<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJNeph</journal-id><journal-title-group><journal-title>Open Journal of Nephrology</journal-title></journal-title-group><issn pub-type="epub">2164-2842</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojneph.2016.64022</article-id><article-id pub-id-type="publisher-id">OJNeph-73067</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Prevalence of Metabolic Syndrome and Associated Factors among Hemodialysis Patients Monitored at the National Teaching Hospital, Hubert Koutoucou Maga in 2015
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jacques</surname><given-names>Vigan</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Adébayo</surname><given-names>S. C. Alassani</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mahoussi</surname><given-names>M. A. Ahissou</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Akomola</surname><given-names>K. Sabi</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ubald</surname><given-names>Assogba-Gbindou</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Vénérand</surname><given-names>Attolou</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>François</surname><given-names>Djrolo</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Endocrinology and Metabolism University Clinic of CNHU-HKM, Cotonou, Benin</addr-line></aff><aff id="aff3"><addr-line>Nephrology Hemodialysis Department, Sylvanus Olympio Teaching Hospital Centre, Lomé, Togo</addr-line></aff><aff id="aff1"><addr-line>Nephrology Hemodialysis University Clinic of Hubert K Maga Teaching Hospital (CNHU-HKM), Cotonou, Benin</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>viques2@yahoo.fr(JV)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>11</day><month>11</month><year>2016</year></pub-date><volume>06</volume><issue>04</issue><fpage>167</fpage><lpage>175</lpage><history><date date-type="received"><day>October</day>	<month>25,</month>	<year>2016</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>December</month>	<year>25,</year>	</date><date date-type="accepted"><day>December</day>	<month>28,</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Introduction: Metabolic syndrome is
   
  one of the main risk factors of cardiovascular disease among hemodialysis patients. Objective: The main objective of this study was
   
  to determine the prevalence and factors associated with metabolic syndrome among hemodialysis patients in Cotonou in 2015. Patients and methods: It was a
   
  cross-sectional, descriptive and analytical
   
  study conducted from 05<sup>th</sup> October to 02<sup>nd</sup> November 2015
   
  at the
   
  National 
  Teaching Hospital,
   Hubert
   
  Koutoucou
   
  Maga of Cotonou.
   
  All patients aged 18 years and above, regularly under hemodialysis for the past 3
   months and who gave their informed consent were included in the study. Those excluded were: currently hospitalized hemodialysis patients, hemodialysis patients hospitalized in the last three months, hemodialysis patients whose general condition deteriorated or unable to answer the questionnaire. Metabolic syndrome was defined according to the International Diabetes Federation’s criteria.
   
  Factors associated with metaboli
  c syndrome
   
  were
   
  sought using logistic regression in
   
  univariate analysis. Confidenc
  e intervals were calculated at 95% and alpha significance threshold at 5%.
   
  Outcomes
  :
   
  In total 165 patients were included in the study.
   
  Male predominance
   
  was observed
  , with 1.27 sex-ratios. Average age was 49.3
   
  &#177; 12.9 years with
   
  extremes ranging from
   18 to 78 years. Metabolic syndrome is observed among 46 patients undergoing hemodialysis or 27.9% prevalence rate. Factors associated with the metabolic syndrome in univariate analysis
   
  were: gender (p
   
  &lt;
   
  0.001), age (p
   
  =
   
  0.007), body mass index (p
   
  =
   
  0.029) and prior diabetes history (p
   
  =
   
  0.011).
   
  Conclusion:
   
  Metabolic syndrome is
   common among hemodialysis patients.
   
  Early screening and fighting against asso
  ciated risk factors are very important.
 
