Department of Psychiatry and Behavioral Neuroscience, Saint Louis University School of Medicine, St. Louis, MO, USA.
Department of Psychiatry and Behavioral Neuroscience, Saint Louis University School of Medicine, St. Louis, MO, USA.
J Affect Disord. 2018 Jan 15;226:245-250. doi: 10.1016/j.jad.2017.09.034. Epub 2017 Sep 30.
Allopurinol is a xanthine oxidase inhibitor commonly used in the treatment of gout. Recent studies have also shown its promise as an adjunctive treatment for manic episodes in bipolar 1 disorder, possibly through mechanisms involving the purinergic pathway. However, its efficacy across studies has been inconsistent, so we conducted a meta-analysis of the published controlled studies with the goal of determining the efficacy profile of allopurinol as an adjunctive treatment for mania in bipolar disorder.
An online search was conducted using PubMed for placebo-controlled, randomized, double-blind, clinical trials (RCTs) using the terms "allopurinol," "bipolar," "mania," "manic," and "YMRS" and a meta-analysis was conducted in accordance with the Preferred Reporting Items for Systematic reviews and Meta-Analyses statement.
Five studies met the criteria for inclusion. Three of the five studies were inpatient treatments, one study was outpatient treatment, and one study had a mixture of both. All studies used allopurinol as an adjunct in treating acute mania in bipolar disorder subjects. Four of the studies showed efficacy in the primary outcome measure between allopurinol vs. placebo groups with significantly reduced YMRS scores while one showed no significant effect size between the allopurinol and placebo groups. The overall effect size for the four studies is d = 0.294. No significant difference in side effects were found between groups for any of the studies.
The data suggest that allopurinol may have some efficacy as an adjunct in reducing mania symptoms during acute manic episodes in patients with bipolar disorder. Adjunctive allopurinol efficacy may be related to the mood stabilizer used. Additional controlled trials with greater sample sizes, homogenous dosing, and consistent treatment modalities are needed to determine optimal clinical application.
别嘌醇是一种黄嘌呤氧化酶抑制剂,常用于治疗痛风。最近的研究还表明,它作为双相情感障碍 1 型躁狂发作的辅助治疗药物具有一定前景,其作用机制可能涉及嘌呤能途径。然而,其在不同研究中的疗效并不一致,因此我们进行了一项荟萃分析,以确定别嘌醇作为双相情感障碍躁狂发作辅助治疗药物的疗效特征。
我们使用 PubMed 在线搜索了安慰剂对照、随机、双盲、临床试验(RCT),使用的术语包括“别嘌醇”、“双相”、“躁狂”、“躁狂”和“YMRS”,并按照系统评价和荟萃分析的首选报告项目进行了荟萃分析。
五项研究符合纳入标准。五项研究中有三项为住院治疗,一项为门诊治疗,一项为混合治疗。所有研究均使用别嘌醇作为辅助药物治疗双相情感障碍患者的急性躁狂症。四项研究显示在主要结局测量中,别嘌醇与安慰剂组之间的疗效差异具有统计学意义,YMRS 评分显著降低,而一项研究显示别嘌醇与安慰剂组之间的效应大小无显著差异。四项研究的总效应大小为 d = 0.294。没有研究发现组间任何不良反应存在显著差异。
数据表明,别嘌醇可能对降低双相情感障碍患者急性躁狂发作期间的躁狂症状具有一定疗效。辅助别嘌醇的疗效可能与使用的心境稳定剂有关。需要进一步开展更多的对照试验,增加样本量、统一剂量和治疗方式,以确定最佳的临床应用。