Predicting Aggressive Multiple Sclerosis With Intrathecal IgM Synthesis Among Patients With a Clinically Isolated Syndrome
To determine the best method to measure intrathecal immunoglobulin (Ig) M synthesis (ITMS), a biomarker of worse prognosis in multiple sclerosis (MS). We compared the ability for predicting a poor evolution of 4 methods assessing ITMS (IgM oligoclonal bands [OCMBs], lipid-specific OCMBs [LS-OCMBs],...
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creator | Monreal, Enric Sainz de la Maza, Susana Costa-Frossard, Lucienne Walo-Delgado, Paulette Zamora, Javier Fernández-Velasco, José Ignacio Villarrubia, Noelia Espiño, Mercedes Lourido, Daniel Lapuente, Paloma Toboso, Inmaculada Álvarez-Cermeño, José Carlos Masjuan, Jaime Villar, Luisa María |
description | To determine the best method to measure intrathecal immunoglobulin (Ig) M synthesis (ITMS), a biomarker of worse prognosis in multiple sclerosis (MS). We compared the ability for predicting a poor evolution of 4 methods assessing ITMS (IgM oligoclonal bands [OCMBs], lipid-specific OCMBs [LS-OCMBs], Reibergram, and IgM index) in patients with a clinically isolated syndrome (CIS).
Prospective study with consecutive patients performed at a referral MS center. We used unadjusted and multivariate Cox regressions for predicting a second relapse, Expanded Disability Status Scale (EDSS) scores of 4 and 6, and development of secondary progressive MS (SPMS).
A total of 193 patients were included, with a median (interquartile range) age of 31 (25-38) years and a median follow-up of 12.9 years. Among all methods, only OCMB, LS-OCMB, and Reibergram significantly identified patients at risk of some of the pre-established outcomes, being LS-OCMB the technique with the strongest associations. Adjusted hazard ratio (aHR) of LS-OCMB for predicting a second relapse was 2.50 (95% CI 1.72-3.64,
< 0.001). The risk of reaching EDSS scores of 4 and 6 and SPMS was significantly higher among patients with LS-OCMB (aHR 2.96, 95% CI 1.54-5.71,
= 0.001; aHR 4.96, 95% CI 2.22-11.07,
< 0.001; and aHR 2.31, 95% CI 1.08-4.93,
= 0.03, respectively).
ITMS predicts an aggressive MS at disease onset, especially when detected as LS-OCMB.
This study provides Class II evidence that lipid-specific IgM oligoclonal bands can predict progression from CIS to MS and a worse disease course over a follow-up of at least 2 years. |
doi_str_mv | 10.1212/NXI.0000000000001047 |
format | Article |
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Prospective study with consecutive patients performed at a referral MS center. We used unadjusted and multivariate Cox regressions for predicting a second relapse, Expanded Disability Status Scale (EDSS) scores of 4 and 6, and development of secondary progressive MS (SPMS).
A total of 193 patients were included, with a median (interquartile range) age of 31 (25-38) years and a median follow-up of 12.9 years. Among all methods, only OCMB, LS-OCMB, and Reibergram significantly identified patients at risk of some of the pre-established outcomes, being LS-OCMB the technique with the strongest associations. Adjusted hazard ratio (aHR) of LS-OCMB for predicting a second relapse was 2.50 (95% CI 1.72-3.64,
< 0.001). The risk of reaching EDSS scores of 4 and 6 and SPMS was significantly higher among patients with LS-OCMB (aHR 2.96, 95% CI 1.54-5.71,
= 0.001; aHR 4.96, 95% CI 2.22-11.07,
< 0.001; and aHR 2.31, 95% CI 1.08-4.93,
= 0.03, respectively).
ITMS predicts an aggressive MS at disease onset, especially when detected as LS-OCMB.
