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Title:The incidence of IgG4-related disease in Slovenia : single-centre experience
Authors:ID Hočevar, Alojzija (Author)
ID Grošelj, Aleš (Author)
ID Hawlina, Gregor (Author)
ID Koželj, Matic (Author)
ID Škoberne, Andrej (Author)
ID Pižem, Jože (Author)
ID Jurčić, Vesna (Author)
Files:.pdf PDF - Presentation file, download (474,84 KB)
MD5: FBB7A141F6116AFC90FB9126814A3247
 
URL URL - Source URL, visit https://www.mdpi.com/2227-9059/13/9/2281
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Background: Data on the incidence of IgG4-related disease (IgG4-RD) are scarce. Our aim was to determine the incidence of IgG4-RD in a well-defined region. Methods: This retrospective study covered the Ljubljana region over the period from January 2012 to December 2024. A review of cases diagnosed with IgG4-RD was performed at several departments of the University Medical Centre Ljubljana—an integrated secondary/tertiary university teaching hospital (rheumatology, nephrology, angiology, gastroenterology, abdominal surgery, ENT surgery, ophthalmology). While IgG4-RD cases at the Department of Rheumatology were collected prospectively, potential cases at other departments were retrieved by searching electronic medical database for the keyword “IgG4”. In addition, the Institute of Pathology, Faculty of Medicine, University of Ljubljana, provided a list of patients with histological features consistent with IgG4-RD. Year-specific incidence rates and an average incidence rate over the 13-year period were determined. Clinical features of patients were analysed. Results: During the observation period, 58 cases of IgG4-RD were diagnosed. Of these, 35 patients were residents of the Ljubljana region, which had an average adult population of 541,600. The estimated average annual incidence rate of IgG4-RD was 5.0 per million (95% confidence interval: 3.5; 6.9), with year-specific incidence rates fluctuating between 1.8 and 9.3 per million adults. The cases were stratified into four phenotypic categories: pancreato-hepato-biliary (17%), retroperitoneal fibrosis-aortitis (43%), head and neck-limited (14%), and Mikulicz syndrome with systemic involvement (26%). Conclusions: The average annual incidence rate of IgG4-RD was 5 per million adults, with the retroperitoneal fibrosis-aortitis phenotype predominating in our cohort.
Keywords:IgG4-related disease, epidemiology, demographic, incidence rate
Publication status:Published
Publication version:Version of Record
Year of publishing:2025
Number of pages:str. 1-8
Numbering:Vol. 13, iss. 9, [article no.] 2281
PID:20.500.12556/DiRROS-24635 New window
UDC:616-002
ISSN on article:2227-9059
DOI:10.3390/biomedicines13092281 New window
COBISS.SI-ID:252958723 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 13. 10. 2025;
Publication date in DiRROS:09.12.2025
Views:92
Downloads:38
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Record is a part of a journal

Title:Biomedicines
Shortened title:Biomedicines
Publisher:MDPI AG
ISSN:2227-9059
COBISS.SI-ID:523006745 New window

Document is financed by a project

Funder:Other - Other funder or multiple funders
Funding programme:Univerzitetni klinični center Ljubljana
Project number:20240008
Name:Klinične in epidemiološke lastnosti z imunoglobulinom IgG4 povezane bolezni

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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.

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