Bendewald Margo J, Wetter David A, Li Xujian, Davis Mark D P
Mayo Medical School, College of Medicine, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA.
Arch Dermatol. 2010 Jan;146(1):26-30. doi: 10.1001/archdermatol.2009.328.
To identify new and existing cases of dermatomyositis and its subtypes in Olmsted County, Minnesota, from 1976 through 2007, and to establish a population-based estimate of the incidence and prevalence of dermatomyositis and amyopathic dermatomyositis.
Retrospective population-based study.
Community-based epidemiology project. Patients Patients with a diagnosis of dermatomyositis were identified from the Rochester Epidemiology Project.
Incidence of dermatomyositis and clinically amyopathic dermatomyositis and risk of malignancy in clinically amyopathic dermatomyositis.
Of the 29 patients identified, 6 (21%) had the clinically amyopathic subtype of dermatomyositis and 22 (76%) were female. Overall age- and sex-adjusted incidence of dermatomyositis including all subtypes was 9.63 (95% confidence interval [CI], 6.09-13.17) per 1 million persons and 2.08 (95% CI, 0.39-3.77) per 1 million persons for clinically amyopathic dermatomyositis. Age- and sex-adjusted prevalence for all subtypes of dermatomyositis was 21.42 (95% CI, 13.07-29.77) per 100,000 persons. Eight patients (28%) had a malignant condition during the study period; the risk of malignancy (odds ratio) for classic dermatomyositis compared with clinically amyopathic dermatomyositis was 4.61 but was not statistically significant (95% CI, 0.22-96.09) (P=.44).
Dermatomyositis is a rare disease, and clinically amyopathic dermatomyositis represents an estimated 20% of all dermatomyositis cases. Larger population-based studies are needed to estimate the risk of malignancy associated with subtypes of dermatomyositis, particularly clinically amyopathic dermatomyositis.
确定1976年至2007年明尼苏达州奥尔姆斯特德县皮肌炎及其亚型的新发病例和现患病例,并基于人群对皮肌炎和无肌病性皮肌炎的发病率和患病率进行估计。
基于人群的回顾性研究。
社区流行病学项目。患者 从罗切斯特流行病学项目中识别出诊断为皮肌炎的患者。
皮肌炎和临床无肌病性皮肌炎的发病率以及临床无肌病性皮肌炎患者发生恶性肿瘤的风险。
在识别出的29例患者中,6例(21%)患有临床无肌病性皮肌炎亚型,22例(76%)为女性。包括所有亚型在内的皮肌炎总体年龄和性别调整发病率为每100万人9.63例(95%置信区间[CI],6.09 - 13.17),临床无肌病性皮肌炎为每100万人2.08例(95% CI,0.39 - 3.77)。皮肌炎所有亚型的年龄和性别调整患病率为每10万人21.42例(95% CI,13.07 - 29.77)。8例患者(28%)在研究期间患有恶性疾病;经典皮肌炎与临床无肌病性皮肌炎相比,发生恶性肿瘤的风险(比值比)为4.61,但无统计学意义(95% CI,0.22 - 96.09)(P = 0.44)。
皮肌炎是一种罕见疾病,临床无肌病性皮肌炎约占所有皮肌炎病例的20%。需要开展更大规模的基于人群的研究来估计与皮肌炎亚型相关的恶性肿瘤风险,尤其是临床无肌病性皮肌炎。