Skip to main content


APOL1 genetic variants, chronic kidney diseases and hypertension in mixed ancestry South Africans

Article metrics



The frequencies of apolipoprotein L1 (APOL1) variants and their associations with chronic kidney disease (CKD) vary substantially in populations from Africa. Moreover, available studies have used very small sample sizes to provide reliable estimates of the frequencies of these variants in the general population. We determined the frequency of the two APOL1 risk alleles (G1 and G2) and investigated their association with renal traits in a relatively large sample of mixed-ancestry South Africans. APOL1 risk variants (G1: rs60910145 and rs73885319; G2: rs71785313) were genotyped in 859 African mixed ancestry individuals using allele-specific TaqMan technology. Glomerular filtration rate (eGFR) was estimated using the Modification of Diet in Renal Disease (MDRD) and Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equations.


The frequencies of rs73885319, rs60910145 and rs71785313 risk alleles were respectively, 3.6 %, 3.4 %, and 5.8 %, resulting in a 1.01 % frequency of the APOL1 two-risk allele (G1:G1 or G1:G2 or G2:G2). The presence of the two-risk allele increased serum creatinine with a corresponding reduction in eGFR (either MDRD or CKD-EPI based). In dominant and log-additive genetic models, significant associations were found between rs71785313 and systolic blood pressure (both p ≤ 0.025), with a significant statistical interaction by diabetes status, p = 0.022, reflecting a negative non-significant effect in nondiabetics and a positive effect in diabetics.


Although the APOL1 variants are not common in the mixed ancestry population of South Africa, the study does provide an indication that APOL1 variants may play a role in conferring an increased risk for renal and cardiovascular risk in this population.


In 2008, through admixture-mapping linkage-disequilibrium genome scan, two landmark studies identified a risk locus on chromosome 22q12.3 which explained the increased burden of nondiabetic end­stage renal disease (ESRD) and focal segmental glomerulosclerosis (FSGS) in individuals of recent African ancestry [1, 2]. These studies provided evidence that genetic variation on the myosin­9 gene (MYH9) conferred most or nearly all of the increased risk for nondiabetic kidney disease in African Americans [1, 2]. However, subsequent reanalysis of chromosome 22q12.3 region utilizing the 1000 Genome Project, identified genetic variants in the apolipoprotein L1 gene (APOL1) which extended beyond MYH9 [3, 4]. These are located 14kbp downstream from the 3’end of MYH9 and the strongest significant association with ESRD was found in a 10-kb region in the last exon of APOL1 [3, 4]. Of the single nucleotide polymorphisms (SNPs) identified, two were nonsynonymous (rs73885139 and rs60910145) designated G1, and one a 6-bp deletion (rs71785313) termed G2. The two missense variants are in almost absolute linkage disequilibrium while the G2 is in complete negative linkage disequilibrium with G1.

The APOL1 is known for its lytic effects on trypanosomes, which cause sleeping sickness in humans [5]. However, one of the Tryanosoma species (T. brucei rhodesiense) overcomes the lytic effects of APOL1 by expressing a serum resistance-associated protein (SRA) [6]. The presence of G1 and G2 polymorphisms in the SRA binding domain are believed to restore the APOL1 ability to kill T. brucei rhodesiense [7], hence the positive selection of the variants in endemic regions, particularly in sub-Saharan Africa. Variation in frequency is substantial within Africa; and therefore the contribution to chronic kidney disease (CKD) is likely to vary [4, 7]. However, at this time the geographic variation in APOL1 association with CKD is unknown, since it has not yet been tested. Therefore, herein, we sought to determine the frequency of APOL1 variants and their association with CKD traits in a South African population with an African ancestry, high prevalence of CKD and poor cardiovascular risk profile.


Two hundred and thirty nine (27.8 %) participants had diabetes and their general characteristics are summarized in Table 1. The overall mean age was 53.1 years, with significant differences between those with and without diabetes (51.0 vs. 58.7 years, p < 0.0001). The eGFR was significantly lower in individuals with diabetes compared to those without diabetes as well as in women vs. men (all p < 0.0001), whilst systolic blood pressure and diastolic blood pressure were significantly elevated in men (both p ≤ 0.016).

