Clinical characteristics of patients with late-onset systemic lupus erythematosus with a disease onset of ≤ 3 months.

IF 1.8 4区 医学 Q3 RHEUMATOLOGY
Lupus Pub Date : 2026-08-24 DOI:10.1177/09612033261481990
Mengxue Yan, Siping Li, Jingyi Lu, Zhichun Liu, Leixi Xue
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Abstract

ObjectivesThis study aimed to explore the clinical characteristics of patients with late-onset systemic lupus erythematosus (SLE) during the initial stage of disease onset and to evaluate disease activity.MethodData from patients with SLE whose disease onset was ≤3 months were retrospectively collected, and the patients were classified into the late- and early-onset SLE groups based on an age cutoff of 50 years.ResultsThis study included 145 patients, including 31 with late-onset SLE and 114 with early-onset SLE. Compared with the early-onset SLE group, the late-onset SLE group had a lower prevalence of rash (25.8% vs. 45.6%, p = 0.040) and anti-dsDNA antibody positivity (54.8% vs. 72.5%, p = 0.027), whereas pericarditis was more frequent (29.0% vs. 12.3%, p = 0.047) and the C3 levels were higher (0.640 [0.400, 0.892] g/L vs. 0.460 [0.324, 0.701] g/L, p = 0.018). As regards disease activity, the SLEDAI 2000 was 10 (8, 20) in the late-onset SLE group and 15 (10, 22) in the early-onset SLE group (p = 0.066), whereas the SLE-DAS was similar between the groups (13.33 [11.50, 28.45] vs 15.48 [8.56, 25.18], p = 0.744). More than half of patients with late-onset SLE received high-dose or intravenous pulse corticosteroid therapy, with no statistically significant difference compared with patients with early-onset SLE.ConclusionsPatients with very early-stage late-onset SLE exhibited distinct clinical and serological features. However, their disease activity was essentially consistent with that of early-onset SLE, and they often require intensive immunosuppressive therapy.

发病≤3个月的迟发性系统性红斑狼疮患者的临床特点
目的探讨迟发性系统性红斑狼疮(SLE)患者发病初期的临床特征,评价疾病活动性。方法回顾性收集发病≤3个月的SLE患者资料,以年龄50岁为截止年龄,分为晚发性SLE组和早发性SLE组。结果本研究纳入145例患者,其中迟发性SLE 31例,早发性SLE 114例。与早发SLE组相比,晚发SLE组皮疹患病率较低(25.8%比45.6%,p = 0.040),抗dsdna抗体阳性率较低(54.8%比72.5%,p = 0.027),心包炎发生率较高(29.0%比12.3%,p = 0.047), C3水平较高(0.640 [0.400,0.892]g/L比0.460 [0.324,0.701]g/L, p = 0.018)。在疾病活动性方面,迟发性SLE组SLEDAI 2000为10(8,20),早发性SLE组SLEDAI 2000为15 (10,22)(p = 0.066),而两组间SLEDAI - das相似(13.33 [11.50,28.45]vs 15.48 [8.56, 25.18], p = 0.744)。超过一半的晚发性SLE患者接受了高剂量或静脉脉冲皮质类固醇治疗,与早发性SLE患者相比无统计学差异。结论极早期迟发性SLE患者具有明显的临床和血清学特征。然而,他们的疾病活动性与早发性SLE基本一致,他们通常需要强化免疫抑制治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lupus
Lupus 医学-风湿病学
CiteScore
4.20
自引率
11.50%
发文量
225
审稿时长
1 months
期刊介绍: The only fully peer reviewed international journal devoted exclusively to lupus (and related disease) research. Lupus includes the most promising new clinical and laboratory-based studies from leading specialists in all lupus-related disciplines. Invaluable reading, with extended coverage, lupus-related disciplines include: Rheumatology, Dermatology, Immunology, Obstetrics, Psychiatry and Cardiovascular Research…
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