Digital repository of Slovenian research organisations

Show document
A+ | A- | SLO | ENG

Title:Functional complement analysis can predict genetic testing results and long-term outcome in patients with complement deficiencies
Authors:Blazina, Štefan (Author)
Debeljak, Maruša (Author)
Košnik, Mitja (Author)
Simčič, Saša (Author)
Stopinšek, Sanja (Author)
Markelj, Gašper (Author)
Toplak, Nataša (Author)
Kopač, Peter (Author)
Zakotnik, Breda (Author)
Pokorn, Marko (Author)
Avčin, Tadej (Author)
Language:English
Tipology:1.01 - Original Scientific Article
Organisation:Logo UKPBAG - University Clinic of Respiratory and Allergic Diseases Golnik
Abstract:Background: Prevalence of complement deficiencies (CDs) is markedly higher in Slovenian primary immunodeficiency (PID) registry in comparison to other national and international PID registries. Objective: The purposes of our study were to confirm CD and define complete and partial CD in registered patients in Slovenia, to evaluate frequency of clinical manifestations, and to assess the risk for characteristic infections separately for subjects with complete and partial CD. Methods: CD was confirmed with genetic analyses in patients with C2 deficiency, C8 deficiency, and hereditary angioedema or with repeated functional complement studies and measurement of complement components in other CD. Results of genetic studies (homozygous subjects vs. heterozygous carriers) and complement functional studies were analyzed to define complete (complement below the level of heterozygous carriers) and partial CD (complement above the level of homozygous patients). Presence of characteristic infections was assessed separately for complete and partial CD. Results: Genetic analyses confirmed markedly higher prevalence of CD in Slovenian PID registry (26% of all PID) than in other national and international PID registries (0.5–6% of all PID). Complement functional studies and complement component concentrations reliably distinguished between homozygous and heterozygous CD carriers. Subjects with partial CD had higher risk for characteristic infections than previously reported. Conclusion: Results of our study imply under-recognition of CD worldwide. Complement functional studies and complement component concentrations reliably predicted risk for characteristic infections in patients with complete or partial CD. Vaccination against encapsulated bacteria should be advocated also for subjects with partial CD and not limited to complete CD.
Keywords:complement deficiency, primary immunodeficiency, laboratory analysis, genetic analysis, clinical manifestations
Year of publishing:2018
Publisher:Frontiers Reserach Foundation
Source:Švica
COBISS_ID:4891564 Link is opened in a new window
UDC:616.9
ISSN on article:1664-3224
OceCobissID:30774233 Link is opened in a new window
DOI:10.3389/fimmu.2018.00500 Link is opened in a new window
Note:Nasl. z nasl. zaslona; Opis vira z dne 17. 8. 2017; Article 500;
Views:748
Downloads:295
Files:.pdf PDF - Presentation file, download (1000,60 KB)
 
Journal:Front. immunol.
Frontiers Research Foundation
 
Metadata:XML RDF-CHPDL DC-XML DC-RDF
Rights:© 2018 Blazina, Debeljak, Košnik, Simčič, Stopinšek, Markelj, Toplak, Kopač, Zakotnik, Pokorn and Avčin
:
  
Hover the mouse pointer over a document title to show the abstract or click on the title to get all document metadata.


Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:21.03.2018

Back