This study provides Class II evidence that lipid-specific IgM oligoclonal bands can predict progression from CIS to MS and a worse disease course over a follow-up of at least 2 years.</description><identifier>ISSN: 2332-7812</identifier><identifier>EISSN: 2332-7812</identifier><identifier>DOI: 10.1212/NXI.0000000000001047</identifier><identifier>PMID: 34301819</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins</publisher><subject>Adult ; Biomarkers - blood ; Biomarkers - cerebrospinal fluid ; Female ; Humans ; Immunoglobulin M - blood ; Immunoglobulin M - cerebrospinal fluid ; Male ; Multiple Sclerosis - blood ; Multiple Sclerosis - cerebrospinal fluid ; Multiple Sclerosis - diagnosis ; Multiple Sclerosis - immunology ; Oligoclonal Bands - blood ; Oligoclonal Bands - cerebrospinal fluid ; Prospective Studies ; Sensitivity and Specificity</subject><ispartof>Neurology : neuroimmunology & neuroinflammation, 2021-09, Vol.8 (5)</ispartof><rights>Lippincott Williams & Wilkins</rights><rights>Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.</rights><rights>Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. 2021 American Academy of Neurology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5049-48751af3f15f7b2cd64395583789829530c606064c89244a0a8ac6851b2594d53</citedby><cites>FETCH-LOGICAL-c5049-48751af3f15f7b2cd64395583789829530c606064c89244a0a8ac6851b2594d53</cites><orcidid>0000-0003-3293-0125</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299514/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8299514/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34301819$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Monreal, Enric</creatorcontrib><creatorcontrib>Sainz de la Maza, Susana</creatorcontrib><creatorcontrib>Costa-Frossard, Lucienne</creatorcontrib><creatorcontrib>Walo-Delgado, Paulette</creatorcontrib><creatorcontrib>Zamora, Javier</creatorcontrib><creatorcontrib>Fernández-Velasco, José Ignacio</creatorcontrib><creatorcontrib>Villarrubia, Noelia</creatorcontrib><creatorcontrib>Espiño, Mercedes</creatorcontrib><creatorcontrib>Lourido, Daniel</creatorcontrib><creatorcontrib>Lapuente, Paloma</creatorcontrib><creatorcontrib>Toboso, Inmaculada</creatorcontrib><creatorcontrib>Álvarez-Cermeño, José Carlos</creatorcontrib><creatorcontrib>Masjuan, Jaime</creatorcontrib><creatorcontrib>Villar, Luisa María</creatorcontrib><title>Predicting Aggressive Multiple Sclerosis With Intrathecal IgM Synthesis Among Patients With a Clinically Isolated Syndrome</title><title>Neurology : neuroimmunology & neuroinflammation</title><addtitle>Neurol Neuroimmunol Neuroinflamm</addtitle><description>To determine the best method to measure intrathecal immunoglobulin (Ig) M synthesis (ITMS), a biomarker of worse prognosis in multiple sclerosis (MS). We compared the ability for predicting a poor evolution of 4 methods assessing ITMS (IgM oligoclonal bands [OCMBs], lipid-specific OCMBs [LS-OCMBs], Reibergram, and IgM index) in patients with a clinically isolated syndrome (CIS).
Prospective study with consecutive patients performed at a referral MS center. We used unadjusted and multivariate Cox regressions for predicting a second relapse, Expanded Disability Status Scale (EDSS) scores of 4 and 6, and development of secondary progressive MS (SPMS).
A total of 193 patients were included, with a median (interquartile range) age of 31 (25-38) years and a median follow-up of 12.9 years. Among all methods, only OCMB, LS-OCMB, and Reibergram significantly identified patients at risk of some of the pre-established outcomes, being LS-OCMB the technique with the strongest associations. Adjusted hazard ratio (aHR) of LS-OCMB for predicting a second relapse was 2.50 (95% CI 1.72-3.64,
< 0.001). The risk of reaching EDSS scores of 4 and 6 and SPMS was significantly higher among patients with LS-OCMB (aHR 2.96, 95% CI 1.54-5.71,
= 0.001; aHR 4.96, 95% CI 2.22-11.07,
< 0.001; and aHR 2.31, 95% CI 1.08-4.93,
= 0.03, respectively).
ITMS predicts an aggressive MS at disease onset, especially when detected as LS-OCMB.
This study provides Class II evidence that lipid-specific IgM oligoclonal bands can predict progression from CIS to MS and a worse disease course over a follow-up of at least 2 years.</description><subject>Adult</subject><subject>Biomarkers - blood</subject><subject>Biomarkers - cerebrospinal fluid</subject><subject>Female</subject><subject>Humans</subject><subject>Immunoglobulin M - blood</subject><subject>Immunoglobulin M - cerebrospinal fluid</subject><subject>Male</subject><subject>Multiple Sclerosis - blood</subject><subject>Multiple Sclerosis - cerebrospinal fluid</subject><subject>Multiple Sclerosis - diagnosis</subject><subject>Multiple Sclerosis - immunology</subject><subject>Oligoclonal Bands - blood</subject><subject>Oligoclonal Bands - cerebrospinal fluid</subject><subject>Prospective Studies</subject><subject>Sensitivity and Specificity</subject><issn>2332-7812</issn><issn>2332-7812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc1u1DAUhSMEolXpGyCUJZsU_yb2Bmk0ohCppZUKgp3lcW4Sg5MMttNqeHocdWintRe2dc_5bN-TZW8xOsMEkw9ff9Zn6GBgxKoX2TGhlBSVwOTlwf4oOw3h1yIinFdl9To7oowiLLA8zv5ee2isiXbs8lXXeQjB3kJ-Obtotw7yG-PAT8GG_IeNfV6P0evYg9Eur7vL_GY3ptNSXg1TQlzraGGMe7XO186ONondLq_D5HSEZvE0fhrgTfaq1S7A6X49yb6ff_q2_lJcXH2u16uLwnDEZMFExbFuaYt5W22IaUpGJeeCVkIKIjlFpkRpMiMkYUwjLbQpBccbwiVrOD3JPt5zt_NmgMbA8gentt4O2u_UpK16Whltr7rpViW65JglwPs9wE9_ZghRDTYYcE6PMM1BpbZyjCkjZZKye6lJTQse2odrMFJLciolp54nl2zvDp_4YPqf0yP3bnIRfPjt5jvwqgftYq8QrkTFEC4IIhjJRC0WsqT_ALXZpDI</recordid><startdate>20210901</startdate><enddate>20210901</enddate><creator>Monreal, Enric</creator><creator>Sainz de la Maza, Susana</creator><creator>Costa-Frossard, Lucienne</creator><creator>Walo-Delgado, Paulette</creator><creator>Zamora, Javier</creator><creator>Fernández-Velasco, José Ignacio</creator><creator>Villarrubia, Noelia</creator><creator>Espiño, Mercedes</creator><creator>Lourido, Daniel</creator><creator>Lapuente, Paloma</creator><creator>Toboso, Inmaculada</creator><creator>Álvarez-Cermeño, José Carlos</creator><creator>Masjuan, Jaime</creator><creator>Villar, Luisa María</creator><general>Lippincott Williams & Wilkins</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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3293-0125</orcidid></search><sort><creationdate>20210901</creationdate><title>Predicting Aggressive Multiple Sclerosis With Intrathecal IgM Synthesis Among Patients With a Clinically Isolated Syndrome</title><author>Monreal, Enric ; Sainz de la Maza, Susana ; Costa-Frossard, Lucienne ; Walo-Delgado, Paulette ; Zamora, Javier ; Fernández-Velasco, José Ignacio ; Villarrubia, Noelia ; Espiño, Mercedes ; Lourido, Daniel ; Lapuente, Paloma ; Toboso, Inmaculada ; Álvarez-Cermeño, José Carlos ; Masjuan, Jaime ; Villar, Luisa María</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5049-48751af3f15f7b2cd64395583789829530c606064c89244a0a8ac6851b2594d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adult</topic><topic>Biomarkers - blood</topic><topic>Biomarkers - cerebrospinal fluid</topic><topic>Female</topic><topic>Humans</topic><topic>Immunoglobulin M - blood</topic><topic>Immunoglobulin M - cerebrospinal fluid</topic><topic>Male</topic><topic>Multiple Sclerosis - blood</topic><topic>Multiple Sclerosis - cerebrospinal fluid</topic><topic>Multiple Sclerosis - diagnosis</topic><topic>Multiple Sclerosis - immunology</topic><topic>Oligoclonal Bands - blood</topic><topic>Oligoclonal Bands - cerebrospinal fluid</topic><topic>Prospective Studies</topic><topic>Sensitivity and Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Monreal, Enric</creatorcontrib><creatorcontrib>Sainz de la Maza, Susana</creatorcontrib><creatorcontrib>Costa-Frossard, Lucienne</creatorcontrib><creatorcontrib>Walo-Delgado, Paulette</creatorcontrib><creatorcontrib>Zamora, Javier</creatorcontrib><creatorcontrib>Fernández-Velasco, José