cyp3a4基因型对肺结核治疗效果的影响

H. A. Poludenko, P. Antonenko, Y. Rozhkovskyi, K. Antonenko, K. Lobashova
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引用次数: 0

摘要

在影响肺结核病程和治疗效果的诸多因素中,患者的遗传特征起着重要的作用。细胞色素(CYP) 3A4/5参与了超过30%的外源药物的代谢。因此,这种酶的活性很大程度上受到相关基因的影响,例如CYP3А4。本研究的目的是探讨CYP3A4多态性对肺结核患者抗结核治疗过程和疗效的预后价值。材料和方法。采用PCR方法对105例新诊断的肺结核患者进行CYP3A4*1B、CYP3A4*1G基因多态性检测,检测CYP3A4酶活性。我们审查了住院治疗开始和结束时的医疗记录,并考虑了结核病病变的形式、程度、消退率和痰检阳性病例的比率。使用Pearson卡方检验对研究数据进行统计分析,以绝对值或相对值表示。结果:105例tb患者中,84例(80%)携带“快速代谢者”(RA)基因型,其余15例(14.3%)和6例(5.7%)分别为“中间代谢者”(IM)和“慢代谢者”(SM)基因型。根据CYP3A4基因型,SM和IM患者的双侧病变以及肺破坏和播散过程以及涂片阳性的发生频率高于RM。例如,IM组的传播频率几乎是RM组的两倍(Р< 0.05;χ2 = 4,44)。在住院治疗结束时,SM患者更常观察到剩余的结核浸润,而实变的消退(66.7%)比IM和RM患者更少(分别为81.5%和80%)。同时,男性患者的结核浸润率高于男性患者(33.3% vs 8.3%, Р< 0.05;χ2 = 4,44)。与此同时,IM组的涂片阳性状态仍然比其他组多。结论。根据CYP3A4基因,“中间代谢物”和“缓慢代谢物”的基因型在结核病治疗开始和住院期结束时都与不利的肺部疾病相关。在肺结核患者中识别CYP3A4基因型,可以分配不利结核病程的高风险组。关键词:肺结核
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE EFFECTIVENESS OF TREATMENT OF PULMONARY TUBERCULOSIS DEPENDING ON CYP3A4 GENOTYPE
Among the factors that can influence the course and effectiveness of the treatment of pulmonary tuberculosis (TB) the genetic characteristics of patients play an important role. It is established that cytochrome (CYP) 3A4/5 is involved in metabolism of more than 30 % of xenobiotics. Consequently, the activity of this enzyme is greatly influenced by responsible genes, such as CYP3А4. The aim of the study was the investigation of prognostic value of CYP3A4 polymorphism on the course and effectiveness of anti-tuberculosis therapy in patients with pulmonary TB. Materials and methods. Using PCR method, a detection of polymorphism of CYP3A4*1B, CYP3A4*1G genes, which determine the activity of CYP3A4 enzyme, was performed in 105 patients with newly diagnosed pulmonary TB. We have revied medical records at the beginning and at the end of inpatient treatment and considered the form, extent, regression rate of TB-lesions, and the rate of smear-positive cases. A statistical analysis of study data, expressed in absolute or relative values, was done using Pearson’s chi-squared test. Results: It was established that out of 105 enrolled TB-patients 84 individuals (80,0%) carried the genotype of “rapid metabolizers” (RA), the rest – 15 (14,3%) and 6 (5,7%) individuals were “intermediate metabolizers” (IM) and “slow metabolizers” (SM) correspondently. According to CYP3A4 genotype in patients with SM and IM the bi-lateral lesions as well as the processes of pulmonary destruction and dissemination, as well as smearpositiveness occurred more frequently than in RM. For example, in IM group the dissemination was observed almost two times more frequently than in RM (Р<0,05; χ2=4,44). At the end of the in-patient treatment in SM remaining TB-infiltrates observed more often, while the resolution of consolidation registered more rarely (66,7%) than in IM and RM (81,0% and 80,0%, correspondently). Also, in SM the TB infiltrates remained more often than in RM (33,3% versus 8,3%, Р<0,05; χ2=4,44). At the same time in IM the smear-positive status remained more often than in other groups. Conclusion. Genotypes of “intermediate metabolizers” and “slow metabolizers” according to CYP3A4 genes were associated with unfavorable pulmonary disease both at initiation and at the end of in-patient phase of the TB treatment. Identification of CYP3A4 genotype in pulmonary TB patients allows allocation of the groups of high risk of unfavorable TB course. Key words: pulmonary tuberculo
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