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Systematic Review of Genomic Associations with Blood Pressure and Hypertension in Populations with African-Ancestry
S Singh1,2, J-T Brandenburg1, A Choudhury1
1Sydney Brenner Institute for Molecular Bioscience (SBIMB), Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Insights
This review highlights the under-representation of African-ancestry individuals in genetic studies for hypertension. Developing African cohorts and harmonizing data are crucial for understanding genetic associations with blood pressure traits in these populations.
Area of Science:
- Genomics
- Population Genetics
- Cardiovascular Disease Epidemiology
Background:
- Hypertension is highly prevalent in individuals of African ancestry.
- African populations are significantly under-represented in large genome-wide association studies (GWAS).
- Inclusion of African participants is vital for understanding genetic associations with blood pressure traits.
Purpose of the Study:
- To critically evaluate existing genetic association studies involving African-ancestry participants.
- To identify knowledge gaps in genomic research related to blood pressure traits in African populations.
- To assess the current landscape of genetic discoveries for blood pressure and hypertension in Africans.
Main Methods:
- Systematic literature review following PRISMA protocol and HuGE Review handbook.
- Searched for original research in English on genetic association studies for blood pressure traits (systolic/diastolic blood pressure, pulse, mean-arterial pressure, hypertension).
- Included studies with African-ancestry participants published between January 2007 and April 2020; narrative synthesis was performed.
Main Results:
- Twelve studies met eligibility criteria; 10 provided genetic association data exclusively from African-ancestry participants.
- Twenty-six single nucleotide polymorphisms (SNPs) showed genome-wide significance across five blood pressure traits.
- Six SNPs demonstrated pleiotropic effects (associated with multiple traits), and 12 SNP associations were novel compared to non-African studies.
Conclusions:
- A significant dearth of genomic association studies exists for African-ancestry populations, particularly within Africa.
- Methodological variations, small sample sizes, and covariate adjustments limit comparisons and discovery in African studies versus European ones.
- Establishing African cohorts with harmonized data and African-centric genomic arrays is essential for advancing research, exemplified by initiatives like H3Africa CHAIR.
Abstract:
Background: Despite hypertension being highly prevalent in individuals with African-ancestry, they are under-represented in large genome-wide association studies. Inclusion of African participants is essential to better understand genetic associations with blood pressure-related traits in Africans. This systematic review critically evaluates existing studies with African-ancestry participants and identifies knowledge gaps. Methods: We followed the PRISMA protocol, HuGE Review handbook to identify literature on original research, in English, on genetic association studies for blood pressure-related traits (systolic and diastolic blood pressure, pulse and mean-arterial pressure, and hypertension) in populations with African-ancestry (January 2007 to April 2020). A narrative synthesis of the evidence was conducted. Results: Twelve studies with African-ancestry participants met the eligibility criteria, within which 10 studies met the additional genetic association data criteria (i.e., reporting only on African-ancestry participants). Across the five blood pressure-related traits, 26 genome-wide significantly associated SNPs were identified, with six SNPs linked to more than one trait, illustrating pleiotropic effects. Among the SNP associations, 12 had not previously been described in non-African studies. Discussion: The limited number of relevant studies highlights the dearth of genomic association studies on participants with African-ancestry, especially those located within Africa. Variations in study methodology, participant inclusion, adjustment for covariates (e.g., antihypertensive medication) and relatively small sample sizes make comparisons challenging, and have resulted in fewer significant associations, compared to large European studies. Regional variation in the prevalence and associated risk factors of hypertension across Africa makes a compelling argument to develop African cohorts to facilitate large genomic studies, using African-centric arrays. Data harmonisation and comparable study designs, such as described in the H3Africa CHAIR initiative, provide a good example toward achieving this goal. Other relevant information: SS and J-TB were funded by the South African National Research Foundation. MR is a South African Research Chair in Genomics and Bioinformatics of African populations hosted by the University of the Witwatersrand, funded by the Department of Science and Innovation, and administered by the NRF. This review was registered at PROSPERO (registration number: CRD42020179221) and OSF (registration DOI: 10.17605/OSF.IO/QT2HA).
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