Treatment Response and GWAS Risk Allele rs2514218 (C) of the Dopamine D2 Receptor Gene in Inpatients with Schizophrenia.

IF 2.3 4区 心理学 Q3 NEUROSCIENCES
Neuropsychobiology Pub Date : 2022-01-01 Epub Date: 2021-09-28 DOI:10.1159/000519155
Margarita A Morozova, Tatyana V Lezheiko, Taissia A Lepilkina, Denis S Burminskiy, Sergey S Potanin, Allan G Beniashvili, George E Rupchev, Vera E Golimbet
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引用次数: 0

Abstract

Introduction: The pathophysiological mechanisms of acute schizophrenia are largely unknown, but it is widely accepted that dopamine D2 receptors (DRD2s) are involved in psychosis treatments for schizophrenic patients. We suggest that genetic variation in these receptors may play a role in patients' responses to commonly used antipsychotics, particularly D2-blockers.

Methods: This study included adult patients with ICD-10 diagnoses of schizophrenia and current acute psychosis who were treated with antipsychotics. All patients underwent genotyping for DRD2 rs2514218 polymorphism. The definition of overall treatment response was based on changes in treatment scheme: no changes indicated a good response, and changes indicated a limited response.

Results: There were 275 inpatients (38.1% of whom were female; mean age = 32.7 years, SD = 11.1 years) who met the inclusion criteria. Of the participants, 99 were good responders (34% of whom were female), and 176 were limited responders (40% of whom were female). No differences in demographic, premorbid, or disease characteristics were found. The number of patients that were homozygous for the risk allele was significantly greater in the limited response group than in the good response group.

Conclusion: Our findings suggest that the risk variant at the DRD2 locus can be used as an indicator for patients' responses to antipsychotics without direct DRD2-blocking, thereby shortening the time needed for drug selection.

住院精神分裂症患者多巴胺D2受体基因rs2514218 (C)的治疗反应与GWAS风险等位基因
急性精神分裂症的病理生理机制在很大程度上尚不清楚,但多巴胺D2受体(DRD2s)参与精神分裂症患者的精神病治疗已被广泛接受。我们认为这些受体的遗传变异可能在患者对常用抗精神病药物,特别是d2受体阻滞剂的反应中起作用。方法:本研究纳入了ICD-10诊断为精神分裂症和当前急性精神病并接受抗精神病药物治疗的成年患者。所有患者均进行DRD2 rs2514218多态性基因分型。总体治疗反应的定义基于治疗方案的变化:无变化表明反应良好,变化表明反应有限。结果:住院患者275例,其中女性占38.1%;平均年龄= 32.7岁,SD = 11.1岁),符合纳入标准。在参与者中,99人反应良好(其中34%是女性),176人反应有限(其中40%是女性)。在人口学、发病前或疾病特征方面没有发现差异。风险等位基因纯合子的患者数量在有限反应组明显大于良好反应组。结论:我们的研究结果表明,DRD2位点的风险变异可以作为患者抗精神病药物反应的指标,而无需直接阻断DRD2,从而缩短了药物选择所需的时间。
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来源期刊
Neuropsychobiology
Neuropsychobiology 医学-精神病学
CiteScore
7.20
自引率
0.00%
发文量
26
审稿时长
6 months
期刊介绍: The biological approach to mental disorders continues to yield innovative findings of clinical importance, particularly if methodologies are combined. This journal collects high quality empirical studies from various experimental and clinical approaches in the fields of Biological Psychiatry, Biological Psychology and Neuropsychology. It features original, clinical and basic research in the fields of neurophysiology and functional imaging, neuropharmacology and neurochemistry, neuroendocrinology and neuroimmunology, genetics and their relationships with normal psychology and psychopathology. In addition, the reader will find studies on animal models of mental disorders and therapeutic interventions, and pharmacoelectroencephalographic studies. Regular reviews report new methodologic approaches, and selected case reports provide hints for future research. ''Neuropsychobiology'' is a complete record of strategies and methodologies employed to study the biological basis of mental functions including their interactions with psychological and social factors.
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