Initial non‐amnestic symptoms relate to faster rate of functional and cognitive decline compared to amnestic symptoms in neuropathologically confirmed dementias

Author:

Pillai Jagan A123,Bena James4,Maly Emily F3,Leverenz James B123

Affiliation:

1. Lou Ruvo Center for Brain Health Cleveland Clinic Cleveland Ohio USA

2. Neurological Institute Cleveland Clinic Cleveland Ohio USA

3. Department of Neurology Cleveland Clinic Cleveland Ohio USA

4. Quantitative Health Sciences Cleveland Clinic Cleveland Ohio USA

Abstract

AbstractIntroductionThe relationship between initial cognitive symptoms and subsequent rate of clinical decline is important in clinical care and the design of dementia clinical trials.MethodsThis retrospective longitudinal, autopsy‐confirmed, cohort study among 2426 participants in the National Alzheimer's Coordinating Center database included Alzheimer's disease (AD) pathology, n = 1187; Lewy body pathology (LBP), n = 331; and mixed pathology (AD‐LBP), n = 904. The predominant initial cognitive symptom was assessed clinically. Linear mixed models evaluated the longitudinal outcome of the Clinical Dementia Rating‐Sum of Boxes (CDR‐SB) score.ResultsNon‐amnestic initial symptoms had a faster rate of decline than amnestic symptoms in all three groups. Language symptoms had a faster rate of decline in all three groups. Executive symptoms had a faster rate of decline than amnestic in AD and AD‐LBP. There was a similar trend for visuospatial symptoms in AD‐LBP.DiscussionInitial cognitive symptoms, despite varied underlying pathology, are a predictor of longitudinal functional outcomes among dementias.Highlights Initial non‐amnestic symptoms had a faster rate of longitudinal cognitive and functional decline on the Clinical Dementia Rating‐Sum of Boxes (CDR‐SB) scores than amnestic symptoms among Alzheimer's disease, Lewy body pathology, and mixed neuropathology. Given the relative size of CDR‐SB changes in Alzheimer's disease clinical trials, clarifying the nature of initial symptoms could be an important variable in ensuring appropriately designed clinical trials.

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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