|Year : 2017 | Volume
| Issue : 2 | Page : 81-87
Prevalence of chronic kidney disease and its risk factors among adults in a semi-urban community of South-East Nigeria
Chimezie Godswill Okwuonu1, Innocent Ijezie Chukwuonye1, Oluseyi Ademola Adejumo2, Emmanuel Idoko Agaba3, Louis Ikechukwu Ojogwu4
1 Department of Internal Medicine, Federal Medical Centre, Nephrology Unit, Umuahia, Abia State, Nigeria
2 Department of Internal Medicine, Kidney Care Centre Ondo, University of Medical Sciences, Ondo City, Nigeria
3 Department of Internal Medicine, Nephrology Unit, Jos University Teaching Hospital, University of Jos, Jos, Nigeria
4 Department of Internal Medicine, Nephrology Unit, University of Benin Teaching Hospital, Benin City, Edo State, Nigeria
|Date of Web Publication||24-Jul-2017|
Chimezie Godswill Okwuonu
Department of Internal Medicine, Federal Medical Centre, Nephrology Unit, Umuahia, Abia State
Source of Support: None, Conflict of Interest: None
Background: Chronic kidney disease (CKD) is an increasingly prevalent problem worldwide. Treatment of end-stage kidney disease is beyond the reach of an average Nigerian. The prevention and early detection are imperative to reducing its burden. Aim: The aim of this study was to determine the prevalence of CKD and some of its risk factors among adults in a representative semi-urban Nigerian population. Subjects and Methods: A cross-sectional study involving 400 randomly selected adults. Participants were assessed using the WHO stepwise approach. Urinary protein-creatinine ratio (PCR) and estimated glomerular filtration rate (GFR) from serum creatinine, among other parameters, were analysed. A PCR ≥200 mg/g was regarded as significant proteinuria while GFR <60 ml/min/1.73 m2 was regarded as reduced GFR. Participants with abnormal PCR and/or reduced GFR were re-evaluated after 3 months to document persistence of these abnormalities. CKD was defined as persistent significant proteinuria and/or reduced GFR for more than 3 months. Results: Data were complete for 328 participants. Persistent significant proteinuria was found in 5.8% while persistently reduced GFR was obtained in 4.6% of participants. Overall, the prevalence of CKD was 7.8%. The prevalence of some established CKD risk factors was old age, 36.3%; hypertension, 36.9%; diabetes mellitus, 7.9%; and family history of kidney disease, 6.4%. The predictors of CKD included old age (adjusted odds ratio = 3.2; confidence interval: 1.10–8.92; P= 0.02), hypertension: 3.5 (1.93–11.90; P= 0.001), family history of kidney disease; 4.5 (3.91–10.23; P= 0.01), generalised obesity 1.3 (1.20–6.21; P= 0.001) and central obesity 3.8 (1.13–12.68; P= 0.003). Conclusion: The prevalence of CKD and some of its risk factors were high. Effective control of the modifiable risk factors identified will assist in reducing the burden of CKD.
Keywords: Chronic kidney disease, diabetes mellitus, glomerular filtration rate, hypertension, proteinuria
|How to cite this article:|
Okwuonu CG, Chukwuonye II, Adejumo OA, Agaba EI, Ojogwu LI. Prevalence of chronic kidney disease and its risk factors among adults in a semi-urban community of South-East Nigeria. Niger Postgrad Med J 2017;24:81-7
|How to cite this URL:|
Okwuonu CG, Chukwuonye II, Adejumo OA, Agaba EI, Ojogwu LI. Prevalence of chronic kidney disease and its risk factors among adults in a semi-urban community of South-East Nigeria. Niger Postgrad Med J [serial online] 2017 [cited 2019 Jan 24];24:81-7. Available from: http://www.npmj.org/text.asp?2017/24/2/81/211459
| Introduction|| |
Chronic kidney disease (CKD) is defined as kidney damage or glomerular filtration rate (GFR) <60 ml/min/1.73 m 2 for more than 3 months with implications for health. The incidence and prevalence of CKD have increased in the recent years in developed and developing nations and are consuming a huge proportion of health-care finances in developed countries while contributing significantly to morbidity, mortality and decreased life expectancy, particularly in developing countries.,,,
There is a paucity of data on CKD from West Africa subregion. In Nigeria, lack of a national registry network and a coordinated national programme on kidney disease have restricted efforts toward the effective planning and control of renal diseases. In addition, it has also affected equitable allocation of resources. Studies aimed at quantifying the magnitude of CKD and determining the risk factors have been conducted in different parts of Nigeria with varying results. Some of these studies were hospital-based, and the definition of chronicity of the disease was based on the duration of suggestive symptoms and radiological evidence of chronic disease process thus assessing advanced stages of CKD in most instances.,, Among the studies that were community-based, most of the studies did not repeat the laboratory investigations after 3 months to confirm CKD based on the generally accepted definition.,,,, The objective of this study was to determine the prevalence of CKD in a semi-urban community in Umuahia, Southeast Nigeria using a marker of kidney damage (proteinuria) and estimated GFR. In addition, the prevalence of some established risk factors for CKD and the predictors of CKD in the community were assessed. This study provides additional data for effective health planning and control of the disease in Nigerian population.
