cada problema ni para una patolog&iacute;a determinada.</font></p>     <p><font face="Verdana" size="2">Se pueden inducir cambios corticales desde actuaciones en distintos puntos de la red o circuito funcional, que producen beneficios cl&iacute;nicos tanto en depresi&oacute;n refractaria, como en el TOC o en la enfermedad de Tourette.</font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">Con el mismo concepto, tampoco conocemos, aunque nos centremos en la misma diana, qu&eacute; pacientes responder&aacute;n bien al tratamiento y quienes no lo har&aacute;n, debido a la variabilidad de los diagn&oacute;sticos cl&iacute;nicos y de la colocaci&oacute;n de los electrodos<sup>51</sup>.</font></p>     <p><font face="Verdana" size="2">Pueden existir diferentes subgrupos de pacientes dentro de cada entidad cl&iacute;nica, lo cual implica que las respuestas pueden ser diferentes. En la actualidad se est&aacute; dedicando una atenci&oacute;n espec&iacute;fica a este problema, para identificar a los que se puedan beneficiar de este tratamiento quir&uacute;rgico. Esto abre un futuro a estudios cl&iacute;nicos, que ahora est&aacute;n en sus comienzos. Actualmente no existe ning&uacute;n estudio doble ciego en ninguna de las patolog&iacute;as referidas que compare resultados entre las distintas dianas quir&uacute;rgicas.</font></p>     <p><font face="Verdana" size="2">La DBS para problemas psiqui&aacute;tricos lleva m&aacute;s de 10 a&ntilde;os desde que se public&oacute; el tratamiento con TOC con DBS-CI y para Tourette la DBS-Voi-CM/Pf tal&aacute;mica, ambos en 1999<sup>84,110</sup>, sin embargo actualmente no se est&aacute;n interviniendo tantos pacientes como para los trastornos del movimiento. Esto puede ser debido a que los resultados no son tan espectaculares como en los previos (50% de pacientes respondedores a los 12 meses y un 30% considerados en remisi&oacute;n) mientras que en la EP, si el paciente es candidato y el electrodo est&aacute; en la diana quir&uacute;rgica, la cirug&iacute;a es predictiva y en el temblor, si el electrodo est&aacute; bien colocado en el Vim, el signo cl&iacute;nico desaparece. Esto no ocurre como hemos visto con la patolog&iacute;a psiqui&aacute;trica. Todo ello lleva a que todav&iacute;a se intervengan pocos casos de pacientes con trastornos psiqui&aacute;tricos y la respuesta cl&iacute;nica al tratamiento quir&uacute;rgico pueda variar dependiendo de los casos y actualmente est&eacute; siendo estudiada por los distintos grupos involucrados en este tipo de terapia.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>Conclusiones</b></font></p>     <p><font face="Verdana" size="2">Los pacientes con trastornos psiqui&aacute;tricos como TOC, depresi&oacute;n y Gilles de la Tourette, refractarios a tratamientos convencionales, pueden ser intervenidos quir&uacute;rgicamente con estimulaci&oacute;n cerebral profunda con una reducci&oacute;n significativa de las escalas de evaluaci&oacute;n y un beneficio cl&iacute;nico. Un porcentaje de pacientes se puede considerar como &quot;curados&quot; o en remisi&oacute;n, ya que no precisan continuar con medicaci&oacute;n y pueden volver a sus actividades diarias.</font></p>     <p><font face="Verdana" size="2">Con los conocimientos que actualmente tenemos, podemos decir que las patolog&iacute;as como la depresi&oacute;n, TOC y SGT se deben a una alteraci&oacute;n del circuito l&iacute;mbico c&oacute;rticoestriado-t&aacute;lamo-cortical.</font></p>     <p><font face="Verdana" size="2">Actualmente no existe ninguna diana superior a otras para tratar quir&uacute;rgicamente estos trastornos psiqui&aacute;tricos y no conocemos ning&uacute;n estudio doble aleatorio entre diferentes dianas, en ninguna de las patolog&iacute;as. Por otro lado y con el mismo concepto una diana puede mejorar diferentes patolog&iacute;as. El circuito patol&oacute;gico de los GB podr&iacute;a ser interrumpido desde diferentes puntos o dianas influyendo sobre diferentes &aacute;reas corticales.</font></p>     <p><font face="Verdana" size="2">No conocemos qu&eacute; pacientes van a responder y quienes no responder&aacute;n al tratamiento quir&uacute;rgico con estimulaci&oacute;n, ya que pueden tratarse de subgrupos cl&iacute;nicos dentro de una misma patolog&iacute;a diagn&oacute;stica.</font></p>     <p><font face="Verdana" size="2">En un futuro, tanto los procedimientos de imagen, PET previo a la cirug&iacute;a, colocaci&oacute;n de electrodos en dianas determinadas con an&aacute;lisis de tractograf&iacute;a podr&iacute;an ayudar en este campo.</font></p>     ]]></body>
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Mov Disord 2002; 17 (Supl 3): 15-21.</font>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=3379296&pid=S1130-1473201100010000100125&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --><p>&nbsp;</p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b><a href="#top"><img border="0" src="/img/revistas/neuro/v22n1/seta.gif" width="15" height="17"></a><a name="bajo"></a>Dirección para correspondencia:</b>    ]]></body>
<body><![CDATA[<br>Dr. Jorge Guridi.    <br>Servicio de Neurocirug&iacute;a.    <br>Cl&iacute;nica Universidad de Navarra. Pio XII sn.    <br>31008 Pamplona  <a href="mailto:jguridi@unav.es">jguridi@unav.es</a></font></p>     <p><font face="Verdana" size="2">Recibido: 23-06-10.    <br>Aceptado: 5-10-10.</font></p>     <p><font face="Verdana" size="2"><u><i>Abreviaturas</u>. AMS: &aacute;rea motora suplementaria. CA: comisura anterior. rCBF: flujo sangu&iacute;neo cerebral regional. CCA: c&oacute;rtex cingular anterior. CI: c&aacute;psula interna. CM/Pf: centro mediano/ parafascicular. COF: c&oacute;rtex orbito-frontal. DA: agonista dopamin&eacute;rgico. DBS: deep brain stimulation. DM: n&uacute;cleo dorsomedial. EP: enfermedad de Parkinson. GB: ganglios basales. GPe: globo p&aacute;lido externo. GPi: globo p&aacute;lido interno. HDRS: Hamilton Depression Rating Scale. ICD: impulse control disease. Nacc: n&uacute;cleo accumbens. NST: n&uacute;cleo subtal&aacute;mico. PET: tomograf&iacute;a por emisi&oacute;n de positrones. SGT: s&iacute;ndrome Gilles de laTourette. SNc: sustancia negra (pars compacta). SNr: sustancia negra (pars reticulata). TEC: terapia electro-convulsiva. TOC: trastorno obsesivo-compulsivo. Voi: ventral oral interno. VS: estriado ventral.</i></font></p>      ]]></body><back>
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