Table 1 Baseline characteristics by diabetes status and gender

The frequency distributions, both genotype and allele, did not differ significantly according to gender and diabetes status. Deletion of the sequence TTATTA of rs71785313 was borderline more frequent in women than in men (6.3 % vs. 3.8 %, p = 0.065), (Table 2). The concomitance of two-risk alleles was observed in 9 individuals (1.01 %) whilst 143 (16.6 %) had one-risk allele (Table 3). In participants with two-risk alleles, serum creatinine was elevated with a corresponding reduction of eGFR (either MDRD or CKD-EPI based) than in those with only one-risk allele or none, but differences did not reach statistical significance. Furthermore, these were still more likely to have higher prevalence of hypertension (Table 3).

Table 2 Genotype distributions, minor allele frequencies, and unadjusted p-values for comparing genotype distributions according to diabetes status and gender
Table 3 Baseline characteristics by allele combination

In a recessive model adjusted for age, sex, diabetes status and hypertension, the G1 risk alleles showed a borderline association with prevalent CKD (CKD-EPI), p = 0.047 (Table 4). On the other hand, in generalized linear and logistics regression models (dominant and log-additive genetic models) adjusted for age, sex, diabetes status and hypertension, none of the genotypes was associated with serum creatinine, urinary albumin/creatinine ratio or prevalent CKD (Table 5 and 6). These genetic models revealed an association between G2 (rs71785313) and systolic blood pressure (both p ≤ 0.025), with a significant statistical interaction by diabetes status, p = 0.025, reflecting a negative non-significant effect in nondiabetics and a positive effect in diabetics.

Table 4 Generalized linear and logistic regression models showing the effects of genes on kidney functions and other continuous predictors (recessive model)
Table 5 Generalized linear and logistic regression models showing the effects of genes on kidney functions and other continuous predictors (dominant model)
Table 6 Generalized linear and logistic regression models showing the effects of genes on kidney functions and other continuous predictors (additive model)


This study aimed to determine the frequency of the two APOL1 risk alleles (G1 and G2) and their association with renal traits in a general South African mixed ancestry population. The findings from this study show that 16.6 % of the participants carried at least one APOL1 risk allele. The G1 risk alleles, rs73885319 and rs60910145 were observed respectively in, 3.6 %, 3.4 % of individuals whilst G2 risk allele carriers were 5.8 %, resulting in a 1.01 % frequency of the APOL1 two-risk allele (G1:G1 or G1:G2 or G2:G2). The presence of two-risk alleles decreased eGFR and the G1 risk alleles showed a borderline association with prevalent CKD (CKD-EPI), p = 0.047. On one hand, the G2 leaned towards an association with systolic blood pressure (p ≤ 0.025), with a significant statistical interaction by diabetes status, p = 0.025 assuming either dominant or log-additive. Our findings in the context of a small sample could also reflect the inadequate statistical power for uncovering some significant associations.

The strong association between APOL1 and non-diabetic kidney diseases has been replicated in several studies [811] since the initial observations reported in African Americans with hypertensive kidney disease and FSGS [3, 4]. This risk is mostly conferred by the presence of two copies of the risk alleles, that is, homozygous or compound heterozygous compared to no or one APOL1 risk variant [3, 4]. In our study, the frequency of the two-risk allele was much lower than that reported in African Americans (13 %) [12], and it was borderline associated with CKD or its markers. Furthermore, carriers of the two-risk allele were more likely to have hypertension. Our findings may be attributed to the non-discriminatory nature of our study in which diabetic and non-diabetic kidney diseases were not analyzed separately and would have resulted in an even smaller number of CKD cases. Nevertheless, our study does provide an indication that APOL1 variants may play a role in conferring a poor renal disease and cardiovascular risk profile in this population. In linear genetic regression models, the G2 risk allele was significantly associated with systolic blood pressure. Emerging data point to an expanding role of APOL1 genetic aberrations implying that they are not limited to kidney diseases, but are also associated with increased risk of cardiovascular disease (CVD) [13]. In two cohorts, the Jackson Heart Study (JHS) and the Women’s Health Initiative (WHI), the APOL1 two-risk allele increased by two-fold the risk for myocardial infarction, stroke, and therapeutic surgical or endovascular interventions in African Americans [13]. Furthermore, APOL1 G2 homozygous individuals were shown to be at an increased risk for stroke compared to G1 two risk alleles [13].

