- Original research article
- Open Access
Prevalence of chronic kidney disease among the high risk population in South-Western Ghana; a cross sectional study
© Ephraim et al. 2015
- Received: 29 April 2014
- Accepted: 28 August 2015
- Published: 3 November 2015
Chronic Kidney Disease (CKD) is a major global health problem. CKD is one of the most common complications of diabetes mellitus and hypertension and carries a risk of cardiovascular morbidity and mortality and progression to end-stage kidney disease.
This study sought to use the 2012 Kidney Disease Improving Global Outcomes (KDIGO) definitions to establish the prevalence and risk factors for CKD among a high risk population in the Sekondi-Takoradi metropolis.
Cross sectional study.
Effia-Nkwanta regional and the Takoradi Government hospitals in South Western Ghana.
Two hundred eight consecutive adults with diabetes, hypertension or both.
Serum creatinine and urine albumin-creatinine ratio respectively. The Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) was used to estimate glomerular filtration rate (GFR).
CKD was classified according to KDIGO.
The prevalence of CKD was 30 %: 27 % in patients with diabetes, 22 % in patients with hypertension only and 74 % in patients with both diabetes and hypertension. GFR category G3a CKD was most prevalent stage (9 %). Albuminuria was highest among people with diabetes (39 %).
A convenience sample of patients attending clinics.
CKD was prevalent in these high-risk patients.
L’insuffisance rénale chronique (IRC) est un problème majeur de santé globale. Elle se révèle l’une des plus fréquentes complications du diabète sucré et de l’hypertension. De plus, l’IRC pose un risque accru pour les patients de souffrir, voire de mourir de cardiopathie, ou alors de voir leur état progresser vers l’insuffisance rénale terminale.
Objectifs de l’étude
L’étude a cherché à établir la prévalence et les facteurs de risque de l’IRC dans la population prédisposée de la métropole de Sekondi-Takoradi (Ghana) en utilisant les définitions proposées par « Kidney Disease Improving Global Outcomes » (KDIGO) en 2012.
Il s’agit d’une étude transversale.
Contexte de l’étude
L’étude a été effectuée sur des patients de l’hôpital régional Effia-Nkwanta et de l’hôpital gouvernemental de Takoradi, dans le sud-ouest du Ghana.
L’étude était constituée d’une cohorte de 208 adultes atteints de diabète, d’hypertension ou d’une comorbidité.
Le rapport albumine-créatinine dans l’urine ainsi que le taux de créatinine sérique ont été mesurés, puis le débit de filtration glomérulaire (GFR) a été déterminé à l’aide de l’équation du « Chronic Kidney Disease Epidemiology Collaboration » (CKD-EPI).
L’IRC a été déterminée selon les critères de KDIGO.
À la suite de cette étude, la prévalence d’IRC a été établie à 30 % parmi les patients de la cohorte. Elle s’établissait à 27 % chez les patients atteints de diabète seulement, 22 % chez les patients atteints d’hypertension seulement et de 74 % chez les patients présentant à la fois du diabète et de l’hypertension. Le stade d’IRC (9 %) le plus prévalent était de catégorie G3a. La prévalence d’albuminurie était plus élevée chez les patients diabétiques (39 %).
Limites de l’étude
Il s’agit d’un échantillon de commodité formé de patients fréquentant les deux cliniques mentionnées plus haut.
La prévalence d’insuffisance rénale chronique était plus élevée chez ce groupe de patients considérés à haut risque.
- Chronic Kidney Disease
- Glomerular Filtration Rate
- Kidney Disease Improve Global Outcome
- Chronic Kidney Disease Epidemiology Collaboration
- Chronic Kidney Disease Prevalence
Chronic Kidney Disease (CKD) is defined as abnormalities of kidney structure or function, present for more than 3 months, with implications for health [1, 2]. It is characterized by either decreased glomerular filtration rate (GFR) or albuminuria, or both, and carries a risk of cardiovascular morbidity and mortality and progression to end-stage renal disease (ESRD) . Chronic kidney disease is thought to be prevalent in sub-Saharan Africa and to be a major public health problem . Resources for recognition and management aiming at reduction in progression are limited, and resources for the treatment of ESRD severely limited .
