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Angioedema without urticaria: novel findings which must be measured in clinical setting.

AbstractPURPOSE OF REVIEW:
Angioedema without urticaria is composed of an increasing subtype's variety and presents a challenging diagnosis. This review summarizes the subtypes recently described and subsequent new findings helpful within their classification.
RECENT FINDINGS:
New methods to measure cleaved high molecular weight kininogen and activated plasma kallikrein have emerged as potential biochemical tests to identify bradykinin-mediated angioedema. Three new subtypes of hereditary angioedema (HAE) with normal C1 inhibitor were described in the past two years: HAE due to mutation in plasminogen gene, in kininogen gene, and in angiopoietin-1 gene; implicating the fibrinolytic and contact systems, and the regulation of vasculature, respectively. The understanding of some mechanisms in angioedema has been improved, compatible to the dominant-negative for some C1 inhibitor variants; furthermore, the increased activation of truncated F12 mutants by plasma kallikrein; and the diminished binding of angiopoietin-1 to its receptor.
SUMMARY:
The validation of biomarkers for the contact system activation could be beneficial in differentiating bradykinin - from histaminergic-mediated angioedema. Currently, the available laboratorial tests are still somewhat restricted to the evaluation of the complement activation and the mediators of nonhistaminergic and nonbradykinin-mediated angioedema remain to be identified.
AuthorsCamila Lopes Veronez, Anete Sevciovic Grumach
JournalCurrent opinion in allergy and clinical immunology (Curr Opin Allergy Clin Immunol) Vol. 20 Issue 3 Pg. 253-260 (06 2020) ISSN: 1473-6322 [Electronic] United States
PMID32073435 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Chemical References
  • ANGPT1 protein, human
  • Angiopoietin-1
  • Biomarkers
  • KNG1 protein, human
  • Kininogens
  • Plasminogen
Topics
  • Angioedemas, Hereditary (diagnosis, genetics, immunology)
  • Angiopoietin-1 (genetics)
  • Biomarkers
  • Complement Activation (genetics)
  • Diagnosis, Differential
  • Humans
  • Kininogens (genetics)
  • Mutation
  • Plasminogen (genetics)

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