Evidence map›Paper›PMID 39925651›Full record

ArticleWellcome open research2024

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

Tsaone Tamuhla, Anna K Coussens, Maleeka Abrahams, Melissa J Blumenthal, Francisco Lakay, Robert J Wilkinson, Catherine Riou, Peter Raubenheimer, Joel A Dave, Nicki Tiffin

Abstract read
In one paragraph

Article in Wellcome open research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Tsaone TamuhlaSouth African Medical Research Council Bioinformatics Unit, South African National Bioinformatics Institute, University of the Western Cape, Cape Town, South Africa.ORCID https://orcid.org/0000-0001-5966-9153
Anna K CoussensWellcome CIDRI-Africa, Faculty of Health Sciences, University of Cape Town, Rondebosch, Western Cape, South Africa.ORCID https://orcid.org/0000-0002-7086-2621
Maleeka AbrahamsDivision of Endocrinology, Department of Medicine, University of Cape Town, Rondebosch, Cape Town, South Africa.
Melissa J BlumenthalInternational Centre for Genetic Engineering and Biotechnology, Cape Town, South Africa.ORCID https://orcid.org/0000-0002-1865-0795
Francisco LakayWellcome CIDRI-Africa, Faculty of Health Sciences, University of Cape Town, Rondebosch, Western Cape, South Africa.
Robert J WilkinsonWellcome CIDRI-Africa, Faculty of Health Sciences, University of Cape Town, Rondebosch, Western Cape, South Africa.ORCID https://orcid.org/0000-0002-2753-1800
Catherine RiouWellcome CIDRI-Africa, Faculty of Health Sciences, University of Cape Town, Rondebosch, Western Cape, South Africa.ORCID https://orcid.org/0000-0001-9679-0745
Peter RaubenheimerDivision of Endocrinology, Department of Medicine, University of Cape Town, Rondebosch, Cape Town, South Africa.ORCID https://orcid.org/0000-0002-5416-1286
Joel A DaveDivision of Endocrinology, Department of Medicine, University of Cape Town, Rondebosch, Cape Town, South Africa.ORCID https://orcid.org/0000-0003-3084-7408
Nicki TiffinSouth African Medical Research Council Bioinformatics Unit, South African National Bioinformatics Institute, University of the Western Cape, Cape Town, South Africa.ORCID https://orcid.org/0000-0001-5083-2735

Funding

Validation and Application of a Model for Human-like TB Latency in RabbitsU19AI111276 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI ALLAND, DAVID, ELLNER, JERROLD J. · 2014 to 2020
$23.3M
Gates Foundation INV-037558NIAID NIH HHS U19 AI111276Wellcome Trust
6 · The paper itself

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.

Indexed as

African genetic dataElectronic routine health datagenotype dataH3Africa Illumina micro-arraypopulation admixtureresource-limited environmentstiered informed consentvirtual cohorts

Identifiers

PMID39925651
PMCPMC11806245

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.