Chronic kidney disease (CKD) is one of the most common complications of diabetes mellitus  and hypertension . Screening for CKD is not routinely performed in many diabetic clinics in sub-Saharan Africa because of limited human resource, diagnostic facilities and the cost of the tests [5–7].
Several studies within sub-Saharan Africa have examined the prevalence of CKD in people at high risk, including those with diabetes and hypertension. Janmohamed et al.,  recorded 84 % prevalence in adult outpatients with diabetes in Tanzania, and Osafo et al.  showed a CKD prevalence of 47 % among Ghanaian patients, mainly from the Greater Accra region, with hypertension. In addition, Sumaili et al.,  recorded 44 % prevalence in patients with hypertension, 39 % in those with diabetes; 16 % in people with obesity and 12 % in those who had human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS). We used the 2012 guidelines of the kidney disease improving global outcomes (KDIGO) to classify CKD among patients with diabetes, hypertension and both and also identified the associated risk factors for CKD in the Sekondi-Takoradi metropolis in south western Ghana.
Study design and study site
A cross-sectional study was conducted at the outpatient diabetes and hypertension clinics of the Effia-Nkwanta Regional hospital (ERH) and the Takoradi Government Hospital (TGH) in the Sekondi-Takoradi metropolis between December 2012 and May 2013. These serve as the major healthcare facilities in the metropolis providing primary, secondary and tertiary healthcare services for a population of 445,000. The healthcare system is accessible to those who contribute or pay the minimum of GH 20.0 yearly premium, equivalent to about three times the daily minimum wage of GH 6.0; about 66 % of the population is covered. In Ghana, patients with diabetes or hypertension receive specialized care in teaching, regional or municipal hospitals since they are the only facilities with the capacity to diagnose and manage this condition. Sekondi-Takoradi is the administrative capital of the Western Region. It has a land area of 385 km2 and is located in the South-Western part of Ghana and about 242 km west of Accra, the capital city of Ghana.
Inclusion and exclusion criteria
We enrolled eligible adult (>18 years) outpatients receiving medical care at the diabetes and hypertension clinics of the hospitals during the study period. Patients diagnosed with high blood pressure or on anti-hypertensive drugs, diabetes or both hypertension and diabetes were included in this study. We excluded patients with other kidney diseases (such as glomerulonephritis, vasculitis, kidney infection, connective tissue disease or adult polycystic kidney disease), those undergoing peritoneal or hemodialysis, and those with inflammatory bowel disease or rheumatoid arthritis. We also excluded people with known hepatitis B or C and HIV/AIDS.
Patient screening, recruitment and data collection
We screened 382 consecutive patients with diabetes, hypertension or both who visited the outpatient department of the two hospitals for routine evaluation. Diabetes was defined as a diagnosis of diabetes or taking a hypoglycaemic drug, and hypertension as a diagnosis of hypertension or taking an anti-hypertensive drug. Information on age, gender, fasting blood glucose, body mass index (BMI), systolic blood pressure and diastolic blood pressure, medication used, duration on medication, and duration of diabetes was obtained using a pre-tested questionnaire and the patient medical records.
Measurement of blood pressure
Trained personnel used a mercury sphygmomanometer (ACCOSON, England) with a standard or a large cuff, appropriate to the patient’s size, to measure blood pressure after patients rested for 5 min, in accordance with recommendations of the American Heart Association Council on High Blood Pressure Research . We report mean values of duplicate measurements.
Body mass index (BMI)
Height (nearest centimetre) and weight (nearest 0.1 kg), without shoes and in light clothing were measured. Participants were weighed on a bathroom scale (Zhongshan Camry Electronic Co. Ltd, Guangdong, China) and their height measured with a wall-mounted ruler. BMI was calculated by dividing weight (kg) by height squared (m2), and categorized according to WHO criteria into normal weight (BMI 18.5–24.9), underweight (<18.5), overweight (25.0–29.9), obese (30.0–39.9) .
Blood sample collection and processing
A 4 ml venous blood sample was collected from each participant and 1 and 3 ml were dispensed into a fluoride oxalate tube and a serum gel separator tube respectively. After centrifugation at 1500 g for 3 min, the plasma and serum were stored in cryovials at −80 °C until assays were performed.
Plasma fasting blood sugar (FBS), serum urea and creatinine were estimated using automated chemistry analyzer (Selectra JR). Estimated glomerular filtration rate (eGFR) was calculated using the CKD-EPI equation using the coefficients for black ethnicity in all .
Urine sample collection and processing
Urine protein was quantitatively estimated using the method of . Estimation of urine creatinine was done using automated analyzer (ENVOY500/BT 3000 chemistry analyzer. Urine protein-creatinine ratio (uPCR) was calculated by the following formula: uPCR (mg/mmol = urine protein (mg/dl)/urine creatinine (mmol/dl). The urine protein/creatinine ratio (uPCR) was reported as mg/mmol. Resources were not available to measure albuminuria. The relationship between uACR and uPCR is not a simple one, so we did not attempt to convert between the two . Instead we report uPCR in uACR categories, recognizing that this leads to overestimation of the proportions of patients with problems.
Analysis was performed using Graphpad prism version 5.0 (GraphPad software, San Diego California USA, www.graphpad.com). Two-sample Student’s t test and chi-squared or Fisher’s exact test, as appropriate, and one-way analysis of variance (ANOVA) were used to compare groups. A P-value ≤0.05 was considered statistically significant.
The study was approved by the University of Cape Coast institutional review board (UCC/IRB) and the committee of ethics of TGH and ERH. Written informed consent was obtained from all participants.
Study procedures including collection of clinical data and the laboratory tests were funded by the authors.
Demographic, clinical and biochemical characteristics of study participants stratified by clinical conditions
Diabetes (n = 120)
Hypertension (n = 65)
Hypertension and diabetes (n = 23)
60.2 ± 10.1
60.8 ± 9.5
60.7 ± 8.6
Age group (years)
Disease Duration (years)
5.4 ± 2.4
5.2 ± 2.3
6.3 ± 3.4
Disease Duration Category
9.7 ± 3.7
5.8 ± 1.4
13.4 ± 4.7
130.3 ± 15.1
145.7 ± 22.8
160.0 ± 17.8
75.1 ± 8.7
85.2 ± 10.2
94.8 ± 12.0
27.5 ± 5.2
27.4 ± 5.0
27.7 ± 5.6
BMI Category n(%)
eGFR, mL/min/1.73 m2
82 ± 32
76 ± 26
61 ± 39
Prevalence of albuminuria, estimated glomerular filtration rate (eGFR) and stages of CKD stratified by clinical conditions
Diabetes (n = 120)
Hypertension (n = 65)
Hypertension and diabetes (n = 23)
Total (n = 208)
p < 0.001
eGFR, mL/min/1.73 m2 n (%)
p < 0.001
CKD n (%)
Stage 1: eGFR ≥90 + Alb
Stage 2: eGFR 60–89 + Alb
Stage 3a: eGFR 45–59
Stage 3b: eGFR 30–44
Stage 4: eGFR15–29
Stage 5: eGFR < 15
Total CKD, n (%)
Prevalence of albuminuria and estimated glomerular filtration rate (eGFR) stratified by clinical conditions
Hypertension and diabetes
Table 3 show the distribution of patients by GFR and albuminuria categories, for those with hypertension, diabetes and both diabetes and hypertension. Overall, 30 % of participants fell into the category defined by KDIGO as ‘very high risk’: 23 % of patients with hypertension, 27 % of patients with diabetes and 74 % of those with both diabetes and hypertension.
Multivariable associations of clinical variables with CKD in high-risk population
OR (95 % CI)
BMI n (%)
Duration on medication
We identified a prevalence of CKD in patients with hypertension of 22 % and in patients with diabetes of 27 %. In patients with both hypertension and diabetes, the prevalence was 74 %, and 26 % had category G4 CKD. Clinical factors associated with a greater risk of CKD were the presence of both hypertension and diabetes, and duration on medication (antidiabetic and antihypertensive).
