<?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>0212-1611</journal-id>
<journal-title><![CDATA[Nutrición Hospitalaria]]></journal-title>
<abbrev-journal-title><![CDATA[Nutr. Hosp.]]></abbrev-journal-title>
<issn>0212-1611</issn>
<publisher>
<publisher-name><![CDATA[Grupo Arán]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0212-16112011000500031</article-id>
<title-group>
<article-title xml:lang="en"><![CDATA[Sagital abdominal diameter, but not waist circumference is strongly associated with glycemia, triacilglycerols and HDL-C levels in overweight adults]]></article-title>
<article-title xml:lang="es"><![CDATA[Diámetro abdominal sagital, pero no la circunferencia de la cintura se asocia fuertemente con la glucemia, triacilglycerols y HDL-C en adultos con sobrepeso]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pimentel]]></surname>
<given-names><![CDATA[G. D.]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Moreto]]></surname>
<given-names><![CDATA[F.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Takahashi]]></surname>
<given-names><![CDATA[M. M.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Portero-Mclellan]]></surname>
<given-names><![CDATA[K. C.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Burini]]></surname>
<given-names><![CDATA[R. C.]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,State University of Campinas (UNICAMP) Faculdade de Ciências Médicas (FCM) Department of Internal Medicine]]></institution>
<addr-line><![CDATA[Campinas SP]]></addr-line>
<country>Brazil</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Sao Paulo State University (UNESP) Botucatu Medical School Center for Nutritional and Exercise Metabolism (CeMENutri)]]></institution>
<addr-line><![CDATA[Botucatu SP]]></addr-line>
<country>Brazil</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>10</month>
<year>2011</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>10</month>
<year>2011</year>
</pub-date>
<volume>26</volume>
<numero>5</numero>
<fpage>1125</fpage>
<lpage>1129</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_arttext&amp;pid=S0212-16112011000500031&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_abstract&amp;pid=S0212-16112011000500031&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_pdf&amp;pid=S0212-16112011000500031&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Aim: To correlate the sagittal abdominal diameter (SAD) and waist circumference (WC) with metabolic syndrome-associated abnormalities in adults. Methods: This cross-sectional study included onehundred twelve adults (M = 27, F = 85) aging 54.0 &plusmn; 11.2 yrs and average body mass index (BMI) of 30.5 &plusmn; 9.0 kg/m². The assessment included blood pressure, plasma and anthropometric measurements. Results: In both men and female, SAD and WC were associated positively with body fat% (r = 0.53 vs r = 0.55), uric acid (r = 0.45 vs r = 0.45), us-PCR (r = 0.50 vs r = 0.44), insulin (r = 0.89 vs r = 0.75), insulin resistance HOMA-IR (r = 0.86 vs r = 0.65), LDL-ox (r = 0.51 vs r = 0.28), GGT (r = 0.70 vs r = 0.61), and diastolic blood pressure (r = 0.35 vs r = 0.33), and negatively with insulin sensibility QUICKI (r = -0.89 vs r = -0.82) and total cholesterol/TG ratio (r = -0.40 vs r = -0.22). Glycemia, TG, and HDL-c were associated significantly only with SAD (r = 0.31; r = 39, r = -0.43, respectively). Conclusion: Though the SAD and WC were associated with numerous metabolic abnormalities, only SAD correlated with dyslipidemia (TG and HDL-c) and hyperglycemia (glycemia).]]></p></abstract>
