Structural connectivity in multiple sclerosis and modeling of disconnection
Background: Multiple sclerosis (MS) is characterized by focal white matter damage, and when the brain is modeled as a network, lesions can be treated as disconnection events. Objective: To evaluate whether modeling disconnection caused by lesions helps explain motor and cognitive impairment in MS. M...
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Veröffentlicht in: | Multiple sclerosis 2020-02, Vol.26 (2), p.220-232 |
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creator | Pagani, Elisabetta Rocca, Maria A De Meo, Ermelinda Horsfield, Mark A Colombo, Bruno Rodegher, Mariaemma Comi, Giancarlo Filippi, Massimo |
description | Background:
Multiple sclerosis (MS) is characterized by focal white matter damage, and when the brain is modeled as a network, lesions can be treated as disconnection events.
Objective:
To evaluate whether modeling disconnection caused by lesions helps explain motor and cognitive impairment in MS.
Methods:
Pathways connecting 116 cortical regions were reconstructed with magnetic resonance imaging (MRI) tractography from diffusion tensors averaged across healthy controls (HCs); maps of pathways were applied to 227 relapse-onset MS patients and 50 HCs to derive structural connectivity. Then, the likelihood of individual connections passing through lesions was used to model disconnection. Patients were grouped according to clinical phenotype (113 relapsing-remitting multiple sclerosis (RRMS), 69 secondary progressive multiple sclerosis (SPMS), 45 benign MS), and then network metrics were compared between groups (analysis of variance (ANOVA)) and correlated with motor and cognitive scores (linear regression).
Results:
Global metrics differentiated RRMS from SPMS and benign MS patients, but not benign from SPMS patients. Nodal connectivity strength replicated global results. After disconnection, few nodes were significantly different between benign MS and RRMS patients. Correlations revealed nodes pertinent to motor and cognitive dysfunctions; these became slightly stronger after disconnection.
Conclusion:
Connectivity did not change greatly after modeled disconnection, suggesting that the brain network is robust against damage caused by MS lesions. |
doi_str_mv | 10.1177/1352458518820759 |
format | Article |
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Multiple sclerosis (MS) is characterized by focal white matter damage, and when the brain is modeled as a network, lesions can be treated as disconnection events.
Objective:
To evaluate whether modeling disconnection caused by lesions helps explain motor and cognitive impairment in MS.
Methods:
Pathways connecting 116 cortical regions were reconstructed with magnetic resonance imaging (MRI) tractography from diffusion tensors averaged across healthy controls (HCs); maps of pathways were applied to 227 relapse-onset MS patients and 50 HCs to derive structural connectivity. Then, the likelihood of individual connections passing through lesions was used to model disconnection. Patients were grouped according to clinical phenotype (113 relapsing-remitting multiple sclerosis (RRMS), 69 secondary progressive multiple sclerosis (SPMS), 45 benign MS), and then network metrics were compared between groups (analysis of variance (ANOVA)) and correlated with motor and cognitive scores (linear regression).
Results:
Global metrics differentiated RRMS from SPMS and benign MS patients, but not benign from SPMS patients. Nodal connectivity strength replicated global results. After disconnection, few nodes were significantly different between benign MS and RRMS patients. Correlations revealed nodes pertinent to motor and cognitive dysfunctions; these became slightly stronger after disconnection.
Conclusion:
Connectivity did not change greatly after modeled disconnection, suggesting that the brain network is robust against damage caused by MS lesions.</description><identifier>ISSN: 1352-4585</identifier><identifier>EISSN: 1477-0970</identifier><identifier>DOI: 10.1177/1352458518820759</identifier><identifier>PMID: 30625050</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Adolescent ; Adult ; Aged ; Benign ; Brain injury ; Brain Mapping - methods ; Cerebral cortex ; Cognitive ability ; Diffusion Magnetic Resonance Imaging - methods ; Female ; Humans ; Image Interpretation, Computer-Assisted - methods ; Lesions ; Magnetic resonance imaging ; Male ; Middle Aged ; Multiple sclerosis ; Multiple Sclerosis - diagnostic imaging ; Multiple Sclerosis - physiopathology ; Nerve Net - diagnostic imaging ; Nerve Net - physiopathology ; Neural networks ; Neural Pathways - diagnostic imaging ; Neural Pathways - physiopathology ; Neuroimaging ; Phenotypes ; Substantia alba ; Variance analysis ; Young Adult</subject><ispartof>Multiple sclerosis, 2020-02, Vol.26 (2), p.220-232</ispartof><rights>The Author(s), 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-537d0ff77ecbd6f8042f41d8837e7675f8c2045123cccf4fa5ce1bfc0986c2383</citedby><cites>FETCH-LOGICAL-c365t-537d0ff77ecbd6f8042f41d8837e7675f8c2045123cccf4fa5ce1bfc0986c2383</cites><orcidid>0000-0003-2358-4320 ; 0000-0002-5485-0479</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/1352458518820759$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/1352458518820759$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30625050$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pagani, Elisabetta</creatorcontrib><creatorcontrib>Rocca, Maria A</creatorcontrib><creatorcontrib>De Meo, Ermelinda</creatorcontrib><creatorcontrib>Horsfield, Mark A</creatorcontrib><creatorcontrib>Colombo, Bruno</creatorcontrib><creatorcontrib>Rodegher, Mariaemma</creatorcontrib><creatorcontrib>Comi, Giancarlo</creatorcontrib><creatorcontrib>Filippi, Massimo</creatorcontrib><title>Structural connectivity in multiple sclerosis and modeling of disconnection</title><title>Multiple sclerosis</title><addtitle>Mult Scler</addtitle><description>Background:
Multiple sclerosis (MS) is characterized by focal white matter damage, and when the brain is modeled as a network, lesions can be treated as disconnection events.
