<?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.2021.111009</article-id><article-id pub-id-type="publisher-id">OJNeph-108127</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>
 
 
  Chronic Kidney Disease in Sub-Saharan Africans: A Study of 462 Patients
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mbengue</surname><given-names>Mansour</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>Ba</surname><given-names>Djenaba</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>Lemrabott</surname><given-names>Tall Ahmed</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>Cissé</surname><given-names>Mouhamadou Moustapha</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>Niang</surname><given-names>Abdou</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Nephrology, Aristide Le Dantec University Hospital, Dakar, Senegal</addr-line></aff><aff id="aff1"><addr-line>Department of Nephrology, Dalal Jamm University Hospital, Dakar, Senegal</addr-line></aff><aff id="aff3"><addr-line>Department of Nephrology, El Hadji Amadou Sakhir Ndiéguéne Hospital, Thiés, Senegal</addr-line></aff><pub-date pub-type="epub"><day>28</day><month>01</month><year>2021</year></pub-date><volume>11</volume><issue>01</issue><fpage>114</fpage><lpage>122</lpage><history><date date-type="received"><day>3,</day>	<month>December</month>	<year>2020</year></date><date date-type="rev-recd"><day>28,</day>	<month>March</month>	<year>2021</year>	</date><date date-type="accepted"><day>31,</day>	<month>March</month>	<year>2021</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>
 
 
  Chronic kidney disease is a global public health problem due to its increasing prevalence as well as its main risk factors such as hypertension and diabetes. However, in Africa, few studies have been done on chronic kidney disease. The aim of our study is to describe the epidemiological, clinical, paraclinical and therapeutic aspects of chronic kidney disease. It was a retrospective and descriptive study carried out from the first of January 2004 to the 31
  <sup>st</sup>
   of December 2013 at Principal hospital in Dakar. Records of any patient aged 18 and over with chronic kidney disease were included. Chronic kidney disease was defined according to the KDIGO 2012 recommendations. Among the 8873 patient records used during our study, 462 presented with chronic kidney disease, which was a hospital prevalence of 5.2%. The sex ratio was 1.61. The mean age of the patients was 58.37 &#177; 19.97 years. There were 75.32% of 
  the patients who were aged 50 and over. The mean serum creatinine was 49.14 
  &#177; 56.83. The mean glomerular filtration rate was 27.47 &#177; 19.86 ml/min/1.73
   
  m
  <sup>2</sup>
  . Chronic renal failure was diagnosed in 92% of patients, including 34.9% in the end-stage of the renal disease. The mean proteinuria was 3.07 &#177; 4.92
   
  g/24
   
  h. Leukocyturia was present in 34.17% of patients. Hematuria was present in 25% of patients. Hypertension and diabetes were the most common causes, found in 61.25% and 35.93% of patients, respectively. Hemodialysis was performed in 49 patients. Peritoneal dialysis was performed in 2 patients. One patient had undergone a kidney transplant. This study establishes the relatively high prevalence of chronic kidney disease and its risk factors including hypertension and diabetes. It also reveals the late diagnosis of chronic kidney disease in our patients.
