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Mild behavioral impairment in Parkinson's disease is associated with altered corticostriatal connectivity

BACKGROUND: Mild behavioral impairment (MBI) is a syndrome characterized by later life onset, sustained neuropsychiatric symptoms as a marker of dementia risk. In Parkinson's disease (PD), MBI has been associated with worse cognitive abilities and increased cortical atrophy. However, the circui...

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Autores principales: Lang, Stefan, Yoon, Eun Jin, Kibreab, Mekale, Kathol, Iris, Cheetham, Jenelle, Hammer, Tracy, Sarna, Justyna, Ismail, Zahinoor, Monchi, Oury
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7152681/
https://www.ncbi.nlm.nih.gov/pubmed/32279019
http://dx.doi.org/10.1016/j.nicl.2020.102252
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author Lang, Stefan
Yoon, Eun Jin
Kibreab, Mekale
Kathol, Iris
Cheetham, Jenelle
Hammer, Tracy
Sarna, Justyna
Ismail, Zahinoor
Monchi, Oury
author_facet Lang, Stefan
Yoon, Eun Jin
Kibreab, Mekale
Kathol, Iris
Cheetham, Jenelle
Hammer, Tracy
Sarna, Justyna
Ismail, Zahinoor
Monchi, Oury
author_sort Lang, Stefan
collection PubMed
description BACKGROUND: Mild behavioral impairment (MBI) is a syndrome characterized by later life onset, sustained neuropsychiatric symptoms as a marker of dementia risk. In Parkinson's disease (PD), MBI has been associated with worse cognitive abilities and increased cortical atrophy. However, the circuit level correlates of MBI have not been investigated in this population. Our objective was to investigate the relationship between MBI and corticostriatal connectivity in PD patients. This emphasis on corticostriatal connectivity was due to the significant role of these circuits in neuropsychiatric and cognitive symptoms across disease conditions. METHODS: Seventy-four non-demented patients with PD were administered the MBI-checklist, and classified as having high MBI (PD-MBI; n = 21) or low MBI scores (PD-noMBI; n = 53). Corticostriatal connectivity was assessed with both an atlas and seed-based analysis. The atlas analysis consisted of calculating the average connectivity between the striatal network and the default mode (DMN), central executive (CEN), and saliency networks (SAN). Structural measurements of cortical thickness and volume were also assessed. PD-MBI and PD-noMBI patients were compared, along with a group of age matched healthy control subjects (HC; n = 28). Subsequently, a seed analysis assessed the relationship of MBI scores with the connectivity of twelve seeds within the striatum while controlling for cognitive ability. A complementary analysis assessed the relationship between striatal connectivity and cognition, while controlling for MBI-C. RESULTS: PD-MBI demonstrated decreased connectivity between the striatum and both the DMN and SAN compared to PD-noMBI and HC. The decreased connectivity between the striatum and the SAN was explained partly by increased atrophy within the SAN in PD-MBI. The seed analysis revealed a relationship between higher MBI scores and lower connectivity of the left caudate head to the dorsal anterior cingulate cortex and left middle frontal gyrus. Higher MBI-C scores were also related to decreased connectivity of the right caudate head with the anterior cingulate cortex, precuneus, and left supramarginal gyrus, as well as increased connectivity to the left hippocampus and right cerebellar hemisphere. Caudate-precuneus connectivity was independently associated with both global behavioural and cognitive scores. CONCLUSION: These results suggest PD-MBI is associated with altered corticostriatal connectivity, particularly between the head of the caudate and cortical regions associated with the DMN and SAN. In particular, caudate-precuneus connectivity is associated with both global behavioral and cognitive symptoms in PD.
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spelling pubmed-71526812020-04-16 Mild behavioral impairment in Parkinson's disease is associated with altered corticostriatal connectivity Lang, Stefan Yoon, Eun Jin Kibreab, Mekale Kathol, Iris Cheetham, Jenelle Hammer, Tracy Sarna, Justyna Ismail, Zahinoor Monchi, Oury Neuroimage Clin Regular Article BACKGROUND: Mild behavioral impairment (MBI) is a syndrome characterized by later life onset, sustained neuropsychiatric symptoms as a marker of dementia risk. In Parkinson's disease (PD), MBI has been associated with worse cognitive abilities and increased cortical atrophy. However, the circuit level correlates of MBI have not been investigated in this population. Our objective was to investigate the relationship between MBI and corticostriatal connectivity in PD patients. This emphasis on corticostriatal connectivity was due to the significant role of these circuits in neuropsychiatric and cognitive symptoms across disease conditions. METHODS: Seventy-four non-demented patients with PD were administered the MBI-checklist, and classified as having high MBI (PD-MBI; n = 21) or low MBI scores (PD-noMBI; n = 53). Corticostriatal connectivity was assessed with both an atlas and seed-based analysis. The atlas analysis consisted of calculating the average connectivity between the striatal network and the default mode (DMN), central executive (CEN), and saliency networks (SAN). Structural measurements of cortical thickness and volume were also assessed. PD-MBI and PD-noMBI patients were compared, along with a group of age matched healthy control subjects (HC; n = 28). Subsequently, a seed analysis assessed the relationship of MBI scores with the connectivity of twelve seeds within the striatum while controlling for cognitive ability. A complementary analysis assessed the relationship between striatal connectivity and cognition, while controlling for MBI-C. RESULTS: PD-MBI demonstrated decreased connectivity between the striatum and both the DMN and SAN compared to PD-noMBI and HC. The decreased connectivity between the striatum and the SAN was explained partly by increased atrophy within the SAN in PD-MBI. The seed analysis revealed a relationship between higher MBI scores and lower connectivity of the left caudate head to the dorsal anterior cingulate cortex and left middle frontal gyrus. Higher MBI-C scores were also related to decreased connectivity of the right caudate head with the anterior cingulate cortex, precuneus, and left supramarginal gyrus, as well as increased connectivity to the left hippocampus and right cerebellar hemisphere. Caudate-precuneus connectivity was independently associated with both global behavioural and cognitive scores. CONCLUSION: These results suggest PD-MBI is associated with altered corticostriatal connectivity, particularly between the head of the caudate and cortical regions associated with the DMN and SAN. In particular, caudate-precuneus connectivity is associated with both global behavioral and cognitive symptoms in PD. Elsevier 2020-03-27 /pmc/articles/PMC7152681/ /pubmed/32279019 http://dx.doi.org/10.1016/j.nicl.2020.102252 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Article
Lang, Stefan
Yoon, Eun Jin
Kibreab, Mekale
Kathol, Iris
Cheetham, Jenelle
Hammer, Tracy
Sarna, Justyna
Ismail, Zahinoor
Monchi, Oury
Mild behavioral impairment in Parkinson's disease is associated with altered corticostriatal connectivity
title Mild behavioral impairment in Parkinson's disease is associated with altered corticostriatal connectivity
title_full Mild behavioral impairment in Parkinson's disease is associated with altered corticostriatal connectivity
title_fullStr Mild behavioral impairment in Parkinson's disease is associated with altered corticostriatal connectivity
title_full_unstemmed Mild behavioral impairment in Parkinson's disease is associated with altered corticostriatal connectivity
title_short Mild behavioral impairment in Parkinson's disease is associated with altered corticostriatal connectivity
title_sort mild behavioral impairment in parkinson's disease is associated with altered corticostriatal connectivity
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7152681/
https://www.ncbi.nlm.nih.gov/pubmed/32279019
http://dx.doi.org/10.1016/j.nicl.2020.102252
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