| Literature DB >> 27105209 |
Robert Zivadinov1,2, Dejan Jakimovski1, Sirin Gandhi1, Rahil Ahmed1, Michael G Dwyer1, Dana Horakova3, Bianca Weinstock-Guttman4, Ralph R H Benedict4, Manuela Vaneckova5, Michael Barnett6, Niels Bergsland1,7.
Abstract
INTRODUCTION: Brain atrophy measurement in multiple sclerosis (MS) has become an important outcome for determining patients at risk for developing physical and cognitive disability. AREAS COVERED: In this article, we discuss the methodological issues related to using this MRI metric routinely, in a clinical setting. Understanding trajectories of annualized whole brain, gray and white matter, thalamic volume loss, and enlargement of ventricular space in specific MS phenotypes is becoming increasingly important. Evidence is mounting that disease-modifying treatments exert a positive effect on slowing brain atrophy progression in MS. Expert Commentary: While there is a need to translate measurement of brain atrophy to clinical routine at the individual patient level, there are still a number of challenges to be met before this can actually happen, including how to account for biological confounding factors and pseudoatrophy, standardize acquisition and analyses parameters, which can influence the accuracy of the assessments.Entities:
Keywords: Multiple sclerosis; biological confounding factors; brain atrophy; clinical routine; cognition; disability; disease-modifying treatment; gray matter; measurement; pseudoatrophy
Mesh:
Year: 2016 PMID: 27105209 DOI: 10.1080/14737175.2016.1181543
Source DB: PubMed Journal: Expert Rev Neurother ISSN: 1473-7175 Impact factor: 4.618