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首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >Adjunctive S-adenosylmethionine (SAMe) in treating non-remittent major depressive disorder: An 8-week double-blind, randomized, controlled trial
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Adjunctive S-adenosylmethionine (SAMe) in treating non-remittent major depressive disorder: An 8-week double-blind, randomized, controlled trial

机译:辅助S-腺苷甲硫氨酸(相同)治疗非备重大抑郁症:8周双盲,随机,受控试验

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There has been increasing interest in nutraceutical augmentation strategies to boost the efficacy of antidepressants. This study assessed whether S-adenosylmethionine (SAMe), a methyl donor that occurs naturally in the body, may be of such benefit. We conducted an 8-week, double-blind RCT in which 107 treatment non-remittent outpatients with DSM-5 diagnosed Major Depressive Disorder (MDD) were randomized to either SAMe or placebo adjunctively to antidepressants. One-carbon cycle nutrients, pertinent single nucleotide polymorphisms (SNPs), and BDNF were also analysed as potential moderators of response. A linear mixed-effects model revealed a significant overall reduction in Montgomery-Asberg Depression Rating Scale (MADRS) score across time, however there was no significant between-group difference observed (p = 0.51). Response rates at Week 8 were 54.3% in the SAMe group and 50.0% in the placebo group, with remission rates 43.5% for SAMe and 38.3% for placebo (all results NS). No effect of SAMe was found on any secondary outcome. Differential response to SAMe was not modified by a range of key genotypes (e.g. COMT), nor reflected in a change of homocysteine, red cell folate, or BDNF. Use of SAMe elicited no significant adverse effects beyond placebo, however it was implicated in one case of serotonin syndrome-like symptoms. This study concludes that 800 mg/day of SAMe is not an effective adjunctive treatment in MDD, and no obvious biomarker reflected any differential response to treatment. Due to such a distinctly high placebo-response (despite rigorous screening), future studies should employ a placebo run-in period and other strategies to minimize placebo response. (c) 2018 Published by Elsevier B.V.
机译:对营养素增强策略的兴趣越来越兴趣,以提高抗抑郁药的疗效。该研究评估了S-腺苷甲硫氨酸(相同),在体内天然发生的甲基供体,可能是这样的益处。我们进行了一个8周的双盲RCT,其中107种治疗非牛仔病毒门诊患者与DSM-5诊断的主要抑郁症(MDD)进行随机化,以与抗抑郁药相同或安慰剂。还分析了一种碳循环营养,相关的单核苷酸多态性(SNP)和BDNF也被分析为潜在的反应剂。线性混合效应模型揭示了蒙哥马利 - Asberg抑郁率(MADRS)得分的显着整体减少,但是观察到的组差异没有显着性(P = 0.51)。第8周的回应率在同一组中为54.3%,安慰剂集团的50.0%,缓解率为43.5%,安慰剂(所有结果NS)为38.3%。任何次要结果都没有发现同样的影响。对同一的差异响应未被一系列关键基因型(例如COMT)修饰,也不反映在同型半胱氨酸,红细胞叶酸或BDNF的变化中。使用同样引发的使用没有显着的安慰剂的不良效果,但是它涉及一种血清素综合征样症状的一种情况。该研究得出结论,同样的800毫克/日不是MDD中有效的辅助治疗,并且没有明显的生物标志物反映了对治疗的任何差异反应。由于这种明显的高安慰剂 - 反应(尽管严格筛查),未来的研究应该采用安慰剂运行期和其他策略,以最大限度地减少安慰剂反应。 (c)2018由elsevier b.v发布。

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