Deakin University, School of Medicine, Barwon Health, P.O. Box 291, Geelong, 3220, Australia.
BMC Med. 2012 Aug 14;10:91. doi: 10.1186/1741-7015-10-91.
N-acetyl cysteine (NAC) is a glutathione precursor that has been shown to have antidepressant efficacy in a placebo-controlled trial. The current study aimed to investigate the maintenance effects of NAC following eight weeks of open-label treatment for bipolar disorder.
The efficacy of a double blind randomized placebo controlled trial of 2 g/day NAC as adjunct maintenance treatment for bipolar disorder was examined. Participants (n = 149) had a Montgomery Asberg Depression Rating Score of ≥12 at trial entry and, after eight weeks of open-label NAC treatment, were randomized to adjunctive NAC or placebo, in addition to treatment as usual. Participants (primarily outpatients) were recruited through public and private services and through newspaper advertisements. Time to intervention for a mood episode was the primary endpoint of the study, and changes in mood symptoms, functionality and quality of life measures were secondary outcomes.
There was a substantial decrease in symptoms during the eight-week open-label NAC treatment phase. During the subsequent double-blind phase, there was minimal further change in outcome measures with scores remaining low. Consequently, from this low plateau, between-group differences did not emerge on recurrence, clinical functioning or quality of life measures.
There were no significant between-group differences in recurrence or symptomatic outcomes during the maintenance phase of the trial; however, these findings may be confounded by limitations.
The trial was registered with the Australian New Zealand Clinical Trials Registry (ACTRN12607000074493).
N-乙酰半胱氨酸(NAC)是一种谷胱甘肽前体,已在安慰剂对照试验中显示出抗抑郁疗效。本研究旨在探讨 NAC 在双相情感障碍为期八周的开放标签治疗后对维持治疗的效果。
研究采用双盲随机安慰剂对照试验,评估每天 2 克 NAC 作为双相情感障碍辅助维持治疗的疗效。入组患者(n=149)在试验开始时的 Montgomery-Asberg 抑郁评定量表(MADRS)评分≥12,在八周的 NAC 开放标签治疗后,随机分配接受辅助 NAC 或安慰剂,同时接受常规治疗。参与者(主要为门诊患者)通过公共和私人服务以及报纸广告招募。心境发作的干预时间是研究的主要终点,心境症状、功能和生活质量测量的变化是次要结果。
在为期八周的 NAC 开放标签治疗阶段,症状有明显减轻。在随后的双盲阶段,随着评分持续较低,结果测量的进一步变化很小。因此,从这个较低的平台来看,在复发、临床功能或生活质量测量方面,组间差异并未出现。
在试验的维持阶段,复发或症状结果没有显著的组间差异;然而,这些发现可能受到限制的影响。
该试验在澳大利亚和新西兰临床试验注册中心(ACTRN12607000074493)注册。