A Synthetic External Control Study Comparing the Clinical Efficacy of Wendan Decoction and 19 Antidepressants.

IF 4.5 2区 医学 Q1 CLINICAL NEUROLOGY International Journal of Neuropsychopharmacology Pub Date : 2023-10-19 DOI:10.1093/ijnp/pyad044
Yuting Yang, Rui Chen, Caixia Li, Qingshan Zheng, Yinghua Lv, Lujin Li, Hongsheng Tan
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Abstract

Background: Wendan decoction (WDD) has been used as a treatment for depression in China since the Tang Dynasty. However, high-quality evidence for this is lacking. This study proposed a novel synthetic external control method to evaluate its clinical efficacy.

Methods: We searched public databases for clinical trials of WDD for major depression. The rate of change of the Hamilton Depression Scale score from baseline was used as an efficacy indicator, and a model-based meta-analysis was performed to analyze the clinical efficacy of WDD. To establish a reference standard for efficacy, the antidepressant efficacy distributions of a placebo and 19 antidepressants were virtually synthesized based on the same conditions as the clinical trial characteristics of WDD.

Results: This study included 5 clinical trials with 177 participants. WDD showed a slow onset, with a time to reach the maximum effect of 9.71 weeks. At 8 weeks, the rate of change in the Hamilton Depression Scale score from baseline was 66.4% (95% CI = 62.3%-70.3%) in the WDD group. The pure effect value of WDD, after deducting the placebo effect, was 26.9% (95%CI = 23.0%-30.9%), which was comparable with 5 types of antidepressants and significantly higher than the others.

Conclusion: The proposed external synthetic control method provides a solution to the bottleneck problem of clinical efficacy evaluation in real-world research on traditional Chinese medicine. WDD has high clinical development value for the treatment of depression, and large-scale randomized controlled trials are recommended to confirm its antidepressant effect.

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温胆汤与19种抗抑郁药临床疗效的综合外对照研究。
背景:自唐代以来,温胆汤在我国一直被用作治疗抑郁症的药物。然而,这方面缺乏高质量的证据。本研究提出了一种新的综合外控方法来评价其临床疗效。方法:我们检索了WDD治疗重度抑郁症的临床试验的公共数据库。汉密尔顿抑郁量表评分与基线的变化率被用作疗效指标,并进行了基于模型的荟萃分析来分析WDD的临床疗效。为了建立疗效参考标准,在与WDD临床试验特征相同的条件下,实际上合成了一种安慰剂和19种抗抑郁药的抗抑郁疗效分布。结果:本研究包括5项临床试验,177名参与者。WDD发病缓慢,达到最大疗效的时间为9.71周。在8周时,汉密尔顿抑郁量表评分与基线相比的变化率为66.4%(95%CI = 62.3%-70.3%)。扣除安慰剂效应后,WDD的纯效应值为26.9%(95%CI = 23.0%-30.9%),与5种抗抑郁药相当,且明显高于其他抗抑郁药。结论:所提出的外部综合控制方法解决了现实中医药研究中临床疗效评价的瓶颈问题。WDD在治疗抑郁症方面具有较高的临床开发价值,建议进行大规模随机对照试验以证实其抗抑郁作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.40
自引率
2.10%
发文量
230
审稿时长
4-8 weeks
期刊介绍: The central focus of the journal is on research that advances understanding of existing and new neuropsychopharmacological agents including their mode of action and clinical application or provides insights into the biological basis of psychiatric disorders and thereby advances their pharmacological treatment. Such research may derive from the full spectrum of biological and psychological fields of inquiry encompassing classical and novel techniques in neuropsychopharmacology as well as strategies such as neuroimaging, genetics, psychoneuroendocrinology and neuropsychology.
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