Bertoli Ana M, Alarcón Graciela S, Calvo-Alén Jaime, Fernández Mónica, Vilá Luis M, Reveille John D
University of Alabama at Birmingham School of Medicine, USA.
Arthritis Rheum. 2006 May;54(5):1580-7. doi: 10.1002/art.21765.
To examine the clinical differences and the type and extent of organ damage in late- versus early-onset systemic lupus erythematosus (SLE).
A nested case-control study was performed in the context of LUMINA (LUpus in MInorities, NAture versus nurture), a large, longitudinal, multiethnic cohort. Patients who developed SLE at or after the age of 50 years were considered cases. Two controls (patients who developed SLE at age < or = 49 years) per case, matched for sex and disease duration, were randomly chosen. Selected baseline socioeconomic/demographic, behavioral, and psychological features, self-reported quality of life, and cumulative clinical data (clinical manifestations, laboratory data, disease activity, damage, and mortality) were compared between cases and controls. Multivariable analyses with late-onset lupus, damage accrual, and mortality as dependent variables were then performed.
Two hundred seventeen patients were studied. Of them, 73 were cases. Cases were more likely to have neurologic involvement, arterial thrombotic events, osteoporosis, and hypertriglyceridemia, while renal involvement and anti-Sm antibodies were less frequent. Disease activity at baseline was lower among cases. Cases also exhibited more cardiovascular and ocular damage. Late-onset lupus was an independent predictor of damage accrual (t-test = 2.23, P = 0.028), any damage at last visit (odds ratio [OR] 23.32, 95% confidence interval [95% CI] 3.98-141.56) (P < 0.001), and mortality (OR 10.74, 95% CI 3.07-37.56) (P < 0.001).
Patients with late-onset lupus exhibit distinct clinical features. Although disease activity tends to be lower in these patients, they tend to accrue more damage and experience higher mortality than patients with early-onset lupus. These findings probably reflect the contribution exerted by other comorbid conditions in the overall impact of lupus in these patients.
探讨晚发型与早发型系统性红斑狼疮(SLE)的临床差异以及器官损害的类型和程度。
在LUMINA(少数族裔狼疮,先天与后天)这一大型、纵向、多民族队列研究的背景下进行巢式病例对照研究。将50岁及以后发病的SLE患者视为病例组。为每个病例随机选取两名对照(年龄≤49岁发病的SLE患者),并按照性别和病程进行匹配。比较病例组和对照组在选定的基线社会经济/人口统计学、行为和心理特征、自我报告的生活质量以及累积临床数据(临床表现、实验室数据、疾病活动度、损害和死亡率)。然后以晚发型狼疮、损害累积和死亡率为因变量进行多变量分析。
共研究了217例患者。其中,73例为病例组。病例组更易出现神经受累、动脉血栓事件、骨质疏松和高甘油三酯血症,而肾脏受累和抗Sm抗体则较少见。病例组基线时的疾病活动度较低。病例组还表现出更多的心血管和眼部损害。晚发型狼疮是损害累积(t检验=2.23,P=0.028)、末次随访时出现任何损害(比值比[OR]23.32,95%置信区间[95%CI]3.98 - 141.56)(P<0.001)以及死亡率(OR 10.74,95%CI 3.07 - 37.56)(P<0.001)的独立预测因素。
晚发型狼疮患者表现出独特的临床特征。尽管这些患者的疾病活动度往往较低,但与早发型狼疮患者相比,他们往往累积更多损害且死亡率更高。这些发现可能反映了其他合并症在狼疮对这些患者的总体影响中所起的作用。