Assessing Progression Independent of Relapse Activity in Multiple Sclerosis Using a Patient-Reported Disability Measure and Self-Administered Neuroperformance Outcomes

Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Beigetragen › Begutachtung

Beitragende

  • Evy M Reinders - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Ariadna Masot-Llima - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Susana Otero-Romero - , Hospital Universitari Vall d'Hebron (Autor:in)
  • René Carvajal - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Álvaro Cobo-Calvo - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Pere Carbonell-Mirabent - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Jordina Beltran - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Maria Jesús Arévalo - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Helena Ariño - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Georgina Arrambide - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Cristina Auger - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Luca Bollo - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Joaquín Castilló - , CIBER - Enfermedades Neurodegenerativas (Autor:in)
  • Manuel Comabella - , CIBER - Enfermedades Neurodegenerativas (Autor:in)
  • Ingrid Galán - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Alexis García-Sarreón - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Andrew Goodman - , University of Rochester Medical Center (Autor:in)
  • Carrie M Hersh - , Lou Ruvo Center for Brain Health (LRCBH) (Autor:in)
  • Delon La Puma - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Le H Hua - , Lou Ruvo Center for Brain Health (LRCBH) (Autor:in)
  • Luciana Midaglia - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Neus Mongay-Ochoa - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Ellen M Mowry - , Johns Hopkins Medicine (Autor:in)
  • Agustín Pappolla - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Breogán Rodríguez-Acevedo - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Jordi Río - , CIBER - Enfermedades Neurodegenerativas (Autor:in)
  • Paula Tagliani - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Ángela Vidal-Jordana - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Andreu Vilaseca - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Ana Zabalza - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Deborah Pareto - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Carlos Nos - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Menno Schoonheim - , Amsterdam University Medical Centers (UMC) (Autor:in)
  • Eva Strijbis - , Amsterdam University Medical Centers (UMC) (Autor:in)
  • Jaume Sastre-Garriga - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Madalina Tivarus - , University of Rochester Medical Center (Autor:in)
  • Tjalf Ziemssen - , Klinik und Poliklinik für Neurologie, Zentrum für klinische Neurowissenschaften (Autor:in)
  • Àlex Rovira - , Hospital Universitari Vall d'Hebron (Autor:in)
  • Xavier Montalban - , The University of Vic - Central University of Catalonia (Autor:in)
  • Mar Tintoré - , The University of Vic - Central University of Catalonia (Autor:in)
  • Carmen Tur - , CIBER - Enfermedades Neurodegenerativas (Autor:in)

Abstract

OBJECTIVE: The objective of this study was to investigate the ability of patient-reported/administered outcomes to capture disability worsening and progression independent of relapse activity (PIRA) in multiple sclerosis (MS).

METHODS: We included patients from the longitudinal multicenter MS PATHS cohort with ≥3 assessments and >6 months follow-up. PIRA was defined on the patient-determined disease steps (PDDS) and self-administered tests assessing walking speed, manual dexterity, and processing speed, in the absence of self-reported relapses. We assessed (i) prevalence of PDDS/self-administered test-based disability worsening and PIRA definitions; (ii) their concurrent validity, through the association with worsening and PIRA definitions based on the expanded disability status scale (EDSS; Barcelona subcohort); and (iii) their clinical meaningfulness, through the correlation with brain magnetic resonance imaging (MRI) and quality-of-life (QoL) data trajectories.

RESULTS: We included 9,088 patients (73% female patients; age = 46.8 years; disease duration = 14.2 years). Over a 3-year follow-up, 4,066 (45%) patients worsened on ≥1 patient-reported/administered outcome, of which 2,357 (58%) developed PIRA. In the Barcelona subcohort (N = 279), 68 (24%) patients developed EDSS-based worsening, of which 30 (44%) developed EDSS-based PIRA; 99 of 279 (35%) worsened on ≥1 patient-reported/administered test, of which 78 of 99 (79%) had PIRA. Worsening (but not PIRA) on PDDS was associated with EDSS-based worsening (odds ratio = 3.03 [1.42; 6.43], p = 0.004). PDDS/self-administered-test-based worsening or PIRA strongly correlated with accelerated brain atrophy and T2 lesion volume increase compared to non-worseners (p < 0.05), and showed worse QoL (p < 0.05).

INTERPRETATION: Despite only partial agreement with EDSS-based definitions, PDDS/self-administered test-based worsening and PIRA definitions were clinically meaningful, by identifying patients with greater brain damage and poorer QoL, supporting their use in clinical practice. ANN NEUROL 2026.

Details

OriginalspracheEnglisch
Seiten (von - bis)525-546
Seitenumfang22
FachzeitschriftAnnals of neurology
Jahrgang100
Ausgabenummer3
Frühes Online-Datum6 Juli 2026
PublikationsstatusVeröffentlicht - Sept. 2026
Peer-Review-StatusJa

Externe IDs

Scopus 105043946938
ORCID /0000-0001-8799-8202/work/222763322

Schlagworte