Although the link between hypertension and CKD is well established, CKD progression is augmented in African Americans compared to their Caucasian counterparts with similar blood pressure control [14, 15]. The APOL1 risk variants have recently been suggested to be the missing link in the accelerated progression of hypertensive CKD despite adequate blood pressure control in African Americans [16]. In the African American Study of Kidney Disease and Hypertension comprising 693 black patients with hypertensive CKD, Parsa et al. [16] used a codominant genetic model to show that patients with the APOL1 two-risk allele had a 2-fold risk of doubling their serum creatinine from baseline or developing incident end-stage renal disease over a 9-year period of follow-up. Furthermore, the progression of CKD in these patients was independent of blood pressure control [16]. The mechanism by which APOL1 risk variants contribute to the pathogenesis of hypertensive CKD has not been elucidated. Several possible mechanisms have been suggested including a role in lipid metabolism since APOL1 is mainly bound to high density lipoprotein [17], and variations in APOL1 circulating levels have been associated with its genetic variants [18, 19]. Another hypothesis relates to the localization of APOL1 protein in kidney vascular endothelium [20, 21]. In view of these studies including ours, a functional role of APOL1 in vasculorpathology, hypertension and kidney disease is worth exploring.

The predominance of APOL1 variants in Africans and populations with an African ancestry is linked to a natural selection, as they protect against trypanosomal infection [5] from a species that is endemic in certain regions of Africa [22]. Another factor is the differing risk of non-diabetic kidney diseases. One example is a study conducted in an Ethiopian population without HIV-associated nephropathy, which showed an absence of the APOL1 G1 and G2 risk alleles [4, 23]. In comparison with other populations from Africa, the frequencies of APOL1 risk alleles are relatively similar [4, 8] except those in Western African populations [4, 911]. Since the Cape region of South Africa is far south of the tsetse fly belt, the moderate frequency of the APOL1 risk alleles is likely due to the African ancestry reported in this population [24].

There are some limitations to be accounted for in the interpretation of our findings. These include a low number of participants with advanced stage CKD, in spite of our large sample, which may have resulted in a reduced statistical power to uncover significant associations. Although other studies from Africa did include patients with advanced CKD, and were consequently adequately powered to capture significant effects of genes on the disease risk, these studies have however used small sample sizes to provide reliable estimates of the frequencies of those gene variants in the general population as we have done. Our study comprised participants with CKD of various etiologies that could have been either diabetic or non-diabetic. Findings could therefore be different if the study was based on a population with a more homogenous type of CKD. Our study was also limited by the heterogeneous nature of the study population, which is of mixed genetic origin with contributions from Europeans, South Asians, Indonesians and a population genetically close to the isiXhosa sub-Saharan Bantu [24], necessitating the use of ancestry informative markers to account for population stratification. Potential population stratification in an unrelated sample is known to cause spurious positive or negative associations in population-based association studies if not accounted for. However, due to financial constraints, this analysis was not conducted, raising the possibility that population admixture interfered with the association analysis. The renal disease markers were based on a single measurement in a cross-sectional study design. The cross-sectional nature of our study precludes drawing causal inferences on the direction of the associations.


In conclusion, our study provides evidence that genetic variants in APOL1 are present in a mixed-ancestry South African population, but their association with renal diseases needs further exploration in patients with non-diabetic kidney diseases.

