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Escalation of Tau Accumulation after a Traumatic Brain Injury: Findings from Positron Emission Tomography
Traumatic brain injury (TBI) has come to be recognized as a risk factor for Alzheimer’s disease (AD), with poorly understood underlying mechanisms. We hypothesized that a history of TBI would be associated with greater tau deposition in elders with high-risk for dementia. A Groups of 20 participants...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313362/ https://www.ncbi.nlm.nih.gov/pubmed/35884683 http://dx.doi.org/10.3390/brainsci12070876 |
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author | Mohamed, Abdalla Z. Cumming, Paul Nasrallah, Fatima A. |
author_facet | Mohamed, Abdalla Z. Cumming, Paul Nasrallah, Fatima A. |
author_sort | Mohamed, Abdalla Z. |
collection | PubMed |
description | Traumatic brain injury (TBI) has come to be recognized as a risk factor for Alzheimer’s disease (AD), with poorly understood underlying mechanisms. We hypothesized that a history of TBI would be associated with greater tau deposition in elders with high-risk for dementia. A Groups of 20 participants with self-reported history of TBI and 100 without any such history were scanned using [(18)F]-AV1451 positron emission tomography as part of the Alzheimer’s Disease Neuroimaging Initiative (ADNI). Scans were stratified into four groups according to TBI history, and by clinical dementia rating scores into cognitively normal (CDR = 0) and those showing cognitive decline (CDR ≥ 0.5). We pursued voxel-based group comparison of [(18)F]-AV1451 uptake to identify the effect of TBI history on brain tau deposition, and for voxel-wise correlation analyses between [(18)F]-AV1451 uptake and different neuropsychological measures and cerebrospinal fluid (CSF) biomarkers. Compared to the TBI-/CDR ≥ 0.5 group, the TBI+/CDR ≥ 0.5 group showed increased tau deposition in the temporal pole, hippocampus, fusiform gyrus, and inferior and middle temporal gyri. Furthermore, the extent of tau deposition in the brain of those with TBI history positively correlated with the extent of cognitive decline, CSF-tau, and CSF-amyloid. This might suggest TBI to increase the risk for tauopathies and Alzheimer’s disease later in life. |
format | Online Article Text |
id | pubmed-9313362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93133622022-07-26 Escalation of Tau Accumulation after a Traumatic Brain Injury: Findings from Positron Emission Tomography Mohamed, Abdalla Z. Cumming, Paul Nasrallah, Fatima A. Brain Sci Article Traumatic brain injury (TBI) has come to be recognized as a risk factor for Alzheimer’s disease (AD), with poorly understood underlying mechanisms. We hypothesized that a history of TBI would be associated with greater tau deposition in elders with high-risk for dementia. A Groups of 20 participants with self-reported history of TBI and 100 without any such history were scanned using [(18)F]-AV1451 positron emission tomography as part of the Alzheimer’s Disease Neuroimaging Initiative (ADNI). Scans were stratified into four groups according to TBI history, and by clinical dementia rating scores into cognitively normal (CDR = 0) and those showing cognitive decline (CDR ≥ 0.5). We pursued voxel-based group comparison of [(18)F]-AV1451 uptake to identify the effect of TBI history on brain tau deposition, and for voxel-wise correlation analyses between [(18)F]-AV1451 uptake and different neuropsychological measures and cerebrospinal fluid (CSF) biomarkers. Compared to the TBI-/CDR ≥ 0.5 group, the TBI+/CDR ≥ 0.5 group showed increased tau deposition in the temporal pole, hippocampus, fusiform gyrus, and inferior and middle temporal gyri. Furthermore, the extent of tau deposition in the brain of those with TBI history positively correlated with the extent of cognitive decline, CSF-tau, and CSF-amyloid. This might suggest TBI to increase the risk for tauopathies and Alzheimer’s disease later in life. MDPI 2022-07-01 /pmc/articles/PMC9313362/ /pubmed/35884683 http://dx.doi.org/10.3390/brainsci12070876 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mohamed, Abdalla Z. Cumming, Paul Nasrallah, Fatima A. Escalation of Tau Accumulation after a Traumatic Brain Injury: Findings from Positron Emission Tomography |
title | Escalation of Tau Accumulation after a Traumatic Brain Injury: Findings from Positron Emission Tomography |
title_full | Escalation of Tau Accumulation after a Traumatic Brain Injury: Findings from Positron Emission Tomography |
title_fullStr | Escalation of Tau Accumulation after a Traumatic Brain Injury: Findings from Positron Emission Tomography |
title_full_unstemmed | Escalation of Tau Accumulation after a Traumatic Brain Injury: Findings from Positron Emission Tomography |
title_short | Escalation of Tau Accumulation after a Traumatic Brain Injury: Findings from Positron Emission Tomography |
title_sort | escalation of tau accumulation after a traumatic brain injury: findings from positron emission tomography |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313362/ https://www.ncbi.nlm.nih.gov/pubmed/35884683 http://dx.doi.org/10.3390/brainsci12070876 |
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