Mandelli Laura, Wang Sheng-Min, Han Changsu, Lee Soo-Jung, Patkar Ashwin A, Masand Prakash S, Pae Chi-Un, Serretti Alessandro
Department of Biomedical and NeuroMotor Sciences, Institute of Psychiatry, University of Bologna, Bologna, Italy.
Department of Psychiatry, The Catholic University of Korea College of Medicine, Seoul, Republic of Korea.
Adv Ther. 2017 Mar;34(3):713-724. doi: 10.1007/s12325-017-0482-2. Epub 2017 Jan 31.
Ample evidence suggested a role of sigma-1 receptor in affective disorders since the interaction of numerous antidepressants with sigma receptors was discovered. A recent study on Japanese subjects found a genetic variant within the encoding gene SIGMAR1 (rs1800866A>C) associated with major depressive disorder (MDD). We aimed to evaluate the same polymorphism in both MDD and bipolar disorder (BD) as well as its relationship to response to treatment with antidepressants and mood stabilizers.
A total of 238 MDD patients treated for an acute episode of depression, 132 BD patients in treatment with mood stabilizers for a manic or mixed episode, and 324 controls were genotyped for rs1800866. At discharge, response to treatments was evaluated in MDD and BD patients by the Hamilton Rating Scale for Depression (HRSD) and the Young Mania Rating Score (YMRS), respectively.
In our Korean sample, allele frequencies were different from those reported in other Asian and non-Asian populations. The CC genotype was associated with BD and, as a trend, with MDD. No significant effect was observed on response to antidepressants in MDD or mood stabilizers in BD, although the CC genotype was more frequent among BD patients experiencing a mixed episode.
The present findings are the first to propose the putative role of genetic variants within SIGMAR1 and sigma-1 receptor in BD. Sigma-1 receptor can modulate a number of central neurotransmitter systems as well as some other signaling pathways (e.g., neurotrophin and growth factor signaling) which are seemingly involved in BD and other mood disorders.
自从发现众多抗抑郁药与σ受体相互作用以来,大量证据表明σ-1受体在情感障碍中发挥作用。最近一项针对日本受试者的研究发现,编码基因SIGMAR1(rs1800866A>C)内的一个基因变异与重度抑郁症(MDD)相关。我们旨在评估该多态性在MDD和双相情感障碍(BD)中的情况,以及它与抗抑郁药和心境稳定剂治疗反应的关系。
对238例因抑郁症急性发作接受治疗的MDD患者、132例因躁狂或混合发作接受心境稳定剂治疗的BD患者以及324名对照者进行rs1800866基因分型。出院时,分别通过汉密尔顿抑郁量表(HRSD)和杨氏躁狂评定量表(YMRS)评估MDD和BD患者的治疗反应。
在我们的韩国样本中,等位基因频率与其他亚洲和非亚洲人群报道的不同。CC基因型与BD相关,并且在MDD中呈一种趋势。在MDD患者对抗抑郁药的反应或BD患者对心境稳定剂的反应方面未观察到显著影响,尽管CC基因型在经历混合发作的BD患者中更常见。
本研究结果首次提出SIGMAR1内基因变异和σ-1受体在BD中的假定作用。σ-1受体可以调节多个中枢神经递质系统以及一些其他信号通路(如神经营养因子和生长因子信号通路),这些通路似乎与BD和其他心境障碍有关。