SIRT1 genetic variation and mortality in type 2 diabetes: interaction with smoking and dietary niacin

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Abstract

SIRT1 protects cells against oxidative stress and aging. Its activity may be modulated by dietary niacin (vitamin 133) intake. We studied the association of SIRT1 genetic variation with mortality in subjects with increased oxidative stress (type 2 diabetes and smokers) in relation to dietary niacin. In 4573 participants from the Rotterdam Study, including 413 subjects with prevalent and 378 with incident type 2 diabetes, three SIRT1 tagging SNPs were genotyped and all-cause mortality was studied (average follow-up] 2 years). We found no association between SIRT1 variation and mortality in the total population or in smokers. In subjects with prevalent type 2 diabetes, homozygous carriers of the most common SIRT1 haplotype, 1, had 1.5 times (95%Cl 1.1-2.1) increased Mortality Fisk compared to noncarriers. This risk further increased among smokers and those with low niacin intake. In the lowest tertile of niacin intake, mortality risk was increased 2.3 (95%Cl 1.1-4.9) and 5.7 (95%CI 2.5-13.1) times for heterozygous and homozygous carriers of haplotype 1. Subjects with incident diabetes showed similar findings but only when they smoked. We conclude that in subjects with type 2 diabetes, SIRT1 genetic variation influences survival in interaction with dietary niacin and smoking. Correction of niacin deficiency and SIRT1 modulators may prolong the life span of patients with diabetes. (c) 2009 Elsevier Inc. All rights reserved.
Original languageUndefined/Unknown
Pages (from-to)836-841
Number of pages6
JournalFree Radical Biology and Medicine
Volume46
Issue number6
DOIs
Publication statusPublished - 2009

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