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亚洲系统性红斑狼疮患者中全身性疾病的高患病率及死亡率

High prevalence of systemic disease and mortality in Asian subjects with systemic lupus erythematosus.

作者信息

Samanta A, Feehally J, Roy S, Nichol F E, Sheldon P J, Walls J

机构信息

Department of Rheumatology, Leicester Royal Infirmary, UK.

出版信息

Ann Rheum Dis. 1991 Jul;50(7):490-2. doi: 10.1136/ard.50.7.490.

Abstract

All patients with systemic lupus erythematosus (SLE) (American Rheumatism Association criteria with positive antinuclear antibody titre) and who attended any of the three general hospitals in Leicester over a 10 year period were ascertained using several complementary sources. Eighty seven subjects (26 Asian, 61 white) were identified. The estimated prevalence of SLE in Leicester is 0.4/1000 for Asian and 0.2/1000 for white subjects. Mean age of onset of the disease was 24 years in Asian and 31 years in white subjects, with both groups showing a female preponderance. Proteinuria (greater than 1 g/24 h) was noted in 15 (58%) Asian and 21 (35%) white subjects; neuropsychiatric disease in 10 (38%) Asian and 8 (13%) white subjects; myalgic symptoms with raised muscle enzymes in 9 (35%) Asian and 3 (5%) white subjects. Nineteen (73%) Asian subjects were positive for extractable nuclear antigens as well, at some stage of their disease, compared with 6 (10%) white subjects. Immunosuppressive treatment was required in 12 (46%) Asian and 12 (20%) white subjects, and deaths of seven Asian and five white subjects were attributed to SLE. These findings show that Asian subjects have a higher prevalence of SLE with greater systemic disease and mortality.

摘要

所有符合美国风湿病协会标准且抗核抗体滴度呈阳性的系统性红斑狼疮(SLE)患者,在10年期间就诊于莱斯特三家综合医院中的任何一家,通过多种互补来源确定了这些患者。共识别出87名受试者(26名亚洲人,61名白人)。莱斯特亚洲人群SLE的估计患病率为0.4/1000,白人为0.2/1000。该疾病的平均发病年龄在亚洲人为24岁,白人为31岁,两组均以女性居多。15名(58%)亚洲人和21名(35%)白人出现蛋白尿(超过1g/24小时);10名(38%)亚洲人和8名(13%)白人患有神经精神疾病;9名(35%)亚洲人和3名(5%)白人有肌痛症状且肌肉酶升高。19名(73%)亚洲受试者在疾病的某个阶段可提取核抗原也呈阳性,相比之下,白人受试者为6名(10%)。12名(46%)亚洲人和12名(20%)白人需要免疫抑制治疗,7名亚洲人和5名白人的死亡归因于SLE。这些发现表明,亚洲受试者SLE患病率更高,系统性疾病和死亡率也更高。

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