Long-term Follow-up of Acute Partial Transverse Myelitis

被引:25
作者
Bourre, Bertrand [1 ]
Zephir, Helene [3 ]
Ongagna, Jean-Claude [4 ]
Cordonnier, Charlotte [3 ]
Collongues, Nicolas [4 ,5 ]
Debette, Stephanie [3 ]
Fleury, Marie-Celine [4 ]
Outerryck, Olivier [3 ]
Hannequin, Didier [1 ,2 ]
Vermersch, Patrick [3 ]
de Seze, Jerome [4 ]
机构
[1] Hop Charles Nicolle, Serv Neurol, F-76031 Rouen, France
[2] INSERM, Rouen, France
[3] Univ Lille Nord France, Strasbourg, France
[4] Hop Civil, Serv Neurol, Strasbourg, France
[5] Lab Imagerie & Neurosci Cognit, Unite Mixte Rech, Strasbourg, France
关键词
DEFINITE MULTIPLE-SCLEROSIS; INTRATHECAL IGM-SYNTHESIS; DEMYELINATING EVENT; DISABILITY; MRI; RISK; MYELOPATHY; CONVERSION; FEATURES; CRITERIA;
D O I
10.1001/archneurol.2011.949
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Acute partial transverse myelitis (APTM) may be the first clinical symptom of multiple sclerosis (MS) or may remain a monophasic event. Objectives: To evaluate the risk of conversion to MS and long-term disability, and to determine prognosis factors for disability. Design: We identified patients with no previous history of neurological disease who experienced APTM between January 1998 and December 2005 and were followed up at 3 university hospitals in France. Data on the patients' demographics and clinical states during follow-up, as well as data on cerebrospinal fluid (CSF) analysis, brain and spinal cord magnetic resonance imaging (MRI), and visual evoked potentials, were analyzed. Setting: Neurology departments of 3 university hospitals in Lille, Strasbourg, and Rouen, France, respectively. Patients: A total of 85 patients with no previous history of neurological disease who experienced APTM. Results: The mean (SD) follow-up period was 104.8 (29.8) months. There were 57 women (67%) and 28 men (33%), with a mean (SD) age at onset of 36.7 (11.7) years. At the end of follow-up, 53 patients (62%) were classified as having MS with a mean (SD) Expanded Disability Status Scale score of 2.6 (1.8), 1 patient (1%) was classified as having postinfectious myelitis, 1 (1%) as having neuromyelitis optica, 1 (1%) as having Sjogren syndrome, and 2((34%) still had APTM of undetermined etiology. Oligoclonal bands in CSF were more frequent in patients with MS (92%) than in patients with APTM of undetermined etiology (38%). Brain MRI results were abnormal in 87% of patients with MS and 27% of patients with APTM of undetermined etiology; visual evoked potentials were abnormal in 43% of patients with MS and 4% of patients with APTM of undetermined etiology. Oligoclonal bands in CSF (odds ratio, 15.76 [95% CI, 2.95-84.24]) and at least 1 MRI-detected brain lesion (odds ratio, 7.74 [95% CI, 2.42-24.74]) were independent predictive factors for conversion to MS. Conclusion: Our study confirms that abnormal brain MRI results and the presence of oligoclonal bands in CSF are 2 independent predictive factors for conversion to MS. No clinical, biological, or MRI factor at onset was predictive of long-term disability.
引用
收藏
页码:357 / 362
页数:6
相关论文
共 19 条
[1]   Comparison of MRI criteria at first presentation to predict conversion to clinically definite multiple sclerosis [J].
Barkhof, F ;
Filippi, M ;
Miller, DH ;
Scheltens, P ;
Campi, A ;
Polman, CH ;
Comi, G ;
Ader, HJ ;
Losseff, N ;
Valk, J .
BRAIN, 1997, 120 :2059-2069
[2]   A longitudinal study of abnormalities on MRI and disability from multiple sclerosis [J].
Brex, PA ;
Ciccarelli, O ;
O'Riordan, JI ;
Sailer, M ;
Thompson, AJ ;
Miller, DH .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (03) :158-164
[3]  
Brodsky M, 2008, ARCH NEUROL-CHICAGO, V65, P727, DOI 10.1001/archneur.65.6.727
[4]   Idiopathic acute transverse myelitis:: a clinical study and prognostic markers in 45 cases [J].
Bruna, J ;
Martínez-Yélamos, S ;
Martínez-Yélamos, A ;
Rubio, F ;
Arbizu, T .
MULTIPLE SCLEROSIS JOURNAL, 2006, 12 (02) :169-173
[5]   Prospective study of patients presenting with acute partial transverse myelopathy [J].
Cordonnier, C ;
de Seze, J ;
Breteau, G ;
Ferriby, D ;
Michelin, E ;
Stojkovic, T ;
Pruvo, JP ;
Vermersch, P .
JOURNAL OF NEUROLOGY, 2003, 250 (12) :1447-1452
[6]   Acute myelopathies -: Clinical, laboratory and outcome profiles in 79 cases [J].
de Seze, J ;
Stojkovic, T ;
Breteau, G ;
Lucas, C ;
Michon-Pasturel, U ;
Gauvrit, JY ;
Hachulla, E ;
Mounier-Vehier, F ;
Pruvo, JP ;
Leys, D ;
Destée, A ;
Hatron, PY ;
Vermersch, P .
BRAIN, 2001, 124 :1509-1521
[7]   Disability and T2 MRI lesions:: a 20-year follow-up of patients with relapse onset of multiple sclerosis [J].
Fisniku, L. K. ;
Brex, P. A. ;
Altmann, D. R. ;
Miszkiel, K. A. ;
Benton, C. E. ;
Lanyon, R. ;
Thompson, A. J. ;
Miller, D. H. .
BRAIN, 2008, 131 :808-817
[8]   LONG-TERM FOLLOW-UP OF ACUTE PARTIAL TRANSVERSE MYELOPATHY [J].
FORD, B ;
TAMPIERI, D ;
FRANCIS, G .
NEUROLOGY, 1992, 42 (01) :250-252
[9]   Discriminatory features of acute transverse myelitis: a retrospective analysis of 45 patients [J].
Harzheim, M ;
Schlegel, U ;
Urbach, H ;
Klockgether, T ;
Schmidt, S .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2004, 217 (02) :217-223
[10]   Intramuscular interferon beta-1a therapy initiated during a first demyelinating event in multiple sclerosis. [J].
Jacobs, LD ;
Beck, RW ;
Simon, JH ;
Kinkel, RP ;
Brownscheidle, CM ;
Murray, TJ ;
Simonian, NA ;
Slasor, PJ ;
Sandrock, AW .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (13) :898-904