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Associations of hippocampal subfields in the progression of cognitive decline related to Parkinson's disease

OBJECTIVE: Hippocampal atrophy has been associated with mild cognitive impairment (MCI) in Parkinson's disease (PD). However, literature on how hippocampal atrophy affects the pathophysiology of cognitive impairment in PD has been limited. Previous studies assessed the hippocampus as an entire...

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Autores principales: Foo, Heidi, Mak, Elijah, Chander, Russell Jude, Ng, Aloysius, Au, Wing Lok, Sitoh, Yih Yian, Tan, Louis C.S., Kandiah, Nagaendran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226850/
https://www.ncbi.nlm.nih.gov/pubmed/28116240
http://dx.doi.org/10.1016/j.nicl.2016.12.008
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author Foo, Heidi
Mak, Elijah
Chander, Russell Jude
Ng, Aloysius
Au, Wing Lok
Sitoh, Yih Yian
Tan, Louis C.S.
Kandiah, Nagaendran
author_facet Foo, Heidi
Mak, Elijah
Chander, Russell Jude
Ng, Aloysius
Au, Wing Lok
Sitoh, Yih Yian
Tan, Louis C.S.
Kandiah, Nagaendran
author_sort Foo, Heidi
collection PubMed
description OBJECTIVE: Hippocampal atrophy has been associated with mild cognitive impairment (MCI) in Parkinson's disease (PD). However, literature on how hippocampal atrophy affects the pathophysiology of cognitive impairment in PD has been limited. Previous studies assessed the hippocampus as an entire entity instead of their individual subregions. We studied the progression of cognitive status in PD subjects over 18 in relation to hippocampal subfields atrophy. METHODS: 65 PD subjects were included. Using the MDS task force criteria, PD subjects were classified as either having no cognitive impairment (PD-NCI) or PD-MCI. We extended the study by investigating the hippocampal subfields atrophy patterns in those who converted from PD-NCI to PD-MCI (PD-converters) compared to those who remained cognitively stable (PD-stable) over 18 months. Freesurfer 6.0 was used to perform the automated segmentation of the hippocampus into thirteen subregions. RESULTS: PD-MCI showed lower baseline volumes in the left fimbria, right CA1, and right HATA; and lower global cognition scores compared to PD-NCI. Baseline right CA1 was also correlated with baseline attention. Over 18 months, decline in volumes of CA2–3 and episodic memory were also seen in PD-converters compared to PD-stable. Baseline volumes of GC-DG, right CA4, left parasubiculum, and left HATA were predictive of the conversion from PD-NCI to PD-MCI. CONCLUSION: The findings from this study add to the anatomical knowledge of hippocampal subregions in PD, allowing us to understand the unique functional contribution of each subfield. Structural changes in the hippocampus subfields could be early biomarkers to detect cognitive impairment in PD.
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spelling pubmed-52268502017-01-23 Associations of hippocampal subfields in the progression of cognitive decline related to Parkinson's disease Foo, Heidi Mak, Elijah Chander, Russell Jude Ng, Aloysius Au, Wing Lok Sitoh, Yih Yian Tan, Louis C.S. Kandiah, Nagaendran Neuroimage Clin Regular Article OBJECTIVE: Hippocampal atrophy has been associated with mild cognitive impairment (MCI) in Parkinson's disease (PD). However, literature on how hippocampal atrophy affects the pathophysiology of cognitive impairment in PD has been limited. Previous studies assessed the hippocampus as an entire entity instead of their individual subregions. We studied the progression of cognitive status in PD subjects over 18 in relation to hippocampal subfields atrophy. METHODS: 65 PD subjects were included. Using the MDS task force criteria, PD subjects were classified as either having no cognitive impairment (PD-NCI) or PD-MCI. We extended the study by investigating the hippocampal subfields atrophy patterns in those who converted from PD-NCI to PD-MCI (PD-converters) compared to those who remained cognitively stable (PD-stable) over 18 months. Freesurfer 6.0 was used to perform the automated segmentation of the hippocampus into thirteen subregions. RESULTS: PD-MCI showed lower baseline volumes in the left fimbria, right CA1, and right HATA; and lower global cognition scores compared to PD-NCI. Baseline right CA1 was also correlated with baseline attention. Over 18 months, decline in volumes of CA2–3 and episodic memory were also seen in PD-converters compared to PD-stable. Baseline volumes of GC-DG, right CA4, left parasubiculum, and left HATA were predictive of the conversion from PD-NCI to PD-MCI. CONCLUSION: The findings from this study add to the anatomical knowledge of hippocampal subregions in PD, allowing us to understand the unique functional contribution of each subfield. Structural changes in the hippocampus subfields could be early biomarkers to detect cognitive impairment in PD. Elsevier 2016-12-12 /pmc/articles/PMC5226850/ /pubmed/28116240 http://dx.doi.org/10.1016/j.nicl.2016.12.008 Text en © 2017 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
Foo, Heidi
Mak, Elijah
Chander, Russell Jude
Ng, Aloysius
Au, Wing Lok
Sitoh, Yih Yian
Tan, Louis C.S.
Kandiah, Nagaendran
Associations of hippocampal subfields in the progression of cognitive decline related to Parkinson's disease
title Associations of hippocampal subfields in the progression of cognitive decline related to Parkinson's disease
title_full Associations of hippocampal subfields in the progression of cognitive decline related to Parkinson's disease
title_fullStr Associations of hippocampal subfields in the progression of cognitive decline related to Parkinson's disease
title_full_unstemmed Associations of hippocampal subfields in the progression of cognitive decline related to Parkinson's disease
title_short Associations of hippocampal subfields in the progression of cognitive decline related to Parkinson's disease
title_sort associations of hippocampal subfields in the progression of cognitive decline related to parkinson's disease
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226850/
https://www.ncbi.nlm.nih.gov/pubmed/28116240
http://dx.doi.org/10.1016/j.nicl.2016.12.008
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