血浆生物活性脂质对酒精使用障碍志愿者渴求的预测价值

IF 4 Q2 NEUROSCIENCES
Cristina Miliano , Luis A. Natividad , Susan Quello , Mike Stoolmiller , Ann M. Gregus , Matthew W. Buczynski , Barbara J. Mason
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引用次数: 0

摘要

背景酒精使用障碍(AUD)是一种慢性复发性疾病,其特点是不顾不良后果地寻求和饮用酒精。尽管有多种治疗方法,但患者的复发率仍然很高。因此,急需能识别渴求增加风险患者的生物标志物。越来越多的临床前和临床证据表明,生物活性脂质信号的干扰与 AUD 患者渴求的神经生物学有关。我们假设这些脂质是预测 AUD 患者酒精渴求的潜在生物标志物。方法本研究使用了 3 项 AUD 临床研究中 157 名参与者的去身份化临床档案数据和相应的血浆标本。结果参与者中有 109 名男性和 48 名女性,他们都符合 DSM-5 重度 AUD 标准。我们发现,血浆中由 12/15 脂氧合酶产生的促炎脂质 12- 和 15-HETE 以及由脂肪酸酰胺水解酶调控的抗炎脂质代谢物棕榈酰乙醇酰胺的水平与戒酒期间的酒精渴求存在不同程度的相关性,预测出更高的渴求,而与人口统计学、酒精使用史和多种治疗方法无关。这些结果为进一步研究和临床评估这些生物标志物提供了一个新的机会,以优化现有的治疗方法并开发治疗 AUD 的新疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Predictive Value of Plasma Bioactive Lipids on Craving in Human Volunteers With Alcohol Use Disorder

Background

Alcohol use disorder (AUD) is a chronic relapsing disorder characterized by alcohol seeking and consumption despite negative consequences. Despite the availability of multiple treatments, patients continue to exhibit high relapse rates. Thus, biomarkers that can identify patients at risk for heightened craving are urgently needed. Mounting preclinical and clinical evidence implicates perturbations in bioactive lipid signaling in the neurobiology of craving in AUD. We hypothesize that these lipids are potential biomarkers for predicting alcohol craving in patients with AUD.

Methods

This study used archival deidentified clinical data and corresponding plasma specimens from 157 participants in 3 clinical studies of AUD. We evaluated plasma levels of 8 lipid species as predictors of craving in response to in vivo alcohol and affective cues during abstinence.

Results

Participants were 109 men and 48 women who met DSM-5 criteria for severe AUD. We found that plasma levels of 12- and 15-HETE, 12/15-lipoxygenase–produced proinflammatory lipids, and palmitoylethanolamide, an anti-inflammatory fatty acid amide hydrolase–regulated lipid metabolite, were differentially correlated with alcohol craving during abstinence, predicting higher craving independent of demographics, alcohol use history, and multiple therapeutic treatments.

Conclusions

Our findings highlight the promise of these lipid metabolites as biomarkers of heightened alcohol craving. The results open a novel opportunity for further research and clinical evaluation of these biomarkers to optimize existing treatments and develop new therapeutics for AUD.

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来源期刊
Biological psychiatry global open science
Biological psychiatry global open science Psychiatry and Mental Health
CiteScore
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