Key result
Specific XPNPEP2, BDKRB2, and neprilysin variants are linked to increased risk of ACE inhibitor-induced angioedema.
Why the study?
Genetic polymorphisms may be associated with ACE inhibitor-induced angioedema, but the quality and reliability of existing studies are uncertain.
Are genetic polymorphisms associated with an increased risk of ACE inhibitor-induced angioedema?
Systematic Review (n=547)
Are genetic polymorphisms associated with an increased risk of ACE inhibitor-induced angioedema?
While certain genetic polymorphisms may increase the risk of ACE inhibitor-induced angioedema, current evidence is limited by the poor methodological quality of existing studies.
Should not yet inform genetic screening or ACE inhibitor selection; leaves open validation in larger, high-quality studies.
Angiotensin-converting enzyme (ACE) converts angiotensin I to angiotensin II which causes vasoconstriction. ACE inhibitors reduce blood pressure by inhibiting ACE. A well-known adverse drug reaction to ACE inhibitors is ACE inhibitor-induced angioedema (ACEi-AE). Angioedema is a swelling of skin and mucosa, which can be fatal if the airway is compromised. We have performed a systematic review of the evidence suggesting that genetic polymorphisms are associated with ACEi-AE and evaluated the methodological approaches of the included studies. The Cochrane Database of Systematic Reviews, Google Scholar, and PubMed were searched. Studies investigating the association between genetic markers and ACEi-AE were included. The Q-genie tool was used to evaluate the quality of the study methodologies. Seven studies were included. With the exception of one whole genome study, all of the included studies were candidate gene association studies. Study quality assessment scores ranged from 36 to 55. One study was found to be of good quality, suggesting that the detected associations may be unreliable. The inferior quality of some studies was due to poor organization, lack of analyses and missing information. Polymorphisms within XPEPNP2, BDKRB2-9/+ 9 and neprilysin genes, were reported to be associated with increased risk of ACEi-AE. However, due to low quality, these associations need to be confirmed in larger studies.
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Ali et al. (2019) conducted a systematic review in ACE inhibitor-induced angioedema (n=547). Genetic polymorphisms (XPEPNP2, BDKRB2-9/+ 9, neprilysin) vs. Patients without the genetic polymorphisms was evaluated on Association between genetic polymorphisms and ACE inhibitor-induced angioedema. Polymorphisms within XPEPNP2, BDKRB2-9/+ 9 and neprilysin genes were associated with an increased risk of ACE inhibitor-induced angioedema, though these findings require confirmation in larger studies due to low study quality.
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