<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1688-0420</journal-id>
<journal-title><![CDATA[Revista Uruguaya de Cardiología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev.Urug.Cardiol.]]></abbrev-journal-title>
<issn>1688-0420</issn>
<publisher>
<publisher-name><![CDATA[Sociedad Uruguaya de Cardiología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1688-04202012000200006</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Perfil autonómico de los pacientes derivados a una clínica de trastornos del sueño: impacto de la CPAP en el sistema nervioso autónomo]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Seaborn]]></surname>
<given-names><![CDATA[Geoffrey EJ]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pang]]></surname>
<given-names><![CDATA[Helen]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Akl]]></surname>
<given-names><![CDATA[Selim G]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Redfearn]]></surname>
<given-names><![CDATA[Damian P]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Simpson]]></surname>
<given-names><![CDATA[Christopher S]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Fitzpatrick]]></surname>
<given-names><![CDATA[Michael]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Munt]]></surname>
<given-names><![CDATA[Peter W]]></given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Baranchuk]]></surname>
<given-names><![CDATA[Adrian]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Kingston General Hospital Cardiac Electrophysiology and Pacing ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2012</year>
</pub-date>
<volume>27</volume>
<numero>2</numero>
<fpage>143</fpage>
<lpage>147</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_arttext&amp;pid=S1688-04202012000200006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_abstract&amp;pid=S1688-04202012000200006&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_pdf&amp;pid=S1688-04202012000200006&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen Introducción: la apnea obstructiva del sueño (AOS) severa ha sido asociada con disfunción autonómica. La presión positiva continua en la vía aérea (CPAP) es el tratamiento estándar para la AOS, aun cuando su impacto sobre la disfunción autonómica no haya sido plenamente investigado. La variabilidad de la frecuencia cardíaca (VFC) es una técnica cuantitativa no invasiva para la evaluación de la actividad autonómica. Nuestro objetivo fue determinar si los pacientes con AOS severa presentan niveles mayores de disfunción autonómica que los pacientes con un índice de apnea-hipopnea (IAH) normal, y si la CPAP mejora los parámetros de VFC a la vez que mejora el IAH. Métodos: todos los pacientes fueron sometidos a una polisomnografía (PSG) completa en una clínica de trastornos del sueño. Se definió como severa a una AOS que tuviera un IAH ³ 30 (eventos por hora), y se definió al grupo control como aquellos que tuvieran un IAH < 5. Se calculó la VFC antes y después de la CPAP, analizando trazados electrocardiogáficos de 10 minutos, conforme las pautas de normalización. Los pacientes con AOS severa fueron tratados con CPAP durante un período de 4-6 semanas (titulados durante la polisomnografía), y los pacientes control no recibieron ninguna intervención entre sus dos registros de electrocardiograma (ECG). Resultados: el estudio incluyó a un total de 20 pacientes con AOS severa y 10 controles. En los pacientes con AOS severa, el IAH se redujo al utilizar CPAP de 38,0 ± 11,0 a 23,0 ± 11,0 (p<0,01). Aparte de una diferencia significativa en el índice de masa corporl (IMC) entre los paciente con AOS y los controles (35,3±4,7 versus 26,6±4,6 kg/m², p<0,01), los grupos fueron comparables en cuanto a edad, condición de hipertensión y género. No hubo ninguna diferencia significativa (p<0,05) en ningún parámetro de VFC entre los pacientes con AOS severa y los controles, ni entre los pacientes con AOS antes y después de CPAP (tabla 2). Conclusión: en una población derivada a una clínica de trastornos del sueño, los pacientes con AOS severa presentaron el mismo perfil autonómico que los pacientes sin AOS. La corrección de AOS mediante CPAP no se acompañó de alteraciones en la actividad autonómica.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Summary Introduction: severe obstructive sleep apnea (OSA) has been associated with autonomic dysfunction. Continuous positive airway pressure (CPAP) is standard treatment for OSA, although its impact on autonomic dysfunction was not fully investigated. Heart rate variability (HRV) is a non-invasive quantitative technique for assessment of autonomic activity. We aimed to determine if patients with severe OSA exhibit greater levels of autonomic dysfunction than patients with normal apnea-hypopnea index (AHI), and if CPAP improves heart rate variability (HRV) parameters while improving AHI. Methods: all patients underwent full polysomnography (PSG) at a Sleep Disorder Clinic. Severe OSA was defined as AHI ³ 30 (events per hour), and control was defined as AHI < 5. HRV was calculated pre and post-CPAP from a 10-minute electrocardiogram (ECG) recording in accordance with guidelines for standardization. Patients with severe OSA were treated with CPAP for a period of 4-6 weeks (titrated during PSG), and control patients underwent no intervention between their two ECG recordings. Results: a total of 20 patients with severe OSA and 10 controls were included (Table 1). In patients with severe OSA, AHI was reduced by CPAP from 38.0 ± 11.0 to 23.0 ± 11.0 (P<0.01). Aside from a significant difference in BMI between OSA patients and controls (35.3±4.7 vs. 26.6±4.6 kg/m², P<0.01), groups were comparable in age, hypertension, and gender. There was no significant difference (P<0.05) in any HRV parameters between patients with severe OSA and controls, and between OSA patients pre- and post-CPAP (table 2). Conclusion: in a population referred to a Sleep Disorder Clinic, patients with severe OSA presented the same autonomic profile as patients with no OSA. Correction of OSA by CPAP was not associated with changes in autonomic activity.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[SÍNDROMES DE LA APNEA DE SUEÑO]]></kwd>
