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Projections of the future course of the primary vCJD epidemic in the UK: inclusion of subclinical infection and the possibility of wider genetic susceptibility

机译:英国主要vCJD流行病未来病程的预测:亚临床感染的纳入以及更广泛的遗传易感性的可能性

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摘要

The incidence of variant Creutzfeldt–Jakob disease (vCJD) in the United Kingdom appears to be in decline, with only four deaths reported this year (to 6 September 2004). However, results of a survey of lymphoreticular tissues have suggested a substantially higher prevalence of vCJD than expected from the clinical data alone. There are two plausible explanations for this discrepancy: first, a proportion of those infected will not develop clinical disease (subclinical infection); and second, the genetic group in which no clinical cases of vCJD have yet occurred is susceptible. Using mathematical models for the primary transmission of bovine spongiform encephalopathy to humans, we explore the impact of these hypotheses on case predictions. Under the first hypothesis, the results suggest relatively few future cases will arise via primary transmission, but that these cases are a small proportion of those infected, with most having subclinical infection. Under the second hypothesis, results suggest a maximum fivefold increase in cases, but this hypothesis is unable to account for the discrepancy between clinical cases and the estimated prevalence. Predictions of future cases of vCJD therefore remain uncertain, particularly given the recent identification of additional cases infected via blood transfusion.
机译:在英国,变异克雅氏病(vCJD)的发病率似乎正在下降,今年(至2004年9月6日)仅报告了四例死亡。然而,一项对淋巴网状组织的调查结果表明,vCJD的患病率比仅根据临床数据所预期的要高得多。对于这种差异,有两个合理的解释:首先,一部分感染者不会发展为临床疾病(亚临床感染);其次,尚未发生vCJD临床病例的遗传群体是易感人群。使用数学模型将牛海绵状脑病主要传播给人类,我们探索了这些假设对病例预测的影响。在第一个假设下,结果表明未来通过原发性传播会出现的病例相对较少,但这些病例只占被感染病例的一小部分,大多数感染是亚临床感染。在第二种假设下,结果表明病例最多增加了五倍,但该假设无法解释临床病例与估计患病率之间的差异。因此,未来vCJD病例的预测仍不确定,特别是考虑到最近发现了其他通过输血感染的病例。

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