Literature DB >> 26320231

Clinically Unsuspected Prion Disease Among Patients With Dementia Diagnoses in an Alzheimer's Disease Database.

Ryan A Maddox1, J L Blase2, N D Mercaldo3, A R Harvey2, L B Schonberger2, W A Kukull4, E D Belay2.   

Abstract

BACKGROUND: Brain tissue analysis is necessary to confirm prion diseases. Clinically unsuspected cases may be identified through neuropathologic testing.
METHODS: National Alzheimer's Coordinating Center (NACC) Minimum and Neuropathologic Data Set for 1984 to 2005 were reviewed. Eligible patients had dementia, underwent autopsy, had available neuropathologic data, belonged to a currently funded Alzheimer's Disease Center (ADC), and were coded as having an Alzheimer's disease clinical diagnosis or a nonprion disease etiology. For the eligible patients with neuropathology indicating prion disease, further clinical information, collected from the reporting ADC, determined whether prion disease was considered before autopsy.
RESULTS: Of 6000 eligible patients in the NACC database, 7 (0.12%) were clinically unsuspected but autopsy-confirmed prion disease cases.
CONCLUSION: The proportion of patients with dementia with clinically unrecognized but autopsy-confirmed prion disease was small. Besides confirming clinically suspected cases, neuropathology is useful to identify unsuspected clinically atypical cases of prion disease.
© The Author(s) 2015.

Entities:  

Keywords:  Alzheimer’s disease; Creutzfeldt–Jakob disease; dementia; diagnosis; prion disease

Mesh:

Year:  2015        PMID: 26320231      PMCID: PMC4651736          DOI: 10.1177/1533317515602218

Source DB:  PubMed          Journal:  Am J Alzheimers Dis Other Demen        ISSN: 1533-3175            Impact factor:   2.035


  9 in total

1.  How to improve the clinical diagnosis of Creutzfeldt-Jakob disease.

Authors:  S Poser; B Mollenhauer; A Kraubeta; I Zerr; B J Steinhoff; A Schroeter; M Finkenstaedt; W J Schulz-Schaeffer; H A Kretzschmar; K Felgenhauer
Journal:  Brain       Date:  1999-12       Impact factor: 13.501

2.  Monitoring the occurrence of emerging forms of Creutzfeldt-Jakob disease in the United States.

Authors:  Ermias D Belay; Ryan A Maddox; Pierluigi Gambetti; Lawrence B Schonberger
Journal:  Neurology       Date:  2003-01-28       Impact factor: 9.910

3.  Creutzfeldt-Jakob disease surveillance and diagnosis.

Authors:  Ermias D Belay; Robert C Holman; Lawrence B Schonberger
Journal:  Clin Infect Dis       Date:  2005-08-12       Impact factor: 9.079

4.  Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation.

Authors:  E J Cochran; D A Bennett; L Cervenáková; K Kenney; B Bernard; N L Foster; D F Benson; L G Goldfarb; P Brown
Journal:  Neurology       Date:  1996-09       Impact factor: 9.910

5.  Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease.

Authors:  Numthip Chitravas; Richard S Jung; Diane M Kofskey; Janis E Blevins; Pierluigi Gambetti; R John Leigh; Mark L Cohen
Journal:  Ann Neurol       Date:  2011-06-14       Impact factor: 10.422

6.  The National Alzheimer's Coordinating Center (NACC) Database: an Alzheimer disease database.

Authors:  Duane L Beekly; Erin M Ramos; Gerald van Belle; Woodrow Deitrich; Amber D Clark; Mary E Jacka; Walter A Kukull
Journal:  Alzheimer Dis Assoc Disord       Date:  2004 Oct-Dec       Impact factor: 2.703

7.  Patients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob disease.

Authors:  H J Tschampa; M Neumann; I Zerr; K Henkel; A Schröter; W J Schulz-Schaeffer; B J Steinhoff; H A Kretzschmar; S Poser
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-07       Impact factor: 10.154

Review 8.  Suggested links between different types of dementias: Creutzfeldt-Jakob disease, Alzheimer disease, and retroviral CNS infections.

Authors:  E E Manuelidis; L Manuelidis
Journal:  Alzheimer Dis Assoc Disord       Date:  1989 Spring-Summer       Impact factor: 2.703

9.  Rapidly progressive neurodegenerative dementias.

Authors:  Keith A Josephs; J Eric Ahlskog; Joseph E Parisi; Bradley F Boeve; Brian A Crum; Caterina Giannini; Ronald C Petersen
Journal:  Arch Neurol       Date:  2009-02
  9 in total
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1.  Probable Creutzfeldt-Jakob Disease Presenting Dementia and Urinary Retention.

Authors:  Yosuke Aiba; Ryuji Sakakibara; Ayako Iimura; Chiaki Inoue; Keiichiro Terayama; Keiko Suzuki; Shuichi Katsuragawa; Fuyuki Tateno; Tsuyoshi Ogata
Journal:  Case Rep Neurol       Date:  2020-06-10

2.  Estimation of the number of inherited prion disease mutation carriers in the UK.

Authors:  Rosie Corbie; Tracy Campbell; Lee Darwent; Peter Rudge; John Collinge; Simon Mead
Journal:  Eur J Hum Genet       Date:  2022-06-27       Impact factor: 5.351

Review 3.  Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases.

Authors:  Eva Bagyinszky; Vo Van Giau; Young Chul Youn; Seong Soo A An; SangYun Kim
Journal:  Neuropsychiatr Dis Treat       Date:  2018-08-14       Impact factor: 2.570

  3 in total

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