Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity.

Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity.
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DOI:
10.1111/j.1474-9726.2009.00493.x
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发表时间:
2009-08
期刊:
影响因子:
7.8
通讯作者:
Study of Osteoporotic Fractures
Study of Osteoporotic Fractures
中科院分区:
生物学1区
文献类型:
--
作者:
Pawlikowska L;Hu D;Huntsman S;Sung A;Chu C;Chen J;Joyner AH;Schork NJ;Hsueh WC;Reiner AP;Psaty BM;Atzmon G;Barzilai N;Cummings SR;Browner WS;Kwok PY;Ziv E;Study of Osteoporotic Fractures

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胰岛素/IGF1信号通路影响几种模式生物的寿命,包括蠕虫、苍蝇和小鼠。为了研究该通路的常见遗传变异是否影响人类寿命,我们从骨质疏松性骨折(SOF)研究中选择了一组老年高加索女性,其中包括293例长寿患者(寿命≥92岁(y),平均±标准差(SD) = 95.3±2.2y)和603例平均寿命对照组(寿命≤79岁,平均=75.7±2.6y),对30个编码胰岛素/IGF1信号通路蛋白的基因中的291个常见变异进行了基因分型。使用单倍型标记方法选择变异进行基因分型。我们发现与寿命相关的变异数量适度过剩。然后,我们在另外两个包含男性和女性的高加索队列中复制了名义上显著的变异:心血管健康研究(CHS)和德系犹太人百岁老人(AJC)。在三个队列的荟萃分析中,AKT1 rs3803304的内含子单核苷酸多态性(SNP)与寿命显著相关(优势比(OR)=0.78(95%可信区间(CI)=0.68-0.89),调整后p=0.043);FOXO3A的两个内含子snp仅在女性中显示出显著的寿命相关性(rs1935949, OR=1.35, 95% CI=1.15-1.57,调整后p=0.0093)。结论:几种胰岛素/IGF1通路基因的常见变异与人类寿命有关。
The insulin/IGF1 signaling pathways affect lifespan in several model organisms, including worms, flies and mice. To investigate whether common genetic variation in this pathway influences lifespan in humans, we genotyped 291 common variants in 30 genes encoding proteins in the insulin/IGF1 signaling pathway in a cohort of elderly Caucasian women selected from the Study of Osteoporotic Fractures (SOF), including 293 long-lived cases (lifespan ≥ 92 years (y), mean ± standard deviation (SD) = 95.3 ± 2.2y) and 603 average-lifespan controls (lifespan ≤ 79y, mean=75.7 ± 2.6y). Variants were selected for genotyping using a haplotype tagging approach. We found a modest excess of variants nominally associated with longevity. We then replicated nominally significant variants in two additional Caucasian cohorts containing both males and females: the Cardiovascular Health Study (CHS) and Ashkenazi Jewish Centenarians (AJC). An intronic single nucleotide polymorphism (SNP) in AKT1, rs3803304, was significantly associated with lifespan in a meta-analysis across the three cohorts (odds ratio (OR)=0.78 (95% confidence interval (CI)=0.68-0.89), adjusted p=0.043); two intronic SNPs in FOXO3A demonstrated a significant lifespan association among women only (rs1935949, OR=1.35, 95% CI=1.15-1.57, adjusted p=0.0093). Conclusion: common variants in several insulin/IGF1 pathway genes are associated with human lifespan.
DOI: 10.1038/nature06258
发表时间: 2007-10-18
期刊: NATURE
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发表时间: 2006-04
期刊: PLOS BIOLOGY
影响因子: 9.8
作者:
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