与精神分裂症严重程度和治疗反应相关的 OXTR 多态性。

IF 3 Q2 PSYCHIATRY Schizophrenia (Heidelberg, Germany) Pub Date : 2024-01-06 DOI:10.1038/s41537-023-00413-5
Xue Lv, Yue-Sen Hou, Zhao-Hui Zhang, Wei-Hua Yue
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引用次数: 0

摘要

精神分裂症特定症状的产生机制尚不清楚,而基因研究使我们有可能从根本上探讨这些问题。考虑到催产素系统与精神分裂症患者明显受损的社会功能之间的关联,我们假设催产素受体基因(OXTR)可能与精神分裂症症状的严重程度和对抗抑郁药的反应有关,并进行了这项探索性定位研究。我们的研究共包括 2363 名精神分裂症患者(男性 1181 人,女性 1182 人),他们被随机分配到 7 个抗精神病药物治疗组,接受为期 6 周的抗精神病药物单药治疗。对他们的血液 DNA 进行了 OXTR 多态性基因分型。他们的症状严重程度由阳性和阴性综合征量表(PANSS)进行评估,并将得分转化为七个因子(阳性、混乱、阴性症状冷漠/逃避、阴性症状表达缺失、敌意、焦虑和抑郁)。计算 PANSS 评分从基线到第 6 周的百分比变化,以量化抗精神病药物反应。我们发现,OXTR 多态性与总体症状(rs237899,β = 1.669,p = 0.019)、敌意症状(rs237899,β = 0.427,p = 0.044)和焦虑症状(rs13316193,β = -0.197,p = 0.038)的严重程度有名义上的相关性。至于治疗反应,OXTR 多态性与负性症状冷漠/逃避的改善有一定关系(rs2268490,β = 2.235,p = 0.0499)。在对多态性进行统计校正后,未发现严重程度或对治疗的反应与 OXTR 多态性之间存在关联。总之,我们的研究结果表明,OXTR 基因与精神分裂症症状的严重程度和改善之间可能存在名义上的显著关联。鉴于本研究的探索性质,这些关联表明了 OXTR 基因在精神分裂症病理中的作用,并可能有助于进一步阐明精神分裂症特定症状的机制,以及开发对特定症状更有效的抗精神病药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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OXTR polymorphisms associated with severity and treatment responses of schizophrenia.

The mechanisms generating specific symptoms of schizophrenia remain unclear and genetic research makes it possible to explore these issues at a fundamental level. Taking into account the associations between the oxytocin system and social functions, which are apparently impaired in schizophrenia patients, we hypothesized that the oxytocin receptor gene (OXTR) might be associated with schizophrenia symptoms in both severity and responses to antipsychotics and did this exploratory positional study. A total of 2363 patients with schizophrenia (1181 males and 1182 females) included in our study were randomly allocated to seven antipsychotic treatment groups and received antipsychotic monotherapy for 6 weeks. Their blood DNA was genotyped for OXTR polymorphisms. Their symptom severity was assessed by Positive and Negative Syndrome Scale (PANSS), and the scores were transformed into seven factors (positive, disorganized, negative symptoms apathy/avolition, negative symptoms deficit of expression, hostility, anxiety and depression). Percentage changes in PANSS scores from baseline to week 6 were calculated to quantify antipsychotic responses. We found that OXTR polymorphisms were nominally associated with the severity of overall symptoms (rs237899, β = 1.669, p = 0.019), hostility symptoms (rs237899, β = 0.427, p = 0.044) and anxiety symptoms (rs13316193, β = -0.197, p = 0.038). As for treatment responses, OXTR polymorphisms were nominally associated with the improvement in negative symptoms apathy/avolition (rs2268490, β = 2.235, p = 0.0499). No association between severity or response to treatment and OXTR polymorphisms was found with statistical correction for multiplicity. Overall, our results highlighted the possibility of nominally significant associations of the OXTR gene with the severity and improvement in schizophrenia symptoms. Given the exploratory nature of this study, these associations are indicative of the role of the OXTR gene in the pathology of schizophrenia and may contribute to further elucidate the mechanism of specific symptoms of schizophrenia and to exploit antipsychotics more effective to specific symptoms.

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