Material and methods

Study participants and procedures

This investigation is based on the Bellville South cohort from Cape town, South Africa that has received study approval from the Research Ethics Committee of the Cape Peninsula University of Technology, Faculty of Health and Wellness Sciences (Reference Number: CPUT/HW-REC 2008/002 and CPUT/HW-REC 2010). The study was conducted according to the Code of Ethics of the World Medical Association (Declaration of Helsinki) [25]. All participants signed written informed consent after all the procedures had been fully explained in the language of their choice. Of the 946 self-reported mixed ancestry participants who took part in the survey, 941 consented for genetic studies. Among the latter, 72 were excluded for missing data on the genetic or renal trait variables. Therefore, 859 had valid data for the current analyses. All participants received a standardized interview and physical examination during which blood pressure was measured according to the World Health Organisation (WHO) guidelines [26] using a semi-automated digital blood pressure monitor (Rossmax PA, USA) on the right arm in a sitting position. Anthropometric measurements were performed three times and their average used for analysis: weight (kg), height (cm), waist (cm) and hip (cm) circumferences. Participants with no history of doctor-diagnosed diabetes mellitus underwent a 75 g oral glucose tolerance test (OGTT) as recommended by the WHO [27]. Further, the following biochemical parameters were determined on the Cobas 6000 Clinical Chemistry instrument (Roche Diagnostics, Germany): fasting plasma glucose, insulin, creatinine, total cholesterol (TC), high density lipoprotein cholesterol (HDL-c), triglycerides (TG), C-reactive protein (CRP), γ-glutamyltransferase (GGT), and glycated haemoglobin (HbA1c) certified by National Glycohaemoglobin Standardisation Programme (NGSP). Low density lipoprotein cholesterol (LDL-c) was calculated using Friedewald’s formula [28]. Urine albumin was determined by the immunoturbidimetric assay (Cobas 6000, Roche Diagnostics, Germany).

SNP genotyping

Genomic DNA was extracted from whole blood samples collected in an EDTA tube. The APOL1 single nucleotide polymorphisms (SNPs) termed G1 (rs73885319; rs60919145) and G2 (rs71785313) were genotyped using high throughput real-time polymerase chain reaction (RT-PCR) on the BioRad Optica (BioRad, USA) platform using Taqman genotyping assay (Applied Biosystems, USA). Conventional polymerase chain reaction followed by direct DNA sequencing was performed for analytical validation of high throughput genotyping.

Definitions and calculations

Body mass index (BMI) was calculated as weight per square meter (kg/m2) and waist-hip-ratio (WHR) as waist/hip circumferences (cm). Type 2 diabetes status was based on a history of doctor-diagnosis, a fasting plasma glucose ≥7.0 mmol/l and/or a 2-hour post-OGTT plasma glucose ≥11.1 mmol/l. Hypertension was based on a history of doctor diagnosed hypertension and/or receiving medications for hypertension or average systolic blood pressure ≥140 mmHg and/or average diastolic blood pressure ≥90 mmHg. Urinary albumin excretion was quantified in term of urinary albumin/creatinine ratio (ACR). Glomerular filtration rate (GFR) was estimated by the 4-variable Modification of Diet in Renal Disease (MDRD) equation applicable to standardised serum creatinine values [29, 30], and the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation [31].

Statistical analysis

General characteristics of the study group are summarized as count and percentage for dichotomous traits, mean and standard deviation (SD) or median and 25th-75th percentiles for quantitative traits. Traits were log-transformed to approximate normality, where necessary, prior to analysis. SNPs were tested for departure from Hardy-Weinberg Equilibrium (HWE) expectation via a chi square goodness of fit test. Linkage disequilibrium (LD) was estimated using the D’ statistic. Linear regression models were used for the analysis of quantitative traits and logistic regression models for dichotomous traits, assuming both dominant and log-additive genetic models for the SNPs. Using linear and logistic models enabled us to adjust all analyses for known confounders as specified everywhere in the results. We investigated the association of each SNP with each trait, overall and tested for heterogeneity by major subgroups by adding the interaction term of major grouping variables and each SNP to a model that contained the main effects of grouping variable and the relevant SNP. Results corresponding to p-values below 5 % are described as significant. Adjustment for multiple testing was conducted via Bonferroni methods. All analyses used the R statistical software (version 3.0.3 [2014-03-06], The R Foundation for statistical computing, Vienna, Austria) and the packages ‘genetics’ and ‘SNPassoc’.


  1. 1.

    Kopp JB, Smith MW, Nelson GW, Johnson RC, Freedman BI, Bowden DW, et al. MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis. Nat Genet. 2008;40:1175–84.

