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Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment
| Content Provider | Semantic Scholar |
|---|---|
| Author | Rasmussen, Eva Rye Hallberg, Pär Baranova, Ekaterina V. Eriksson, Niclas Karawajczyk, Malgorzata Johansson, Caroline Cavalli, Marco Maroteau, Cyrielle Veluchamy, Abirami Islander, Gunilla Hugosson, S. Terreehorst, Ingrid Asselbergs, Folkert W. Norling, Pia Johansson, H. Kohnke, Hugo Syvänen, A. C. Siddiqui, Moneeza Kalhan Lang, Chim C. Magnusson, Patrik K. E. Yue, Qun-Ying Wadelius, Claes Buchwald, Christian Von Bygum, Anette Alfirevic, Ana Zee, Anke H. Maitland-Van Der Palmer, Colin N. A. Wadelius, Mia |
| Copyright Year | 2020 |
| Abstract | Angioedema in the mouth or upper airways is a feared adverse reaction to angiotensin-converting enzyme inhibitor (ACEi) and angiotensin receptor blocker (ARB) treatment, which is used for hypertension, heart failure and diabetes complications. This candidate gene and genome-wide association study aimed to identify genetic variants predisposing to angioedema induced by these drugs. The discovery cohort consisted of 173 cases and 4890 controls recruited in Sweden. In the candidate gene analysis, ETV6, BDKRB2, MME, and PRKCQ were nominally associated with angioedema (p < 0.05), but did not pass Bonferroni correction for multiple testing (p < 2.89 × 10−5). In the genome-wide analysis, intronic variants in the calcium-activated potassium channel subunit alpha-1 (KCNMA1) gene on chromosome 10 were significantly associated with angioedema (p < 5 × 10−8). Whilst the top KCNMA1 hit was not significant in the replication cohort (413 cases and 599 ACEi-exposed controls from the US and Northern Europe), a meta-analysis of the replication and discovery cohorts (in total 586 cases and 1944 ACEi-exposed controls) revealed that each variant allele increased the odds of experiencing angioedema 1.62 times (95% confidence interval 1.05–2.50, p = 0.030). Associated KCNMA1 variants are not known to be functional, but are in linkage disequilibrium with variants in transcription factor binding sites active in relevant tissues. In summary, our data suggest that common variation in KCNMA1 is associated with risk of angioedema induced by ACEi or ARB treatment. Future whole exome or genome sequencing studies will show whether rare variants in KCNMA1 or other genes contribute to the risk of ACEi- and ARB-induced angioedema. |
| Starting Page | 1 |
| Ending Page | 14 |
| Page Count | 14 |
| File Format | PDF HTM / HTML |
| PubMed reference number | 32080354 |
| Journal | Medline |
| Alternate Webpage(s) | https://discovery.ucl.ac.uk/id/eprint/10094777/1/s41397-020-0165-2.pdf |
| Alternate Webpage(s) | https://doi.org/10.1038/s41397-020-0165-2 |
| Journal | The Pharmacogenomics Journal |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |
