The CYP2C19*2 and CYP2C19*17 Polymorphisms Influence Responses to Clozapine for the Treatment of Schizophrenia

被引:16
|
作者
Rodrigues-Silva, Christielly [1 ]
Semedo, Agostinho Tavares [1 ]
da Silva Neri, Hiasmin Franciely [1 ]
Vianello, Rosana Pereira [2 ]
Galaviz-Hernandez, Carlos [3 ]
Sosa-Macias, Martha [3 ]
de Brito, Rodrigo Bernini [1 ,4 ]
Ghedini, Paulo Cesar [1 ]
机构
[1] Univ Fed Goias, Inst Biol Sci, Dept Pharmacol, Goiania, Go, Brazil
[2] Empresa Brasileira Pesquisa Agr Embrapa, Santo Antonio De Goias, Go, Brazil
[3] CIIDIR Durango, Acad Genom, Inst Politecn Nacl, Durango, Mexico
[4] Brain Inst Med Clin, Bueno Med Ctr Bldg, Goiania, Go, Brazil
关键词
schizophrenia; CYP2C19*2; CYP2C19*17; treatment response; clozapine; DRUG RESPONSE; CYP2C19; METABOLISM;
D O I
10.2147/NDT.S228103
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Clozapine (CLZ) is the gold standard drug for treatment-refractory schizophrenia (TRS). However, approximately 30% of patients partially respond to CLZ, defining this subset with super refractory schizophrenia (SRS). Alterations in enzyme activity may affect CLZ responses; the CYP3A4, CYP1A2 and CYP2C19 genes are primarily responsible for CLZ metabolism. Objective: The aim of this study was to assess if CYP2C19 variants were associated with TRS or SRS. Methods: CYP2C19*2 loss-of-function and CYP2C19*17 gain-of-function polymorphism genotype testing were performed in 108 individuals undergoing pharmacological treatment for TRS or SRS. DNA was extracted and polymorphisms were analyzed by polymerase chain reaction (PCR) and sequencing. Results: CYP2C19*17 had positive correlations with SRS and lower Brief Psychiatric Rating Scale (BPRS) scores for TRS. In addition, CYP2C19*2 was associated with lower CLZ dosages for TRS. Conclusion: These results show that CYP2C19*2 and CYP2C19*17 polymorphisms influence CLZ responses during schizophrenia treatment.
引用
收藏
页码:427 / 432
页数:6
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