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Late-onset systemic lupus erythematosus in Northwestern Spain: Differences with early-onset systemic lupus erythematosus and literature review

机译:西班牙西北部迟发性系统性红斑狼疮:与早发性系统性红斑狼疮的区别和文献综述

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摘要

To further investigate into the epidaemiology of systemic lupus erythematosus (SLE) in Southern Europe, we have assessed the incidence, clinical spectrum and survival of patients diagnosed with late-onset SLE (age ≥ 50 years) according to the 1982 American College of Rheumatology (ACR) classification criteria at the single hospital for a well-defined population of Lugo, Northwestern (NW) Spain. Between January 1987 and December 2006, 51 (39.3%) of the 150 patients diagnosed as having SLE fulfilled definitions for late-onset SLE. The predominance of women among late-onset SLE (4:1) was reduced when compared with that observed in early-onset SLE (7:1). However, the incidence of late-onset SLE was significantly higher in women (4.2 [95% confidence interval (CI): 3.1-5.6] per 100,000 population) than in men (1.3 [95% CI: 0.6-2.2] per 100,000 population) (p < 0.001). As observed in early-onset SLE, the most frequent clinical manifestation in patients with late-onset SLE was arthritis (71.2%). Renal disease was less common in late-onset SLE (13.5%) than in early-onset SLE (26.4%); p = 0.07). In contrast, secondary Sj?gren syndrome was more commonly found in the older age-group (27.1% versus 12.1%; p = 0.03). A non-significantly increased incidence of serositis was also observed in late-onset SLE patients (33.9% versus 22.0%; p = 0.13). Hypocomplementaemia (72.9% versus 91.2%) and positive results for anti-DNA and anti-Sm (49.2% and 6.8% versus 68.1% and 23.1, respectively) were significantly less common in late-onset SLE patients than in early-onset SLE. The probability of survival was reduced in late-onset SLE (p < 0.001). With respect to this, the 10-year and 15-year survival probability were 74.9 % and 63.3% in the late-onset SLE group and 96.3% and 91.0% in patients with early-onset SLE, respectively. In conclusion, our results confirm that in NW Spain SLE is not uncommon in individuals 50 years and older. In keeping with earlier studies, late-onset SLE patients from NW Spain have some clinical and laboratory differences with respect to those individuals with early-onset SLE. Our data support the claim of a reduced probability of survival in the older age-group of SLE patients.
机译:为了进一步调查南欧系统性红斑狼疮(SLE)的流行病学,我们根据1982年美国风湿病学会(美国西班牙西北(NW)Lugo明确人群的单一医院的分类标准。在1987年1月至2006年12月之间,被诊断患有SLE的150例患者中有51例(39.3%)符合迟发性SLE的定义。与早发性SLE(7:1)相比,晚发性SLE(4:1)中女性的优势有所降低。但是,女性(每10万人口中4.2 [95%置信区间(CI):3.1-5.6])的发病率明显高于男性(每10万人口中1.3 [95%CI:0.6-2.2]) )(p <0.001)。正如在早发性SLE中观察到的那样,迟发性SLE患者中最常见的临床表现是关节炎(71.2%)。肾病在发病较晚的SLE(13.5%)较发病较早的SLE(26.4%)少。 p = 0.07)。相比之下,继发性干燥综合征在老年人群中更常见(27.1%对12.1%; p = 0.03)。在晚期SLE患者中也观察到浆膜炎的发生率没有显着增加(33.9%对22.0%; p = 0.13)。低互补性贫血(72.9%对91.2%)以及抗DNA和抗Sm阳性结果(分别为49.2%和6.8%对68.1%和23.1)在早期SLE患者中较不常见。迟发性SLE患者生存率降低(p <0.001)。对此,晚期SLE组的10年和15年生存率分别为74.9%和63.3%,早期SLE组的分别为96.3%和91.0%。总之,我们的结果证实,在西班牙西北部,SLE在50岁以上的人群中并不罕见。与早期研究一致,西班牙西北地区的晚期SLE患者与那些早期SLE患者在临床和实验室方面存在差异。我们的数据支持SLE患者年龄较大的存活率降低的主张。

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