Faster cognitive decline in dementia due to Alzheimer disease with clinically undiagnosed Lewy body disease

Autor: Charles H. Adler, Bryan M. Spann, Brett Cutler, Sandra A. Jacobson, Bryan K. Woodruff, Javon Oliver, Lisa R. Nicholson, Geoffrey L. Ahern, Eric M. Reiman, Michael Malek-Ahmadi, Steven Z. Rapscak, Richard J. Caselli, Jiong Shi, Kewei Chen, Christine Belden, Edward Zamrini, John N. Caviness, Marwan N. Sabbagh, Jasmine Curry, Michael J. Glass, David Shprecher, Lucia I. Sue, Richard Arce, Douglas G. Walker, Anthony Intorcia, Lih-Fen Lue, Geidy E. Serrano, Kathy E. Long, Holly A. Shill, Michael Callan, Erika Driver-Dunckley, Pierre N. Tariot, Shyamal H. Mehta, Thomas G. Beach, Kathryn J. Davis, Jessica E. Walker
Rok vydání: 2019
Předmět:
Male
Social Sciences
Kaplan-Meier Estimate
Disease
Alzheimer's Disease
Pathology and Laboratory Medicine
0302 clinical medicine
Animal Cells
Medicine and Health Sciences
Prevalence
Psychology
Cognitive decline
Neuropathology
Cognitive Impairment
Neurons
0303 health sciences
Movement Disorders
Multidisciplinary
Cognitive Neurology
Parkinsonism
Neurodegenerative Diseases
Parkinson Disease
Neurology
Medicine
Female
Cellular Types
Alzheimer's disease
Research Article
Lewy Body Disease
medicine.medical_specialty
Science
Cognitive Neuroscience
03 medical and health sciences
Diagnostic Medicine
Neuropsychology
Alzheimer Disease
Internal medicine
Mental Health and Psychiatry
mental disorders
medicine
Humans
Dementia
Cognitive Dysfunction
Neuropsychological Testing
Aged
030304 developmental biology
Behavior
business.industry
Dementia with Lewy bodies
Biology and Life Sciences
Cell Biology
medicine.disease
Comorbidity
Anatomical Pathology
Cellular Neuroscience
Cognitive Science
Lewy Bodies
business
030217 neurology & neurosurgery
Neuroscience
Zdroj: PLoS ONE
PLoS ONE, Vol 14, Iss 6, p e0217566 (2019)
ISSN: 1932-6203
Popis: BackgroundNeuropathology has demonstrated a high rate of comorbid pathology in dementia due to Alzheimer's disease (ADD). The most common major comorbidity is Lewy body disease (LBD), either as dementia with Lewy bodies (AD-DLB) or Alzheimer's disease with Lewy bodies (AD-LB), the latter representing subjects with ADD and LBD not meeting neuropathological distribution and density thresholds for DLB. Although it has been established that ADD subjects with undifferentiated LBD have a more rapid cognitive decline than those with ADD alone, it is still unknown whether AD-LB subjects, who represent the majority of LBD and approximately one-third of all those with ADD, have a different clinical course.MethodsSubjects with dementia included those with "pure" ADD (n = 137), AD-DLB (n = 64) and AD-LB (n = 114), all with two or more complete Mini Mental State Examinations (MMSE) and a full neuropathological examination.ResultsLinear mixed models assessing MMSE change showed that the AD-LB group had significantly greater decline compared to the ADD group (β = -0.69, 95% CI: -1.05, -0.33, pConclusionsThe probable cause of LBD clinical detection failure is the lack of a sufficient set of characteristic core clinical features. Core DLB clinical features were not more common in AD-LB as compared to ADD. Clinical identification of ADD with LBD would allow stratified analyses of ADD clinical trials, potentially improving the probability of trial success.
Databáze: OpenAIRE