Chavan Bir S, Kaur Gurjit, Gupta Deepti, Aneja Jitender
Department of Psychiatry, Government Medical College and Hospital, Chandigarh, India.
Department of Physiology, Government Medical College and Hospital, Chandigarh, India.
Indian J Psychol Med. 2018 Jul-Aug;40(4):335-342. doi: 10.4103/IJPSYM.IJPSYM_83_18.
Risperidone is one of commonly utilized antipsychotic in clinical practice. Various metabolizing enzymes effect the plasma levels of risperidone and its active metabolite and thus its clinical efficacy. So, we attempted to evaluate the relationship between CYP2D610 (rs1065852) and CYP2D64 (rs3892097) gene polymorphism and the plasma concentration of risperidone and its metabolite in patients with schizophrenia.
It was a 12-week prospective study carried out in patients diagnosed with schizophrenia. The dose of risperidone was increased weekly by 1 mg and rating of psychopathology was done using Positive and Negative Syndrome Scale (PANSS). Quantification of plasma level of risperidone and 9-hydroxyrisperidone was carried out at week 6 and 12 of treatment. The *4 and *10 alleles of CYP2D6 were genotyped and their effect on metabolism of risperidone was assessed.
The number of CYP2D64 alleles affected the plasma levels of risperidone, 9-hydroxyrisperidone at 6 weeks of treatment but not at 12 weeks. On the other hand, the number of mutated alleles for CYP2D610 influenced the dose corrected plasma concentration of risperidone and active moiety at 12 weeks of treatment. The ratio of plasma concentration of risperidone and 9-hydroxyrisperidone was more than one in all study participants, thus, suggesting that they were poor metabolizers of risperidone.
The polymorphism of CYP2D6*10 affects the steady state plasma concentration of risperidone in Indian patients with schizophrenia.
利培酮是临床实践中常用的抗精神病药物之一。多种代谢酶影响利培酮及其活性代谢产物的血浆水平,进而影响其临床疗效。因此,我们试图评估细胞色素P450 2D6(CYP2D6)10(rs1065852)和CYP2D64(rs3892097)基因多态性与精神分裂症患者利培酮及其代谢产物血浆浓度之间的关系。
这是一项针对诊断为精神分裂症患者的为期12周的前瞻性研究。利培酮剂量每周增加1mg,并使用阳性和阴性症状量表(PANSS)对精神病理学进行评分。在治疗的第6周和第12周对利培酮和9-羟基利培酮的血浆水平进行定量。对CYP2D6的4和10等位基因进行基因分型,并评估它们对利培酮代谢的影响。
CYP2D64等位基因的数量影响治疗6周时利培酮和9-羟基利培酮的血浆水平,但在12周时不影响。另一方面,CYP2D610突变等位基因的数量影响治疗12周时利培酮和活性部分的剂量校正血浆浓度。所有研究参与者中利培酮和9-羟基利培酮的血浆浓度比值均大于1,因此,表明他们是利培酮的代谢不良者。
CYP2D6*10基因多态性影响印度精神分裂症患者利培酮的稳态血浆浓度。