Epidemiological determinants of the pattern and magnitude of the vCJD epidemic in Great Britain

被引:73
作者
Ghani, AC [1 ]
Ferguson, NM [1 ]
Donnelly, CA [1 ]
Hagenaars, TJ [1 ]
Anderson, RM [1 ]
机构
[1] Univ Oxford, Dept Zool, Wellcome Trust Ctr Epidemiol Infect Dis, Oxford OX1 3PS, England
基金
英国惠康基金;
关键词
vCJD; BSE; prediction; epidemic size; mathematical model;
D O I
10.1098/rspb.1998.0596
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Understanding the epidemiology and aetiology of new-variant Creutzfeldt-Jakob (vCJD) disease in humans has become increasingly important given the scientific evidence linking it to bovine spongiform encephalopathy (BSE) in cattle and hence the wide exposure of the population of Great Britain (GB) to potentially infectious tissue. The recent analysis undertaken to determine the risk to the population from dorsal route ganglia illustrated the danger in presenting point estimates rather than ranges of scenarios in the face of uncertainty. We present a mathematical template that relates the past pattern of the BSE epidemic in cattle to the future course of any vCJD epidemic in humans, and use extensive scenario analysis to explore the wide range of possible outcomes given the uncertainty in epidemiological determinants. We demonstrate that the average number of humans infected by one infectious bovine and the incubation period distribution are the two epidemiological factors that have the greatest impact on epidemic size and duration. Using the time-series of the BSE epidemic and the cases seen to date, we show that the minimum length of the incubation period is approximately nine years, and that at least 20% of the cases diagnosed to date were exposed prior to 1986. We also demonstrate that the current age distribution of vCJD cases can only arise if younger people were either exposed to a greater extent, more susceptible to infection, or have shorter incubation periods. Extensive scenario analyses show that given the information currently available, the very high degree of uncertainty in the future size of the epidemic will remain for the next 3-5 years. Furthermore, we demonstrate that this uncertainty is unlikely to be reduced by mass screening for late-stage infection.
引用
收藏
页码:2443 / 2452
页数:10
相关论文
共 44 条
  • [1] Transmission dynamics and epidemiology of BSE in British cattle
    Anderson, RM
    Donnelly, CA
    Ferguson, NM
    Woolhouse, MEJ
    Watt, CJ
    Udy, HJ
    MaWhinney, S
    Dunstan, SP
    Southwood, TRE
    Wilesmith, JW
    Ryan, JBM
    Hoinville, LJ
    Hillerton, JE
    Austin, AR
    Wells, GAH
    [J]. NATURE, 1996, 382 (6594) : 779 - 788
  • [2] ASHER DM, 1973, S 4 INT C PRIM, V4, P43
  • [3] BARLOW RM, 1990, VET REC, V126, P111
  • [4] EXPERIMENTAL KURU IN SPIDER MONKEY - HISTOPATHOLOGICAL AND ULTRASTRUCTURAL STUDIES OF BRAIN DURING EARLY STAGES OF INCUBATION
    BECK, E
    BAK, IJ
    CHRIST, JF
    GAJDUSEK, DC
    GIBBS, CJ
    HASSLER, R
    [J]. BRAIN, 1975, 98 (DEC) : 595 - &
  • [5] Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent
    Bruce, ME
    Will, RG
    Ironside, JW
    McConnell, I
    Drummond, D
    Suttie, A
    McCardle, L
    Chree, A
    Hope, J
    Birkett, C
    Cousens, S
    Fraser, H
    Bostock, CJ
    [J]. NATURE, 1997, 389 (6650) : 498 - 501
  • [6] Phenotype-genotype studies in kuru:: Implications for new variant Creutzfeldt-Jakob disease
    Cervenáková, L
    Goldfarb, LG
    Garruto, R
    Lee, HS
    Gajdusek, DC
    Brown, P
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) : 13239 - 13241
  • [7] Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD
    Collinge, J
    Sidle, KCL
    Meads, J
    Ironside, J
    Hill, AF
    [J]. NATURE, 1996, 383 (6602) : 685 - 690
  • [8] GENETIC PREDISPOSITION TO IATROGENIC CREUTZFELDT-JAKOB DISEASE
    COLLINGE, J
    PALMER, MS
    DRYDEN, AJ
    [J]. LANCET, 1991, 337 (8755) : 1441 - 1442
  • [9] UNALTERED SUSCEPTIBILITY TO BSE IN TRANSGENIC MICE EXPRESSING HUMAN PRION PROTEIN
    COLLINGE, J
    PALMER, MS
    SIDLE, KCL
    HILL, AF
    GOWLAND, I
    MEADS, J
    ASANTE, E
    BRADLEY, R
    DOEY, LJ
    LANTOS, PL
    [J]. NATURE, 1995, 378 (6559) : 779 - 783
  • [10] COMER PJ, 1997, ASSESSMENT RISK POSS