Polymorphisms in the superoxidase dismutase genes reveal no association with human longevity in Germans: a case-control association study

被引:9
作者
Gentschew, Liljana [1 ]
Flachsbart, Friederike [1 ]
Kleindorp, Rabea [1 ]
Badarinarayan, Nandini [1 ]
Schreiber, Stefan [1 ,2 ,3 ]
Nebel, Almut [1 ]
机构
[1] Univ Kiel, Inst Clin Mol Biol, D-24105 Kiel, Germany
[2] Univ Hosp Schleswig Holstein, Clin Internal Med 1, Kiel, Germany
[3] Univ Kiel, Popgen Biobank, D-24105 Kiel, Germany
关键词
SOD; Aging; Centenarians; SNP; Case-control association; GENOME-WIDE ASSOCIATION; LIFE-SPAN; OXIDATIVE STRESS; EXTREME LONGEVITY; NULL MUTATION; MN-SOD; DAMAGE; SURVIVAL; FOXO3A; AGE;
D O I
10.1007/s10522-013-9470-3
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 role of superoxide dismutases (SODs) in aging and oxidative stress regulation has been widely studied and there is growing evidence that imbalances in these processes influence lifespan in several species. In humans, genetic polymorphisms in SOD genes may play an important role in the development of age-related diseases and genetic variation in SOD2 is thought to be associated with longevity. These observations prompted us to perform a case-control association study using a comprehensive haplotype tagging approach for the three SOD genes (SOD1, SOD2, SOD3) by testing a total of 19 SNPs in our extensive collection of 1,612 long-lived individuals (centenarians and nonagenarians) and 1,104 younger controls. Furthermore, we intended to replicate the previous association of the SOD2 SNP rs4880 with longevity observed in a Danish cohort. In our study, no association was detected between the tested SNPs and the longevity phenotype, neither in the entire long-lived sample set nor in the centenarian subgroup analysis. Our results suggest that there is no considerable influence of sequence variation in the SOD genes on human longevity in Germans.
引用
收藏
页码:719 / 727
页数:9
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