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2
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Contribution of genetic polymorphisms on functional status at very old age: a gene-based analysis of 38 genes (311 SNPs) in the oxidative stress pathway.基因多态性对高龄功能状态的影响:基于氧化应激途径中38个基因(311个单核苷酸多态性)的分析
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10
Exploring the role of genetic variability and lifestyle in oxidative stress response for healthy aging and longevity.探讨遗传变异和生活方式在氧化应激反应中对健康衰老和长寿的作用。
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本文引用的文献

1
Cross-national differences in grip strength among 50+ year-old Europeans: results from the SHARE study.50岁及以上欧洲人的握力跨国差异:来自SHARE研究的结果。
Eur J Ageing. 2009 Aug 11;6(3):227-236. doi: 10.1007/s10433-009-0128-6. eCollection 2009 Sep.
2
Human longevity and variation in GH/IGF-1/insulin signaling, DNA damage signaling and repair and pro/antioxidant pathway genes: cross sectional and longitudinal studies.人类长寿与 GH/IGF-1/胰岛素信号、DNA 损伤信号和修复以及促/抗氧化途径基因的变化:横断面和纵向研究。
Exp Gerontol. 2012 May;47(5):379-87. doi: 10.1016/j.exger.2012.02.010. Epub 2012 Mar 3.
3
Further support to the uncoupling-to-survive theory: the genetic variation of human UCP genes is associated with longevity.进一步支持解偶联生存理论:人类 UCP 基因的遗传变异与长寿有关。
PLoS One. 2011;6(12):e29650. doi: 10.1371/journal.pone.0029650. Epub 2011 Dec 27.
4
Two variants located in the upstream enhancer region of human UCP1 gene affect gene expression and are correlated with human longevity.两个位于人 UCP1 基因上游增强子区域的变异体影响基因表达,并与人类长寿相关。
Exp Gerontol. 2011 Nov;46(11):897-904. doi: 10.1016/j.exger.2011.07.011. Epub 2011 Jul 30.
5
Frailty phenotypes in the elderly based on cluster analysis: a longitudinal study of two Danish cohorts. Evidence for a genetic influence on frailty.基于聚类分析的老年人衰弱表型:丹麦两个队列的纵向研究。基因对衰弱影响的证据。
Age (Dordr). 2012 Jun;34(3):571-82. doi: 10.1007/s11357-011-9257-x. Epub 2011 May 13.
6
A common polymorphism in the UCP3 promoter influences hand grip strength in elderly people.UCP3 启动子中的常见多态性影响老年人的握力。
Biogerontology. 2011 Jun;12(3):265-71. doi: 10.1007/s10522-011-9321-z. Epub 2011 Feb 20.
7
Comprehensive fine mapping of chr12q12-14 and follow-up replication identify activin receptor 1B (ACVR1B) as a muscle strength gene.全面精细定位 chr12q12-14,并进行后续复制,确定激活素受体 1B(ACVR1B)为肌肉力量基因。
Eur J Hum Genet. 2011 Feb;19(2):208-15. doi: 10.1038/ejhg.2010.173. Epub 2010 Nov 10.
8
Mitochondrial uncoupling and lifespan.线粒体解偶联与寿命。
Mech Ageing Dev. 2010 Jul-Aug;131(7-8):463-72. doi: 10.1016/j.mad.2010.03.010. Epub 2010 Apr 2.
9
Commonly studied polymorphisms in inflammatory cytokine genes show only minor effects on mortality and related risk factors in nonagenarians.在 90 岁以上的人群中,常见的炎症细胞因子基因多态性研究仅显示出对死亡率和相关危险因素的微小影响。
J Gerontol A Biol Sci Med Sci. 2010 Mar;65(3):225-35. doi: 10.1093/gerona/glp210. Epub 2010 Jan 18.
10
Variation in the UCP2 and UCP3 genes associates with abdominal obesity and serum lipids: the Finnish Diabetes Prevention Study.UCP2和UCP3基因变异与腹型肥胖及血脂相关:芬兰糖尿病预防研究
BMC Med Genet. 2009 Sep 21;10:94. doi: 10.1186/1471-2350-10-94.

UCP3 多态性、握力表现与老年生存:两项丹麦中老年队列的关联分析。

UCP3 polymorphisms, hand grip performance and survival at old age: association analysis in two Danish middle aged and elderly cohorts.

机构信息

Department of Cell Biology, University of Calabria, Ponte Pietro Bucci cubo 4C, 87036 Rende (CS), Italy.

出版信息

Mech Ageing Dev. 2012 Aug;133(8):530-7. doi: 10.1016/j.mad.2012.06.004. Epub 2012 Jun 26.

DOI:10.1016/j.mad.2012.06.004
PMID:22743239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3629378/
Abstract

An efficient uncoupling process is generally considered to have a protective effect on the aging muscle by slowing down its age-related decay. Genetic polymorphisms in the Uncoupling Protein 3 (UCP3) gene, whose product is mainly expressed in skeletal muscle, were suggested to be associated with hand grip (HG) performances in elderly populations. Considering the population specificity of the quality of aging, we aimed to add further support to this evidence by analyzing the association between four SNPs in the UCP3 gene and relative haplotypes in two large cohorts of middle aged (N=708) and oldest old Danes (N=908). We found that the variability at rs1685354 and rs11235972 was associated with HG levels both at single and haplotypic level in both cohorts. Furthermore, taking advantage of large cohort and period survival data of the oldest cohort, we tested the association of each SNP with survival at 10years from the baseline visit. Interestingly, we found that allele A at rs11235972, associated in this cohort with lowest HG scores, influences also the survival patterns, with people carrying this allele showing higher mortality rates. On the whole, our work supports the role of UCP3 gene in functional status and survival at old age.

摘要

一种有效的解偶联过程通常被认为对衰老肌肉具有保护作用,可减缓其与年龄相关的衰退。解偶联蛋白 3(UCP3)基因的遗传多态性,其产物主要在骨骼肌中表达,被认为与老年人群的手握力(HG)表现有关。考虑到衰老质量的人群特异性,我们旨在通过分析 UCP3 基因中的四个单核苷酸多态性(SNP)与两个丹麦中年(N=708)和最年长队列(N=908)中相对单倍型之间的关联,为这一证据提供更多支持。我们发现,rs1685354 和 rs11235972 的变异性与两个队列中单倍型和单倍型水平的 HG 水平均相关。此外,利用最大队列和最长队列的生存数据,我们测试了每个 SNP 与基线随访 10 年后生存的关联。有趣的是,我们发现,与该队列中 HG 评分最低相关的 rs11235972 等位基因 A 也影响了生存模式,携带该等位基因的人死亡率更高。总的来说,我们的工作支持 UCP3 基因在功能状态和老年生存中的作用。