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接受华法林治疗的伊朗人群中烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H)醌氧化还原酶1(NQO1)基因甲基化/表达与出血发生率之间的关联

Association Between NAD(P)H Quinone Oxidoreductase 1 (NQO1) Gene Methylation/Expression and Bleeding Incidence Among an Iranian Population Undergoing Warfarin Therapy.

作者信息

Hosseini Maryam Sadat, Pourgholi Leyla, Ziaee Shayan, Pourgholi Mitra, Mandegary Ali, Boroumand Mohammadali

机构信息

Department of Molecular Pathology, Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran.

Department of Clinical Biochemistry, Faculty of Medicine, Babol University of Medical Sciences, Babol, Iran.

出版信息

Indian J Hematol Blood Transfus. 2024 Jul;40(3):517-521. doi: 10.1007/s12288-023-01726-2. Epub 2024 Feb 24.

Abstract

Increased bleeding tendency is a common and challenging complication of warfarin therapy which results in extensive pharmacogenomic studies in order to develop a personalized dosing approach and minimize the risk of related side effects. Here we aimed to explore the potential role of NQO1 gene expression in warfarin response in a group of Iranian patients. We also evaluated the NQO1 promoter methylation and its association with mRNA expression. A total of 87 patients on warfarin therapy including 34 cases with drug-induced bleeding events and 53 matched controls without bleedings were included in the study. The expression of NQO1 was examined by real-time q-PCR and the methylation status of its promoter region was analyzed using methyQESD technique. There was a significant association between the reduced NQO1 gene expression and susceptibility to bleeding before (OR = 1.92, 95% CI = 1.23-3.00,  = 0.004) and following adjustment for hypertriglyceridemia (OR = 2.22, 95% CI = 1.33-3.69,  = 0.002). Furthermore, a medium negative correlation was observed between NQO1 expression and its promoter methylation ( = - 0.382,  = 0.001). The lower expression of NQO1 which partly arises from increased methylation of promoter region, may predispose warfarin treated patients to bleeding events.

摘要

出血倾向增加是华法林治疗常见且具有挑战性的并发症,这促使开展广泛的药物基因组学研究,以制定个性化给药方案并将相关副作用风险降至最低。在此,我们旨在探讨NQO1基因表达在一组伊朗患者对华法林反应中的潜在作用。我们还评估了NQO1启动子甲基化及其与mRNA表达的关联。本研究共纳入87例接受华法林治疗的患者,其中34例发生药物性出血事件,53例未出血的匹配对照。通过实时定量PCR检测NQO1的表达,并使用甲基化QESD技术分析其启动子区域的甲基化状态。在调整高甘油三酯血症之前(OR = 1.92,95% CI = 1.23 - 3.00,P = 0.004)和之后(OR = 2.22,95% CI = 1.33 - 3.69,P = 0.002),NQO1基因表达降低与出血易感性之间存在显著关联。此外,观察到NQO1表达与其启动子甲基化之间存在中等程度的负相关(r = - 0.382,P = 0.001)。NQO1表达降低部分源于启动子区域甲基化增加,这可能使接受华法林治疗的患者易发生出血事件。

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