Autonomic dysfunction in multiple sclerosis: cervical spinal cord atrophy correlates

Citation
J. De Seze et al., Autonomic dysfunction in multiple sclerosis: cervical spinal cord atrophy correlates, J NEUROL, 248(4), 2001, pp. 297-303
Citations number
41
Categorie Soggetti
Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROLOGY
ISSN journal
03405354 → ACNP
Volume
248
Issue
4
Year of publication
2001
Pages
297 - 303
Database
ISI
SICI code
0340-5354(200104)248:4<297:ADIMSC>2.0.ZU;2-A
Abstract
Autonomic dysfunction has rarely been studied in patients suffering from mu ltiple sclerosis (MS). Some hypotheses have concerned the pathophysiology, especially with regard to a possible spinal cord origin. However, there hav e been no previous studies on autonomic dysfunction in MS and spinal cord l esions. This study assessed the frequency of autonomic dysfunction (AD) in MS and the correlation to spinal cord magnetic resonance imaging (MRI) find ings. We prospectively studied 75 MS patients (25 with relapsing-remitting forms, 25 with secondary progressive forms and 25 with primary progressive forms). We performed sympathetic skin response, R-R interval variability an d orthostatic hypotension testing. Spinal cord MRI was performed to detect demyelinating lesions (sagittal and axial plane) or spinal cord atrophy. Cl inical and laboratory evidence of AD was found in 84% and 56% of MS patient s, respectively. The correlation of the latter with disability was evaluate d using the Extended Disability Status Scale. AD was more frequent in prima ry progressive MS than in the other two forms. AD was correlated with spina l cord cross-sectional area reduction but not with spinal cord hyperintensi ties. This study confirms that the frequency of AD in MS, especially in pri mary progressive forms, has until now been underestimated. Furthermore, AD appears to be more closely related to axonal loss, as demonstrated by spina l cord atrophy, than to demyelinating lesions.