The contribution of demyelination to axonal loss in multiple sclerosis

被引:172
作者
DeLuca, G. C.
Williams, K.
Evangelou, N.
Ebers, G. C.
Esiri, M. M.
机构
[1] Univ Oxford, Dept Clin Neurol, Oxford, England
[2] Oxford Radcliffe NHS Trust, Dept Neuropathol, Oxford, England
[3] Univ Hosp NHS Trust, Queens Med Ctr, Dept Neurol, Nottingham, England
关键词
demyelination; axon; axonal degeneration; multiple sclerosis; neuropathology;
D O I
10.1093/brain/awl074
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The traditional notion that multiple sclerosis is a primary demyelinating disease has led to a plaque-centred view of both aetiology and the pathogenesis of disease progression. The presence of axonal loss has received increasing recognition. However, the relative roles of demyelination and axonal loss have not been fully clarified in multiple sclerosis nor have their possible interrelationships been elucidated. Post-mortem material from the cerebrum, brainstem and spinal cord of 55 multiple sclerosis patients (29 males) with an age range of 25-83 years (mean = 57.5 years) and length of disease history ranging from 2 to 43 years (mean = 17.1 years) was stained for myelin. Plaque load was calculated by summing the relative proportion of plaque area compared with total white matter area of the corticospinal and sensory tracts at each level. This was related to estimates of axonal density and of total axon number in these tracts in the spinal cord. Our results indicate that plaque load did not correlate with brain weight. Unexpectedly, after adjusting for sex, age and duration of disease, correlations between total plaque load and axonal loss in both the corticospinal tract and sensory tracts were weak or absent at each level investigated. Since there was little correlation between plaque load and axonal loss, the possibility that demyelination is not the primary determinant of spinal cord axonal loss warrants consideration.
引用
收藏
页码:1507 / 1516
页数:10
相关论文
共 47 条
[31]   Spinal cord atrophy and disability in multiple sclerosis - A new reproducible and sensitive MRI method with potential to monitor disease progression [J].
Losseff, NA ;
Webb, SL ;
ORiordan, JI ;
Page, R ;
Wang, L ;
Barker, GJ ;
Tofts, PS ;
McDonald, WI ;
Miller, DH ;
Thompson, AJ .
BRAIN, 1996, 119 :701-708
[32]   Axonal changes in chronic demyelinated cervical spinal cord plaques [J].
Lovas, G ;
Szilágyi, N ;
Majtényi, K ;
Palkovits, M ;
Komoly, S .
BRAIN, 2000, 123 :308-317
[33]   IMMUNOGENESIS OF MULTIPLE SCLEROSIS PLAQUE [J].
LUMSDEN, CE .
BRAIN RESEARCH, 1971, 28 (03) :365-&
[34]   Correlates of MS disability assessed in vivo using aggregates of MR quantities [J].
Mainero, C ;
De Stefano, N ;
Iannucci, G ;
Sormani, MP ;
Guidi, L ;
Federico, A ;
Bartolozzi, ML ;
Comi, G ;
Filippi, M .
NEUROLOGY, 2001, 56 (10) :1331-1334
[35]   Axonal loss results in spinal-cord atrophy, electrophysiological abnormalities and neurological deficits following demyelination in a chronic inflammatory model of multiple sclerosis [J].
McGavern, DB ;
Murray, PD ;
Rivera-Quiñones, C ;
Schmelzer, JD ;
Low, PA ;
Rodriguez, M .
BRAIN, 2000, 123 :519-531
[36]   CERVICAL CORD IN MULTIPLE-SCLEROSIS [J].
OPPENHEIMER, DR .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1978, 4 (02) :151-162
[37]   PATTERNS OF OLIGODENDROGLIA PATHOLOGY IN MULTIPLE-SCLEROSIS [J].
OZAWA, K ;
SUCHANEK, G ;
BREITSCHOPF, H ;
BRUCK, W ;
BUDKA, H ;
JELLINGER, K ;
LASSMANN, H .
BRAIN, 1994, 117 :1311-1322
[38]   Disability profile of MS did not change over 10 years in a population-based prevalence cohort [J].
Pittock, SJ ;
Mayr, WT ;
McClelland, RL ;
Jorgensen, NW ;
Weigand, SD ;
Noseworthy, JH ;
Rodriguez, M .
NEUROLOGY, 2004, 62 (04) :601-606
[39]   PATHOGENESIS OF MULTIPLE-SCLEROSIS - A CRITICAL REAPPRAISAL [J].
POSER, CM .
ACTA NEUROPATHOLOGICA, 1986, 71 (1-2) :1-10
[40]   MULTIPLE-SCLEROSIS - REMYELINATION OF NASCENT LESIONS [J].
PRINEAS, JW ;
BARNARD, RO ;
KWON, EE ;
SHARER, LR ;
CHO, ES .
ANNALS OF NEUROLOGY, 1993, 33 (02) :137-151