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Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey

Objectives To carry out a further survey of archived appendix samples to understand better the differences between existing estimates of the prevalence of subclinical infection with prions after the bovine spongiform encephalopathy epizootic and to see whether a broader birth cohort was affected, an...

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Autores principales: Gill, O Noel, Spencer, Yvonne, Richard-Loendt, Angela, Kelly, Carole, Dabaghian, Reza, Boyes, Lynnette, Linehan, Jacqueline, Simmons, Marion, Webb, Paul, Bellerby, Peter, Andrews, Nick, Hilton, David A, Ironside, James W, Beck, Jon, Poulter, Mark, Mead, Simon, Brandner, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3805509/
https://www.ncbi.nlm.nih.gov/pubmed/24129059
http://dx.doi.org/10.1136/bmj.f5675
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author Gill, O Noel
Spencer, Yvonne
Richard-Loendt, Angela
Kelly, Carole
Dabaghian, Reza
Boyes, Lynnette
Linehan, Jacqueline
Simmons, Marion
Webb, Paul
Bellerby, Peter
Andrews, Nick
Hilton, David A
Ironside, James W
Beck, Jon
Poulter, Mark
Mead, Simon
Brandner, Sebastian
author_facet Gill, O Noel
Spencer, Yvonne
Richard-Loendt, Angela
Kelly, Carole
Dabaghian, Reza
Boyes, Lynnette
Linehan, Jacqueline
Simmons, Marion
Webb, Paul
Bellerby, Peter
Andrews, Nick
Hilton, David A
Ironside, James W
Beck, Jon
Poulter, Mark
Mead, Simon
Brandner, Sebastian
author_sort Gill, O Noel
collection PubMed
description Objectives To carry out a further survey of archived appendix samples to understand better the differences between existing estimates of the prevalence of subclinical infection with prions after the bovine spongiform encephalopathy epizootic and to see whether a broader birth cohort was affected, and to understand better the implications for the management of blood and blood products and for the handling of surgical instruments. Design Irreversibly unlinked and anonymised large scale survey of archived appendix samples. Setting Archived appendix samples from the pathology departments of 41 UK hospitals participating in the earlier survey, and additional hospitals in regions with lower levels of participation in that survey. Sample 32 441 archived appendix samples fixed in formalin and embedded in paraffin and tested for the presence of abnormal prion protein (PrP). Results Of the 32 441 appendix samples 16 were positive for abnormal PrP, indicating an overall prevalence of 493 per million population (95% confidence interval 282 to 801 per million). The prevalence in those born in 1941-60 (733 per million, 269 to 1596 per million) did not differ significantly from those born between 1961 and 1985 (412 per million, 198 to 758 per million) and was similar in both sexes and across the three broad geographical areas sampled. Genetic testing of the positive specimens for the genotype at PRNP codon 129 revealed a high proportion that were valine homozygous compared with the frequency in the normal population, and in stark contrast with confirmed clinical cases of vCJD, all of which were methionine homozygous at PRNP codon 129. Conclusions This study corroborates previous studies and suggests a high prevalence of infection with abnormal PrP, indicating vCJD carrier status in the population compared with the 177 vCJD cases to date. These findings have important implications for the management of blood and blood products and for the handling of surgical instruments.
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spelling pubmed-38055092013-10-24 Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey Gill, O Noel Spencer, Yvonne Richard-Loendt, Angela Kelly, Carole Dabaghian, Reza Boyes, Lynnette Linehan, Jacqueline Simmons, Marion Webb, Paul Bellerby, Peter Andrews, Nick Hilton, David A Ironside, James W Beck, Jon Poulter, Mark Mead, Simon Brandner, Sebastian BMJ Research Objectives To carry out a further survey of archived appendix samples to understand better the differences between existing estimates of the prevalence of subclinical infection with prions after the bovine spongiform encephalopathy epizootic and to see whether a broader birth cohort was affected, and to understand better the implications for the management of blood and blood products and for the handling of surgical instruments. Design Irreversibly unlinked and anonymised large scale survey of archived appendix samples. Setting Archived appendix samples from the pathology departments of 41 UK hospitals participating in the earlier survey, and additional hospitals in regions with lower levels of participation in that survey. Sample 32 441 archived appendix samples fixed in formalin and embedded in paraffin and tested for the presence of abnormal prion protein (PrP). Results Of the 32 441 appendix samples 16 were positive for abnormal PrP, indicating an overall prevalence of 493 per million population (95% confidence interval 282 to 801 per million). The prevalence in those born in 1941-60 (733 per million, 269 to 1596 per million) did not differ significantly from those born between 1961 and 1985 (412 per million, 198 to 758 per million) and was similar in both sexes and across the three broad geographical areas sampled. Genetic testing of the positive specimens for the genotype at PRNP codon 129 revealed a high proportion that were valine homozygous compared with the frequency in the normal population, and in stark contrast with confirmed clinical cases of vCJD, all of which were methionine homozygous at PRNP codon 129. Conclusions This study corroborates previous studies and suggests a high prevalence of infection with abnormal PrP, indicating vCJD carrier status in the population compared with the 177 vCJD cases to date. These findings have important implications for the management of blood and blood products and for the handling of surgical instruments. BMJ Publishing Group Ltd. 2013-10-15 /pmc/articles/PMC3805509/ /pubmed/24129059 http://dx.doi.org/10.1136/bmj.f5675 Text en © Gill et al 2013 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/.
spellingShingle Research
Gill, O Noel
Spencer, Yvonne
Richard-Loendt, Angela
Kelly, Carole
Dabaghian, Reza
Boyes, Lynnette
Linehan, Jacqueline
Simmons, Marion
Webb, Paul
Bellerby, Peter
Andrews, Nick
Hilton, David A
Ironside, James W
Beck, Jon
Poulter, Mark
Mead, Simon
Brandner, Sebastian
Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey
title Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey
title_full Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey
title_fullStr Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey
title_full_unstemmed Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey
title_short Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey
title_sort prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3805509/
https://www.ncbi.nlm.nih.gov/pubmed/24129059
http://dx.doi.org/10.1136/bmj.f5675
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