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CYP2C9 基因分析与巴基斯坦癫痫患者药物反应的关系。

Genetic Analysis of CYP2C9 with Reference to Drug Response in Epilepsy Patients of Pakistan.

机构信息

Institute of Zoology, University of the Punjab Lahore, Lahore, Pakistan.

Department of Neurology, University Medical Center Göttingen, Robert-Koch-Straße 40, 37075 Göttingen, Germany.

出版信息

Genet Res (Camb). 2022 Jan 29;2022:1451007. doi: 10.1155/2022/1451007. eCollection 2022.

Abstract

Epilepsy is a major global issue. Epilepsy patients are treated with AED (antiepileptic drugs). Interindividual variability in drug response has been documented in several studies. The resistance to drug response may be attributed to genetic polymorphism. The current study was undertaken to investigate the CYP2C9 gene polymorphism associated with antiepileptic drug (AED) resistance in the Pakistani population. The current study included 337 individuals including 100 control subjects, 110 drug-resistant subjects, and 127 drug responders. Genomic DNA was isolated from blood, and amplification of rs1799853 (430C > T) and rs1057910 was carried out by polymerase chain reaction. Genotypes of CYP2C9 SNPs were determined by Sanger's sequencing. Astounding results were observed in the current study that none of the well-known reported SNPs of CYP2C9 was found in our Pakistani cohorts. However, a novel missense variant (c.374G > A) was found only in drug-resistant patients of the current study. According to the analysis performed by PolyPhen-2, it was observed that this nonsynonymous substitution is likely to be pathogenic. The results of our study demonstrated that rs1799853 and rs1057910 may be involved in drug resistance in the Pakistani population. However, some other variants on CYP2C9 may play a critical role in AED resistance that needs to be explored.

摘要

癫痫是一个全球性的重大问题。抗癫痫药物(AED)用于治疗癫痫患者。多项研究已经证实了药物反应的个体间差异。药物反应的耐药性可能归因于遗传多态性。本研究旨在探讨与巴基斯坦人群抗癫痫药物(AED)耐药相关的 CYP2C9 基因多态性。本研究包括 337 人,其中 100 名对照,110 名耐药患者,127 名药物反应者。从血液中提取基因组 DNA,通过聚合酶链反应扩增 rs1799853(430C>T)和 rs1057910。通过 Sanger 测序确定 CYP2C9 SNP 的基因型。本研究令人惊讶地发现,我们的巴基斯坦队列中未发现任何已知的 CYP2C9 报告 SNP。然而,在本研究的耐药患者中仅发现了一个新的错义变异(c.374G>A)。根据 PolyPhen-2 进行的分析,观察到这种非同义取代很可能是致病的。我们的研究结果表明,rs1799853 和 rs1057910 可能与巴基斯坦人群的耐药性有关。然而,CYP2C9 上的其他一些变异可能在 AED 耐药中发挥关键作用,需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5821/8817865/a3cdd4efb83f/GR2022-1451007.001.jpg

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