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循环中的生长分化因子11(GDF11)水平会随着年龄增长而降低,但在肥胖和2型糖尿病患者中保持不变。

Circulating GDF11 levels are decreased with age but are unchanged with obesity and type 2 diabetes.

作者信息

Añón-Hidalgo Juan, Catalán Victoria, Rodríguez Amaia, Ramírez Beatriz, Silva Camilo, Galofré Juan C, Salvador Javier, Frühbeck Gema, Gómez-Ambrosi Javier

机构信息

Metabolic Research Laboratory, Clínica Universidad de Navarra, Pamplona, Spain.

CIBER Fisiopatología de la Obesidad y Nutrición (CIBEROBN), Instituto de Salud Carlos III, Pamplona, Spain.

出版信息

Aging (Albany NY). 2019 Mar 21;11(6):1733-1744. doi: 10.18632/aging.101865.

Abstract

Growth differentiation factor 11 (GDF11) is a member of the transforming growth factor β (TGFβ) superfamily which declines with age and exerts anti-aging regenerative effects in skeletal muscle in mice. However, recent data in humans and mice are conflicting casting doubts about its true functional actions. The aim of the present study was to compare the circulating concentrations of GDF11 in individuals of different ages as well as body weight and glycemic status. Serum concentrations of GDF11 were measured by ELISA in 319 subjects. There was a significant increase in GDF11 concentrations in people in the 41-50 y group and a decline in the elder groups (61-70 and 71-80 y groups, =0.008 for the comparison between all age groups). However, no significant correlation between fat-free mass index (FFMI), a formula used to estimate the amount of muscle mass in relation to height, and logGDF11 was observed (=0.08, =0.197). Moreover, no significant differences in circulating concentrations of GDF11 regarding obesity or glycemic status were found. Serum GDF11 concentrations in humans decrease in older ages being unaltered in obesity and T2D. Further studies should determine the exact pathophysiological role of GDF11 in aging.

摘要

生长分化因子11(GDF11)是转化生长因子β(TGFβ)超家族的成员,其水平随年龄增长而下降,并在小鼠骨骼肌中发挥抗衰老再生作用。然而,最近在人类和小鼠中的数据相互矛盾,令人对其真正的功能作用产生怀疑。本研究的目的是比较不同年龄、体重和血糖状态个体的循环GDF11浓度。采用酶联免疫吸附测定法(ELISA)测量了319名受试者的血清GDF11浓度。41 - 50岁组人群的GDF11浓度显著升高,而老年组(61 - 70岁和71 - 80岁组)则下降(所有年龄组之间比较,P = 0.008)。然而,未观察到用于估计与身高相关的肌肉量的无脂肪质量指数(FFMI)与logGDF11之间存在显著相关性(P = 0.08,r = 0.197)。此外,未发现肥胖或血糖状态对GDF11循环浓度有显著差异。人类血清GDF11浓度在老年时降低,在肥胖和2型糖尿病中未改变。进一步的研究应确定GDF11在衰老过程中的确切病理生理作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cd4/6461177/e5e0af5e36ae/aging-11-101865-g001.jpg

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