Spinal cord involvement in multiple sclerosis: A correlative MRI and high-resolution HLA-DRB1 genotyping study

Abstract Background There have been few magnetic resonance imaging (MRI) studies of the spinal cord in large multiple sclerosis (MS) patient cohorts and little is known about correlations between cord lesions and human leukocyte antigen (HLA) alleles. Objective To investigate the spectrum of MRI cha...

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Veröffentlicht in:Journal of the neurological sciences 2011-01, Vol.300 (1), p.114-119
Hauptverfasser: Qiu, Wei, Raven, Sonja, James, Ian, Luo, Yuebei, Wu, Jingshan, Castley, Alison, Christiansen, Frank T, Carroll, William M, Mastaglia, Frank L, Kermode, Allan G
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container_end_page 119
container_issue 1
container_start_page 114
container_title Journal of the neurological sciences
container_volume 300
creator Qiu, Wei
Raven, Sonja
James, Ian
Luo, Yuebei
Wu, Jingshan
Castley, Alison
Christiansen, Frank T
Carroll, William M
Mastaglia, Frank L
Kermode, Allan G
description Abstract Background There have been few magnetic resonance imaging (MRI) studies of the spinal cord in large multiple sclerosis (MS) patient cohorts and little is known about correlations between cord lesions and human leukocyte antigen (HLA) alleles. Objective To investigate the spectrum of MRI changes in the spinal cord in MS and associations with the HLA-DRB1 genotype. Methods Two hundred and fifty two consecutive MS patients from the Perth Demyelinating Diseases Database had MRI of the spinal cord and brain and high-resolution HLA-DRB1 genotyping. The numbers, locations, shape and segmental extent of cord lesions were analysed and were correlated with carriage of individual HLA-DRB1 alleles and diplotypes. Results Focal cord lesions were present in 82.9% of cases, with numbers being maximal in the cervical cord and increasing with disease duration. Focal lesions were usually round or oval in shape but in 35% of cases subpial wedge-shaped lesions were present. Diffuse cord involvement was present in 10% of cases and correlated with carriage of HLA-DRB1*1501 and with higher disability. Carriage of the minor allele HLA-DRB1*0701 was significantly associated with numbers of wedge-shaped lesions and lesions in the cervical cord, while HLA-DRB1*1104 and DRB1*0103 were significantly associated respectively with higher and lower numbers of thoracic cord lesions. HLA-DRB1*1501 and the HLA-DRB1*11 sub-alleles DRB1*1101 and DRB1*1104 were significantly associated with the segmental length of cord lesions. Conclusions Our study is the first to investigate the frequency of subpial wedge-shaped lesions in the cord in vivo and has provided preliminary evidence that HLA-DRB1 alleles may play a role in determining the severity and extent of spinal cord involvement in MS.
doi_str_mv 10.1016/j.jns.2010.09.006
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Objective To investigate the spectrum of MRI changes in the spinal cord in MS and associations with the HLA-DRB1 genotype. Methods Two hundred and fifty two consecutive MS patients from the Perth Demyelinating Diseases Database had MRI of the spinal cord and brain and high-resolution HLA-DRB1 genotyping. The numbers, locations, shape and segmental extent of cord lesions were analysed and were correlated with carriage of individual HLA-DRB1 alleles and diplotypes. Results Focal cord lesions were present in 82.9% of cases, with numbers being maximal in the cervical cord and increasing with disease duration. Focal lesions were usually round or oval in shape but in 35% of cases subpial wedge-shaped lesions were present. Diffuse cord involvement was present in 10% of cases and correlated with carriage of HLA-DRB1*1501 and with higher disability. Carriage of the minor allele HLA-DRB1*0701 was significantly associated with numbers of wedge-shaped lesions and lesions in the cervical cord, while HLA-DRB1*1104 and DRB1*0103 were significantly associated respectively with higher and lower numbers of thoracic cord lesions. HLA-DRB1*1501 and the HLA-DRB1*11 sub-alleles DRB1*1101 and DRB1*1104 were significantly associated with the segmental length of cord lesions. Conclusions Our study is the first to investigate the frequency of subpial wedge-shaped lesions in the cord in vivo and has provided preliminary evidence that HLA-DRB1 alleles may play a role in determining the severity and extent of spinal cord involvement in MS.</description><identifier>ISSN: 0022-510X</identifier><identifier>EISSN: 1878-5883</identifier><identifier>DOI: 10.1016/j.jns.2010.09.006</identifier><identifier>PMID: 20884011</identifier><identifier>CODEN: JNSCAG</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Alleles ; Biological and medical sciences ; Diplotypes ; Female ; Genotype ; HLA-DR Antigens - genetics ; HLA-DRB1 alleles ; HLA-DRB1 Chains ; Humans ; Magnetic Resonance Imaging - methods ; Male ; Medical sciences ; Middle Aged ; MRI ; Multiple sclerosis ; Multiple Sclerosis - diagnosis ; Multiple Sclerosis - genetics ; Multiple Sclerosis - pathology ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Neurology ; Spinal Cord - pathology ; Spinal cord lesions</subject><ispartof>Journal of the neurological sciences, 2011-01, Vol.300 (1), p.114-119</ispartof><rights>Elsevier B.V.