  2. 2.

    Kao WH, Klag MJ, Meoni LA, Reich D, Berthier-Schaad Y, Li M, et al. Family Investigation of Nephropathy and Diabetes Research Group: MYH9 is associated with nondiabetic end-stage renal disease in African Americans. Nat Genet. 2008;40:1185–92.

  3. 3.

    Genovese G, Friedman DJ, Ross MD, Lecordier L, Uzureau P, Freedman BI, et al. Association of trypanolytic APOL1 variants with kidney disease in African-Americans. Science. 2010;329:841–5.

  4. 4.

    Tzur S, Rosset S, Shemer R, Yudkovsky G, Selig S, Tarekegn A, et al. Missense mutations in the APOL1 gene are highly as- sociated with end-stage kidney disease risk previously attributed to the MYH9 gene. Hum Genet. 2010;128:345–50.

  5. 5.

    Vanhamme L, Paturiaux-Hanocq F, Poelvoorde P, Nolan DP, Lins L, Van Den Abbeele J, et al. Apolipoprotein L-I is the trypanosome lytic factor of human serum. Nature. 2003;422:83–7.

  6. 6.

    Stephens NA, Hajduk SL. Endosomal localization of the serum resistance-asso- ciated protein in African trypanosomes confers human infectivity. Eukaryot Cell. 2011;10:1023–33.

  7. 7.

    Thomson R, Genovese G, Canon C, Kovacsics D, Higgins MK, Carrington M, et al. Evolution of the primate trypanolytic factor APOL1. Proc Natl Acad Sci U S A. 2014;11:E2130–9.

  8. 8.

    Genovese G, Friedman DJ, Pollak MR. APOL1 variants and kidney disease in people of recent African ancestry. Nat Rev Nephrol. 2013;9:240–4.

  9. 9.

    Tayo BO, Kramer H, Salako BL, Gottesman O, McKenzie CA, Ogunniyi A, et al. Genetic 19 variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians. Int Urol Nephrol. 2013;45:485–94.

  10. 10.

    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;12:123–8.

  11. 11.

    Wasser WG, Tzur S, Wolday D, Adu D, Baumstein D, Rosset S, et al. Population genetics of chronic kidney disease: the evolving story of APOL1. J Nephrol. 2012;25:603–18.

  12. 12.

    Tzur S, Rosset S, Skorecki K, Wasser WG. APOL1 allelic variants are associated with lower age of dialysis initiation and thereby in- creased dialysis vintage in African- and His- panic-Americans with non-diabetic end- stage kidney disease. Nephrol Dial Transplant. 2012;27:1498–505.

  13. 13.

    Ito K, Bick AG, Flannick J, Friedman DJ, Genovese G, Parfenov MG, et al. Increased burden of cardiovascular disease in carriers of APOL1 genetic variants. Circ Res. 2014;114:845–50.

  14. 14.

    Rostand SG, Brown G, Kirk KA, Rutsky EA, Dustan HP. Renal insufficiency in treated essential hypertension. N Engl J Med. 1989;320:684–8.

  15. 15.

    Appel LJ, Wright Jr JT, Greene T, Kusek JW, Lewis JB, Wang X, et al. African American Study of Kidney Disease and Hypertension Collaborative Research Group: Long-term effects of renin- angiotensin system-blocking therapy and a low blood pressure goal on progression of hypertensive chronic kidney disease in African Americans. Arch Intern Med. 2008;168:832–9.

  16. 16.

    Parsa A, Kao WH, Xie D, Astor BC, Li M, Hsu CY, et al. AASK Study Investigators; CRIC Study Investigators: APOL1 risk variants, race, and progression of chronic kidney disease. N Engl J Med. 2013;369:2183–96.

  17. 17.

    Duchateau PN, Pullinger CR, Cho MH, Eng C, Kane JP. Apoli- poprotein L gene family: tissue-specific expression, splicing, pro- moter regions; discovery of a new gene. J Lipid Res. 2001;42:620–30.

  18. 18.

    Bentley AR, Doumatey AP, Chen G, Huang H, Zhou J, Shriner D, et al. Variation in APOL1 contributes to Ancestry-level differences in HDLc-kidney function association. Int J Nephrol. 2012;2012:748984.