<kwd lng="es"><![CDATA[FRECUENCIA CARDÍACA]]></kwd>
<kwd lng="es"><![CDATA[PRESIÓN DE LAS VÍAS AÉREAS POSITIVA CONTINUA]]></kwd>
<kwd lng="en"><![CDATA[CONTINUOUS POSITIVE AIRWAY PRESSURE]]></kwd>
<kwd lng="en"><![CDATA[SLEEP APNEA SYNDROMES]]></kwd>
<kwd lng="en"><![CDATA[HEART RATEY]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[       <basefont size="3"> <multicol gutter="18" cols="2"></multicol>     <p align="left"><font face="Verdana" size="2"><b>Art&iacute;culo original    <br>      &nbsp;</b></font></p>          <p align="left"><font face="Verdana" size="2">pnea del sue&ntilde;o y sistema nervioso aut&oacute;nomo&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2"> Geoffrey EJ Seaborn, Helen Pang, Selim G Akl, y colaboradores&nbsp; </font></p>          <p align="left"><font face="Verdana" size="4"> <b>Autonomic profile of patients referred to a sleep disorder clinic: impact  of CPAP on the autonomic nervous system</b>&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2"> Geoffrey EJ Seaborn, Helen Pang, Selim G Akl, Damian P Redfearn, Christopher S Simpson, Michael Fitzpatrick, Peter W Munt, Adrian Baranchuk&nbsp;<font size="2"><basefont size="3"> </font></font> </p>          <p align="left"><font face="Verdana" size="2"> Correspondencia: Dr Adrian Baranchuk, MD FACC FRCPC. Associate Professor   of Medicine. Cardiac Electrophysiology and Pacing. Kingston General Hospital   K7L 2V7. Queen's University.    <br>        Correo electr&oacute;nico: </font> <font color="#1f1a17" face="Verdana" size="2"> <a href="mailto:barancha@kgh.kari.net">barancha@kgh.kari.net</a></font><font face="Verdana" size="2">    <br>        Recibido   mayo 22, 2012; aceptado junio 19, 2012.&nbsp; </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2"> <b>Resumen&nbsp;</b> </font></p>          <p align="left"><font face="Verdana" size="2"> <b>Introducci&oacute;n:</b> la apnea obstructiva del sue&ntilde;o (AOS) severa ha sido asociada  con disfunci&oacute;n auton&oacute;mica. La presi&oacute;n positiva continua en la v&iacute;a a&eacute;rea  (CPAP) es el tratamiento est&aacute;ndar para la AOS, aun cuando su impacto sobre  la disfunci&oacute;n auton&oacute;mica no haya sido plenamente investigado. La variabilidad  de la frecuencia card&iacute;aca (VFC) es una t&eacute;cnica cuantitativa no invasiva  para la evaluaci&oacute;n de la actividad auton&oacute;mica. Nuestro objetivo fue determinar  si los pacientes con AOS severa presentan niveles mayores de disfunci&oacute;n  auton&oacute;mica que los pacientes con un &iacute;ndice de apnea-hipopnea (IAH) normal,  y si la CPAP mejora los par&aacute;metros de VFC a la vez que mejora el IAH.    <br>      <b>M&eacute;todos:</b>  todos los pacientes fueron sometidos a una polisomnograf&iacute;a (PSG) completa  en una cl&iacute;nica de trastornos del sue&ntilde;o. Se defini&oacute; como severa a una AOS  que tuviera un IAH &sup3; 30 (eventos por hora), y se defini&oacute; al grupo control  como aquellos que tuvieran un IAH &lt; 5. Se calcul&oacute; la VFC antes y despu&eacute;s  de la CPAP, analizando trazados electrocardiog&aacute;ficos de 10 minutos, conforme  las pautas de normalizaci&oacute;n. Los pacientes con AOS severa fueron tratados  con CPAP durante un per&iacute;odo de 4-6 semanas (titulados durante la polisomnograf&iacute;a),  y los pacientes control no recibieron ninguna intervenci&oacute;n entre sus dos  registros de electrocardiograma (ECG).    <br>      <b>Resultados: </b>el estudio incluy&oacute; a  un total de 20 pacientes con AOS severa y 10 controles. En los pacientes  con AOS severa, el IAH se redujo al utilizar CPAP de 38,0 &plusmn; 11,0 a 23,0  &plusmn; 11,0 (p&lt;0,01). Aparte de una diferencia significativa en el &iacute;ndice de  masa corporl (IMC) entre los paciente con AOS y los controles (35,3&plusmn;4,7  versus 26,6&plusmn;4,6 kg/m<sup>2</sup>, p&lt;0,01), los grupos fueron comparables en cuanto  a edad, condici&oacute;n de hipertensi&oacute;n y g&eacute;nero. No hubo ninguna diferencia  significativa (p&lt;0,05) en ning&uacute;n par&aacute;metro de VFC entre los pacientes con  AOS severa y los controles, ni entre los pacientes con AOS antes y despu&eacute;s  de CPAP (tabla 2).    <br>      <b>Conclusi&oacute;n:</b> en una poblaci&oacute;n derivada a una cl&iacute;nica de  trastornos del sue&ntilde;o, los pacientes con AOS severa presentaron el mismo  perfil auton&oacute;mico que los pacientes sin AOS. La correcci&oacute;n de AOS mediante  CPAP no se acompa&ntilde;&oacute; de alteraciones en la actividad auton&oacute;mica.&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2">     <br>      </font></p>          <p align="left"> <font face="Verdana" size="2"><b>Palabras clave:    <br>      </b>&nbsp;&nbsp;&nbsp;&nbsp;S&Iacute;NDROMES DE LA APNEA DE SUE&Ntilde;O    <br>      &nbsp;&nbsp;&nbsp;&nbsp;FRECUENCIA CARD&Iacute;ACA    ]]></body>
