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Genetics of diabetic kidney disease: A follow-up study in the Arab population of the United Arab Emirates.
- Source :
-
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2019 Dec; Vol. 7 (12), pp. e985. Date of Electronic Publication: 2019 Sep 30. - Publication Year :
- 2019
-
Abstract
- Background: Two genome-wide association studies in European and Japanese populations reported on new loci for diabetic kidney disease (DKD), including FTO. In this study, we have replicated these investigations on a cohort of 410 Type 2 diabetes mellitus (T2DM) patients of Arab origin from the United Arab Emirates (UAE).<br />Methods and Results: The cohort included 145 diabetic patients diagnosed with DKD and 265 diabetics free of the disease. In general, we were able to confirm the association between the FTO locus and DKD, as reported in the Japanese population. Specifically, there were significant associations with two single nucleotide polymorphisms (SNPs), namely rs1421086 (p = .013, OR = 1.52 depending on allele G, 95% CI: 1.09-2.11) and rs17817449 (p = .0088, OR = 1.55 depending on allele C, 95% CI: 1.12-2.14) of the FTO locus. Both SNPs were in linkage disequilibrium with rs56094641, also as reported in the Japanese population. While the alleles of both SNPs, which increase the risk of DKD, were associated with higher Body Mass Index (BMI), their associations with DKD were independent of the BMI effects.<br />Conclusions: This study confirms that FTO is a multiethnic locus for DKD which is independent from any influence of BMI and/or obesity.<br /> (© 2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc.)
- Subjects :
- Aged
Body Mass Index
Case-Control Studies
Cross-Sectional Studies
Female
Genetic Association Studies
Humans
Linkage Disequilibrium
Male
Middle Aged
United Arab Emirates ethnology
Alpha-Ketoglutarate-Dependent Dioxygenase FTO genetics
Arabs genetics
Diabetic Nephropathies genetics
Polymorphism, Single Nucleotide
Subjects
Details
- Language :
- English
- ISSN :
- 2324-9269
- Volume :
- 7
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Molecular genetics & genomic medicine
- Publication Type :
- Academic Journal
- Accession number :
- 31568687
- Full Text :
- https://doi.org/10.1002/mgg3.985