Objective:
To evaluate whether modeling disconnection caused by lesions helps explain motor and cognitive impairment in MS.
Methods:
Pathways connecting 116 cortical regions were reconstructed with magnetic resonance imaging (MRI) tractography from diffusion tensors averaged across healthy controls (HCs); maps of pathways were applied to 227 relapse-onset MS patients and 50 HCs to derive structural connectivity. Then, the likelihood of individual connections passing through lesions was used to model disconnection. Patients were grouped according to clinical phenotype (113 relapsing-remitting multiple sclerosis (RRMS), 69 secondary progressive multiple sclerosis (SPMS), 45 benign MS), and then network metrics were compared between groups (analysis of variance (ANOVA)) and correlated with motor and cognitive scores (linear regression).
Results:
Global metrics differentiated RRMS from SPMS and benign MS patients, but not benign from SPMS patients. Nodal connectivity strength replicated global results. After disconnection, few nodes were significantly different between benign MS and RRMS patients. Correlations revealed nodes pertinent to motor and cognitive dysfunctions; these became slightly stronger after disconnection.
Conclusion:
Connectivity did not change greatly after modeled disconnection, suggesting that the brain network is robust against damage caused by MS lesions.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Benign</subject><subject>Brain injury</subject><subject>Brain Mapping - methods</subject><subject>Cerebral cortex</subject><subject>Cognitive ability</subject><subject>Diffusion Magnetic Resonance Imaging - methods</subject><subject>Female</subject><subject>Humans</subject><subject>Image Interpretation, Computer-Assisted - methods</subject><subject>Lesions</subject><subject>Magnetic resonance imaging</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - diagnostic imaging</subject><subject>Multiple Sclerosis - physiopathology</subject><subject>Nerve Net - diagnostic imaging</subject><subject>Nerve Net - physiopathology</subject><subject>Neural networks</subject><subject>Neural Pathways - diagnostic imaging</subject><subject>Neural Pathways - physiopathology</subject><subject>Neuroimaging</subject><subject>Phenotypes</subject><subject>Substantia alba</subject><subject>Variance analysis</subject><subject>Young Adult</subject><issn>1352-4585</issn><issn>1477-0970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1LAzEQxYMotlbvnmTBi5fVydcme5TiFxY8qOdlm03KlmxSk12h_70pbRUKnmZgfu_NzEPoEsMtxkLcYcoJ45JjKQkIXh6hMWZC5FAKOE59Gueb-QidxbgEACEoP0UjCgXhwGGMXt_7MKh-CLXNlHdOq779bvt11rqsG2zfrqzOorI6-NjGrHZN1vlG29YtMm-ypo17lXfn6MTUNuqLXZ2gz8eHj-lzPnt7epnez3JFC97nnIoGjBFCq3lTGAmMGIYbKanQohDcSEWAcUyoUsowU3Ol8dwoKGWhCJV0gm62vqvgvwYd-6pLZ2hra6f9ECuCRUkJUGAJvT5Al34ILl1XEcpZwXFKJ1GwpVT6MgZtqlVouzqsKwzVJujqMOgkudoZD_NON7-CfbIJyLdArBf6b-u_hj8mnYUr</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Pagani, Elisabetta</creator><creator>Rocca, Maria A</creator><creator>De Meo, Ermelinda</creator><creator>Horsfield, Mark A</creator><creator>Colombo, Bruno</creator><creator>Rodegher, Mariaemma</creator><creator>Comi, Giancarlo</creator><creator>Filippi, Massimo</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2358-4320</orcidid><orcidid>https://orcid.org/0000-0002-5485-0479</orcidid></search><sort><creationdate>202002</creationdate><title>Structural connectivity in multiple sclerosis and modeling of disconnection</title><author>Pagani, Elisabetta ; Rocca, Maria A ; De Meo, Ermelinda ; Horsfield, Mark A ; Colombo, Bruno ; Rodegher, Mariaemma ; Comi, Giancarlo ; Filippi, Massimo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-537d0ff77ecbd6f8042f41d8837e7675f8c2045123cccf4fa5ce1bfc0986c2383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Benign</topic><topic>Brain injury</topic><topic>Brain Mapping - methods</topic><topic>Cerebral cortex</topic><topic>Cognitive ability</topic><topic>Diffusion Magnetic Resonance Imaging - methods</topic><topic>Female</topic><topic>Humans</topic><topic>Image Interpretation, Computer-Assisted - methods</topic><topic>Lesions</topic><topic>Magnetic resonance