Show simple item record

dc.contributor.authorLin, S
dc.contributor.authorGreen, H
dc.contributor.authorHendy, P
dc.contributor.authorHeerasing, N
dc.contributor.authorChanchlani, N
dc.contributor.authorHamilton, B
dc.contributor.authorWalker, G
dc.contributor.authorHeap, G
dc.contributor.authorHobart, J
dc.contributor.authorMartin, R
dc.contributor.authorColes, A
dc.contributor.authorIrving, P
dc.contributor.authorChung-Faye, G
dc.contributor.authorCummings, F
dc.contributor.authorLytvyak, E
dc.contributor.authorAndersen, V
dc.contributor.authorWood, A
dc.contributor.authorTyrrell, J
dc.contributor.authorBeaumont, R
dc.contributor.authorWeedon, M
dc.contributor.authorKennedy, N
dc.contributor.authorSpiers, A
dc.contributor.authorHarrower, T
dc.contributor.authorGoodhand, J
dc.contributor.authorAhmad, T
dc.date.accessioned2020-04-30T09:58:39Z
dc.date.issued2020-05-04
dc.identifier.issn1873-9946
dc.identifier.issn1876-4479
dc.identifier.urihttp://hdl.handle.net/10026.1/15613
dc.description.abstract

<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Background</jats:title> <jats:p>Anti-TNF exposure has been linked to demyelination events. We sought to describe the clinical features of demyelination events following anti-TNF treatment and to test whether affected patients were genetically predisposed to multiple sclerosis [MS].</jats:p> </jats:sec> <jats:sec> <jats:title>Methods</jats:title> <jats:p>We conducted a case-control study to describe the clinical features of demyelination events following anti-TNF exposure. We compared genetic risk scores [GRS], calculated using carriage of 43 susceptibility loci for MS, in 48 cases with 1219 patients exposed to anti-TNF who did not develop demyelination.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>Overall, 39 [74%] cases were female. The median age [range] of patients at time of demyelination was 41.5 years [20.7–63.2]. The median duration of anti-TNF treatment was 21.3 months [0.5-99.4] and 19 [36%] patients were receiving concomitant immunomodulators. Most patients had central demyelination affecting the brain, spinal cord, or both. Complete recovery was reported in 12 [23%] patients after a median time of 6.8 months [0.1–28.7]. After 33.0 months of follow-up, partial recovery was observed in 29 [55%] patients, relapsing and remitting episodes in nine [17%], progressive symptoms in three [6%]: two [4%] patients were diagnosed with MS. There was no significant difference between MS GRS scores in cases (mean -3.5 × 10–4, standard deviation [SD] 0.0039) and controls [mean -1.1 × 10–3, SD 0.0042] [p = 0.23].</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions</jats:title> <jats:p>Patients who experienced demyelination events following anti-TNF exposure were more likely female, less frequently treated with an immunomodulator, and had a similar genetic risk to anti-TNF exposed controls who did not experience demyelination events. Large prospective studies with pre-treatment neuroimaging are required to identify genetic susceptibility loci.</jats:p> </jats:sec>

dc.format.extent1653-1661
dc.format.mediumPrint
dc.languageen
dc.language.isoen
dc.publisherOxford University Press (OUP)
dc.subjectDemyelination
dc.subjectanti-TNF
dc.titleClinical features and genetic risk of demyelination following anti-TNF treatment
dc.typejournal-article
dc.typeJournal Article
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000606032500002&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue12
plymouth.volume14
plymouth.publication-statusPublished
plymouth.journalJournal of Crohn's and Colitis
dc.identifier.doi10.1093/ecco-jcc/jjaa104
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Medical School
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA03 Allied Health Professions, Dentistry, Nursing and Pharmacy
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CCT&PS
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeEngland
dcterms.dateAccepted2020-04-29
dc.rights.embargodate2021-5-4
dc.identifier.eissn1876-4479
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1093/ecco-jcc/jjaa104
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2020-05-04
rioxxterms.typeJournal Article/Review


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record


All items in PEARL are protected by copyright law.
Author manuscripts deposited to comply with open access mandates are made available in accordance with publisher policies. Please cite only the published version using the details provided on the item record or document. In the absence of an open licence (e.g. Creative Commons), permissions for further reuse of content should be sought from the publisher or author.
Theme by 
Atmire NV