Department of Psychiatry, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Department of Anesthesiology, Chi Mei Medical Center, Tainan, Taiwan.
BMJ Ment Health. 2024 Nov 18;27(1):e301165. doi: 10.1136/bmjment-2024-301165.
The optimal dose of lurasidone for bipolar depression is unclear. This study examined its dose-response relationship for efficacy, acceptability, and metabolic/endocrine profiles.
Five databases and grey literature published until 1 August 2024, were systematically reviewed. The outcomes included efficacy (changes in depression, anxiety, clinical global impression, disability and quality of life), acceptability (dropout, manic switch, suicidality and side effects) and metabolic/endocrine profiles (changes in body weight, glucose, lipid and prolactin levels). Effect sizes were calculated using a one-step dose-response meta-analysis, expressed as standardised mean differences (SMDs), risk ratios (RRs) and mean differences (MDs) with 95% CIs.
Five randomised clinical trials (2032 patients, mean treatment duration 6 weeks) indicated that the optimal therapeutic dose of lurasidone (40-60 mg) improved depression (50 mg: SMD -0.60 (95% CI -0.30, -0.89)), anxiety (50 mg: -0.32 (95% CI -0.21, -0.42)), clinical global impression (50 mg: -0.67 (95% CI -0.30, -1.03)) and disability (50 mg: -0.38 (95% CI -0.08, -0.69)). Side effects increased with higher doses (50 mg: RR 1.15 (95% CI 1.05, 1.25); 100 mg: 1.18 (95% CI 1.02, 1.36)), but dropout, manic switch and suicidality did not show a dose-effect relationship. Weight increased at doses<60 mg (40 mg: MD 0.38 (95% CI 0.16, 0.60) kg), while blood glucose levels rose at doses>70 mg (100 mg: 3.16 (95% CI 0.76, 5.57) mg/dL). Prolactin levels increased in both males (50 mg: 3.21 (95% CI 1.59, 4.84) ng/mL; 100 mg: 5.61 (95% CI 2.42, 8.81)) and females (50 mg: 6.64 (95% CI 3.50, 9.78); 100 mg: 5.33 (95% CI 0.67, 10.00)).
A daily dose of 40-60 mg of lurasidone is a reasonable choice for bipolar depression treatment.
INPLASY202430069.
对于双相情感障碍的抑郁发作,拉鲁色酮的最佳剂量尚不清楚。本研究旨在考察其疗效、可接受性和代谢/内分泌特征的剂量反应关系。
系统检索了截至 2024 年 8 月 1 日的五个数据库和灰色文献。结果包括疗效(抑郁、焦虑、临床总体印象、残疾和生活质量的变化)、可接受性(脱落、躁狂发作、自杀意念和副作用)和代谢/内分泌特征(体重、血糖、血脂和催乳素水平的变化)。使用一步剂量反应荟萃分析计算效应大小,以标准化均数差值(SMD)、风险比(RR)和均值差(MD)表示,并带有 95%置信区间(CI)。
五项随机临床试验(2032 名患者,平均治疗时间为 6 周)表明,拉鲁色酮的最佳治疗剂量(40-60mg)可改善抑郁(50mg:SMD-0.60[95%CI-0.30,-0.89])、焦虑(50mg:-0.32[95%CI-0.21,-0.42])、临床总体印象(50mg:-0.67[95%CI-0.30,-1.03])和残疾(50mg:-0.38[95%CI-0.08,-0.69])。副作用随剂量增加而增加(50mg:RR 1.15[95%CI 1.05,1.25];100mg:1.18[95%CI 1.02,1.36]),但脱落、躁狂发作和自杀意念与剂量无相关性。体重在<60mg 剂量时增加(40mg:MD 0.38[95%CI 0.16,0.60]kg),而血糖水平在>70mg 剂量时升高(100mg:3.16[95%CI 0.76,5.57]mg/dL)。男性(50mg:3.21[95%CI 1.59,4.84]ng/mL;100mg:5.61[95%CI 2.42,8.81])和女性(50mg:6.64[95%CI 3.50,9.78];100mg:5.33[95%CI 0.67,10.00])的催乳素水平均升高。
拉鲁色酮每天 40-60mg 是治疗双相情感障碍抑郁发作的合理选择。
INPLASY202430069。