Pauluci Renata, Noto Ana Regina, Curado Daniela Fernandez, Siqueira-Campos Miguel, Bezerra Andréia Gomes, Galduróz José Carlos Fernandes
Departamento de Psicobiologia, Universidade Federal de São Paulo, São Paulo, Brazil.
Front Psychiatry. 2022 Apr 8;13:826448. doi: 10.3389/fpsyt.2022.826448. eCollection 2022.
Recent studies have sought to identify the possible benefits of the intake of omega-3, an important component of neuronal membranes, for the treatment of alcohol use disorder.
The objective of the present study was to evaluate whether omega-3 supplementation is protective against alcohol use disorder relapse after hospital discharge.
A randomized, double-blind, placebo-controlled study was carried out with severe alcohol dependence. Male inpatients were randomized to treatment with omega-3 ( = 59) or placebo ( = 52) for 3 months, participants were assessed after discharge at 1 month (T1), 2 months (T2), 3 months (T3), and 6 months (T4) with assessments made using self-report instruments. The primary outcomes were the possible reduction with assessments made using self-report instruments. The primary outcomes were the possible reduction in the number, intensity of relapses, amount of consumption in each relapse and number of days of consumption during relapses; as secondary outcomes were assessed symptoms of anxiety, depression, degree of dependence, compulsion, and craving.
The groups were similar regarding consumption amount parameters and propensity to relapse; however, an effect of treatment with omega-3 was found on the number of days of drinking at 2 months [ = 0.65 (0.09; 1, 21), = 0.01] and 3 months [ = 2.6 (1.61; 3.58), < 0.001] after discharge, favoring the intervention group. The effect was not maintained at follow up of 6 months. No differences were found in psychiatric symptoms and severity of addiction.
Despite the major limitations of the present study, the group that received omega-3 had a lower number of days of consumption of standard doses of alcohol in the evaluations of 60 and 90 days after discharge. More robust studies are needed to confirm or refute these findings. Brazilian Registry of Clinical Trials: n° RBR-48mkgz7 (URL: https://ensaiosclinicos.gov.br/rg/RBR-48mkgz7).
近期研究试图确定摄入ω-3(神经元膜的重要组成部分)对治疗酒精使用障碍可能带来的益处。
本研究的目的是评估补充ω-3是否对出院后酒精使用障碍复发具有预防作用。
对重度酒精依赖患者开展了一项随机、双盲、安慰剂对照研究。男性住院患者被随机分为ω-3治疗组(n = 59)或安慰剂组(n = 52),治疗3个月,出院后1个月(T1)、2个月(T2)、3个月(T3)和6个月(T4)使用自我报告工具进行评估。主要结局是使用自我报告工具评估可能出现的复发次数、复发强度、每次复发的饮酒量以及复发期间饮酒天数的减少情况;作为次要结局评估的是焦虑、抑郁症状、依赖程度、强迫行为和渴望程度。
两组在饮酒量参数和复发倾向方面相似;然而,发现ω-3治疗对出院后2个月[β = 0.65(0.09;1.21),P = 0.01]和3个月[β = 2.6(1.61;3.58),P < 0.001]的饮酒天数有影响,干预组更具优势。6个月随访时该效果未持续存在。在精神症状和成瘾严重程度方面未发现差异。
尽管本研究存在重大局限性,但接受ω-3治疗的组在出院后60天和90天的评估中标准剂量酒精的饮酒天数较少。需要更有力的研究来证实或反驳这些发现。巴西临床试验注册:编号RBR-48mkgz7(网址:https://ensaiosclinicos.gov.br/rg/RBR-48mkgz7)