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人类长寿与 11p15.5:对 1321 名百岁老人的研究。

Human longevity and 11p15.5: a study in 1321 centenarians.

机构信息

Centro Interdipartimentale 'L.Galvani' per Studi Integrati di Bioinformatica, Biofisica e Biocomplessità - Alma Mater Studiorum Università di Bologna, Italy.

出版信息

Eur J Hum Genet. 2009 Nov;17(11):1515-9. doi: 10.1038/ejhg.2009.54. Epub 2009 Apr 15.

Abstract

The 11p15.5 chromosomal region (2.8 Mb) is of particular interest as it encloses five genes (HRAS1, SIRT3, TH, INS and IGF2), the variability of which was found to be associated with life extension by association studies. Mostly important, the above genes are homologous of genes that modulate lifespan in model organisms. We scanned the area in four European sample groups for a total of 1321 centenarians and 1140 younger subjects, who shared with centenarians ethnicity and geographical origin, with a set of 239 SNPs. No significant results (P<0.05) have been found on the earlier associated loci (ie, TH, IGF2, INS and HRAS1), and this study could not confirm the earlier findings on each of those genes. A meta-analysis was carried out on the SIRT3 SNP data; a total number of 2461 samples were included, but no positive association was found except for one SNP having a significant effect (rs939915). The same meta-analysis approach has been applied to the other 229 markers, and six SNPs have been found significant for the frequent genotype (rs4073591, DEAF1-rs4073590, KRTAP5-6-rs11040489, rs4930001, TSPAN32-rs800140 and rs16928120). This experience, although unable to confirm the earlier findings of the literature, highlights all the common difficulties of such studies in human longevity. Despite the rather negative findings presented here, the results derived from unprecedented studies involving such a large number of centenarians should be disseminated, thus contributing to set up adequate strategies to disentangle complex and likely heterogeneous phenotypes.

摘要

11p15.5 号染色体区域(2.8Mb)特别引人注目,因为它包含五个基因(HRAS1、SIRT3、TH、INS 和 IGF2),通过关联研究发现,这些基因的变异性与寿命延长有关。最重要的是,上述基因与调节模式生物寿命的基因具有同源性。我们在四个欧洲样本组中对该区域进行了扫描,共对 1321 名百岁老人和 1140 名年龄较小的受试者进行了检测,这些受试者与百岁老人具有相同的种族和地理来源,共检测了 239 个 SNP。在之前与这些基因相关的基因座(即 TH、IGF2、INS 和 HRAS1)上没有发现显著的结果(P<0.05),本研究无法证实之前关于这些基因的发现。对 SIRT3 SNP 数据进行了荟萃分析;共纳入了 2461 个样本,但除了一个具有显著影响的 SNP(rs939915)外,没有发现阳性关联。同样的荟萃分析方法也应用于其他 229 个标记物,发现了 6 个 SNP 与常见基因型显著相关(rs4073591、DEAF1-rs4073590、KRTAP5-6-rs11040489、rs4930001、TSPAN32-rs800140 和 rs16928120)。尽管这一经验无法证实文献中的早期发现,但它突出了人类长寿研究中此类研究的所有共同困难。尽管这里提出的结果相当消极,但应传播从前所未有的研究中获得的结果,这些研究涉及如此多的百岁老人,从而有助于制定适当的策略来理清复杂且可能异质的表型。

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本文引用的文献

2
The impact of mitochondrial DNA on human lifespan: a view from studies on centenarians.
Biotechnol J. 2008 Jun;3(6):740-9. doi: 10.1002/biot.200800046.
4
WHAP: haplotype-based association analysis.
Bioinformatics. 2007 Jan 15;23(2):255-6. doi: 10.1093/bioinformatics/btl580. Epub 2006 Nov 21.
6
The unusual genetics of human longevity.
Sci Aging Knowledge Environ. 2006 Jun 28;2006(10):pe20. doi: 10.1126/sageke.2006.10.pe20.
7
Multiple testing in the context of haplotype analysis revisited: application to case-control data.
Ann Hum Genet. 2005 Nov;69(Pt 6):747-56. doi: 10.1111/j.1529-8817.2005.00198.x.
8
Calorie restriction--the SIR2 connection.
Cell. 2005 Feb 25;120(4):473-82. doi: 10.1016/j.cell.2005.01.029.

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