 
</p></abstract><kwd-group><kwd>Chronic Kidney Disease</kwd><kwd> Hypertension</kwd><kwd> Diabetes</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Chronic kidney disease (CKD) is a global public health problem due to its increasing prevalence as well as its major risk factors which are hypertension and diabetes. Therefore, it contributes significantly to morbidity and mortality and the reduction in life expectancy. Mortality and morbidity are significant because the most affected patients do not access renal replacement therapy. In 2015, more than one over 10 adults was suffering from CKD and more than 600 million worldwide [<xref ref-type="bibr" rid="scirp.108127-ref1">1</xref>]. In 2013, a study estimated that 956,200 deaths worldwide were directly attributable to CKD, which was an increase of 134.6% from 1990 [<xref ref-type="bibr" rid="scirp.108127-ref2">2</xref>]. However, the data available on CKD in countries with limited resources are patchy and come from a few isolated studies [<xref ref-type="bibr" rid="scirp.108127-ref3">3</xref>]. A recent study in Senegal showed CKD prevalence of 4.9% [<xref ref-type="bibr" rid="scirp.108127-ref4">4</xref>]. This study was carried out with the aim of determining the epidemiological, clinical, paraclinical and therapeutic aspects in patients with CKD.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>This was a retrospective and descriptive study carried out over a period of ten years, extending from the first of January 2004 to the 31<sup>st</sup> of December 2013 at Principal Hospital in Dakar. Records of any patient aged 18 and over with CKD were included. The CKD was defined according to the 2012 KDIGO (kidney disease improving global outcomes) recommendations [<xref ref-type="bibr" rid="scirp.108127-ref5">5</xref>]. Patients with acute renal failure or any incomplete or inoperable patient records were not included in the study. Sociodemographic, clinical and paraclinical characteristics were studied. Glomerular filtration rate (GFR) was calculated according to the MDRD (Modification of diet in Renal Disease) formula [<xref ref-type="bibr" rid="scirp.108127-ref6">6</xref>]. Data were collected from patient medical records using pre-established forms. The data were entered and analyzed using a questionnaire developed with the Epi info 7 software and analyzed with the SPSS version 18 software.</p></sec><sec id="s3"><title>3. Results</title><p>During our study period, 8873 records were collected, among which 462 presented a CKD, for a hospital prevalence of 5.2%. There were 285 men and 177 women, for a sex ratio of 1.61. The mean age of the patients was 58.37 &#177; 19.97 years (<xref ref-type="table" rid="table1">Table 1</xref>). There were 348 (75.32%) patients who were aged 50 years and older (<xref ref-type="fig" rid="fig1">Figure 1</xref>). Twenty-seven patients (5.85%) had a history of herbal medicine use. The reasons for consultation were mainly represented by edema of the lower limbs (25.10%), vomiting (13.63%) and dyspnea (22.29%) (<xref ref-type="table" rid="table2">Table 2</xref>). Three hundred and eighteen patients (68.83%) had systolic hypertension. Two hundred and seventy patients (58.44%) had diastolic hypertension. The mean blood urea level was 1.18 g/L &#177; 0.95. The mean serum creatinine was 49.14 mg/L &#177; 56.83. The mean GFR was 27.47 &#177; 19.86 ml/min/1.73 m<sup>2</sup>. Chronic renal failure was diagnosed in 92% of patients, including 34.9% in the end-stage of the renal disease (ESRD) (<xref ref-type="fig" rid="fig2">Figure 2</xref>). There were 82.8% of our patients who had anemia. Hypocalcaemia was observed in 51.62% of patients. Hyperphosphatemia was present in 48.37% of</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Demographical and clinical characteristics of participants (Data are expressed as mean &#177; standard deviation or number and percentage)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Mean and percentages</th></tr></thead><tr><td