Prevalence of anti-synthetase antibodies among systemic sclerosis patients

被引:1
|
作者
Garra, Wakar [1 ,2 ]
Levy, Yair [1 ,2 ]
机构
[1] Meir Med Ctr, Dept Internal Med E, IL-4428164 Kefar Sava, Israel
[2] Tel Aviv Univ, Sackler Sch Med, Tel Aviv, Israel
关键词
Systemic sclerosis; Anti synthetase antibodies; Interstitial lung disease; Myositis antibodies; FORCED VITAL CAPACITY; ANTISYNTHETASE SYNDROME; PULMONARY-HYPERTENSION; LUNG-DISEASE; SCLERODERMA; AUTOANTIBODIES; PREDICTORS; MORTALITY; SURVIVAL;
D O I
10.1016/j.ejim.2023.07.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: we aimed to estimate the prevalence of Amino acyl-transfer ribonucleic acid synthetase antibodies (Anti-ARS); myositis specific antibodies, among patients with systemic sclerosis (SSc), to evaluate the clinical associations of anti-ARS antibodies in SSc patients and to identify risk factors for development of interstitial lung disease (ILD) in SSc. Methods: A prospective study of 71 systemic sclerosis patients in our rheumatology clinic in Israel. Sera were tested for myositis antibodies. Data on patients clinical and serological manifestations and treatment were collected and compared according to anti-ARS antibodies and ILD. Results: Prevalence of anti-ARS antibodies was 6% (4/71) with anti PL-7, anti- OJ and Jo-1 positivity. Anti Ro-52 was found in 27%, anti-PM/Scl 75, anti-PM/Scl 100 and anti-SRP in 6%, anti-Ku in 3%, anti-Mi-2 beta and antiMi-2 alfa in 4%, anti- NXP2 and anti-TIF1gamma in 1%. ILD complication was observed in 42% of patients and was associated with anti RNAP-III, anti Scl-70 and Anti-ARS antibodies. In multiple logistic regression, anti Scl70 was associated with 6-fold higher risk for ILD. Conclusion: Anti-ARS antibodies were observed in 6% of SSc patients. All of them had ILD. Due to the low prevalence of anti-ARS, this study could not describe clinical associations of anti-ARS antibodies in SSc patients.
引用
收藏
页码:98 / 102
页数:5
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