<abstract abstract-type="short" xml:lang="es"><p><![CDATA[Objetivo: Correlacionar el diámetro abdominal sagital (DAS) y la circunferencia de la cintura (CC) con las anomalías asociadas al síndrome metabólico en adultos. Métodos: Este estudio transversal incluyó a 112 adultos (H = 27, M = 85) con edad de 54,0 &plusmn; 11,2 años y un promedio de índice de masa corporal (IMC) de 30,5 &plusmn; 9,0 kg/m². La evaluación incluía la presión sanguínea y medidas plasmáticas y antropométricas. Resultados: Tanto en hombres como mujeres, DAS y CC se asociaban positivamente con el % grasa corporal (r = 0,53 vs r = 0,55), el ácido úrico (r = 0,45 vs r = 0,45), la us-PCR (r = 0,50 vs r = 0,44), la insulina (r = 0,89 vs r = 0,75), la resistencia a la insulina HOMA-IR (r = 0,86 vs r = 0,65), la LDL-ox (r = 0,51 vs r = 0,28), GGT (r = 0,70 vs r = 0,61), y la presión sanguínea diastólica (r = 0,35 vs r = 0,33), y negativamente con la sensibilidad a la insulina QUICKI (r = -0,89 vs r = -0,82) y el cociente colesterol total/TG (r = -0,40 vs r = -0,22). La glucemia, los TG, y la HDL-c se asociaban significativamente sólo con DAS (r = 0,31; r = 0,39, r = -0,43, respectivamente). Conclusión: Aunque DAS y CC se asociaban con numerosas anomalías metabólicas, sólo DAS se correlacionaba con la dislipemia (TG y HDL-c) y la hiperglucemia (glucemia).]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Sagital abdominal diameter]]></kwd>
<kwd lng="en"><![CDATA[Waist circumference]]></kwd>
<kwd lng="en"><![CDATA[Hyperglycemia]]></kwd>
<kwd lng="en"><![CDATA[Dyslipidemia]]></kwd>
<kwd lng="en"><![CDATA[Inflammation]]></kwd>
<kwd lng="en"><![CDATA[Anthropometric measurements]]></kwd>
<kwd lng="es"><![CDATA[Diámetro abominal sagital]]></kwd>
<kwd lng="es"><![CDATA[Circunferencia de la cintura]]></kwd>
<kwd lng="es"><![CDATA[Hiperglucemia]]></kwd>
<kwd lng="es"><![CDATA[Dislipemia]]></kwd>
<kwd lng="es"><![CDATA[Inflamación]]></kwd>
<kwd lng="es"><![CDATA[Medidas antropométricas]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p><font face="Verdana" size="2"><a name="top"></a><b>ORIGINAL</b></font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="4"><b>Sagital abdominal diameter, but not waist circumference is strongly associated with glycemia, triacilglycerols and HDL-Clevels in overweight adults</b></font></p>     <p><font face="Verdana" size="4"><b>Diámetro abdominal sagital, pero no la circunferencia de la cintura se asocia fuertemente con la glucemia, triacilglycerols y HDL-C en adultos con sobrepeso</b></font></p>     <p>&nbsp;</p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>G. D. Pimentel<sup>1,2</sup>, F. Moreto<sup>2</sup>, M. M. Takahashi<sup>2</sup>, K. C. Portero-Mclellan<sup>2</sup> and R. C. Burini<sup>2</sup></b></font></p>     <p><font face="Verdana" size="2"><sup>1</sup>Department of Internal Medicine. FCM. State University of Campinas (UNICAMP). Campinas. SP. Brazil.    <br><sup>2</sup>Botucatu Medical School. Center for Nutritional and Exercise Metabolism (CeMENutri). Department of Public Health. Sao Paulo State University (UNESP). Botucatu. SP. Brazil.</font></p>     <p><font face="Verdana" size="2">This work was funded by grants from the Sao Paulo State Research Foundation (FAPESP, Brazil) and CAPES, Brazil. We declare that there are no conflicts of interest.</font></p>     ]]></body>
<body><![CDATA[<p><a href="#bajo"><font face="Verdana" size="2">Correspondence</font></a></p>     <p>&nbsp;</p>     <p>&nbsp;</p> <hr size="1">     <p><font face="Verdana" size="2"><b>ABSTRACT</b></font></p>     <p><font face="Verdana" size="2"><b>Aim:</b> To correlate the sagittal abdominal diameter (SAD) and waist circumference (WC) with metabolic syndrome-associated abnormalities in adults.    <br><b>Methods:</b> This cross-sectional study included onehundred twelve adults (M = 27, F = 85) aging 54.0 &plusmn; 11.2 yrs and average body mass index (BMI) of 30.5 &plusmn; 9.0 kg/m<sup>2</sup>. The assessment included blood pressure, plasma and anthropometric measurements.    <br><b>Results:</b> In both men and female, SAD and WC were associated positively with body fat% (r = 0.53 <i>vs</i> r = 0.55), uric acid (r = 0.45 <i>vs</i> r = 0.45), us-PCR (r = 0.50 <i>vs</i> r = 0.44), insulin (r = 0.89 <i>vs</i> r = 0.75), insulin resistance HOMA-IR (r = 0.86 <i>vs</i> r = 0.65), LDL-ox (r = 0.51 <i>vs</i> r = 0.28), GGT (r = 0.70 <i>vs</i> r = 0.61), and diastolic blood pressure (r = 0.35 <i>vs</i> r = 0.33), and negatively with insulin sensibility QUICKI (r = -0.89 <i>vs</i> r = -0.82) and total cholesterol/TG ratio (r = -0.40 <i>vs</i> r = -0.22). Glycemia, TG, and HDL-c were associated significantly only with SAD (r = 0.31; r = 39, r = -0.43, respectively).    <br><b>Conclusion:</b> Though the SAD and WC were associated with numerous metabolic abnormalities, only SAD correlated with dyslipidemia (TG and HDL-c) and hyperglycemia (glycemia).</font></p>     <p><font face="Verdana" size="2"><b>Key words:</b> Sagital abdominal diameter. Waist circumference. Hyperglycemia. Dyslipidemia. Inflammation. Anthropometric measurements.</font></p> <hr size="1">     <p><font face="Verdana" size="2"><b>RESUMEN</b></font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2"><b>Objetivo:</b> Correlacionar el diámetro abdominal sagital (DAS) y la circunferencia de la cintura (CC) con las anomalías asociadas al síndrome metabólico en adultos.    <br><b>Métodos:</b> Este estudio transversal incluyó a 112 adultos (H = 27, M = 85) con edad de 54,0 &plusmn; 11,2 años y un promedio de índice de masa corporal (IMC) de 30,5 &plusmn; 9,0 kg/m<sup>2</sup>. La evaluación incluía la presión sanguínea y medidas plasmáticas y antropométricas.    <br><b>Resultados:</b> Tanto en hombres como mujeres, DAS y CC se asociaban positivamente con el % grasa corporal (r = 0,53 <i>vs</i> r = 0,55), el ácido úrico (r = 0,45 <i>vs</i> r = 0,45), la us-PCR (r = 0,50 <i>vs</i> r = 0,44), la insulina (r = 0,89 <i>vs</i> r = 0,75), la resistencia a la insulina HOMA-IR (r = 0,86 <i>vs</i> r = 0,65), la LDL-ox (r = 0,51 <i>vs</i> r = 0,28), GGT (r = 0,70 <i>vs</i> r = 0,61), y la presión sanguínea diastólica (r = 0,35 <i>vs</i> r = 0,33), y negativamente con la sensibilidad a la insulina QUICKI (r = -0,89 <i>vs</i> r = -0,82) y el cociente colesterol total/TG (r = -0,40 <i>vs</i> r = -0,22). La glucemia, los TG, y la HDL-c se asociaban significativamente sólo con DAS (r = 0,31; r = 0,39, r = -0,43, respectivamente).    <br><b>Conclusión:</b> Aunque DAS y CC se asociaban con numerosas anomalías metabólicas, sólo DAS se correlacionaba con la dislipemia (TG y HDL-c) y la hiperglucemia (glucemia).</font></p>     <p><font face="Verdana" size="2"><b>Palabras clave:</b> Diámetro abominal sagital. Circunferencia de la cintura. Hiperglucemia. Dislipemia. Inflamación. Medidas antropométricas.</font></p> <hr size="1">     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>Introduction</b></font></p>     <p><font face="Verdana" size="2">The "gold standard" measurements of visceral or intraabdominal obesity are obtained by computed tomography, dual-energy-X ray absorptiometry, or magnetic resonance imaging. However, they are expensive and dual-energy-X ray absorptiometry and computed tomography involves radiation exposure. Though, it is impractical for epidemiologic purposes, in the context of primary care, or in clinic routine.<sup>1,2</sup></font></p>     <p><font face="Verdana" size="2">Indirect anthropometric estimates of body composition have proven usefulness for clinical practice and epidemiologic surveys because they are simple, noninvasive, and cheap. Several studies indicate that measures of abdominal fat are better predictors of metabolic syndrome (MS) and inflammation than total body adiposity as assessed by body mass index (BMI) in adults.