糖皮质激素拮抗剂是抗精神病药物引起的体重增加的潜在治疗选择吗?

IF 0.4 Q4 PHARMACOLOGY & PHARMACY Journal of Pharmacology & Pharmacotherapeutics Pub Date : 2021-04-01 DOI:10.4103/jpp.jpp_33_21
Wisam Al Jumaili, C. Trivedi, K. Shah, M. Adnan, Z. Mansuri, S. Jain
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引用次数: 0

摘要

目的:评价米非司酮作为抗精神病药致体重增加的新治疗方式的有效性和安全性。方法:我们检索截至2021年3月的数据库,检索已发表的英文文献,包括医学主题标题为“米非司酮”、“受体、糖皮质激素”、“体重增加”、“超重”、“肥胖”、“体重变化”、“抗精神病药物”、“糖皮质激素受体阻滞剂”、“糖皮质激素受体拮抗剂”。我们确定了两项临床和四项临床前研究使用米非司酮作为治疗方式。结果:奥氮平临床试验结果显示,奥氮平联合安慰剂组从基线到第14天的平均体重增加(3.2±0.9 kg)大于奥氮平联合米非司酮组(2.0±1.2 kg)和米非司酮联合安慰剂组(2.0±0.7 kg),利培酮联合米非司酮临床试验中也观察到类似的效果。结论:米非司酮在AIWG的治疗中具有一定的潜力。糖皮质激素拮抗剂是抑制这种副作用的可行选择。基于这种作用机制,有必要进行大规模的临床研究,以确定药物的安全性和有效性。
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Is a Glucocorticoid Antagonist a Potential Treatment Alternative for Antipsychotic-Induced Weight Gain?
Objective: To evaluate the efficacy and safety of mifepristone as a new treatment modality for antipsychotic-induced weight gain. Methods: We searched databases up to March 2021, for the published English-language literature including a Medical Subject Heading “Mifepristone,” “Receptors, Glucocorticoid,” “Weight gain,” “Overweight,” “Obesity,” “Body Weight Change,” “Antipsychotics Agents,” “Glucocorticoid Receptor Blocker,” “Glucocorticoid Receptor antagonist.” We identified two clinical and four preclinical studies utilizing mifepristone as a treatment modality. Results: The results of the olanzapine clinical trial showed that mean increase in weight from baseline to day 14 was greater in the olanzapine with the placebo group (3.2 ± 0.9 kg) than the olanzapine with mifepristone group (2.0 ± 1.2 kg) and the mifepristone with placebo (2.0 ± 0.7 kg), and a similar effect was observed in the risperidone with mifepristone clinical trial. Conclusions: Mifepristone shows potential in the management of AIWG. Glucocorticoid antagonists can be a viable alternative to curb this side effect. Large-scale clinical studies are warranted to determine the medication's safety and efficacy based on this mechanism of action.
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