Clinical Validity of Anti-Proteinase 3 Antibodies in Patients with Inflammatory Bowel Disease: A Short Meta-Analysis.

Autor: Andalucía C; Research and Development, Headquarters & Technology Center Autoimmunity, Werfen, San Diego, CA 92121, USA., Martínez-Prat L; Research and Development, Headquarters & Technology Center Autoimmunity, Werfen, San Diego, CA 92121, USA., Bentow C; Research and Development, Headquarters & Technology Center Autoimmunity, Werfen, San Diego, CA 92121, USA., Aure MA; Research and Development, Headquarters & Technology Center Autoimmunity, Werfen, San Diego, CA 92121, USA., Horn MP; Department of Clinical Chemistry, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland., Mahler M; Research and Development, Headquarters & Technology Center Autoimmunity, Werfen, San Diego, CA 92121, USA.
Jazyk: angličtina
Zdroj: Diagnostics (Basel, Switzerland) [Diagnostics (Basel)] 2023 Dec 16; Vol. 13 (24). Date of Electronic Publication: 2023 Dec 16.
DOI: 10.3390/diagnostics13243682
Abstrakt: Anti-neutrophil cytoplasmic antibodies (ANCA) directed to proteinase 3 (PR3) represent highly established markers for patients with ANCA-associated vasculitis (AAV). PR3-ANCA have also demonstrated utility in the management of inflammatory bowel disease (IBD). More specifically, PR3-ANCA discriminate individuals with ulcerative colitis (UC) from Crohn's disease (CD) patients and are associated with disease severity, activity, and treatment non-response. Here, we aim to summarize the current data on the diagnostic utility of PR3-ANCA in IBD. A structured, systematic literature review, including three electronic databases, was conducted on June 6th, 2023, to identify studies assessing the diagnostic accuracy of the QUANTA Flash ® PR3 assay in UC vs. CD patients. Electronic searches were supplemented by hand searching. A hierarchical, bivariate, mixed-effect meta-analysis was conducted using the metandi function, as per the Cochrane collaboration recommendations. Study quality was assessed using the QUADAS-2 tool, which considers the risk of bias and applicability. Six out of a hundred and eleven citations met the inclusion criteria and reported QUANTA Flash ® PR3 diagnostic accuracy in UC vs. CD (UC, n = 667, CD, n = 682 patients). The sensitivity/specificity point estimate for UC was 34.9%/95.9%. This resulted in a Diagnostic Odds Ratio (DOR) of 12.6. The risk of bias was low in the index test and reference standard domains. Four of the six studies (67%) showed an unclear risk of bias in patient selection and in flow and timing domains. All studies had low concerns about applicability in all the domains. PR3-ANCA measured with the QUANTA Flash ® PR3 assay represent novel diagnostic markers in IBD and enables discrimination between UC and CD.
Databáze: MEDLINE
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