Wang Zuowei, Li Xujuan, Li Ningning, Huang Leping, Liu Jiawen, Yang Bixiu, Shi Jingquan, Fei Yue, Ji Xunming, Gao Keming, Ren Ming
Division of Mood Disorders, Hongkou District Mental Health Center, Shanghai, China.
School of Medicine, Shanghai University, Shanghai, China.
Front Psychiatry. 2020 Jun 18;11:570. doi: 10.3389/fpsyt.2020.00570. eCollection 2020.
A substantial proportion of patients with major depressive disorder (MDD) does not respond or cannot tolerate to currently available treatments. This study was to assess the safety and tolerability of Remote Limb Ischemic Preconditioning (RLIPC) as an adjunctive therapy in patients with MDD.
Enrolled patients underwent RLIPC, five cycles of simultaneous bilateral arm ischemia, 5 min and followed by reperfusion of each cycle, and once daily for eight consecutive weeks. Depression and anxiety severity, and quality of life were assessed every 2 weeks. Descriptive analysis was used for safety and tolerability data.
Thirty-seven participants completed at least one RLIPC. Twenty-four of them (64.9%) completed the study. Twelve patients prematurely discontinued the study due to poor adherence, and one due to a mild side effect. The changes in HRSD-17, GAD-7 and QOL-6 total scores from baseline to the endpoint were significant from the end of second week treatment onwards. The responder and remission rates were 59.46% (22/37) and 54.05% (20/37) at the endpoint, respectively.
RLIPC was safe and well tolerated, and may be effective in reducing depressive symptoms in patients with MDD. Large studies are warranted to test its efficacy and safety as monotherapy or adjunctive therapy in the treatment of MDD.
相当一部分重度抑郁症(MDD)患者对目前可用的治疗方法无反应或无法耐受。本研究旨在评估远程肢体缺血预处理(RLIPC)作为MDD患者辅助治疗的安全性和耐受性。
入选患者接受RLIPC治疗,即五个周期的双侧手臂同时缺血,每个周期5分钟,随后进行再灌注,连续八周每天一次。每2周评估一次抑郁和焦虑严重程度以及生活质量。对安全性和耐受性数据进行描述性分析。
37名参与者完成了至少一次RLIPC治疗。其中24人(64.9%)完成了研究。12名患者因依从性差提前终止研究,1名患者因轻微副作用提前终止研究。从治疗第二周结束起,HRSD-17、GAD-7和QOL-6总分从基线到终点的变化具有显著性。终点时缓解率和治愈率分别为59.46%(22/37)和54.05%(20/37)。
RLIPC安全且耐受性良好,可能对减轻MDD患者的抑郁症状有效。有必要开展大型研究以检验其作为MDD单一疗法或辅助疗法的疗效和安全性。