</rights><rights>2010 Elsevier B.V.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c469t-8162ff6c3048c8582d68ef134d24768b025cf5821a08dc9320b014eb85ab49e43</citedby><cites>FETCH-LOGICAL-c469t-8162ff6c3048c8582d68ef134d24768b025cf5821a08dc9320b014eb85ab49e43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022510X10004429$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23725377$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20884011$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qiu, Wei</creatorcontrib><creatorcontrib>Raven, Sonja</creatorcontrib><creatorcontrib>James, Ian</creatorcontrib><creatorcontrib>Luo, Yuebei</creatorcontrib><creatorcontrib>Wu, Jingshan</creatorcontrib><creatorcontrib>Castley, Alison</creatorcontrib><creatorcontrib>Christiansen, Frank T</creatorcontrib><creatorcontrib>Carroll, William M</creatorcontrib><creatorcontrib>Mastaglia, Frank L</creatorcontrib><creatorcontrib>Kermode, Allan G</creatorcontrib><title>Spinal cord involvement in multiple sclerosis: A correlative MRI and high-resolution HLA-DRB1 genotyping study</title><title>Journal of the neurological sciences</title><addtitle>J Neurol Sci</addtitle><description>Abstract Background There have been few magnetic resonance imaging (MRI) studies of the spinal cord in large multiple sclerosis (MS) patient cohorts and little is known about correlations between cord lesions and human leukocyte antigen (HLA) alleles. Objective To investigate the spectrum of MRI changes in the spinal cord in MS and associations with the HLA-DRB1 genotype. Methods Two hundred and fifty two consecutive MS patients from the Perth Demyelinating Diseases Database had MRI of the spinal cord and brain and high-resolution HLA-DRB1 genotyping. The numbers, locations, shape and segmental extent of cord lesions were analysed and were correlated with carriage of individual HLA-DRB1 alleles and diplotypes. Results Focal cord lesions were present in 82.9% of cases, with numbers being maximal in the cervical cord and increasing with disease duration. Focal lesions were usually round or oval in shape but in 35% of cases subpial wedge-shaped lesions were present. Diffuse cord involvement was present in 10% of cases and correlated with carriage of HLA-DRB1*1501 and with higher disability. Carriage of the minor allele HLA-DRB1*0701 was significantly associated with numbers of wedge-shaped lesions and lesions in the cervical cord, while HLA-DRB1*1104 and DRB1*0103 were significantly associated respectively with higher and lower numbers of thoracic cord lesions. HLA-DRB1*1501 and the HLA-DRB1*11 sub-alleles DRB1*1101 and DRB1*1104 were significantly associated with the segmental length of cord lesions. Conclusions Our study is the first to investigate the frequency of subpial wedge-shaped lesions in the cord in vivo and has provided preliminary evidence that HLA-DRB1 alleles may play a role in determining the severity and extent of spinal cord involvement in MS.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alleles</subject><subject>Biological and medical sciences</subject><subject>Diplotypes</subject><subject>Female</subject><subject>Genotype</subject><subject>HLA-DR Antigens - genetics</subject><subject>HLA-DRB1 alleles</subject><subject>HLA-DRB1 Chains</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>MRI</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - diagnosis</subject><subject>Multiple Sclerosis - genetics</subject><subject>Multiple Sclerosis - pathology</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Neurology</subject><subject>Spinal Cord - pathology</subject><subject>Spinal cord lesions</subject><issn>0022-510X</issn><issn>1878-5883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkl2L1DAUhoMo7rj6A7yR3IhXHU_StE0VhHFd3YURYVfBu5Cmp7OpmXRM2oH595syo4IX4lU-eM4H7_sS8pzBkgErX_fL3sclh_SGeglQPiALJiuZFVLmD8kCgPOsYPD9jDyJsYdESFk_JmccpBTA2IL425312lEzhJZavx_cHrfox3Sn28mNdueQRuMwDNHGN3Q1kwGdHu0e6eeba6p9S-_s5i4LGAc3jXbw9Gq9yj7cvGd0g34YD2nEhsZxag9PyaNOu4jPTuc5-fbx8uvFVbb-8un6YrXOjCjrMZOs5F1XmhyENLKQvC0ldiwXLRdVKRvghenSN9MgW1PnHBpgAhtZ6EbUKPJz8urYdxeGnxPGUW1tNOic9jhMUcmCiVIWxX-QnHGAXBaJZEfSJC1iwE7tgt3qcFAM1OyH6lXyQ81-KKhVUjvVvDh1n5ottr8rfhmQgJcnQEejXRe0Nzb-4fKKF3lVJe7tkcOk2t5iUNFY9AZbG9CMqh3sP9d491e1cdbbNPAHHjD2wxRSCKJiKnIF6nYOzpwbliIjBK_ze-VIvDU</recordid><startdate>20110115</startdate><enddate>20110115</enddate><creator>Qiu, Wei</creator><creator>Raven, Sonja</creator><creator>James, Ian</creator><creator>Luo, Yuebei</creator><creator>Wu, Jingshan</creator><creator>Castley, Alison</creator><creator>Christiansen, Frank T</creator><creator>Carroll, William M</creator><creator>Mastaglia, Frank L</creator><creator>Kermode, Allan