<sup>3-7</sup></font></p>     <p><font face="Verdana" size="2">In adult populations, the waist circumference (WC) is the most commonly used indicator of abdominal adiposity and is the main pathological finding in MS.<sup>8,9</sup> However, the reliability of this measure in people with subcutaneous fat has been questioned<sup>10</sup> because these individuals appear "tummy apron".</font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">Sagittal abdominal diameter (SAD) is highly correlated with visceral adipose tissue assessment by computed tomography.<sup>11</sup> Methodologically the SAD would be better measurement than the WC, because the sliding of subcutaneous fat to the waist sides when the measurement is taken orthostatically.<sup>3-5,12</sup></font></p>     <p><font face="Verdana" size="2">The aim of this study was to correlate two anthropometric measurements (WC and SAD) with MS-associated abnormalities in adults.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>Materials and methods</b></font></p>     <p><font face="Verdana" size="2"><i>Subjects and methods</i></font></p>     <p><font face="Verdana" size="2">This descriptive and cross-sectional study was conducted in patients clinically selected for lifestyle modification program "Mexa-se Pro-Saúde" (2006- 2008). One hundred twelve patients (85 female and 27 male) participated of study. The criterion for exclusion was only subjects with liver, kidney, heart, or peripheral vascular disease, as well as chronic alcoholic.</font></p>     <p><font face="Verdana" size="2">This study was conducted according to the guidelines laid down in the Declaration of Helsinki and all procedures involving human subjects were approved by the Ethics Committee of Sao Paulo State University (UNESP, Brazil) n<sup>o</sup> 170/2005. Written informed consent was obtained from all subjects.</font></p>     <p><font face="Verdana" size="2"><i>Anthropometric measurements</i></font></p>     <p><font face="Verdana" size="2">Height was measured to nearest 0.5 cm. Body weight was measured to the nearest 0.1 kg without shoes in light indoor clothing. BMI was calculated as the ratio of body weight (kg) divided by height (m) squared. WC was measured in a supine position between the lowest rib and the iliac crest.<sup>13</sup></font></p>     <p><font face="Verdana" size="2">Body fat percentage (%BF) was calculated from the resistance value (ohms) informed by bioelectric impedance analysis (BIA) (Biodynamics<sup>&reg;</sup> 450 model) and subsequent application in the equation recommended by Segal et al.<sup>14</sup> In order to reduce possible changes in water status, the participants were demanded to follow the recommendations: of avoiding drinking alcoholic beverages as well as caffeine for 24 hours before the test, fasting for 4 hours before the test, avoid intense exercising for at least 12 hours before the test, and let know about the use of medicine based on diuretics (in this case, the participants were not submitted to the test).<sup>13</sup></font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">The SAD was measured with a portable, sliding beam, abdominal caliper (Holtain, Ltd.; Dyfed, Wales, UK). The caliper´s upper arm was brought down to just above an abdominal mark made midway between the iliac crests, a location that approximates to the L4-L5 interspace. The subject was asked to inhale and exhale gently, and the arm of the caliper was brought down to touch the abdominal mark without compression.