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虚弱的代谢谱分析、与2型糖尿病的关联以及与遗传易感性的相互作用。

Metabolic profiling of frailty, associations with type 2 diabetes and interaction with genetic susceptibility.

作者信息

Wang Yuxiang, Chen Shuang, Li Yue, Lu Qi, Li Rui, Chen Jun-Xiang, Zhang Ji-Juan, Yu Hancheng, Xu Hanrui, Xie Jinchi, Li Xianli, Liu Gang, Pan An, Geng Tingting, Liao Yun-Fei

机构信息

Department of Endocrinology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.

Department of Epidemiology and Biostatistics, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.

出版信息

Cardiovasc Diabetol. 2025 May 24;24(1):226. doi: 10.1186/s12933-025-02776-8.

Abstract

BACKGROUND

Individuals with frailty are at increased risk of type 2 diabetes (T2D), but the underlying mechanisms are unclear. We aimed to investigate whether the frailty-T2D association is mediated by alterations in the metabolome and assess potential interaction with genetic susceptibility to diabetes.

METHODS

This retrospective analysis, using data from a large prospective population-based cohort, included a total of 197,502 adults with baseline metabolomics data from the UK Biobank. Frailty was defined using the Fried frailty phenotype according to five components. Elastic net regression was applied to create a frailty-related metabolic signature. We assessed hazard ratios (HR) and its 95% confidence interval (CI) of incident T2D in relation to the baseline metabolic signature of frailty and examined the mediating role of the metabolic signature in the effect of frailty on T2D. Additive interaction between the metabolic signature and polygenic risk score for T2D (PRS-T2D) on the incidence of T2D was assessed as relative excess risk due to interaction (RERI).

RESULTS

Compared with non-frailty, the HR (95% CI) of incident T2D in pre-frailty and frailty was 1.33 (1.26, 1.40) and 1.59 (1.46, 1.74), respectively. The metabolic signature of frailty (comprised of 53 metabolites) was positively associated with T2D risk (HR per standard deviation increment: 1.45; 95% CI: 1.42, 1.48), and explained 31.0% (95% CI: 25.8, 36.8) of the association between frailty and T2D. An additive interaction between metabolic signature of frailty and PRS-T2D was found (RERI: 9.43; 95% CI: 6.06, 12.80).

CONCLUSIONS

The increased risk of T2D in individuals with frailty may be mediated through effects on the metabolome, and the influence of such metabolic alterations on diabetes risk may be amplified in individuals with genetic susceptibility to T2D.

摘要

背景

虚弱个体患2型糖尿病(T2D)的风险增加,但其潜在机制尚不清楚。我们旨在研究虚弱与T2D之间的关联是否由代谢组改变介导,并评估与糖尿病遗传易感性的潜在相互作用。

方法

这项回顾性分析使用了来自一个大型前瞻性人群队列的数据,共纳入了197,502名来自英国生物银行且有基线代谢组学数据的成年人。根据五个组成部分,使用Fried虚弱表型定义虚弱。应用弹性网络回归创建与虚弱相关的代谢特征。我们评估了与虚弱基线代谢特征相关的T2D发病风险比(HR)及其95%置信区间(CI),并研究了代谢特征在虚弱对T2D影响中的中介作用。评估了虚弱代谢特征与T2D多基因风险评分(PRS-T2D)之间对T2D发病率的相加相互作用,作为交互作用导致的相对超额风险(RERI)。

结果

与非虚弱个体相比,虚弱前期和虚弱个体发生T2D的HR(95%CI)分别为1.33(1.26,1.40)和1.59(1.46,1.74)。虚弱的代谢特征(由53种代谢物组成)与T2D风险呈正相关(每标准差增加的HR:1.45;95%CI:1.42,1.48),并解释了虚弱与T2D之间关联的31.0%(95%CI:25.8,36.8)。发现虚弱代谢特征与PRS-T2D之间存在相加相互作用(RERI:9.43;95%CI:6.06,12.80)。

结论

虚弱个体患T2D风险的增加可能通过对代谢组的影响介导,并且这种代谢改变对糖尿病风险的影响在具有T2D遗传易感性的个体中可能会被放大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2fe/12102881/83be70ef66ed/12933_2025_2776_Fig1_HTML.jpg

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