</p></abstract><kwd-group><kwd>Benin</kwd><kwd> Associated Factors</kwd><kwd> Hemodialysis Patients</kwd><kwd> Prevalence</kwd><kwd> Metabolic Syndrome</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Chronic kidney disease is a real public health problem [<xref ref-type="bibr" rid="scirp.73067-ref1">1</xref>] . Hemodialysis patients are faced with the risk of cardiovascular diseases which are the first cause of mortality among this population. Cardiovascular diseases’ index varies from 25% to 60% among patients with chronic renal disease [<xref ref-type="bibr" rid="scirp.73067-ref2">2</xref>] . These cardiovascular diseases claim 44% of deaths among hemodialysis patients [<xref ref-type="bibr" rid="scirp.73067-ref3">3</xref>] . The risk of hemodialysis patients’ death is 5 to 20 times higher compared to the general population [<xref ref-type="bibr" rid="scirp.73067-ref4">4</xref>] .</p><p>Metabolic syndrome is an entity that brings together in the same individual, several metabolic abnormalities which predispose him to cardiovascular risks. Metabolic syndrome is itself one of the main risk factors for cardiovascular diseases [<xref ref-type="bibr" rid="scirp.73067-ref5">5</xref>] .</p><p>The prevalence of metabolic syndrome among the general population is 13.3% in China in 2006 [<xref ref-type="bibr" rid="scirp.73067-ref6">6</xref>] , 22% in the United States in 2012 [<xref ref-type="bibr" rid="scirp.73067-ref5">5</xref>] . Jalalzadeh observed among hemodialysis patients in Iran in 2011, 28.7% prevalence; P&#233;rez in Spain in 2014, 29% and Maoujoud in Morocco recorded in 2011, 44% [<xref ref-type="bibr" rid="scirp.73067-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref9">9</xref>] . This prevalence within hemodialysis population may reach 70% [<xref ref-type="bibr" rid="scirp.73067-ref10">10</xref>] . Metabolic syndrome triples the risk of developing cardiovascular disease [<xref ref-type="bibr" rid="scirp.73067-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref11">11</xref>] , and increases two-fold mortality among hemodialysis patients [<xref ref-type="bibr" rid="scirp.73067-ref12">12</xref>] .</p><p>In Benin, the prevalence of the metabolic syndrome among chronic hemodialysis patients is unknown. The factors associated with metabolic syndrome among these patients have not yet been identified. This justifies the interest in this study on the metabolic syndrome among hemodialysis patients at the National Teaching Hospital Hubert Koutoukou Maga (CNHU-HKM) of Cotonou.</p></sec><sec id="s2"><title>2. Objectives</title><sec id="s2_1"><title>2.1. General Objective</title><p>・ Study metabolic syndrome among hemodialysis patients monitored in CNHU- HKM.</p></sec><sec id="s2_2"><title>2.2. Specific Objectives</title><p>・ Determine metabolic syndrome prevalence among patients undergoing hemodialysis.</p><p>・ Identify factors associated with metabolic syndrome among hemodialysis patients.</p></sec></sec><sec id="s3"><title>3. Patients and Methods</title><p>It was a cross-sectional, descriptive and analytical study conducted from 05<sup>th</sup> October to 02<sup>nd</sup> November 2015 at the Nephrology-Hemodialysis University Clinic of The National Teaching Hospital, Hubert Koutoukou Maga of Cotonou.</p><p>This National University Teaching Hospital is the referral hospital for the whole country. Nephrology-Hemodialysis University Clinic received 60 - 80 new patients per year, which are then distributed mostly in other public or private dialysis centers of the country.</p><p>Patients included in the study were at least 18 years old, under hemodialysis for at least the past three months and who gave their informed consent. The following were excluded from the study: currently hospitalized hemodialysis patients, hemodialysis patients hospitalized in the last three months, hemodialysis patients unable to answer the questionnaire.</p><p>Metabolic syndrome was defined according to International Diabetes Federation (IDF) which includes the following components [<xref ref-type="bibr" rid="scirp.73067-ref13">13</xref>] :</p><p>・ Waist size or abdominal circumference is above or equal to 94 cm among men and above or equal to 80 cm among women,</p><p>・ Blood pressure is above or equal to 130/85 mmHg or specific treatment of hypertension,</p><p>・ Fasting plasma glucose above or equal to 1, 1 g/L or specific treatment,</p><p>・ Fasting triglyceridemia above or equal to 1, 50 g/L or specific treatment,</p><p>・ HDL cholesterol levels below 0.40 g/l among men or below 0.50 g/L among women or specific treatment.</p><p>Metabolic syndrome occurs with a patient if his/her waist size is high and associated with at least two other criteria [<xref ref-type="bibr" rid="scirp.73067-ref13">13</xref>] .