| Subjects and Methods|| |
Study design and area
This was a cross-sectional study conducted in Olokoro, a semi-urban community in Umuahia South Local Government Area of Abia State Nigeria.
Adults who were 18 years or older constituted the study population. A previous community-based study by Okoye et al. obtained a CKD prevalence of 27.2%. The sample size for this study was extrapolated from that value with 95% confidence and 5% error margin using the appropriate formula for study population > 10,000 giving us 304 participants. This number was increased to 400 to make allowance for 10% possible non-responders and increase the scope of the study. Adults who were <18 years and those who did not give informed consent were excluded from the study. Furthermore, those with clinical suspicion of urinary tract infection, females who were pregnant or menstruating at the time of the study and non-permanent residents were excluded from the study.
A multistage systematic sampling technique was used. According to the National Population Commission (NPC) of Nigeria census of 2006, the estimated population of Olokoro community, projected to 2014, was 52,712. There are 212 enumeration areas (EAs) in Olokoro, and these served as sampling units for the purpose of this study. Fifty-three EAs (representing 25% of the total EAs) were selected randomly by balloting. The population of adults from 18 years and above in the selected EA was estimated using the NPC figures of 2006 projected to 2014. This gave 4,108. Dividing this estimated population (4108) by the sample size (400) gave the sampling interval for systematic selection of participants which was approximately 1:10. Hence one in every ten adults was enroled for the study. Selected houses where every 10th adult was residing were given unique numbers for identification. The Kish conversion sheet was used to select the participant for the study in each household. In situ ations where selected EAs were not contiguous, the first house in the next EA was regarded as a continuation of the previous EA and the selection procedure continued.
The methodology used in this study was based on the World Health Organization's recommended STEPS approach to chronic disease surveillance with some modifications.
This is a simple, standardised method for collecting, analysing and disseminating data in WHO member countries. The STEPS approach focuses on obtaining core data on the established risk factors that determine the major disease burden and is designed to help countries build and strengthen their surveillance capacity. The STEPS Instrument covers three different levels or 'steps' of risk factor assessment. These steps are questionnaire, physical measurements and biochemical measurements. Estimation of serum creatinine and repetition of measurements was not part of the original STEPS instrument but was added in this study to correctly define the output variable of interest (CKD). Hence, this constituted a modification of to the original STEPS instrument.
The study was carried out in three phases. In the pilot phase, the study was pre-tested in ten percent of the sample size in a different EA. In the second phase, health talk was delivered at four different traditional meeting grounds in EAs selected for the study. Attendees were informed of the study and those residing in selected houses would be expected to willingly participate in the study.
A pre-tested semi-structured questionnaire was administered to each participant by a trained research assistant. Information about age, occupation, educational level, sex, marital status, religion, lifestyle (alcohol, smoking and consumption pattern of fruits and vegetables), family history of kidney disease, hypertension and diabetes, use of herbal medications, non-steroidal anti-inflammatory drugs and skin lightening cosmetics were obtained. Physical measurements obtained included blood pressure, weight, height, waist and hip circumference.
