Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/37810
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dc.contributor.authorRosenfeld, Jeffreyen_UK
dc.contributor.authorAbrahams, Sharonen_UK
dc.contributor.authorMcHutchinson, Carolineen_UK
dc.contributor.authorAjroud-Driss, Sendaen_UK
dc.contributor.authorWeber, Markusen_UK
dc.contributor.authorPaganoni, Sabrinaen_UK
dc.contributor.authorMitsumoto, Hiroshien_UK
dc.contributor.authorGenge, Angelaen_UK
dc.contributor.authorGrosskreutz, Julianen_UK
dc.contributor.authorVan Den Berg, Leonarden_UK
dc.contributor.authorAndrews, Jinsyen_UK
dc.contributor.authorKiernan, Matthew Cen_UK
dc.date.accessioned2026-01-27T01:08:50Z-
dc.date.available2026-01-27T01:08:50Z-
dc.date.issued2025-12-08en_UK
dc.identifier.urihttp://hdl.handle.net/1893/37810-
dc.description.abstractThe heterogeneity among the amyotrophic lateral sclerosis (ALS)/MND patient population is well recognized but not well understood. Such heterogeneity may represent a significant confound in our current and prior clinical trials as certain subgroups of patients might have a selective response (or resistance) to a novel therapeutic. The basis on which to segregate the patient population is, however, unclear. The ALS/MND Committee of the World Federation of Neurology (WFN) convened a symposium to discuss various strategies that might be considered for separating (stratifying) the population to further study. The results of that conference are presented here as a white paper, reflecting current understanding of several of the various criteria that could be implemented to divide the patient population as presented and discussed at that meeting. Consideration of grouping patients based on phenotype, cognitive involvement, imaging, or electrophysiology is presented here.en_UK
dc.language.isoenen_UK
dc.publisherInforma UK Limiteden_UK
dc.relationRosenfeld J, Abrahams S, McHutchinson C, Ajroud-Driss S, Weber M, Paganoni S, Mitsumoto H, Genge A, Grosskreutz J, Van Den Berg L, Andrews J & Kiernan MC (2025) Utility of patient subgrouping in ALS clinical trials: a World Federation of Neurology white paper. <i>Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration</i>. https://doi.org/10.1080/21678421.2025.2593308en_UK
dc.rights© 2025 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.en_UK
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_UK
dc.subjectALS heterogeneityen_UK
dc.subjectclinical trial designen_UK
dc.subjectALS subtypesen_UK
dc.subjectstratificationen_UK
dc.subjectsubgroupingen_UK
dc.titleUtility of patient subgrouping in ALS clinical trials: a World Federation of Neurology white paperen_UK
dc.typeJournal Articleen_UK
dc.identifier.doi10.1080/21678421.2025.2593308en_UK
dc.identifier.pmid41361897en_UK
dc.citation.jtitleAmyotrophic Lateral Sclerosis and Frontotemporal Degenerationen_UK
dc.citation.issn2167-8421en_UK
dc.citation.issn2167-8421en_UK
dc.citation.peerreviewedRefereeden_UK
dc.type.statusVoR - Version of Recorden_UK
dc.contributor.funderUniversity of Stirlingen_UK
dc.author.emailcaroline.mchutchison@stir.ac.uken_UK
dc.citation.date08/12/2025en_UK
dc.contributor.affiliationLoma Linda University Healthen_UK
dc.contributor.affiliationUniversity of Edinburghen_UK
dc.contributor.affiliationPsychologyen_UK
dc.contributor.affiliationNorthwestern Universityen_UK
dc.contributor.affiliationHOCH, Kantonsspital St.Gallen, Muskelzentrum/ALS Clinicen_UK
dc.contributor.affiliationMassachusetts General Hospitalen_UK
dc.contributor.affiliationColumbia Universityen_UK
dc.contributor.affiliationMcGill Universityen_UK
dc.contributor.affiliationUniversity of Lubecken_UK
dc.contributor.affiliationUtrecht Universityen_UK
dc.contributor.affiliationColumbia Universityen_UK
dc.contributor.affiliationNeuroscience Research Australia (NeuRA)en_UK
dc.identifier.isiWOS:001635221800001en_UK
dc.identifier.scopusid105024896314en_UK
dc.identifier.wtid2217653en_UK
dc.contributor.orcid0000-0003-0103-8580en_UK
dc.date.accepted2025-11-17en_UK
dcterms.dateAccepted2025-11-17en_UK
dc.date.filedepositdate2025-12-10en_UK
rioxxterms.apcnot requireden_UK
rioxxterms.versionVoRen_UK
local.rioxx.authorRosenfeld, Jeffrey|en_UK
local.rioxx.authorAbrahams, Sharon|en_UK
local.rioxx.authorMcHutchinson, Caroline|0000-0003-0103-8580en_UK
local.rioxx.authorAjroud-Driss, Senda|en_UK
local.rioxx.authorWeber, Markus|en_UK
local.rioxx.authorPaganoni, Sabrina|en_UK
local.rioxx.authorMitsumoto, Hiroshi|en_UK
local.rioxx.authorGenge, Angela|en_UK
local.rioxx.authorGrosskreutz, Julian|en_UK
local.rioxx.authorVan Den Berg, Leonard|en_UK
local.rioxx.authorAndrews, Jinsy|en_UK
local.rioxx.authorKiernan, Matthew C|en_UK
local.rioxx.projectProject ID unknown|University of Stirling|en_UK
local.rioxx.freetoreaddate2026-01-26en_UK
local.rioxx.licencehttp://creativecommons.org/licenses/by/4.0/|2026-01-26|en_UK
local.rioxx.filenameUtility of patient subgrouping in ALS clinical trials a World Federation of Neurology white paper.pdfen_UK
local.rioxx.filecount1en_UK
local.rioxx.source2167-8421en_UK
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