Next-generation biomarkers for alcohol consumption and alcohol use disorder diagnosis, prognosis, and treatment: A critical review.

IF 3 Q2 SUBSTANCE ABUSE Alcohol (Hanover, York County, Pa.) Pub Date : 2024-11-12 DOI:10.1111/acer.15476
Shaunna L Clark, Emily E Hartwell, Doo-Sup Choi, John H Krystal, Robert O Messing, Laura B Ferguson
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Abstract

This critical review summarizes the current state of omics-based biomarkers in the alcohol research field. We first provide definitions and background information on alcohol and alcohol use disorder (AUD), biomarkers, and "omic" technologies. We next summarize using (1) genetic information as risk/prognostic biomarkers for the onset of alcohol-related problems and the progression from regular drinking to problematic drinking (including AUD), (2) epigenetic information as diagnostic biomarkers for AUD and risk biomarkers for alcohol consumption, (3) transcriptomic information as diagnostic biomarkers for AUD, risk biomarkers for alcohol consumption, and (4) metabolomic information as diagnostic biomarkers for AUD, risk biomarkers for alcohol consumption, and predictive biomarkers for response to acamprosate in subjects with AUD. In the final section, the clinical implications of the findings are discussed, and recommendations are made for future research.

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用于酒精消费和酒精使用障碍诊断、预后和治疗的新一代生物标志物:重要综述。
这篇重要综述总结了酒精研究领域基于 omics 的生物标志物的现状。我们首先提供有关酒精和酒精使用障碍(AUD)、生物标志物和 "奥米克 "技术的定义和背景信息。接下来,我们总结了以下几种生物标志物的使用情况:(1) 遗传信息作为酒精相关问题发病的风险/诊断生物标志物,以及从经常饮酒到问题饮酒(包括 AUD)的进展情况;(2) 表观遗传信息作为 AUD 的诊断生物标志物和酒精消费的风险生物标志物、(3) 作为 AUD 诊断生物标志物和饮酒风险生物标志物的转录组信息;以及 (4) 作为 AUD 诊断生物标志物、饮酒风险生物标志物和 AUD 患者对阿坎酸反应的预测生物标志物的代谢组信息。最后一节讨论了研究结果的临床意义,并对今后的研究提出了建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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