MRI measures show significant cerebellar gray matter volume loss in multiple sclerosis and are associated with cerebellar dysfunction

Author:

Anderson VM1,Fisniku LK1,Altmann DR2,Thompson AJ3,Miller DH1

Affiliation:

1. Nuclear Magnetic Resonance Research Unit, Institute of Neurology, University College London, Queen Square, London, UK; Department of Neuroinflammation, Institute of Neurology, University College London, Queen Square, London, UK

2. Nuclear Magnetic Resonance Research Unit, Institute of Neurology, University College London, Queen Square, London, UK; Medical Statistics Unit, London School of Hygiene and Tropical Medicine, London, UK

3. Nuclear Magnetic Resonance Research Unit, Institute of Neurology, University College London, Queen Square, London, UK; Department of Brain Repair and Rehabilitation, Institute of Neurology, University College London, Queen Square, London, UK

Abstract

Background Regional atrophy measures may offer useful information about the causes of specific clinical deficits in multiple sclerosis (MS). Objective To determine the magnitude of cerebellar gray and white matter (GM and WM) atrophy in patients with clinically isolated syndromes (CIS) and MS, and their role in clinical manifestations of cerebellar damage. Methods T1-weighted volumetric magnetic resonance imaging (MRI) of 73 patients [29 CIS, 33 relapsing–remitting MS (RRMS), 11 secondary progressive MS (SPMS)] was compared with 25 controls. GM and WM regions were generated using SPM5 and cerebellar regions delineated. Linear regression was used to investigate differences in tissue-specific cerebellar volumes between groups and the association with clinical measures. Results Mean cerebellar GM volume (CGMV) was 100.1 cm3 in controls, 96.4 cm3 in CIS patients, 91.8 cm3 in RRMS patients, and 88.8 cm3 in SPMS patients. Mean cerebellar WM volumes (CWMV) were 21.3 cm3, 20.4 cm3, 19.9 cm3, and 18.8 cm3, respectively. CGMV was reduced by 4.8 cm3 ( P = 0.054) in RRMS patients, and 8.5 cm3 ( P = 0.012) in SPMS patients, relative to controls. Only patients with SPMS showed a borderline significant reduction in CWMV compared with controls (mean 2.1 cm3, P = 0.053). CGMV was significantly smaller in patients assessed as having cerebellar dysfunction compared with patients who had normal cerebellar function. Significant associations of CGMV and CWMV with performance on the nine-hole peg test were also observed. Conclusion Clinically relevant GM atrophy occurs in the cerebellum of MS patients and is more prominent than WM atrophy. As such, it may provide complementary data to other regional atrophy and intrinsic tissue measures.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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