Suppr超能文献

一项多中心、随机、双盲、安慰剂对照试验,旨在研究日本传统药物加味逍遥散对更年期症状的影响:KOSMOS研究。

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Investigate the Effects of Kamishoyosan, a Traditional Japanese Medicine, on Menopausal Symptoms: The KOSMOS Study.

作者信息

Takamatsu Kiyoshi, Ogawa Mariko, Obayashi Satoshi, Takeda Takashi, Terauchi Masakazu, Higuchi Tsuyoshi, Kato Kiyoko, Kubota Toshiro

机构信息

Department of Obstetrics and Gynecology, Tokyo Dental College Ichikawa General Hospital, Chiba, Japan.

Department of Obstetrics and Gynecology, Dokkyo Medical University, Tochigi, Japan.

出版信息

Evid Based Complement Alternat Med. 2021 Feb 26;2021:8856149. doi: 10.1155/2021/8856149. eCollection 2021.

Abstract

OBJECTIVE

The KOSMOS study, a multicenter, randomized, double-blind, placebo-controlled trial, investigated the effects and safety of kamishoyosan (TJ-24), a traditional Japanese medicine, in the treatment of climacteric disorder.

METHODS

Japanese women with climacteric disorder were administered a placebo during a 4-week run-in period, after which they were classified as placebo responders (R group) if their score on the modified Questionnaire for the Assessment of Climacteric Symptoms in Japanese Women (m-QACS) with excitability and irritability as the primary outcome improved by ≥ 3 points and as placebo nonresponders (NR group) otherwise. Members of the NR group were randomly allocated to receive either TJ-24 or placebo. After 12 weeks, their m-QACS scores, anxiety and depression, sleep, and overall quality of life (QOL) were compared.

RESULTS

The TJ-24 and placebo arms in the NR group included 20 patients each. The change in the m-QACS scores of members of the NR group for excitability and irritability at 12 weeks versus baseline was -3.1 ± 1.7 in the TJ-24 arm, a significant decrease, but compared with -2.7 ± 2.2 in the placebo arm, no significant difference was between two arms. However, the proportion of participants whose score improved by ≥3 points was significantly higher in the TJ-24 arm. In the subgroup analysis of premenopausal women, the changes in the score for excitability and irritability were significantly larger in the TJ-24 arm. The incidence of adverse drug reactions or adverse events did not differ between the two arms, and no serious events were reported.

CONCLUSION

Although no significant difference was identified for the primary outcome, a significantly higher proportion of patients who received TJ-24 displayed improvement. Its high level of safety and effects on excitability and irritability in premenopausal women suggest that TJ-24 may be a useful treatment.

摘要

目的

KOSMOS研究是一项多中心、随机、双盲、安慰剂对照试验,旨在研究日本传统药物加味逍遥散(TJ - 24)治疗更年期障碍的疗效和安全性。

方法

患有更年期障碍的日本女性在为期4周的导入期服用安慰剂,之后,如果她们以兴奋性和易怒性为主要结局的改良日本女性更年期症状评估问卷(m - QACS)得分提高≥3分,则被归类为安慰剂反应者(R组),否则为安慰剂无反应者(NR组)。NR组的成员被随机分配接受TJ - 24或安慰剂。12周后,比较她们的m - QACS得分、焦虑和抑郁、睡眠以及总体生活质量(QOL)。

结果

NR组中TJ - 24组和安慰剂组各有20名患者。NR组成员在12周时与基线相比,TJ - 24组兴奋性和易怒性的m - QACS得分变化为 - 3.1±1.7,显著下降,但与安慰剂组的 - 2.7±2.2相比,两组之间无显著差异。然而,TJ - 24组得分提高≥3分的参与者比例显著更高。在绝经前女性的亚组分析中,TJ - 组兴奋性和易怒性得分的变化显著更大。两组之间药物不良反应或不良事件的发生率没有差异,也未报告严重事件。

结论

虽然主要结局未发现显著差异,但接受TJ - 24治疗的患者中有显著更高比例的人病情有所改善。其高安全性以及对绝经前女性兴奋性和易怒性的影响表明,TJ - 24可能是一种有效的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c96/7935592/ad8bb397252d/ECAM2021-8856149.001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验