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接受治疗的艾滋病病毒感染者中情绪障碍和脑源性神经营养因子与饮酒轨迹的关系

Mood Disorders and BDNF Relationship with Alcohol Drinking Trajectories among PLWH Receiving Care.

作者信息

Míguez-Burbano María José, Espinoza Luis, Vargas Mayra, LaForest Diana

机构信息

School of Integrated Science and Humanity, Florida International University, Miami, FL, USA.

Department of Medicine, University of Miami School of Medicine, Miami, FL, USA.

出版信息

J Alcohol Drug Depend. 2014 May;2(2):148. doi: 10.4172/2329-6488.1000148. Epub 2014 Feb 10.

Abstract

BACKGROUND

Despite the excessive rates of Hazardous Alcohol Use (HAU) among people living with HIV (PLWH), although largely speculated, psychological and physiological components associated with HAU, has not been actively measured. Therefore, the present study was geared toward determining: 1) the rates of mood disorders and its relationship with HAU, and 2) to assess the impact of Brain Derived Neurotrophic Factor (BDNF), a well-known regulator of alcohol and mood disorders.

METHODS

For this study, participants of the longitudinal PADS Study n=400, were followed over time. Alcohol use (Alcohol Use Disorders Identification Test -AUDIT- and the Alcohol Dependence Scale -ADS) and moods (depression, anxiety, and stress) were assessed repeatedly.

RESULTS

A cluster analyses shows three distinctive trajectories. The first one, revealed a group with increased drinking (Cluster 1: n=140), constant alcohol intake (Cluster 2: n = 60), and one with decreased consumption (Cluster 3: n =120). Analyses discovered higher AUDIT scores across the clusters with Cluster 1 being followed by Clusters 2 and 3 (1: 14.5 ± 8 vs. 2=8.7 ± 7.5 vs. 3= 6.6 ± 4.2, p = 0.001). Women in Clusters 1 and 2 had higher levels of stress (1:21 ± 7.5; 2:19.3 ± 7) and lower BDNF levels (7904 ± 1248 pg/ml and 10405 ± 909 pg/mL) than their counterparts in Cluster 3 (PSS: 3: 16.6 ±5, p = 0.02 BDNF: 10828 ± 1127 pg/mL, p = 0.08). Men in Cluster 1 differed in terms of stress (19.8 ± 7 vs. 21 ± 7.5 score) and BDNF levels (Cluster 1: 5204 ± 818 vs. Cluster 2: 7656 ± 843 pg/ml, p = 0.002) but not in the number of years living with HIV. The proportion of subjects with multiple mood comorbidities was disturbingly higher (26%), and all were members of Cluster 1. Multiple logistic regression analyses indicated that participants reporting high relative to low levels of perceived stress, dual mood comorbidity, altered BDNF levels and low income increased the likelihood of being a member of Cluster 1.

CONCLUSION

This study found that stress and overlaying psychiatric comorbidities are linked with persistent alcohol use. Findings suggest that BDNF and social support seems to be a logical target as it seems to be the bridge linking mood disorders and alcohol consumption.

摘要

背景

尽管人类免疫缺陷病毒感染者(PLWH)中有害酒精使用(HAU)率过高,但与HAU相关的心理和生理因素,虽多有推测,但尚未得到积极测量。因此,本研究旨在确定:1)情绪障碍的发生率及其与HAU的关系,以及2)评估脑源性神经营养因子(BDNF)的影响,BDNF是一种众所周知的酒精和情绪障碍调节因子。

方法

在本研究中,对纵向PADS研究的400名参与者进行了长期跟踪。对酒精使用情况(酒精使用障碍识别测试 - AUDIT - 和酒精依赖量表 - ADS)和情绪(抑郁、焦虑和压力)进行了反复评估。

结果

聚类分析显示出三种不同的轨迹。第一种显示一组饮酒量增加(第1组:n = 140),一组酒精摄入量恒定(第2组:n = 60),另一组饮酒量减少(第3组:n = 120)。分析发现各聚类的AUDIT评分较高,第1组之后依次是第2组和第3组(1组:14.5 ± 8 vs. 2组 = 8.7 ± 7.5 vs. 3组 = 6.6 ± 4.2,p = 0.001)。第1组和第2组中的女性比第3组中的女性有更高的压力水平(1组:21 ± 7.5;2组:19.3 ± 7)和更低的BDNF水平(7904 ± 1248 pg/ml和10405 ± 909 pg/mL)(PSS:3组:16.6 ± 5,p = 0.02;BDNF:10828 ± 1127 pg/mL,p = 0.08)。第1组中的男性在压力(19.8 ± 7 vs. 21 ± 7.5分)和BDNF水平方面存在差异(第1组:5204 ± 818 vs. 第2组:7656 ± 843 pg/ml,p = 0.002),但在感染HIV的年限方面没有差异。患有多种情绪共病的受试者比例高得惊人(26%),且均为第1组成员。多项逻辑回归分析表明,报告感知压力水平高相对于低、双重情绪共病、BDNF水平改变和低收入的参与者更有可能成为第1组成员。

结论

本研究发现压力和叠加的精神共病与持续饮酒有关。研究结果表明,BDNF和社会支持似乎是一个合理的靶点,因为它似乎是连接情绪障碍和酒精消费的桥梁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71b/4612491/8077da35f9d3/nihms706248f1.jpg

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