</p><p>The waist circumference was measured at the end of hemodialysis session, in sitting position, with a measuring tape, placed in the middle of the distance between the iliac crest and the lower costal margin, on the narrowest abdominal section.</p><p>Other variables sought were socio-demographic data (age, gender, profession, marital status); medical history (diabetes, hypertension); lifestyle (alcohol abuse, and level of physical activity), dialysis parameters (usual number of hours of dialysis per session, frequency of dialysis per week, type of arterio-venous fistula or catheter, duration under hemodialysis, percentage of urea reduction) and biological data.</p><p>Patients practicing less than 30 minutes of physical activity per day were considered as inactive. Otherwise, they were considered active. Anemia is defined by a rate of hemoglobin below 10 g/dl according kidney Disease Improving Global Outcome (KDIGO) guideline [<xref ref-type="bibr" rid="scirp.73067-ref14">14</xref>] . Urea reduction percentage (URP) was calculated on the ratio of the difference between blood urea nitrogen before dialysis and the one after dialysis on blood urea nitrogen before dialysis multiplied by 100. The URP is considered as normal when it is above or equal to 60%. With regard to biological data, blood sampling was made for each patient at the beginning of one of the he-modialysis sessions in the morning.</p><p>Associated factors were sought by using logistic regression in univariate analysis. Data entry and analysis were performed using Epi Data 3.1. P-value below 0.05 was considered significant.</p></sec><sec id="s4"><title>4. Results</title><sec id="s4_1"><title>4.1. General Characteristics of the Population</title><p>The study population comprised 165 hemodialysis patients. Male predominance was noted with 1.27 sex-ratio. Average age was 49.3 &#177; 12.9 years with extremes ranging from 18 to 78 years. Hypertension (HTA) was observed among 103 patients (62.4%). Arterio- venous fistula (AVF) was the privileged vascular access, and it was observed among 140 patients (84.8%). Average BMI of patients was 22.5 &#177; 6.8 kg/m&#178; with extremes ranging from 14.5 to 62.14 kg/m<sup>2</sup>. <xref ref-type="table" rid="table1">Table 1</xref> shows the general characteristics of hemodialysis patients.</p></sec><sec id="s4_2"><title>4.2. Metabolic Syndrome Prevalence</title><p>Metabolic syndrome was observed among 46 hemodialysis patients or 27.9% prevalence. The average waist size of patients was 87.7 &#177; 12.4 cm with extremes ranging from 64 to 130 cm. Average systolic blood pressures was 147 &#177; 25.73 mmHg with extremes ranging from 81 to 234 mmHg and average diastolic blood pressure was 76.03 &#177; 19.06 mmHg with extremes ranging from 10 to 111 mmHg. Average HDL rate was 0.47 &#177; 0.14 g/L with extremes ranging from 0.10 to 0.87 g/l. Average triglyceridemia was 1.17 &#177; 0.75 g/L with extremes ranging from 0.30 to 5.92 g/L. Average glycemia was 0.97 &#177; 0.35 g/L with extremes ranging from 0.6 to 2.60 g/l. The most frequently metabolic syndrome criteria observed were blood pressure above or equal to 130/85 mm Hg (66.67%), followed by HDL hypocholesterolemia (45.5%). <xref ref-type="table" rid="table2">Table 2</xref> shows metabolic syndrome prevalence and metabolic syndrome criteria among hemodialysis patients.</p></sec><sec id="s4_3"><title>4.3. Factors Associated with Metabolic Syndrome</title><p>Factors associated with metabolic syndrome in univariate analysis were gender (p &lt; 0.001), age (p = 0.007), body mass index (p = 0.029), and diabetes history (p = 0.011). <xref ref-type="table" rid="table3">Table 3</xref> shows factors associated with metabolic syndrome among hemodialysis patients in univariate analysis.</p></sec></sec><sec id="s5"><title>5. Discussion</title><sec id="s5_1"><title>5.1. Metabolic Syndrome Prevalence</title><p>In this study, the definition of metabolic syndrome is based on IDF criterion, which is a reliable definition of metabolic syndrome. It is the most used and practical in the sense that the excess abdominal fat estimated through waist size is considered as a vital criterion [<xref ref-type="bibr" rid="scirp.73067-ref13">13</xref>] .