All participants provided mid-stream urine in plain bottles after education on the procedure for collection. Furthermore, 10 ml of blood was collected from each person in different sample bottles specific for the required test. Serum and urine creatinine were measured by Jaffe's alkaline picrate kinetic method. In this method, creatinine reacts with alkaline picrate to produce a red coloured complex; the rate of red-coloured complex formation is directly proportional to the creatinine concentration. The concentration of albumin in urine was measured by sulphosalicylic acid colorimetric assay. In this method, the sulphosalicylic acid (anion) precipitates the protein (cation) in a sample of urine. The turbidity formed is proportional to the concentration of the protein and is measured with a spectrophotometer at 500 nm. Analyses were done using the Selectra Jnr Auto Analyzer. All samples were analysed at the main laboratory of Federal Medical Centre Umuahia Abia State, which is about 25 km away from the different areas of sample collection.
In the third phase of the study, individuals with reduced kidney function or significant proteinuria were revisited after 3 months to detect persistence of these abnormalities. A subject was adjudged to have CKD if he/she had the following at two separate visits 3 months apart;
- Significant proteinuria (Protein/creatinine ratio ≥200 mg/g) and/or
- GFR <60 ml/min/1.73 m2
Participants with CKD were further classified into five stages as follows:
- Stage 1 - GFR ≥90 ml/min/1.73 m 2 with persistent significant proteinuria
- Stage 2 - GFR 60–89 ml/min/1.73 m 2 with persistent significant proteinuria
- Stage 3 - GFR 30–59 ml/min/1.73 m 2 with or without persistent significant proteinuria
- Stage 4 - GFR 15–29 ml/min/1.73 m 2 with or without persistent significant proteinuria
- Stage 5 - GFR <15 ml/min/1.73 m 2 with or without persistent significant proteinuria.
The study commenced on 1st June 2014 and ended on 11th September 2014.
Definition of terms
Old age was regarded as age ≥60 years in both sexes according to the World Health Organization's working definition for older persons in Africa. Individuals with protein/creatinine ratio ≥200 mg/g were regarded as having significant proteinuria. Obesity indices, hypertension and diabetes mellitus were defined according to standard criteria.,,, A participant was regarded to have family history of kidney disease if he/she has a first-degree relative (parent, child or sibling) who is suffering from kidney disease or died of a kidney disease. For the purpose of this study, significant intake of herbal medications was regarded as any history of weekly intake of herbal preparation for 1 month or more either currently or in the past while analgesic abuse was regarded as a cumulative lifetime use of more than 5000 pills of analgesics. This was calculated from multiplying the average number of pills consumed in a week by the duration of use in years.
The GFR was estimated from serum creatinine measurements using the modification of diet in renal disease formula (MDRD-4 parameter equation). This formula has been shown to be a reliable alternative to measured creatinine clearance in Nigerian patients with CKD. Reduced kidney function was regarded as estimated GFR <60 ml/min/1.73 m 2.
The study was approved by the Human Resource and Ethics Committee of Federal Medical Centre Umuahia Abia State Nigeria.
The data were analysed using the Statistical Package for Social Sciences software, version 21.0 (2012, IBM Corporation, Armonk, NY, USA). The Data were presented as means ± standard deviation for continuous variables and as proportions for categorical variables. The Chi-square test was used for the comparison of and to test associations between categorical variables with Fisher's exact test where cells contained <5 observations. The Student's t-test was used to compare the means of two groups. All P< 0.05 were regarded as statistically significant. Participants with CKD were compared with those without CKD across the domains of risk factors investigated to find out the significant variables or correlates. This was followed by multivariate analysis, where the significant variables (potential predictor variables) identified were included in a binary logistic regression to identify variables which are independent risk factors or predictors of CKD.
| Results|| |
A total of 328 participants completed the study; the remaining 72 participants who took part in the study did not complete either their questionnaire or investigations and were excluded from the analysis. [Table 1] shows the sociodemographic characteristics of the participants. Mean age was 54.8 ± 12.8 years
One hundred and seventy-nine (54.6%) participants had a normal body mass index, overweight was found in 104 (31.7%) while obesity was found in 38 (11.6%) participants. [Table 2] shows the prevalence of risk factors for CKD among the participants and their gender distribution.
|Table 2: Prevalence and gender distribution of risk factors for chronic kidney disease|
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Significant proteinuria was detected in 32 (9.8%) participants at first assessment while 19 (5.8%) had persistent proteinuria on re-assessment after 3 months. There were more females (13, 4.0%) with persistent significant proteinuria than males (6, 1.8%). The prevalence increased with age from 0.6% in the 18–30 years age group to 3.0% in the >60 years age group (P = 0.009 for trend across group).
