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  • Mathey, Carina M (author)

Molecular Genetic Screening in Patients With ACE Inhibitor/Angiotensin Receptor Blocker-Induced Angioedema to Explore the Role of Hereditary Angioedema Genes

  • Article/chapterEnglish2022

Publisher, publication year, extent ...

  • 2022-07-18
  • Frontiers Media S.A.2022
  • electronicrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:uu-491743
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-491743URI
  • https://doi.org/10.3389/fgene.2022.914376DOI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Angioedema is a relatively rare but potentially life-threatening adverse reaction to angiotensin-converting enzyme inhibitors (ACEi) and angiotensin receptor blockers (ARBs). As with hereditary forms of angioedema (HAE), this adverse reaction is mediated by bradykinin. Research suggests that ACEi/ARB-induced angioedema has a multifactorial etiology. In addition, recent case reports suggest that some ACEi/ARB-induced angioedema patients may carry pathogenic HAE variants. The aim of the present study was to investigate the possible association between ACEi/ARB-induced angioedema and HAE genes via systematic molecular genetic screening in a large cohort of ACEi/ARB-induced angioedema cases. Targeted re-sequencing of five HAE-associated genes (SERPING1, F12, PLG, ANGPT1, and KNG1) was performed in 212 ACEi/ARB-induced angioedema patients recruited in Germany/Austria, Sweden, and Denmark, and in 352 controls from a German cohort. Among patients, none of the identified variants represented a known pathogenic variant for HAE. Moreover, no significant association with ACEi/ARB-induced angioedema was found for any of the identified common [minor allele frequency (MAF) >5%] or rare (MAF < 5%) variants. However, several non-significant trends suggestive of possible protective effects were observed. The lowest p-value for an individual variant was found in PLG (rs4252129, p.R523W, p = 0.057, p.adjust > 0.999, Fisher's exact test). Variant p.R523W was found exclusively in controls and has previously been associated with decreased levels of plasminogen, a precursor of plasmin which is part of a pathway directly involved in bradykinin production. In addition, rare, potentially functional variants (MAF < 5%, Phred-scaled combined annotation dependent depletion score >10) showed a nominally significant enrichment in controls both: 1) across all five genes; and 2) in the F12 gene alone. However, these results did not withstand correction for multiple testing. In conclusion, our results suggest that HAE-associated mutations are, at best, a rare cause of ACEi/ARB-induced angioedema. Furthermore, we were unable to identify a significant association between ACEi/ARB-induced angioedema and other variants in the investigated genes. Further studies with larger sample sizes are warranted to draw more definite conclusions concerning variants with limited effect sizes, including protective variants.

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Added entries (persons, corporate bodies, meetings, titles ...)

  • Maj, Carlo (author)
  • Scheer, Annika B (author)
  • Fazaal, Julia (author)
  • Wedi, Bettina (author)
  • Wieczorek, Dorothea (author)
  • Amann, Philipp M (author)
  • Löffler, Harald (author)
  • Koch, Lukas (author)
  • Schöffl, Clemens (author)
  • Dickel, Heinrich (author)
  • Ganjuur, Nomun (author)
  • Hornung, Thorsten (author)
  • Forkel, Susann (author)
  • Greve, Jens (author)
  • Wurpts, Gerda (author)
  • Hallberg, Pär,1974-Uppsala universitet,Klinisk farmakogenomik och osteoporos,Science for Life Laboratory, SciLifeLab,Klinisk farmakogenomik och osteoporos, Clinical pharmacogenomics and osteoporosis(Swepub:uu)pahal677 (author)
  • Bygum, Anette (author)
  • Von Buchwald, Christian (author)
  • Karawajczyk, MalgorzataUppsala universitet,Klinisk kemi(Swepub:uu)malgkara (author)
  • Steffens, Michael (author)
  • Stingl, Julia (author)
  • Hoffmann, Per (author)
  • Heilmann-Heimbach, Stefanie (author)
  • Mangold, Elisabeth (author)
  • Ludwig, Kerstin U (author)
  • Rasmussen, Eva R (author)
  • Wadelius, MiaUppsala universitet,Klinisk farmakogenomik och osteoporos,Science for Life Laboratory, SciLifeLab(Swepub:uu)miawadel (author)
  • Sachs, Bernhardt (author)
  • Nöthen, Markus M (author)
  • Forstner, Andreas J (author)
  • Uppsala universitetKlinisk farmakogenomik och osteoporos (creator_code:org_t)

Related titles

  • In:Frontiers in Genetics: Frontiers Media S.A.131664-8021

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