Angioedema associated with dipeptidyl peptidase-IV inhibitors.

Q2 Medicine
Nicoletta Cassano, Eustachio Nettis, Elisabetta Di Leo, Francesca Ambrogio, Gino A Vena, Caterina Foti
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引用次数: 0

Abstract

Background: Dipeptidyl peptidase-IV (DPP-IV) inhibitors, also known as gliptins, are a class of oral antidiabetic agents. Postmarketing reports have documented the occurrence of angioedema in patients treated with gliptins and it was found that these drugs increased the risk of angioedema in patients concurrently treated with angiotensin-converting enzyme inhibitors (ACEIs). The aim of this manuscript is to provide an overview of the risk of angioedema associated with gliptins.

Methods: The keywords used for the literature search in the PubMed database included "angioedema" and "dipeptidyl peptidase", "gliptins", or the name of each DPP-IV inhibitor. Articles in English published up to December 2020 were taken into consideration.

Results: The available data appear to rule out a higher risk of angioedema associated with gliptin monotherapy and have revealed an increased susceptibility in patients simultaneously treated with gliptins and ACEIs. However, one single multicenter phase IV trial and case reports, even if very limited in number, have shown that angioedema can also occur during treatment with DPP-IV inhibitors without the concomitant use of ACEIs. The involvement of other drugs and drug interactions has occasionally been suggested. In a few patients, deficiency of enzymes involved in bradykinin catabolism was detected and this finding can constitute a risk factor for angioedema exacerbated by treatment with DPP-IV inhibitors.

Conclusions: This risk of angioedema associated with the use of gliptins has mostly been related to the concurrent administration of ACEIs, and has been considered rare, but it might be underestimated and underreported. The role of additional risk factors or drug interactions deserves further investigations. Caution should be taken when considering the use of DPP-IV inhibitors in patients treated with ACEIs or presenting with other known risk factors for angioedema.

与二肽基肽酶-IV 抑制剂相关的血管性水肿。
背景:二肽基肽酶-IV(DPP-IV)抑制剂,又称格列汀类药物,是一类口服抗糖尿病药物。上市后的报告记录了使用格列汀类药物治疗的患者发生血管性水肿的情况,并且发现这类药物会增加同时使用血管紧张素转换酶抑制剂(ACEIs)治疗的患者发生血管性水肿的风险。本手稿旨在概述格列汀类药物引起血管性水肿的风险:在PubMed数据库中进行文献检索时使用的关键词包括 "血管性水肿 "和 "二肽基肽酶"、"格列汀类 "或每种DPP-IV抑制剂的名称。结果:现有数据似乎排除了与格列汀单药治疗相关的较高血管性水肿风险,并揭示了同时接受格列汀类药物和 ACEIs 治疗的患者更易发生血管性水肿。然而,一项单一的多中心 IV 期试验和病例报告(尽管数量非常有限)显示,在使用 DPP-IV 抑制剂治疗期间,如果没有同时使用 ACEIs,也会出现血管性水肿。偶尔也有人认为与其他药物和药物相互作用有关。在少数患者中,发现了缓激肽分解酶的缺乏,这一发现可能是DPP-IV抑制剂治疗加重血管性水肿的危险因素:使用格列汀类药物引起血管性水肿的风险主要与同时服用 ACEIs 有关,一直被认为是罕见的,但这种风险可能被低估和报告不足。其他风险因素或药物相互作用的作用值得进一步研究。在考虑对接受 ACEIs 治疗或存在其他已知血管性水肿风险因素的患者使用 DPP-IV 抑制剂时,应谨慎行事。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical and Molecular Allergy
Clinical and Molecular Allergy Medicine-Immunology and Allergy
CiteScore
8.20
自引率
0.00%
发文量
11
审稿时长
13 weeks
期刊介绍: Clinical and Molecular Allergy is an open access, peer-reviewed, online journal that publishes research on human allergic and immunodeficient disease (immune deficiency not related to HIV infection/AIDS). The scope of the journal encompasses all aspects of the clinical, genetic, molecular and inflammatory aspects of allergic-respiratory (Type 1 hypersensitivity) and non-AIDS immunodeficiency disorders. However, studies of allergic/hypersensitive aspects of HIV infection/AIDS or drug desensitization protocols in AIDS are acceptable. At the basic science level, this includes original work and reviews on the genetic and molecular mechanisms underlying the inflammatory response.
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