Osafo and colleagues  reported a 47 % prevalence of CKD among patients with hypertension in Ghana, in a multicenter study conducted predominantly among people with hypertension in the Greater Accra area (known for a high prevalence of hypertension). This is higher than the overall prevalence of 30 % among our study participants, and 22 % in people with hypertension. The difference may, in part, be owing to our having used the CKD-Epi  equation rather the MDRD equation, which was used in the study by Osafo and colleagues. MDRD is known to overestimate the prevalence of CKD compared with CKD-Epi, and this has also been shown by Kitiyakara and colleagues in their study of the high risk population in South East Asia . In all patients with diabetes (with or without hypertension) we observed a prevalence of 48 %, which is lower than the 80 % prevalence observed among African adults with diabetes in a cross-sectional study conducted in Tanzania by Janmohamed and colleagues . Again this is not directly comparable, with differences arising from their use of Cockroft-Gault equation to calculate the eGFR (which overestimates true GFR and underestimates prevalence); and urine albumin concentration as a measure of proteinuria (which is the recommended method of assessing proteinuria; our use of uPCR overestimates prevalence) but both these differences would result in a tendency for our prevalence by our methods to be higher than by their methods; so it may be that true differences exist. However, neither study used IDMS calibrated creatinine measurement and the direction of biases resulting from this limitation cannot be assessed.
Osafo and colleagues  observed a 51 % prevalence of CKD in patients with coexistent diabetes and hypertension, based on data from 712 participants in a multicenter study in Accra, Ghana, and we observed 74 % prevalence of CKD in our participants. Since their use of the MDRD formula would have biased their findings towards a greater incidence of CKD, it is possible that the prevalence is truly higher in this group in Ghana.
Good blood pressure control and ACE inhibitors are known to have a reno-protective effect, particularly in people with albuminuria . In our study, 30 % overall, 11.1 % of people with diabetes and hypertension, 9.2 % of people with albuminuria and hypertension received ACE inhibitor therapy. We are unable to determine from our study to what extent this relatively low prevalence represents true contraindications or previous adverse effects, or whether this is a possible missed treatment opportunity that results from the economic costs of the drug (most of which are borne by the patients) or a reluctance on the part of physicians to prescribe ACE inhibitors without access to repeated monitoring of renal function (laboratory tests are paid for by the patient).
Our study has several limitations. First our findings cannot be generalized to other low income and low resource countries because it was not community based and was conducted within a population at risk of developing CKD with genetic and cultural differences. Further, there may be differences in the practices that lead to a patient being identified as having hypertension or diabetes, and differences in access to treatments for, and monitoring of those conditions. The study was conducted in the Sekondi-Takoradi metropolis. It is likely that there would be significant variation in prevalence rates in other urban and rural towns in the Western region and across Ghana as a whole. This study is also limited by the small sample size, use of the single measurement of serum creatinine (whereas to truly fulfill definitions of CKD, two measurements at least 3 months apart are needed), and by our lack of standardization of serum creatinine to isotope mass dilution spectrophotometry (IMDS). Third, although the CKD-EPI eGFR equation has been used in previous studies in this population [8, 18, 19] it has not been validated for use in the black Ghanaian population. Strengths of our study are the consecutive sampling and completeness of data collection.
CKD was detected among 30 % of this high-risk population. Further research is needed into optimal approaches to screening and treatment, including research on the effects of lowering economic barriers to known effective treatments. This is particularly important in resource-constrained practice settings such as ours, because the impact of the development of end-stage renal disease when dialysis cannot be provided is so much greater.
The authors appreciate the contributions Mr. Samuel K. Danquah and the staff and management of the Effia Nkwanta Regional Hospital (ENRH) and the Takoradi Government Hospital (TGH) especially the Laboratory Department in making this work a success. We also appreciate the contributions of the humble people of the Sekondi-Takoradi metropolis for availing themselves for this research.
