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基于人群的前瞻性研究(特雷维索长寿研究--TRELONG)表明,胰岛素样生长因子 1 受体多态性 rs2229765 和循环白细胞介素-6 水平影响男性的长寿。

Insulin-like growth factor 1 receptor polymorphism rs2229765 and circulating interleukin-6 level affect male longevity in a population-based prospective study (Treviso Longeva--TRELONG).

机构信息

Department of Neuroscience, "Mario Negri" Institute for Pharmacological Research, via La Masa, Milan, Italy.

出版信息

Aging Male. 2011 Dec;14(4):257-64. doi: 10.3109/13685538.2011.607521.

Abstract

Insulin-like growth factor 1 (IGF-1) signaling modulation has been associated with increased lifespan in model organisms, while high levels of circulating interleukin-6 (IL-6) are a marker of disability and mortality. In the prospective, population-based "Treviso Longeva"--TRELONG Study from Italy (n = 668, age range 70-105.5 years at baseline, followed for seven years) we investigated the effects of survival on the IGF-1 receptor (IGF-1R) gene polymorphism rs2229765, the IL-6 gene promoter polymorphism rs1800795, and plasma concentrations of IGF-1 and IL-6, alone or in combination. We found a sex-dependent effect for the IGF-1R rs2229765 polymorphism, as male carriers of the homozygous A/A genotype survived longer, while the IL-6 rs1800795 genotype did not influence overall or sex-specific longevity. Higher IL-6 levels were more detrimental for survival among males than females, while IGF-1 had no dose-response effect. These findings sustain the hypothesis that sex-specific longevity relies on detectable differences in genetic and biochemical parameters between males and females.

摘要

胰岛素样生长因子 1(IGF-1)信号转导的调节与模型生物寿命的延长有关,而循环白细胞介素 6(IL-6)水平升高是残疾和死亡的标志。在来自意大利的前瞻性、基于人群的“特雷维索长寿”--TRELONG 研究中(n = 668,基线时年龄范围为 70-105.5 岁,随访 7 年),我们研究了生存对 IGF-1 受体(IGF-1R)基因多态性 rs2229765、IL-6 基因启动子多态性 rs1800795 以及 IGF-1 和 IL-6 血浆浓度的影响,单独或联合。我们发现 IGF-1R rs2229765 多态性存在性别依赖性效应,因为纯合 A/A 基因型的男性携带者存活时间更长,而 IL-6 rs1800795 基因型并不影响整体或性别特异性长寿。较高的 IL-6 水平对男性的生存影响大于女性,而 IGF-1 没有剂量反应效应。这些发现支持这样一种假设,即性别特异性长寿依赖于男性和女性之间遗传和生化参数的可检测差异。

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