</p><p>Metabolic syndrome prevalence among hemodialysis patients was 27.9% in Spain and Russia while similar results were reported by Perez and Radojica [<xref ref-type="bibr" rid="scirp.73067-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref15">15</xref>] . In their studies, metabolic syndrome prevalence was respectively 29% and 29.8% in hemodialysis patients [<xref ref-type="bibr" rid="scirp.73067-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref15">15</xref>] . Alfonso et al. and Bonet et al. used NCEP-ATP III (National Cholesterol Education Program Adult Treatment Panel III) criteria and still recorded among hemodialysis patient a prevalence close to that of our study, respectively 25%</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> General characteristics of hemodialysis patients monitored at CNHU-HKM in 2015</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Number (N = 165)</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Gender</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Female</td><td align="center" valign="middle" >72</td><td align="center" valign="middle" >43.6</td></tr><tr><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >93</td><td align="center" valign="middle" >56.4</td></tr><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&lt;40 years</td><td align="center" valign="middle" >42</td><td align="center" valign="middle" >25.5</td></tr><tr><td align="center" valign="middle" >≥40 years</td><td align="center" valign="middle" >123</td><td align="center" valign="middle" >74.5</td></tr><tr><td align="center" valign="middle" >Level of Education</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Illiterate</td><td align="center" valign="middle" >24</td><td align="center" valign="middle" >14.5</td></tr><tr><td align="center" valign="middle" >Literate</td><td align="center" valign="middle" >141</td><td align="center" valign="middle" >85.5</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Level of physical activity</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Inactive</td><td align="center" valign="middle" >139</td><td align="center" valign="middle" >84.3</td></tr><tr><td align="center" valign="middle" >Active</td><td align="center" valign="middle" >26</td><td align="center" valign="middle" >15.8</td></tr><tr><td align="center" valign="middle" >History</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >HTA</td><td align="center" valign="middle" >103</td><td align="center" valign="middle" >62.4</td></tr><tr><td align="center" valign="middle" >Diabetes</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >18.2</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Dialysis parameters</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle"  colspan="2"  >Number of session per week</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >2</td><td align="center" valign="middle" >146</td><td align="center" valign="middle" >88.5</td></tr><tr><td align="center" valign="middle" >3</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >11.5</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Duration of each session</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >4 h</td><td align="center" valign="middle" >71</td><td align="center" valign="middle" >43.0</td></tr><tr><td align="center" valign="middle" >&gt;4 h</td><td align="center" valign="middle" >94</td><td align="center" valign="middle" >57.0</td></tr><tr><td align="center" valign="middle" >Vascular access</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >AVF*</td><td align="center" valign="middle" >140</td><td align="center" valign="middle" >84.8</td></tr><tr><td align="center" valign="middle" >Catheter</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >15.2</td></tr><tr><td align="center" valign="middle" >URP**</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&lt;60%</td><td align="center" valign="middle" >42</td><td align="center" valign="middle" >25.5</td></tr><tr><td align="center" valign="middle" >≥60%</td><td align="center" valign="middle" >123</td><td align="center" valign="middle" >74.5</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Duration under dialysis</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&lt;60 months</td><td align="center" valign="middle" >46</td><td align="center" valign="middle" >27.9</td></tr><tr><td align="center" valign="middle" >≥60 months</td><td align="center" valign="middle" >119</td><td align="center" valign="middle" >72.1</td></tr><tr><td align="center" valign="middle"  colspan="2"  >Body Mass Index</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&lt; 18</td><td align="center" valign="middle" >32</td><td align="center" valign="middle" >19.4</td></tr><tr><td align="center" valign="middle" >[18 - 25]</td><td align="center" valign="middle" >102</td><td align="center" valign="middle" >61.8</td></tr><tr><td align="center" valign="middle" >[25 - 30]</td><td align="center" valign="middle" >21</td><td align="center" valign="middle" >12.7</td></tr><tr><td align="center" valign="middle" >≥30</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >06.1</td></tr></tbody></table></table-wrap><p>*Arterio-venous fistula, **Percentage of urea reduction.