<body><![CDATA[<br>      &nbsp;&nbsp;&nbsp;&nbsp;PRESI&Oacute;N  DE LAS V&Iacute;AS A&Eacute;REAS POSITIVA CONTINUA    <br>          <br>      &nbsp; </font></p>     <font face="Verdana" size="2">         <br>      </font>          <p align="left"><font face="Verdana" size="2"> <b>Summary&nbsp;</b> </font></p>          <p align="left"><font face="Verdana" size="2"> <b>Introduction:</b> severe obstructive sleep apnea (OSA) has been associated  with autonomic dysfunction. Continuous positive airway pressure (CPAP)  is standard treatment for OSA, although its impact on autonomic dysfunction  was not fully investigated. Heart rate variability (HRV) is a non-invasive  quantitative technique for assessment of autonomic activity. We aimed to  determine if patients with severe OSA exhibit greater levels of autonomic  dysfunction than patients with normal apnea-hypopnea index (AHI), and if  CPAP improves heart rate variability (HRV) parameters while improving AHI.    <br>      <b>Methods:</b>  all patients underwent full polysomnography (PSG) at a Sleep Disorder Clinic.  Severe OSA was defined as AHI &sup3; 30 (events per hour), and control was defined  as AHI &lt; 5. HRV was calculated pre and post-CPAP from a 10-minute electrocardiogram  (ECG) recording in accordance with guidelines for standardization. Patients  with severe OSA were treated with CPAP for a period of 4-6 weeks (titrated  during PSG), and control patients underwent no intervention between their  two ECG recordings.    <br>      <b>Results: </b>a total of 20 patients with severe OSA and  10 controls were included (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#tab1">Table 1</a></font><font face="Verdana" size="2">). In patients with severe OSA, AHI was  reduced by CPAP from 38.0 &plusmn; 11.0 to 23.0 &plusmn; 11.0 (P&lt;0.01). Aside from a  significant difference in BMI between OSA patients and controls (35.3&plusmn;4.7  vs. 26.6&plusmn;4.6 kg/m<sup>2</sup>, P&lt;0.01), groups were comparable in age, hypertension,  and gender. There was no significant difference (P&lt;0.05) in any HRV parameters  between patients with severe OSA and controls, and between OSA patients pre- and post-CPAP (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#tab2">table 2</a></font><font face="Verdana" size="2">). </font> <basefont size="3"> </p>          <p align="left">&nbsp;</p>          <p align="left"><font face="Verdana" size="2">    ]]></body>
<body><![CDATA[<br>        <b>Conclusion:</b> in a population referred to a   Sleep Disorder Clinic, patients with severe OSA presented the same autonomic   profile as patients with no OSA. Correction of OSA by CPAP was not associated   with changes in autonomic activity.&nbsp; </font></p>           <p>  <multicol gutter="18" cols="2"></multicol> </p>         <p align="left"><font face="Verdana" size="2"><b>Key words:    <br>      </b>&nbsp;&nbsp;&nbsp;&nbsp;CONTINUOUS POSITIVE AIRWAY PRESSURE    <br>      &nbsp;&nbsp;&nbsp;&nbsp;SLEEP APNEA SYNDROMES    <br>      &nbsp;&nbsp;&nbsp;&nbsp;HEART  RATEY    <br>           <br>      &nbsp; </font></p>      <font face="Verdana" size="2">          <br>      </font>          <p align="left"><font face="Verdana" size="2"> <b>Introduction&nbsp;</b> </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2"> It is estimated that 1 in 5 adults have at least mild obstructive sleep  apnea (OSA) </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#1">1</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".1"></a>, a condition that is associated with hypertension </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#2">2</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".2"></a>,  cardiac arrhythmia </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#3">3</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".3"></a>, stroke </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#4">4</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".4"></a>, congestive heart failure </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#5">5</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".5"></a>, daytime  sleepiness </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#6">6</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".6"></a>, abnormal brain morphology </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#7">7</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".7"></a>, diabetes mellitus </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#8">8</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".8"></a>, and  autonomic dysfunction </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#9">9</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".9"></a>. Continuous positive airway pressure (CPAP) is  standard treatment for OSA. Heart rate variability (HRV) analysis is a  non-invasive and quantitative technique for assessment of autonomic activity.  We hypothesized that patients with severe OSA may exhibit greater levels  of autonomic dysfunction than patients with normal apnea-hypopnea index  (AHI), and that CPAP may improve HRV parameters while improving AHI.&nbsp; </font></p>     <font face="Verdana" size="2">         <br>      </font>          <p align="left"><font face="Verdana" size="2"> <b>Methods&nbsp;</b> </font></p>          <p align="left"><font face="Verdana" size="2"> All patients underwent full polysomnography (PSG) at a Sleep Disorder Clinic.  