align="center" valign="middle" >Age (years)</td><td align="center" valign="middle" >58.37 &#177; 19.97</td></tr><tr><td align="center" valign="middle" >Sex ratio (men/women)</td><td align="center" valign="middle" >1.61 (285/177)</td></tr><tr><td align="center" valign="middle" >Systolic hypertension (%)</td><td align="center" valign="middle" >68.39</td></tr><tr><td align="center" valign="middle" >Diastolic hypertension (%)</td><td align="center" valign="middle" >58.44</td></tr><tr><td align="center" valign="middle" >Obesity (%)</td><td align="center" valign="middle" >33%</td></tr><tr><td align="center" valign="middle" >Mean blood urea (g/L)</td><td align="center" valign="middle" >1.18 &#177; 0.95</td></tr><tr><td align="center" valign="middle" >Mean serum creatinine (mg/L)</td><td align="center" valign="middle" >49.14 &#177; 56.83</td></tr><tr><td align="center" valign="middle" >Mean eGFR (ml/min/1.73m<sup>2</sup>)</td><td align="center" valign="middle" >27.47 &#177; 19.86</td></tr><tr><td align="center" valign="middle" >Anemia (%)</td><td align="center" valign="middle" >82.8</td></tr><tr><td align="center" valign="middle" >Hypocalcaemia (%)</td><td align="center" valign="middle" >51.62</td></tr><tr><td align="center" valign="middle" >Hyperphosphatemia (%)</td><td align="center" valign="middle" >48.37</td></tr><tr><td align="center" valign="middle" >Hyperkalaemia (%)</td><td align="center" valign="middle" >47.8</td></tr><tr><td align="center" valign="middle" >Hyponatremia (%)</td><td align="center" valign="middle" >30.39</td></tr><tr><td align="center" valign="middle" >Total hypercholesterolemia (%)</td><td align="center" valign="middle" >76.5</td></tr><tr><td align="center" valign="middle" >LDL hypercholesterolemia (%)</td><td align="center" valign="middle" >76.5</td></tr><tr><td align="center" valign="middle" >Hypertriglyceridemia (%)</td><td align="center" valign="middle" >23.96</td></tr><tr><td align="center" valign="middle" >HDL dyslipidemia (%)</td><td align="center" valign="middle" >31.9</td></tr><tr><td align="center" valign="middle" >Hyperuricemia (%)</td><td align="center" valign="middle" >76.44</td></tr><tr><td align="center" valign="middle" >mean proteinuria (g/24h)</td><td align="center" valign="middle" >3.07 &#177; 4.92</td></tr><tr><td align="center" valign="middle" >Leukocyturia (%)</td><td align="center" valign="middle" >34.17</td></tr><tr><td align="center" valign="middle" >Hematuria (%)</td><td align="center" valign="middle" >25</td></tr></tbody></table></table-wrap><p>eGFR = estimated glomerular filtration rate according to 4-variables MDRD equation; HDL = Hight density lipoproteins; LDL = Low density lipoproteins.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> The different reasons for consultation</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Functional signs</th><th align="center" valign="middle" >Number of patientsn (%)</th></tr></thead><tr><td align="center" valign="middle" >Edema</td><td align="center" valign="middle" >116 (25.10)</td></tr><tr><td align="center" valign="middle" >Nausea</td><td align="center" valign="middle" >12 (2.59)</td></tr><tr><td align="center" valign="middle" >Vomiting</td><td align="center" valign="middle" >63 (13.63)</td></tr><tr><td align="center" valign="middle" >Haematemesis</td><td align="center" valign="middle" >4 (0.86)</td></tr><tr><td align="center" valign="middle" >Pollakiuria</td><td align="center" valign="middle" >17 (3.67)</td></tr><tr><td align="center" valign="middle" >Haematuria</td><td align="center" valign="middle" >2 (0.43)</td></tr><tr><td align="center" valign="middle" >Dyspnea</td><td align="center" valign="middle" >103 (22.29)</td></tr><tr><td align="center" valign="middle" >Hiccups</td><td align="center" valign="middle" >11 (2.38)</td></tr><tr><td align="center" valign="middle" >Pruritus</td><td align="center" valign="middle" >13 (2.81)</td></tr><tr><td align="center" valign="middle" >Other signs</td><td align="center" valign="middle" >87 (18.83)</td></tr></tbody></table></table-wrap><p>patients. Hyperkalaemia