Reduced kidney function (estimated GFR <60 ml/min/1.63 m 2) was found in 44 (13.4%) participants at first assessment. Only 15 participants (4.6%) had persistently low GFR at re-assessment 3 months later. Slightly more than half of participants (54.3%) had GFR ≥90 ml/min.
Overall, CKD was found in 25 participants giving a crude prevalence of 7.6%. According to stages of CKD, there were 2.4% of the participants in stage 1, 0.6% in stage 2, 3% in stage 3, 1.2% in stage 4 and 0.3% in stage 5.
The predictors of CKD included old age (adjusted odds ratio = 3.2; confidence interval: 1.10–8.92; P= 0.02), hypertension: 3.5 (1.93–11.90; P= 0.001), family history of kidney disease; 4.5 (3.91–10.23; P= 0.01), generalised obesity; 1.3 (1.20–6.21; P= 0.001) and central obesity; 3.8 (1.13–12.68; P= 0.003) [Table 3]. [Table 4] compares this current study with some other community-based studies on magnitude of CKD and its risk factors.
|Table 3: Univariate analysis to determine the risk factors for chronic kidney disease among the study participants|
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|Table 4: Multivariate analysis to determine predictors of chronic kidney disease among the participants|
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| Discussion|| |
The mean age of the participants in this study was higher than 29.5 years recorded from NHANES III study. It is also higher than 40.29 ± 16 years obtained in a screening of CKD and its risk factors in Kano Nigeria  and 39.37 ± 14 years reported in a similar survey in Jos Nigeria. This suggests that in terms of age, the sample in this study had a higher age when compared to those in other studies and perhaps, the general population. The implication of this observation to this study is that some findings need to be interpreted with caution. Increasing age is a well-documented risk factor for hypertension and CKD. The preponderance of the elderly population in this study might have contributed to the high prevalence of hypertension and CKD observed in this study. Diabetes mellitus was detected in 7.9% of the participants. This is comparable to 10.4% obtained in a similar survey in Jos Nigeria  and 5.9% obtained in Enugu Nigeria.
The prevalence of CKD in this study was 7.6%. This is lower than 11% and 16% obtained in the AusDiab  and NHANES III  studies, respectively. It is also lower than the prevalence observed in some earlier studies in Nigeria ,, This may be because persistence of markers of CKD after 3 months was not demonstrated in some of these studies; hence, there may be overestimation of the prevalence of CKD in such studies. The prevalence of CKD observed in this study is similar to 6.3% observed in a study conducted in Shimoga district in Southern India  and 10.4% obtained by Afolabi et al. in South-western Nigeria. Markers of CKD were also re-assessed in these studies and may account for this similarity in prevalence of CKD.
Old age is also a risk factor for CKD in both univariate and multivariate analyses in this study, and this is in agreement with earlier studies., The implication of this is that as our population ages, there is need to intensify screening strategies for CKD to detect early stages of the disease for more effective intervention. Participants with hypertension had a 3.5-fold increased risk of having CKD than their normotensive counterparts. This is in keeping with previous reports from a survey of CKD and its risk factors among the Australian Aborigines, NHANES III study among non-institutionalised adults in the USA  and a similar study by Okoye et al. in Benin City, Nigeria.
The family history of kidney disease was identified as an independent risk factor of CKD in this study. Among the 21 participants with positive family history of kidney disease, 8 (38%) were found to have a CKD. This is higher than 14.6% reported from China , and 9.5% in KEAPS study conducted in Yorkshire, Northern England. This suggests that genetic factors may be contributing significantly to the prevalence of CKD obtained in this study. This is not surprising because Ulasi et al. had earlier documented that APOL1 genetic risk variants are common in the Igbo population of South-Eastern Nigeria and are also highly associated with non-diabetic CKD in this area. These APOL1 risk variants have been shown to be strongly associated with an increased risk for non-diabetic kidney disease including HIV nephropathy, primary non-monogenic focal and segmental glomerulosclerosis and hypertension-attributed nephropathy among African ancestry populations in the USA.
