• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

对抗抑郁药反应不足的日本重度抑郁症患者症状和功能的最小临床重要差异评估:一项关于日本重度抑郁症患者布雷哌唑增效治疗长期研究的分析

Assessment of minimum clinically important difference in symptoms and functionality of Japanese patients with major depressive disorder following inadequate response to antidepressants: a analysis of the long-term study of brexpiprazole augmentation therapy in Japanese patients with major depressive disorder.

作者信息

Hori Hikaru, Shiosakai Masako, Shibasaki Yoshiyuki, Yamato Kentaro, Zhang Yilong

机构信息

Department of Psychiatry, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

Clinical Development, Headquarters of Clinical Development, Otsuka Pharmaceutical Co., Ltd., Tokyo, Japan.

出版信息

Front Psychiatry. 2025 Mar 26;16:1556470. doi: 10.3389/fpsyt.2025.1556470. eCollection 2025.

DOI:10.3389/fpsyt.2025.1556470
PMID:40206646
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11979183/
Abstract

BACKGROUND AND OBJECTIVES

The aim of this study was to apply the minimum clinically important difference (MCID) concept to clinical results for Japanese patients with major depressive disorder following inadequate response to antidepressants, and to explore the disparity in what physicians and patients considered important in the treatment of depression.

METHODS

The original study was a 52-week, open-label, multicenter study on the administration of 2 mg/d of brexpiprazole as adjunctive therapy for patients with major depressive disorder. Here, we conducted a analysis to determine the MCID in Montgomery-Åsberg Depression Rating Scale (MADRS), Sheehan Disability Scale (SDS), and EQ-5D-5L-derived utility score. We compared the area under the curve (AUC) and correlation coefficients for the MADRS, SDS, and utility scores between the physicians' and patients' responses.

RESULTS

The MCIDs for this patient group were 4.89-4.94 for the MADRS score, 31.15-35.10% for the MADRS improvement rate, 0.69-2.14 for the SDS score, and 0.045-0.195 for the utility score. The MCIDs for the SDS and utility scores derived from the patient-perspective anchor were almost twice as high as those from the physician-perspective anchor. The utility score had the highest AUC and correlation coefficient for the patient-perspective anchor, while the MADRS score did for the physician-perspective anchor.

CONCLUSIONS

The MCIDs for the MADRS, SDS, and EQ-5D-5L -derived utility scores were estimated. Physicians focus more on depressive symptoms and prioritize symptom severity over improvements in functionality and activities of daily life, in contrast to patients, who prioritize such improvements.

摘要

背景与目的

本研究旨在将最小临床重要差异(MCID)概念应用于对抗抑郁药反应不佳的日本重度抑郁症患者的临床结果,并探讨医生和患者在抑郁症治疗中认为重要的方面的差异。

方法

原研究是一项为期52周的开放标签、多中心研究,对重度抑郁症患者给予每日2mg的布雷哌唑作为辅助治疗。在此,我们进行了一项分析,以确定蒙哥马利-阿斯伯格抑郁评定量表(MADRS)、希恩残疾量表(SDS)和EQ-5D-5L衍生效用评分的MCID。我们比较了医生和患者反应之间MADRS、SDS和效用评分的曲线下面积(AUC)和相关系数。

结果

该患者组的MADRS评分的MCID为4.89 - 4.94,MADRS改善率的MCID为31.15% - 35.10%,SDS评分的MCID为0.69 - 2.14,效用评分的MCID为0.045 - 0.195。从患者视角锚定得出的SDS和效用评分的MCID几乎是从医生视角锚定得出的MCID的两倍。效用评分在患者视角锚定方面具有最高的AUC和相关系数,而MADRS评分在医生视角锚定方面具有最高的AUC和相关系数。

结论

估计了MADRS、SDS和EQ-5D-5L衍生效用评分的MCID。与患者优先考虑功能和日常生活活动的改善相比,医生更关注抑郁症状,并将症状严重程度置于优先地位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/980a/11979183/ebf2dec8a8b5/fpsyt-16-1556470-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/980a/11979183/f6550e4e1fdf/fpsyt-16-1556470-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/980a/11979183/ebf2dec8a8b5/fpsyt-16-1556470-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/980a/11979183/f6550e4e1fdf/fpsyt-16-1556470-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/980a/11979183/ebf2dec8a8b5/fpsyt-16-1556470-g002.jpg