was present in 47.8% of patients. Hyponatremia was present in 30.39% of patients. Hypercholesterolemia was present in 55.3% of patients. LDL hypercholesterolemia was present in 76.5% of patients. Hypertriglyceridemia was present in 23.96% of patients. HDL dyslipidemia was present in 31.9% of patients. Hyperuricemia was present in 76.44% of patients. The mean proteinuria was 3.07 &#177; 4.92 g/24 h. Leukocyturia was present in 34.17% of patients. Hematuria was present in 25% of patients. Obesity was found in 33% of the patients. Smoking was noted in 6% of patients. Hypertension and diabetes were the most common causes, found in 283 patients (61.25%) and 166 patients (35.93%), respectively (<xref ref-type="table" rid="table3">Table 3</xref>). Kidney biopsy was indicated and performed in 23 patients, 10 of whom presented with focal segmental hyalinosis. Hemodialysis was performed in 49 patients. The mean duration of the sessions was 3.83 &#177; 0.44 hours with extremes of 2 and 4 hours. Peritoneal dialysis was performed in 2 patients. One patient had undergone a kidney transplant.</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Causes of CKD in other studies</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Causes</th><th align="center" valign="middle" >Number of patients N = 462 (%)</th></tr></thead><tr><td align="center" valign="middle" >Hypertension</td><td align="center" valign="middle" >214 (46.32)</td></tr><tr><td align="center" valign="middle" >Diabetes</td><td align="center" valign="middle" >97 (20.99)</td></tr><tr><td align="center" valign="middle" >Mixed nephropathy (Hypertension et Diabetes)</td><td align="center" valign="middle" >69 (15.00)</td></tr><tr><td align="center" valign="middle" >Lupus nephritis</td><td align="center" valign="middle" >2 (0.43)</td></tr><tr><td align="center" valign="middle" >HIV</td><td align="center" valign="middle" >1 (0.21)</td></tr><tr><td align="center" valign="middle" >Focal segmental glomerulosclerosis</td><td align="center" valign="middle" >10 (2.16)</td></tr><tr><td align="center" valign="middle" >Membranous nephropathy</td><td align="center" valign="middle" >12 (2.59)</td></tr><tr><td align="center" valign="middle" >Amyloidosis</td><td align="center" valign="middle" >8 (1.72)</td></tr><tr><td align="center" valign="middle" >Minimal change disease</td><td align="center" valign="middle" >4 (0.86)</td></tr><tr><td align="center" valign="middle" >Obstructive uropathy</td><td align="center" valign="middle" >3 (0.65)</td></tr><tr><td align="center" valign="middle" >Autosomal dominant polycystic kidney disease</td><td align="center" valign="middle" >24 (5.19)</td></tr><tr><td align="center" valign="middle" >Hemopathy</td><td align="center" valign="middle" >4 (0.86)</td></tr><tr><td align="center" valign="middle" >Urinary lithiasis</td><td align="center" valign="middle" >6 (1.29)</td></tr><tr><td align="center" valign="middle" >undetermined</td><td align="center" valign="middle" >8 (1.73)</td></tr></tbody></table></table-wrap></sec><sec id="s4"><title>4. Discussion</title><p>In the world, the prevalence of CKD is estimated at 10% but there are many variations between countries [<xref ref-type="bibr" rid="scirp.108127-ref7">7</xref>]. In sub-Saharan Africa, the epidemiology of CKD in the general population is difficult to estimate probably due to possible confusion caused by the heterogeneity of the populations studied, design and methods used to define CKD. By comparing our study with the other studies presented in <xref ref-type="table" rid="table4">Table 4</xref>, we see that the prevalence of CKD varies from one country to another and within the same country [<xref ref-type="bibr" rid="scirp.108127-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.108127-ref8">8</xref>] - [<xref ref-type="bibr" rid="scirp.108127-ref14">14</xref>]. In our study, the mean patient age was 58.37 &#177; 19.97 years and more than 70% of our patients were over 50 years old. Our study is consistent with results found in other studies. This could be explained on the one hand by the physiological decline of GFR which is observed in these advanced ages. This is currently even a topic of discussion because it leads some authors to think about redefining CKD in older ages. On the other hand, improvement in life expectancy of the population could also explain this predominance of CKD in subjects over 50 years of age [<xref ref-type="bibr" rid="scirp.108127-ref15">15</xref>].</p><p>Hypertension (61.25%) and diabetes (35.93%) were the two major risk factors associated with CKD in our series. Studies done in several countries had also found hypertension to be the leading cause of CKD [<xref ref-type="bibr" rid="scirp.108127-ref16">16</xref>]. This is the case of studies that were done in Cameroon and the United States where hypertension was found in 84.6% [<xref ref-type="bibr" rid="scirp.108127-ref17">17</xref>] and 86.1% [<xref ref-type="bibr" rid="scirp.108127-ref18">18</xref>] respectively. This high frequency of hypertension can be explained by behavioral changes namely smoking, sedentary lifestyle, an unsuitable diet (high in salt and fat) [<xref ref-type="bibr" rid="scirp.108127-ref16">16</xref>]. Hypertension in general is more common in black people due to the genetic predisposition linked to the presence of a polymorphism in the Apol 1 gene which codes for apolipoprotein 1</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> prevalence of CKD in other studies</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Studies</th><th align="center" valign="middle" >Prevalence</th></tr></thead><tr><td align="center" valign="middle" >NHANES III (USA) [<xref ref-type="bibr" rid="scirp.108127-ref8">8</xref>]</td><td align="center" valign="middle" >11</td></tr><tr><td align="center" valign="middle" >KEEP (USA) [<xref ref-type="bibr" rid="scirp.108127-ref9">9</xref>]</td><td align="center" valign="middle" >27.2</td></tr><tr><td align="center" valign="middle" >NEOERICA (UK) [<xref ref-type="bibr" rid="scirp.108127-ref8">8</xref>]</td><td align="center" valign="middle" >11</td></tr><tr><td align="center" valign="middle" >AusDiab (Australie) [<xref ref-type="bibr" rid="scirp.108127-ref8">8</xref>]</td><td align="center" valign="middle" >10</td></tr><tr><td align="center" valign="middle" >Pekin (Chine) [<xref ref-type="bibr" rid="scirp.108127-ref10">10</xref>]</td><td align="center" valign="middle" >13</td></tr><tr><td align="center" valign="middle" >SEEK (India) [<xref ref-type="bibr" rid="scirp.108127-ref11">11</xref>]</td><td align="center" valign="middle" >17.2</td></tr><tr><td align="center" valign="middle" >Norway [<xref ref-type="bibr" rid="scirp.108127-ref12">12</xref>]</td><td align="center" valign="middle" >10.2</td></tr><tr><td align="center" valign="middle" >Saint Louis (Senegal) [<xref ref-type="bibr" rid="scirp.108127-ref4">4</xref>]</td><td align="center" valign="middle" >4.9</td></tr><tr><td align="center" valign="middle" >Ghana [<xref ref-type="bibr" rid="scirp.108127-ref13">13</xref>]</td><td align="center" valign="middle" >13.2</td></tr><tr><td align="center" valign="middle" >Kinshasa [<xref ref-type="bibr" rid="scirp.108127-ref11">11</xref>]</td><td align="center" valign="middle" >12.4</td></tr><tr><td align="center" valign="middle" >Gueoul (Senegal) [<xref ref-type="bibr" rid="scirp.108127-ref14">14</xref>]</td><td align="center" valign="middle" >36.5</td></tr><tr><td align="center" valign="middle" >Our study</td><td align="center" valign="middle" >5.2</td></tr></tbody></table></table-wrap><p>[<xref ref-type="bibr" rid="scirp.108127-ref19">19</xref>]. Hypertension is a risk factor for progression associated with CKD. And this has been reported in the studies done in Morocco [<xref ref-type="bibr" rid="scirp.108127-ref20">20</xref>], Lebanon [<xref ref-type="bibr" rid="scirp.108127-ref21">21</xref>] and Germany [<xref ref-type="bibr" rid="scirp.108127-ref22">22</xref>]. The kidney, which is often the cause of hypertension, can in turn be