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Anterolateral entorhinal cortex thickness as a new biomarker for early detection of Alzheimer's disease
INTRODUCTION: Loss of entorhinal cortex (EC) layer II neurons represents the earliest Alzheimer's disease (AD) lesion in the brain. Research suggests differing functional roles between two EC subregions, the anterolateral EC (aLEC) and the posteromedial EC (pMEC). METHODS: We use joint label fu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447874/ https://www.ncbi.nlm.nih.gov/pubmed/32875052 http://dx.doi.org/10.1002/dad2.12068 |
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author | Holbrook, Andrew J. Tustison, Nicholas J. Marquez, Freddie Roberts, Jared Yassa, Michael A. Gillen, Daniel L. |
author_facet | Holbrook, Andrew J. Tustison, Nicholas J. Marquez, Freddie Roberts, Jared Yassa, Michael A. Gillen, Daniel L. |
author_sort | Holbrook, Andrew J. |
collection | PubMed |
description | INTRODUCTION: Loss of entorhinal cortex (EC) layer II neurons represents the earliest Alzheimer's disease (AD) lesion in the brain. Research suggests differing functional roles between two EC subregions, the anterolateral EC (aLEC) and the posteromedial EC (pMEC). METHODS: We use joint label fusion to obtain aLEC and pMEC cortical thickness measurements from serial magnetic resonance imaging scans of 775 ADNI‐1 participants (219 healthy; 380 mild cognitive impairment; 176 AD) and use linear mixed‐effects models to analyze longitudinal associations among cortical thickness, disease status, and cognitive measures. RESULTS: Group status is reliably predicted by aLEC thickness, which also exhibits greater associations with cognitive outcomes than does pMEC thickness. Change in aLEC thickness is also associated with cerebrospinal fluid amyloid and tau levels. DISCUSSION: Thinning of aLEC is a sensitive structural biomarker that changes over short durations in the course of AD and tracks disease severity—it is a strong candidate biomarker for detection of early AD. |
format | Online Article Text |
id | pubmed-7447874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74478742020-08-31 Anterolateral entorhinal cortex thickness as a new biomarker for early detection of Alzheimer's disease Holbrook, Andrew J. Tustison, Nicholas J. Marquez, Freddie Roberts, Jared Yassa, Michael A. Gillen, Daniel L. Alzheimers Dement (Amst) Neuroimaging INTRODUCTION: Loss of entorhinal cortex (EC) layer II neurons represents the earliest Alzheimer's disease (AD) lesion in the brain. Research suggests differing functional roles between two EC subregions, the anterolateral EC (aLEC) and the posteromedial EC (pMEC). METHODS: We use joint label fusion to obtain aLEC and pMEC cortical thickness measurements from serial magnetic resonance imaging scans of 775 ADNI‐1 participants (219 healthy; 380 mild cognitive impairment; 176 AD) and use linear mixed‐effects models to analyze longitudinal associations among cortical thickness, disease status, and cognitive measures. RESULTS: Group status is reliably predicted by aLEC thickness, which also exhibits greater associations with cognitive outcomes than does pMEC thickness. Change in aLEC thickness is also associated with cerebrospinal fluid amyloid and tau levels. DISCUSSION: Thinning of aLEC is a sensitive structural biomarker that changes over short durations in the course of AD and tracks disease severity—it is a strong candidate biomarker for detection of early AD. John Wiley and Sons Inc. 2020-08-25 /pmc/articles/PMC7447874/ /pubmed/32875052 http://dx.doi.org/10.1002/dad2.12068 Text en © 2020 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, Inc. on behalf of Alzheimer's Association This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Neuroimaging Holbrook, Andrew J. Tustison, Nicholas J. Marquez, Freddie Roberts, Jared Yassa, Michael A. Gillen, Daniel L. Anterolateral entorhinal cortex thickness as a new biomarker for early detection of Alzheimer's disease |
title | Anterolateral entorhinal cortex thickness as a new biomarker for early detection of Alzheimer's disease |
title_full | Anterolateral entorhinal cortex thickness as a new biomarker for early detection of Alzheimer's disease |
title_fullStr | Anterolateral entorhinal cortex thickness as a new biomarker for early detection of Alzheimer's disease |
title_full_unstemmed | Anterolateral entorhinal cortex thickness as a new biomarker for early detection of Alzheimer's disease |
title_short | Anterolateral entorhinal cortex thickness as a new biomarker for early detection of Alzheimer's disease |
title_sort | anterolateral entorhinal cortex thickness as a new biomarker for early detection of alzheimer's disease |
topic | Neuroimaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447874/ https://www.ncbi.nlm.nih.gov/pubmed/32875052 http://dx.doi.org/10.1002/dad2.12068 |
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