Severe OSA was defined as an AHI &sup3; 30 (events per hour). Control was defined  as AHI &lt; 5. Patients with diabetes mellitus (DM), implantable devices,  cardiac abnormalities, beta- and calcium-blocking medications, or anti-arrhythmic  agents were excluded from the analysis. Nightly CPAP compliance was confirmed  for patients with severe OSA. A 10-minute high-resolution Holter ECG recording  was collected pre and post 4-6 weeks of CPAP, titrated during PSG, in OSA  patients. In control subjects, a 10-minute Holter ECG was collected pre  and post 4-6 weeks following PSG in order to gauge analysis reproducibility,  with no intervention between the two recordings. Automated R-wave detection  was performed using the Myoelectric Control Development Toolbox </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#10">10</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".10"></a>. HRV  analysis was carried out in accordance with guidelines for standardization  using MATLAB (2010a, The MathWorks, Nantick, MA) </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#11">11</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".11"></a>. Written, informed  consent was obtained from every patient in accordance with a protocol approved  by the Queen&rsquo;s University Health Sciences Ethics Committee.&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2"> Statistical analysis&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2"> All results are expressed as mean &plusmn; standard deviation. The power of each  frequency band is reported in log-normalized ms2. The very-low frequency  (VLF) and ultra-low frequency (ULF) power-spectral components are absent  due to their measurement not being appropriate in the relatively short-term  recordings used in our analysis. In order to compare patient groups before  and after the 4-6 week follow-up period, results were tested for normality  using one-sample Kolmogorov-Smirnov tests, and, depending on the outcome,  were then subjected either to unpaired t-tests or Wilcoxon rank sum tests  with a minimum significant probability value of P&lt;0.05. All statistical  analysis was performed using MATLAB (2010a, The MathWorks, Nantick, MA).&nbsp; </font></p>     <font face="Verdana" size="2">         <br>      </font>          <p align="left"><font face="Verdana" size="2"> <b>Results&nbsp;</b> </font></p>          <p align="left"><font face="Verdana" size="2"> Patients with severe OSA (n=20 patients) and control subjects (n=10 patients)  were included in the analysis. In patients with severe OSA, the AHI was  reduced by CPAP from 38.0 &plusmn; 11.0 to 23.0 &plusmn; 11.0 episodes/hour; P&lt;0.01.  Aside from a significant difference in BMI between OSA patients and patients  with AHI&lt;5 (35.3 &plusmn; 4.7 vs. 26.6 &plusmn; 4.6 kg/m<sup>2</sup>; P&lt;0.01), groups were comparable  in age, gender, hypertension, and smoking (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#tab1">table 1</a></font><font face="Verdana" size="2">). There was no significant  difference in any HRV parameters between patients with severe OSA and controls,  or between OSA patients before and after CPAP (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#tab2">table 2</a></font><font face="Verdana" size="2">).&nbsp; </font></p>     <font face="Verdana" size="2">     <a name="tab1"></a><img style="width: 520px; height: 204px;" alt="" src="/img/revistas/ruc/v27n2/2a06t1.JPG">    <br>     </font>         ]]></body>
<body><![CDATA[<p>   <basefont size="3"> </p>       <font face="Verdana" size="2">     <a name="tab2"></a><img style="width: 543px; height: 237px;" alt="" src="/img/revistas/ruc/v27n2/2a06t2.JPG">    <br>       </font>         <p align="left"><font face="Verdana" size="2"> <b>Discussion&nbsp;</b> </font></p>          <p align="left"><font face="Verdana" size="2"> Our results contrast many of those presented in the literature. Investigators  have reported that over 24 hours, patients with OSA have greater sympathetic </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#12">12</a></font><font face="Verdana" size="2">,</font><font color="#1f1a17" face="Verdana" size="2"><a href="#13">13</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".12"></a><a name=".13"></a> and lesser parasympathetic influence </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#14">14</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".14"></a> on heart rate than control  subjects, as well less time-domain HRV </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#15">15</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".15"></a>. CPAP has been shown to reduce  blood pressure, as well as sympathetic influence on heart rate, over 24  hours </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#9">9</a></font><font face="Verdana" size="2">,</font><font color="#1f1a17" face="Verdana" size="2"><a href="#16">16</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".16"></a>. In addition, Babaeizadeh and colleagues have described a  method for detecting and quantifying apneic episodes by measuring changes  in HRV over time </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#17">17</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".17"></a>. There are a number of factors that we suspect may  have contributed to our unexpected results.