mdr1基因多态性在疼痛综合征非甾体类抗炎药的应用中的作用

Zafar B. Abdashimov
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引用次数: 0

摘要

介绍。在许多药物,特别是非甾体抗炎药物的排泄中,一个关键的作用是有一种转运蛋白糖蛋白P,由MDR1基因编码。因此,糖蛋白P基因多态性对这些药物药代动力学的影响有助于预测临床后果。的目标。本研究的目的是研究编码糖蛋白P的MDR1基因多态性标记C1236T和C3435T与疼痛综合征患者不良药物反应发生的关系。材料和方法。本研究纳入69例疼痛综合征患者,根据有无药物不良反应分为2组:疼痛综合征NLR+ - 20例和NLR - - 49例。研究了22例有药物不良反应(ADR+)患者和47例无药物不良反应(ADR-)的疼痛综合征患者中MDR1基因多态性标记物C3435T的相关性。分子遗传学研究是在国家遗传研究所医学遗传学实验室和乌兹别克斯坦共和国卫生部PC的基础上进行的。结果和讨论。在基因分型过程中发现,MDR1基因多态性标记物C3435T等位基因的发生情况和基因型在被检查组患者之间存在显著差异,这取决于药物不良反应。结论。MDR1基因多态性标记物C3435T与疼痛综合征药物不良反应的发生、TT基因型和T等位基因的相关性可能是遗传危险因素(OR=4.0和8.25;95% CI分别为1.78-9.09和2.56-26.57),易导致疼痛综合征患者出现不良药物反应。因此,有必要进一步研究MDR1基因多态性标记物C3435T的基因分型,以提高非甾体抗炎药治疗的有效性和安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE ROLE OF POLYMORPHISM OF THE MDR1 GENE FOR THE APPOINTMENT OF NONSTEROIDAL ANTI-INFLAMMATORY DRUGS IN PAIN SYNDROME
Introduction. One of the key roles in the excretion of a number of drugs, in particular nonsteroidal anti- inflammatory drugs, has a transport protein glycoprotein P, encoded by the MDR1 gene. In this connection, the influence of genetic polymorphism of glycoprotein P on the pharmacokinetics of these drugs contributes to the prediction of clinical consequences. Aim. The aim of the current study was to study the associations of polymorphic markers C1236T and C3435T of the MDR1 gene encoding glycoprotein P with the development of undesirable drug reactions in patients with pain syndrome. Material and methods. The study included 69 patients with pain syndrome and were divided into 2 groups depending on the presence of adverse drug reactions: NLR+ - 20 patients and NLR - - 49 patients with pain syndrome. The association of the polymorphic marker C3435T of the MDR1 gene was also studied among 22 patients with adverse drug reactions (ADR+) and 47 patients with pain syndrome without the presence of adverse drug reactions (ADR-). Molecular genetic studies were carried out on the basis of the Laboratory of medical genetics of NIIG and the PC of the Ministry of Health of the Republic of Uzbekistan. Results and discussion. During the genotyping, it was found that the occurrence of alleles and genotypes of the polymorphic marker C3435T of the MDR1 gene had significantly significant differences among the patients of the examined groups, depending on adverse drug reactions. Conclusion. The association of the polymorphic marker C3435T of the MDR1 gene with the development of undesirable drug reactions in pain syndrome, the TT genotype and the T allele may be genetic risk factors (OR=4.0 and 8.25; 95% CI 1.78-9.09 and 2.56-26.57, respectively) predisposing to the development of undesirable drug reactions in patients with pain syndrome. Therefore, further study is necessary in order to carry out genotyping of the polymorphic marker C3435T of the MDR1 gene to increase the effectiveness and safety of therapy of nonsteroidal anti-inflammatory drugs.
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