摘要
目的考察还原叶酸载体基因(RFC1)G80A基因多态性与甲氨蝶呤治疗异位妊娠所致药物不良反应间的相关性。方法收集经甲氨蝶呤治疗后发生药物不良反应的异位妊娠患者104例,用聚合酶链式反应(PCR)与DNA测序技术检测所有患者RFC1 G80A基因分型,分析不同基因型患者甲氨蝶呤治疗后的药物不良反应发生率。结果104例患者的RFC1 G80A基因型分布符合Hardy-Weinberg平衡。AA型患者的口腔溃疡风险是AG型患者的2.46倍,差异有统计学意义(P<0.05)。AA型患者的肝功能异常风险是GG型患者的3.02倍,差异有统计学意义(P<0.05)。RFC1 G80A中AA型、AG型、GG型患者的消化道反应发生率分别为24.14%,10.00%,16.00%,骨髓抑制发生率分别为20.69%,10.00%,12.00%,不同基因型患者的消化道反应和骨髓抑制发生率比较差异无统计学意义(P>0.05)。结论异位妊娠患者的RFC1 G80A基因多态性与甲氨蝶呤所致口腔溃疡与肝功能异常存在相关性。
Objective To evaluate the relationship between the genetic polymorphisms of reduced folate carrier (RFC1) and the incidence of adverse drug reactions of methotrexate in patients with ectopic pregnancy. Methods 104 ectopic pregnancy patients treated with methotrexate were collected. The genetic polymorphisms of RFC1 G80A were analyzed by PCR and DNA sequencing. The relationship between adverse drug reactions of methotrexate and the genetic polymorphisms were analyzed. Results RFC1 G80A polymorphisms were found to be in Hardy- Weinberg equilibrium. There was a significant difference in the incidence of mucositis and hepatic impair among the patients with different genotypes of RFC1 G80A (P 〈 0.05 ), while there was no difference in the inci- dence of gastrointestinal reaction and myelosuppression (P 〉 0. 05 ). The incidence rate of gastrointestinal reaction in patients with AA, AG, GG were 24. 14% , 10. 00% and 16. 00%, respectively. The incidence rate of myelosuppression in patients with AA, AG, GG were 20. 69%, 10.00% and 12.00%, respectively. Conclusion RFC1 G80A was linked with the incidence of mucositis and hepatic impair in ectopic pregnancy patients with methotrexate therapy.
出处
《中国临床药理学杂志》
CAS
CSCD
北大核心
2016年第16期1474-1476,共3页
The Chinese Journal of Clinical Pharmacology
基金
福建省临床重点专科建设基金资助项目(闽卫科教[2012]149号)
福建省卫生厅青年科研课题基金资助项目(2013-2-12)