<sup>3</sup></font></p>     <p><font face="Verdana" size="2"><i>Clinical and biochemical measurements</i></font></p>     <p><font face="Verdana" size="2">Blood pressure was measured in the participant´s right arm after a 5 minutes rest by using an indirect auscultation with a mercury sphygmomanometer. Systolic and diastolic blood pressure was defined as Korotkoff phases 1 and 5, respectively.</font></p>     <p><font face="Verdana" size="2">Blood samples were drawn from an antecubital vein, and all serum and plasma samples were immediately chilled, kept on ice, centrifuged, and stored at -80<sup>o</sup>C until analyzed. Fasting glucose, total cholesterol, high-density lipoprotein (HDL-c), triacilglycerols (TG), &gamma;-glutamyl transferase (GGT) and uric acid were quantified by commercial kits by enzymatic colorimetry assay (Labtest Diagnostica, MG, Brazil) in a semi-automatic spectrophotometry. Low-density lipoprotein (LDL-c) was calculated by the equation LDL-c = total cholesterol-(HDLc-TG/5)<sup>15</sup> and LDL-c subclass by the equation (TG/HDL-c ratio)<sup>16</sup> which is a good predictive factor for oxidized-LDL-c. Fasting insulin was assayed by immunochemical luminescence using commercial kits (DPC Medlab) in automated equipment (Immulite 2000R; DPC Medlab). The insulin resistance was calculated by the Homeostasis Model Assessment of insulin resistance (HOMA-IR) and for insulin sensitivity the QUICKI formula.<sup>17</sup></font></p>     <p><font face="Verdana" size="2">Plasma by ultra-sensitivity C-reactive protein (us- CRP) was measured using Immulite Kit (DPC&acirc; Medlab-Diagnostic Products Corporation, Los Angeles, CA).</font></p>     <p><font face="Verdana" size="2"><i>Statistical analysis</i></font></p>     <p><font face="Verdana" size="2">Data are presented as means and standard deviations. The normality of the distribution within each sex group was tested for all the variables using the Kolmogorov-Smirnov test. Pearson´s correlations were used to verify a possible association between WC and SAD with metabolic abnormalities and comparisons between sexes were performed with <i>Student´s</i> unpaired t test. All statistical analyses were performed by using SPSS for Windows (version 12.0; SPSS Inc, Chicago, IL). P &lt; 0.05 was considered as statistically significant.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>Results</b></font></p>     <p><font face="Verdana" size="2">Participants showed an age averaging (mean&plusmn;Sd) 54.0 &plusmn; 11.2 years, BMI of 30.5 &plusmn; 9.0 kg/m<sup>2</sup>, SAD of 22.4 &plusmn; 3.9 cm (23.7 &plusmn; 3.0 cm for male and 22.0 &plusmn; 4.0 cm for female, p = 0.14), and WC of 96.3 &plusmn; 13.7 cm (101.0 &plusmn; 14.8 cm for male and 95.4 &plusmn; 13.4 cm for female, p = 0.17) (<a target="_blank" href="/img/revistas/nh/v26n5/31_original_30_t1.gif">table I</a>). Uric acid was the only measure that differed between genders. Other general characteristics of subjects studied are shown in <a target="_blank" href="/img/revistas/nh/v26n5/31_original_30_t1.gif">table I</a>.</font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">SAD and WC were associated positively (<a target="_blank" href="/img/revistas/nh/v26n5/31_original_30_f1.gif">fig. 1</a>) with body fat% (r = 0.53 <i>vs</i> r = 0.55), uric acid (r = 0.45 <i>vs</i> r = 0.45), us-PCR (r = 0.50 <i>vs</i> r = 0.44), insulin (r = 0.89 <i>vs</i> r = 0.75), HOMA-IR (r = 0.86 <i>vs</i> r = 0.65), oxidized-LDL-c (r = 0.51 <i>vs</i> r = 0.28), GGT (r = 0.70 <i>vs</i> r = 0.61), and diastolic blood pressure (r = 0.35 <i>vs</i> r = 0.33), and negatively (<a target="_blank" href="/img/revistas/nh/v26n5/31_original_30_f1.gif">fig. 1</a>) with insulin sensibility QUICKI (r = -0.89 <i>vs</i> r = -0.82) and total cholesterol/ TG ratio (r = -0.40 <i>vs</i> r = -0.22). Glycemia, TG, and HDL-c were associated significantly only with SAD (r = 0.31; r = 0.39, r = -0.43, respectively).Total cholesterol and LDL-c were not associated with neither adiposity indicators.