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Genome-wide association study and polygenic score assessment of insulin resistance.

Authors :
Aliyu, Usama
Umlai, Umm-Kulthum Ismail
Toor, Salman M.
Elashi, Asma A.
Al-Sarraj, Yasser A.
Abou-Samra, Abdul Badi
Suhre, Karsten
Albagha, Omar M. E.
Source :
Frontiers in Endocrinology; 2024, p1-11, 11p
Publication Year :
2024

Abstract

Insulin resistance (IR) and beta cell dysfunction are the major drivers of type 2 diabetes (T2D). Genome-Wide Association Studies (GWAS) on IR have been predominantly conducted in European populations, while Middle Eastern populations remain largely underrepresented. We conducted a GWAS on the indices of IR (HOMA2-IR) and beta cell function (HOMA2-%B) in 6,217 nondiabetic individuals from the Qatar Biobank (QBB; Discovery cohort; n = 2170, Replication cohort; n = 4047) with and without body mass index (BMI) adjustment. We also developed polygenic scores (PGS) for HOMA2-IR and compared their performance with a previously derived PGS for HOMA-IR (PGS003470). We replicated 11 loci that have been previously associated with HOMA-IR and 24 loci that have been associated with HOMA-%B, at nominal statistical significance. We also identified a novel locus associated with beta cell function near VEGFC gene, tagged by rs61552983 (P = 4.38 × 10<superscript>-8</superscript>). Moreover, our best performing PGS (Q-PGS4; Adj R² = 0.233 ± 0.014; P = 1.55 x 10<superscript>-3</superscript>) performed better than PGS003470 (Adj R² = 0.194 ± 0.014; P = 5.45 x 10<superscript>-2</superscript>) in predicting HOMA2-IR in our dataset. This is the first GWAS on HOMA2 and the first GWAS conducted in the Middle East focusing on IR and beta cell function. Herein, we report a novel locus in VEGFC that is implicated in beta cell dysfunction. Inclusion of under-represented populations in GWAS has potentials to provide important insights into the genetic architecture of IR and beta cell function. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16642392
Database :
Complementary Index
Journal :
Frontiers in Endocrinology
Publication Type :
Academic Journal
Accession number :
178112005
Full Text :
https://doi.org/10.3389/fendo.2024.1384103