Martins Bradford S, Fogelman Nia, Tate Marshall, Hermes Gretchen H, Sinha Rajita
Yale Stress Center, Yale University, New Haven, Connecticut, USA.
Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut, USA.
Alcohol Clin Exp Res (Hoboken). 2024 Mar;48(3):507-515. doi: 10.1111/acer.15263. Epub 2024 Jan 23.
Alcohol use disorder (AUD) is associated with significant liver pathology marked by elevated liver enzymes. Prazosin, an alpha1-noradrenergic antagonist significantly improves alcohol drinking outcomes in individuals with alcohol withdrawal symptoms (AW), but effects on liver enzymes are unknown. We assessed the effects of prazosin treatment on the liver enzymes alanine transaminase (ALT), aspartate transaminase (AST), and gamma-glutamyltransferase (GGT) in individuals with AUD.
Participants (N=100) with AUD were enrolled in a 12-week randomized controlled trial and received either placebo or 16 mg/day of prazosin. Whole blood was drawn from 92 participants to measure liver enzyme levels every 4 weeks, and severity of AW was assessed weekly. Analysis predicting liver function outcomes used linear mixed effects models.
Controlling for alcohol consumption, a significant AW × treatment effect was seen for ALT (p < 0.05), AST (p < 0.05) and GGT (p < 0.01). Additionally, AST (b = 0.2, p < 0.01), ALT (b = 0.2, p < 0.05), and GGT (b = 0.3, p < 0.01) were elevated in individuals with higher AW in the placebo but not in the prazosin group (AST: p > 0.66; ALT: p > 0.65). Only in the prazosin group were lower GGT levels associated with higher withdrawal severity (b = -0.16, p < 0.05).
We found an interaction of alcohol withdrawal symptoms and prazosin treatment on liver enzyme levels, which were not influenced by week in the trial or the amount of alcohol consumed. Together, these findings suggest that prazosin treatment reduces liver enzymes over the course of AUD treatment among individuals with significant AW, though replication to establish clinical utility is needed.
酒精使用障碍(AUD)与以肝酶升高为特征的显著肝脏病理改变相关。哌唑嗪是一种α1-去甲肾上腺素能拮抗剂,可显著改善有酒精戒断症状(AW)个体的饮酒结局,但对肝酶的影响尚不清楚。我们评估了哌唑嗪治疗对AUD个体肝酶丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)和γ-谷氨酰转移酶(GGT)的影响。
100名AUD参与者参加了一项为期12周的随机对照试验,接受安慰剂或每日16毫克哌唑嗪治疗。每4周从92名参与者中采集全血以测量肝酶水平,每周评估AW的严重程度。预测肝功能结局的分析采用线性混合效应模型。
在控制饮酒量的情况下,ALT(p < 0.05)、AST(p < 0.05)和GGT(p < 0.01)出现了显著的AW×治疗效应。此外,安慰剂组中AW较高的个体AST(b = 0.2,p < 0.01)、ALT(b = 0.2,p < 0.05)和GGT(b = 0.3,p < 0.01)升高,但哌唑嗪组未升高(AST:p > 0.66;ALT:p > 0.65)。仅在哌唑嗪组中,较低的GGT水平与较高的戒断严重程度相关(b = -0.16,p < 0.05)。
我们发现酒精戒断症状与哌唑嗪治疗对肝酶水平存在相互作用,这不受试验周数或饮酒量的影响。总之,这些发现表明,在有显著AW的个体中,哌唑嗪治疗在AUD治疗过程中可降低肝酶水平,不过需要重复研究以确立其临床实用性。