SIRT1 gene, age-related diseases, and mortality:: The Leiden 85-plus Study

被引:67
|
作者
Kuningas, Maris [1 ,2 ]
Putters, Marielle [1 ]
Westendorp, Rudi G. J. [1 ]
Slagboorn, P. Eline [3 ]
van Heemst, Diana [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Gerontol & Geriatr, NL-2300 RC Leiden, Netherlands
[2] Univ Tartu, Inst Mol & Cell Biol, Dept Biotechnol, EE-50090 Tartu, Estonia
[3] Leiden Univ, Med Ctr, Dept Med Stat, Sect Mol Epidemiol, NL-2300 RC Leiden, Netherlands
关键词
D O I
10.1093/gerona/62.9.960
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The (Silent Information Regulator 2) Sir2 gene has been shown to regulate the life span of several model organisms. In mammals, the evolutionarily conserved homologue (Sirtuin 1) SIRT1 regulates neuroprotection, metabolism, and cell survival in response to stress. Based on these data, we hypothesized that SIRT1 might influence the prevalence of age-related diseases and modify the life span of humans. In order to test this, we genotyped five single nucleotide polymorphisms (SNPs) in 1245 participants of the population-based Leiden 85-plus Study. SIRT1 haplotypes were assessed and tested for association with the risks of mortality, metabolic profile, age-related diseases, and cognitive functioning. These analyses revealed a trend for lower cardiovascular mortality for haplotype 2 and rs3758391. SNP carriers. In further analyses, this trend was not supported by intermediate phenotypes, albeit the rs3758391 T-allele carriers had better cognitive functioning. In conclusion, our results indicate a role for SIRT1 in cognitive functioning, but the role in life span remains to be elucidated.
引用
收藏
页码:960 / 965
页数:6
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