Literature DB >> 9660576

Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993-95. European Union (EU) Collaborative Study Group of Creutzfeldt-Jakob disease (CJD).

C M van Duijn1, N Delasnerie-Lauprêtre, C Masullo, I Zerr, R de Silva, D P Wientjens, J P Brandel, T Weber, V Bonavita, M Zeidler, A Alpérovitch, S Poser, E Granieri, A Hofman, R G Will.   

Abstract

BACKGROUND: Creutzfeldt-Jakob disease (CJD) is a transmissible spongiform encephalopathy. Genetic and iatrogenic forms have been recognised but most are sporadic and of unknown cause. We have studied risk factors for CJD as part of the 1993-95 European Union collaborative studies of CJD in Europe.
METHODS: The 405 patients with definite or probable CJD who took part in our study had taken part in population-based studies done between 1993 and 1995 in Belgium, France, Germany, Italy, the Netherlands, and the UK. Data on putative risk factors from these patients were compared with data from 405 controls.
FINDINGS: We found evidence for familial aggregation of CJD with dementia due to causes other than CJD (relative risk [RR] 2.26, 95% CI 1.31-3.90). No significant increased risk of CJD in relation to a history of surgery and blood transfusion was shown. There was no evidence for an association between the risk of CJD and the consumption of beef, veal, lamb, cheese, or milk. No association was found with occupational exposure to animals or leather. The few positive findings of the study include increased risk in relation to consumption of raw meat (RR 1.63 [95% CI 1.18-2.23]) and brain (1.68 [1.18-2.39]), frequent exposure to leather products (1.94 [1.13-3.33]), and exposure to fertiliser consisting of hoofs and horns (2.32 [1.38-2.91]). Additional analyses, for example stratification by country and of exposures pre-1985 and post-1985, suggest that these results should be interpreted with great caution.
INTERPRETATION: Within the limits of the retrospective design of the study, our findings suggest that genetic factors other than the known CJD mutations may play an important part in CJD. Iatrogenic transmission of disease seems rare in this large population-based sample of patients with CJD. There is little evidence for an association between the risk of CJD and either animal exposure, or consumption of processed bovine meat or milk products for the period studied.

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Year:  1998        PMID: 9660576     DOI: 10.1016/s0140-6736(97)09468-3

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  35 in total

1.  The effect of stress on the onset and progression of Creutzfeldt-Jakob disease: results of a German pilot case-control study.

Authors:  C Laske; O Gefeller; A Pfahlberg; I Zerr; A Schröter; S Poser
Journal:  Eur J Epidemiol       Date:  1999-08       Impact factor: 8.082

Review 2.  Risk of acquiring Creutzfeldt-Jakob disease from blood transfusions: systematic review of case-control studies.

Authors:  K Wilson; C Code; M N Ricketts
Journal:  BMJ       Date:  2000-07-01

3.  Why aren't we more ahead? The risk of variant Creutzfeldt-Jakob disease from eating bovine spongiform encephalopathy-infected foods: still undetermined.

Authors:  Miquel Porta; Alfredo Morabia
Journal:  Eur J Epidemiol       Date:  2004       Impact factor: 8.082

4.  Ophthalmic surgery and Creutzfeldt-Jakob disease.

Authors:  P S-Juan; H J T Ward; R De Silva; R S G Knight; R G Will
Journal:  Br J Ophthalmol       Date:  2004-04       Impact factor: 4.638

5.  Transmission of elk and deer prions to transgenic mice.

Authors:  Gültekin Tamgüney; Kurt Giles; Essia Bouzamondo-Bernstein; Patrick J Bosque; Michael W Miller; Jiri Safar; Stephen J DeArmond; Stanley B Prusiner
Journal:  J Virol       Date:  2006-09       Impact factor: 5.103

Review 6.  Prion diseases: current understanding of epidemiology and pathogenesis, and therapeutic advances.

Authors:  Maria Caramelli; Giuseppe Ru; Pierluigi Acutis; Gianluigi Forloni
Journal:  CNS Drugs       Date:  2006       Impact factor: 5.749

7.  Prion protein gene M129 allele is a risk factor for Alzheimer's disease.

Authors:  M Gacia; K Safranow; M Styczyńska; K Jakubowska; B Pepłońska; M Chodakowska-Zebrowska; I Przekop; A Słowik; E Golańska; K Hułas-Bigoszewska; D Chlubek; D Religa; C Zekanowski; M Barcikowska
Journal:  J Neural Transm (Vienna)       Date:  2006-08-08       Impact factor: 3.575

8.  The quandary of Creutzfeldt-Jakob disease.

Authors:  B Larke
Journal:  CMAJ       Date:  1998-10-06       Impact factor: 8.262

9.  Genomic and post-genomic analyses of human prion diseases.

Authors:  Maurizio Pocchiari; Anna Poleggi; Serena Principe; Silvia Graziano; Franco Cardone
Journal:  Genome Med       Date:  2009-06-22       Impact factor: 11.117

10.  Classic scrapie in sheep with the ARR/ARR prion genotype in Germany and France.

Authors:  Martin H Groschup; Caroline Lacroux; Anne Buschmann; Gesine Lühken; Jacinthe Mathey; Martin Eiden; Séverine Lugan; Christine Hoffmann; Juan Carlos Espinosa; Thierry Baron; Juan Maria Torres; Georg Erhardt; Olivier Andreoletti
Journal:  Emerg Infect Dis       Date:  2007-08       Impact factor: 6.883

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