G</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20110115</creationdate><title>Spinal cord involvement in multiple sclerosis: A correlative MRI and high-resolution HLA-DRB1 genotyping study</title><author>Qiu, Wei ; Raven, Sonja ; James, Ian ; Luo, Yuebei ; Wu, Jingshan ; Castley, Alison ; Christiansen, Frank T ; Carroll, William M ; Mastaglia, Frank L ; Kermode, Allan G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c469t-8162ff6c3048c8582d68ef134d24768b025cf5821a08dc9320b014eb85ab49e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Alleles</topic><topic>Biological and medical sciences</topic><topic>Diplotypes</topic><topic>Female</topic><topic>Genotype</topic><topic>HLA-DR Antigens - genetics</topic><topic>HLA-DRB1 alleles</topic><topic>HLA-DRB1 Chains</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>MRI</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - diagnosis</topic><topic>Multiple Sclerosis - genetics</topic><topic>Multiple Sclerosis - pathology</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Neurology</topic><topic>Spinal Cord - pathology</topic><topic>Spinal cord lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qiu, Wei</creatorcontrib><creatorcontrib>Raven, Sonja</creatorcontrib><creatorcontrib>James, Ian</creatorcontrib><creatorcontrib>Luo, Yuebei</creatorcontrib><creatorcontrib>Wu, Jingshan</creatorcontrib><creatorcontrib>Castley, Alison</creatorcontrib><creatorcontrib>Christiansen, Frank T</creatorcontrib><creatorcontrib>Carroll, William M</creatorcontrib><creatorcontrib>Mastaglia, Frank L</creatorcontrib><creatorcontrib>Kermode, Allan G</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Journal of the neurological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qiu, Wei</au><au>Raven, Sonja</au><au>James, Ian</au><au>Luo, Yuebei</au><au>Wu, Jingshan</au><au>Castley, Alison</au><au>Christiansen, Frank T</au><au>Carroll, William M</au><au>Mastaglia, Frank L</au><au>Kermode, Allan G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spinal cord involvement in multiple sclerosis: A correlative MRI and high-resolution HLA-DRB1 genotyping study</atitle><jtitle>Journal of the neurological sciences</jtitle><addtitle>J Neurol Sci</addtitle><date>2011-01-15</date><risdate>2011</risdate><volume>300</volume><issue>1</issue><spage>114</spage><epage>119</epage><pages>114-119</pages><issn>0022-510X</issn><eissn>1878-5883</eissn><coden>JNSCAG</coden><abstract>Abstract Background There have been few magnetic resonance imaging (MRI) studies of the spinal cord in large multiple sclerosis (MS) patient cohorts and little is known about correlations between cord lesions and human leukocyte antigen (HLA) alleles. Objective To investigate the spectrum of MRI changes in the spinal cord in MS and associations with the HLA-DRB1 genotype. Methods Two hundred and fifty two consecutive MS patients from the Perth Demyelinating Diseases Database had MRI of the spinal cord and brain and high-resolution HLA-DRB1 genotyping. The numbers, locations, shape and segmental extent of cord lesions were analysed and were correlated with carriage of individual HLA-DRB1 alleles and diplotypes. Results Focal cord lesions were present in 82.9% of cases, with numbers being maximal in the cervical cord and increasing with disease duration. Focal lesions were usually round or oval in shape but in 35% of cases subpial wedge-shaped lesions were present. Diffuse cord involvement was present in 10% of cases and correlated with carriage of HLA-DRB1*1501 and with higher disability. Carriage of the minor allele HLA-DRB1*0701 was significantly associated with numbers of wedge-shaped lesions and lesions in the cervical cord, while HLA-DRB1*1104 and DRB1*0103 were significantly associated respectively with higher and lower numbers of thoracic cord lesions. HLA-DRB1*1501 and the HLA-DRB1*11 sub-alleles DRB1*1101 and DRB1*1104 were significantly associated with the segmental length of cord lesions. Conclusions Our study is the first to investigate the frequency of subpial wedge-shaped lesions in the cord in vivo and has provided preliminary evidence that HLA-DRB1 alleles may play a role in determining the severity and extent of spinal cord involvement in MS.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>20884011</pmid><doi>10.1016/j.jns.2010.09.006</doi><tpages>6</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Aged, 80 and over
Alleles
Biological and medical sciences
Diplotypes
Female
Genotype
HLA-DR Antigens - genetics
HLA-DRB1 alleles
HLA-DRB1 Chains
Humans
Magnetic Resonance Imaging - methods
Male
Medical sciences
Middle Aged
MRI
Multiple sclerosis
Multiple Sclerosis - diagnosis
Multiple Sclerosis - genetics
Multiple Sclerosis - pathology
Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis
Neurology
Spinal Cord - pathology
Spinal cord lesions
title Spinal cord involvement in multiple sclerosis: A correlative MRI and high-resolution HLA-DRB1 genotyping study
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