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米尔立诺利特,一种选择性糖皮质激素受体调节剂,对健康受试者奥氮平相关体重增加的影响:概念验证研究。

Effect of Miricorilant, a Selective Glucocorticoid Receptor Modulator, on Olanzapine-Associated Weight Gain in Healthy Subjects: A Proof-of-Concept Study.

机构信息

From Corcept Therapeutics, Menlo Park, CA.

Jade Consultants (Cambridge) Ltd, Cambridge, United Kingdom.

出版信息

J Clin Psychopharmacol. 2021;41(6):632-637. doi: 10.1097/JCP.0000000000001470.

DOI:10.1097/JCP.0000000000001470
PMID:34369902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8575171/
Abstract

PURPOSE

Antipsychotic medications, including olanzapine, are associated with substantial weight gain and metabolic disturbances. We sought to determine whether coadministration of miricorilant, a selective glucocorticoid receptor modulator, with olanzapine can ameliorate these effects.

METHODS

Sixty-six healthy men were enrolled in a 2-week, randomized, double-blind, placebo-controlled trial. The primary objective was to evaluate changes in body weight after 14 days coadministration of olanzapine (10 mg) + miricorilant (600 mg) compared with olanzapine (10 mg) + placebo. Secondary objectives included evaluating (a) the safety and tolerability of the combination; (b) the effects of the combination on glucose, insulin, insulin resistance, and triglycerides; and (c) the impact of the combination on hepatic enzymes.

RESULTS

Subjects administered olanzapine + miricorilant gained less weight than subjects administered olanzapine + placebo (mean weight gain on day 15, 3.91 kg vs 4.98 kg; difference between groups, -1.07 kg; 95% confidence interval, -1.94 to -0.19; P = 0.017]). Compared with the placebo group, coadministration of miricorilant with olanzapine was associated with smaller increases in insulin (difference, -3.74 mIU/L; P = 0.007), homeostatic model assessment of insulin resistance (difference, -0.47; P = 0.007), triglycerides (difference, -0.29 mmol/L; P = 0.057), aspartate aminotransferase (difference, -32.24 IU/L; P = 0.009), and alanine aminotransferase (difference, -49.99 IU/L; P = 0.030).

CONCLUSIONS

Miricorilant may provide a promising option for ameliorating the detrimental effects of olanzapine, and investigation of this medication in patients affected by antipsychotic-induced weight gain is warranted. Two phase 2 studies of miricorilant in patients with recent and long-standing antipsychotic-induced weight gain are currently in progress.

摘要

目的

包括奥氮平在内的抗精神病药物会导致体重显著增加和代谢紊乱。我们旨在确定联合使用米立莫利单抗(一种选择性糖皮质激素受体调节剂)是否可以改善这些影响。

方法

66 名健康男性参与了一项为期 2 周的随机、双盲、安慰剂对照试验。主要目的是评估在奥氮平(10 毫克)+米立莫利单抗(600 毫克)联合治疗 14 天后体重的变化,与奥氮平(10 毫克)+安慰剂相比。次要目标包括评估(a)联合用药的安全性和耐受性;(b)联合用药对血糖、胰岛素、胰岛素抵抗和甘油三酯的影响;以及(c)联合用药对肝酶的影响。

结果

服用奥氮平+米立莫利单抗的受试者体重增加少于服用奥氮平+安慰剂的受试者(第 15 天的体重增加,3.91 公斤与 4.98 公斤;两组间差异,-1.07 公斤;95%置信区间,-1.94 至 -0.19;P = 0.017])。与安慰剂组相比,米立莫利单抗联合奥氮平治疗与胰岛素(差异,-3.74 mIU/L;P = 0.007)、稳态模型评估的胰岛素抵抗(差异,-0.47;P = 0.007)、甘油三酯(差异,-0.29 mmol/L;P = 0.057)、天冬氨酸氨基转移酶(差异,-32.24 IU/L;P = 0.009)和丙氨酸氨基转移酶(差异,-49.99 IU/L;P = 0.030)的增加较小。

结论

米立莫利单抗可能为改善奥氮平的有害影响提供一种有前途的选择,值得在受抗精神病药引起的体重增加影响的患者中进行这种药物的研究。目前正在进行两项米立莫利单抗治疗近期和长期抗精神病药引起的体重增加患者的 2 期研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/8575171/d1b896a22267/jcp-41-632-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/8575171/d1b896a22267/jcp-41-632-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dab4/8575171/d1b896a22267/jcp-41-632-g001.jpg

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