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Magnetic resonance elastography of frontotemporal dementia

PURPOSE: To investigate the feasibility of utilizing brain stiffness as a potential biomarker for behavioral variant frontotemporal dementia (bvFTD) patients. Magnetic resonance elastography (MRE) is a noninvasive technique for evaluating the mechanical properties of brain tissue in vivo. MRE has de...

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Autores principales: Huston, John, Murphy, Matthew C., Boeve, Bradley F., Fattahi, Nikoo, Arani, Arvin, Glaser, Kevin J., Manduca, Armando, Jones, David T., Ehman, Richard L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696917/
https://www.ncbi.nlm.nih.gov/pubmed/26130216
http://dx.doi.org/10.1002/jmri.24977
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author Huston, John
Murphy, Matthew C.
Boeve, Bradley F.
Fattahi, Nikoo
Arani, Arvin
Glaser, Kevin J.
Manduca, Armando
Jones, David T.
Ehman, Richard L.
author_facet Huston, John
Murphy, Matthew C.
Boeve, Bradley F.
Fattahi, Nikoo
Arani, Arvin
Glaser, Kevin J.
Manduca, Armando
Jones, David T.
Ehman, Richard L.
author_sort Huston, John
collection PubMed
description PURPOSE: To investigate the feasibility of utilizing brain stiffness as a potential biomarker for behavioral variant frontotemporal dementia (bvFTD) patients. Magnetic resonance elastography (MRE) is a noninvasive technique for evaluating the mechanical properties of brain tissue in vivo. MRE has demonstrated decreased brain stiffness in patients with Alzheimer's disease. MATERIALS AND METHODS: We examined five male subjects with bvFTD and nine cognitively normal age‐matched male controls (NC) with brain 3T MRE. Stiffness was calculated in nine regions of interest (ROIs): whole brain (entire cerebrum excluding cerebellum), frontal lobes, occipital lobes, parietal lobes, temporal lobes, deep gray matter / white matter (GM/WM; insula, deep gray nuclei and white matter tracts), cerebellum, sensorimotor cortex (pre‐ and postcentral gyri), and a composite region labeled FT (frontal and temporal lobes excluding the pre‐ and postcentral gyri). RESULTS: Significantly lower stiffness values were observed in the whole brain (P = 0.007), frontal lobe (P = 0.001), and temporal lobes (P = 0.005) of bvFTD patients compared to NC. No significant stiffness differences were observed in any other ROIs of bvFTD patients compared to NC (P > 0.05). These results demonstrate that statistically significant brain softening occurs in the frontal and temporal lobes of bvFTD patients, which corresponds to the expected pathophysiology of bvFTD. CONCLUSION: Future studies evaluating the feasibility of brain MRE for early disease detection and monitoring disease progression could shed new insights into understanding the mechanisms involved in bvFTD. J. Magn. Reson. Imaging 2016;43:474–478.
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spelling pubmed-46969172016-02-26 Magnetic resonance elastography of frontotemporal dementia Huston, John Murphy, Matthew C. Boeve, Bradley F. Fattahi, Nikoo Arani, Arvin Glaser, Kevin J. Manduca, Armando Jones, David T. Ehman, Richard L. J Magn Reson Imaging Original Research – Neuro PURPOSE: To investigate the feasibility of utilizing brain stiffness as a potential biomarker for behavioral variant frontotemporal dementia (bvFTD) patients. Magnetic resonance elastography (MRE) is a noninvasive technique for evaluating the mechanical properties of brain tissue in vivo. MRE has demonstrated decreased brain stiffness in patients with Alzheimer's disease. MATERIALS AND METHODS: We examined five male subjects with bvFTD and nine cognitively normal age‐matched male controls (NC) with brain 3T MRE. Stiffness was calculated in nine regions of interest (ROIs): whole brain (entire cerebrum excluding cerebellum), frontal lobes, occipital lobes, parietal lobes, temporal lobes, deep gray matter / white matter (GM/WM; insula, deep gray nuclei and white matter tracts), cerebellum, sensorimotor cortex (pre‐ and postcentral gyri), and a composite region labeled FT (frontal and temporal lobes excluding the pre‐ and postcentral gyri). RESULTS: Significantly lower stiffness values were observed in the whole brain (P = 0.007), frontal lobe (P = 0.001), and temporal lobes (P = 0.005) of bvFTD patients compared to NC. No significant stiffness differences were observed in any other ROIs of bvFTD patients compared to NC (P > 0.05). These results demonstrate that statistically significant brain softening occurs in the frontal and temporal lobes of bvFTD patients, which corresponds to the expected pathophysiology of bvFTD. CONCLUSION: Future studies evaluating the feasibility of brain MRE for early disease detection and monitoring disease progression could shed new insights into understanding the mechanisms involved in bvFTD. J. Magn. Reson. Imaging 2016;43:474–478. John Wiley and Sons Inc. 2015-06-30 2016-02 /pmc/articles/PMC4696917/ /pubmed/26130216 http://dx.doi.org/10.1002/jmri.24977 Text en © 2015 The Authors Journal of Magnetic Resonance Imaging published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/3.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research – Neuro
Huston, John
Murphy, Matthew C.
Boeve, Bradley F.
Fattahi, Nikoo
Arani, Arvin
Glaser, Kevin J.
Manduca, Armando
Jones, David T.
Ehman, Richard L.
Magnetic resonance elastography of frontotemporal dementia
title Magnetic resonance elastography of frontotemporal dementia
title_full Magnetic resonance elastography of frontotemporal dementia
title_fullStr Magnetic resonance elastography of frontotemporal dementia
title_full_unstemmed Magnetic resonance elastography of frontotemporal dementia
title_short Magnetic resonance elastography of frontotemporal dementia
title_sort magnetic resonance elastography of frontotemporal dementia
topic Original Research – Neuro
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4696917/
https://www.ncbi.nlm.nih.gov/pubmed/26130216
http://dx.doi.org/10.1002/jmri.24977
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