Deciphering Lipidomics Landscape of Urine Extracellular Vesicles in Alcohol Use Disorder Patients

脂类学 脂质体 细胞外小泡 尿 酒精使用障碍 化学 饮酒量 脂质代谢 代谢组学 细胞外 胞外囊泡 生物化学 药理学 生物信息学 诊断生物标志物 医学 代谢组 酒精摄入量 生物标志物 生物流体 生物 脂泡
作者
Blanca Martín-Urdiales,Carla Perpiñá-Clérigues,Susana Mellado,Maura Rojas-Pirela,M. Sánchez,David Puertas-Miranda,Francisco García‐García,Miguel Marcos,María Pascual
出处
期刊:Journal of Proteome Research [American Chemical Society]
卷期号:24 (11): 5653-5663 被引量:1
标识
DOI:10.1021/acs.jproteome.5c00515
摘要

Urine extracellular vesicles (EVs) have garnered increasing interest in recent years, as their lipid content represents a promising source of noninvasive biomarkers. Alcohol use disorder (AUD) is one of the most common psychiatric disorders and is a major contributor to morbidity and mortality. Accordingly, there is growing interest in assessing prior alcohol consumption and evaluating the severity of liver or brain injury, particularly through noninvasive methods. In this study, we employed a novel approach based on urine EVs and a highly sensitive lipidomics strategy to characterize lipid species in male AUD patients as well as to evaluate the differential functional roles and enzymatic activity networks of urine EV lipids. Our results demonstrate, for the first time, that the lipidomic profiling of urine EVs in male AUD patients is characterized by an enrichment of fatty acyls and glycerophospholipids, with FA 22:0 emerging as a potential biomarker. Notably, increased acyl chain saturation and elevated levels of long-chain fatty acids (22-24 carbons) suggest links to AUD-associated inflammation, cancer, and metabolic dysfunction. These findings advance the understanding of the urine EV lipidome and may contribute to the identification of novel lipid targets and the development of noninvasive biomarkers in AUD.
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