Arroyo-Ávila Mariangelí, Santiago-Casas Yesenia, McGwin Gerald, Cantor Ryan S, Petri Michelle, Ramsey-Goldman Rosalind, Reveille John D, Kimberly Robert P, Alarcón Graciela S, Vilá Luis M, Brown Elizabeth E
Division of Rheumatology, Department of Medicine, University of Puerto Rico Medical Sciences Campus, PO Box 365067, San Juan, PR, 00936-5067, USA.
Clin Rheumatol. 2015 Jul;34(7):1217-23. doi: 10.1007/s10067-015-2941-y. Epub 2015 Apr 22.
The aim of this study was to determine the association of anti-Sm antibodies with clinical manifestations, comorbidities, and disease damage in a large multi-ethnic SLE cohort. SLE patients (per American College of Rheumatology criteria), age ≥16 years, disease duration ≤10 years at enrollment, and defined ethnicity (African American, Hispanic or Caucasian), from a longitudinal US cohort were studied. Socioeconomic-demographic features, cumulative clinical manifestations, comorbidities, and disease damage (as per the Systemic Lupus International Collaborating Clinics Damage Index [SDI]) were determined. The association of anti-Sm antibodies with clinical features was examined using multivariable logistic regression analyses adjusting for age, gender, ethnicity, disease duration, level of education, health insurance, and smoking. A total of 2322 SLE patients were studied. The mean (standard deviation, SD) age at diagnosis was 34.4 (12.8) years and the mean (SD) disease duration was 9.0 (7.9) years; 2127 (91.6%) were women. Anti-Sm antibodies were present in 579 (24.9%) patients. In the multivariable analysis, anti-Sm antibodies were significantly associated with serositis, renal involvement, psychosis, vasculitis, Raynaud's phenomenon, hemolytic anemia, leukopenia, lymphopenia, and arterial hypertension. No significant association was found for damage accrual. In this cohort of SLE patients, anti-Sm antibodies were associated with several clinical features including serious manifestations such as renal, neurologic, and hematologic disorders as well as vasculitis.
本研究的目的是确定在一个大型多民族系统性红斑狼疮(SLE)队列中,抗Sm抗体与临床表现、合并症及疾病损害之间的关联。对来自美国一个纵向队列的SLE患者(符合美国风湿病学会标准)进行研究,这些患者年龄≥16岁,入组时疾病病程≤10年,且种族明确(非裔美国人、西班牙裔或白种人)。确定了社会经济人口学特征、累积临床表现、合并症及疾病损害(根据系统性红斑狼疮国际协作临床损害指数[SDI])。使用多变量逻辑回归分析,对年龄、性别、种族、疾病病程、教育程度、医疗保险和吸烟情况进行校正,以检验抗Sm抗体与临床特征之间的关联。共研究了2322例SLE患者。诊断时的平均(标准差,SD)年龄为34.4(12.8)岁,平均(SD)疾病病程为9.0(7.9)年;2127例(91.6%)为女性。579例(24.9%)患者存在抗Sm抗体。在多变量分析中,抗Sm抗体与浆膜炎、肾脏受累、精神病、血管炎、雷诺现象、溶血性贫血、白细胞减少、淋巴细胞减少和动脉高血压显著相关。未发现与疾病损害累积有显著关联。在这个SLE患者队列中,抗Sm抗体与多种临床特征相关,包括肾脏、神经和血液系统疾病以及血管炎等严重表现。