4.7 Article

Treatment Effect on Brain Atrophy Correlates with Treatment Effect on Cognition in Multiple Sclerosis

Journal

ANNALS OF NEUROLOGY
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1002/ana.26751

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The objective of this study was to assess the mediating effect of treatment on MRI-derived measures of brain atrophy and focal lesions on cognitive outcomes in MS clinical trials. The study analyzed published randomized trials in MS lasting at least 2 years and found that treatment effect on cognitive performance was strongly associated with the treatment effect on brain atrophy, but not with active MRI lesions. These results suggest that brain atrophy can be a main outcome measure for clinical trials targeting cognitive impairment and neurodegeneration in MS.
Objective: The purpose of this study was to evaluate the extent to which treatment effect on magnetic resonance imaging (MRI)-derived measures of brain atrophy and focal lesions can mediate, at the trial level, the treatment effect on cognitive outcomes in multiple sclerosis (MS). Methods: We collected all published randomized clinical trials in MS lasting at least 2 years and including as end points: active MRI lesions (defined as new/enlarging T2 lesions), brain atrophy (defined as a change in brain volume between month 12 and month 24), and change in cognitive performance (assessed by the Paced Auditory Serial Addition Test [PASAT]). Relative reductions were used to quantify the treatment effect on MRI markers (lesions and atrophy), whereas the standardized mean difference (Hedges g) between baseline and follow-up cognitive assessment was used to quantify the treatment effects on cognition. A linear regression, weighted for trial size, was used to assess the relationship between the treatment effects on MRI markers and cognition. Results: Fourteen trials including more than 8,813 patients with MS were included in the meta-regression. Treatment effect on cognition was strongly associated with the treatment effect on brain atrophy (R-2 = 0.79, p < 0.001), but was not correlated with the treatment effect on active MRI lesions (R-2 = 0.16, p = 0.14). Interpretation: Results reported here suggest that brain atrophy, a well-established MRI marker in MS clinical trials, can be used as a main outcome for clinical trials with drugs targeting cognitive impairment and neurodegeneration.

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