Incubation period of Creutzfeldt-Jakob disease in human growth hormone recipients in France
- PMID: 10522872
- DOI: 10.1212/wnl.53.6.1197
Incubation period of Creutzfeldt-Jakob disease in human growth hormone recipients in France
Abstract
Objective: To estimate the statistical distribution of the incubation period of Creutzfeldt-Jakob disease (CJD) in human growth hormone (hGH) recipients in France.
Background: Published papers suggest that the median incubation period of hGH-related CJD is approximately 15 years, but there are as yet no statistical data that support this assertion.
Methods: Of the 1,361 hGH recipients who were included in this study, 55 had developed CJD at the time of the study. Individual data on hGH treatment history were available. Different mathematical models were used to estimate the statistical distribution of the incubation period. One main feature of the models was to take into account the occurrence of future CJD cases.
Results: Models showed that the mean incubation period was 9 to 10 years, and the 95th percentile of the distribution was 15 to 16 years. Data and models indicated that the incubation period was significantly shorter in homozygotes at codon 129 of the prion protein gene than in heterozygotes.
Conclusions: The short mean incubation period of CJD in French hGH recipients may be due to high infectivity in hormone lots. Estimates of the 95th percentile indicate that the number of hGH-related CJD cases may continue to increase in the coming years.
Similar articles
-
Creutzfeldt-Jakob disease risk in Slovak recipients of human pituitary growth hormone.Bratisl Lek Listy. 1999 Apr;100(4):187-91. Bratisl Lek Listy. 1999. PMID: 10914140
-
Prion strains associated with iatrogenic CJD in French and UK human growth hormone recipients.Acta Neuropathol Commun. 2021 Aug 28;9(1):145. doi: 10.1186/s40478-021-01247-x. Acta Neuropathol Commun. 2021. PMID: 34454616 Free PMC article.
-
A statistical model to identify the contaminated lots implicated in iatrogenic transmission of Creutzfeldt-Jakob disease among French human growth hormone recipients.Am J Epidemiol. 1998 Mar 15;147(6):597-604. doi: 10.1093/oxfordjournals.aje.a009492. Am J Epidemiol. 1998. PMID: 9521187
-
The French surveillance network of Creutzfeldt-Jakob disease. Epidemiological data in France and worldwide.Transfus Clin Biol. 2013 Sep;20(4):395-7. doi: 10.1016/j.tracli.2013.02.029. Epub 2013 Apr 12. Transfus Clin Biol. 2013. PMID: 23587616 Review.
-
Iatrogenic Creutzfeldt-Jakob disease at the millennium.Neurology. 2000 Oct 24;55(8):1075-81. doi: 10.1212/wnl.55.8.1075. Neurology. 2000. PMID: 11071481 Review.
Cited by
-
Genetic aspects of human prion diseases.Front Neurol. 2022 Oct 5;13:1003056. doi: 10.3389/fneur.2022.1003056. eCollection 2022. Front Neurol. 2022. PMID: 36277922 Free PMC article. Review.
-
Factors determining the pattern of the variant Creutzfeldt-Jakob disease (vCJD) epidemic in the UK.Proc Biol Sci. 2003 Apr 7;270(1516):689-98. doi: 10.1098/rspb.2002.2313. Proc Biol Sci. 2003. PMID: 12713742 Free PMC article.
-
Bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease: background, evolution, and current concerns.Emerg Infect Dis. 2001 Jan-Feb;7(1):6-16. doi: 10.3201/eid0701.010102. Emerg Infect Dis. 2001. PMID: 11266289 Free PMC article.
-
Identification of multiple quantitative trait loci linked to prion disease incubation period in mice.Proc Natl Acad Sci U S A. 2001 May 22;98(11):6279-83. doi: 10.1073/pnas.101130398. Epub 2001 May 15. Proc Natl Acad Sci U S A. 2001. PMID: 11353827 Free PMC article.
-
Modeling of Neurodegenerative Diseases: 'Step by Step' and 'Network' Organization of the Complexes of Model Systems.Int J Mol Sci. 2022 Dec 29;24(1):604. doi: 10.3390/ijms24010604. Int J Mol Sci. 2022. PMID: 36614047 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical