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Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes
OBJECTIVE: Brainstem segmentation has been useful in identifying potential imaging biomarkers for diagnosis and progression in atypical parkinsonian syndromes (APS). However, the majority of work has been performed using manual segmentation, which is time consuming for large cohorts. METHODS: We inv...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Movement Disorder Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987532/ https://www.ncbi.nlm.nih.gov/pubmed/31552724 http://dx.doi.org/10.14802/jmd.19030 |
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author | Bocchetta, Martina Iglesias, Juan Eugenio Chelban, Viorica Jabbari, Edwin Lamb, Ruth Russell, Lucy L. Greaves, Caroline V. Neason, Mollie Cash, David M. Thomas, David L. Warren, Jason D. Woodside, John Houlden, Henry Morris, Huw R. Rohrer, Jonathan D. |
author_facet | Bocchetta, Martina Iglesias, Juan Eugenio Chelban, Viorica Jabbari, Edwin Lamb, Ruth Russell, Lucy L. Greaves, Caroline V. Neason, Mollie Cash, David M. Thomas, David L. Warren, Jason D. Woodside, John Houlden, Henry Morris, Huw R. Rohrer, Jonathan D. |
author_sort | Bocchetta, Martina |
collection | PubMed |
description | OBJECTIVE: Brainstem segmentation has been useful in identifying potential imaging biomarkers for diagnosis and progression in atypical parkinsonian syndromes (APS). However, the majority of work has been performed using manual segmentation, which is time consuming for large cohorts. METHODS: We investigated brainstem involvement in APS using an automated method. We measured the volume of the medulla, pons, superior cerebellar peduncle (SCP) and midbrain from T1-weighted MRIs in 67 patients and 42 controls. Diagnoses were corticobasal syndrome (CBS, n = 14), multiple system atrophy (MSA, n = 16: 8 with parkinsonian syndrome, MSA-P; 8 with cerebellar syndrome, MSA-C), progressive supranuclear palsy with a Richardson’s syndrome (PSP-RS, n = 12), variant PSP (n = 18), and APS not otherwise specified (APS-NOS, n = 7). RESULTS: All brainstem regions were smaller in MSA-C (19–42% volume difference, p < 0.0005) and in both PSP groups (18–33%, p < 0.0005) than in controls. MSA-P showed lower volumes in all regions except the SCP (15–26%, p < 0.0005). The most affected region in MSA-C and MSA-P was the pons (42% and 26%, respectively), while the most affected regions in both the PSP-RS and variant PSP groups were the SCP (33% and 23%, respectively) and midbrain (26% and 24%, respectively). The brainstem was less affected in CBS, but nonetheless, the pons (14%, p < 0.0005), midbrain (14%, p < 0.0005) and medulla (10%, p = 0.001) were significantly smaller in CBS than in controls. The brainstem was unaffected in APS-NOS. CONCLUSION: Automated methods can accurately quantify the involvement of brainstem structures in APS. This will be important in future trials with large patient numbers where manual segmentation is unfeasible. |
format | Online Article Text |
id | pubmed-6987532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Korean Movement Disorder Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-69875322020-02-14 Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes Bocchetta, Martina Iglesias, Juan Eugenio Chelban, Viorica Jabbari, Edwin Lamb, Ruth Russell, Lucy L. Greaves, Caroline V. Neason, Mollie Cash, David M. Thomas, David L. Warren, Jason D. Woodside, John Houlden, Henry Morris, Huw R. Rohrer, Jonathan D. J Mov Disord Original Article OBJECTIVE: Brainstem segmentation has been useful in identifying potential imaging biomarkers for diagnosis and progression in atypical parkinsonian syndromes (APS). However, the majority of work has been performed using manual segmentation, which is time consuming for large cohorts. METHODS: We investigated brainstem involvement in APS using an automated method. We measured the volume of the medulla, pons, superior cerebellar peduncle (SCP) and midbrain from T1-weighted MRIs in 67 patients and 42 controls. Diagnoses were corticobasal syndrome (CBS, n = 14), multiple system atrophy (MSA, n = 16: 8 with parkinsonian syndrome, MSA-P; 8 with cerebellar syndrome, MSA-C), progressive supranuclear palsy with a Richardson’s syndrome (PSP-RS, n = 12), variant PSP (n = 18), and APS not otherwise specified (APS-NOS, n = 7). RESULTS: All brainstem regions were smaller in MSA-C (19–42% volume difference, p < 0.0005) and in both PSP groups (18–33%, p < 0.0005) than in controls. MSA-P showed lower volumes in all regions except the SCP (15–26%, p < 0.0005). The most affected region in MSA-C and MSA-P was the pons (42% and 26%, respectively), while the most affected regions in both the PSP-RS and variant PSP groups were the SCP (33% and 23%, respectively) and midbrain (26% and 24%, respectively). The brainstem was less affected in CBS, but nonetheless, the pons (14%, p < 0.0005), midbrain (14%, p < 0.0005) and medulla (10%, p = 0.001) were significantly smaller in CBS than in controls. The brainstem was unaffected in APS-NOS. CONCLUSION: Automated methods can accurately quantify the involvement of brainstem structures in APS. This will be important in future trials with large patient numbers where manual segmentation is unfeasible. The Korean Movement Disorder Society 2020-01 2019-09-26 /pmc/articles/PMC6987532/ /pubmed/31552724 http://dx.doi.org/10.14802/jmd.19030 Text en Copyright © 2020 The Korean Movement Disorder Society This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Bocchetta, Martina Iglesias, Juan Eugenio Chelban, Viorica Jabbari, Edwin Lamb, Ruth Russell, Lucy L. Greaves, Caroline V. Neason, Mollie Cash, David M. Thomas, David L. Warren, Jason D. Woodside, John Houlden, Henry Morris, Huw R. Rohrer, Jonathan D. Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes |
title | Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes |
title_full | Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes |
title_fullStr | Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes |
title_full_unstemmed | Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes |
title_short | Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes |
title_sort | automated brainstem segmentation detects differential involvement in atypical parkinsonian syndromes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6987532/ https://www.ncbi.nlm.nih.gov/pubmed/31552724 http://dx.doi.org/10.14802/jmd.19030 |
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