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Clinical Outcome Evaluations and CBT Response Prediction in Myotonic Dystrophy

Authors :
Jeffrey C. Glennon
Benedikt Schoser
Hanns Lochmüller
Guillaume Bassez
Peter A C 't Hoen
Kees Okkersen
Daniël van As
Baziel G.M. van Engelen
Hans Knoop
Radboud University Medical Center [Nijmegen]
Unité clinique de pathologie neuromusculaire [CHU Pitié-Salpêtrière]
Institut de Myologie
Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Ludwig Maximilian University [Munich] (LMU)
Children's Hospital of Eastern Ontario Research Institute
The Ottawa Hospital
University of Ottawa [Ottawa]
University College Dublin [Dublin] (UCD)
University of Amsterdam [Amsterdam] (UvA)
APH - Mental Health
Medical Psychology
Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
HAL-SU, Gestionnaire
Source :
Journal of Neuromuscular Diseases, 8, 6, pp. 1031-1046, Journal of Neuromuscular Diseases, Journal of Neuromuscular Diseases, IOS Press, 2021, 8 (6), pp.1031-1046. ⟨10.3233/jnd-210634⟩, Journal of neuromuscular diseases, 8(6), 1031-1046. IOS Press, Journal of Neuromuscular Diseases, 8, 1031-1046, Journal of Neuromuscular Diseases, 2021, 8 (6), pp.1031-1046. ⟨10.3233/jnd-210634⟩
Publication Year :
2021

Abstract

BackgroundThe European OPTIMISTIC clinical trial has demonstrated a significant, yet heterogenous effect of Cognitive Behavioural Therapy (CBT) for Myotonic Dystrophy type 1 (DM1) patients. One of its remaining aims was the assessment of efficacy and adequacy of clinical outcome measures, including the relatively novel primary trial outcome, the DM1-Activ-c questionnaire.ObjectivesAssessment of the relationship between the Rasch-built DM1-Activ-c questionnaire and 26 commonly used clinical outcome measurements. Identification of variables associated with CBT response in DM1 patients.MethodsRetrospective analysis of the to date largest clinical trial in DM1 (OPTIMISTIC), comprising of 255 genetically confirmed DM1 patients randomized to either standard care or CBT with optionally graded exercise therapy. Correlations of 27 different outcome measures were calculated at baseline (cross-sectional) and of their respective intervention induced changes (longitudinal). Bootstrap enhanced Elastic-Net (BeEN) regression was validated and implemented to select variables associated with CBT response.ResultsIn cross-sectional data, DM1-Activ-c correlated significantly with the majority of other outcome measures, including Six Minute Walk Test and Myotonic Dystrophy Health Index. Fewer and weaker significant longitudinal correlations were observed. Nine variables potentially associated with CBT response were identified, including measures of disease severity, executive cognitive functioning and perceived social support.ConclusionsThe DM1-Activ-c questionnaire appears to be a well suited cross-sectional instrument to assess a variety of clinically relevant dimensions in DM1. Yet, apathy and experienced social support measures were less well captured. CBT response was heterogenous, requiring careful selection of outcome measures for different disease aspects.

Details

ISSN :
22143599 and 22143602
Database :
OpenAIRE
Journal :
Journal of Neuromuscular Diseases, 8, 6, pp. 1031-1046, Journal of Neuromuscular Diseases, Journal of Neuromuscular Diseases, IOS Press, 2021, 8 (6), pp.1031-1046. ⟨10.3233/jnd-210634⟩, Journal of neuromuscular diseases, 8(6), 1031-1046. IOS Press, Journal of Neuromuscular Diseases, 8, 1031-1046, Journal of Neuromuscular Diseases, 2021, 8 (6), pp.1031-1046. ⟨10.3233/jnd-210634⟩
Accession number :
edsair.doi.dedup.....bb2e98d864b62985a792e473a98fe6cf