Cousens S N, Zeidler M, Esmonde T F, De Silva R, Wilesmith J W, Smith P G, Will R G
Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine.
BMJ. 1997 Aug 16;315(7105):389-95. doi: 10.1136/bmj.315.7105.389.
To identify changes in the occurrence of Creutzfeldt-Jakob disease that might be related to the epidemic of bovine spongiform encephalopathy.
Epidemiological surveillance of the United Kingdom population for Creutzfeldt-Jakob disease based on (a) referral of suspected cases by neurologists, neuropathologists, and neurophysiologists and (b) death certificates.
England and Wales during 1970-84, and whole of the United Kingdom during 1985-96.
All 662 patients identified as sporadic cases of Creutzfeldt-Jakob disease.
Age distribution of patients, age specific time trends of disease, occupational exposure to cattle, potential exposure to causative agent of bovine spongiform encephalopathy.
During 1970-96 there was an increase in the number of sporadic cases of Creutzfeldt-Jakob disease recorded yearly in England and Wales. The greatest increase was among people aged over 70. There was a statistically significant excess of cases among dairy farm workers and their spouses and among people at increased risk of contact with live cattle infected with bovine spongiform encephalopathy. During 1994-6 there were six deaths from sporadic Creutzfeldt-Jakob disease in the United Kingdom in patients aged under 30.
The increase in the incidence of sporadic Creutzfeldt-Jakob disease and the high incidence in dairy farmers in the United Kingdom may be unrelated to bovine spongiform encephalopathy. The most striking change in the pattern of Creutzfeldt-Jakob disease in the United Kingdom after the epidemic of bovine spongiform encephalopathy is provided by the incidence in a group of exceptionally young patients with a consistent and unusual neuropathological profile. The outcome of mouse transmission studies and the future incidence of the disease in the United Kingdom and elsewhere, will be important in judging whether the agent causing bovine spongiform encephalopathy has infected humans.
确定克雅氏病发病率的变化,这些变化可能与牛海绵状脑病的流行有关。
对英国人群进行克雅氏病的流行病学监测,监测基于:(a)神经科医生、神经病理学家和神经生理学家转诊的疑似病例,以及(b)死亡证明。
1970 - 1984年在英格兰和威尔士,1985 - 1996年在整个联合王国。
所有662例被确诊为散发性克雅氏病的患者。
患者的年龄分布、特定年龄组疾病的时间趋势、职业性接触牛的情况、潜在接触牛海绵状脑病病原体的情况。
1970 - 1996年期间,英格兰和威尔士每年记录的散发性克雅氏病病例数有所增加。增幅最大的是70岁以上人群。在奶牛场工人及其配偶以及接触感染牛海绵状脑病活牛风险增加的人群中,病例数有统计学意义的过量。1994 - 1996年期间,联合王国有6例30岁以下的散发性克雅氏病患者死亡。
英国散发性克雅氏病发病率的增加以及奶农中的高发病率可能与牛海绵状脑病无关。牛海绵状脑病流行后,英国克雅氏病模式最显著的变化是一组异常年轻患者的发病率,他们具有一致且不寻常的神经病理学特征。小鼠传播研究的结果以及该疾病在联合王国和其他地区未来的发病率,对于判断导致牛海绵状脑病的病原体是否已感染人类至关重要。