医学
免疫性血小板减少症
内科学
入射(几何)
胃肠病学
发病机制
自身抗体
血小板
关节炎
肌酐
免疫学
抗体
物理
光学
作者
Fan Dai,Guomei Yang,Peishi Rao,Puqi Wu,Rongjuan Chen,Yuechi Sun,Yun Peng,Hongyan Qian,Bin Wang,Shiju Chen,Yuan Liu,Guixiu Shi
标识
DOI:10.3389/fmed.2020.00138
摘要
Objective: Clinical characteristics of immune thrombocytopenia (ITP) associated with primary Sjögren's syndrome (pSS) have not been clearly defined. This study aimed to evaluate the prevalence and characteristics of secondary ITP in patients with pSS. Methods: A total of 291 pSS patients in our hospital were retrospectively analyzed. Clinical manifestations and laboratory findings were compared between pSS patients with and without ITP. Results: The prevalence of secondary ITP in pSS patients was 12.03%. Compared to pSS patients without ITP, pSS patients with ITP were younger and had higher disease activity. The prevalence of interstitial lung diseases (ILD) was significantly lower in pSS patients with ITP (30.43% vs 54.95%; P=0.029), and it was the same with arthritis (17.14% vs 39.11%; P=0.014) and dry eye (33.33% vs 54.17%, P=0.027) compared with those without ITP. Serum creatinine level was lower in pSS patients with ITP (P=0.009), while positivity of anti-histone autoantibodies was higher in pSS patients with ITP (P=0.025). Conclusion: This study revealed that patients with pSS-ITP had some distinct characteristics. The lower incidence of ILD and arthritis among pSS patients with ITP indicated potential active roles of platelets in the pathogenesis of fibrosis or inflammatory arthritis.
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