Atrophied Brain T2 Lesion Volume at MRI Is Associated with Disability Progression and Conversion to Secondary

Antonia Valentina Genovese1, Jesper Hagemeier1, Niels Bergsland1

  • 1From the Buffalo Neuroimaging Analysis Center (A.V.G., J.H., N.B., D.J., M.G.D., D.P.R., R.Z.) and Jacobs MS Center (A.A.L., D.H., C.K.), Department of Neurology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, 100 High St, Buffalo, NY 14203; Institute of Radiology, Department of Clinical Surgical Diagnostic and Pediatric Sciences, University of Pavia, Pavia, Italy (A.V.G.); and Center for Biomedical Imaging at Clinical Translational Science Institute (M.G.D., B.W., R.Z.), University at Buffalo, State University of New York, Buffalo, NY.

Radiology
|September 25, 2019
PubMed

Insights

Atrophied T2 lesion volume on MRI is a strong indicator of multiple sclerosis disability progression and conversion to secondary progressive MS. This imaging marker helps predict disease worsening and disease course changes.

Area of Science:

  • Neurology
  • Radiology
  • Medical Imaging

Background:

  • Atrophied T2 lesion volume on MRI quantifies the replacement of T2 lesions by cerebrospinal fluid spaces in multiple sclerosis (MS).
  • Understanding imaging markers associated with disease progression is crucial for managing MS.

Purpose of the Study:

  • To investigate the association between atrophied T2 lesion volume and the development of disability progression (DP) in MS.
  • To examine the relationship between atrophied T2 lesion volume and conversion to secondary progressive MS (SPMS).

Main Methods:

  • Retrospective study of 1612 participants with MS, clinically isolated syndrome, or as healthy controls, followed for 5 years.
  • MRI measurements included T2 lesion volume, atrophied T2 lesion volume, percentage brain volume change (PBVC), and percentage ventricular volume change (PVVC).
  • Disability progression and SPMS conversion were defined using standardized guidelines; statistical analyses included ANCOVA and Cox regression.

Main Results:

  • Patients who converted to DP showed significantly higher atrophied T2 lesion volume compared to non-converters.
  • Atrophied T2 lesion volume was independently associated with both disability progression (HR, 1.23; P < .001) and conversion to SPMS (HR, 1.16; P = .008) in Cox regression analysis.
  • Other MRI measures like PBVC, PVVC, and T2 lesion volume change were not consistently associated with DP or SPMS conversion.

Conclusions:

  • Atrophied brain T2 lesion volume is a reliable MRI marker for predicting disability progression in multiple sclerosis.
  • This imaging metric serves as a robust predictor of conversion to a secondary progressive disease course in MS patients.

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