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精神分裂症迟发性运动障碍的药物遗传学:和毒蕈碱受体的作用。

Pharmacogenetics of tardive dyskinesia in schizophrenia: The role of and muscarinic receptors.

机构信息

Mental Health Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Tomsk, Russian Federation.

National Research Tomsk Polytechnic University, Tomsk, Russian Federation.

出版信息

World J Biol Psychiatry. 2020 Jan;21(1):72-77. doi: 10.1080/15622975.2018.1548780. Epub 2019 Jan 9.

Abstract

Acetylcholine M (muscarinic) receptors are possibly involved in tardive dyskinesia (TD). The authors tried to verify this hypothesis by testing for possible associations between two muscarinic receptor genes ( and ) polymorphisms and TD in patients with schizophrenia. A total of 472 patients with schizophrenia were recruited. TD was assessed cross-sectionally using the Abnormal Involuntary Movement Scale. Fourteen allelic variants of and were genotyped using Applied Biosystems amplifiers (USA) and the MassARRAY System by Agena Bioscience. The prevalence of the rs1824024*GG genotype of the gene was lower in TD patients compared to the group without it (χ2 = 6.035,  = 0.049). This suggested that this genotype has a protective effect for the development of TD (OR = 0.4, 95% CI: 0.19-0.88). When age, gender, duration of schizophrenia and dosage of antipsychotic treatment were added as covariates in regression analysis, the results did not reach statistical significance. This study did identify associations between variations and TD; the results of logistic regression analysis with covariates suggest that the association is, however, likely to be secondary to other concomitant factors.

摘要

乙酰胆碱 M (毒蕈碱) 受体可能与迟发性运动障碍 (TD) 有关。作者试图通过检测两种毒蕈碱受体基因 (和) 多态性与精神分裂症患者 TD 之间的可能关联来验证这一假设。共招募了 472 名精神分裂症患者。使用异常不自主运动量表对 TD 进行横断面评估。使用 Applied Biosystems 扩增仪(美国)和 Agena Bioscience 的 MassARRAY 系统对和基因的 14 个等位基因变体进行基因分型。与无该基因型的患者相比,基因 rs1824024*GG 基因型的 TD 患者的患病率较低(χ2=6.035,=0.049)。这表明该基因型对 TD 的发生具有保护作用(OR=0.4,95%CI:0.19-0.88)。当将年龄、性别、精神分裂症持续时间和抗精神病药物治疗剂量作为回归分析中的协变量添加时,结果未达到统计学意义。本研究确实确定了与 TD 相关的基因变异;然而,协变量逻辑回归分析的结果表明,这种关联很可能是其他伴随因素的次要因素。

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