{"title":"抗整合素αvβ6自身抗体作为轴性脊柱炎患者溃疡性结肠炎的生物标志物","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":"{\"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}","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
摘要
抗整合素αvβ6自身抗体(AIA)最近被描述为溃疡性结肠炎(UC)的信息生物标志物,与非炎症性肠病(IBD)患者相比,显示出高敏感性和特异性。鉴于轴性脊柱炎(AxSpA)和IBD之间的关联,我们试图评估AIA作为AxSpA合并或不合并IBD患者生物标志物的潜力。方法采用已建立的ELISA方案,我们测量了(i) AxSpA和UC (n=18), (ii) AxSpA和克罗恩病(CD) (n=29), (iii) AxSpA单独(n=48)和健康对照(HC) (n=48)患者血清中的AIA水平。比较患者组间AIA吸光度值,比较临床变量与AIA阳性的关系。结果与单独使用AxSpA的患者相比,AxSpA和UC患者的平均吸光度和AIA阳性率显著增加。对于AxSpA患者UC的诊断,AIAs的敏感性为55.6%,特异性为89.6%,受试者工作特征分析的曲线下面积为0.83。AIA阳性与AxSpA和UC患者的IBD家族史相关。令人惊讶的是,与aia阴性患者相比,aia阳性患者的平均CRP和BASDAI降低。在检查一系列样本时,我们观察到10例AIA阳性患者中有3例变为AIA阴性,而AIA阴性到AIA阳性的转变没有观察到。结论:aia被证明有潜力作为AxSpA患者UC的诊断测试,特别是那些有IBD家族史的患者。据我们所知,这是迄今为止在AxSpA中检验AIA的第一项研究。
Anti-Integrin αvβ6 Autoantibodies as a Biomarker for Ulcerative Colitis in Patients With Axial Spondyloarthritis.
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.