HTR2C promoter polymorphisms are associated with risperidone efficacy in Chinese female patients

被引:8
作者
Liu, Bao-Cheng [1 ,2 ,3 ]
Zhang, Jing [1 ,2 ,3 ]
Wang, Lei [1 ,2 ,3 ]
Li, Xing-Wang [1 ,2 ,3 ]
Wang, Yang [1 ,2 ,3 ]
Wei, Zhi Yun [1 ,2 ,3 ]
Ji, Jue [1 ,2 ,3 ]
Yang, Feng-Ping [1 ,2 ,3 ]
Wan, Chun-Ling [1 ,2 ,3 ]
Xu, Yi-Feng [4 ]
Feng, Guo-Yin [4 ]
He, Lin [2 ,3 ,5 ]
He, Guang [1 ,2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, BioX Ctr, Key Lab Genet Dev & Neuropsychiat Disorders, Minist Educ, Shanghai 200030, Peoples R China
[2] Fudan Univ, Inst Biomed Sci, Shanghai 200032, Peoples R China
[3] Chinese Acad Sci, Inst Nutr Sci, Shanghai Inst Biol Sci, Shanghai 200031, Peoples R China
[4] Shanghai Inst Mental Hlth, Shanghai 200030, Peoples R China
[5] Shanghai Jiao Tong Univ, BioX Life Sci Ctr, Shanghai 200030, Peoples R China
基金
中国国家自然科学基金;
关键词
HTR2C; pharmacogenomics; risperidone; schizophrenia; treatment response; 5-HT2C RECEPTOR GENE; SEROTONIN 2C RECEPTOR; INDUCED WEIGHT-GAIN; LINKAGE DISEQUILIBRIUM; TARDIVE-DYSKINESIA; METABOLIC SYNDROME; CLINICAL-RESPONSE; DOPAMINE D-3; SCHIZOPHRENIA; PHARMACOGENETICS;
D O I
10.2217/PGS.10.23
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims: A number of studies demonstrate that the polymorphisms in the 5' region of HTR2C play a pivotal role in antipsychotic drug efficacy. Since risperidone is an antagonist of HTR2C, polymorphic variations in HTR2C may explain variability in response to risperidone treatment. We analyzed HTR2C polymorphisms for association with efficacy of risperidone monotherapy. Materials & methods: We genotyped five SNPs distributed throughout the HTR2C gene and examined them for association using the Brief Psychiatric Rating Scale score in 130 Chinese schizophrenic patients following an 8-week period of risperidone monotherapy. All the patients were receiving the atypical antipsychotic drug treatment for the first time and had a 4-week medication-free period before research began. Results: We found rs518147, rs1023574 and rs9698290 were significantly associated with risperidone treatment in female patients (F = 4.75, degrees of freedom = 2 and p = 0.011; F = 4.329, degrees of freedom = 2 and p = 0.016; F = 4.188, degrees of freedom = 2 and p = 0.019, respectively) and they were also found to be in one linkage disequilibrium block. Conclusion: Our results indicate that variants in the HTR2C promoter region are likely to affect the risperidone therapeutic effect in female mainland patients. It may be helpful to investigate a combination of other clinical factors to predict atypical antipsychotic efficacy.
引用
收藏
页码:685 / 692
页数:8
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