Obesity is a major driver of the current epidemic of CKD and waist-to-hip ratio reliably reflects visceral fat in CKD patients. Generalised obesity and central obesity were significantly associated with CKD in this study. This is in agreement with earlier studies.,
Male gender has been reported as a risk factor for CKD but this gender difference in association with CKD was not apparent in this study. This does not agree with the findings of many other studies, in which the male gender was reported to be a non-modifiable risk factor for CKD., Some young males refused blood sampling and hence did not complete the study. This may have affected the result of this study in this regard. Non-completion of the study by males for various reasons had earlier been reported by Okoye et al. in Benin City Nigeria  and in a study of CKD in Beijing China.
The available data did not identify diabetes mellitus as a risk factor for CKD in this present study. This is in agreement with earlier studies , in Nigeria and may be because the prevalence of diabetes among participants in this study is low. Thus, its effect on kidney function may not be appreciable compared to hypertension and old age.
This study did not show any significant relationship between CKD and cigarette smoking. There are some studies which showed that cigarette smoking is a risk factor for the development and progression of CKD , while others have not strongly linked it with kidney disease., The reason for this apparent conflict may be because some studies that linked smoking to kidney function did so indirectly. Such studies established the link between smoking and microalbuminuria (a marker of glomerular damage) and hence indirectly linked it with CKD; this inference may not always be true. The relationship between smoking and CKD, therefore, deserves further study. Alcohol consumption was not found to have a significant association with CKD in this study. This is similar to studies by Stengel et al. and Vupputuri and Sandler, in which alcohol consumption was not associated with CKD. Some studies in Nigeria , did not also find any such association between alcohol consumption and CKD.
Limitations of the study
Few participants in this study did not report their age accurately; they estimated their ages based on events surrounding their birth. Furthermore, non-refusal of blood collection by some male counterparts reduced the number of participants that completed the study; however, allowance was made for such occurrences during the sample size estimation.
| Conclusion|| |
The prevalence of CKD and some of its risk factors were high in the community. The independent risk factors for CKD observed included old age, family history of kidney disease, hypertension, generalised obesity and central obesity. Based on the outcome of this study, we recommend the development of a well-structured health education programme in the community. Urgent attention needs to be paid to the risk factors for CKD and to instituting interventions to slow the progression of kidney diseases in this Nigerian community.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
National Kidney Foundation. KDIGO 2012 clinical practice guideline for the evaluation and management of chronic kidney disease. Kidney Int Suppl 2013;3:19-62.
Alebiosu CO, Ayodele OE. The global burden of chronic kidney disease and the way forward. Ethn Dis 2005;15:418-23.
Coresh J, Astor BC, Greene T, Eknoyan G, Levey AS. Prevalence of chronic kidney disease and decreased kidney function in the adult US population: Third National Health and Nutrition Examination Survey. Am J Kidney Dis 2003;41:1-12.
Hillege HL, Fidler V, Diercks GF, van Gilst WH, de Zeeuw D, van Veldhuisen DJ, et al.
Urinary albumin excretion predicts cardiovascular and noncardiovascular mortality in general population. Circulation 2002;106:1777-82.
Chadban SJ, Briganti EM, Kerr PG, Dunstan DW, Welborn TA, Zimmet PZ, et al.
Prevalence of kidney damage in Australian adults: The AusDiab kidney study. J Am Soc Nephrol 2003;14 7 Suppl 2:S131-8.
Ulasi II, Ijoma CK. The enormity of chronic kidney disease in Nigeria: The situation in a teaching hospital in South-East Nigeria. J Trop Med 2010;2010:501957.
Arogundade FA, Sanusi AA, Hassan MO, Akinsola A. The pattern, clinical characteristics and outcome of ESRD in Ile-Ife, Nigeria: Is there a change in trend? Afr Health Sci 2011;11:594-601.
