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Single-subject classification of presymptomatic frontotemporal dementia mutation carriers using multimodal MRI

BACKGROUND: Classification models based on magnetic resonance imaging (MRI) may aid early diagnosis of frontotemporal dementia (FTD) but have only been applied in established FTD cases. Detection of FTD patients in earlier disease stages, such as presymptomatic mutation carriers, may further advance...

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Autores principales: Feis, Rogier A., Bouts, Mark J.R.J., Panman, Jessica L., Jiskoot, Lize C., Dopper, Elise G.P., Schouten, Tijn M., de Vos, Frank, van der Grond, Jeroen, van Swieten, John C., Rombouts, Serge A.R.B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543025/
https://www.ncbi.nlm.nih.gov/pubmed/30827922
http://dx.doi.org/10.1016/j.nicl.2019.101718
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author Feis, Rogier A.
Bouts, Mark J.R.J.
Panman, Jessica L.
Jiskoot, Lize C.
Dopper, Elise G.P.
Schouten, Tijn M.
de Vos, Frank
van der Grond, Jeroen
van Swieten, John C.
Rombouts, Serge A.R.B.
author_facet Feis, Rogier A.
Bouts, Mark J.R.J.
Panman, Jessica L.
Jiskoot, Lize C.
Dopper, Elise G.P.
Schouten, Tijn M.
de Vos, Frank
van der Grond, Jeroen
van Swieten, John C.
Rombouts, Serge A.R.B.
author_sort Feis, Rogier A.
collection PubMed
description BACKGROUND: Classification models based on magnetic resonance imaging (MRI) may aid early diagnosis of frontotemporal dementia (FTD) but have only been applied in established FTD cases. Detection of FTD patients in earlier disease stages, such as presymptomatic mutation carriers, may further advance early diagnosis and treatment. In this study, we aim to distinguish presymptomatic FTD mutation carriers from controls on an individual level using multimodal MRI-based classification. METHODS: Anatomical MRI, diffusion tensor imaging (DTI) and resting-state functional MRI data were collected in 55 presymptomatic FTD mutation carriers (8 microtubule-associated protein Tau, 35 progranulin, and 12 chromosome 9 open reading frame 72) and 48 familial controls. We calculated grey and white matter density features from anatomical MRI scans, diffusivity features from DTI, and functional connectivity features from resting-state functional MRI. These features were applied in a recently introduced multimodal behavioural variant FTD (bvFTD) classification model, and were subsequently used to train and test unimodal and multimodal carrier-control models. Classification performance was quantified using area under the receiver operator characteristic curves (AUC). RESULTS: The bvFTD model was not able to separate presymptomatic carriers from controls beyond chance level (AUC = 0.582, p = 0.078). In contrast, one unimodal and several multimodal carrier-control models performed significantly better than chance level. The unimodal model included the radial diffusivity feature and had an AUC of 0.642 (p = 0.032). The best multimodal model combined radial diffusivity and white matter density features (AUC = 0.684, p = 0.004). CONCLUSIONS: FTD mutation carriers can be separated from controls with a modest AUC even before symptom-onset, using a newly created carrier-control classification model, while this was not possible using a recent bvFTD classification model. A multimodal MRI-based classification score may therefore be a useful biomarker to aid earlier FTD diagnosis. The exclusive selection of white matter features in the best performing model suggests that the earliest FTD-related pathological processes occur in white matter.
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spelling pubmed-65430252019-08-28 Single-subject classification of presymptomatic frontotemporal dementia mutation carriers using multimodal MRI Feis, Rogier A. Bouts, Mark J.R.J. Panman, Jessica L. Jiskoot, Lize C. Dopper, Elise G.P. Schouten, Tijn M. de Vos, Frank van der Grond, Jeroen van Swieten, John C. Rombouts, Serge A.R.B. Neuroimage Clin Article BACKGROUND: Classification models based on magnetic resonance imaging (MRI) may aid early diagnosis of frontotemporal dementia (FTD) but have only been applied in established FTD cases. Detection of FTD patients in earlier disease stages, such as presymptomatic mutation carriers, may further advance early diagnosis and treatment. In this study, we aim to distinguish presymptomatic FTD mutation carriers from controls on an individual level using multimodal MRI-based classification. METHODS: Anatomical MRI, diffusion tensor imaging (DTI) and resting-state functional MRI data were collected in 55 presymptomatic FTD mutation carriers (8 microtubule-associated protein Tau, 35 progranulin, and 12 chromosome 9 open reading frame 72) and 48 familial controls. We calculated grey and white matter density features from anatomical MRI scans, diffusivity features from DTI, and functional connectivity features from resting-state functional MRI. These features were applied in a recently introduced multimodal behavioural variant FTD (bvFTD) classification model, and were subsequently used to train and test unimodal and multimodal carrier-control models. Classification performance was quantified using area under the receiver operator characteristic curves (AUC). RESULTS: The bvFTD model was not able to separate presymptomatic carriers from controls beyond chance level (AUC = 0.582, p = 0.078). In contrast, one unimodal and several multimodal carrier-control models performed significantly better than chance level. The unimodal model included the radial diffusivity feature and had an AUC of 0.642 (p = 0.032). The best multimodal model combined radial diffusivity and white matter density features (AUC = 0.684, p = 0.004). CONCLUSIONS: FTD mutation carriers can be separated from controls with a modest AUC even before symptom-onset, using a newly created carrier-control classification model, while this was not possible using a recent bvFTD classification model. A multimodal MRI-based classification score may therefore be a useful biomarker to aid earlier FTD diagnosis. The exclusive selection of white matter features in the best performing model suggests that the earliest FTD-related pathological processes occur in white matter. Elsevier 2019-03-01 /pmc/articles/PMC6543025/ /pubmed/30827922 http://dx.doi.org/10.1016/j.nicl.2019.101718 Text en © 2019 The Author(s) 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 Article
Feis, Rogier A.
Bouts, Mark J.R.J.
Panman, Jessica L.
Jiskoot, Lize C.
Dopper, Elise G.P.
Schouten, Tijn M.
de Vos, Frank
van der Grond, Jeroen
van Swieten, John C.
Rombouts, Serge A.R.B.
Single-subject classification of presymptomatic frontotemporal dementia mutation carriers using multimodal MRI
title Single-subject classification of presymptomatic frontotemporal dementia mutation carriers using multimodal MRI
title_full Single-subject classification of presymptomatic frontotemporal dementia mutation carriers using multimodal MRI
title_fullStr Single-subject classification of presymptomatic frontotemporal dementia mutation carriers using multimodal MRI
title_full_unstemmed Single-subject classification of presymptomatic frontotemporal dementia mutation carriers using multimodal MRI
title_short Single-subject classification of presymptomatic frontotemporal dementia mutation carriers using multimodal MRI
title_sort single-subject classification of presymptomatic frontotemporal dementia mutation carriers using multimodal mri
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543025/
https://www.ncbi.nlm.nih.gov/pubmed/30827922
http://dx.doi.org/10.1016/j.nicl.2019.101718
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