Cognitive Impairment and Its Structural Correlates in the Parkinsonian Subtype of Multiple System Atrophy

Background/Aims: Previous studies indicate that patients with the parkinsonian subtype of multiple system atrophy (MSA-P) experience cognitive impairment. This study aimed to identify the existence of cognitive impairments and the different topographic patterns of morphological changes in MSA-P by m...

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Veröffentlicht in:Neuro-degenerative diseases 2015-08, Vol.15 (5), p.294-300
Hauptverfasser: Kim, Ji Sun, Yang, Jin-ju, Lee, Dong-Kyun, Lee, Jong-min, Youn, Jinyoung, Cho, Jin Whan
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container_end_page 300
container_issue 5
container_start_page 294
container_title Neuro-degenerative diseases
container_volume 15
creator Kim, Ji Sun
Yang, Jin-ju
Lee, Dong-Kyun
Lee, Jong-min
Youn, Jinyoung
Cho, Jin Whan
description Background/Aims: Previous studies indicate that patients with the parkinsonian subtype of multiple system atrophy (MSA-P) experience cognitive impairment. This study aimed to identify the existence of cognitive impairments and the different topographic patterns of morphological changes in MSA-P by means of imaging analysis, and also whether these morphological changes could be associated with cognitive dysfunctions in MSA-P. Methods: We recruited 15 nondemented probable MSA-P patients and 32 normal controls (NC) for neuropsychological testing and MRI. We analyzed morphological changes using cortical thickness analysis, voxel-based morphometry (VBM) and cerebellar volumetry. Multiple linear regression analysis was performed to evaluate the correlation of each cognitive score with the mean thickness of significant cortical-thinning clusters, mean gray-matter density of VBM clusters and cerebellar volume. Results: The scores on the Digit Span Test, the Seoul Verbal Learning Test (immediate and delayed), the phonemic Controlled Oral Word Association Test and the Stroop color test were significantly lower in the MSA-P group than in the NC group. We found two clusters exhibiting significant cortical thinning in the right paracentral lobule and parahippocampal gyrus. VBM analysis revealed significant gray-matter atrophy in the MSA-P group in the bilateral basal ganglia, cerebellum and temporal and frontal cortical areas. Multiple linear regression analysis demonstrated that cognitive dysfunction correlated significantly with thinning in the neocortex, cerebellum and striatum. Conclusions: Our data demonstrate that cortical and cerebellar atrophy and striatal degeneration are associated with cognitive impairment in patients with MSA-P.
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This study aimed to identify the existence of cognitive impairments and the different topographic patterns of morphological changes in MSA-P by means of imaging analysis, and also whether these morphological changes could be associated with cognitive dysfunctions in MSA-P. Methods: We recruited 15 nondemented probable MSA-P patients and 32 normal controls (NC) for neuropsychological testing and MRI. We analyzed morphological changes using cortical thickness analysis, voxel-based morphometry (VBM) and cerebellar volumetry. Multiple linear regression analysis was performed to evaluate the correlation of each cognitive score with the mean thickness of significant cortical-thinning clusters, mean gray-matter density of VBM clusters and cerebellar volume. Results: The scores on the Digit Span Test, the Seoul Verbal Learning Test (immediate and delayed), the phonemic Controlled Oral Word Association Test and the Stroop color test were significantly lower in the MSA-P group than in the NC group. We found two clusters exhibiting significant cortical thinning in the right paracentral lobule and parahippocampal gyrus. VBM analysis revealed significant gray-matter atrophy in the MSA-P group in the bilateral basal ganglia, cerebellum and temporal and frontal cortical areas. Multiple linear regression analysis demonstrated that cognitive dysfunction correlated significantly with thinning in the neocortex, cerebellum and striatum. Conclusions: Our data demonstrate that cortical and cerebellar atrophy and striatal degeneration are associated with cognitive impairment in patients with MSA-P.