医学
抗抑郁药
胰岛素抵抗
内科学
罗格列酮
2型糖尿病
葡萄糖稳态
二甲双胍
不利影响
药理学
安慰剂
随机对照试验
内分泌学
吡格列酮
肿瘤科
糖尿病
胰岛素
替代医学
病理
海马体
作者
Romain Colle,Solenn de Larminat,Samuel Rotenberg,Franz Hozer,P. Hardy,Céline Verstuyft,Bruno Fève,Emmanuelle Corruble
出处
期刊:Pharmacopsychiatry
[Thieme Medical Publishers (Germany)]
日期:2016-12-15
卷期号:50 (02): 49-55
被引量:65
标识
DOI:10.1055/s-0042-120120
摘要
Introduction: Selective agonists of the nuclear transcription factor peroxisome proliferator-activated receptor-gamma (PPAR-γ) are used for the treatment of type 2 diabetes. We reviewed their efficacy and safety for the treatment of major depression and the association of their potential antidepressant effects with changes in biomarkers of metabolism and inflammation. Methods: From 8 studies, 4 open-label trials, and 4 randomized controlled trials (RCT) (3 vs. placebo and 1 vs. metformin), 448 patients with major depression were included, of which 209 patients received PPAR-γ agonists (pioglitazone or rosiglitazone) for 6-12 weeks, either alone or in add-on therapy to conventional treatments. Results: PPAR-γ agonists have antidepressant effects in the 4 open-label studies and in 3 out of 4 RCT. No major adverse event was reported. Improvement in depression scores was associated with improvement in 3 biomarkers of insulin resistance (homeostatic model assessment [HOMA-IR], oral glucose tolerance test, and fasting plasma glucose) and 1 biomarker of inflammation (interleukin-6) among 21 biomarkers studied. Conclusion: PPAR-γ agonists may have antidepressant properties, which need to be assessed in further studies of major depressive episodes.
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