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Clinical and MRI models predicting amyloid deposition in progressive aphasia and apraxia of speech

Beta-amyloid (Aβ) deposition can be observed in primary progressive aphasia (PPA) and progressive apraxia of speech (PAOS). While it is typically associated with logopenic PPA, there are exceptions that make predicting Aβ status challenging based on clinical diagnosis alone. We aimed to determine wh...

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Autores principales: Whitwell, Jennifer L., Weigand, Stephen D., Duffy, Joseph R., Strand, Edythe A., Machulda, Mary M., Senjem, Matthew L., Gunter, Jeffrey L., Lowe, Val J., Jack, Clifford R., Josephs, Keith A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752814/
https://www.ncbi.nlm.nih.gov/pubmed/26937376
http://dx.doi.org/10.1016/j.nicl.2016.01.014
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author Whitwell, Jennifer L.
Weigand, Stephen D.
Duffy, Joseph R.
Strand, Edythe A.
Machulda, Mary M.
Senjem, Matthew L.
Gunter, Jeffrey L.
Lowe, Val J.
Jack, Clifford R.
Josephs, Keith A.
author_facet Whitwell, Jennifer L.
Weigand, Stephen D.
Duffy, Joseph R.
Strand, Edythe A.
Machulda, Mary M.
Senjem, Matthew L.
Gunter, Jeffrey L.
Lowe, Val J.
Jack, Clifford R.
Josephs, Keith A.
author_sort Whitwell, Jennifer L.
collection PubMed
description Beta-amyloid (Aβ) deposition can be observed in primary progressive aphasia (PPA) and progressive apraxia of speech (PAOS). While it is typically associated with logopenic PPA, there are exceptions that make predicting Aβ status challenging based on clinical diagnosis alone. We aimed to determine whether MRI regional volumes or clinical data could help predict Aβ deposition. One hundred and thirty-nine PPA (n = 97; 15 agrammatic, 53 logopenic, 13 semantic and 16 unclassified) and PAOS (n = 42) subjects were prospectively recruited into a cross-sectional study and underwent speech/language assessments, 3.0 T MRI and C11-Pittsburgh Compound B PET. The presence of Aβ was determined using a 1.5 SUVR cut-point. Atlas-based parcellation was used to calculate gray matter volumes of 42 regions-of-interest across the brain. Penalized binary logistic regression was utilized to determine what combination of MRI regions, and what combination of speech and language tests, best predicts Aβ (+) status. The optimal MRI model and optimal clinical model both performed comparably in their ability to accurately classify subjects according to Aβ status. MRI accurately classified 81% of subjects using 14 regions. Small left superior temporal and inferior parietal volumes and large left Broca's area volumes were particularly predictive of Aβ (+) status. Clinical scores accurately classified 83% of subjects using 12 tests. Phonological errors and repetition deficits, and absence of agrammatism and motor speech deficits were particularly predictive of Aβ (+) status. In comparison, clinical diagnosis was able to accurately classify 89% of subjects. However, the MRI model performed well in predicting Aβ deposition in unclassified PPA. Clinical diagnosis provides optimum prediction of Aβ status at the group level, although regional MRI measurements and speech and language testing also performed well and could have advantages in predicting Aβ status in unclassified PPA subjects.
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spelling pubmed-47528142016-03-02 Clinical and MRI models predicting amyloid deposition in progressive aphasia and apraxia of speech Whitwell, Jennifer L. Weigand, Stephen D. Duffy, Joseph R. Strand, Edythe A. Machulda, Mary M. Senjem, Matthew L. Gunter, Jeffrey L. Lowe, Val J. Jack, Clifford R. Josephs, Keith A. Neuroimage Clin Regular Article Beta-amyloid (Aβ) deposition can be observed in primary progressive aphasia (PPA) and progressive apraxia of speech (PAOS). While it is typically associated with logopenic PPA, there are exceptions that make predicting Aβ status challenging based on clinical diagnosis alone. We aimed to determine whether MRI regional volumes or clinical data could help predict Aβ deposition. One hundred and thirty-nine PPA (n = 97; 15 agrammatic, 53 logopenic, 13 semantic and 16 unclassified) and PAOS (n = 42) subjects were prospectively recruited into a cross-sectional study and underwent speech/language assessments, 3.0 T MRI and C11-Pittsburgh Compound B PET. The presence of Aβ was determined using a 1.5 SUVR cut-point. Atlas-based parcellation was used to calculate gray matter volumes of 42 regions-of-interest across the brain. Penalized binary logistic regression was utilized to determine what combination of MRI regions, and what combination of speech and language tests, best predicts Aβ (+) status. The optimal MRI model and optimal clinical model both performed comparably in their ability to accurately classify subjects according to Aβ status. MRI accurately classified 81% of subjects using 14 regions. Small left superior temporal and inferior parietal volumes and large left Broca's area volumes were particularly predictive of Aβ (+) status. Clinical scores accurately classified 83% of subjects using 12 tests. Phonological errors and repetition deficits, and absence of agrammatism and motor speech deficits were particularly predictive of Aβ (+) status. In comparison, clinical diagnosis was able to accurately classify 89% of subjects. However, the MRI model performed well in predicting Aβ deposition in unclassified PPA. Clinical diagnosis provides optimum prediction of Aβ status at the group level, although regional MRI measurements and speech and language testing also performed well and could have advantages in predicting Aβ status in unclassified PPA subjects. Elsevier 2016-01-20 /pmc/articles/PMC4752814/ /pubmed/26937376 http://dx.doi.org/10.1016/j.nicl.2016.01.014 Text en © 2016 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
Whitwell, Jennifer L.
Weigand, Stephen D.
Duffy, Joseph R.
Strand, Edythe A.
Machulda, Mary M.
Senjem, Matthew L.
Gunter, Jeffrey L.
Lowe, Val J.
Jack, Clifford R.
Josephs, Keith A.
Clinical and MRI models predicting amyloid deposition in progressive aphasia and apraxia of speech
title Clinical and MRI models predicting amyloid deposition in progressive aphasia and apraxia of speech
title_full Clinical and MRI models predicting amyloid deposition in progressive aphasia and apraxia of speech
title_fullStr Clinical and MRI models predicting amyloid deposition in progressive aphasia and apraxia of speech
title_full_unstemmed Clinical and MRI models predicting amyloid deposition in progressive aphasia and apraxia of speech
title_short Clinical and MRI models predicting amyloid deposition in progressive aphasia and apraxia of speech
title_sort clinical and mri models predicting amyloid deposition in progressive aphasia and apraxia of speech
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752814/
https://www.ncbi.nlm.nih.gov/pubmed/26937376
http://dx.doi.org/10.1016/j.nicl.2016.01.014
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