相似文献

1
Assessment of minimum clinically important difference in symptoms and functionality of Japanese patients with major depressive disorder following inadequate response to antidepressants: a analysis of the long-term study of brexpiprazole augmentation therapy in Japanese patients with major depressive disorder.对抗抑郁药反应不足的日本重度抑郁症患者症状和功能的最小临床重要差异评估:一项关于日本重度抑郁症患者布雷哌唑增效治疗长期研究的分析
Front Psychiatry. 2025 Mar 26;16:1556470. doi: 10.3389/fpsyt.2025.1556470. eCollection 2025.
2
A Multicenter, Open-Label Study to Evaluate the Long-term Safety and Efficacy of Adjunctive Brexpiprazole 2 mg Daily in Japanese Patients with Major Depressive Disorder.一项多中心、开放性标签研究,旨在评估每日 2 毫克布瑞哌唑辅助治疗日本重度抑郁症患者的长期安全性和疗效。
CNS Drugs. 2024 Dec;38(12):1003-1016. doi: 10.1007/s40263-024-01124-w. Epub 2024 Oct 18.
3
Adjunctive brexpiprazole 1 mg and 2 mg daily for Japanese patients with major depressive disorder following inadequate response to antidepressants: a phase 2/3, randomized, double-blind (BLESS) study.在抗抑郁药治疗反应不足的日本重度抑郁症患者中,每日联合使用 1 毫克和 2 毫克的布瑞哌唑作为辅助治疗:一项 2/3 期、随机、双盲(BLESS)研究。
Psychiatry Clin Neurosci. 2024 Feb;78(2):113-122. doi: 10.1111/pcn.13615. Epub 2023 Dec 1.
4
Efficacy and safety of adjunctive brexpiprazole 2 mg in major depressive disorder: a phase 3, randomized, placebo-controlled study in patients with inadequate response to antidepressants.辅助使用2毫克布雷哌唑治疗重度抑郁症的疗效和安全性:一项针对对抗抑郁药反应不足患者的3期随机安慰剂对照研究。
J Clin Psychiatry. 2015 Sep;76(9):1224-31. doi: 10.4088/JCP.14m09688.
5
Adjunctive brexpiprazole 1 and 3 mg for patients with major depressive disorder following inadequate response to antidepressants: a phase 3, randomized, double-blind study.辅助使用1毫克和3毫克的布瑞哌唑治疗对抗抑郁药反应不足的重度抑郁症患者:一项3期随机双盲研究。
J Clin Psychiatry. 2015 Sep;76(9):1232-40. doi: 10.4088/JCP.14m09689.
6
Minimal clinically important change in the MADRS anhedonia factor score: A pooled analysis of open-label studies with vortioxetine in patients with major depressive disorder.MADRS 快感缺失因子评分的最小临床有意义变化:在伴有重性抑郁障碍的患者中,使用沃替西汀进行开放性研究的汇总分析。
J Affect Disord. 2024 Oct 15;363:430-435. doi: 10.1016/j.jad.2024.07.070. Epub 2024 Jul 18.
7
Who Benefits From Hip Arthroplasty or Knee Arthroplasty? Preoperative Patient-reported Outcome Thresholds Predict Meaningful Improvement.哪些人能从髋关节置换术或膝关节置换术中获益?术前患者报告的结局阈值可预测有意义的改善。
Clin Orthop Relat Res. 2024 May 1;482(5):867-881. doi: 10.1097/CORR.0000000000002994. Epub 2024 Feb 21.
8
A Randomized, Placebo-Controlled Study of the Efficacy and Safety of Fixed-Dose Brexpiprazole 2 mg/d as Adjunctive Treatment of Adults With Major Depressive Disorder.一项随机、安慰剂对照研究评估了固定剂量 2 毫克 Brexpiprazole 作为辅助治疗成人重度抑郁症的疗效和安全性。
J Clin Psychiatry. 2018 May 22;79(4):17m12058. doi: 10.4088/JCP.17m12058.
9
Efficacy and safety of flexibly dosed brexpiprazole for the adjunctive treatment of major depressive disorder: a randomized, active-referenced, placebo-controlled study.灵活剂量的布雷哌唑辅助治疗重度抑郁症的疗效和安全性:一项随机、活性对照、安慰剂对照研究。
Curr Med Res Opin. 2018 Apr;34(4):633-642. doi: 10.1080/03007995.2018.1430220. Epub 2018 Jan 25.
10
Validation and Functional Relevance of the Short Form of the Perceived Deficits Questionnaire for Depression for Japanese Patients with Major Depressive Disorder.日本重度抑郁症患者抑郁感知缺陷问卷简表的效度及功能相关性
Neuropsychiatr Dis Treat. 2022 Nov 2;18:2507-2517. doi: 10.2147/NDT.S381647. eCollection 2022.

