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Susceptibility Loci for Type 2 Diabetes in the Ethnically Endogamous Indian Sindhi Population: A Pooled Blood Genome-Wide Association Study.

Pipal KV, Mamtani M, Patel AA et al.

35893037 PubMed ID
GWAS Study Type
1402 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PK
Pipal KV
MM
Mamtani M
PA
Patel AA
JS
Jaiswal SG
JM
Jaisinghani MT
KH
Kulkarni H
Chapter II

Abstract

Summary of the research findings

Type 2 diabetes (T2D) is a complex metabolic derangement that has a strong genetic basis. There is substantial population-specificity in the association of genetic variants with T2D. The Indian urban Sindhi population is at a high risk of T2D. The genetic basis of T2D in this population is unknown. We interrogated 28 pooled whole blood genomes of 1402 participants from the Diabetes In Sindhi Families In Nagpur (DISFIN) study using Illumina's Global Screening Array. From a total of 608,550 biallelic variants, 140 were significantly associated with T2D after adjusting for comorbidities, batch effects, pooling error, kinship status and pooling variation in a random effects multivariable logistic regression framework. Of the 102 well-characterized genes that these variants mapped onto, 70 genes have been previously reported to be associated with T2D to varying degrees with known functional relevance. Excluding open reading frames, intergenic non-coding elements and pseudogenes, our study identified 22 novel candidate genes in the Sindhi population studied. Our study thus points to the potential, interesting candidate genes associated with T2D in an ethnically endogamous population. These candidate genes need to be fully investigated in future studies.

418 Sindhi ancestry cases from endogamous families, 984 Sindhi ancestry controls from endogamous families

Chapter III

Study Statistics

Key metrics and study information

1402
Total Participants
GWAS
Study Type
No
Replicated
South Asian
Ancestry
India
Recruitment Country
Chapter IV

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