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Assessment of disease progression in dysferlinopathy: A 1-year cohort study.

dc.contributor.authorMoore, Ursula
dc.contributor.authorJacobs, Marni
dc.contributor.authorJames, Meredith K
dc.contributor.authorMayhew, Anna G
dc.contributor.authorFernandez-Torron, Roberto
dc.contributor.authorFeng, Jia
dc.contributor.authorCnaan, Avital
dc.contributor.authorEagle, Michelle
dc.contributor.authorBettinson, Karen
dc.contributor.authorRufibach, Laura E
dc.contributor.authorLofra, Robert Muni
dc.contributor.authorBlamire, Andrew M
dc.contributor.authorCarlier, Pierre G
dc.contributor.authorMittal, Plavi
dc.contributor.authorLowes, Linda Pax
dc.contributor.authorAlfano, Lindsay
dc.contributor.authorRose, Kristy
dc.contributor.authorDuong, Tina
dc.contributor.authorBerry, Katherine M
dc.contributor.authorMontiel-Morillo, Elena
dc.contributor.authorPedrosa-Hernandez, Irene
dc.contributor.authorHolsten, Scott
dc.contributor.authorSanjak, Mohammed
dc.contributor.authorAshida, Ai
dc.contributor.authorSakamoto, Chikako
dc.contributor.authorTateishi, Takayuki
dc.contributor.authorYajima, Hiroyuki
dc.contributor.authorCanal, Aurelie
dc.contributor.authorOllivier, Gwenn
dc.contributor.authorDecostre, Valerie
dc.contributor.authorMendez, Juan Bosco
dc.contributor.authorSanchez-Aguilera-Praxedes, Nieves
dc.contributor.authorThiele, Simone
dc.contributor.authorSiener, Catherine
dc.contributor.authorShierbecker, Jeanine
dc.contributor.authorFlorence, Julaine M
dc.contributor.authorVandevelde, Bruno
dc.contributor.authorDeWolf, Brittney
dc.contributor.authorHutchence, Meghan
dc.contributor.authorGee, Richard
dc.contributor.authorPrügel, Juliana
dc.contributor.authorMaron, Elke
dc.contributor.authorHilsden, Heather
dc.contributor.authorLochmüller, Hanns
dc.contributor.authorGrieben, Ulrike
dc.contributor.authorSpuler, Simone
dc.contributor.authorTesi Rocha, Carolina
dc.contributor.authorDay, John W
dc.contributor.authorJones, Kristi J
dc.contributor.authorBharucha-Goebel, Diana X
dc.contributor.authorSalort-Campana, Emmanuelle
dc.contributor.authorHarms, Matthew
dc.contributor.authorPestronk, Alan
dc.contributor.authorKrause, Sabine
dc.contributor.authorSchreiber-Katz, Olivia
dc.contributor.authorWalter, Maggie C
dc.contributor.authorParadas, Carmen
dc.contributor.authorHogrel, Jean-Yves
dc.contributor.authorStojkovic, Tanya
dc.contributor.authorTakeda, Shin'ichi
dc.contributor.authorMori-Yoshimura, Madoka
dc.contributor.authorBravver, Elena
dc.contributor.authorSparks, Susan
dc.contributor.authorDiaz-Manera, Jordi
dc.contributor.authorBello, Luca
dc.contributor.authorSemplicini, Claudio
dc.contributor.authorPegoraro, Elena
dc.contributor.authorMendell, Jerry R
dc.contributor.authorBushby, Kate
dc.contributor.authorStraub, Volker
dc.contributor.groupJain COS Consortium
dc.date.accessioned2023-01-25T10:27:50Z
dc.date.available2023-01-25T10:27:50Z
dc.date.issued2019-01-09
dc.description.abstractTo assess the ability of functional measures to detect disease progression in dysferlinopathy over 6 months and 1 year. One hundred ninety-three patients with dysferlinopathy were recruited to the Jain Foundation's International Clinical Outcome Study for Dysferlinopathy. Baseline, 6-month, and 1-year assessments included adapted North Star Ambulatory Assessment (a-NSAA), Motor Function Measure (MFM-20), timed function tests, 6-minute walk test (6MWT), Brooke scale, Jebsen test, manual muscle testing, and hand-held dynamometry. Patients also completed the ACTIVLIM questionnaire. Change in each measure over 6 months and 1 year was calculated and compared between disease severity (ambulant [mild, moderate, or severe based on a-NSAA score] or nonambulant [unable to complete a 10-meter walk]) and clinical diagnosis. The functional a-NSAA test was the most sensitive to deterioration for ambulant patients overall. The a-NSAA score was the most sensitive test in the mild and moderate groups, while the 6MWT was most sensitive in the severe group. The 10-meter walk test was the only test showing significant change across all ambulant severity groups. In nonambulant patients, the MFM domain 3, wrist flexion strength, and pinch grip were most sensitive. Progression rates did not differ by clinical diagnosis. Power calculations determined that 46 moderately affected patients are required to determine clinical effectiveness for a hypothetical 1-year clinical trial based on the a-NSAA as a clinical endpoint. Certain functional outcome measures can detect changes over 6 months and 1 year in dysferlinopathy and potentially be useful in monitoring progression in clinical trials. NCT01676077.
dc.description.versionSi
dc.identifier.citationMoore U, Jacobs M, James MK, Mayhew AG, Fernandez-Torron R, Feng J, et al. Assessment of disease progression in dysferlinopathy: A 1-year cohort study. Neurology. 2019 Jan 28;92(5):e461-e474.
dc.identifier.doi10.1212/WNL.0000000000006858
dc.identifier.essn1526-632X
dc.identifier.pmcPMC6369904
dc.identifier.pmid30626655
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369904/pdf
dc.identifier.unpaywallURLhttps://n.neurology.org/content/neurology/92/5/e461.full.pdf
dc.identifier.urihttp://hdl.handle.net/10668/13402
dc.issue.number5
dc.journal.titleNeurology
dc.journal.titleabbreviationNeurology
dc.language.isoen
dc.organizationÁrea de Gestión Sanitaria Sur de Sevilla
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen del Rocío
dc.organizationHospital Universitario Virgen del Rocío
dc.organizationAGS - Sur de Sevilla
dc.page.numbere461-e474
dc.provenanceRealizada la curación de contenido 12/03/2025
dc.publisherWolters Kluwer Health
dc.pubmedtypeJournal Article
dc.relation.publisherversionhttps://www.neurology.org/doi/10.1212/WNL.0000000000006858?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%20%200pubmed
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectHumans
dc.subjectWalk Test
dc.subjectOutcome Assessment, Health Care
dc.subjectMuscles
dc.subject.decsPacientes
dc.subject.decsDiagnóstico clínico
dc.subject.decsFuerza de la mano
dc.subject.decsMuñeca
dc.subject.decsGravedad del paciente
dc.subject.decsProgresión de la enfermedad
dc.subject.decsResultado del tratamiento
dc.subject.decsMúsculos
dc.subject.decsPoder psicológico
dc.subject.meshWrist
dc.subject.meshDysferlinopathy
dc.subject.meshTreatment Outcome
dc.subject.meshDisease Progression
dc.subject.meshHand Strength
dc.titleAssessment of disease progression in dysferlinopathy: A 1-year cohort study.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number92
dspace.entity.typePublication

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