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>Discussion</b></font></p>     <p><font face="Verdana" size="2">The relative utility of several estimates of fat distribution has been controversial. Some investigators have proposed that WC is a better indicator of abdominal fat distribution than is waist-hip ratio, because it requires only one measurement and is more highly correlated with visceral fat<sup>9,18</sup> and yet is suggest that predictive equation for evaluation of abdominal obesity based on bioelectrical impedance may be very useful in the clinical practice.<sup>19</sup> SAD has been proposed to be even better than WC. However, no large or consistent difference between SAD and WC has been found in relation to visceral fat.<sup>18</sup> The present study and others<sup>3-5,13</sup> suggest that the SAD may be also a strong predictor of blood metabolic abnormalities.</font></p>     <p><font face="Verdana" size="2">Petersson et al.<sup>5</sup> demonstrated that every onecentimeter increase in SAD was associated with an increase of CRP by 0.41 mg/l, corresponding to an increased mean CRP level by 16%. This estimation is of clinical importance once elevated levels of serum CRP are associated with the MS and cardiovascular diseases.<sup>20,21</sup> Other studies have obtained a stronger association for SAD to insulin resistance,<sup>22</sup> cardiovascular risk<sup>4</sup> and MS<sup>22</sup> than WC, BMI and waist-hip ratio.</font></p>     <p><font face="Verdana" size="2">In a previous study<sup>23</sup> we established the cut-off points for SAD that corresponded to altered WC (WC &gt; 102 cm for men and &gt; 88 cm for women). The established points were 23.1 cm for men and 20.1 cm for women. Here we showed that either WC or SAD correlated well with plasma markers of metabolic abnormalities.</font></p>     <p><font face="Verdana" size="2">Recently, López de la Torre<sup>24</sup> demonstrated that both female and male and adults and elderly with high WC values are associated with diabetes. However, in the present study only SAD correlated with the MS components (TG, glycemia and HDL-c). Thus, the SAD could be seeing as an appropriate method to be used for MS diagnosis purpose.</font></p>     <p><font face="Verdana" size="2">In summary, this study shown that both SAD and WC associated with numerous metabolic abnormalities. However, only SAD correlated with glycemia, TG and HDL-c, indicating that the SAD is a strong indicator of dyslipidemia and hyperglycemia. Thus, we suggesting that SAD measurement should be adopt in clinical practice and epidemiological studies.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>Author contributions</b></font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">The work presented here was carried out in collaboration between all authors. GDP and RCB defined the research theme. GDP, KCPM, MMT and RCB designed methods and experiments. GDP wrote the manuscript, analyzed the data and interpreted the results. FM performed the plasma biochemistry analysis. All authors have given final approval of submitted version.</font></p>     <p>&nbsp;</p>     <p><font face="Verdana" size="2"><b>References</b></font></p>     <!-- ref --><p><font face="Verdana" size="2">1. Fuller NJ, Jebb SA, Laskey MA, Coward WA, Elia M. 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Brazil.    <br>E-mail: <a href="mailto:gupimentel@yahoo.com.br">gupimentel@yahoo.com.br</a></font></p>     ]]></body>
<body><![CDATA[<p><font face="Verdana" size="2">Recibido: 2-II-2011.    <br>1<sup>a</sup> Revisión: 6-III-2011.    <br>Aceptado: 9-III-2011.</font></p>      ]]></body><back>
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