Implementation of a genotyped African population cohort, with virtual follow-up: A feasibility study in the Western Cape Province, South Africa.

Q1 Medicine Wellcome Open Research Pub Date : 2025-01-13 eCollection Date: 2024-01-01 DOI:10.12688/wellcomeopenres.23009.2
Tsaone Tamuhla, Anna K Coussens, Maleeka Abrahams, Melissa J Blumenthal, Francisco Lakay, Robert J Wilkinson, Catherine Riou, Peter Raubenheimer, Joel A Dave, Nicki Tiffin
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Abstract

Background: There is limited knowledge regarding African genetic drivers of disease due to prohibitive costs of large-scale genomic research in Africa.

Methods: We piloted a scalable virtual genotyped cohort in South Africa that was affordable in this resource-limited context, cost-effective, scalable virtual genotyped cohort in South Africa, with participant recruitment using a tiered informed consent model and DNA collection by buccal swab. Genotype data was generated using the H3Africa Illumina micro-array, and phenotype data was derived from routine health data of participants. We demonstrated feasibility of nested case control genome wide association studies using these data for phenotypes type 2 diabetes mellitus (T2DM) and severe COVID-19.

Results: 2267346 variants were analysed in 459 participant samples, of which 229 (66.8%) are female. 78.6% of SNPs and 74% of samples passed quality control (QC). Principal component analysis showed extensive ancestry admixture in study participants. Of the 343 samples that passed QC, 93 participants had T2DM and 63 had severe COVID-19. For 1780 previously published COVID-19-associated variants, 3 SNPs in the pre-imputation data and 23 SNPS in the imputed data were significantly associated with severe COVID-19 cases compared to controls (p<0.05). For 2755 published T2DM associated variants, 69 SNPs in the pre-imputation data and 419 SNPs in the imputed data were significantly associated with T2DM cases when compared to controls (p<0.05).

Conclusions: The results shown here are illustrative of what will be possible as the cohort expands in the future. Here we demonstrate the feasibility of this approach, recognising that the findings presented here are preliminary and require further validation once we have a sufficient sample size to improve statistical significance of findings.We implemented a genotyped population cohort with virtual follow up data in a resource-constrained African environment, demonstrating feasibility for scale up and novel health discoveries through nested case-control studies.

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非洲人口基因分型队列的实施和虚拟随访:南非西开普省的可行性研究。
背景:由于在非洲进行大规模基因组研究的费用过高,关于非洲疾病的遗传驱动因素的知识有限。方法:我们在南非试点了一个可扩展的虚拟基因型队列,该队列在南非资源有限的情况下是负担得起的,具有成本效益,可扩展的虚拟基因型队列,参与者招募使用分层知情同意模型和通过口腔拭子收集DNA。基因型数据使用H3Africa Illumina微阵列生成,表型数据来自参与者的常规健康数据。我们利用这些数据证明了巢式病例对照全基因组关联研究对2型糖尿病(T2DM)和严重COVID-19表型的可行性。结果:在459份参与者样本中分析了2267346个变异,其中229个(66.8%)为女性。78.6%的snp和74%的样品通过质量控制(QC)。主成分分析显示,研究参与者存在广泛的血统混杂。在通过QC的343个样本中,93名参与者患有T2DM, 63名参与者患有严重的COVID-19。对于先前发表的1780个与COVID-19相关的变异,与对照组相比,预代入数据中的3个snp和代入数据中的23个snp与严重的COVID-19病例显著相关(结论:这里显示的结果说明了随着未来队列的扩大,可能出现的情况。在这里,我们证明了这种方法的可行性,认识到这里提出的发现是初步的,一旦我们有足够的样本量来提高发现的统计意义,就需要进一步验证。我们在资源受限的非洲环境中实施了一个具有虚拟随访数据的基因分型人群队列,通过嵌套病例对照研究证明了扩大规模和新健康发现的可行性。
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来源期刊
Wellcome Open Research
Wellcome Open Research Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
5.50
自引率
0.00%
发文量
426
审稿时长
1 weeks
期刊介绍: Wellcome Open Research publishes scholarly articles reporting any basic scientific, translational and clinical research that has been funded (or co-funded) by Wellcome. Each publication must have at least one author who has been, or still is, a recipient of a Wellcome grant. Articles must be original (not duplications). All research, including clinical trials, systematic reviews, software tools, method articles, and many others, is welcome and will be published irrespective of the perceived level of interest or novelty; confirmatory and negative results, as well as null studies are all suitable. See the full list of article types here. All articles are published using a fully transparent, author-driven model: the authors are solely responsible for the content of their article. Invited peer review takes place openly after publication, and the authors play a crucial role in ensuring that the article is peer-reviewed by independent experts in a timely manner. Articles that pass peer review will be indexed in PubMed and elsewhere. Wellcome Open Research is an Open Research platform: all articles are published open access; the publishing and peer-review processes are fully transparent; and authors are asked to include detailed descriptions of methods and to provide full and easy access to source data underlying the results to improve reproducibility.
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