Literature DB >> 16849160

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

Paul Clarke1, Azra C Ghani.   

Abstract

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.

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Year:  2005        PMID: 16849160      PMCID: PMC1578257          DOI: 10.1098/rsif.2004.0017

Source DB:  PubMed          Journal:  J R Soc Interface        ISSN: 1742-5662            Impact factor:   4.118


  38 in total

1.  Predicted vCJD mortality in Great Britain.

Authors:  A C Ghani; N M Ferguson; C A Donnelly; R M Anderson
Journal:  Nature       Date:  2000-08-10       Impact factor: 49.962

2.  Retrospective study of prion-protein accumulation in tonsil and appendix tissues.

Authors:  J W Ironside; D A Hilton; A Ghani; N J Johnston; L Conyers; L M McCardle; D Best
Journal:  Lancet       Date:  2000-05-13       Impact factor: 79.321

3.  Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease.

Authors:  A Alperovitch; I Zerr; M Pocchiari; E Mitrova; J de Pedro Cuesta; I Hegyi; S Collins; H Kretzschmar; C van Duijn; R G Will
Journal:  Lancet       Date:  1999-05-15       Impact factor: 79.321

4.  Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease.

Authors:  L Cervenáková; L G Goldfarb; R Garruto; H S Lee; D C Gajdusek; P Brown
Journal:  Proc Natl Acad Sci U S A       Date:  1998-10-27       Impact factor: 11.205

5.  Tonsillar biopsy and PrPSc detection in the preclinical diagnosis of scrapie.

Authors:  B E Schreuder; L J van Keulen; M E Vromans; J P Langeveld; M A Smits
Journal:  Vet Rec       Date:  1998-05-23       Impact factor: 2.695

6.  Prion immunoreactivity in appendix before clinical onset of variant Creutzfeldt-Jakob disease.

Authors:  D A Hilton; E Fathers; P Edwards; J W Ironside; J Zajicek
Journal:  Lancet       Date:  1998-08-29       Impact factor: 79.321

7.  Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.

Authors:  P Parchi; A Giese; S Capellari; P Brown; W Schulz-Schaeffer; O Windl; I Zerr; H Budka; N Kopp; P Piccardo; S Poser; A Rojiani; N Streichemberger; J Julien; C Vital; B Ghetti; P Gambetti; H Kretzschmar
Journal:  Ann Neurol       Date:  1999-08       Impact factor: 10.422

8.  Reversible conversion of monomeric human prion protein between native and fibrilogenic conformations.

Authors:  G S Jackson; L L Hosszu; A Power; A F Hill; J Kenney; H Saibil; C J Craven; J P Waltho; A R Clarke; J Collinge
Journal:  Science       Date:  1999-03-19       Impact factor: 47.728

9.  Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent.

Authors:  M E Bruce; R G Will; J W Ironside; I McConnell; D Drummond; A Suttie; L McCardle; A Chree; J Hope; C Birkett; S Cousens; H Fraser; C J Bostock
Journal:  Nature       Date:  1997-10-02       Impact factor: 49.962

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

Authors:  A C Ghani; N M Ferguson; C A Donnelly; T J Hagenaars; R M Anderson
Journal:  Proc Biol Sci       Date:  1998-12-22       Impact factor: 5.349

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  16 in total

1.  Is there the potential for an epidemic of variant Creutzfeldt-Jakob disease via blood transfusion in the UK?

Authors:  Paul Clarke; Robert G Will; Azra C Ghani
Journal:  J R Soc Interface       Date:  2007-08-22       Impact factor: 4.118

2.  Factors determining the potential for onward transmission of variant Creutzfeldt-Jakob disease via surgical instruments.

Authors:  Tini Garske; Hester J T Ward; Paul Clarke; Robert G Will; Azra C Ghani
Journal:  J R Soc Interface       Date:  2006-12-22       Impact factor: 4.118

3.  B cells and platelets harbor prion infectivity in the blood of deer infected with chronic wasting disease.

Authors:  Candace K Mathiason; Jeanette Hayes-Klug; Sheila A Hays; Jenny Powers; David A Osborn; Sallie J Dahmes; Karl V Miller; Robert J Warren; Gary L Mason; Glenn C Telling; Alan J Young; Edward A Hoover
Journal:  J Virol       Date:  2010-03-10       Impact factor: 5.103

4.  Interventions to reduce the risk of surgically transmitted Creutzfeldt-Jakob disease: a cost-effective modelling review.

Authors:  Matt Stevenson; Lesley Uttley; Jeremy E Oakley; Christopher Carroll; Stephen E Chick; Ruth Wong
Journal:  Health Technol Assess       Date:  2020-02       Impact factor: 4.014

5.  Prevalence of sheep infected with classical scrapie in Great Britain: integrating multiple sources of surveillance data for 2002.

Authors:  Simon Gubbins
Journal:  J R Soc Interface       Date:  2008-11-06       Impact factor: 4.118

6.  Blood transfusion and spread of variant Creutzfeldt-Jakob disease.

Authors:  Klaus Dietz; Günter Raddatz; Jonathan Wallis; Norbert Müller; Inga Zerr; Hans-Peter Duerr; Hans Lefèvre; Erhard Seifried; Johannes Löwer
Journal:  Emerg Infect Dis       Date:  2007-01       Impact factor: 6.883

7.  Uncertainty in the tail of the variant Creutzfeldt-Jakob disease epidemic in the UK.

Authors:  Tini Garske; Azra C Ghani
Journal:  PLoS One       Date:  2010-12-23       Impact factor: 3.240

8.  All clinically-relevant blood components transmit prion disease following a single blood transfusion: a sheep model of vCJD.

Authors:  Sandra McCutcheon; Anthony Richard Alejo Blanco; E Fiona Houston; Christopher de Wolf; Boon Chin Tan; Antony Smith; Martin H Groschup; Nora Hunter; Valerie S Hornsey; Ian R MacGregor; Christopher V Prowse; Marc Turner; Jean C Manson
Journal:  PLoS One       Date:  2011-08-17       Impact factor: 3.240

9.  Human prion disease and relative risk associated with chronic wasting disease.

Authors:  Samantha Mawhinney; W John Pape; Jeri E Forster; C Alan Anderson; Patrick Bosque; Michael W Miller
Journal:  Emerg Infect Dis       Date:  2006-10       Impact factor: 6.883

10.  Prevalence of disease related prion protein in anonymous tonsil specimens in Britain: cross sectional opportunistic survey.

Authors:  Jonathan P Clewley; Carole M Kelly; Nick Andrews; Kelly Vogliqi; Gary Mallinson; Maria Kaisar; David A Hilton; James W Ironside; Philip Edwards; Linda M McCardle; Diane L Ritchie; Reza Dabaghian; Helen E Ambrose; O Noel Gill
Journal:  BMJ       Date:  2009-05-21
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