CP14
Cognitive Evolution in Tysabri Treated Multiple Sclerosis Patients

Friday, May 29, 2015
Griffin Hall
Francois H Jacques, MD , Clinique Neuro-Outaouais, Gatineau, QC, Canada
Brian T Harel, PhD , Cogstate, New Haven, CT
Adrian J Schembri, DPsych , Cogstate, Melbourne, Australia
Chantal Paquette, BScN , Clinique Neuro-Outaouais, Gatineau, QC, Canada
Brigitte Bilodeau, BSc , Clinique Neuro-Outaouais, Gatineau, QC, Canada
Pawel Kalinowski, PhD , Cogstate, Melbourne, Australia



Background:

Cognitive dysfunction affects up to 65% of MS patients and progresses over time. Natalizumab has shown to be superior to placebo in preserving cognitive function for the first two years of therapy.

Objectives:

The objectives of this study are to understand the impact of natalizumab on cognition beyond two years of therapy and to investigate whether baseline characteristics are predictive of clinical response.

Methods:

This is a single-center, 24-month, observational study. Sixty-three patients treated with natalizumab were assessed prior to monthly infusions using a Cogstate battery and the SDMT. A Beck Depression Index (BDI) was administered every 4 months. Patient demographics, including EDSS, MSSS, education level, age, MS disease duration, BDI scores, natalizumab treatment duration and presence of cognitive impairment, were collected at baseline. A linear mixed model was conducted with duration of natalizumab therapy as a between-subjects factor (<=2 or >2 years), assessment as a within-subjects factor, and MSSS as a covariate. All patients in the <=2 years group were treated with natalizumab for less than two years prior to baseline. All patients in the >2 years group were treated with natalizumab for at least two years prior to the baseline (mean 3.6 years).

Results:

There were no statistically significant differences between the key demographic variables aside for the MSSS (p=.0074). No patient showed evidence of sustained cognitive deterioration over the 24 month period. Irrespective of time on natalizumab, significant improvements were observed at the group level in executive function, verbal memory and working memory, whereas processing speed and attention remained unchanged. Impaired cognition or any other baseline parameter did not influence the trajectory of cognitive change over 24 months.

Conclusions:

Our results suggest that natalizumab preserves cognitive function, including the ability to learn, for 4 years and beyond of continuous therapy. This occurs irrespective of baseline characteristics.