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用于区分酒精使用障碍个体与社交饮酒者及未饮酒者的血浆代谢生物标志物。

Plasma metabolic biomarkers for discriminating individuals with alcohol use disorders from social drinkers and alcohol-naive subjects.

作者信息

Mostafa Hamza, Amin Arwa M, Teh Chin-Hoe, Murugaiyah Vikneswaran A/L, Arif Nor Hayati, Ibrahim Baharudin

机构信息

School of Pharmaceutical Sciences, Universiti Sains Malaysia, Malaysia.

Bruker (Malaysia) Sdn Bhd, Malaysia.

出版信息

J Subst Abuse Treat. 2017 Jun;77:1-5. doi: 10.1016/j.jsat.2017.02.015. Epub 2017 Mar 1.

Abstract

BACKGROUND

Alcohol use disorders (AUD) is a phase of alcohol misuse in which the drinker consumes excessive amount of alcohol and have a continuous urge to consume alcohol which may lead to various health complications. The current methods of alcohol use disorders diagnosis such as questionnaires and some biomarkers lack specificity and sensitivity. Metabolomics is a novel scientific field which may provide a novel method for the diagnosis of AUD by using a sensitive and specific technique such as nuclear magnetic resonance (NMR).

METHODS

A cross sectional study was conducted on three groups: individuals with alcohol use disorders (n=30), social drinkers (n=54) and alcohol-naive controls (n=60). H NMR-based metabolomics was used to obtain the metabolic profiles of plasma samples. Data were processed by multivariate principal component analysis (PCA) and orthogonal partial least squares-discriminant analysis (OPLS-DA) followed by univariate and multivariate logistic regressions to produce the best fit-model for discrimination between groups.

RESULTS

The OPLS-DA model was able to distinguish between the AUD group and the other groups with high sensitivity, specificity and accuracy of 64.29%, 98.17% and 91.24% respectively. The logistic regression model identified two biomarkers in plasma (propionic acid and acetic acid) as being significantly associated with alcohol use disorders. The reproducibility of all biomarkers was excellent (0.81-1.0).

CONCLUSIONS

The applied plasma metabolomics technique was able to differentiate the metabolites between AUD and the other groups. These metabolites are potential novel biomarkers for diagnosis of alcohol use disorders.

摘要

背景

酒精使用障碍(AUD)是酒精滥用的一个阶段,在此阶段饮酒者摄入过量酒精,并持续有饮酒冲动,这可能导致各种健康并发症。目前用于诊断酒精使用障碍的方法,如问卷调查和一些生物标志物,缺乏特异性和敏感性。代谢组学是一个新兴的科学领域,它可能通过使用核磁共振(NMR)等敏感且特异的技术,为酒精使用障碍的诊断提供一种新方法。

方法

对三组人群进行了横断面研究:酒精使用障碍患者(n = 30)、社交饮酒者(n = 54)和从未饮酒的对照者(n = 60)。基于氢核磁共振的代谢组学用于获取血浆样本的代谢谱。数据通过多变量主成分分析(PCA)和正交偏最小二乘判别分析(OPLS - DA)进行处理,随后进行单变量和多变量逻辑回归,以生成区分各组的最佳拟合模型。

结果

OPLS - DA模型能够以高灵敏度、特异性和准确性区分AUD组与其他组,灵敏度、特异性和准确性分别为64.29%、98.17%和91.24%。逻辑回归模型确定血浆中的两种生物标志物(丙酸和乙酸)与酒精使用障碍显著相关。所有生物标志物的重现性都非常好(0.81 - 1.0)。

结论

所应用的血浆代谢组学技术能够区分AUD组与其他组之间的代谢物。这些代谢物是诊断酒精使用障碍的潜在新型生物标志物。

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