Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Department of Pharmacotherapeutics and Informatics, Fujita Health University School of Medicine, Toyoake, Aichi, Japan.
Neuropsychopharmacol Rep. 2024 Mar;44(1):216-220. doi: 10.1002/npr2.12376. Epub 2023 Aug 30.
The question remains to be elucidated: "Is treatment with antidepressants at doses approved in Japan effective for Japanese patients with MDD?" It is crucial to confirm this in order to provide appropriate treatments for Japanese patients with major depressive disorder (MDD). Therefore, we conducted a systematic review and random-effects pairwise meta-analysis including these nine double-blind, randomized, placebo-controlled trials.
We calculated the standardized mean difference (SMD) and risk ratio (RR) with a 95% confidence interval (95% CI).
Pooled newer antidepressants outperformed placebo regarding improvement of depressive symptom scale scores [SMD (95% CI) = -0.20 (-0.27, -0.12), p < 0.00001], response to treatment [RR (95% CI) = 1.23 (1.13, 1.32), p < 0.00001], and remission rate [RR (95% CI) = 1.30 (1.16, 1.45), p < 0.00001]. Although all-cause discontinuation was not significantly different between the treatment groups, the pooled antidepressant group showed a higher discontinuation rate due to adverse event [RR (95% CI) = 1.60 (1.13, 2.26), p = 0.007] and a higher incidence of at least one adverse event than the placebo group [RR (95% CI) = 1.13 (1.08, 1.18), p < 0.00001].
We concluded that newer antidepressants are effective for Japanese adults with MDD although the clinicians must monitor the health conditions of these individuals.
仍需要阐明的问题是:“以日本批准的剂量使用抗抑郁药治疗日本 MDD 患者是否有效?”为了为日本重度抑郁症(MDD)患者提供适当的治疗,这一点至关重要。因此,我们进行了一项系统评价和随机效应成对荟萃分析,其中包括这九项双盲、随机、安慰剂对照试验。
我们计算了标准化均数差(SMD)和风险比(RR)及其 95%置信区间(95%CI)。
与安慰剂相比,新型抗抑郁药在改善抑郁症状量表评分方面表现出优势[SMD(95%CI)=-0.20(-0.27,-0.12),p<0.00001]、对治疗的反应[RR(95%CI)=1.23(1.13,1.32),p<0.00001]和缓解率[RR(95%CI)=1.30(1.16,1.45),p<0.00001]。尽管治疗组之间的全因停药率没有显著差异,但合并的抗抑郁药组因不良事件而停药的比例更高[RR(95%CI)=1.60(1.13,2.26),p=0.007],且至少发生一次不良事件的发生率高于安慰剂组[RR(95%CI)=1.13(1.08,1.18),p<0.00001]。
我们的结论是,新型抗抑郁药对日本成年人 MDD 有效,尽管临床医生必须监测这些患者的健康状况。