Your browser doesn't support javascript.
loading
Association Between Cognitive Trajectories and Disability Progression in Patients With Relapsing-Remitting Multiple Sclerosis.
Merlo, Daniel; Stankovich, Jim; Bai, Claire; Kalincik, Tomas; Zhu, Chao; Gresle, Melissa; Lechner-Scott, Jeannette; Kilpatrick, Trevor; Barnett, Michael; Taylor, Bruce; Darby, David; Butzkueven, Helmut; Van der Walt, Anneke.
Afiliación
  • Merlo D; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Stankovich J; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Bai C; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Kalincik T; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Zhu C; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Gresle M; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Lechner-Scott J; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Kilpatrick T; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Barnett M; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Taylor B; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Darby D; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Butzkueven H; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
  • Van der Walt A; From the Department of Neuroscience (D.M., J.S., C.Z., M.G., H.B., A.V.d.W.), Central Clinical School, Monash University; CORe (C.B., T. Kalincik), Department of Medicine at RMH, University of Melbourne; Department of Neurology (T. Kalincik, T. Kilpatrick), Royal Melbourne Hospital, Parkville; Depar
Neurology ; 97(20): e2020-e2031, 2021 11 16.
Article en En | MEDLINE | ID: mdl-34556562
ABSTRACT
BACKGROUND AND

OBJECTIVES:

Longitudinal cognitive trajectories in multiple sclerosis are heterogeneous and difficult to measure. We aimed to identify discrete longitudinal reaction time trajectories in relapsing-remitting multiple sclerosis using a computerized cognitive battery and to assess the association between trajectories of reaction time and disability progression.

METHODS:

All participants serially completed computerized reaction time tasks measuring psychomotor speed, visual attention, and working memory. Participants completed at least 3 testing sessions over a minimum of 180 days. Longitudinal reaction times were modeled with latent class mixed models to identify groups of individuals sharing similar latent characteristics. Optimal models were validated for consistency and baseline associations with class membership tested using multinomial logistic regression. Interclass differences in the probability of reaction time worsening and the probability of 6-month confirmed disability progression were assessed with survival analysis.

RESULTS:

A total of 460 people with relapsing-remitting multiple sclerosis were included in the analysis. For each task of the MSReactor battery, the optimal model comprised 3 latent classes. All MSReactor tasks could identify a group with high probability of reaction time slowing. The visual attention and working memory tasks could identify a group of participants who were 3.7 and 2.6 times more likely to experience a 6-month confirmed disability progression, respectively. Participants could be classified into predicted cognitive trajectories after just 5 tests with 64% to 89% accuracy.

DISCUSSION:

Latent class modeling of longitudinal cognitive data collected by a computerized battery identified patients with worsening reaction times and increased risk of disability progression. Slower baseline reaction time, age, and disability increased assignment into this trajectory. Monitoring of cognition in clinical practice with computerized tests may enable detection of cognitive change trajectories and people with relapsing-remitting multiple sclerosis at risk of disability progression.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos del Conocimiento / Esclerosis Múltiple Recurrente-Remitente / Evaluación de la Discapacidad Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Neurology Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos del Conocimiento / Esclerosis Múltiple Recurrente-Remitente / Evaluación de la Discapacidad Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Neurology Año: 2021 Tipo del documento: Article