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Prevalence and characteristics of metabolic syndrome components among hemodialysis patients monitored at CNHU-HKM in 2015</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Number (N = 165)</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Metabolic Syndrome</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >46</td><td align="center" valign="middle" >27.9</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >119</td><td align="center" valign="middle" >72.1</td></tr><tr><td align="center" valign="middle"  colspan="3"  >Metabolic syndrome criteria</td></tr><tr><td align="center" valign="middle" >Waist size</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >High</td><td align="center" valign="middle" >74</td><td align="center" valign="middle" >44.8</td></tr><tr><td align="center" valign="middle" >Normal</td><td align="center" valign="middle" >91</td><td align="center" valign="middle" >55.2</td></tr><tr><td align="center" valign="middle" >Blood pressure (mmHg)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&lt;130/85</td><td align="center" valign="middle" >55</td><td align="center" valign="middle" >33.3</td></tr><tr><td align="center" valign="middle" >≥130/85</td><td align="center" valign="middle" >110</td><td align="center" valign="middle" >66.7</td></tr><tr><td align="center" valign="middle" >Glucose (g/L)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Normal</td><td align="center" valign="middle" >106</td><td align="center" valign="middle" >64.3</td></tr><tr><td align="center" valign="middle" >Abnormal</td><td align="center" valign="middle" >59</td><td align="center" valign="middle" >35.7</td></tr><tr><td align="center" valign="middle" >HDL hypocholesterolemiea</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >75</td><td align="center" valign="middle" >45.5</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >90</td><td align="center" valign="middle" >54.5</td></tr><tr><td align="center" valign="middle" >Hypertriglyceridemia</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >42</td><td align="center" valign="middle" >25.5</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >123</td><td align="center" valign="middle" >74.5</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Factors associated with metabolic syndrome among hemodialysis patients monitored at CNHU-HKM in 2015 (univariate analysis)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Metabolic syndrome N (%)</th><th align="center" valign="middle" >No metabolic syndrome N (%)</th><th align="center" valign="middle" >RC [95% CI]</th><th align="center" valign="middle"  colspan="2"  >P</th></tr></thead><tr><td align="center" valign="middle" >Gender</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >&lt;0.001</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Male</td><td align="center" valign="middle" >15 (16.1)</td><td align="center" valign="middle" >78 (83.9)</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Female</td><td align="center" valign="middle" >31 (43.1)</td><td align="center" valign="middle" >41 (56.9)</td><td align="center" valign="middle" >2.66 [1.56 - 4.55]</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.007</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&lt;40 years</td><td align="center" valign="middle" >5 (11.9)</td><td align="center" valign="middle" >37 (88.1)</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >≥40 years</td><td align="center" valign="middle" >41 (33.3)</td><td align="center" valign="middle" >82 (66.7)</td><td align="center" valign="middle" >5 [1.43 - 11.11]</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle"  colspan="3"  >Body Mass Index</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.029</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&lt;25 kg/m<sup>2</sup></td><td align="center" valign="middle" >28 (20.9)</td><td align="center" valign="middle" >106 (79.1)</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >≥25 kg/m<sup>2</sup></td><td align="center" valign="middle" >18 (58)</td><td align="center" valign="middle" >13 (42)</td><td align="center" valign="middle" >2.5 [1.11 - 5]</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle"  colspan="2"  >Diabetes history</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.011</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >32 (23.7)</td><td align="center" valign="middle" >103 (76.3)</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >14 (46.7)</td><td align="center" valign="middle" >16 (53.3)</td><td align="center" valign="middle" >2.8 [1.2 - 6.3]</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><p>and 34.3% [<xref ref-type="bibr" rid="scirp.73067-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref16">16</xref>] . In UCAR study, metabolic syndrome prevalence based on IDF criteria was 36% [<xref ref-type="bibr" rid="scirp.73067-ref17">17</xref>] . Higher metabolic syndrome prevalence among hemodialysis patients 52% was reported by Chang et al. [<xref ref-type="bibr" rid="scirp.73067-ref5">5</xref>] . In that study metabolic syndrome was defined based on NCEP-ATP III criteria. Similarly, in Nakagawa, Kubrusly, Maoujoud and Tu’s studies, metabolic syndrome prevalence was much higher with respectively 38.3%, 42.6%, 44%, and 63.1% [<xref ref-type="bibr" rid="scirp.73067-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref19">19</xref>] . This disparity could be explained by differences between sample size, race, dietary habits, culture and defining criteria of metabolic syndrome. Furthermore, these different studies took place respectively in Japan, Brazil, Morocco, Taiwan and their respective sample size was 133, 115, 25, 377 patients. Vogt et al. observed among the general population varied metabolic syndrome 51%, 66.3%, and 75.3% respectively following the criteria of NCEP ATP III, IDF and harmonized criteria [<xref ref-type="bibr" rid="scirp.73067-ref20">20</xref>] .</p><p>The most frequent metabolic syndrome criteria observed were high blood pressure followed by HDL hypocholesterolemia. Bonet et al. reported similar results with high blood pressure among 65% of hemodialysis patients and HDL hypocholesterolemia among 52.7% patients [<xref ref-type="bibr" rid="scirp.73067-ref11">11</xref>] .</p></sec><sec id="s5_2"><title>5.2. Factors Associated with Metabolic Syndrome</title><p>Gender was associated with metabolic syndrome, and female subjects were 2.6 times more exposed to the risk of developing metabolic syndrome (RC [95% CI] = 2.66 [1.56- 4.55]; p &lt; 0.001). This same association was reported by Chen (p &lt; 0.0001) who usedas criteria for metabolic syndrome definition, NCEP-ATPIII [<xref ref-type="bibr" rid="scirp.73067-ref21">21</xref>] .</p><p>In our study, age is associated with metabolic syndrome among hemodialysis patients and patients aged above 40 years were 5 times more exposed to the risk of developing metabolic syndrome (RC [95% CI] = 5 [1.43 - 11,11]; p = 0.007). Age is also associated with metabolic syndrome in the studies of Radojica (p = 0.001), Kubrusly (p = 0.004) and Chen (p &lt; 0.0001) [<xref ref-type="bibr" rid="scirp.73067-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref21">21</xref>] .</p><p>Diabetes history is associated with metabolic syndrome (RC [95% CI] = 2.8 [1.2 - 6.3]; p = 0.011). It is similar in the studies of Jalalzadeh (p &lt; 0.001) and Radojica (p = 0.04) [<xref ref-type="bibr" rid="scirp.73067-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref15">15</xref>] . However, in Gorsane’s study, diabetes was not associated with metabolic syndrome [<xref ref-type="bibr" rid="scirp.73067-ref10">10</xref>] .</p><p>Body mass index (BMI) is associated with metabolic syndrome among hemodialysis patients, and patients with BMI ≥25 kg/m<sup>2</sup> were 2.5 times more exposed to the risk of developing metabolic syndrome (RC [95% CI] = 2.5 [1.11 - 5]; p = 0.029). This association was observed in the studies of Jalalzadeh (p &lt; 0.001), Radojica (p = 0.001) and Chen (p &lt; 0.0001) [<xref ref-type="bibr" rid="scirp.73067-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.73067-ref21">21</xref>] . In contrast, in Maoujoud’s study carried out in Morocco, BMI is not associated with metabolic syndrome (p = 0.098) [<xref ref-type="bibr" rid="scirp.73067-ref9">9</xref>] .</p></sec></sec><sec id="s6"><title>6. Conclusion</title><p>Metabolic syndrome is common among hemodialysis patients. Early screening and fighting against the risk factors are necessary. It is important to introduce a dietician in these hemodialysis patients’ support team in order to prevent cardiovascular complications.</p></sec><sec id="s7"><title>Declaration of Conflict of Interest</title><p>The authors declare not to have any conflict of interest in connection with this article.</p></sec><sec id="s8"><title>Cite this paper</title><p>Vigan, J., Alassani, A.S.C., Ahissou, M.M.A., Sabi, A.K., Assogba- Gbindou, U., Attolou, V. and Djrolo, F. (2016) Prevalence of Metabolic Syndrome and Associated Factors among Hemodialysis Patients Monitored at the National Teaching Hospital, Hubert Koutoucou Maga in 2015. Open Journal of Nephrology, 6, 167-175. http://dx.doi.org/10.4236/ojneph.2016.64022</p></sec></body><back><ref-list><title>References</title><ref id="scirp.73067-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Levey, A.S., Eckardt, K.U., Tsukamoto, Y., Levin, A., Coresh, J., Rossert, J. et al. (2005) Definition and Classification of Chronic Kidney Disease: Improving Global Outcomes (KDIGO). Kidney International, 67, 2089-2100. https://doi.org/10.1111/j.1523-1755.2005.00365.x</mixed-citation></ref><ref id="scirp.73067-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Yildiz, G., Duman, A., Aydin, H., Yilmaz, A., Hür, E., Magden, K., et al. (2013) Evaluation of Association between Atherogenic Index of Plasma and Intima-Media Thickness of the Carotid Artery for Subclinic Atherosclerosis in Patients on Maintenance Hemodialysis. 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