Alebiosu CO, Ayodele OO, Abbas A, Olutoyin AI. Chronic renal failure at the Olabisi Onabanjo University Teaching Hospital, Sagamu, Nigeria. Afr Health Sci 2006;6:132-8.
Nalado AM. Prevalence of Chronic Kidney Disease and Its Risk Factors among Adults in a Rural Population of Kano. A Dissertation Submitted to Faculty of Internal Medicine, West African College of Physicians for the Award of the Fellowship of the College (FWACP; Internal Medicine); October, 2010.
Olatise OO. Community-Based Screening for Chronic Kidney Disease and Its Risk Factors amongst Adults in Howlshe. Jos: A Dissertation Submitted to Faculty of Internal Medicine, National Postgraduate Medical College of Nigeria for the Award of Fellowship of the College (FMCP; Nephrology Subspecialty); November, 2009.
Oluyombo R, Ayodele OE, Akinwusi PO, Okunola OO, Akinsola A, Arogundade FA, et al.
A community study of the prevalence, risk factors and pattern of chronic kidney disease in Osun State, South West Nigeria. West Afr J Med 2013;32:85-92.
Okoye CO, Oviasu E, Ojogwu LI. Prevalence of chronic kidney disease and its risk factors among adults in a rural population in Edo state, Nigeria. J US China Med Sci 2011;8:471-81.
Ulasi II, Ijoma CK, Onodugo OD, Arodiwe BE, Ifebunandu NA, Okoye JU. Towards prevention of chronic kidney disease in Nigeria: A community-based study in South East Nigeria. Kidney Int Suppl 2013;3:195-201.
Araoye MO. Research Methodology with Statistics for Health and Social Sciences. Ilorin: Nathadex Publication; 2004. p. 115-20.
Federal Republic of Nigeria. Legal Notice on Publication of 2006 Census Final Results, Official Gazette. Vol. 96. Abuja: National Population Commission; 2009. p. 1-103.
Lustgarten JA, Wenk RE. Simple, rapid, kinetic method for serum creatinine measurement. Clin Chem 1972;18:1419-22.
Levey AS, Coresh J, Balk E, Kausz AT, Levin A, Steffes MW, et al.
National Kidney Foundation practice guidelines for chronic kidney disease: Evaluation, classification, and stratification. Ann Intern Med 2003;139:137-47.
International Society of Nephrology. Program for detection and management of chronic kidney disease, hypertension, diabetes and cardiovascular disease in developing countries (KHDC PROGRAM). Brussels: International Society of Nephrology; 2005.
World Health Organization. Report of a WHO Consultation on Obesity. Obesity Preventing and Managing the Global Epidemic. Geneva, Switzerland: World Health Organization; 1997.
World Health Organization. Definition, Diagnosis and Classification of Diabetes Mellitus and Its Complications. Report of a WHO Consultation. Geneva: World Health Organization; 1999.
Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults. Executive summary of the third report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (adult treatment panel III). JAMA 2001;285:2486-97.
McClellan WM, Satko SG, Gladstone E, Krisher JO, Narva AS, Freedman BI. Individuals with a family history of ESRD are a high-risk population for CKD: Implications for targeted surveillance and intervention activities. Am J Kidney Dis 2009;53 3 Suppl 3:S100-6.
Agaba EI, Agaba PA, Wigwe CM. Use and abuse of analgesics in Nigeria: A community survey. Niger J Med 2004;13:379-82.
Levey AS, Bosch JP, Lewis JB, Greene T, Rogers N, Roth D. A more accurate method to estimate glomerular filtration rate from serum creatinine: A new prediction equation. Modification of Diet in Renal Disease Study Group. Ann Intern Med 1999;130:461-70.
Agaba EI, Wigwe CM, Agaba PA, Tzamaloukas AH. Performance of the Cockcroft-Gault and MDRD equations in adult Nigerians with chronic kidney disease. Int Urol Nephrol 2009;41:635-42.
Ogah OS, Madukwe OO, Onyeonoro UU, Chukwuonye II, Ukegbu AU, Akhimien MO, et al
. Cardiovascular risk factors and non-communicable diseases in Abia state, Nigeria: Report of a community-based survey. Int J Med Biomed Res2013;2:57-68.
