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Metabolic Signature of Insulin Resistance and Risk of Alzheimer's Disease.

JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES(2025)

Rovira i Virgili Univ URV | Univ Int Catalunya UIC | Pablo Olavide Univ UPO

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Abstract
Background Substantial evidence supports the relationship between peripheral insulin resistance (IR) and the development of Alzheimer's disease (AD)-dementia. However, the mechanisms explaining these associations are only partly understood. We aimed to identify a metabolic signature of IR associated with the progression from mild cognitive impairment (MCI) to AD-dementia. Methods This is a case-control study on 400 MCI subjects, free of type 2 diabetes, within the ACE cohort, including individuals ATN + and ATN-. After a median of 2.1 years of follow-up, 142 subjects converted to AD-dementia. IR was assessed using the homeostasis model assessment for insulin resistance (HOMA-IR). A targeted multiplatform approach profiled over 600 plasma metabolites. Elastic net penalized linear regression with 10-fold cross-validation was employed to select those metabolites associated with HOMA-IR. The prediction ability of the signature was assessed using support vector machine and performance metrics. The metabolic signature was associated with AD-dementia risk using a multivariable Cox regression model. Using counterfactual-based mediation analysis, we investigated the mediation role of the metabolic signature between HOMA-IR and AD-dementia. The metabolic pathways in which the metabolites were involved were identified using MetaboAnalyst. Results The metabolic signature comprised 18 metabolites correlated with HOMA-IR. After adjustments by confounders, the signature was associated with increased AD-dementia risk (HR = 1.234; 95% CI = 1.019-1.494; p < .05). The metabolic signature mediated 35% of the total effect of HOMA-IR on AD-dementia risk. Significant metabolic pathways were related to glycerophospholipid and tyrosine metabolism. Conclusions We have identified a blood-based metabolic signature that reflects IR and may enhance our understanding of the biological mechanisms through which IR affects AD-dementia.
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Biomarkers,Blood,Dementia,Metabolomics
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要点】:本研究发现了一种与胰岛素抵抗相关的血液代谢特征,该特征与轻度认知障碍向阿尔茨海默病痴呆的进展有关,并介导了胰岛素抵抗对阿尔茨海默病痴呆风险的部分影响。

方法】:研究采用弹性网惩罚线性回归和10倍交叉验证方法,在无2型糖尿病的400名轻度认知障碍参与者中,分析超过600种血浆代谢物,以确定与胰岛素抵抗相关的代谢特征。

实验】:在一项针对ACE队列中ATN+和ATN-的轻度认知障碍个体的病例对照研究中,经过2.1年的中位随访,142名参与者发展为阿尔茨海默病痴呆。实验使用了弹性网回归和交叉验证来识别代谢特征,并通过支持向量机评估了其预测能力,同时使用多变量Cox回归模型和反事实中介分析来评估代谢特征与阿尔茨海默病痴呆风险之间的关系。结果显示,该代谢特征包含了18种与HOMA-IR相关的代谢物,并与阿尔茨海默病痴呆风险增加相关(HR = 1.234; 95% CI = 1.019-1.494; p < .05)。该代谢特征介导了胰岛素抵抗对阿尔茨海默病痴呆风险总效应的35%。显著代谢途径与甘油磷脂和酪氨酸代谢相关。