Association Studies of DRD2 and COMT Gene Polymorphisms withRisperidone-induced Amenorrhea in Female Schizophrenia Patients

Chengye Hou, Jintian Xu, Jing Yan, Zheng Zhao, Yan Sun, Zhiyong Li, Yang Shen, Yichen Huang, Songnian Hu, Ying Liang
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Abstract

Object: To study the association between dopamine D2 receptor (DRD2) and catechol-O-methyltransferase (COMT) gene polymorphisms and the risperidone-induced amenorrhea resulted from hyperprolactinemia in female schizophrenia patients. Patients and methods: According to International Diagnostic and Classification of Diseases tenth edition (ICD-10) criteria, 45 Chinese female schizophrenic patients (25 patients with amenorrhea, and 20 patients with eumenorrhea) were recruited by trained psychiatrists in this study. Sanger sequencing was utilized to determine the DRD2 and COMT genotypes from peripheral venous blood samples. Results: There were no significant differences between amenorrhea patients and eumenorrhea patients in age, disease courses and risperidone dosages (P>0.05). Also, no significant differences were observed in rs6277, rs1079598 and rs4680 polymorphisms between the two groups. Conclusion: These results suggest that DRD2 rs6277, rs1079598 and COMT rs4680 gene polymorphisms show no significant correlation with risperidone-induced amenorrhea in Chinese female schizophrenia patients.
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女性精神分裂症患者DRD2和COMT基因多态性与利培酮所致闭经的相关性研究
目的:探讨女性精神分裂症患者多巴胺D2受体(DRD2)和儿茶酚胺-O-甲基转移酶(COMT)基因多态性与利培酮所致高泌乳素血症闭经的关系。患者和方法:根据国际疾病诊断与分类第十版(ICD-10)标准,本研究招募了45名中国女性精神分裂症患者(25名闭经患者和20名痛经患者),由受过培训的精神科医生进行研究。Sanger测序用于确定外周静脉血样本中的DRD2和COMT基因型。结果:闭经患者与痛经患者在年龄、病程、利培酮剂量等方面差异无统计学意义(P>0.05),rs6277、rs1079598、rs4680多态性在两组间也无统计学意义。结论:DRD2 rs6277、rs1079598和COMT rs4680基因多态性与利培酮诱发的中国女性精神分裂症患者闭经无显著相关性。
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