Non-genetic factors associated with ACE-inhibitor and angiotensin receptor blocker-induced angioedema

IF 4.6 2区 医学 Q2 ALLERGY
Diana Dubrall, Nora L. Branding, Carina M. Mathey, Anna M. Weber, Michael Steffens, Maike Below, Matthias Schmid, Bettina Wedi, Dorothea Wieczorek, Philipp M. Amann, Harald Löffler, Lukas Koch, Clemens Schöffl, Heinrich Dickel, Nomun Ganjuur, Thorsten Hornung, Timo Buhl, Emel Aygören-Pürsün, Gerda Wurpts, Jens Greve, Markus M. Nöthen, Andreas J. Forstner, Bernhardt Sachs
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Abstract

Background

Angioedema (AE) rarely occurs as a potentially life-threatening adverse drug reaction (ADR) to angiotensin-converting enzyme inhibitors (ACEi) or angiotensin receptor blockers (ARB). The aim of the present study was to investigate non-genetic association factors with ACEi-/ARB-induced angioedema in the European ADR database EudraVigilance and the database of the vARIANCE study.

Methods

The cohort of the vARIANCE study comprised 114 patients who suffered from ACEi- or ARB-induced angioedema. In addition, 171 angioedema reports and 4650 reports on other ADRs of ACEi/ARB were identified in the ADR database EudraVigilance with the latter serving as a reference group. Odds ratios were calculated and a logistic regression analysis was performed using angioedema versus reference reports.

Results

Increased age, smoking, allergies and a history of previous angioedema were identified as associated factors for ACEi-/ARB-induced angioedema. In most patients, the swelling affected the face, lips and tongue. In the vARIANCE study, about 70% of angioedema occurred after 1 year of treatment. For one in two patients in the vARIANCE study (84.2% with ACEi treatment) and one in three patients from the EudraVigilance reports (59.6% with ARB treatment), the angioedema resulted in hospitalization.

Conclusions

We found small to moderate associations with certain individual patient-related factors in this pharmaco-epidemiological study. As a future perspective, combining non-genetic association factors with corresponding genetic data might provide an option to compose stronger and individual risk scores.

Abstract Image

与ace抑制剂和血管紧张素受体阻滞剂诱导的血管性水肿相关的非遗传因素
血管水肿(AE)很少作为血管紧张素转换酶抑制剂(ACEi)或血管紧张素受体阻滞剂(ARB)的潜在危及生命的药物不良反应(ADR)发生。本研究的目的是在欧洲不良反应数据库EudraVigilance和方差研究数据库中调查与ACEi-/ arb诱导的血管性水肿相关的非遗传因素。方法方差研究的队列包括114例ACEi或arb诱导的血管性水肿患者。此外,在ADR数据库EudraVigilance中发现171例血管性水肿报告和4650例ACEi/ARB其他ADR报告,后者作为参照组。计算优势比,并将血管性水肿与参考报告进行logistic回归分析。结果年龄增加、吸烟、过敏和既往血管性水肿史被确定为ACEi-/ arb诱导血管性水肿的相关因素。在大多数患者中,肿胀影响到面部、嘴唇和舌头。在方差研究中,约70%的血管性水肿发生在治疗1年后。方差研究中有1 / 2的患者(ACEi治疗组为84.2%)和EudraVigilance报告中有1 / 3的患者(ARB治疗组为59.6%)因血管性水肿而住院。结论:在这项药物流行病学研究中,我们发现与某些个体患者相关因素有小到中等程度的关联。从未来的角度来看,将非遗传相关因素与相应的遗传数据相结合可能会提供一种选择,以组成更强的个体风险评分。
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来源期刊
Clinical and Translational Allergy
Clinical and Translational Allergy Immunology and Microbiology-Immunology
CiteScore
7.50
自引率
4.50%
发文量
117
审稿时长
12 weeks
期刊介绍: Clinical and Translational Allergy, one of several journals in the portfolio of the European Academy of Allergy and Clinical Immunology, provides a platform for the dissemination of allergy research and reviews, as well as EAACI position papers, task force reports and guidelines, amongst an international scientific audience. Clinical and Translational Allergy accepts clinical and translational research in the following areas and other related topics: asthma, rhinitis, rhinosinusitis, drug hypersensitivity, allergic conjunctivitis, allergic skin diseases, atopic eczema, urticaria, angioedema, venom hypersensitivity, anaphylaxis, food allergy, immunotherapy, immune modulators and biologics, animal models of allergic disease, immune mechanisms, or any other topic related to allergic disease.
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