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作 者:钱卿[1] 胡楠[1] 周华[2] 凌静[1] 陈荣[1] 邹素兰[1] 王莉英[1] QIAN Qing;HU Nan;ZHOU Hua;LING Jing;CHEN Rong;ZOU Sulan;WANG Liying(Department of Pharmacy;Department of Nephrology,the First People's Hospital of Changzhou,Changzhou 213003,China)
机构地区:[1]常州市第一人民医院药学部,常州213003 [2]常州市第一人民医院肾内科,常州213003
出 处:《药学与临床研究》2021年第6期430-434,共5页Pharmaceutical and Clinical Research
基 金:常州市科技计划(应用基础研究)指导性项目(2017329);常州市应用基础研究指导性项目(CJ20199010)。
摘 要:目的:考察谷胱甘肽硫转移酶(GST)和乙醛脱氢酶(ALDH)基因多态性对环磷酰胺(CTX)方案治疗膜性肾病的效果与不良反应的影响,为精准治疗及药学监护提供参考。方法:采用CTX方案的膜性肾病患者共65例,收集其临床资料、实验室数据及不良反应报告;采集患者全血提取DNA,以聚合酶链式反应(PCR)-直接测序法检测GSTP1 A313G(rs1695)、ALDH3A1(rs2228100)的基因型。结果:CTX方案治疗膜性肾病患者的完全缓解率为41.5%,部分缓解率为36.9%,未缓解率为21.5%。单因素分析显示,性别、体重、GSTP1 rs1695基因型对疗效存在显著影响(P=0.003;P=0.032;P=0.047);多因素分析显示,性别是疗效的独立影响因素(P=0.017)。GSTP1rs1695、ALDH3A1 rs2228100基因多态性与肝损伤或感染之间无统计学相关性。结论:GSTP1rs1695基因型对膜性肾病患者CTX方案的疗效并非独立影响因素,有待更大样本的临床研究来进一步验证。Objective:To investigate the effects of glutathione S transferases(GST)and aldehyde dehydrogenase(ALDH)polymorphisms on the efficacy and adverse reactions of cyclophosphamide(CTX)in patients with membrane nephropathy(MN),in order to provide reference and guidance for precision treatment and pharmaceutical monitoring.Methods:A retrospective study was carried out including 65 patients with MN treated with CTX.Clinical data,laboratory data and adverse reaction reports were collected;Meanwhile,whole blood samples were collected to extract DNA for genotyping the polymorphisms of GSTP1 A313G(rs1695)and ALDH3A1 rs2228100 by a polymerase chain reaction(PCR)-direct sequencing method.Results:The complete remission rate was 41.5%,the partial remission rate was 36.9%,and the nonremission rate was 21.5%.Univariate analysis showed that gender,body weight and GSTP1(rs1695)genotype had significant effects on remission(P=0.003;P=0.032;P=0.047).In multivariate analysis,gender was an independent factor of total remission(P=0.017),GSTP1(rs1695)genotype was not an independent factor,but the difference of remission rate showed a trend that GSTP1(rs1695)A/A was more likely to have poor remission(P=0.052).No association between polymorphisms of GSTP1(rs1695)/ALDH3A1(rs2228100)and liver injury or infection was observed.Conclusion:GSTP1(rs1695)genotype may affect the efficacy of CTX regimen in patients with MN.Identification of this genotype may provide a basis for clinical individualized treatment.
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