Cousens S N, Harries-Jones R, Knight R, Will R G, Smith P G, Matthews W B
Department of Epidemiology and Population Sciences, London School of Hygiene and Tropical Medicine, United Kingdom.
J Neurol Neurosurg Psychiatry. 1990 Jun;53(6):459-65. doi: 10.1136/jnnp.53.6.459.
Two hundred and sixty seven patients with a definite or probable diagnosis of Creutzfeldt-Jakob disease (CJD) were identified in an attempt to ascertain all cases of the disease in England and Wales in the period 1970-84. No evidence of space-time clustering of dates and places of onset was found for these cases. Two age- and sex-matched controls were selected for 72 of the 122 cases diagnosed in the period 1980-84 and life histories of places of residence were obtained for these cases and the controls. No evidence was found that cases had lived closer to each other than had controls at any time in their lives, except that there was an excess of cases born in London. The study does not provide supportive evidence for case-to-case transmission of CJD being an important component in the aetiology of the disease.
为了确定1970年至1984年间英格兰和威尔士所有克雅氏病(CJD)病例,共识别出267例确诊或疑似克雅氏病患者。未发现这些病例的发病日期和地点存在时空聚集现象。在1980年至1984年间确诊的122例病例中,为其中72例选取了年龄和性别匹配的对照,并获取了这些病例及对照的居住史。除了出生在伦敦的病例过多外,未发现病例在其生命中的任何时候比对照彼此住得更近。该研究没有为克雅氏病在病例间传播是该疾病病因的重要组成部分提供支持性证据。