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Brain Advance Access originally published online on March 3, 2004
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Brain, Vol. 127, No. 5, 1101-1107, 2004
© 2004 Guarantors of Brain
doi: 10.1093/brain/awh126

Early development of multiple sclerosis is associated with progressive grey matter atrophy in patients presenting with clinically isolated syndromes

Catherine M. Dalton1, Declan T. Chard1, Gerard R. Davies1, Katherine A. Miszkiel2, Dan R. Altmann1,4, Kryshani Fernando1, Gordon T. Plant3, Alan J. Thompson1 and David H. Miller1

1 NMR Research Unit, Institute of Neurology, 2 Lysholm Department of Neuroradiology, National Hospital for Neurology and Neurosurgery, 3 Moorfields Eye Hospital and 4 Medical Statistics Unit, London School of Hygiene and Tropical Medicine, London, UK

Correspondence to: Professor D. H. Miller, NMR Research Group, Institute of Neurology, Queen Square, London WC1N 3BG, UK E-mail: d.miller{at}ion.ucl.ac.uk

While brain atrophy occurs early in the clinical course of multiple sclerosis, exactly how early, which tissues are affected and the rate at which early atrophy occurs are unclear. Regional brain atrophy was investigated in 58 patients recruited within 3 months of onset of a clinically isolated syndrome (CIS) suggestive of multiple sclerosis, who were followed-up for 3 years. At 3 years, 31 subjects had developed multiple sclerosis as defined by the McDonald criteria, while 27 had not (13 had MRI-visible brain lesions and 14 did not). In those who developed multiple sclerosis, the mean decrease in grey matter fractional volume (GMF, as a fraction of total intracranial volume) was –0.017 (–3.3%) and was significantly larger than in the combined lesion-positive and lesion-negative CIS subjects [–0.005 (–1.1%), P = 0.001]. No decrease in white matter fractional volumes (WMF) was seen. Change in GMF correlated only modestly with the change in T2 lesion volume from baseline to year 3 (r = –0.428, P = 0.004). These results suggest that progressive grey matter, but not white matter, atrophy is seen in the earliest clinically observable stages of relapse onset multiple sclerosis, and this is only moderately related to lesion accumulation. Longer-term follow-up is required to determine whether early grey matter atrophy is associated with subsequent disability or cognitive impairment.

Key Words: multiple sclerosis; clinically isolated syndrome; grey matter; white matter; atrophy

Abbreviations: BPF= brain parenchymal fraction; CIS = clinically isolated syndrome; EDSS = Expanded Disability Status Score; GM = grey matter; GMF = grey matter fraction; NAWM = normal-appearing white matter; VV = ventricular volume; WM = white matter; WMF = white matter fraction

Received September 16, 2003. Revised December 1, 2003. Accepted December 23, 2003.


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