a victim of the latter through its repercussions (fibrous endarteritis and arteriosclerosis). As a result, hypertension is a factor in the progression of CKD. When transmitted to the glomerular capillaries, it aggravates intraglomerular hypertension and precipitates the development of CKD. This transmission is facilitated by the almost constant vasodilation of the afferent arteriole. Administration of antihypertensive drugs to animals with nephron reduction and arterial hypertension to a greater or lesser extent decreases glomerular sclerosis and the progression of CKD [<xref ref-type="bibr" rid="scirp.108127-ref23">23</xref>]. In our study, diabetes was found in 35.93% of cases. These results were similar to those found in Morocco (41.5%) and higher than results previously found in Senegal (12.7%) and Nigeria (5.9%) [<xref ref-type="bibr" rid="scirp.108127-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.108127-ref24">24</xref>]. The increase in the prevalence of diabetes in developing countries seems to be explained by the rapid urbanization which is associated with a more sedentary lifestyle and the prevalence of obesity which is 33.9% in our work.</p><p>In our study, patients were diagnosed with CKD late. In fact, 92% of patients were diagnosed with chronic renal failure, including 34.9% with ESRD. The challenge in our countries must be a diagnosis at the early stages, especially in patients at risk, particularly hypertensive and diabetic patients.</p></sec><sec id="s5"><title>5. Conclusion</title><p>This study establishes the relatively high prevalence of CKD and its risk factors including hypertension and diabetes. It also reveals the late diagnosis of chronic kidney disease in our patients. Developing action plans for the prevention of CKD and its early diagnosis would be beneficial for better health of the population. However, these data cannot be extrapolated to the general population as this is a retrospective study limited to one establishment.</p></sec><sec id="s6"><title>Statement of Ethics</title><p>All patient information was anonymised and the written consent for publication of the study was obtained from the patients. The research was conducted ethically in accordance with the World Health Association Declaration of Helsinki and was approved by the local ethics committee.</p></sec><sec id="s7"><title>Funding Sources</title><p>This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.</p></sec><sec id="s8"><title>Author Contributions</title><p>Mansour Mbengue reviewed the literature and wrote the first draft of the manuscript. All authors reviewed and edited the manuscript and approved the final version of the manuscript.</p></sec><sec id="s9"><title>Limitations</title><p>The retrospective design of our study represents a limitation. Kidney function was not measured 3 months later to ascertain chronicity of the disease and to roll out acute kidney injuries.</p></sec><sec id="s10"><title>Conflicts of Interest</title><p>The authors have no conflicts of interest to declare.</p></sec><sec id="s11"><title>Cite this paper</title><p>Mansour, M., Djenaba, B., Ahmed, L.T., Moustapha, C.M. and Abdou, N. (2021) Chronic Kidney Disease in Sub-Saharan Africans: A Study of 462 Patients. Open Journal of Nephrology, 11, 114-122. https://doi.org/10.4236/ojneph.2021.111009</p></sec></body><back><ref-list><title>References</title><ref id="scirp.108127-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Ulasi, I.I., Ijoma, C.K., Onodugo, O.D., et al. (2013) Towards Prevention of Chronic Kidney Disease in Nigeria: A Community-Based Study in Southeast Nigeria. Kidney International, 3, S195-S201.</mixed-citation></ref><ref id="scirp.108127-ref2"><label>2</label><mixed-citation publication-type="book" xlink:type="simple">Combe, C. and Kourilsky, O. (2014) Maladie rénale chronique: Chronic Kidney Disease. In: Kanfer, A., Kourilsky, O., Peraldi, M.N. and Christian Combe, C., Eds., Néphrologie et troubles hydro électrolytiques, Elsevier Masson, Paris, 279-334. 
