{"title":"Anti-Integrin αvβ6 Autoantibodies as a Biomarker for Ulcerative Colitis in Patients With Axial Spondyloarthritis.","authors":"Enoch Yau,Tina Chim,Melissa Lim,Robert D Inman","doi":"10.3899/jrheum.2024-1296","DOIUrl":null,"url":null,"abstract":"OBJECTIVE\r\nAnti-integrin αvβ6 autoantibodies (AIA) have recently been described as an informative biomarker for ulcerative colitis (UC), demonstrating a high sensitivity and specificity compared to patients without inflammatory bowel disease (IBD). Given the association between axial spondyloarthritis (AxSpA) and IBD, we sought to evaluate the potential of AIA as a biomarker in AxSpA patients with or without concurrent IBD.\r\n\r\nMETHODS\r\nUsing an established ELISA protocol, we measured AIA levels in sera of patients with (i) AxSpA and UC (n=18), (ii) AxSpA and Crohn's Disease (CD) (n=29), (iii) AxSpA alone (n=48), and healthy controls (HC) (n=48). AIA absorbance values were compared between patient groups and clinical variables were compared with AIA positivity.\r\n\r\nRESULTS\r\nPatients with AxSpA and UC showed a significant increase in mean absorbance and AIA positivity rate compared with AxSpA alone. For the diagnosis of UC among AxSpA patients, AIAs had a sensitivity of 55.6% and specificity of 89.6%, and receiver operating characteristic analysis yielded an area under curve value of 0.83. AIA positivity was associated with a family history of IBD in patients with AxSpA and UC. Surprisingly, AIA-positive patients had decreased mean CRP and BASDAI compared with AIA-negative patients. Examining serial samples, we observed that 3 of 10 AIA positive patients became AIA-negative, whereas AIA-negative to AIA-positive transitions were not observed.\r\n\r\nCONCLUSION\r\nAIA demonstrated potential as a diagnostic test for UC within AxSpA patients, particularly those with a family history of IBD. To our knowledge, this is the first study to date examining AIA in AxSpA.","PeriodicalId":501812,"journal":{"name":"The Journal of Rheumatology","volume":"35 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Rheumatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3899/jrheum.2024-1296","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
OBJECTIVE
Anti-integrin αvβ6 autoantibodies (AIA) have recently been described as an informative biomarker for ulcerative colitis (UC), demonstrating a high sensitivity and specificity compared to patients without inflammatory bowel disease (IBD). Given the association between axial spondyloarthritis (AxSpA) and IBD, we sought to evaluate the potential of AIA as a biomarker in AxSpA patients with or without concurrent IBD.
METHODS
Using an established ELISA protocol, we measured AIA levels in sera of patients with (i) AxSpA and UC (n=18), (ii) AxSpA and Crohn's Disease (CD) (n=29), (iii) AxSpA alone (n=48), and healthy controls (HC) (n=48). AIA absorbance values were compared between patient groups and clinical variables were compared with AIA positivity.
RESULTS
Patients with AxSpA and UC showed a significant increase in mean absorbance and AIA positivity rate compared with AxSpA alone. For the diagnosis of UC among AxSpA patients, AIAs had a sensitivity of 55.6% and specificity of 89.6%, and receiver operating characteristic analysis yielded an area under curve value of 0.83. AIA positivity was associated with a family history of IBD in patients with AxSpA and UC. Surprisingly, AIA-positive patients had decreased mean CRP and BASDAI compared with AIA-negative patients. Examining serial samples, we observed that 3 of 10 AIA positive patients became AIA-negative, whereas AIA-negative to AIA-positive transitions were not observed.
CONCLUSION
AIA demonstrated potential as a diagnostic test for UC within AxSpA patients, particularly those with a family history of IBD. To our knowledge, this is the first study to date examining AIA in AxSpA.