Risk of Prion Disease Transmission through Bovine-Derived Bone Substitutes:
A Systematic Review
Yeoungsug Kim DDS1, Hessam Nowzari DDS; PhD2,*, Sandra K. Rich MPH,
PhD3
Article first published online: 15 DEC 2011
DOI: 10.1111/j.1708-8208.2011.00407.x
© 2011 Wiley Periodicals, Inc.
Issue
Clinical Implant Dentistry and Related Research
Clinical Implant Dentistry and Related Research
Volume 15, Issue 5, pages 645–653, October 2013
Additional Information(Hide All)
How to CiteAuthor InformationPublication History
How to Cite
Kim, Y., Nowzari, H. and Rich, S. K. (2013), Risk of Prion Disease
Transmission through Bovine-Derived Bone Substitutes: A Systematic Review.
Clinical Implant Dentistry and Related Research, 15: 645–653. doi:
10.1111/j.1708-8208.2011.00407.x
Author Information 1 Resident, Advanced Education in Periodontics Program,
Herman Ostrow School of Dentistry, University of Southern California, Los
Angeles, CA, USA
2 professor, Clinical Dentistry and director, Advanced Education in
Periodontics Program, Herman Ostrow School of Dentistry, University of Southern
California, Los Angeles, CA, USA
3 associate professor, Advanced Education in Periodontics Program, Herman
Ostrow School of Dentistry, University of Southern California, Los Angeles, CA,
USA
*Dr. Hessam Nowzari, Herman Ostrow School of Dentistry, University of
Southern California, Norris Dental Science Center-DEN, 925W. 34th Street, Room
119, Los Angeles, CA 90089-0641, USA; e-mail: nowzari@usc.edu
Publication History Issue published online: 7 OCT 2013 Article first
published online: 15 DEC 2011
Keywords:
anorganic bovine bone substitutes; BSE diagnostic test; BSE prion
inactivation; BSE prion infectivity; protein; PrP(27-30); PrPSc
ABSTRACT
Background: Despite the causal association between variant Creutzfeldt –
Jakob disease and bovine spongiform encephalopathy (BSE), bovine origin graft
materials are widely used during dental surgical procedures. The aim of this
study was to assess the risk of BSE transmission through anorganic bovine bone
substitutes.
Methods: Electronic database of MEDLINE was searched to identify relevant
studies regarding our focused questions, presence of BSE prion infectivity in
raw bovine bone, BSE prion inactivation by bone substitute manufacturing
process, protein contents in anorganic bovine bone substitutes, and validity of
current BSE diagnostic methods. Search terms yielded 1,704 titles. After
title/abstract screening and duplicates removal, 36 full-text articles were
screened for inclusion.
Results: A total of 16 studies were included in the final analysis. No
eligible studies were identified regarding the efficacy of BSE prion
inactivation by the treatments used for anorganic bovine bone manufacturing. BSE
infectivity and PrPSc, pathological prion, were detected in bovine bone marrow
and serum samples. Proteins were detected in Tutoplast® (bovine), Bio-Oss®, and
tibia samples treated at the similar condition for Bio-Oss deproteinization.
Inconsistent results of different BSE diagnostic tests were not unusual findings
(Iwata et al. 2006; Arnold et al. 2007; Murayama et al. 2010), and a study by
Balkema-Buschmann and colleagues showed an apparent discrepancy between BSE
infectivity and detection of PrP(27-30), the current surrogate marker for prion
disease infectivity.
Conclusion: This review indicates that bovine-derived graft biomaterials
may carry a risk of prion transmission to patients.
Thursday, January 17, 2013
TSE guidance, surgical, dental, blood risk factors, Part 4 Infection control of CJD, vCJD and other human prion diseases in healthcare and community settings (updated January 2013)
http://transmissiblespongiformencephalopathy.blogspot.com/2013/01/tse-guidance-surgical-dental-blood-risk.html
Tuesday, October 29, 2013
VARIANT CJD PRESENTS DIFFERENTLY IN OLDER PATIENTS
Monday, October 14, 2013
Researchers estimate one in 2,000 people in the UK carry variant CJD proteins
http://creutzfeldt-jakob-disease.blogspot.com/2013/10/researchers-estimate-one-in-2000-people.html
Researchers estimate one in 2,000 people in the UK carry variant CJD proteins
http://creutzfeldt-jakob-disease.blogspot.com/2013/10/researchers-estimate-one-in-2000-people.html
WHAT about the sporadic CJD TSE proteins
?
WE now know that some cases of sporadic CJD are linked to atypical BSE
and atypical Scrapie, so why are not MORE concerned about the sporadic CJD, and
all it’s sub-types $$$
Sunday, August 11, 2013
Creutzfeldt-Jakob Disease CJD cases rising North America updated report August 2013
Creutzfeldt-Jakob Disease CJD cases rising North America with Canada seeing an extreme increase of 48% between 2008 and 2010
http://creutzfeldt-jakob-disease.blogspot.com/2013/08/creutzfeldt-jakob-disease-cjd-cases.html
Creutzfeldt-Jakob Disease CJD cases rising North America updated report August 2013
Creutzfeldt-Jakob Disease CJD cases rising North America with Canada seeing an extreme increase of 48% between 2008 and 2010
http://creutzfeldt-jakob-disease.blogspot.com/2013/08/creutzfeldt-jakob-disease-cjd-cases.html
Sunday, October 13, 2013
CJD TSE Prion Disease Cases in Texas by Year, 2003-2012
http://creutzfeldt-jakob-disease.blogspot.com/2013/10/cjd-tse-prion-disease-cases-in-texas-by.html
CJD TSE Prion Disease Cases in Texas by Year, 2003-2012
http://creutzfeldt-jakob-disease.blogspot.com/2013/10/cjd-tse-prion-disease-cases-in-texas-by.html
Wednesday, September 25, 2013
Cleaning, disinfection and sterilization of surface prion contamination
http://creutzfeldt-jakob-disease.blogspot.com/2013/09/cleaning-disinfection-and-sterilization.html
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