N. Kawaguchi, K. Nakatani, A. Uzawa, Y. Nemoto, K. Himuro, S. Kuwabara
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引用次数: 2
摘要
目的:探讨细胞色素P450 (CYP) 3A5 (A6986G, CYP3A5*3)多态性对重症肌无力(MG)患者血清他克莫司和环孢素(CyA)水平的影响。方法:74例MG患者接受他克莫司(65例)或CyA(22例)治疗。提取基因组DNA,用特异性引物扩增,在自动AB13100 DNA测序仪上对PCR产物进行直接测序,确认CYP3A5等位基因。测定他克莫司和CyA血谷水平(C0)。采用MG-ADL量表评估临床残疾。结果:对于他克莫司C0, CYP3A5*3/*3基因型与CYP3A5*1/*3基因型的相关性高于CYP3A5*1/*3基因型(7.1 ng/ml vs 2.9 ng/ml;P<0.0001)和CYP3A*1/*1 (7.1 ng/ml vs 1.3 ng/ml;P < 0.0004)。CYP3A5*3/*3或CYP3A5*1/*3的MG患者MG- adl平均评分的改善往往比CYP3A5*1/*1的MG患者更好。对于CyA浓度,CYP3A5基因型无显著影响。结论:在MG患者中,CYP3A5多态性显著影响他克莫司的血清水平从而影响治疗效果,但对CyA无显著影响。他克莫司维持剂量的确定应考虑CYP3A5多态性。
Polymorphisms of CYP3A5 Affect Serum Levels and Maintenance Doses of Tacrolimus in Myasthenia Gravis Patients
Objectives: To evaluate the influences of polymorphisms of cytochrome P450 (CYP) 3A5 (A6986G, CYP3A5*3) on serum levels of tacrolimus and cyclosporine (CyA) in patients with myasthenia gravis (MG). Methods: This study included 74 MG patients treated with tacrolimus (n=65) or CyA (n=22). Genomic DNA was extracted and amplified with specific primers, and CYP3A5 alleles were confirmed by direct sequencing of PCR products on an automated AB13100 DNA sequencer. We measured blood trough level (C0) of tacrolimus and CyA. Clinical disabilities were evaluated with the MG-ADL scale. Results: For tacrolimus C0, the CYP3A5*3/*3 genotype was associated with higher levels than the CYP3A5*1/*3 genotypes (7.1 ng/ml versus 2.9 ng/ml; P<0.0001) and CYP3A*1/*1 (7.1 ng/ml versus 1.3 ng/ml; P<0.0004). The improvement in the mean MG-ADL scores tended to be better in MG patients with the CYP3A5*3/*3 or CYP3A5*1/*3 than those with CYP3A5*1/*1. For the CyA concentrations, CYP3A5 genotypes did not have significant effects. Conclusion: In MG patients, CYP3A5 polymorphism significantly affects serum levels of tacrolimus and thereby treatment effects, but not those of CyA. The maintenance dose of tacrolimus should be determined considering CYP3A5 polymorphism.