Human Prion Diseases in the United States
Publication Date
January 01, 2010
Journal
PLOS ONE
Authors
Robert C. Holman, Ermias D. Belay, Krista Y. Christensen, Ryan A. Maddox, et al
Volume
5
Issue
1
Pages
e8521
DOI
https://dx.plos.org/10.1371/journal.pone.0008521
Publisher URL
http://journals.plos.org/plosone/article?id=10.1371%2Fjournal.pone.0008521
PubMed
http://www.ncbi.nlm.nih.gov/pubmed/20049325
PubMed Central
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797136
Europe PMC
http://europepmc.org/abstract/MED/20049325
Web of Science
000273225000004
Scopus
77649141798
Mendeley
http://www.mendeley.com/research/human-prion-diseases-united-states-2
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Mendeley | Further Information

{"title"=>"Human prion diseases in the United States", "type"=>"journal", "authors"=>[{"first_name"=>"Robert C.", "last_name"=>"Holman", "scopus_author_id"=>"7202041884"}, {"first_name"=>"Ermias D.", "last_name"=>"Belay", "scopus_author_id"=>"6603872304"}, {"first_name"=>"Krista Y.", "last_name"=>"Christensen", "scopus_author_id"=>"8621393900"}, {"first_name"=>"Ryan A.", "last_name"=>"Maddox", "scopus_author_id"=>"7102210328"}, {"first_name"=>"Arialdi M.", "last_name"=>"Minino", "scopus_author_id"=>"6506670417"}, {"first_name"=>"Arianne M.", "last_name"=>"Folkema", "scopus_author_id"=>"35621663200"}, {"first_name"=>"Dana L.", "last_name"=>"Haberling", "scopus_author_id"=>"23481667700"}, {"first_name"=>"Teresa A.", "last_name"=>"Hammett", "scopus_author_id"=>"7003606820"}, {"first_name"=>"Kenneth D.", "last_name"=>"Kochanek", "scopus_author_id"=>"7003366877"}, {"first_name"=>"James J.", "last_name"=>"Sejvar", "scopus_author_id"=>"7003834515"}, {"first_name"=>"Lawrence B.", "last_name"=>"Schonberger", "scopus_author_id"=>"7006620345"}], "year"=>2010, "source"=>"PLoS ONE", "identifiers"=>{"pui"=>"358372617", "issn"=>"19326203", "doi"=>"10.1371/journal.pone.0008521", "scopus"=>"2-s2.0-77649141798", "pmid"=>"20049325", "sgr"=>"77649141798"}, "id"=>"3c7bb07b-fdac-3b79-8e0f-f25d1d11dff9", "abstract"=>"BACKGROUND: Prion diseases are a family of rare, progressive, neurodegenerative disorders that affect humans and animals. The most common form of human prion disease, Creutzfeldt-Jakob disease (CJD), occurs worldwide. Variant CJD (vCJD), a recently emerged human prion disease, is a zoonotic foodborne disorder that occurs almost exclusively in countries with outbreaks of bovine spongiform encephalopathy. This study describes the occurrence and epidemiology of CJD and vCJD in the United States.\\n\\nMETHODOLOGY/PRINCIPAL FINDINGS: Analysis of CJD and vCJD deaths using death certificates of US residents for 1979-2006, and those identified through other surveillance mechanisms during 1996-2008. Since CJD is invariably fatal and illness duration is usually less than one year, the CJD incidence is estimated as the death rate. During 1979 through 2006, an estimated 6,917 deaths with CJD as a cause of death were reported in the United States, an annual average of approximately 247 deaths (range 172-304 deaths). The average annual age-adjusted incidence for CJD was 0.97 per 1,000,000 persons. Most (61.8%) of the CJD deaths occurred among persons >or=65 years of age for an average annual incidence of 4.8 per 1,000,000 persons in this population. Most deaths were among whites (94.6%); the age-adjusted incidence for whites was 2.7 times higher than that for blacks (1.04 and 0.40, respectively). Three patients who died since 2004 were reported with vCJD; epidemiologic evidence indicated that their infection was acquired outside of the United States.\\n\\nCONCLUSION/SIGNIFICANCE: Surveillance continues to show an annual CJD incidence rate of about 1 case per 1,000,000 persons and marked differences in CJD rates by age and race in the United States. Ongoing surveillance remains important for monitoring the stability of the CJD incidence rates, and detecting occurrences of vCJD and possibly other novel prion diseases in the United States.", "link"=>"http://www.mendeley.com/research/human-prion-diseases-united-states-2", "reader_count"=>55, "reader_count_by_academic_status"=>{"Unspecified"=>1, "Professor > Associate Professor"=>2, "Researcher"=>5, "Student > Ph. D. Student"=>9, "Student > Postgraduate"=>7, "Student > Master"=>9, "Other"=>2, "Student > Bachelor"=>18, "Lecturer > Senior Lecturer"=>1, "Professor"=>1}, "reader_count_by_user_role"=>{"Unspecified"=>1, "Professor > Associate Professor"=>2, "Researcher"=>5, "Student > Ph. D. Student"=>9, "Student > Postgraduate"=>7, "Student > Master"=>9, "Other"=>2, "Student > Bachelor"=>18, "Lecturer > Senior Lecturer"=>1, "Professor"=>1}, "reader_count_by_subject_area"=>{"Unspecified"=>1, "Biochemistry, Genetics and Molecular Biology"=>8, "Agricultural and Biological Sciences"=>22, "Medicine and Dentistry"=>12, "Neuroscience"=>2, "Arts and Humanities"=>1, "Physics and Astronomy"=>2, "Chemistry"=>1, "Psychology"=>1, "Social Sciences"=>2, "Immunology and Microbiology"=>2, "Earth and Planetary Sciences"=>1}, "reader_count_by_subdiscipline"=>{"Medicine and Dentistry"=>{"Medicine and Dentistry"=>12}, "Neuroscience"=>{"Neuroscience"=>2}, "Chemistry"=>{"Chemistry"=>1}, "Social Sciences"=>{"Social Sciences"=>2}, "Physics and Astronomy"=>{"Physics and Astronomy"=>2}, "Psychology"=>{"Psychology"=>1}, "Immunology and Microbiology"=>{"Immunology and Microbiology"=>2}, "Earth and Planetary Sciences"=>{"Earth and Planetary Sciences"=>1}, "Agricultural and Biological Sciences"=>{"Agricultural and Biological Sciences"=>22}, "Biochemistry, Genetics and Molecular Biology"=>{"Biochemistry, Genetics and Molecular Biology"=>8}, "Unspecified"=>{"Unspecified"=>1}, "Arts and Humanities"=>{"Arts and Humanities"=>1}}, "reader_count_by_country"=>{"Canada"=>1, "Austria"=>1, "Brazil"=>1, "Portugal"=>1}, "group_count"=>3}

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