&nbsp; </font></p>           <p>&nbsp;</p>      <multicol gutter="18" cols="2"></multicol>     <p align="left"><font face="Verdana" size="2"> Our study is limited by a relatively modest sample size, with only 20 patients  with severe OSA and 10 control subjects. It is conceivable that we may  observe a trend in HRV over time with further enrolment. In addition, control  subjects were similar to patients with severe OSA in demographic indices,  apart from a difference in BMI and AHI. It may be the case that both these  groups exhibit attenuated HRV compared with healthy control subjects who  have not been referred for PSG. Other factors may also have played a role,  such as the duration of the 4-6 week follow-up period. Perhaps if this  was extended, a significant improvement in HRV indices may have taken place,  possibly due to reverse autonomic remodeling. It may also be the case that  changes in HRV are more pronounced during sleep, with levels returning  to baseline during the day when our ECG recordings were collected for analysis.  Other investigators have observed a significant improvement over a comparable  follow-up during morning wakefulness, however </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#18">18</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"><a name=".18"></a>. Finally, and perhaps  most importantly, we employed a practical 10-minute ECG recording during  clinic follow up, as opposed to the 24-hour recording more commonly reported  in the literature. It has been reported that HRV results are dependent  on the length of the ECG recording analyzed </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#11">11</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">. However, it is nonetheless  intriguing that short-term HRV measured during routine follow-up is not  improved by CPAP in patients with severe OSA.&nbsp; </font></p>       <font face="Verdana" size="2">         <br>        </font>          <p align="left"><font face="Verdana" size="2"> <b>Conclusion&nbsp;</b> </font></p>             <p><font face="Verdana" size="2"> In a population referred to a sleep disorder clinic, patients with severe  OSA exhibited similar heart rate variability to control subjects with normal  AHI during the day. In patients with severe OSA, an improvement in AHI  via 4-6 weeks of CPAP therapy was not associated with an improvement in  HRV indices.&nbsp;</font></p>      <multicol gutter="18" cols="2"></multicol>      <p> <font face="Verdana"> <a href="/img/revistas/ruc/v27n2/2a06f1.JPG"><font size="2">Figure 1</font></a><font size="2">. Results of time-domain HRV analysis. Results are listed as mean &plusmn; standard deviation.</p>        </font></font><font face="Verdana" size="2">      <a href="/img/revistas/ruc/v27n2/2a06f2.JPG">Figure 2</a>. Results of frequency-domain HRV analysis. Results are listed as mean &plusmn; standard deviation.     ]]></body>
<body><![CDATA[<br>     &nbsp;</font><multicol gutter="18" cols="2"></multicol><font face="Verdana" size="2">   </font>     <p align="left"><font face="Verdana" size="2"> <b>Acknowledgements&nbsp;</b> </font></p>          <p align="left"><font face="Verdana" size="2"> Financial support to the first author from the Queen&rsquo;s University Faculty  of Arts and Science is gratefully acknowledged.&nbsp; </font></p>       <font face="Verdana" size="2">         <br>        </font>          <p align="left"><font face="Verdana" size="2"> <b>Bibliography&nbsp;</b> </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="1"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.18">1</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Young T, Peppard P, Gottlieb D.</b> Epidemiology of obstructive sleep apnea.  Am J Respir Crit Care Med 2002; 165: 1217-39.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="2"></a> </font><font color="#1f1a17" face="Verdana" size="2"><a href="#.2"> 2</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Worsnop C, Naughton M, Barter C, Morgan T, Anderson A, Pierce R.</b> The  prevalence of obstructive sleep apnea in hypertensives. Am J Respir Crit  Care Med 1998; 157: 111-5&nbsp;     </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="3"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.3">3</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Baranchuk A. </b>Sleep apnea, cardiac arrhythmias and conduction disorders.  J Electrocardiol. In press 2012&nbsp;     </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="4"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.4">4</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Wessendorf T, Teschler H, Wang Y, Konietzko N, Thilmann A. </b>Sleep-disordered  breathing among patients with first-ever stroke. &nbsp;J Neurol 2000; 247: 41-7.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="5"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.5">5</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Sin D, Fitzgerald F, Parker J, Newton G, Floras J. </b>Risk factors for central  and obstructive sleep apnea in 450 men and women with congestive heart  failure. Am J Respir Crit Care Med 1999;160: 1101-6.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="6"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.6">6</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Johns M. </b>Daytime sleepiness, snoring, and obstructive sleep apnea. the  epworth sleepiness scale. Chest 1993; 103: 30-6.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="7"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.7">7</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Morrell M, McRobbie D, Quest R, Cummin A, Ghiassi R, Corfield D. </b>Changes  in brain morphology associated with obstructive sleep apnea. Sleep Med  2003; 4:4 51-4.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="8"></a> </font><font color="#1f1a17" face="Verdana" size="2"><a href="#.8"> 8</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Tasali E, Mokhlesi B, Van Cauter E.</b> Obstructive sleep apnea and type  2 diabetes: Interacting epidemics. Chest 2008; 133: 496-506.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"><a name="9"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.9">9</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Somers V, Dyken M, Clary M, Abboud F.</b> Sympathetic neural mechanisms in  obstructive sleep apnea. J Clin Invest 1995; 96: 1897-904.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"> <a name="10"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.10">10</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Chan ADC, Green GC.</b> Myoelectric control development toolbox. 30th Conference  of the Canadian Medical and Biological Engineering Society. Toronto: CMBES;  2007.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"> <a name="11"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.11">11</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Task force of the European Society of Cardiology and the North American  Society of Pacing and Electrophysiology. </b>Heart rate variability: standards  of measurement, physiological interpretation, and clinical use. Circulation  1996;93: 1043-65.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"> <a name="12"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.12">12</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Mansfield D, Kaye D, La Rocca H, Solin P, Esler M, Naughton M. </b>Raised  sympathetic nerve activity in heart failure and central sleep apnea is  due to heart failure severity. Circulation 2003;107: 1396-400.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"> <a name="13"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.13">13</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Shimizu T, Takahashi Y, Kogawa S, Takahashi K, Kanbayashi T, Saito Y,  et al. </b>Muscle sympathetic nerve activity during apneic episodes in patients  with obstructive sleep apnea syndrome. Electroencephalogr Clin Neurophysiol.  1994;93:345-52.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"> <a name="14"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.14">14</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Jo J, Blasi A, Valladares E, Juarez R, Baydur A, Khoo M.</b> Model-based  assessment of autonomic control in obstructive sleep apnea syndrome during  sleep. Am J Respir Crit Care Med 2003; 167: 128-36.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"> <a name="15"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.15">15</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Narkiewicz K, Somers V. </b>Sympathetic nerve activity in obstructive sleep  apnoea. Acta Physiol Scand 2003; 177: 385-90.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"> <a name="16"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.16">16</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Roche F, Court-Fortune I, Pichot V, Duverney D, Costes F, Emonot A,  et al.</b> Reduced cardiac sympathetic autonomic tone after long-term nasal  continuous positive airway pressure in obstructive sleep apnea syndrome.  Clin Physiol 1999; 19: 127-34.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"> <a name="17"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.17">17</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Babaeizadeh S, White D, Pittman S, Zhou S.</b> Automatic detection and quantification  of sleep apnea using heart rate variability. J Electrocardiol 2010; 43:  535-41.    &nbsp; </font></p>          <!-- ref --><p align="left"><font face="Verdana" size="2"> <a name="18"></a> </font><font color="#1f1a17" face="Verdana" size="2"> <a href="#.18">18</a></font><font face="Verdana" size="2">.&nbsp;&nbsp;&nbsp;&nbsp;<b>Gilman M, Floras J, Kengo U, Yasuyuki K, Leung R, Bradley T. </b>Continuous  positive airway pressure increases heart rate variability in heart failure  patients with obstructive sleep apnoea. Clin Sci (Lond) 2008; 114: 243-9.    &nbsp; </font></p>           <p> <font face="Verdana" size="2"> <a href="MasterFrame2_%283%29_40.htm"></a>  </font>  <multicol gutter="18" cols="2"></multicol> </p>         <p align="left"><font face="Verdana" size="2"> Perfil auton&oacute;mico de los pacientes derivados a una cl&iacute;nica de trastornos      <br>      del sue&ntilde;o: impacto de la CPAP     <br>      en el sistema nervioso aut&oacute;nomo&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2"> Geoffrey EJ Seaborn, Helen Pang, Selim G Akl, Damian P Redfearn,     <br>      Christopher  S Simpson, Michael Fitzpatrick, Peter W Munt, Adri&aacute;n Baranchuk&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2"> <b>Introducci&oacute;n&nbsp;</b> </font></p>          <p align="left"><font face="Verdana" size="2"> Se estima que uno de cada cinco adultos tiene por lo menos una apnea del  sue&ntilde;o obstructiva (AOS) leve </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#1">1</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">, una afecci&oacute;n que se acompa&ntilde;a de hipertensi&oacute;n  </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#2">2</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">, arritmia card&iacute;aca </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#3">3</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">, accidente cerebrovascular </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#4">4</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">, insuficiencia  