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A genome-wide association study identifies genetic determinants of hemoglobin glycation index with implications across sex and ethnicity.
- Source :
-
Frontiers in endocrinology [Front Endocrinol (Lausanne)] 2024 Oct 28; Vol. 15, pp. 1473329. Date of Electronic Publication: 2024 Oct 28 (Print Publication: 2024). - Publication Year :
- 2024
-
Abstract
- Introduction: We investigated the genetic determinants of variation in the hemoglobin glycation index (HGI), an emerging biomarker for the risk of diabetes complications.<br />Methods: We conducted a genome-wide association study (GWAS) for HGI in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial ( N = 7,913) using linear regression and additive genotype encoding on variants with minor allele frequency greater than 3%. We conducted replication analyses of top findings in the Atherosclerosis Risk in Communities (ARIC) study with inverse variance-weighted meta-analysis. We followed up with stratified GWAS analyses by sex and self-reported race.<br />Results: In ACCORD, we identified single nucleotide polymorphisms (SNPs) associated with HGI, including a peak with the strongest association at the intergenic SNP rs73407935 (7q11.22) ( P = 5.8e-10) with a local replication in ARIC. In black individuals, the variant rs10739419 on chromosome 9 in the Whirlin ( WHRN ) gene formally replicated (meta- P = 2.2e-9). The SNP-based heritability of HGI was 0.39 ( P < 1e-10). HGI had significant sex-specific associations with SNPs in or near GALNT11 in women and HECW2 in men. Finally, in Hispanic participants, we observed genome-wide significant associations with variants near USF1 and NXNL2/SPIN1 .<br />Discussion: Many HGI-associated SNPs were distinct from those associated with fasting plasma glucose or HbA1c, lending further support for HGI as a distinct biomarker of diabetes complications. The results of this first evaluation of the genetic etiology of HGI indicate that it is highly heritable and point to heterogeneity by sex and race.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2024 House, Breeyear, Akhtari, Evans, Buse, Hempe, Doria, Mychaleckyi, Fonseca, Shi, Li, Liu, Kelly, Rotroff and Motsinger-Reif.)
- Subjects :
- Humans
Male
Female
Middle Aged
Sex Factors
Diabetes Mellitus, Type 2 genetics
Diabetes Mellitus, Type 2 metabolism
Ethnicity genetics
Aged
Biomarkers blood
Genotype
Genetic Predisposition to Disease
Genome-Wide Association Study
Polymorphism, Single Nucleotide
Glycated Hemoglobin analysis
Glycated Hemoglobin metabolism
Glycated Hemoglobin genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1664-2392
- Volume :
- 15
- Database :
- MEDLINE
- Journal :
- Frontiers in endocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 39530122
- Full Text :
- https://doi.org/10.3389/fendo.2024.1473329