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Clinical Features of Patients with Alzheimer's Disease and a History of Traumatic Brain Injury

INTRODUCTION: Traumatic brain injury (TBI) has been associated with a greater risk of developing Alzheimer's disease (AD). Less is known about the clinical features of AD patients with TBI history. The objective of this study was to examine whether a history of TBI and specific injury character...

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Autores principales: van Amerongen, Suzan, Caton, Dewi K., Pijnenburg, Yolande A.L., Scheltens, Philip, Vijverberg, Everard G.B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574209/
https://www.ncbi.nlm.nih.gov/pubmed/36262422
http://dx.doi.org/10.1159/000526243
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author van Amerongen, Suzan
Caton, Dewi K.
Pijnenburg, Yolande A.L.
Scheltens, Philip
Vijverberg, Everard G.B.
author_facet van Amerongen, Suzan
Caton, Dewi K.
Pijnenburg, Yolande A.L.
Scheltens, Philip
Vijverberg, Everard G.B.
author_sort van Amerongen, Suzan
collection PubMed
description INTRODUCTION: Traumatic brain injury (TBI) has been associated with a greater risk of developing Alzheimer's disease (AD). Less is known about the clinical features of AD patients with TBI history. The objective of this study was to examine whether a history of TBI and specific injury characteristics are associated with differences in age of disease onset, cognitive features, and neuropsychiatric symptoms (NPSs) in AD patients. METHODS: Biomarker-proven AD patients (CSF or amyloid PET) were selected from the Amsterdam Dementia Cohort. TBI events were classified by age at injury (TBI <25 or ≥25 years) and TBI severity (loss of consciousness, multiple events). Cognitive composite scores were calculated from results of a neuropsychological test battery. NPSs were assessed with the Neuropsychiatric Inventory Questionnaire (NPI-Q). Linear regression analyses were utilized to examine associations between TBI, TBI characteristics, and clinical outcome measures. RESULTS: Among the 1,755 selected AD patients (mean age = 65.2 years), 166 (9.5%) had documented ≥1 TBI in their medical history. Overall, TBI history was not related to differences in age of disease onset, but age at injury <25 years old was associated with 2.3 years earlier age at symptom onset (B = −2.34, p = 0.031). No significant associations were found between TBI history or TBI characteristics and differences in cognition or NPSs. CONCLUSION: Our results underscore previous findings on the vulnerability of the brain during critical maturation phases and suggest that an early TBI may contribute to lower resilience to neurodegenerative changes.
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spelling pubmed-95742092022-10-18 Clinical Features of Patients with Alzheimer's Disease and a History of Traumatic Brain Injury van Amerongen, Suzan Caton, Dewi K. Pijnenburg, Yolande A.L. Scheltens, Philip Vijverberg, Everard G.B. Dement Geriatr Cogn Dis Extra Research Article INTRODUCTION: Traumatic brain injury (TBI) has been associated with a greater risk of developing Alzheimer's disease (AD). Less is known about the clinical features of AD patients with TBI history. The objective of this study was to examine whether a history of TBI and specific injury characteristics are associated with differences in age of disease onset, cognitive features, and neuropsychiatric symptoms (NPSs) in AD patients. METHODS: Biomarker-proven AD patients (CSF or amyloid PET) were selected from the Amsterdam Dementia Cohort. TBI events were classified by age at injury (TBI <25 or ≥25 years) and TBI severity (loss of consciousness, multiple events). Cognitive composite scores were calculated from results of a neuropsychological test battery. NPSs were assessed with the Neuropsychiatric Inventory Questionnaire (NPI-Q). Linear regression analyses were utilized to examine associations between TBI, TBI characteristics, and clinical outcome measures. RESULTS: Among the 1,755 selected AD patients (mean age = 65.2 years), 166 (9.5%) had documented ≥1 TBI in their medical history. Overall, TBI history was not related to differences in age of disease onset, but age at injury <25 years old was associated with 2.3 years earlier age at symptom onset (B = −2.34, p = 0.031). No significant associations were found between TBI history or TBI characteristics and differences in cognition or NPSs. CONCLUSION: Our results underscore previous findings on the vulnerability of the brain during critical maturation phases and suggest that an early TBI may contribute to lower resilience to neurodegenerative changes. S. Karger AG 2022-09-16 /pmc/articles/PMC9574209/ /pubmed/36262422 http://dx.doi.org/10.1159/000526243 Text en Copyright © 2022 by The Author(s). Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense), applicable to the online version of the article only. Usage and distribution for commercial purposes requires written permission.
spellingShingle Research Article
van Amerongen, Suzan
Caton, Dewi K.
Pijnenburg, Yolande A.L.
Scheltens, Philip
Vijverberg, Everard G.B.
Clinical Features of Patients with Alzheimer's Disease and a History of Traumatic Brain Injury
title Clinical Features of Patients with Alzheimer's Disease and a History of Traumatic Brain Injury
title_full Clinical Features of Patients with Alzheimer's Disease and a History of Traumatic Brain Injury
title_fullStr Clinical Features of Patients with Alzheimer's Disease and a History of Traumatic Brain Injury
title_full_unstemmed Clinical Features of Patients with Alzheimer's Disease and a History of Traumatic Brain Injury
title_short Clinical Features of Patients with Alzheimer's Disease and a History of Traumatic Brain Injury
title_sort clinical features of patients with alzheimer's disease and a history of traumatic brain injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574209/
https://www.ncbi.nlm.nih.gov/pubmed/36262422
http://dx.doi.org/10.1159/000526243
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