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Cortical thinning pattern according to differential nigrosome involvement in patients with Parkinson’s disease
The pathological hallmark of Parkinson’s disease (PD) is the progressive degeneration of dopaminergic neurons in the substantia nigra pars compacta, where the dopaminergic neurons form five clusters called nigrosomes 1–5 (N1–N5). N1 is the largest and considered to be the most affected by PD, follow...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7451416/ https://www.ncbi.nlm.nih.gov/pubmed/32828029 http://dx.doi.org/10.1016/j.nicl.2020.102382 |
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author | Shin, Na-Young Kim, Bo-Hyun Yun, Eunkyeong Yoon, Uicheul Lee, Jong-Min Sung, Young Hee Kim, Eung Yeop |
author_facet | Shin, Na-Young Kim, Bo-Hyun Yun, Eunkyeong Yoon, Uicheul Lee, Jong-Min Sung, Young Hee Kim, Eung Yeop |
author_sort | Shin, Na-Young |
collection | PubMed |
description | The pathological hallmark of Parkinson’s disease (PD) is the progressive degeneration of dopaminergic neurons in the substantia nigra pars compacta, where the dopaminergic neurons form five clusters called nigrosomes 1–5 (N1–N5). N1 is the largest and considered to be the most affected by PD, followed by N2, N4, N3, and N5. Recently, an MRI study suggested a sequential progression of loss from N1 to N4. As the extent of cortical thinning widens as PD progresses, we aimed to define cortical thinning patterns according to the differential involvement of N1 and N4 in PD patients. Cortical thickness was analyzed in 83 PD patients (29 with N1 loss on at least one side of the brain, but no N4 loss; and 54 with N4 loss on at least one side) and 35 healthy subjects with age, sex, disease duration, and intracranial volume as covariates. On patient-wise analysis, for areas with more cortical thinning than the controls, PD patients with N4 loss had wider cortical thinning involving more dorsolateral prefrontal cortex and temporal areas than PD patients with only N1 loss, but cortical thinning did not significantly differ between these two patient groups. However, cortical thinning was more apparent in hemisphere-level analysis with statistically significant clusters being found more in hemispheres with N4 loss than hemispheres with N1 loss in PD patients compared to normal hemispheres of the controls. Cortical thinning occurred in a similar propagation pattern to that seen with PD progression, supporting past hypotheses on the sequential progression of nigrosome loss from N1 to N4. |
format | Online Article Text |
id | pubmed-7451416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-74514162020-09-02 Cortical thinning pattern according to differential nigrosome involvement in patients with Parkinson’s disease Shin, Na-Young Kim, Bo-Hyun Yun, Eunkyeong Yoon, Uicheul Lee, Jong-Min Sung, Young Hee Kim, Eung Yeop Neuroimage Clin Regular Article The pathological hallmark of Parkinson’s disease (PD) is the progressive degeneration of dopaminergic neurons in the substantia nigra pars compacta, where the dopaminergic neurons form five clusters called nigrosomes 1–5 (N1–N5). N1 is the largest and considered to be the most affected by PD, followed by N2, N4, N3, and N5. Recently, an MRI study suggested a sequential progression of loss from N1 to N4. As the extent of cortical thinning widens as PD progresses, we aimed to define cortical thinning patterns according to the differential involvement of N1 and N4 in PD patients. Cortical thickness was analyzed in 83 PD patients (29 with N1 loss on at least one side of the brain, but no N4 loss; and 54 with N4 loss on at least one side) and 35 healthy subjects with age, sex, disease duration, and intracranial volume as covariates. On patient-wise analysis, for areas with more cortical thinning than the controls, PD patients with N4 loss had wider cortical thinning involving more dorsolateral prefrontal cortex and temporal areas than PD patients with only N1 loss, but cortical thinning did not significantly differ between these two patient groups. However, cortical thinning was more apparent in hemisphere-level analysis with statistically significant clusters being found more in hemispheres with N4 loss than hemispheres with N1 loss in PD patients compared to normal hemispheres of the controls. Cortical thinning occurred in a similar propagation pattern to that seen with PD progression, supporting past hypotheses on the sequential progression of nigrosome loss from N1 to N4. Elsevier 2020-08-13 /pmc/articles/PMC7451416/ /pubmed/32828029 http://dx.doi.org/10.1016/j.nicl.2020.102382 Text en © 2020 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 | Regular Article Shin, Na-Young Kim, Bo-Hyun Yun, Eunkyeong Yoon, Uicheul Lee, Jong-Min Sung, Young Hee Kim, Eung Yeop Cortical thinning pattern according to differential nigrosome involvement in patients with Parkinson’s disease |
title | Cortical thinning pattern according to differential nigrosome involvement in patients with Parkinson’s disease |
title_full | Cortical thinning pattern according to differential nigrosome involvement in patients with Parkinson’s disease |
title_fullStr | Cortical thinning pattern according to differential nigrosome involvement in patients with Parkinson’s disease |
title_full_unstemmed | Cortical thinning pattern according to differential nigrosome involvement in patients with Parkinson’s disease |
title_short | Cortical thinning pattern according to differential nigrosome involvement in patients with Parkinson’s disease |
title_sort | cortical thinning pattern according to differential nigrosome involvement in patients with parkinson’s disease |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7451416/ https://www.ncbi.nlm.nih.gov/pubmed/32828029 http://dx.doi.org/10.1016/j.nicl.2020.102382 |
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