Predictors of recurrence following an initial episode of transverse myelitis

OBJECTIVE:This study sought to identify factors that increased the risk of recurrence after an initial transverse myelitis (TM) presentation. METHODS:Retrospective cohort study of 192 patients initially presenting with TM of unknown etiology. Patients diagnosed with multiple sclerosis during the fir...

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Veröffentlicht in:Neurology : neuroimmunology & neuroinflammation 2014-06, Vol.1 (1), p.e4-e4
Hauptverfasser: Kimbrough, Dorlan J, Mealy, Maureen A, Simpson, Alexandra, Levy, Michael
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container_title Neurology : neuroimmunology & neuroinflammation
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creator Kimbrough, Dorlan J
Mealy, Maureen A
Simpson, Alexandra
Levy, Michael
description OBJECTIVE:This study sought to identify factors that increased the risk of recurrence after an initial transverse myelitis (TM) presentation. METHODS:Retrospective cohort study of 192 patients initially presenting with TM of unknown etiology. Patients diagnosed with multiple sclerosis during the first myelitis episode were excluded. Demographic and laboratory data were analyzed for associations with recurrence. RESULTS:One hundred ten of 192 patients (57%) eventually developed recurrent symptoms69 (63%) neuromyelitis optica (NMO) or NMO spectrum disorder, 34 (31%) non-NMO recurrent TM, and 7 (6%) systemic autoimmune disease. Multiple independent risk factors for recurrence were identifiedAfrican American race (risk ratio 1.60, p < 0.001, 95% confidence interval 1.26–2.03; similarly noted hereafter), female sex (1.88, p = 0.007, 1.19–2.98), longitudinally extensive myelitis at onset (1.34, p = 0.036, 1.01–1.78), Sjogren syndrome antigen A (1.89, p = 0.003, 1.44–2.48), vitamin D insufficiency (4.00, p < 0.001, 1.60–10.0), antinuclear antibody titer ≥1:160 (1.69, p = 0.006, 1.23–2.32), and the presence of inflammatory markers (e.g., immunoglobulin G index) in the CSF (2.14, p < 0.001, 1.44–3.17). CONCLUSIONS:Sex, race, and serologic biomarkers warrant consideration when assessing risk of TM recurrence. Male sex and Caucasian American race were independently associated with risk of monophasic idiopathic TM. Recurrence risk in female and African American patients appears driven by a greater likelihood of developing NMO or NMO spectrum disorder.
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METHODS:Retrospective cohort study of 192 patients initially presenting with TM of unknown etiology. Patients diagnosed with multiple sclerosis during the first myelitis episode were excluded. Demographic and laboratory data were analyzed for associations with recurrence. RESULTS:One hundred ten of 192 patients (57%) eventually developed recurrent symptoms69 (63%) neuromyelitis optica (NMO) or NMO spectrum disorder, 34 (31%) non-NMO recurrent TM, and 7 (6%) systemic autoimmune disease. Multiple independent risk factors for recurrence were identifiedAfrican American race (risk ratio 1.60, p &lt; 0.001, 95% confidence interval 1.26–2.03; similarly noted hereafter), female sex (1.88, p = 0.007, 1.19–2.98), longitudinally extensive myelitis at onset (1.34, p = 0.036, 1.01–1.78), Sjogren syndrome antigen A (1.89, p = 0.003, 1.44–2.48), vitamin D insufficiency (4.00, p &lt; 0.001, 1.60–10.0), antinuclear antibody titer ≥1:160 (1.69, p = 0.006, 1.23–2.32), and the presence of inflammatory markers (e.g., immunoglobulin G index) in the CSF (2.14, p &lt; 0.001, 1.44–3.17). CONCLUSIONS:Sex, race, and serologic biomarkers warrant consideration when assessing risk of TM recurrence. Male sex and Caucasian American race were independently associated with risk of monophasic idiopathic TM. Recurrence risk in female and African American patients appears driven by a greater likelihood of developing NMO or NMO spectrum disorder.</description><identifier>ISSN: 2332-7812</identifier><identifier>EISSN: 2332-7812</identifier><identifier>DOI: 10.1212/NXI.0000000000000004</identifier><identifier>PMID: 25340060</identifier><language>eng</language><publisher>United States: American Academy of Neurology</publisher><ispartof>Neurology : neuroimmunology &amp; neuroinflammation, 2014-06, Vol.1 (1), p.e4-e4</ispartof><rights>2014 American Academy of Neurology</rights><rights>2014 American Academy of Neurology 2014 American Academy of Neurology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5044-bda3b7f5016b53ca0a97edbff00d4c7bd0442320ce60094a6631b74d032439f03</citedby><cites>FETCH-LOGICAL-c5044-bda3b7f5016b53ca0a97edbff00d4c7bd0442320ce60094a6631b74d032439f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202674/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202674/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25340060$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kimbrough, Dorlan J</creatorcontrib><creatorcontrib>Mealy, Maureen A</creatorcontrib><creatorcontrib>Simpson, Alexandra</creatorcontrib><creatorcontrib>Levy, Michael</creatorcontrib><title>Predictors of recurrence following an initial episode of transverse myelitis</title><title>Neurology : neuroimmunology &amp; neuroinflammation</title><addtitle>Neurol Neuroimmunol Neuroinflamm</addtitle><description>OBJECTIVE:This