Clinical Profile of Patients with Primary Sjögren's Syndrome with Non-Identified Antinuclear Autoantibodies

被引:3
作者
Parisis, Dorian [1 ,2 ]
Sarrand, Julie [1 ]
Cabrol, Xavier [1 ,2 ]
Delporte, Christine [2 ]
Soyfoo, Muhammad S. [1 ]
机构
[1] Univ Libre Bruxelles, Erasme Hosp, Hop Univ Bruxelles HUB, Dept Rheumatol, B-1070 Brussels, Belgium
[2] Univ Libre Bruxelles, Fac Med, Lab Pathophysiol & Nutr Biochem, B-1070 Brussels, Belgium
基金
欧盟地平线“2020”;
关键词
Sj & ouml; gren's syndrome; autoantibodies; rheumatoid factor; systemic manifestations; corticosteroids; PRIMARY SJOGRENS-SYNDROME; CLASSIFICATION CRITERIA; AMERICAN-COLLEGE; DATA-DRIVEN; CONSENSUS; DISEASE; COHORT;
D O I
10.3390/diagnostics14090935
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives-The aim of the present study was to characterize the clinical phenotype of patients with primary Sj & ouml;gren's syndrome (pSS) with non-identified antinuclear antibodies (ANA) in comparison with that of patients with pSS with negative ANA, positive typical ANA (anti-Ro/SSA and/or La/SSB) and positive atypical ANA. Methods-We conducted an observational, retrospective monocentric study at the Erasme University Hospital (Brussels, Belgium). Two hundred and thirty-three patients fulfilling the 2002 American-European Consensus Group criteria for pSS were included in this study. The patients were subdivided according to their ANA profile and demographics. The clinical and biological data of each subgroup were compared. Moreover, the relationships between these data and the ANA profiles were determined by multiple correspondence analysis. Results-In our cohort, 42 patients (18%) presented a non-identified ANA-positive profile. No statistically significant difference could be observed between non-identified ANA patients and ANA-negative patients in terms of age and/or ESSDAI score at diagnosis. There were significantly more frequent articular manifestations, positive rheumatoid factor (RF), and the use of corticosteroids in anti-Ro/SSA-positive patients compared to ANA-negative (p <= 0.0001) and non-identified ANA-positive patients (p <= 0.01). However, a significantly higher proportion of RF positivity and corticosteroid treatment was observed in non-identified ANA-positive patients compared to ANA-negative patients (p < 0.05). Conclusions-For the first time to our knowledge, our study has characterized the clinical phenotype of patients with pSS with non-identified ANA at diagnosis. The non-identified ANA-positive patients featured mostly a clinical phenotype similar to that of the ANA-negative patients. On the other hand, the non-identified ANA-positive patients were mainly distinguished from the ANA-negative patients by a greater proportion of RF positivity and the need for corticosteroid use due to articular involvement.
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