  19. 19.

    Freedman BI, Langefeld CD, Murea M, Ma L, Otvos JD, Turner J, et al. Apolipoprotein L1 nephropathy risk variants associate with HDL subfraction concentration in African Americans. Nephrol Dial Transplant. 2011;26:3805–10.

  20. 20.

    Monajemi H, Fontijn RD, Pannekoek H, Horrevoets AJ. The apolipoprotein L gene cluster has emerged recently in evolution and is expressed in human vascular tissue. Genomics. 2002;79:539–46.

  21. 21.

    Madhavan SM, O’Toole JF, Konieczkowski M, Ganesin S, Bruggeman LA, Sedor JR. APOL1 localization in normal kidney and non-diabetic kidney disease. J Am Soc Nephrol. 2011;22:2119–28.

  22. 22.

    World Health Organization. Control and surveillance of African trypanosomiasis. Report of a WHO Expert Committee. WHO Technical Report Series 881. Geneva: World Health Organization; 1998.

  23. 23.

    Behar DM, Kedem E, Rosset S, Haileselassie Y, Tzur S, Kra-Oz Z, et al. Absence of APOL1 risk variants protects against HIV-associated nephropathy in the Ethiopian population. Am J Nephrol. 2011;34:452–9.

  24. 24.

    Patterson N, Petersen DC, van der Ross RE, Sudoyo H, Glashoff RH, Marzuki S, et al. Genetic structure of a unique admixed population: implications for medical research. Hum Mol Genet. 2010;19:411–9.

  25. 25.

    Zemlin AE, Matsha TE, Hassan MS, Erasmus RT. HbA1c of 6.5% to diagnose diabetes mellitus – does it work for us? –the Bellville South Africa study. PLoS One. 2011;6:e22558.

  26. 26.

    Chalmers J, MacMahon S, Mancia G, Whitworth J, Beilin L, Hansson L, et al. 1999 World Health Organization-International Society of Hypertension Guidelines for the management of hypertension. Guidelines sub-committee of the World Health Organization. Clin Exp Hypertens. 1999;21:1009–60.

  27. 27.

    Alberti KG, Zimmet PZ. Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet Med. 1998;15:539–53.

  28. 28.

    Friedewald WT, Levy RI, Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972;18:499–502.

  29. 29.

    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.

  30. 30.

    Levey AS, Coresh J, Greene T, Stevens LA, Zhang YL, Hendriksen S, et al. Chronic Kidney Disease Epidemiology Collaboration: Using standardized serum creatinine values in the modification of diet in renal disease study equation for estimating glomerular filtration rate. Ann Intern Med. 2006;145:247–54.

  31. 31.

    Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro III AF, Feldman HI, et al. CKD-EPI (Chronic Kidney Disease Epidemiology Collaboration): A new equation to estimate glomerular filtration rate. Ann Intern Med. 2009;150:604–12.

Download references


We thank the Bellville South community for participating in the study. The research was funded by the Cape Peninsula University of Technology, South Africa and University of Stellenbosch, South Africa.

Author information

Correspondence to Tandi E Matsha.

Additional information

Competing interest

The authors declare that they have no competing interests.

Authors’ contributions

TEM: Conception, design, interpretation of data, drafting, revising the article and final approval of the version to be published. APK: Design, analysis and interpretation of data, revising the article and final approval of the version to be published. KLM: Analysis and interpretation of data, revising the article and final approval of the version to be published. YYY: Revising and providing intellectual content of critical importance to the work described and final approval of the version to be published RTE: Conception, revising and providing intellectual content of critical importance to the work described and final approval of the version to be published. All authors read and approved the final manuscript.

Rights and permissions

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Matsha, T.E., Kengne, A.P., Masconi, K.L. et al. APOL1 genetic variants, chronic kidney diseases and hypertension in mixed ancestry South Africans. BMC Genet 16, 69 (2015) doi:10.1186/s12863-015-0228-6

Download citation


  • Africa
  • APOL1 polymorphisms
  • Chronic kidney diseases
  • Blood pressure
  • MDRD