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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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. 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><subject>Aged</subject><subject>Atrophy</subject><subject>Brain - pathology</subject><subject>Care and treatment</subject><subject>Cerebellum</subject><subject>Cognition disorders</subject><subject>Cognition Disorders - etiology</subject><subject>Complications and side effects</subject><subject>Diagnosis</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medical examination</subject><subject>Middle Aged</subject><subject>Multiple System Atrophy - complications</subject><subject>Multiple System Atrophy - pathology</subject><subject>Multiple System Atrophy - psychology</subject><subject>Neocortex</subject><subject>Neuroimaging</subject><subject>Neuropsychological Tests</subject><subject>Original Paper</subject><subject>Parkinsonian Disorders - complications</subject><subject>Parkinsonian Disorders - pathology</subject><subject>Parkinsonian Disorders - psychology</subject><issn>1660-2854</issn><issn>1660-2862</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqN0s1rFDEUAPBBFFurB-8igYLoYWu-Z3Jctn4s1A9YPQ9p5s1u2kwyJhlh_3tTto5WepAcEl5-75FHXlU9J_iMEKHeYow5w0qwB9UxkRIvaCPpw_ks-FH1JKUrjKmqFXlcHVFJMcWSHVd2FbbeZvsT0HoYtY0D-Iy079A6J7TJcTJ5itqhVYgRnM6QkPUo7wB91fHa-hS81R5tpsu8HwGFHn2aXLajA7TZpwwDWuYYxt3-afWo1y7Bs9v9pPr-_t231cfFxZcP69XyYmEkVXnRGYlrQokgtdK9EJx0HDAD0XdEkp7XgqtGAxhDGya00Eoorg2vOZRI17GT6vWh7hjDjwlSbgebDDinPYQptaRusKC0ZP0Hxaq8ReCm0NN_6FWYoi-NFEWJqhtZqz9qqx201vchR21uirZLyWpGSPmmos7uUWV1MFgTPPS2xO8kvPorYQfa5V0Kbso2-HQXvjlAE0NKEfp2jHbQcd8S3N6MSjuPSrEvbzuaLgfoZvl7Ngp4cQDXOm4hzmDOP733-vP5-UG0Y9ezXwMDyi4</recordid><startdate>20150801</startdate><enddate>20150801</enddate><creator>Kim, Ji Sun</creator><creator>Yang, Jin-ju</creator><creator>Lee, Dong-Kyun</creator><creator>Lee, Jong-min</creator><creator>Youn, Jinyoung</creator><creator>Cho, Jin Whan</creator><general>S. 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pathology</topic><topic>Care and treatment</topic><topic>Cerebellum</topic><topic>Cognition disorders</topic><topic>Cognition Disorders - etiology</topic><topic>Complications and side effects</topic><topic>Diagnosis</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medical examination</topic><topic>Middle Aged</topic><topic>Multiple System Atrophy - complications</topic><topic>Multiple System Atrophy - pathology</topic><topic>Multiple System Atrophy - psychology</topic><topic>Neocortex</topic><topic>Neuroimaging</topic><topic>Neuropsychological Tests</topic><topic>Original Paper</topic><topic>Parkinsonian Disorders - complications</topic><topic>Parkinsonian Disorders - pathology</topic><topic>Parkinsonian Disorders - psychology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Neuro-degenerative diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Ji Sun</au><au>Yang, Jin-ju</au><au>Lee, Dong-Kyun</au><au>Lee, Jong-min</au><au>Youn, Jinyoung</au><au>Cho, Jin Whan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cognitive Impairment and Its Structural Correlates in the Parkinsonian Subtype of Multiple System Atrophy</atitle><jtitle>Neuro-degenerative diseases</jtitle><addtitle>Neurodegener Dis</addtitle><date>2015-08-01</date><risdate>2015</risdate><volume>15</volume><issue>5</issue><spage>294</spage><epage>300</epage><pages>294-300</pages><issn>1660-2854</issn><eissn>1660-2862</eissn><abstract>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.</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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