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Genes associated with Type 2 Diabetes and vascular complications
Author(s) -
Alberto Montesanto,
Anna Rita Bonfigli,
Paolina Crocco,
Paolo Garagnani,
María De Luca,
Massimo Boemi,
Elena Marasco,
Chiara Pirazzini,
Cristina Giuliani,
Claudio Franceschi,
Giuseppe Passarino,
Roberto Testa,
Fabiola Olivieri,
Giuseppina Rose
Publication year - 2018
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.101375
Subject(s) - type 2 diabetes , single nucleotide polymorphism , diabetes mellitus , candidate gene , genetic predisposition , medicine , nephropathy , bioinformatics , diabetic retinopathy , biology , disease , endocrinology , gene , genetics , genotype
Type 2 Diabetes (T2D) is a chronic disease associated with a number of micro- and macrovascular complications that increase the morbidity and mortality of patients. The risk of diabetic complications has a strong genetic component. To this end, we sought to evaluate the association of 40 single nucleotide polymorphisms (SNPs) in 21 candidate genes with T2D and its vascular complications in 503 T2D patients and 580 healthy controls. The genes were chosen because previously reported to be associated with T2D complications and/or with the aging process. We replicated the association of T2D risk with I GF2BP rs4402960 and detected novel associations with TERT rs2735940 and rs2736098. The addition of these SNPs to a model including traditional risk factors slightly improved risk prediction. After stratification of patients according to the presence/absence of vascular complications, we found significant associations of variants in the CAT , FTO , and UCP1 genes with diabetic retinopathy and nephropathy. Additionally, a variant in the ADIPOQ gene was found associated with macrovascular complications. Notably, these genes are involved in some way in mitochondrial biology and reactive oxygen species regulation. Hence, our findings strongly suggest a potential link between mitochondrial oxidative homeostasis and individual predisposition to diabetic vascular complications.

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