study sought to identify factors that increased the risk of recurrence after an initial transverse myelitis (TM) presentation. METHODS:Retrospective cohort study of 192 patients initially presenting with TM of unknown etiology. Patients diagnosed with multiple sclerosis during the first myelitis episode were excluded. Demographic and laboratory data were analyzed for associations with recurrence. RESULTS:One hundred ten of 192 patients (57%) eventually developed recurrent symptoms69 (63%) neuromyelitis optica (NMO) or NMO spectrum disorder, 34 (31%) non-NMO recurrent TM, and 7 (6%) systemic autoimmune disease. Multiple independent risk factors for recurrence were identifiedAfrican American race (risk ratio 1.60, p &lt; 0.001, 95% confidence interval 1.26–2.03; similarly noted hereafter), female sex (1.88, p = 0.007, 1.19–2.98), longitudinally extensive myelitis at onset (1.34, p = 0.036, 1.01–1.78), Sjogren syndrome antigen A (1.89, p = 0.003, 1.44–2.48), vitamin D insufficiency (4.00, p &lt; 0.001, 1.60–10.0), antinuclear antibody titer ≥1:160 (1.69, p = 0.006, 1.23–2.32), and the presence of inflammatory markers (e.g., immunoglobulin G index) in the CSF (2.14, p &lt; 0.001, 1.44–3.17). CONCLUSIONS:Sex, race, and serologic biomarkers warrant consideration when assessing risk of TM recurrence. Male sex and Caucasian American race were independently associated with risk of monophasic idiopathic TM. Recurrence risk in female and African American patients appears driven by a greater likelihood of developing NMO or NMO spectrum disorder.</description><issn>2332-7812</issn><issn>2332-7812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNpdkU1LxDAQhoMoKuo_EOnRS3Xy0WT3Ioj4BYt6UPAW0nTqRrPNmrQu_nuzrN-5JDDPPBnmJWSfwhFllB3fPF4fwd8j1sg245yVakTZ-q_3FtlL6TkTlFWVkmqTbLGKCwAJ22RyF7Fxtg8xFaEtItohRuwsFm3wPixc91SYrnCd653xBc5dCg0u0T6aLr1hTFjM3tHnetolG63xCfc-7x3ycHF-f3ZVTm4vr89OJ6WtQIiybgyvVVsBlXXFrQEzVtjUbQvQCKvqJkOMM7AoAcbCSMlprUQDnAk-boHvkJOVdz7UM2wsdnkYr-fRzUx818E4_bfSual-Cm9aMGBSiSw4_BTE8Dpg6vXMJYvemw7DkDSVVAqlxqMlKlaojSGliO33NxT0Mguds9D_s8htB79H_G762vyPdxF8n7f44ocFRj1F4_upBqpGSgAtGVCRcQrlyvsBPpyVIg</recordid><startdate>201406</startdate><enddate>201406</enddate><creator>Kimbrough, Dorlan J</creator><creator>Mealy, Maureen A</creator><creator>Simpson, Alexandra</creator><creator>Levy, Michael</creator><general>American Academy of Neurology</general><general>Lippincott Williams &amp; Wilkins</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201406</creationdate><title>Predictors of recurrence following an initial episode of transverse myelitis</title><author>Kimbrough, Dorlan J ; Mealy, Maureen A ; Simpson, Alexandra ; Levy, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5044-bda3b7f5016b53ca0a97edbff00d4c7bd0442320ce60094a6631b74d032439f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kimbrough, Dorlan J</creatorcontrib><creatorcontrib>Mealy, Maureen A</creatorcontrib><creatorcontrib>Simpson, Alexandra</creatorcontrib><creatorcontrib>Levy, Michael</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neurology : neuroimmunology &amp; neuroinflammation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kimbrough, Dorlan J</au><au>Mealy, Maureen A</au><au>Simpson, Alexandra</au><au>Levy, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predictors of recurrence following an initial episode of transverse myelitis</atitle><jtitle>Neurology : neuroimmunology &amp; neuroinflammation</jtitle><addtitle>Neurol Neuroimmunol Neuroinflamm</addtitle><date>2014-06</date><risdate>2014</risdate><volume>1</volume><issue>1</issue><spage>e4</spage><epage>e4</epage><pages>e4-e4</pages><issn>2332-7812</issn><eissn>2332-7812</eissn><abstract>OBJECTIVE:This study sought to identify factors that increased the risk of recurrence after an initial transverse myelitis (TM) presentation. METHODS:Retrospective cohort study of 192 patients initially presenting with TM of unknown etiology. Patients diagnosed with multiple sclerosis during the first myelitis episode were excluded. Demographic and laboratory data were analyzed for associations with recurrence. RESULTS:One hundred ten of 192 patients (57%) eventually developed recurrent symptoms69 (63%) neuromyelitis optica (NMO) or NMO spectrum disorder, 34 (31%) non-NMO recurrent TM, and 7 (6%) systemic autoimmune disease. Multiple independent risk factors for recurrence were identifiedAfrican American race (risk ratio 1.60, p &lt; 0.001, 95% confidence interval 1.26–2.03; similarly noted hereafter), female sex (1.88, p = 0.007, 1.19–2.98), longitudinally extensive myelitis at onset (1.34, p = 0.036, 1.01–1.78), Sjogren syndrome antigen A (1.89, p = 0.003, 1.44–2.48), vitamin D insufficiency (4.00, p &lt; 0.001, 1.60–10.0), antinuclear antibody titer ≥1:160 (1.69, p = 0.006, 1.23–2.32), and the presence of inflammatory markers (e.g., immunoglobulin G index) in the CSF (2.14, p &lt; 0.001, 1.44–3.17). CONCLUSIONS:Sex, race, and serologic biomarkers warrant consideration when assessing risk of TM recurrence. Male sex and Caucasian American race were independently associated with risk of monophasic idiopathic TM. 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title Predictors of recurrence following an initial episode of transverse myelitis
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