Pharmacopsychiatry 2017; 50(02): 49-55
DOI: 10.1055/s-0042-120120
Review
© Georg Thieme Verlag KG Stuttgart · New York

PPAR-γ Agonists for the Treatment of Major Depression: A Review

Autoren

  • R. Colle*

    1   University Paris-Sud, Le Kremlin Bicêtre, France
    2   INSERM, UMRS 1178, Le Kremlin Bicêtre, France
    3   Hôpital Bicêtre, Hôpitaux Universitaires Paris-Sud, Assistance Publique-Hôpitaux de Paris, Le Kremlin Bicêtre, France
    4   Département de Psychiatrie, Le Kremlin Bicêtre, France
  • D. de Larminat*

    1   University Paris-Sud, Le Kremlin Bicêtre, France
    2   INSERM, UMRS 1178, Le Kremlin Bicêtre, France
    3   Hôpital Bicêtre, Hôpitaux Universitaires Paris-Sud, Assistance Publique-Hôpitaux de Paris, Le Kremlin Bicêtre, France
    4   Département de Psychiatrie, Le Kremlin Bicêtre, France
  • S. Rotenberg

    1   University Paris-Sud, Le Kremlin Bicêtre, France
    2   INSERM, UMRS 1178, Le Kremlin Bicêtre, France
    3   Hôpital Bicêtre, Hôpitaux Universitaires Paris-Sud, Assistance Publique-Hôpitaux de Paris, Le Kremlin Bicêtre, France
    4   Département de Psychiatrie, Le Kremlin Bicêtre, France
  • F. Hozer

    1   University Paris-Sud, Le Kremlin Bicêtre, France
    2   INSERM, UMRS 1178, Le Kremlin Bicêtre, France
    3   Hôpital Bicêtre, Hôpitaux Universitaires Paris-Sud, Assistance Publique-Hôpitaux de Paris, Le Kremlin Bicêtre, France
    4   Département de Psychiatrie, Le Kremlin Bicêtre, France
  • P. Hardy

    1   University Paris-Sud, Le Kremlin Bicêtre, France
    2   INSERM, UMRS 1178, Le Kremlin Bicêtre, France
    3   Hôpital Bicêtre, Hôpitaux Universitaires Paris-Sud, Assistance Publique-Hôpitaux de Paris, Le Kremlin Bicêtre, France
    4   Département de Psychiatrie, Le Kremlin Bicêtre, France
  • C. Verstuyft

    1   University Paris-Sud, Le Kremlin Bicêtre, France
    3   Hôpital Bicêtre, Hôpitaux Universitaires Paris-Sud, Assistance Publique-Hôpitaux de Paris, Le Kremlin Bicêtre, France
    5   INSERM UMR_S1184, Centre IMVA
    6   Service de Génétique moléculaire, Pharmacogénétique et Hormonologie
  • B. Fève*

    7   Sorbonne Universités, Université Pierre et Marie Curie, Centre de Recherche Saint-Antoine, INSERM UMR_S938, Paris, France
    8   Institut Hospitalo-Universitaire ICAN, Paris, France
    9   Service d’Endocrinologie, Assistance Publique des Hôpitaux de Paris, Hôpital Saint-Antoine, Paris, France
  • E. Corruble*

    1   University Paris-Sud, Le Kremlin Bicêtre, France
    2   INSERM, UMRS 1178, Le Kremlin Bicêtre, France
    3   Hôpital Bicêtre, Hôpitaux Universitaires Paris-Sud, Assistance Publique-Hôpitaux de Paris, Le Kremlin Bicêtre, France
    4   Département de Psychiatrie, Le Kremlin Bicêtre, France
Weitere Informationen

Publikationsverlauf

received 08. September 2016
revised 26. September 2016

accepted 25. Oktober 2016

Publikationsdatum:
15. Dezember 2016 (online)

Abstract

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.

* These authors contributed equally to this work.


* These authors co-directed this work.