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Abstract Details

Clinical Profiles of Arteriosclerosis and Alzheimer’s Disease at Mild Cognitive Impairment and Early Dementia in a National Neuropathology Cohort
Aging, Dementia, and Behavioral Neurology
P11 - Poster Session 11 (8:00 AM-9:00 AM)
10-005

We sought to evaluate differences in clinical profiles at mild cognitive impairment (MCI) and early dementia stages between those with arteriosclerosis alone (pARTE), Alzheimer's disease (AD) alone (pAD), and AD with arteriosclerosis (ADARTE) using retrospective clinical data on autopsy-confirmed cases from the National Alzheimer’s Coordinating Center (NACC) database.

AD and cerebral small vessel disease are common causes of dementia. They often co-exist but can be difficult to distinguish and their exact clinical interaction is unclear.

We defined groups of pARTE (n=34), pAD (n=189), and ADARTE (n=256) from NACC neuropathology diagnoses. Subjects included had moderate to severe arteriosclerosis and/or ABC score for AD of 2-3, without other major neuropathology. We compared demographics, vascular risk factors, cognitive testing, and neuropsychiatric symptoms across neuropathology groups and subgroups of apolipoprotein (APOE) allele variants at first evaluation with Global Clinical Dementia Rating (CDR) score of 0.5 and 1.0, corresponding to MCI and early dementia stages respectively.

At CDR 0.5, the only difference was that pARTE subjects were older, with later onset of cognitive decline. Evaluating for APOE genotype effects, APOE4 associated with worse Logical Memory Delayed Recall in pAD and ADARTE groups, but not in pARTE. Differences among the three groups were more apparent at CDR 1.0. The pAD subjects were younger with earlier onset of cognitive decline than the other two groups. The pARTE subjects had higher Geriatric Depression Scale scores and better Logical Memory Delayed Recall performance. Diabetes was the most distinguishing vascular risk factor, with higher prevalence in pARTE. APOE4 associated with worse Trail-Making Test performance in ADARTE.

Clinical differences between pARTE, pAD, and ADARTE emerge at early dementia rather than MCI. Diabetes plays a more prominent role in pARTE dementia. APOE4 allele has varied associations within neuropathology groups at different stages.

Authors/Disclosures
Dixon Yang, MD (Rush University Medical Center)
PRESENTER
Dr. Yang has nothing to disclose.
Arjun V. Masurkar, MD (NYU Langone Medical Center) The institution of Dr. Masurkar has received research support from NIH. The institution of Dr. Masurkar has received research support from Alzheimer's Association. The institution of Dr. Masurkar has received research support from BrightFocus Foundation. Dr. Masurkar has received personal compensation in the range of $500-$4,999 for serving as a IRGP Advisory Council Member with Alzheimer's Association. Dr. Masurkar has a non-compensated relationship as a Steering Committee Member with Alzheimer's Disease Cooperative Study that is relevant to Âé¶¹´«Ã½Ó³»­ interests or activities.