imaging</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - diagnostic imaging</topic><topic>Multiple Sclerosis - physiopathology</topic><topic>Nerve Net - diagnostic imaging</topic><topic>Nerve Net - physiopathology</topic><topic>Neural networks</topic><topic>Neural Pathways - diagnostic imaging</topic><topic>Neural Pathways - physiopathology</topic><topic>Neuroimaging</topic><topic>Phenotypes</topic><topic>Substantia alba</topic><topic>Variance analysis</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pagani, Elisabetta</creatorcontrib><creatorcontrib>Rocca, Maria A</creatorcontrib><creatorcontrib>De Meo, Ermelinda</creatorcontrib><creatorcontrib>Horsfield, Mark A</creatorcontrib><creatorcontrib>Colombo, Bruno</creatorcontrib><creatorcontrib>Rodegher, Mariaemma</creatorcontrib><creatorcontrib>Comi, Giancarlo</creatorcontrib><creatorcontrib>Filippi, Massimo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Multiple sclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pagani, Elisabetta</au><au>Rocca, Maria A</au><au>De Meo, Ermelinda</au><au>Horsfield, Mark A</au><au>Colombo, Bruno</au><au>Rodegher, Mariaemma</au><au>Comi, Giancarlo</au><au>Filippi, Massimo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural connectivity in multiple sclerosis and modeling of disconnection</atitle><jtitle>Multiple sclerosis</jtitle><addtitle>Mult Scler</addtitle><date>2020-02</date><risdate>2020</risdate><volume>26</volume><issue>2</issue><spage>220</spage><epage>232</epage><pages>220-232</pages><issn>1352-4585</issn><eissn>1477-0970</eissn><abstract>Background:
Multiple sclerosis (MS) is characterized by focal white matter damage, and when the brain is modeled as a network, lesions can be treated as disconnection events.
Objective:
To evaluate whether modeling disconnection caused by lesions helps explain motor and cognitive impairment in MS.
Methods:
Pathways connecting 116 cortical regions were reconstructed with magnetic resonance imaging (MRI) tractography from diffusion tensors averaged across healthy controls (HCs); maps of pathways were applied to 227 relapse-onset MS patients and 50 HCs to derive structural connectivity. Then, the likelihood of individual connections passing through lesions was used to model disconnection. Patients were grouped according to clinical phenotype (113 relapsing-remitting multiple sclerosis (RRMS), 69 secondary progressive multiple sclerosis (SPMS), 45 benign MS), and then network metrics were compared between groups (analysis of variance (ANOVA)) and correlated with motor and cognitive scores (linear regression).
Results:
Global metrics differentiated RRMS from SPMS and benign MS patients, but not benign from SPMS patients. Nodal connectivity strength replicated global results. After disconnection, few nodes were significantly different between benign MS and RRMS patients. Correlations revealed nodes pertinent to motor and cognitive dysfunctions; these became slightly stronger after disconnection.
Conclusion:
Connectivity did not change greatly after modeled disconnection, suggesting that the brain network is robust against damage caused by MS lesions.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>30625050</pmid><doi>10.1177/1352458518820759</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0003-2358-4320</orcidid><orcidid>https://orcid.org/0000-0002-5485-0479</orcidid></addata></record> |
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subjects | Adolescent Adult Aged Benign Brain injury Brain Mapping - methods Cerebral cortex Cognitive ability Diffusion Magnetic Resonance Imaging - methods Female Humans Image Interpretation, Computer-Assisted - methods Lesions Magnetic resonance imaging Male Middle Aged Multiple sclerosis Multiple Sclerosis - diagnostic imaging Multiple Sclerosis - physiopathology Nerve Net - diagnostic imaging Nerve Net - physiopathology Neural networks Neural Pathways - diagnostic imaging Neural Pathways - physiopathology Neuroimaging Phenotypes Substantia alba Variance analysis Young Adult |
title | Structural connectivity in multiple sclerosis and modeling of disconnection |
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