Key result
Genome-wide analysis links novel CSMD1 variants and SNP rs500766 to ACEI-induced angioedema.
Why the study?
Despite African Americans having a 5-fold increased risk of angiotensin-converting enzyme inhibitor-induced angioedema (AE-ACEI), there were no published genome-wide association studies from Africa.
What genetic variants are associated with angiotensin-converting enzyme inhibitor-induced angioedema in African and diverse populations?
Case-Control (n=1,378)
Yes
What genetic variants are associated with angiotensin-converting enzyme inhibitor-induced angioedema in African and diverse populations?
This GWAS and meta-analysis identified novel genetic variants and replicated known SNPs associated with ACE inhibitor-induced angioedema, highlighting the importance of including diverse African populations in pharmacogenomic research.
May inform risk stratification for ACEI angioedema in African ancestry patients; extends prior GWAS by identifying CSMD1 variants and replicating rs500766.
Background: Angiotensin-converting enzyme inhibitor-induced angioedema (AE-ACEI) is a life-threatening adverse event; globally, it is the most common cause of emergency presentations with angioedema. Several genome-wide association studies (GWASs) have found genomic associations with AE-ACEI. However, despite African Americans having a 5-fold increased risk of AE-ACEI, there are no published GWASs from Africa. Objective: The aim of this study was to conduct a GWAS of AE-ACEI in a South African population and perform a meta-analysis with an African American and European American population. Methods: The GWAS included 202 South African adults with a history of AE-ACEI and 513 controls without angioedema following angiotensin-converting enzyme inhibitor (ACEI) treatment for at least 2 years. A meta-analysis was conducted with GWAS summary statistics from an African American and European American cohort (from the Vanderbilt-Marshfield cohort, which consisted of 174 case patients and 489 controls). Results: (CUB and sushi multiple domains 1) gene, which has been linked to ACEI cough, providing replication at the gene level but with novel lead SNPs. The study also replicated SNP rs500766 on chromosome 10, which was previously found to be associated with AE-ACEI. Conclusions: Our results highlight the importance of African populations for detection of novel variants in replication studies. Further increased sampling across the continent and matched functional work are needed to confirm the importance of genetic variation in understanding the biology of AE-ACEI.
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Mugo et al. (2025) conducted a case-control in Angiotensin-converting enzyme inhibitor-induced angioedema (AE-ACEI) (n=1,378). Angiotensin-converting enzyme inhibitor (ACEI) vs. ACEI without angioedema was evaluated on Genomic associations with AE-ACEI. A genome-wide association study and meta-analysis identified novel lead SNPs in the CSMD1 gene and replicated the association of SNP rs500766 with ACEI-induced angioedema.
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