https://doi.org/10.1016/B978-2-294-73759-6.00014-6</mixed-citation></ref><ref id="scirp.108127-ref3"><label>3</label><mixed-citation publication-type="book" xlink:type="simple">Olson, J.L. and Laszik, Z.G. (2007) Diabetic Nephropathy. In: Jennette, J.C., Oison, J.L., Schwartz, M.M. and Silva, F.G., Eds., Heptinstall’s Pathology of the Kidney, 6th Edition, Lippincott Williams &amp; Wilkins, Philadelphie, 803-852.</mixed-citation></ref><ref id="scirp.108127-ref4"><label>4</label><mixed-citation publication-type="book" xlink:type="simple">Mount, D.B. and Yu, A.S.L. (2008) Transport of Inorganic Solutes: Sodium, Chloride, Potassium, Magnesium, Calcium and Phosphate. In: Brenner, B.M. and Levine, A.S., Eds., Brenner and Rector’s The Kidney, Saunders Elsevier, Philadelphia, 156-200.</mixed-citation></ref><ref id="scirp.108127-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Cordonnier, D., Corticelli, P., Maynard, C., Halimi, S. and Pinel, N. (1994) Nephropathies diabétiques. EMC (éditions Médicales Elsevier SAS) Néphrologie, 18-066-P-10.</mixed-citation></ref><ref id="scirp.108127-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Larsen, C.P., Beggs, M.L., Saeed, M. and Walker, P.D. (2013) Apolipoprotein L1 Risk Variants Associate with Systemic Lupus Erythematosus-Associated Collapsing Glomerulopathy. Journal of the American Society of Nephrology, 24, 722-725. 
https://doi.org/10.1681/ASN.2012121180</mixed-citation></ref><ref id="scirp.108127-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Madhav, V.R., Yang, Q., Changchun, W. and Bakris, G. (2008) Hypertension and CKD: Kidney Early Evaluation Program (KEEP) and National Health and Nutrition Examination Survey (NHANES), 1999-2004. American Journal of Kidney Diseases, 51, S30-S37. https://doi.org/10.1053/j.ajkd.2007.12.012</mixed-citation></ref><ref id="scirp.108127-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Kaze-Folefack, F., Nono, A., Halle, M.P. and Ashuntantang, G. (2013) Sévérité et contr&amp;#244;le de l’hypertension artérielle au cours de la maladie rénale chronique au Cameroun. La Revue Médicale de Madagascar, 3, 318-323</mixed-citation></ref><ref id="scirp.108127-ref9"><label>9</label><mixed-citation publication-type="book" xlink:type="simple">Tostivint, I. (2010) Comment ralentir la dégradation de la fonction rénale chez le patient insuffisant rénal. In: Deray, G. and Bitker, M.-O., Eds., Séminaire d’uro-néphrologie, XXXVI ème série 2010, Groupe hospitalier Pitié-Salpêtrière  Paris, 23-24.</mixed-citation></ref><ref id="scirp.108127-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Steven, V.D.V., Akinyi, H., Oti, S., et al. (2013) African Population and Health Research Center 2013. [En ligne]. http://www.carmma.org/</mixed-citation></ref><ref id="scirp.108127-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Faye, M., Lemrabott, A.T., Cissé, M., Fall, K., Keita, Y., Ngaide, A.A., et al. (2017) Prevalence and Risk Factors of Chronic Kidney Disease in an African Semi-Urban Area: Results from a Cross-Sectional Survey in Gueoul, Senegal. Saudi Journal of Kidney Disease and Transplantation, 28, 1389-1396. 
https://doi.org/10.4103/1319-2442.220878</mixed-citation></ref><ref id="scirp.108127-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Eastwood, J.B., Kerry, S.M., Plange-Rhule, J., Micah, F.B., Antwi, S., Boa, F.G., Banerjee, D. and Cappuccio, F.P. (2010) Assessment of GFR by Four Methods in Adults in Ashanti, Ghana: The need for an eGFR Equation for Lean African Populations. Nephrology Dialysis Transplantation, 25, 2178-2187.  
