Towards a personalized treatment in depression: endocannabinoids, inflammation and stress response

被引:23
|
作者
Zajkowska, Zuzanna E. [1 ]
Englund, Amir [2 ]
Zunszain, Patricia A. [1 ]
机构
[1] Kings Coll London, Sect Stress Psychiat & Immunol, Dept Psychol Med, Inst Psychiat, London SE5 9NU, England
[2] Kings Coll London, Inst Psychiat, London SE5 8AF, England
关键词
antidepressant; CNR1; CNR2; COX-2; FAAH; FKBP5; GR; HPA axis; IL-1; immune; inflammatory; polymorphism; GLUCOCORTICOID-RECEPTOR POLYMORPHISMS; ANTIDEPRESSANT TREATMENT RESPONSE; PITUITARY-ADRENAL AXIS; MAJOR DEPRESSION; MOOD DISORDERS; CNR1; GENE; CANNABINOID RECEPTORS; RESISTANT DEPRESSION; CITALOPRAM TREATMENT; FKBP5; POLYMORPHISMS;
D O I
10.2217/pgs.14.40
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The complex nature of depression is mirrored by difficulties in tailoring its treatment. Key underlying mechanisms of this mental disorder include elevated inflammation and a dysregulated hypothalamic-pituitary-adrenal (HPA) axis. More recently, the endocannabinoid system has been proposed as another important component in the pathogenesis of depression, and strong evidence suggests that all three systems communicate with each other. A growing number of genetic studies have investigated polymorphisms in depression in each of these systems separately. However, no study to date has looked at these genes in conjunction. In this article we will review the crosstalk between the endocannabinoid system, immune system and HPA axis; and discuss the evidence of gene polymorphisms and their relation to the risk of depression and its treatment. We propose future directions where genes of these three systems are considered from a joint perspective to improve prediction of treatment response, taking into account potentially overlooked genetic variations.
引用
收藏
页码:687 / 698
页数:12
相关论文
共 50 条
  • [1] Pharmacogenomic Testing and Personalized Treatment of Depression
    Perlis, Roy H.
    CLINICAL CHEMISTRY, 2014, 60 (01) : 53 - 59
  • [2] Deep Brain Stimulation for Treatment-Resistant Depression: Towards a More Personalized Treatment Approach
    Roet, Milaine
    Boonstra, Jackson
    Sahin, Erdi
    Mulders, Anne E. P.
    Leentjens, Albert F. G.
    Jahanshahi, Ali
    JOURNAL OF CLINICAL MEDICINE, 2020, 9 (09) : 1 - 19
  • [3] Gene-Environment Interaction in Major Depression and Antidepressant Treatment Response
    Keers, Robert
    Uher, Rudolf
    CURRENT PSYCHIATRY REPORTS, 2012, 14 (02) : 129 - 137
  • [4] Abnormalities in neuroendocrine stress response in psychosis: the role of endocannabinoids
    Appiah-Kusi, E.
    Leyden, E.
    Parmar, S.
    Mondelli, V.
    McGuire, P.
    Bhattacharyya, S.
    PSYCHOLOGICAL MEDICINE, 2016, 46 (01) : 27 - 45
  • [5] Inflammation and clinical response to treatment in depression: A meta-analysis
    Strawbridge, R.
    Arnone, D.
    Danese, A.
    Papadopoulos, A.
    Vives, A. Herane
    Cleare, A. J.
    EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2015, 25 (10) : 1532 - 1543
  • [6] New trends in personalized treatment of depression
    Sampogna, Gaia
    Toni, Claudia
    Catapano, Pierluigi
    Della Rocca, Bianca
    Di Vincenzo, Matteo
    Luciano, Mario
    Fiorillo, Andrea
    CURRENT OPINION IN PSYCHIATRY, 2024, 37 (01) : 3 - 8
  • [7] Perspective of Personalized Drug Treatment in Depression
    Ising, Marcus
    Scheuer, Sandra
    Belcredi, Petra
    Uhr, Manfred
    Holsboer, Florian
    BIOLOGICAL PSYCHIATRY, 2018, 83 (09) : S375 - S376
  • [8] Choosing Treatment for Depression in Older Adults and Evaluating Response
    Arean, Patricia A.
    Niu, Grace
    CLINICS IN GERIATRIC MEDICINE, 2014, 30 (03) : 535 - +
  • [9] Stress-Related Immune Markers in Depression: Implications for Treatment
    Hughes, Martina M.
    Connor, Thomas J.
    Harkin, Andrew
    INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2016, 19 (06) : 1 - 19
  • [10] The Relationship between Stress, Inflammation, and Depression
    Kim, Il-Bin
    Lee, Jae-Hon
    Park, Seon-Cheol
    BIOMEDICINES, 2022, 10 (08)