Scott Susanne I, Andersen Michelle Fog, Aagaard Lise, Buchwald Christian Von, Rasmussen Eva R
Department of Otorhinolaryngology and Maxillofacial Surgery, Zealand University Hospital, Lykkebaekvej 1, 4600 Koge, Denmark.
Department of Orthopaedic Surgery, Nordsjaellands Hospital, Dyrehavevej 29, 3400 Hillerod, Denmark.
Curr Diabetes Rev. 2018;14(4):327-333. doi: 10.2174/1573399813666170214113856.
Angioedema is a potentially fatal adverse drug reaction of some medications, as swellings of the upper airways can cause death by asphyxiation. Angiotensin converting enzymeinhibitors are widely known to cause angioedema but less is known about the association between dipeptidyl peptidase-4 inhibitors (gliptins) and angioedema. Dipeptidyl peptidase-4 inhibitors are antidiabetic drugs used to improve glycaemic control. They, as a class effect, inadvertently affect the degradation of the vasoactive kinins bradykinin and substance P, both of which can cause angioedema due to vasodilatation and increase in vascular permeability in the capillaries.
To assess the risk and pathomechanism of angioedema due to inhibition of dipeptidyl peptidase- 4 inhibitors when used as monotherapy and in combination with angiotensin converting enzymeinhibitors.
PubMed, Embase, the Cochrane Library, PubMed Central, Web of Science, Google Scholar and clinicaltrials.gov were searched using different combinations of keywords "angioedema", "dipeptidyl peptidase 4", "dipeptidyl peptidase 4 inhibitors", "gliptins", "bradykinin", "substance P" and "angiotensin converting enzyme-inhibitors". Original research papers were preferably used as references and their bibliographies were used to further the search for original research results.
Both angiotensin converting enzyme and dipeptidyl peptidase-4 are major enzymes in the degradation pathway of bradykinin and substance P, and when inhibited pharmacologically - especially at the same time - the theoretical risk of angioedema is increased due to accumulation of vasoactive kinins.
Treatment with dipeptidyl peptidase-4 inhibitors must be carefully considered and monitored especially during concurrent treatment with angiotensin converting enzyme-inhibitors or when treating patients with a known predisposition to angioedema.
血管性水肿是某些药物潜在的致命性不良反应,因为上呼吸道肿胀可导致窒息死亡。众所周知,血管紧张素转换酶抑制剂会引起血管性水肿,但关于二肽基肽酶-4抑制剂(格列汀类)与血管性水肿之间的关联,人们了解较少。二肽基肽酶-4抑制剂是用于改善血糖控制的抗糖尿病药物。作为一类药物效应,它们会意外影响血管活性激肽缓激肽和P物质的降解,这两种激肽均可因血管舒张和毛细血管通透性增加而导致血管性水肿。
评估二肽基肽酶-4抑制剂单药治疗及与血管紧张素转换酶抑制剂联合使用时引起血管性水肿的风险和发病机制。
使用“血管性水肿”“二肽基肽酶4”“二肽基肽酶-4抑制剂”“格列汀类”“缓激肽”“P物质”和“血管紧张素转换酶抑制剂”等关键词的不同组合,对PubMed、Embase、Cochrane图书馆、PubMed Central、科学网、谷歌学术和clinicaltrials.gov进行检索。优先使用原始研究论文作为参考文献,并利用其参考文献进一步检索原始研究结果。
血管紧张素转换酶和二肽基肽酶-4都是缓激肽和P物质降解途径中的主要酶,当受到药物抑制时,尤其是同时受到抑制时,由于血管活性激肽的积累,血管性水肿的理论风险会增加。
使用二肽基肽酶-4抑制剂进行治疗时必须谨慎考虑并进行监测,尤其是在与血管紧张素转换酶抑制剂同时治疗期间,或治疗已知有血管性水肿倾向的患者时。