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Deformation based morphometry study of longitudinal MRI changes in behavioral variant frontotemporal dementia
OBJECTIVE: To objectively quantify how cerebral volume loss could assist with clinical diagnosis and clinical trial design in the behavioural variant of frontotemporal dementia (bvFTD). METHODS: We applied deformation-based morphometric analyses with robust registration to precisely quantify the mag...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879994/ https://www.ncbi.nlm.nih.gov/pubmed/31795051 http://dx.doi.org/10.1016/j.nicl.2019.102079 |
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author | Manera, Ana L. Dadar, Mahsa Collins, D. Louis Ducharme, Simon |
author_facet | Manera, Ana L. Dadar, Mahsa Collins, D. Louis Ducharme, Simon |
author_sort | Manera, Ana L. |
collection | PubMed |
description | OBJECTIVE: To objectively quantify how cerebral volume loss could assist with clinical diagnosis and clinical trial design in the behavioural variant of frontotemporal dementia (bvFTD). METHODS: We applied deformation-based morphometric analyses with robust registration to precisely quantify the magnitude and pattern of atrophy in patients with bvFTD as compared to cognitively normal controls (CNCs), to assess the progression of atrophy over one year follow up and to generate clinical trial sample size estimates to detect differences for the structures most sensitive to change. This study included 203 subjects - 70 bvFTD and 133 CNCs - with a total of 482 timepoints from the Frontotemporal Lobar Degeneration Neuroimaging Initiative. RESULTS: Deformation based morphometry (DBM) revealed significant atrophy in the frontal lobes, insula, medial and anterior temporal regions bilaterally in bvFTD subjects compared to controls with outstanding subcortical involvement. We provide detailed information on regional changes per year. In both cross-sectional analysis and over a one-year follow-up period, ventricle expansion was the most prominent differentiator of bvFTD from controls and a sensitive marker of disease progression. CONCLUSIONS: Automated measurement of ventricular expansion is a sensitive and reliable marker of disease progression in bvFTD to be used in clinical trials for potential disease modifying drugs, as well as possibly to implement in clinical practice. Ventricular expansion measured with DBM provides the lowest published estimated sample size for clinical trial design to detect significant differences over one and two years. |
format | Online Article Text |
id | pubmed-6879994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68799942019-11-29 Deformation based morphometry study of longitudinal MRI changes in behavioral variant frontotemporal dementia Manera, Ana L. Dadar, Mahsa Collins, D. Louis Ducharme, Simon Neuroimage Clin Regular Article OBJECTIVE: To objectively quantify how cerebral volume loss could assist with clinical diagnosis and clinical trial design in the behavioural variant of frontotemporal dementia (bvFTD). METHODS: We applied deformation-based morphometric analyses with robust registration to precisely quantify the magnitude and pattern of atrophy in patients with bvFTD as compared to cognitively normal controls (CNCs), to assess the progression of atrophy over one year follow up and to generate clinical trial sample size estimates to detect differences for the structures most sensitive to change. This study included 203 subjects - 70 bvFTD and 133 CNCs - with a total of 482 timepoints from the Frontotemporal Lobar Degeneration Neuroimaging Initiative. RESULTS: Deformation based morphometry (DBM) revealed significant atrophy in the frontal lobes, insula, medial and anterior temporal regions bilaterally in bvFTD subjects compared to controls with outstanding subcortical involvement. We provide detailed information on regional changes per year. In both cross-sectional analysis and over a one-year follow-up period, ventricle expansion was the most prominent differentiator of bvFTD from controls and a sensitive marker of disease progression. CONCLUSIONS: Automated measurement of ventricular expansion is a sensitive and reliable marker of disease progression in bvFTD to be used in clinical trials for potential disease modifying drugs, as well as possibly to implement in clinical practice. Ventricular expansion measured with DBM provides the lowest published estimated sample size for clinical trial design to detect significant differences over one and two years. Elsevier 2019-11-05 /pmc/articles/PMC6879994/ /pubmed/31795051 http://dx.doi.org/10.1016/j.nicl.2019.102079 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Manera, Ana L. Dadar, Mahsa Collins, D. Louis Ducharme, Simon Deformation based morphometry study of longitudinal MRI changes in behavioral variant frontotemporal dementia |
title | Deformation based morphometry study of longitudinal MRI changes in behavioral variant frontotemporal dementia |
title_full | Deformation based morphometry study of longitudinal MRI changes in behavioral variant frontotemporal dementia |
title_fullStr | Deformation based morphometry study of longitudinal MRI changes in behavioral variant frontotemporal dementia |
title_full_unstemmed | Deformation based morphometry study of longitudinal MRI changes in behavioral variant frontotemporal dementia |
title_short | Deformation based morphometry study of longitudinal MRI changes in behavioral variant frontotemporal dementia |
title_sort | deformation based morphometry study of longitudinal mri changes in behavioral variant frontotemporal dementia |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879994/ https://www.ncbi.nlm.nih.gov/pubmed/31795051 http://dx.doi.org/10.1016/j.nicl.2019.102079 |
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