Goh Kah Kheng, Chen Chun-Hsin, Lu Mong-Liang
Department of Psychiatry, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Psychiatric Research Center, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan.
J Psychopharmacol. 2025 Mar 24:2698811251326945. doi: 10.1177/02698811251326945.
Antipsychotic treatment is commonly associated with hyperprolactinemia, leading to menstrual disturbances, sexual dysfunction, and decreased bone mineral density. Nearly all antipsychotic drugs can elevate prolactin levels, affecting up to 70% of patients with schizophrenia. We aim to evaluate the potential therapeutic role of metformin in reducing hyperprolactinemia among these patients.
We systematically searched PubMed, CNKI, Embase, Cochrane, and Web of Science through January 31, 2024, for randomized controlled trials (RCTs) evaluating metformin's effect on prolactin levels in patients with schizophrenia. Data were extracted and synthesized using random-effects meta-analysis.
This meta-analysis included 10 RCTs with 1046 participants (584 received metformin and 462 received placebo or no treatment). Metformin significantly reduced prolactin levels compared to control groups (SMD = -0.98, 95% CI: -1.62, -0.35, = 0.002; transformed MD = -34.88 ng/mL, 95% CI: -57.65, -12.46). Subgroup analyses indicated that higher doses (1500 mg), shorter treatment durations (<24 weeks), higher BMI (>25 kg/m²), and longer illness duration (>1 year) were associated with more significant prolactin reductions. Metformin was well tolerated with no significant increase in adverse events or all-cause discontinuation rates compared to the control group.
This meta-analysis suggests that metformin shows potential as a treatment for antipsychotic-induced hyperprolactinemia, with a favorable tolerability profile in patients with schizophrenia, particularly at higher doses, shorter treatment durations, higher BMI, and longer illness duration. Despite the robustness of the findings, high heterogeneity necessitates cautious interpretation. Future research should explore demographic and clinical factors influencing the response to metformin for optimizing treatment.
抗精神病药物治疗通常与高催乳素血症相关,可导致月经紊乱、性功能障碍和骨密度降低。几乎所有抗精神病药物均可升高催乳素水平,影响多达70%的精神分裂症患者。我们旨在评估二甲双胍在降低这些患者高催乳素血症方面的潜在治疗作用。
我们系统检索了截至2024年1月31日的PubMed、CNKI、Embase、Cochrane和Web of Science,以查找评估二甲双胍对精神分裂症患者催乳素水平影响的随机对照试验(RCT)。使用随机效应荟萃分析提取和综合数据。
该荟萃分析纳入了10项RCT,共1046名参与者(584名接受二甲双胍治疗,462名接受安慰剂或未治疗)。与对照组相比,二甲双胍显著降低了催乳素水平(标准化均数差= -0.98,95%可信区间:-1.62,-0.35,P = 0.002;转换后的均数差= -34.88 ng/mL,95%可信区间:-57.65,-12.46)。亚组分析表明,更高剂量(1500 mg)、更短治疗时长(<24周)、更高体重指数(>25 kg/m²)和更长病程(>1年)与更显著的催乳素降低相关。与对照组相比,二甲双胍耐受性良好,不良事件或全因停药率无显著增加。
该荟萃分析表明,二甲双胍显示出治疗抗精神病药物所致高催乳素血症的潜力,在精神分裂症患者中具有良好的耐受性,尤其是在更高剂量、更短治疗时长、更高体重指数和更长病程的情况下。尽管研究结果具有稳健性,但高异质性需要谨慎解读。未来的研究应探索影响二甲双胍反应的人口统计学和临床因素,以优化治疗。