Neuropsychiatric Symptoms in Patients With Pathologically Confirmed Comorbid Alzheimer Disease and Frontotemporal Lobar Degeneration

Comorbid presence of ADNC and FTLD neuropathology, compared with each pathology alone, was associated with a greater likelihood of presenting with known neuropsychiatric symptoms of the other disease, irrespective of patients' clinical syndrome. Findings highlight the potential clinical diagnostic value of antemortem behavioral symptoms in identifying patients with comorbid pathology, although conclusions are limited by the cross-sectional nature of the neuropsychiatric data.

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Publication Details

Journal
Neurology
Published
2026-03-05
DOI
https://doi.org/10.1212/wnl.0000000000214750
Citations
1
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
Field-Weighted Citation Impact
33.12
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article

Neuropsychiatric Symptoms in Patients With Pathologically Confirmed Comorbid Alzheimer Disease and Frontotemporal Lobar Degeneration

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1 citations
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Dementia and Cognitive Impairment Research
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article

Neuropsychiatric Symptoms in Patients With Pathologically Confirmed Comorbid Alzheimer Disease and Frontotemporal Lobar Degeneration

Molly Split, Daliah Ross, Zachary J. Kunicki, Rachel Keszycki, Sarah Prieto, Masood Manoochehri, Alyssa N. De Vito, Edward D Huey, Megan S. Barker
article en
1 citations

Abstract

Comorbid presence of ADNC and FTLD neuropathology, compared with each pathology alone, was associated with a greater likelihood of presenting with known neuropsychiatric symptoms of the other disease, irrespective of patients' clinical syndrome. Findings highlight the potential clinical diagnostic value of antemortem behavioral symptoms in identifying patients with comorbid pathology, although conclusions are limited by the cross-sectional nature of the neuropsychiatric data.

NeurologyVol. 106(7)
Northwestern University (US), Providence College (US), Brown University (US), Butler Hospital (US), Alzheimer’s Disease Neuroimaging Initiative (US)
Zero hunger
Openalex Percentile: Top 0%
Dementia and Cognitive Impairment Research
33.12
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