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Cardiovascular Risk in Black South Africans (CRIBSA) Study

South Africa
Reference ID
CRIBSAStudy
Producer(s)
Elvis Ndonwi, Keren de Buys, Don Matshazi, Naomi Levitt, Carl Lombard, Glenda Davison, Tandi Matsha, Andre Pascal Kengne, Sian Hemmings, Nasheeta Peer
Collections
Non-communicable Disease
Metadata
Documentation in PDF DDI/XML JSON
Created on
Jan 28, 2025
Last modified
Jan 28, 2025
Page views
4021
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    CRIBSAStudy

    Title

    Cardiovascular Risk in Black South Africans (CRIBSA) Study

    Country
    Name Country code
    South Africa RSA
    Abstract

    Background: Our study investigated the association between transcription factor 7-like 2 (TCF7L2-rs7903146), angiotensin convertase enzyme (ACE-rs4646994), angiotensinogen (AGT-rs699), angiotensin II type 1 receptor (AGT1R-rs5186), fat mass and obesity-associated (FTO-rs17817499) and melanocortin 4 receptor (MC4R-rs17782313, rs12970134 and rs229616) single nucleotide polymorphisms (SNPs) with type 2 diabetes (T2D), obesity and hypertension in a Black South African population.

    Methods: This cross-sectional study involved 560 Black South Africans aged 25 to 74 years. Participant demographic and lifestyle characteristics were self-reported; anthropometry and blood pressures (BP) measured; oral glucose tolerance tests used to diagnose T2D; and SNPs genotyped by polymerase chain reaction. The Benjamini-Hochberg method was used to control for multiple hypothesis testing, using a significance threshold of 0.12.

    Results: Systolic BP was significantly higher in carriers of the G/G genotype of rs229616 within the MC4R gene compared to carriers of the G/A genotype (p = 0.006). In the same gene, logistic regression analysis showed that carriers of the minor C/C genotype of the rs17782313 SNP had a significantly higher risk of hypertension (OR = 1.37, p = 0.023). Moreover, carriers of the minor T/T genotype of the TCF7L2 rs7903146 SNP had a lower risk of T2D (OR = 0.66, p = 0.043).

    Conclusion: TCF7L2-rs7903146 (C/C genotype) and MC4R-17782313 (C/C genotype) SNPs are potential genetic risk factors for T2D and hypertension in the Black South African population. Replicating these findings and exploring the role played by these genetic variants in downstream molecular pathways could aid in risk stratification and facilitate personalized approaches to healthcare delivery.

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    Primary investigators
    Name Affiliation
    Elvis Ndonwi SAMRC/CPUT, Cardiometabolic Health Research Unit, Department of Biomedical Sciences, Cape Peninsula University of Technology
    Keren de Buys SAMRC/Stellenbosch University Genomics of Brain Disorders Research Unit, Stellenbosch University
    Don Matshazi SAMRC/CPUT, Cardiometabolic Health Research Unit, Department of Biomedical Sciences, Cape Peninsula University of Technology
    Naomi Levitt Chronic Disease Initiative for Africa, Department of Medicine, University of Cape Town
    Carl Lombard Biostatistics Research Unit, South African Medical Research Council
    Glenda Davison SAMRC/CPUT, Cardiometabolic Health Research Unit, Department of Biomedical Sciences, Cape Peninsula University of Technology
    Tandi Matsha SAMRC/CPUT, Cardiometabolic Health Research Unit, Department of Biomedical Sciences, Cape Peninsula University of Technology
    Andre Pascal Kengne NCDRU, South African Medical Research Council
    Sian Hemmings Stellenbosch University Genomics of Brain Disorders Research Unit, Stellenbosch University
    Nasheeta Peer NCDRU, South African Medical Research Council
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