Université de Paris, Institute of Psychiatry and Neuroscience of Paris (IPNP), INSERM U1266, Team Vulnerability of Psychiatric and Addictive Disorders, 75014, Paris, France.
Assistance Publique-Hôpitaux de Paris (APHP), Corentin Celton Hospital, Department of Psychiatry, 92130, Issy-les-Moulineaux, France.
Transl Psychiatry. 2020 Nov 5;10(1):378. doi: 10.1038/s41398-020-01067-y.
Polymorphisms of genes involved in the hypothalamic-pituitary-adrenocortical (HPA) axis have been associated with response to several antidepressant treatments in patients suffering of depression. These pharmacogenetics findings have been reported from independent cohorts of patients mostly treated with selective serotonin reuptake inhibitors, tricyclic antidepressant, and mirtazapine. Tianeptine, an atypical antidepressant, recently identified as a mu opioid receptor agonist, which prevents and reverses the stress induced by glucocorticoids, has been investigated in this present pharmacogenetics study. More than 3200 Caucasian outpatients with a major depressive episode (MDE) from real-life settings were herein analyzed for clinical response to tianeptine, a treatment initiated from 79.5% of the subjects, during 6-8 weeks follow-up, assessing polymorphisms targeting four genes involved in the HPA axis (NR3C1, FKPB5, CRHR1, and AVPR1B). We found a significant association (p < 0.001) between CRHR1 gene variants rs878886 and rs16940665, or haplotype rs878886C-rs16940665T, and tianeptine antidepressant response and remission according to the hospital anxiety and depression scale. Analyses, including a structural equation model with simple mediation, suggest a moderate effect of sociodemographic characteristics and depressive disorder features on treatment response in individuals carrying the antidepressant responder allele rs8788861 (allele C). These findings suggest direct pharmacological consequences of CRHR1 polymorphisms in the antidepressant tianeptine response and remission, in MDE patients. This study replicates the association of the CRHR1 gene, involved in the HPA axis, with (1) a specificity attributed to treatment response, (2) a lower risk of chance finding, and in (3) an ecological situation.
涉及下丘脑-垂体-肾上腺(HPA)轴的基因多态性与抑郁症患者对几种抗抑郁治疗的反应有关。这些药物遗传学发现已在大多数接受选择性 5-羟色胺再摄取抑制剂、三环抗抑郁药和米氮平治疗的独立患者队列中报道。噻奈普汀是一种新型抗抑郁药,最近被鉴定为μ阿片受体激动剂,可预防和逆转糖皮质激素引起的应激,在本药物遗传学研究中进行了研究。对来自真实环境的 3200 多名高加索门诊患者进行了主要抑郁发作(MDE)的临床反应分析,这些患者接受噻奈普汀治疗,起始治疗时间为 79.5%的患者,随访 6-8 周,评估了四个参与 HPA 轴的基因(NR3C1、FKPB5、CRHR1 和 AVPR1B)的靶向多态性。我们发现 CRHR1 基因变体 rs878886 和 rs16940665,或单倍型 rs878886C-rs16940665T,与汉密尔顿焦虑和抑郁量表的噻奈普汀抗抑郁反应和缓解之间存在显著关联(p<0.001)。包括简单中介结构方程模型在内的分析表明,携带抗抑郁反应等位基因 rs8788861(等位基因 C)的个体的社会人口统计学特征和抑郁障碍特征对治疗反应有中等影响。这些发现表明,CRHR1 多态性在 MDE 患者中直接影响噻奈普汀的抗抑郁反应和缓解。这项研究复制了参与 HPA 轴的 CRHR1 基因与(1)归因于治疗反应的特异性,(2)降低机会发现的风险,以及(3)生态情况的关联。