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dc.contributor.authorBagnato, Francesca
dc.contributor.authorSati, Pascal
dc.contributor.authorHemond, Christopher C
dc.contributor.authorElliott, Colm
dc.contributor.authorGauthier, Susan A
dc.contributor.authorHarrison, Daniel M
dc.contributor.authorMainero, Caterina
dc.contributor.authorOh, Jiwon
dc.contributor.authorPitt, David
dc.contributor.authorShinohara, Russell T
dc.contributor.authorSmith, Seth A
dc.contributor.authorTrapp, Bruce
dc.contributor.authorAzevedo, Christina J
dc.contributor.authorCalabresi, Peter A
dc.contributor.authorHenry, Roland G
dc.contributor.authorLaule, Cornelia
dc.contributor.authorOntaneda, Daniel
dc.contributor.authorRooney, William D
dc.contributor.authorSicotte, Nancy L
dc.contributor.authorReich, Daniel S
dc.contributor.authorAbsinta, Martina
dc.date.accessioned2024-10-18T13:43:08Z
dc.date.available2024-10-18T13:43:08Z
dc.date.issued2024-01-16
dc.identifier.citationBagnato F, Sati P, Hemond CC, Elliott C, Gauthier SA, Harrison DM, Mainero C, Oh J, Pitt D, Shinohara RT, Smith SA, Trapp B, Azevedo CJ, Calabresi PA, Henry RG, Laule C, Ontaneda D, Rooney WD, Sicotte NL, Reich DS, Absinta M. Imaging chronic active lesions in multiple sclerosis: a consensus statement. Brain. 2024 Sep 3;147(9):2913-2933. doi: 10.1093/brain/awae013. PMID: 38226694; PMCID: PMC11370808.en_US
dc.identifier.eissn1460-2156
dc.identifier.doi10.1093/brain/awae013en_US
dc.identifier.pmid38226694
dc.identifier.urihttp://hdl.handle.net/20.500.14038/53896
dc.description.abstractChronic active lesions (CAL) are an important manifestation of chronic inflammation in multiple sclerosis and have implications for non-relapsing biological progression. In recent years, the discovery of innovative MRI and PET-derived biomarkers has made it possible to detect CAL, and to some extent quantify them, in the brain of persons with multiple sclerosis, in vivo. Paramagnetic rim lesions on susceptibility-sensitive MRI sequences, MRI-defined slowly expanding lesions on T1-weighted and T2-weighted scans, and 18-kDa translocator protein-positive lesions on PET are promising candidate biomarkers of CAL. While partially overlapping, these biomarkers do not have equivalent sensitivity and specificity to histopathological CAL. Standardization in the use of available imaging measures for CAL identification, quantification and monitoring is lacking. To fast-forward clinical translation of CAL, the North American Imaging in Multiple Sclerosis Cooperative developed a consensus statement, which provides guidance for the radiological definition and measurement of CAL. The proposed manuscript presents this consensus statement, summarizes the multistep process leading to it, and identifies the remaining major gaps in knowledge.en_US
dc.language.isoen
dc.relation.ispartofBrainen_US
dc.relation.urlhttps://doi.org/10.1093/brain/awae013en_US
dc.rights© The Author(s) 2024. Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com. Elements of this work were written by employees of the US Government.en_US
dc.subjectMRI-defined slowly evolving lesionsen_US
dc.subjectchronic active lesionsen_US
dc.subjectironen_US
dc.subjectmicrogliaen_US
dc.subjectmultiple sclerosisen_US
dc.subjectparamagnetic rim lesionsen_US
dc.subjectUMCCTS fundingen_US
dc.titleImaging chronic active lesions in multiple sclerosis: a consensus statementen_US
dc.typeJournal Articleen_US
dc.source.journaltitleBrain : a journal of neurology
dc.source.volume147
dc.source.issue9
dc.source.beginpage2913
dc.source.endpage2933
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryEngland
dc.identifier.journalBrain : a journal of neurology
dc.contributor.departmentNeurologyen_US


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