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一项系统评价:评估已获许可的减肥药物治疗精神分裂症和精神病患者的抗精神病药引起的体重增加和肥胖。

A systematic review of licensed weight-loss medications in treating antipsychotic-induced weight gain and obesity in schizophrenia and psychosis.

机构信息

Liaison Mental Health Service, Royal Oldham Hospital, Pennine Care NHS Foundation Trust, United Kingdom.

Liaison Mental Health Service, Royal Oldham Hospital, Pennine Care NHS Foundation Trust, United Kingdom; School of Psychiatry, Health Education England North West, United Kingdom; Manchester Metropolitan University, United Kingdom.

出版信息

Gen Hosp Psychiatry. 2022 Sep-Oct;78:58-67. doi: 10.1016/j.genhosppsych.2022.07.006. Epub 2022 Jul 14.

Abstract

BACKGROUND

Schizophrenia and antipsychotic use are associated with clinically significant weight gain and subsequent increased mortality. Despite weight loss medications (WLMs) licensed by regulatory bodies (FDA, EMA, and MHRA) being available, current psychiatric guidelines recommend off-label alternatives, which differ from non-psychiatric guidelines for obesity.

OBJECTIVE

Evaluate the efficacy of licensed WLMs on treating antipsychotic-induced weight gain (AIWG) and obesity in schizophrenia and psychosis (OSP).

METHOD

A literature search was conducted using Medline, EMBASE, PsycINFO and Cochrane Library online databases for human studies using licensed WLMs to treat AIWG and OSP.

RESULTS

Three RCTs (two liraglutide, one naltrexone-bupropion), one unpublished open-label trial (naltrexone-bupropion), and seven observational studies (five liraglutide, one semaglutide, one multiple WLMs) were identified. Results for liraglutide showed statistically significant improvement in weight, BMI, waist circumference, HbA1c, cholesterol, and LDL readings on meta-analysis. Evidence was mixed for naltrexone-bupropion with no detailed studies conducted for setmelanotide, or stimulants.

CONCLUSION

Evidence is strongest for liraglutide compared to other licensed WLMs. The findings, particularly the inclusion of human trial data, provide evidence for liraglutide use in treating AIWG and OSP, which would better align psychiatric practice with non-psychiatric practices around obesity. The findings also identify continued literature gaps regarding other licensed WLMs.

摘要

背景

精神分裂症和抗精神病药物的使用与临床显著的体重增加以及随后的死亡率增加有关。尽管监管机构(FDA、EMA 和 MHRA)批准了减肥药物(WLMs),但目前的精神科指南推荐使用非标签替代品,这些替代品与肥胖的非精神科指南不同。

目的

评估已批准的 WLMs 治疗精神分裂症和精神病(OSP)中抗精神病药物引起的体重增加(AIWG)和肥胖的疗效。

方法

使用 Medline、EMBASE、PsycINFO 和 Cochrane Library 在线数据库,对使用已批准的 WLMs 治疗 AIWG 和 OSP 的人类研究进行文献检索。

结果

共确定了三项 RCT(两项利拉鲁肽,一项纳曲酮-安非他酮)、一项未发表的开放标签试验(纳曲酮-安非他酮)和七项观察性研究(五项利拉鲁肽、一项司美格鲁肽、一项多种 WLMs)。利拉鲁肽的荟萃分析结果显示体重、BMI、腰围、HbA1c、胆固醇和 LDL 读数均有统计学意义上的改善。纳曲酮-安非他酮的证据不一,对 setmelanotide 或兴奋剂没有详细的研究。

结论

与其他已批准的 WLMs 相比,利拉鲁肽的证据最强。这些发现,特别是纳入了人体试验数据,为利拉鲁肽治疗 AIWG 和 OSP 提供了证据,这将使精神病学实践与肥胖的非精神病学实践更好地保持一致。这些发现还确定了其他已批准的 WLMs 方面持续存在的文献空白。

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