</description><identifier>ISSN: 1660-2854</identifier><identifier>EISSN: 1660-2862</identifier><identifier>DOI: 10.1159/000430953</identifier><identifier>PMID: 26202063</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Aged ; Atrophy ; Brain - pathology ; Care and treatment ; Cerebellum ; Cognition disorders ; Cognition Disorders - etiology ; Complications and side effects ; Diagnosis ; Female ; Humans ; Male ; Medical examination ; Middle Aged ; Multiple System Atrophy - complications ; Multiple System Atrophy - pathology ; Multiple System Atrophy - psychology ; Neocortex ; Neuroimaging ; Neuropsychological Tests ; Original Paper ; Parkinsonian Disorders - complications ; Parkinsonian Disorders - pathology ; Parkinsonian Disorders - psychology</subject><ispartof>Neuro-degenerative diseases, 2015-08, Vol.15 (5), p.294-300</ispartof><rights>2015 S. Karger AG, Basel</rights><rights>2015 S. Karger AG, Basel.</rights><rights>COPYRIGHT 2015 S. Karger AG</rights><rights>Copyright S. Karger AG Aug 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c629t-dc6071215179af5541d4e03e5fd161f475498aeecc2835a5a9594ac474ec28dd3</citedby><cites>FETCH-LOGICAL-c629t-dc6071215179af5541d4e03e5fd161f475498aeecc2835a5a9594ac474ec28dd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,2430,27928,27929</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26202063$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Ji Sun</creatorcontrib><creatorcontrib>Yang, Jin-ju</creatorcontrib><creatorcontrib>Lee, Dong-Kyun</creatorcontrib><creatorcontrib>Lee, Jong-min</creatorcontrib><creatorcontrib>Youn, Jinyoung</creatorcontrib><creatorcontrib>Cho, Jin Whan</creatorcontrib><title>Cognitive Impairment and Its Structural Correlates in the Parkinsonian Subtype of Multiple System Atrophy</title><title>Neuro-degenerative diseases</title><addtitle>Neurodegener Dis</addtitle><description>Background/Aims: Previous studies indicate that patients with the parkinsonian subtype of multiple system atrophy (MSA-P) experience cognitive impairment. 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This study aimed to identify the existence of cognitive impairments and the different topographic patterns of morphological changes in MSA-P by means of imaging analysis, and also whether these morphological changes could be associated with cognitive dysfunctions in MSA-P. Methods: We recruited 15 nondemented probable MSA-P patients and 32 normal controls (NC) for neuropsychological testing and MRI. We analyzed morphological changes using cortical thickness analysis, voxel-based morphometry (VBM) and cerebellar volumetry. Multiple linear regression analysis was performed to evaluate the correlation of each cognitive score with the mean thickness of significant cortical-thinning clusters, mean gray-matter density of VBM clusters and cerebellar volume. Results: The scores on the Digit Span Test, the Seoul Verbal Learning Test (immediate and delayed), the phonemic Controlled Oral Word Association Test and the Stroop color test were significantly lower in the MSA-P group than in the NC group. We found two clusters exhibiting significant cortical thinning in the right paracentral lobule and parahippocampal gyrus. VBM analysis revealed significant gray-matter atrophy in the MSA-P group in the bilateral basal ganglia, cerebellum and temporal and frontal cortical areas. Multiple linear regression analysis demonstrated that cognitive dysfunction correlated significantly with thinning in the neocortex, cerebellum and striatum. Conclusions: Our data demonstrate that cortical and cerebellar atrophy and striatal degeneration are associated with cognitive impairment in patients with MSA-P.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>26202063</pmid><doi>10.1159/000430953</doi><tpages>7</tpages></addata></record>
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subjects Aged
Atrophy
Brain - pathology
Care and treatment
Cerebellum
Cognition disorders
Cognition Disorders - etiology
Complications and side effects
Diagnosis
Female
Humans
Male
Medical examination
Middle Aged
Multiple System Atrophy - complications
Multiple System Atrophy - pathology
Multiple System Atrophy - psychology
Neocortex
Neuroimaging
Neuropsychological Tests
Original Paper
Parkinsonian Disorders - complications
Parkinsonian Disorders - pathology
Parkinsonian Disorders - psychology
title Cognitive Impairment and Its Structural Correlates in the Parkinsonian Subtype of Multiple System Atrophy
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