University of Western Ontario, London, Ontario, Canada.
J Rheumatol. 2010 Jan;37(1):38-44. doi: 10.3899/jrheum.080957. Epub 2009 Dec 15.
There is controversy whether older-onset systemic lupus erythematosus (SLE) is associated with a different, more benign disease course than in younger-onset SLE. Our objective was to characterize the clinical features and prognosis of late-onset SLE in a large, multicenter cohort.
We studied adult-onset lupus in the 1000 Canadian Faces of Lupus cohort (n = 1528) of whom 10.5% had onset at age > or = 50 years versus a control group with onset at < 50 years.
Disease duration was different in early- and late-onset groups (15 yrs in early vs 9.3 yrs in late; p < 0.001). Caucasians were represented more in the later-onset SLE group (55.6% vs 74.5%), while Asians and Blacks were more prevalent in the younger group. Younger-onset SLE subjects fulfilled more American College of Rheumatology criteria for SLE (< 50 yrs: 5.98 +/- 1.68; > or = 50 yrs: 5.24 +/- 1.44; p < 0.0001). Despite an equal prevalence of anti-dsDNA, the younger-onset group more often had positive anti-Smith autoantibody, ribonucleoprotein, and hypocomplementemia, and more nephritis, rash, and cytopenias than the older-onset group. However, disease activity and damage accrual were higher in the older-onset group. The older patients received less prednisone and immunosuppressives (current and ever-use). As expected, comorbidity was higher in the older-onset SLE group.
This study suggests that older age-onset SLE is not benign. There may be an interaction between lupus and age in which, although there is less lupus nephritis in the elderly, more disease activity and damage are present.
关于老年发病的系统性红斑狼疮(SLE)是否与较年轻发病者相比具有不同的、更良性的病程仍存在争议。我们的目的是在一个大型多中心队列中描述老年发病 SLE 的临床特征和预后。
我们研究了 1000 例加拿大狼疮面孔队列(n = 1528)中的成人发病狼疮,其中 10.5%的患者发病年龄≥50 岁,与发病年龄<50 岁的对照组相比。
早发和晚发组的疾病持续时间不同(早发组为 15 年,晚发组为 9.3 年;p <0.001)。晚发组更多的是白种人(55.6%比 74.5%),而亚洲人和黑人在年轻组中更为常见。年轻组的 SLE 患者符合更多的美国风湿病学会 SLE 标准(<50 岁:5.98±1.68;≥50 岁:5.24±1.44;p <0.0001)。尽管抗双链 DNA 抗体的阳性率相同,但年轻组更常出现抗 Smith 抗体、核糖核蛋白和低补体血症,以及更多的肾炎、皮疹和细胞减少症,而非老年组。然而,老年组的疾病活动度和损伤进展更高。老年患者接受的泼尼松和免疫抑制剂(当前和既往使用)更少。正如预期的那样,老年 SLE 组的合并症更多。
本研究表明,老年发病的 SLE 并非良性。狼疮和年龄之间可能存在相互作用,尽管老年人的狼疮肾炎较少,但存在更多的疾病活动度和损伤。