4.1 Review

Clinical relevance of brain atrophy assessment in multiple sclerosis. Implications for its use in a clinical routine

期刊

EXPERT REVIEW OF NEUROTHERAPEUTICS
卷 16, 期 7, 页码 777-793

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/14737175.2016.1181543

关键词

Multiple sclerosis; brain atrophy; gray matter; measurement; pseudoatrophy; biological confounding factors; disability; cognition; disease-modifying treatment; clinical routine

资金

  1. Teva Neuroscience
  2. Biogen Idec
  3. EMD Serono
  4. Questcor Pharmaceuticals
  5. Genzyme
  6. Bracco
  7. Claret Medical
  8. Novartis
  9. Czech Ministry of Education [PRVOUK-P26/LF1/4]
  10. Czech Science Foundation [GA CR 16-03322S]
  11. Merck
  12. Bayer
  13. Sanofi Genzyme
  14. Teva
  15. Teva Pharmaceuticals
  16. GenzymeSanofi
  17. Acorda
  18. Shire Pharmaceuticals
  19. Czech Ministry of Health [RVO-VFN64165/2012]
  20. Merck Serono

向作者/读者索取更多资源

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.

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