Association Between Clinical Measures and Florbetapir F18 PET Neuroimaging in Mild or Moderate Alzheimer’s Disease Dementia

The authors conducted a retrospective, cross-sectional analysis comparing baseline neuropsychiatric and other clinical characteristics in 199 expert-diagnosed mild and moderate Alzheimer’s dementia patients participating in industry-sponsored clinical trials of an investigational therapy, where 18%...

Full description

Saved in:
Bibliographic Details
Published inThe journal of neuropsychiatry and clinical neurosciences Vol. 26; no. 3; pp. 214 - 220
Main Authors Witte, Michael M, Trzepacz, Paula, Case, Michael, Yu, Peng, Hochstetler, Helen, Quinlivan, Mitchell, Sundell, Karen, Henley, David
Format Journal Article
LanguageEnglish
Published United States American Psychiatric Association 2014
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The authors conducted a retrospective, cross-sectional analysis comparing baseline neuropsychiatric and other clinical characteristics in 199 expert-diagnosed mild and moderate Alzheimer’s dementia patients participating in industry-sponsored clinical trials of an investigational therapy, where 18% lacked florbetapir positron emission tomography (PET) evidence of Alzheimer’s neuropathology. Clinical diagnosis of Alzheimer’s disease (AD) is challenging, with 20% or more of patients misdiagnosed, even by expert clinicians. The authors conducted a retrospective, cross-sectional analysis comparing baseline neuropsychiatric and other clinical characteristics in 199 expert-diagnosed mild and moderate AD dementia patients participating in industry-sponsored clinical trials of an investigational therapy, where 18% lacked florbetapir positron emission tomography (PET) evidence of AD neuropathology. Significant differences were found only for cognition and ApoE ε4 status, but the large degree of score overlap would preclude using these measures to predict AD misdiagnosis. This study highlights the value of amyloid PET when evaluating patients with seemingly typical AD.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0895-0172
1545-7222
DOI:10.1176/appi.neuropsych.12120402