首页> 外文期刊>American journal of psychiatry >l-Methylfolate as Adjunctive Therapy for SSRI-Resistant Major Depression: Results of Two Randomized, Double-Blind, Parallel-Sequential Trials.
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l-Methylfolate as Adjunctive Therapy for SSRI-Resistant Major Depression: Results of Two Randomized, Double-Blind, Parallel-Sequential Trials.

机译:l-甲基叶酸作为抗SSRI的主要抑郁症的辅助治疗:两项随机,双盲,并行顺序试验的结果。

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OBJECTIVE The authors conducted two multicenter sequential parallel comparison design trials to investigate the effect of l-methylfolate augmentation in the treatment of major depressive disorder in patients who had a partial response or no response to selective serotonin reuptake inhibitors (SSRIs). METHOD In the first trial, 148 outpatients with SSRI-resistant major depressive disorder were enrolled in a 60-day study divided into two 30-day periods. Patients were randomly assigned, in a 2:3:3 ratio, to receive l-methylfolate for 60 days (7.5 mg/day for 30 days followed by 15 mg/day for 30 days), placebo for 30 days followed by l-methylfolate (7.5 mg/day) for 30 days, or placebo for 60 days. SSRI dosages were kept constant throughout the study. In the second trial, with 75 patients, the design was identical to the first, except that the l-methylfolate dosage was 15 mg/day during both 30-day periods. RESULTS In the first trial, no significant difference was observed in outcomes between the treatment groups. In the second trial, adjunctive l-methylfolate at 15 mg/day showed significantly greater efficacy compared with continued SSRI therapy plus placebo on both primary outcome measures (response rate and degree of change in depression symptom score) and two secondary outcome measures of symptom severity. The number needed to treat for response was approximately six in favor of adjunctive l-methylfolate at 15 mg/day. l-Methylfolate was well tolerated, with rates of adverse events no different from those reported with placebo. CONCLUSIONS Adjunctive l-methylfolate at 15 mg/day may constitute an effective, safe, and relatively well tolerated treatment strategy for patients with major depressive disorder who have a partial response or no response to SSRIs.
机译:目的作者进行了两项多中心顺序平行比较设计试验,以研究对选择性5-羟色胺再摄取抑制剂(SSRIs)有部分反应或无反应的患者,使用l-甲基叶酸增强剂治疗主要抑郁症的效果。方法在第一项试验中,对148名SSRI耐药的重度抑郁症患者进行了为期60天的研究,分为两个30天。以2:3:3的比例随机分配患者接受l-甲基叶酸治疗60天(7.5 mg /天,持续30天,然后15 mg /天,持续30天),安慰剂治疗30天,然后接受l-甲基叶酸治疗(7.5毫克/天)30天,或安慰剂60天。在整个研究中,SSRI剂量保持恒定。在第二项试验中,有75名患者,其设计与第一项试验相同,不同之处在于在30天的两天内,l-甲基叶酸的剂量均为15 mg /天。结果在第一项试验中,各治疗组之间的结果均未观察到显着差异。在第二项试验中,与持续SSRI治疗加安慰剂相比,15mg /天的辅助l-甲基叶酸在主要结局指标(缓解率和抑郁症状评分变化的程度)和两项症状严重程度的二级结局指标中均显示出明显更高的疗效。需要治疗的数量大约为六种,以15 mg / day的辅助l-甲基叶酸治疗。 1-甲基叶酸耐受性良好,不良事件发生率与安慰剂无差异。结论对于每天对SSRIs有部分反应或无反应的重度抑郁症患者,每天15 mg的辅助l-甲基叶酸可能是一种有效,安全且耐受性较好的治疗策略。

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