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Common variants in SIRT1 and human longevity in a Chinese population

Rong Lin, Dongjing Yan, Yunxia Zhang, Xiaoping Liao, Gu Gong, Junjie Hu, Yun‐Xin Fu, Wangwei Cai

BMC Medical Genetics · 2016 · ▲ 23 citations

Abstract

BACKGROUND: The silent information regulator SIR2/SIRT1gene has been demonstrated as regulating lifespan in many model organisms, including yeast, worms, fruit flies and rodents. SIRT1, the human homolog of SIR2, is considered a candidate gene as a modifier of human life expectancy. METHODS: In the current study we included 616 long-lived individuals and 846 matched younger controls to investigate associations between 8 common single nucleotide polymorphisms (SNPs) (i.e., rs12778366, rs3758391, rs3740051, rs33957861, rs7896005, rs12413112, rs11599176 and rs4746720) in the SIRT1 gene and human longevity. RESULTS: The 8 SNPs had strong linkage disequilibrium (LD) and were in an LD block, which was characterized by 4 common haplotypes that capture 99.3% of the genetic variation present within it. We found no evidence for statistically significant associations between the tested SIRT1 SNPs and longevity at the allele, genotype or haplotype levels. CONCLUSIONS: Current findings show that several common variants in SIRT1 are not associated with human longevity.

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Provenance

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OpenAlex
DOI
10.1186/s12881-016-0293-3
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2026-10-23 MST

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APA
Lin, R., Yan, D., Zhang, Y., Liao, X., Gong, G., Hu, J., Fu, Y., &amp; Cai, W. (2016). Common variants in SIRT1 and human longevity in a Chinese population. <em>BMC Medical Genetics</em>. https://doi.org/10.1186/s12881-016-0293-3
Vancouver
Lin R, Yan D, Zhang Y, Liao X, Gong G, Hu J, et al. Common variants in SIRT1 and human longevity in a Chinese population. BMC Medical Genetics. 2016. doi:10.1186/s12881-016-0293-3.
BibTeX
@article{rong2016Common, title = {Common variants in SIRT1 and human longevity in a Chinese population}, author = {Rong Lin and Dongjing Yan and Yunxia Zhang and Xiaoping Liao and Gu Gong and Junjie Hu and Yun‐Xin Fu and Wangwei Cai}, journal = {BMC Medical Genetics}, year = {2016}, doi = {10.1186/s12881-016-0293-3}, }

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