https://doi.org/10.1093/ndt/gfp765</mixed-citation></ref><ref id="scirp.108127-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Sumaili, E.K., Krzesinski, J.M., Cohen, E.P. and Nseka, N.M. (2010) Epidemiology of Chronic Kidney Disease in the Democratic Republic of Congo: Review of Cross Sectional Studies from Kinshasa, the Capital. Néphrologie &amp; Thérapeutique, 6, 232-239.  
https://doi.org/10.1016/j.nephro.2010.03.008</mixed-citation></ref><ref id="scirp.108127-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Singh, A.K., Farag, Y.M., Mittal, B.V., Karai Subramanian, K., Ram Keithi Reddy, S., Acharya, V.N., et al. (2013) Epidemiology and Risk Factors of Chronic Kidney Disease in India—Results from the SEEK (Screening and Early Evaluation of Kidney Disease) Study. BMC Nephrology, 14, Article No. 114. 
https://doi.org/10.1186/1471-2369-14-114</mixed-citation></ref><ref id="scirp.108127-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Zhang, L., Wang, F., Wang, L., Wang, W., Liu, B., Liu, J., et al. (2012) Prevalence of Chronic Kidney Disease in China: A Cross-Sectional Survey. Lancet, 379, 815-822. 
https://doi.org/10.1016/S0140-6736(12)60033-6</mixed-citation></ref><ref id="scirp.108127-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Jurkovitz, C.T., Qiu, Y., Wang, C., Gilbertson, D.T. and Brown, W.W. (2008) The Kidney Early Evaluation Program (KEEP): Program Design and Demographic Characteristics of the Population. American Journal of Kidney Diseases, 51, S3-S12. 
https://doi.org/10.1053/j.ajkd.2007.12.022</mixed-citation></ref><ref id="scirp.108127-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Nahas, M.E.L. (2005) The Global Challenge of Chronic Kidney Disease. Kidney International, 68, 2918-2929. https://doi.org/10.1111/j.1523-1755.2005.00774.x</mixed-citation></ref><ref id="scirp.108127-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">James, M.T., Hemmelgarn, B.R. and Tonelli, M. (2010) Early Recognition and Prevention of Chronic Kidney Disease. Lancet, 375, 1296-1309.  
https://doi.org/10.1016/S0140-6736(09)62004-3</mixed-citation></ref><ref id="scirp.108127-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">(2012) Kidney Disease Improval Global Outcomes KDIGO Clinical Practice Guideline for Anemia in Chronic kidney disease. Kidney International, 2, 288-291.</mixed-citation></ref><ref id="scirp.108127-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Levin, A., Stevens, P.E., Bilous, R.W., Coresh, J., De Francisco, A.L.M., De Jong, P.E., et al. (2013) Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group. KDIGO 2012 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease. Kidney International, 3, 1-150.</mixed-citation></ref><ref id="scirp.108127-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Seck, S.M., Doupa, D. and Gueye, L. (2014) Enquête de prévalence de la maladie rénale chronique dans la région Nord du Sénégal. Pan African Medical Journal, 18, 307. https://doi.org/10.1016/j.nephro.2014.07.128</mixed-citation></ref><ref id="scirp.108127-ref22"><label>22</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Bamgboye</surname><given-names> E.L. </given-names></name>,<etal>et al</etal>. (<year>2006</year>)<article-title>End-Stage Renal Disease in Sub-Saharan Africa</article-title><source> Ethnicity &amp; Disease</source><volume> 16</volume>,<fpage> S2</fpage>-<lpage>5</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.108127-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Mills, K.T., Xu, Y., Zhang, W., Bundy, J.D., Chen, C.-S., Kelly, T.N., et al. (2015) A Systematic Analysis of World-Wide Population-Based Data on the Global Burden of Chronic Kidney Disease in 2010. Kidney International, 88, 950-957. 
https://doi.org/10.1038/ki.2015.230</mixed-citation></ref><ref id="scirp.108127-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Fondation du rein (2015) Dossier de presse de la journée mondiale du rein Mars 2015. [Enligne]. http://www.fondation-du-rein.org</mixed-citation></ref></ref-list></back></article>