card&iacute;aca congestiva </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#5">5</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">, somnolencia diurna </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#6">6</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">, morfolog&iacute;a encef&aacute;lica  anormal </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#7">7</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">, diabetes mellitus </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#8">8</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">, y disfunci&oacute;n auton&oacute;mica </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#9">9</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">. La presi&oacute;n  positiva continua en la v&iacute;a a&eacute;rea (CPAP) es el tratamiento est&aacute;ndar para  la AOS. El an&aacute;lisis de la variabilidad de la frecuencia card&iacute;aca (VFC)  es una t&eacute;cnica no invasiva y cuantitativa para la evaluaci&oacute;n de la actividad  auton&oacute;mica. Nuestra hip&oacute;tesis fue que los pacientes con AOS severa pueden  presentar mayores niveles de disfunci&oacute;n auton&oacute;mica que los pacientes con  un &iacute;ndice de apnea-hipopnea (IAH) normal, y que la CPAP puede mejorar los  par&aacute;metros de VFC a la vez que mejora el IAH.&nbsp; </font></p>       <font face="Verdana" size="2">         <br>        </font>          ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2"> <b>M&eacute;todos&nbsp;</b> </font></p>          <p align="left"><font face="Verdana" size="2"> Todos los pacientes fueron sometidos a una polisomnograf&iacute;a (PSG) en una  cl&iacute;nica de trastornos del sue&ntilde;o. La AOS severa fue definida como aquella  que tuviera un IAH &sup3; 30 (eventos por hora). El control fue definido como  aquel que presentara un IAH &lt; 5. No se incluy&oacute; en el an&aacute;lisis a los pacientes  portadores de diabetes mellitus (DM), dispositivos implantables, anomal&iacute;as  card&iacute;acas, o que estuvieran recibiendo medicaci&oacute;n betabloqueante, bloqueantes  del calcio o agentes antiarr&iacute;tmicos. Para los pacientes con AOS severa  se confirm&oacute; el cumplimiento nocturno de CPAP. En los pacientes con AOS  se registr&oacute; un trazado de ECG Holter de alta resoluci&oacute;n de 10 minutos de  duraci&oacute;n antes y despu&eacute;s de las 4-6 semanas de CPAP, titul&aacute;ndose durante  la PSG. En los sujetos control se recogi&oacute; un ECG Holter de 10 minutos antes  y despu&eacute;s de las 4-6 semanas luego de PSG, para medir la reproducibilidad  del an&aacute;lisis sin que mediara ninguna intervenci&oacute;n entre los dos trazados.  Se realiz&oacute; la detecci&oacute;n automatizada de la onda R utilizando la bater&iacute;a  de desarrollo de control mioel&eacute;ctrico </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#10">10</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">. El an&aacute;lisis de la VFC se realiz&oacute;  siguiendo las directrices para normalizaci&oacute;n, utilizando MATLAB (2010a,  The MathWorks, Nantick, MA) </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#11">11</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">. Se obtuvo consentimiento informado escrito  de todos los pacientes, conforme el protocolo aprobado por el Comit&eacute; de  &Eacute;tica de las Ciencias de la Salud de la Universidad de Queen&rsquo;s.&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2"> An&aacute;lisis estad&iacute;sticos&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2"> Todos los resultados est&aacute;n expresados como media &plusmn; desviaci&oacute;n est&aacute;ndar.  El poder de cada banda de frecuencia se informa en ms<sup>2</sup> normalizados logar&iacute;tmicamente.  Faltan los componentes del espectro de potencia de frecuencia muy baja  (FMB) y frecuencia ultra baja (FUB) debido a que su medici&oacute;n no es apropiada  en los registros de los plazos relativamente cortos utilizados en nuestro  an&aacute;lisis. Para comparar los grupos de pacientes antes y despu&eacute;s del per&iacute;odo  de seguimiento de 4-6 semanas, se confirm&oacute; la anormalidad de los resultados  utilizando pruebas de Kolmogorov-Smirnov de una muestra, y, seg&uacute;n fuera  el resultado, luego se los someti&oacute;, ya sea a pruebas de suma de los rangos  de Wilcoxon o a pruebas no apareadas con un valor de probabilidad significativo  m&iacute;nimo de p&lt;0,05. Todos los an&aacute;lisis estad&iacute;sticos se realizaron utilizando  MATLAB (2010a, The MathWorks, Nantick, MA).&nbsp; </font></p>       <font face="Verdana" size="2">         <br>        </font>          <p align="left"><font face="Verdana" size="2"> <b>Resultados&nbsp;</b> </font></p>          <p align="left"><font face="Verdana" size="2"> En el an&aacute;lisis se incluyeron pacientes con AOS severa (n=20 pacientes)  y sujetos control (n=10 pacientes). En pacientes con AOS severa, al utilizar  CPAP, se redujo el IAH desde 38,0 &plusmn; 11,0 a 23,0 &plusmn; 11,0 episodios/hora;  p&lt;0,01. Aparte de la diferencia significativa en el IMC entre los pacientes  con AOS y los pacientes con IAH&lt;5 (35,3 &plusmn; 4,7 versus 26,6 &plusmn; 4,6 kg/m<sup>2</sup>;  p&lt;0,01), los grupos fueron comparables en cuanto a edad, g&eacute;nero, hipertensi&oacute;n  y tabaquismo (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#tab1">tabla 1</a></font><font face="Verdana" size="2">). No hubo diferencia significativa en ninguno de  los par&aacute;metros de la VFC entre los pacientes con AOS severa y los controles,  o entre los pacientes con AOS antes y despu&eacute;s de CPAP (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#tab2">tabla 2</a></font><font face="Verdana" size="2">).&nbsp; </font></p>       <font face="Verdana" size="2">         <br>         </font>           <p>&nbsp;</p>      <multicol gutter="18" cols="2"></multicol>     <p align="left"><font face="Verdana" size="2"> <b>Discusi&oacute;n&nbsp;</b> </font></p>          ]]></body>