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- Stevens PE, Levin A. Evaluation and management of chronic kidney disease: synopsis of the kidney disease: improving global outcomes 2012 clinical practice guideline. Ann Intern Med. 2013;158(11):825–30.Google Scholar
- Kidney Disease: Improving Global Outcomes (KDIGO) CKD Work Group. KDIGO clinical practice guideline for the evaluation and management of chronic kidney disease. Kidney Int Suppl. 2013;3:1–150.Google Scholar
- Hallan SI, Dahl K, Oien CM, Grootendorst DC, Aasberg A, Holmen J, et al. Screening strategies for chronic kidney disease in the general population: follow-up of cross sectional health survey. BMJ. 2006;333(7577):1047.PubMed CentralView ArticlePubMedGoogle Scholar
- Naicker S. End-stage renal disease in sub-Saharan Africa. Ethn Dis. 2009;19(1 Suppl 1):S1-13–15.Google Scholar
- Gill GV, Mbanya JC, Ramaiya KL, Tesfaye S. A sub-Saharan African perspective of diabetes. Diabetologia. 2009;52(1):8–16.View ArticlePubMedGoogle Scholar
- Perico N, Remuzzi G. Chronic kidney disease in sub-Saharan Africa: a public health priority. Lancet Glob Health. 2014;2(3):e124–5.View ArticlePubMedGoogle Scholar
- Janmohamed MN, Kalluvya SE, Mueller A, Kabangila R, Smart LR, Downs JA, et al. Prevalence of chronic kidney disease in diabetic adult out-patients in Tanzania. BMC Nephrol. 2013;14:183.PubMed CentralView ArticlePubMedGoogle Scholar
- Osafo C, Mate-Kole M, Affram K, Adu D. Prevalence of chronic kidney disease in hypertensive patients in Ghana. Ren Fail. 2011;33(4):388–92.View ArticlePubMedGoogle Scholar
- Sumaili EK, Cohen EP, Zinga CV, Krzesinski JM, Pakasa NM, Nseka NM. High prevalence of undiagnosed chronic kidney disease among at-risk population in Kinshasa, the Democratic Republic of Congo. BMC Nephrol. 2009;10:18.PubMed CentralView ArticlePubMedGoogle Scholar
- Pickering TG, Hall JE, Appel LJ, Falkner BE, Graves J, Hill MN, Jones DW, Kurtz T, Sheps SG, Roccella EJ: Recommendations for blood pressure measurement in humans and experimental animals: Part 1: blood pressure measurement in humans: a statement for professionals from the Subcommittee of Professional and Public Education of the American Heart Association Council on High Blood Pressure Research. Hypertension 2005;45(1):142–161.Google Scholar
- WHO. Physical status: the use and interpretation of anthropometry, Report of a WHO expert committee. In: Technical report series, vol. 854. Geneva: WHO; 1995.Google Scholar
- Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro 3rd AF, Feldman HI, et al. A new equation to estimate glomerular filtration rate. Ann Intern Med. 2009;150(9):604–12.PubMed CentralView ArticlePubMedGoogle Scholar
- Pesce MA, Strande CS. A new micromethod for determination of protein in cerebrospinal fluid and urine. Clin Chem. 1973;19:1265–1267.PubMedGoogle Scholar
- Johnson DW, Jones GR, Mathew TH, Ludlow MJ, Chadban SJ, Usherwood T, et al. Chronic kidney disease and measurement of albuminuria or proteinuria: a position statement. Med J Aust. 2012;197(4):224–5.Google Scholar
- Kitiyakara C, Yamwong S, Vathesatogkit P, Chittamma A, Cheepudomwit S, Vanavanan S, et al. The impact of different GFR estimating equations on the prevalence of CKD and risk groups in a Southeast Asian cohort using the new KDIGO guidelines. BMC Nephrol. 2012;13:1.PubMed CentralView ArticlePubMedGoogle Scholar
- Baltatzi M, Savopoulos C, Hatzitolios A: Role of angiotensin converting enzyme inhibitors and angiotensin receptor blockers in hypertension of chronic kidney disease and renoprotection. Study results. Hippokratia 2011, 15(Suppl 1):27–32Google Scholar
- van der Meer V, Wielders HPM, Grootendorst DC, de Kanter JS, Sijpkens YWJ, Assendelft WJJ, et al. Chronic kidney disease in patients with diabetes mellitus type 2 or hypertension in general practice. Br J Gen Pract. 2010;60:884–90.PubMed CentralView ArticlePubMedGoogle Scholar
- Owiredu W, Ephraim R, Amidu N, Eghan Jnr BA, Quaye L. Predictive performance of renal function equations among Ghanaians presenting with chronic kidney disease. J Med Sci. 2008;8:491–7.View ArticleGoogle Scholar
- Eastwood JB, Kerry SM, Plange-Rhule J, Micah FB, Antwi S, Boa FG, et al. Assessment of GFR by four methods in adults in Ashanti, Ghana: the need for an eGFR equation for lean African populations. Nephrol Dial Transplant. 2010;25(7):2178–87.PubMed CentralView ArticlePubMedGoogle Scholar