Maciel Gabriel, Crowson Cynthia S, Matteson Eric L, Cornec Divi
Mayo Clinic College of Medicine, Rochester, Minnesota, and Hospital Maciel, Montevideo, Uruguay.
Mayo Clinic College of Medicine, Rochester, Minnesota.
Arthritis Care Res (Hoboken). 2017 Oct;69(10):1612-1616. doi: 10.1002/acr.23173. Epub 2017 Aug 31.
To report the point prevalence of primary Sjögren's syndrome (SS) in the first US population-based study.
Cases of all potential primary SS patients living in Olmsted County, Minnesota, on January 1, 2015, were retrieved using Rochester Epidemiology Project resources, and ascertained by manual medical records review. Primary SS cases were defined according to physician diagnosis. The use of diagnostic tests was assessed and the performance of classification criteria was evaluated. The number of prevalent cases in 2015 was also projected based on 1976-2005 incidence data from the same source population.
A total of 106 patients with primary SS were included in the study: 86% were female, with a mean ± SD age of 64.6 ± 15.2 years, and a mean ± SD disease duration of 10.5 ± 8.4 years. A majority were anti-SSA positive (75%) and/or anti-SSB positive (58%), but only 22% met American-European Consensus Group or American College of Rheumatology criteria, because the other tests required for disease classification (ocular dryness objective assessment, salivary gland functional or morphologic tests, or salivary gland biopsy) were rarely performed in clinical practice. According to the physician diagnosis, the age- and sex-adjusted prevalence of primary SS was 10.3 per 10,000 inhabitants, but according to classification criteria, this prevalence was only 2.2 per 10,000. The analysis based on previous incidence data projected a similar 2015 prevalence rate of 11.0 per 10,000.
The prevalence of primary SS in this geographically well-defined population was estimated to be between 2 and 10 per 10,000 inhabitants. Physicians rarely used tests included in the classification criteria to diagnose the disease in this community setting.
在首个基于美国人群的研究中报告原发性干燥综合征(SS)的时点患病率。
利用罗切斯特流行病学项目资源检索出2015年1月1日居住在明尼苏达州奥尔姆斯特德县的所有潜在原发性SS患者病例,并通过人工查阅病历确定。原发性SS病例根据医生诊断定义。评估诊断测试的使用情况,并评价分类标准的性能。还根据来自同一源人群的1976 - 2005年发病率数据预测了2015年的现患病例数。
该研究共纳入106例原发性SS患者:86%为女性,平均年龄±标准差为64.6±15.2岁,平均病程±标准差为10.5±8.4年。大多数患者抗SSA阳性(75%)和/或抗SSB阳性(58%),但只有22%符合欧美共识组或美国风湿病学会标准,因为疾病分类所需的其他测试(眼部干燥客观评估、唾液腺功能或形态学测试或唾液腺活检)在临床实践中很少进行。根据医生诊断,原发性SS的年龄和性别调整患病率为每10000居民10.3例,但根据分类标准,该患病率仅为每10000居民2.2例。基于既往发病率数据的分析预测2015年患病率相似,为每10000居民11.0例。
在这个地理界定明确的人群中,原发性SS的患病率估计为每10000居民2至10例。在这个社区环境中,医生很少使用分类标准中包含的测试来诊断该疾病。