本文引用的文献

1
A Multicenter, Open-Label Study to Evaluate the Long-term Safety and Efficacy of Adjunctive Brexpiprazole 2 mg Daily in Japanese Patients with Major Depressive Disorder.一项多中心、开放性标签研究,旨在评估每日 2 毫克布瑞哌唑辅助治疗日本重度抑郁症患者的长期安全性和疗效。
CNS Drugs. 2024 Dec;38(12):1003-1016. doi: 10.1007/s40263-024-01124-w. Epub 2024 Oct 18.
2
Adjunctive brexpiprazole 1 mg and 2 mg daily for Japanese patients with major depressive disorder following inadequate response to antidepressants: a phase 2/3, randomized, double-blind (BLESS) study.在抗抑郁药治疗反应不足的日本重度抑郁症患者中,每日联合使用 1 毫克和 2 毫克的布瑞哌唑作为辅助治疗:一项 2/3 期、随机、双盲(BLESS)研究。
Psychiatry Clin Neurosci. 2024 Feb;78(2):113-122. doi: 10.1111/pcn.13615. Epub 2023 Dec 1.
3
Implementation of a shared decision-making training program for clinicians based on the major depressive disorder guidelines in Japan: A multi-center cluster randomized trial.基于日本重度抑郁症指南为临床医生实施的共同决策培训项目:一项多中心整群随机试验。
Front Psychiatry. 2022 Aug 12;13:967750. doi: 10.3389/fpsyt.2022.967750. eCollection 2022.
4
Establishing the minimal clinically important difference of the EQ-5D-3L in older adults with a history of falls.确定有跌倒史的老年人中 EQ-5D-3L 的最小临床重要差异。
Qual Life Res. 2022 Nov;31(11):3293-3303. doi: 10.1007/s11136-022-03231-x. Epub 2022 Aug 23.
5
Prevalence of Suicidality in Major Depressive Disorder: A Systematic Review and Meta-Analysis of Comparative Studies.重度抑郁症中自杀倾向的患病率:一项比较研究的系统评价和荟萃分析
Front Psychiatry. 2021 Sep 16;12:690130. doi: 10.3389/fpsyt.2021.690130. eCollection 2021.
6
Assessment of the Minimum Clinically Important Difference in Symptoms and Functions of Patients With Acute Schizophrenia: A Analysis of an Open-Label, Single-Arm Multicenter Study.急性精神分裂症患者症状和功能的最小临床重要差异评估:一项开放标签、单臂多中心研究的分析
Front Psychiatry. 2021 May 3;12:653916. doi: 10.3389/fpsyt.2021.653916. eCollection 2021.
7
How much change is enough? Evidence from a longitudinal study on depression in UK primary care.变化多少才算足够?来自英国初级保健中抑郁纵向研究的证据。
Psychol Med. 2022 Jul;52(10):1875-1882. doi: 10.1017/S0033291720003700. Epub 2020 Nov 3.
8
User's guide to correlation coefficients.相关系数用户指南。
Turk J Emerg Med. 2018 Aug 7;18(3):91-93. doi: 10.1016/j.tjem.2018.08.001. eCollection 2018 Sep.
9
Patient centric measures for a patient centric era: Agreement and convergent between ratings on The Patient Global Impression of Improvement (PGI-I) scale and the Clinical Global Impressions - Improvement (CGI-S) scale in bipolar and major depressive disorder.以患者为中心的时代的患者中心措施:双相情感障碍和重度抑郁症患者的整体改善印象量表(PGI-I)评分与临床整体印象-改善量表(CGI-S)评分之间的一致性和趋同。
Eur Psychiatry. 2018 Sep;53:17-22. doi: 10.1016/j.eurpsy.2018.05.006. Epub 2018 May 30.
10
Moderate/severe Depression (MADRS) Can Affect the Quality of Life and Outcome Among Patients Admitted to Breast Cancer Diagnosis Unit.中度/重度抑郁症(MADRS)会影响乳腺癌诊断科室收治患者的生活质量及预后。
Anticancer Res. 2017 May;37(5):2641-2647. doi: 10.21873/anticanres.11611.