Incidence and risk factors of antidepressant withdrawal symptoms: a meta-analysis and systematic review.

IF 9.6 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Psychiatry Pub Date : 2024-10-11 DOI:10.1038/s41380-024-02782-4
Mi-Mi Zhang, Xuan Tan, Yong-Bo Zheng, Na Zeng, Zhe Li, Mark Abie Horowitz, Xue-Zhu Feng, Ke Wang, Zi-Yi Li, Wei-Li Zhu, Xinyu Zhou, Peng Xie, Xiujun Zhang, Yumei Wang, Jie Shi, Yan-Ping Bao, Lin Lu, Su-Xia Li
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Abstract

Antidepressants are among the most extensively prescribed psychotropic drugs worldwide. Discontinuation induced withdrawal symptoms have been reported for almost all antidepressants. The incidence of antidepressant withdrawal syndrome (AWS) and other characteristics remain unknown. We searched the PubMed, Embase, PsycINFO, MEDLINE, CINAHL, and Cochrane Central Register of Controlled Trials databases from inception to December 31, 2023. Randomized double-blinded trials, longitudinal or cross-sectional studies that reported the incidence and other characteristics of antidepressant withdrawal symptoms were included. The pooled incidence of AWS was calculated by a random effects model. We included 35 studies, of which 2 studies just provided incidence of specific withdrawal symptoms, and 4 studies only described other characteristics. The pooled incidence of AWS from all available studies was 42.9%, from 11 RCTs was 44.4%, in studies in which the treatment duration was mostly 8-12 weeks, which usually appear within 2 weeks, and were generally measured for <4 weeks. The incidence in selective serotonin-norepinephrine reuptake inhibitors was the lowest (29.7%), followed by selective serotonin reuptake inhibitors (45.6%) and tricyclic antidepressants (59.7%), without significant differences (p = 0.221). Treatment duration showed a dose-response to the incidence of AWS (6-12 W: 35.1%, 12-24 W: 42.7%, >24 W: 51.4%). The half-life did not show such a simple dose-dependent relationship. The pooled estimate was robust regardless whether withdrawal symptoms were measured in RCTs or observational studies (including face-to-face and online survey studies). Tapering the dose reduced the incidence of AWS compared with abrupt stoppage (34.5% vs 42.5%), without a significant difference (p = 0.484). Risk factors for withdrawal symptoms included being female, younger, experiencing adverse effects early in treatment, taking higher doses or longer duration of medication, abrupt cessation of drugs, and those with a lower clearance of drugs or with serotonin 1A receptor gene variation. The findings suggest the incidence of AWS are common and some clinical characteristics and risk factors which can help clinicians identify who is at greater risk of experiencing AWS. Discontinuation studies on long-term antidepressant users with long follow-up periods are required in the future.

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抗抑郁药戒断症状的发生率和风险因素:荟萃分析和系统综述。
抗抑郁药是全世界处方量最大的精神药物之一。据报道,几乎所有抗抑郁药物都有因停药引起的戒断症状。抗抑郁药戒断综合征(AWS)的发病率及其他特征仍不为人所知。我们检索了 PubMed、Embase、PsycINFO、MEDLINE、CINAHL 和 Cochrane Central Register of Controlled Trials 等数据库中从开始到 2023 年 12 月 31 日的数据。纳入了报告抗抑郁药戒断症状发生率和其他特征的随机双盲试验、纵向或横断面研究。通过随机效应模型计算出AWS的总发生率。我们共纳入了 35 项研究,其中 2 项研究仅提供了特定戒断症状的发生率,4 项研究仅描述了其他特征。从所有可用研究中汇总的戒断症状发生率为 42.9%,从 11 项研究中汇总的戒断症状发生率为 44.4%,在这些研究中,治疗持续时间大多为 8-12 周,戒断症状通常在 2 周内出现,一般在 24 小时内测量:51.4%)。半衰期并未显示出如此简单的剂量依赖关系。无论戒断症状是在 RCT 还是观察性研究(包括面对面研究和在线调查研究)中测量得出,汇总的估计值都是可靠的。与突然停药相比,逐渐减少剂量降低了戒断症状的发生率(34.5% vs 42.5%),但差异不显著(p = 0.484)。出现戒断症状的风险因素包括女性、年轻、治疗初期出现不良反应、服药剂量较大或服药时间较长、突然停药、药物清除率较低或血清素 1A 受体基因变异。研究结果表明,AWS的发病率很高,一些临床特征和风险因素可以帮助临床医生识别哪些人更容易发生AWS。今后需要对长期服用抗抑郁药的患者进行停药研究,并进行长期随访。
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
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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