O'Hare AM, Choi AI, Bertenthal D, Bacchetti P, Garg AX, Kaufman JS, et al.
Age affects outcomes in chronic kidney disease. J Am Soc Nephrol 2007;18:2758-65.
Anupama YJ, Uma G. Prevalence of chronic kidney disease among adults in a rural community in South India: Results from the kidney disease screening (KIDS) project. Indian J Nephrol 2014;24:214-21.
] [Full text]
Afolabi MO, Abioye-Kuteyi AE, Arogundade FA, Bello IS. Prevalence of chronic kidney disease in a Nigerian family practice population. SA Fam Pract 2009;51:132-7.
Fox CS, Larson MG, Leip EP, Culleton B, Wilson PW, Levy D. Predictors of new-onset kidney disease in a community-based population. JAMA 2004;291:844-50.
McDonald SP, Maguire GP, Hoy WE. Renal function and cardiovascular risk markers in a remote Australian Aboriginal community. Nephrol Dial Transplant 2003;18:1555-61.
Wei X, Li ZI, Chen W, Mao H, Li Z, Dong X, et al
. Prevalence and risk factors of chronic kidney disease in first-degree relatives of chronic kidney disease patients in Southern Chinan Nephrology 2012;17:123-30.
Kong X, Liu L, Zuo L, Yuan P, Li Z, Li W, et al.
Association between family members of dialysis patients and chronic kidney disease: A multicenter study in China. BMC Nephrol 2013;14:19.
Bello AK, Peters J, Wight J, de Zeeuw D, El Nahas M; European Kidney Institute. A population-based screening for microalbuminuria among relatives of CKD patients: The Kidney Evaluation and Awareness Program in Sheffield (KEAPS). Am J Kidney Dis 2008;52:434-43.
Ulasi II, Tzur S, Wasser WG, Shemer R, Kruzel E, Feigin E, et al.
High population frequencies of APOL1 risk variants are associated with increased prevalence of non-diabetic chronic kidney disease in the Igbo people from South-Eastern Nigeria. Nephron Clin Pract 2013;123:123-8.
Zoccali C, Torino C, Tripepi G, Mallamaci F. Assessment of obesity in chronic kidney disease: What is the best measure? Curr Opin Nephrol Hypertens 2012;21:641-6.
Iseki K. Body mass index and the risk of chronic renal failure: The Asian experience. Contrib Nephrol 2006;151:42-56.
Kalaitzidis RG, Siamopoulos KC. The role of obesity in kidney disease: Recent findings and potential mechanisms. Int Urol Nephrol 2011;43:771-84.
Iseki K. The okinawa screening program. J Am Soc Nephrol 2003;14 7 Suppl 2:S127-30.
Halbesma N, Brantsma AH, Bakker SJ, Jansen DF, Stolk RP, De Zeeuw D, et al.
Gender differences in predictors of the decline of renal function in the general population. Kidney Int 2008;74:505-12.
Zhang L, Zuo L, Xu G, Wang F, Wang M, Wang S, et al.
Community-based screening for chronic kidney disease among populations older than 40 years in Beijing. Nephrol Dial Transplant 2007;22:1093-9.
Bleyer AJ, Shemanski LR, Burke GL, Hansen KJ, Appel RG. Tobacco, hypertension, and vascular disease: Risk factors for renal functional decline in an older population. Kidney Int 2000;57:2072-9.
Stengel B, Tarver-Carr ME, Powe NR, Eberhardt MS, Brancati FL. Lifestyle factors, obesity and the risk of chronic kidney disease. Epidemiology 2003;14:479-87.
Vupputuri S, Sandler DP. Lifestyle risk factors and chronic kidney disease. Ann Epidemiol 2003;13:712-20.
Haroun MK, Jaar BG, Hoffman SC, Comstock GW, Klag MJ, Coresh J. Risk factors for chronic kidney disease: A prospective study of 23,534 men and women in Washington County, Maryland. J Am Soc Nephrol 2003;14:2934-41.
[Table 1], [Table 2], [Table 3], [Table 4]
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