Ignacio</creatorcontrib><creatorcontrib>Villarrubia, Noelia</creatorcontrib><creatorcontrib>Espiño, Mercedes</creatorcontrib><creatorcontrib>Lourido, Daniel</creatorcontrib><creatorcontrib>Lapuente, Paloma</creatorcontrib><creatorcontrib>Toboso, Inmaculada</creatorcontrib><creatorcontrib>Álvarez-Cermeño, José Carlos</creatorcontrib><creatorcontrib>Masjuan, Jaime</creatorcontrib><creatorcontrib>Villar, Luisa María</creatorcontrib><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>PubMed Central (Full Participant titles)</collection><jtitle>Neurology : neuroimmunology & neuroinflammation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Monreal, Enric</au><au>Sainz de la Maza, Susana</au><au>Costa-Frossard, Lucienne</au><au>Walo-Delgado, Paulette</au><au>Zamora, Javier</au><au>Fernández-Velasco, José Ignacio</au><au>Villarrubia, Noelia</au><au>Espiño, Mercedes</au><au>Lourido, Daniel</au><au>Lapuente, Paloma</au><au>Toboso, Inmaculada</au><au>Álvarez-Cermeño, José Carlos</au><au>Masjuan, Jaime</au><au>Villar, Luisa María</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predicting Aggressive Multiple Sclerosis With Intrathecal IgM Synthesis Among Patients With a Clinically Isolated Syndrome</atitle><jtitle>Neurology : neuroimmunology & neuroinflammation</jtitle><addtitle>Neurol Neuroimmunol Neuroinflamm</addtitle><date>2021-09-01</date><risdate>2021</risdate><volume>8</volume><issue>5</issue><issn>2332-7812</issn><eissn>2332-7812</eissn><abstract>To determine the best method to measure intrathecal immunoglobulin (Ig) M synthesis (ITMS), a biomarker of worse prognosis in multiple sclerosis (MS). We compared the ability for predicting a poor evolution of 4 methods assessing ITMS (IgM oligoclonal bands [OCMBs], lipid-specific OCMBs [LS-OCMBs], Reibergram, and IgM index) in patients with a clinically isolated syndrome (CIS).
Prospective study with consecutive patients performed at a referral MS center. We used unadjusted and multivariate Cox regressions for predicting a second relapse, Expanded Disability Status Scale (EDSS) scores of 4 and 6, and development of secondary progressive MS (SPMS).
A total of 193 patients were included, with a median (interquartile range) age of 31 (25-38) years and a median follow-up of 12.9 years. Among all methods, only OCMB, LS-OCMB, and Reibergram significantly identified patients at risk of some of the pre-established outcomes, being LS-OCMB the technique with the strongest associations. Adjusted hazard ratio (aHR) of LS-OCMB for predicting a second relapse was 2.50 (95% CI 1.72-3.64,
< 0.001). The risk of reaching EDSS scores of 4 and 6 and SPMS was significantly higher among patients with LS-OCMB (aHR 2.96, 95% CI 1.54-5.71,
= 0.001; aHR 4.96, 95% CI 2.22-11.07,
< 0.001; and aHR 2.31, 95% CI 1.08-4.93,
= 0.03, respectively).
ITMS predicts an aggressive MS at disease onset, especially when detected as LS-OCMB.
This study provides Class II evidence that lipid-specific IgM oligoclonal bands can predict progression from CIS to MS and a worse disease course over a follow-up of at least 2 years.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins</pub><pmid>34301819</pmid><doi>10.1212/NXI.0000000000001047</doi><orcidid>https://orcid.org/0000-0003-3293-0125</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biomarkers - blood Biomarkers - cerebrospinal fluid Female Humans Immunoglobulin M - blood Immunoglobulin M - cerebrospinal fluid Male Multiple Sclerosis - blood Multiple Sclerosis - cerebrospinal fluid Multiple Sclerosis - diagnosis Multiple Sclerosis - immunology Oligoclonal Bands - blood Oligoclonal Bands - cerebrospinal fluid Prospective Studies Sensitivity and Specificity |
title | Predicting Aggressive Multiple Sclerosis With Intrathecal IgM Synthesis Among Patients With a Clinically Isolated Syndrome |
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