The Molecular Biology Laboratory, Hangzhou Seventh People's Hospital, Hangzhou, 310013, China.
Mental Health Center, Zhejiang University School of Medicine, Hangzhou, 310013, China.
Sci Rep. 2021 Nov 30;11(1):23150. doi: 10.1038/s41598-021-02628-x.
Valproic acid is an anticonvulsant, which is also widely used for treating psychiatric disorders. Some clinical trials have demonstrated benefits of valproic acid augmentation therapy in schizophrenia. Interindividual variability in valproic acid dose and serum concentration may reflect functional consequences of genetic polymorphisms in genes encoding drug-metabolizing enzymes. The aim of this study was to determine the relationship between serum concentrations of valproic acid and single nucleotide polymorphisms of the cytochrome P450 (CYP) 2C19 gene in patients with schizophrenia. All patients had been receiving fixed dose of valproic acid for at least 2 weeks. The daily doses were 0.5-1.5 g. No other drugs except olanzapine were coadministered. Serum concentrations of valproic acid were measured using the ultra-high performance liquid chromatography method with mass-spectrometric detection. The CYP2C19 (CYP2C192 G681A rs4244285 and CYP2C193 G636A rs4986893) genotypes were identified by real-time PCR analyses. The mean concentration/dose ratios of valproic acid were significantly higher in patients with CYP2C19 *1/*2 genotype (P < 0.01) or CYP2C19 *2/*3 genotype (P < 0.01) than in those with CYP2C12 *1/*1 genotype. The mean concentration/dose ratios of valproic acid were significantly higher in patients with 1 (P < 0.01) or 2 (P < 0.01) mutated alleles for CYP2C19 than in those without mutated alleles. And the post hoc analysis revealed that the result has acceptable statistical (power (1 - β) = 0.8486 at type I level of 0.05) to support the observed significant associations for CYP2C19 SNPs and serum C/D ratios of valproic acid. The findings of this study suggest that the genetic polymorphisms of CYP2C19 significantly affect the steady-state serum concentrations of valproic acid in Chinese Han population. The determination of the CYP2C19 genotypes may be useful for dosing adjustment in schizophrenia patients on valproic acid therapy.
丙戊酸是一种抗惊厥药物,也广泛用于治疗精神疾病。一些临床试验表明,丙戊酸增效治疗在精神分裂症中有获益。丙戊酸剂量和血清浓度的个体间差异可能反映了编码药物代谢酶的基因中的遗传多态性的功能后果。本研究的目的是确定精神分裂症患者丙戊酸血清浓度与细胞色素 P450(CYP)2C19 基因单核苷酸多态性之间的关系。所有患者均接受固定剂量丙戊酸治疗至少 2 周,剂量为 0.5-1.5g,除奥氮平外未合并使用其他药物。采用超高效液相色谱法-质谱联用检测法测定丙戊酸血清浓度。采用实时 PCR 分析确定 CYP2C19(CYP2C192 G681A rs4244285 和 CYP2C193 G636A rs4986893)基因型。CYP2C19*1/2 基因型(P<0.01)或 CYP2C192/3 基因型(P<0.01)患者的丙戊酸浓度/剂量比值显著高于 CYP2C121/*1 基因型患者。CYP2C19 存在 1 个(P<0.01)或 2 个(P<0.01)突变等位基因的患者的丙戊酸浓度/剂量比值显著高于无突变等位基因的患者。事后分析显示,该结果具有可接受的统计学(功率(1-β)=0.8486,I 型错误率为 0.05),支持 CYP2C19 SNP 与丙戊酸血清 C/D 比值之间的观察到的显著相关性。本研究结果表明,CYP2C19 基因多态性显著影响中国汉族人群丙戊酸的稳态血清浓度。确定 CYP2C19 基因型可能有助于调整丙戊酸治疗的精神分裂症患者的剂量。