Sjögren's syndrome: a community-based study of prevalence and impact.

E Thomas, E M Hay, A Hajeer, A J Silman
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引用次数: 273

Abstract

Objective: Using the European Community (EC) criteria for classification Vitali et al. Arthritis Rheum 1993;36:340 7, we report the prevalence estimates of Sjogren's syndrome (SS) from a general population and present the first population data to assess the impact of the syndrome.

Methods: A cross-sectional population-based survey performed on 1000 adults, aged 18-75 yr, randomly selected from a population register. Responders to the initial postal phase were invited for an interview. The five criteria measured at interview were: (1) the reporting of subjective oral symptoms lasting for > 3 months; (2) the reporting of subjective ocular symptoms lasting for >3 months; (3) Schirmer-I test; (4) unstimulated salivary flow; (5) autoantibodies [Ro (SS-A), La (SS-B), rheumatoid factor (RF), antinuclear antibodies (ANA)]. SS was diagnosed if at least four of these five criteria were positive. The MOS Short-form 36 (SF-36), General Health Questionnaire (GHQ) and the Health and Fatigue Questionnaire (HFQ) were completed by subjects after the interview, and scores were compared between those with and without a diagnosis of SS.

Results: A total of 341 subjects completed both the postal questionnaire and home visit. A diagnosis of SS could be given to 13 subjects. After adjusting for the presence of possible bias due to non-response, our best estimate of the prevalence of SS in the study population was 33 per 1000 subjects (95% CI 22 44). The prevalence of the disorder was higher in females (38; 95% CI 27-52) and for those subjects aged > or = 55 yr (46; 95% CI 34-61). Those subjects diagnosed positively were more impaired for each of the eight dimensions of the SF-36 than those without a diagnosis, and also suffered from higher levels of depression and fatigue.

Conclusions: SS affects approximately 3-4% of adults and in the general population appears to be associated with a clinically significant impairment of a subject's health and well-being.

Sjögren's综合征:患病率和影响的社区研究。
目的:利用欧共体(EC)标准对Vitali等人进行分类。风湿病1993;36:340,我们报告了普通人群中干燥综合征(SS)的患病率估计,并提出了第一个评估该综合征影响的人群数据。方法:对1000名年龄在18-75岁的成年人进行横断面人口调查,随机从人口登记册中选择。最初邮寄阶段的答复者被邀请进行面谈。访谈时测量的5项标准是:(1)报告主观口腔症状持续> 3个月;(2)报告主观眼部症状持续>3个月;(3) Schirmer-I检验;(4)无刺激唾液流;(5)自身抗体[Ro (SS-A), La (SS-B),类风湿因子(RF),抗核抗体(ANA)]。如果这五项标准中至少有四项为阳性,则诊断为SS。访谈结束后,对被试进行问卷调查(SF-36)、一般健康问卷(GHQ)和健康与疲劳问卷(HFQ),并比较被试和未被诊断为ss的被试的得分。结果:共341名被试完成了邮寄问卷和家访问卷。13例被诊断为SS。在调整了由于无反应而可能存在的偏倚后,我们对研究人群中SS患病率的最佳估计是每1000名受试者中有33名(95% CI 22.44)。女性的患病率更高(38;95% CI 27-52),对于年龄>或= 55岁的受试者(46;95% ci 34-61)。那些被诊断为阳性的受试者在SF-36的八个维度上都比那些没有被诊断为阳性的人受损更严重,而且抑郁和疲劳的程度也更高。结论:SS影响大约3-4%的成年人,在一般人群中似乎与受试者健康和福祉的临床显著损害有关。
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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