Unraveling the neuroimaging predictors for motor dysfunction in long- standing multiple sclerosis

作者:Daams Marita*; Steenwijk Martijn D; Wattjes Mike P; Geurts Jeroen J G; Uitdehaag Bernard M J; Tewarie Prejaas K; Balk Lisanne J; Pouwels Petra J W; Killestein Joep; Barkhof Frederik
来源:Neurology, 2015, 85(3): 248-255.
DOI:10.1212/WNL.0000000000001756

摘要

Objective:To find the strongest neuroimaging predictors for motor dysfunction using conventional and quantitative imaging measures focusing on the corticospinal tract (CST) in a large cohort of patients with long-standing multiple sclerosis (MS).Methods:In this cross-sectional study, a wide spectrum of neuroimaging measures at the whole-brain, cervical, and CST level were analyzed in 195 patients with MS and 54 healthy controls. Motor function was assessed using the Expanded Disability Status Scale (EDSS), 9-Hole Peg Test, Timed 25-Foot Walk Test, and Multiple Sclerosis Walking Scale. Associations between damage in different parts of the motor system and motor functioning were assessed using stepwise linear regression.Results:Patients had an average disease duration of 19.98 (6.99) years and a median EDSS score of 4 (range: 1.0-8.0). EDSS score was associated with number of infratentorial and cervical cord lesions, lesion volume in the CST, and mean upper cervical cord area (adjusted R-2 = 0.403). Timed 25-Foot Walk Test score was associated with number of infratentorial lesions and cerebellar volume (adjusted R-2 = 0.150), 9-Hole Peg Test score with number of infratentorial lesions and thickness of the cortex connected to the CST (adjusted R-2 = 0.245), and Multiple Sclerosis Walking Scale with number of infratentorial and cervical lesions, thickness of the cortex connected to the CST, and mean upper cervical cord area (adjusted R-2 = 0.354).Conclusions:Motor dysfunction in MS has a complex substrate that cannot be ascribed to a single neuroimaging finding, but is the consequence of infratentorial and spinal cord damage, as well as damage in the CST.

  • 出版日期2015-7-21