Evidence map›Paper›PMID 26635871›Full record

ArticleFrontiers in genetics2015

Evaluation of Genome Wide Association Study Associated Type 2 Diabetes Susceptibility Loci in Sub Saharan Africans.

Adebowale A Adeyemo, Fasil Tekola-Ayele, Ayo P Doumatey, Amy R Bentley, Guanjie Chen, Hanxia Huang, Jie Zhou, Daniel Shriner, Olufemi Fasanmade, Godfrey Okafor and 15 more

Abstract read
In one paragraph

Article in Frontiers in genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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

40 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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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

25 authors.

Adebowale A AdeyemoCenter for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.
Fasil Tekola-AyeleCenter for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.
Ayo P DoumateyCenter for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.
Amy R BentleyCenter for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.
Guanjie ChenCenter for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.
Hanxia HuangCenter for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.
Jie ZhouCenter for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.
Daniel ShrinerCenter for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.
Olufemi FasanmadeDepartment of Medicine, University of Lagos Lagos, Nigeria.
Godfrey OkaforDepartment of Medicine, University of Nigeria Teaching Hospital Enugu, Nigeria.
Benjamin EghanDepartment of Medicine, University of Science and Technology Kumasi, Ghana.
Kofi Agyenim-BoatengDepartment of Medicine, University of Science and Technology Kumasi, Ghana.
Jokotade AdeleyeDepartment of Medicine, College of Medicine, University of Ibadan Ibadan, Nigeria.
Williams BalogunDepartment of Medicine, College of Medicine, University of Ibadan Ibadan, Nigeria.
Abdel ElkahlounNational Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.
Settara ChandrasekharappaNational Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.
Samuel OwusuDepartment of Medicine and Therapeutics, University of Ghana Medical School Accra, Ghana.
Albert AmoahDepartment of Medicine and Therapeutics, University of Ghana Medical School Accra, Ghana.
Joseph AcheampongDepartment of Medicine, University of Science and Technology Kumasi, Ghana.
Thomas JohnsonDepartment of Medicine, University of Lagos Lagos, Nigeria.
Johnnie OliDepartment of Medicine, University of Nigeria Teaching Hospital Enugu, Nigeria.
Clement AdebamowoInstitute of Human Virology, School of Medicine, University of Maryland Baltimore, MD, USA.
Francis CollinsNational Institutes of Health Bethesda, MD, USA.
Georgia DunstonNational Human Genome Center at Howard University Washington, DC, USA.
Charles N RotimiCenter for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health Bethesda, MD, USA.

Funding

Genetic epidemiology of complex diseasesZIAHG200362 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI ROTIMI, CHARLES · 2009 to 2025
$54.7M
Genetic analysis of type II diabetes in Finnish populationZIAHG000024 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI ERDOS, MICHAEL · 2009 to 2025
$38.2M
PROTEOMICS CORE FACILITYG12MD007597 · NIMHD · HOWARD UNIVERSITY · PI SOUTHERLAND, WILLIAM M. · 2012 to 2018
$14.8M
POSITIONAL CLONING OF THE MEN1 GENEZIAHG000029 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI CHANDRASEKHARAPPA, SETTARA · 2009 to 2025
$13.3M
International Partnership for Interdisciplinary Research TrainingD43TW009112 · FIC · UNIVERSITY OF CHICAGO · PI OLOPADE, CHRISTOPHER O, OLOPADE, OLUFUNMILAYO F. · 2012 to 2016
$1.1M
STUDIES OF THE NATURAL HISTORY AND TREATMENT OF CHRONIC HEPATITIS BZ01DK054001 · NIDDK · DIABETES, DIGESTIVE, KIDNEY DISEASES · PI HOOFNAGLE, JAY H. · 1992 to 2005
–
MINORITY INTERNATIONAL RESEARCH TRAINING GRANTT37TW000041 · FIC · HOWARD UNIVERSITY · PI ADAMS-CAMPBELL, LUCILE L · 1993 to 1998
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FIC NIH HHS D43 TW009112FIC NIH HHS T37 TW000041Intramural NIH HHS Z01 DK054001Intramural NIH HHS ZIA HG200362NIMHD NIH HHS G12 MD007597
6 · The paper itself

Abstract

Genome wide association studies (GWAS) for type 2 diabetes (T2D) undertaken in European and Asian ancestry populations have yielded dozens of robustly associated loci. However, the genomics of T2D remains largely understudied in sub-Saharan Africa (SSA), where rates of T2D are increasing dramatically and where the environmental background is quite different than in these previous studies. Here, we evaluate 106 reported T2D GWAS loci in continental Africans. We tested each of these SNPs, and SNPs in linkage disequilibrium (LD) with these index SNPs, for an association with T2D in order to assess transferability and to fine map the loci leveraging the generally reduced LD of African genomes. The study included 1775 unrelated Africans (1035 T2D cases, 740 controls; mean age 54 years; 59% female) enrolled in Nigeria, Ghana, and Kenya as part of the Africa America Diabetes Mellitus (AADM) study. All samples were genotyped on the Affymetrix Axiom PanAFR SNP array. Forty-one of the tested loci showed transferability to this African sample (p < 0.05, same direction of effect), 11 at the exact reported SNP and 30 others at SNPs in LD with the reported SNP (after adjustment for the number of tested SNPs). TCF7L2 SNP rs7903146 was the most significant locus in this study (p = 1.61 × 10(-8)). Most of the loci that showed transferability were successfully fine-mapped, i.e., localized to smaller haplotypes than in the original reports. The findings indicate that the genetic architecture of T2D in SSA is characterized by several risk loci shared with non-African ancestral populations and that data from African populations may facilitate fine mapping of risk loci. The study provides an important resource for meta-analysis of African ancestry populations and transferability of novel loci.

Indexed as

fine-mappinggenetic associationreplicationsub Saharan Africatype 2 diabetes

Identifiers

PMID26635871
PMCPMC4656823

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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.