<body><![CDATA[<p align="left"><font face="Verdana" size="2"> Nuestros resultados contrastan muchos de los resultados presentados en  la literatura. Otros investigadores han comunicado que en el transcurso  de 24 horas, la frecuencia card&iacute;aca de los pacientes con AOS tiene una  mayor influencia simp&aacute;tica </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#12">12</a></font><font face="Verdana" size="2">,</font><font color="#1f1a17" face="Verdana" size="2"><a href="#13">13</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"> y una menor influencia parasimp&aacute;tica  </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#14">14</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"> que la de los sujetos control, as&iacute; como menos dominio VFC-tiempo </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#15">15</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">.  Se ha demostrado que CPAP reduce la presi&oacute;n arterial, as&iacute; como su influencia  simp&aacute;tica sobre la frecuencia card&iacute;aca en el transcurso de 24 horas </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#9">9</a></font><font face="Verdana" size="2">,</font><font color="#1f1a17" face="Verdana" size="2"><a href="#16">16</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">.  Adem&aacute;s, Babaeizadeh y colaboradores han descrito un m&eacute;todo para detectar  y cuantificar episodios apneicos midiendo cambios en la VFC con el tiempo  </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#17">17</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">. Hay una serie de factores que sospechamos puedan haber contribuido  a nuestros resultados inesperados.&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2"> Nuestro estudio se ve acotado por un tama&ntilde;o de muestra relativamente modesto:  solo 20 pacientes con AOS severa y 10 sujetos control. Es concebible que  si sigui&eacute;ramos registrando pacientes en la evaluaci&oacute;n, observar&iacute;amos una  tendencia en la VFC con el tiempo. Adem&aacute;s, los sujetos control fueron similares  a los pacientes con AOS severa en lo que respecta a sus &iacute;ndices demogr&aacute;ficos,  aparte de su diferencia en IMC y en el IAH. Es posible que ambos grupos  presenten una VFC atenuada comparado con sujetos-control sanos que no han  sido derivados para PSG. Tambi&eacute;n es posible que hayan incidido otros factores,  tales como la duraci&oacute;n del per&iacute;odo de seguimiento de 4-6 semanas. Tal vez  si esto se extendiera podr&iacute;a observarse una mejor&iacute;a significativa de los  &iacute;ndices de VFC, posiblemente debido a una remodelaci&oacute;n auton&oacute;mica inversa.  Tambi&eacute;n puede ser que los cambios de la VFC sean m&aacute;s pronunciados durante  el sue&ntilde;o, retornando los niveles al nivel basal durante el d&iacute;a, que es  cuando se recogieron nuestros registros de ECG utilizados en el an&aacute;lisis. </font><sup><font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#18">18</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2"> Sin embargo, otros investigadores han observado una mejor&iacute;a significativa  en un seguimiento comparable durante la vigilia matutina. Finalmente, y  tal vez lo que es m&aacute;s importante, es que empleamos un trazado de ECG durante  solo 10 minutos, en vez del registro de 24 horas utilizado m&aacute;s com&uacute;nmente  en la literatura. Est&aacute; descrito que los resultados de la VFC dependen de  la duraci&oacute;n del trazado de ECG analizado </font><sup> <font face="Verdana" size="2"> (</font><font color="#1f1a17" face="Verdana" size="2"><a href="#11">11</a></font><font face="Verdana" size="2">)</font></sup><font face="Verdana" size="2">. Sin embargo, no deja de  ser intrigante que en pacientes con AOS severa, la VFC de corto plazo medida  durante un seguimiento de rutina no mejore con CPAP.&nbsp; </font></p>       <font face="Verdana" size="2">         <br>        </font>          <p align="left"><font face="Verdana" size="2"> <b>Conclusi&oacute;n&nbsp;</b> </font></p>          <p align="left"><font face="Verdana" size="2"> En una poblaci&oacute;n derivada a una cl&iacute;nica de trastornos del sue&ntilde;o los pacientes  con AOS severa presentaron una variabilidad de la frecuencia card&iacute;aca similar  a la de los sujetos control con un IAH normal durante el d&iacute;a. En pacientes  con AOS severa, la mejor&iacute;a del IAH con CPAP por 4-6 semanas de duraci&oacute;n,  no se acompa&ntilde;&oacute; de una mejor&iacute;a de los &iacute;ndices de VFC.&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2"> Agradecimientos&nbsp; </font></p>          <p align="left"><font face="Verdana" size="2"> Queremos agradecer el apoyo financiero que recibi&oacute; el primer autor por  parte de Queen&rsquo;s University Faculty of Arts and Science.&nbsp; </font></p>           <p>  </p>          ]]></body><back>
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