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POS1487 (2023)
CLINICAL SIGNIFICANCE OF DIFFERENT PROFILES OF ANTI-Ro ANTIBODIES IN CONNECTIVE TISSUE DISEASES
Y. Chen1,1,1,1, H. T. Yang1,1,1,1, D. Liu1,1,1
1Shenzhen People’s Hospital, Department of Rheumatology and Immunology, Shenzhen, China

 

Background Anti-Ro60 and anti-Ro52 antibodies are associated with different connective tissue diseases (CTDs) [1]. However, the clinical significance of anti-Ro antibodies is not always consistent among different global regions.

Objectives To investigate the clinical characteristics of patients with anti-Ro antibodies.

Methods A total of 1596 inpatients with anti-Ro antibodies were included in the study. Demographic, clinical, and serological data were compared between individuals with different profiles of anti-Ro antibodies: patients with anti-Ro52 antibodies alone, patients with anti-Ro60 antibodies alone, and patients with combined anti-Ro52 and anti-Ro60 antibodies.

Results Of the 1596 patients, 1362 (85.3%) were female, the mean age was 45.5 years, and systemic lupus erythematosus (SLE) (46.0%) and Sjogren’s syndrome (SS) (19.0%) were the most common CTD diagnoses. Among the patients with anti-Ro52 antibodies alone, idiopathic inflammatory myopathy (18.8%) and SLE (17.6%) were the most common CTD diagnoses. The coexistent autoantibodies of this group were significantly lower compared with those of the other two groups, while the presence of anti-Jo1 antibodies were significantly higher compared with those of the other two groups (3.7% vs. 0.6% vs. 1.9%, p=0.029) (Figure 1). In addition, the patients with isolated anti-Ro52 antibodies were more likely to suffer from interstitial lung disease (35.5% vs.11.3% vs.13.7%, p<0.0001) and pulmonary arterial hypertension (10.1% vs. 5.3% vs. 3.6%, p=0.001) compared with the other two groups of patients (Table 1). Compared with patients with isolated anti-Ro52 or anti-Ro60 antibodies, the patients with combined anti-Ro52 and anti-Ro60 antibodies were more likely to suffer from xerophthalmia and xerostomia. Furthermore, hypocomplementemia, hyperglobulinemia, and proteinuria were particularly prevalent in patients with anti-Ro60 antibodies.

Conclusion Different profiles of anti-Ro antibodies were significantly associated with clinical phenotypic features in CTDs, indicating the potential diagnostic and prognostic value of these antibodies in clinical practice.

Reference [1]Lee A Y S, J H Reed, and T P Gordon. Anti-Ro60 and anti-Ro52/TRIM21: Two distinct autoantibodies in systemic autoimmune diseases. J Autoimmun, 2021 Nov;124:102724.

Image/graph:

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Figure 1 Comparison of autoantibody profiles in patients with positive anti-Ro antibodies

TABLE 1 Comparison of clinical features in patients with connective tissue diseases

Parameters (n, %) Groups p values
All: n=1319 Group A: Ro52 alone n=169 Group B: Ro60 alone n=283 Group C: Ro60 and Ro52 n=867 Group A vs. group B Group A vs. group C Group B vs. group C Overall
Skin rash 349(26.5) 40(23.7) 101(35.7) 208(24.0) 0.008 0.928 <0.0001 <0.0001
Arthralgia 512(38.8) 72(42.6) 164(58.0) 276(31.8) 0.002 0.007 <0.0001 <0.0001
Myalgia 80(6.1) 16(9.5) 26(9.2) 38(4.4) 0.921 0.007 0.002 0.002
Xerophthalmia 277(21.0) 31(18.3) 39(13.8) 207(23.9) 0.160 0.118 <0.0001 0.001
Xerostomia 310(23.5) 34(20.1) 47(16.6) 229(26.4) 0.346 0.085 0.001 0.002
Anemia 375(28.4) 39(23.1) 78(27.6) 258(29.8) 0.292 0.079 0.481 0.198
Leukocytopenia 295(22.4) 28(16.6) 61(21.6) 206(23.8) 0.197 0.041 0.446 0.114
Thrombocytopenia 128(9.7) 11(6.5) 27(9.5) 90(10.4) 0.261 0.121 0.685 0.297
Proteinuria 208(15.8) 10(5.9) 53(18.7) 145(16.7) <0.0001 <0.0001 0.438 0.001
Hematuria 99(7.5) 3(1.8) 29(10.2) 67(7.7) 0.001 0.005 0.183 0.004
ILD 211(16.0) 60(35.5) 32(11.3) 119(13.7) <0.0001 <0.0001 0.296 <0.0001
PAH 63(4.8) 17(10.1) 15(5.3) 31(3.6) 0.056 <0.0001 0.199 0.001
RP 88(6.7) 18(10.7) 22(7.8) 48(5.5) 0.297 0.013 0.172 0.036

ILD: interstitial lung disease; PAH: pulmonary arterial hypertension; RP: Raynaud’s phenomenon

Acknowledgements: NIL.

Disclosure of Interests None Declared.

Keywords: Autoantibodies, Clinical trials, Organ damage

DOI: 10.1136/annrheumdis-2023-eular.639


Citation: , volume 82, supplement 1, year 2023, page 1099
Session: SLE, Sjön’s and APS - clinical aspects (other than treatment) (Poster View)