Suppr超能文献

CYP2C9、VKORC1和CYP4F2基因变异对土耳其华法林剂量调整影响的解读

Interpretation of the effect of CYP2C9, VKORC1 and CYP4F2 variants on warfarin dosing adjustment in Turkey.

作者信息

Kocael Ahmet, Eronat Allison Pınar, Tüzüner Mete Bora, Ekmekçi Ahmet, Orhan Ahmet Lütfullah, İkizceli İbrahim, Yılmaz-Aydoğan Hülya, Öztürk Oğuz

机构信息

Department of General Surgery, Cerrahpasa Medical Faculty, Istanbul University, Istanbul, Turkey.

Department of Molecular Medicine, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.

出版信息

Mol Biol Rep. 2019 Apr;46(2):1825-1833. doi: 10.1007/s11033-019-04634-9. Epub 2019 Feb 2.

Abstract

It was aimed to underline the importance and explain the meaning of genetic testing in warfarin dosing and investigate and evaluate the contributions of the CYP2C9, VKORC1, and CYP4F2 variants in a Turkish population. Two hundred patients were genotyped for CYP2C9 (rs1799853, rs1057910 and rs56165452), VKORC1 (rs9934438, rs8050894, rs9923231, rs7294 and rs2359612) and CYP4F2 (rs2108622), yet, only 127 patients were found suitable for further evaluation in terms of their personal response to warfarin due to long term usage and available INR and dose usage information. The DNA sequences were determined by the ABI PRISM 3100 Genetic Analyzer to 3130xl System (Applied Biosystems, Foster City, California). Warfarin dose application suggestions by warfaringdosing.org, FDA and MayoClinic were followed. Dose requirements in the Turkish population were found higher than the suggested doses by warfarindosing.org. The multivariate logistic regression analysis reveals the utilization of VCORC1 genetic evaluation is valuable in warfarin dosing (low and moderate vs. high) in this study (p < 0.001). The present study provides findings for clinicians to adapt the genetic data to the daily practice. We observed that the VKORC1 variant showed a more potent impact in warfarin dosing in this study.

摘要

旨在强调基因检测在华法林剂量调整中的重要性并解释其意义,同时调查和评估CYP2C9、VKORC1和CYP4F2基因变异在土耳其人群中的作用。对200名患者进行了CYP2C9(rs1799853、rs1057910和rs56165452)、VKORC1(rs9934438、rs8050894、rs9923231、rs7294和rs2359612)以及CYP4F2(rs2108622)基因分型,但由于长期用药以及可用的国际标准化比值(INR)和剂量使用信息,仅发现127名患者适合根据其对华法林的个人反应进行进一步评估。DNA序列由ABI PRISM 3100遗传分析仪至3130xl系统(应用生物系统公司,加利福尼亚州福斯特城)测定。遵循了warfaringdosing.org、美国食品药品监督管理局(FDA)和梅奥诊所的华法林剂量应用建议。发现土耳其人群的剂量需求高于warfarindosing.org建议的剂量。多因素逻辑回归分析显示,在本研究中,VKORC1基因评估在华法林剂量调整(低、中剂量与高剂量)中具有重要价值(p < 0.001)。本研究为临床医生将基因数据应用于日常实践提供了研究结果。我们观察到,在本研究中,VKORC1基因变异在华法林剂量调整中显示出更强的影响。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验