Antimyelin antibodies and the risk of relapse in patients with a primary demyelinating event

被引:44
作者
Rauer, S
Euler, B
Reindl, M
Berger, T
机构
[1] Univ Freiburg, Neurol Klin & Poliklin, D-79106 Freiburg, Germany
[2] Univ Hosp Freiburg, Dept Neurol, Freiburg, Germany
[3] Innsbruck Med Univ, Dept Clin Neurol, Innsbruck, Austria
关键词
D O I
10.1136/jnnp.2005.077784
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Aim: To investigate whether the presence of serum antibodies against myelin oligodendrocyte glycoprotein (MOG) and myelin basic protein (MBP) in patients with a clinically isolated syndrome (CIS) predicts the interval to develop more frequently and earlier a first relapse (clinically definite multiple sclerosis: CDMS) than seronegative patients. Methods: Sera from 45 patients with a CIS and positive intrathecal IgG-synthesis were retrospectively tested for the presence of IgM antibodies against both MOG and MBP. Antibodies were detected by immunoblot using recombinant MOG (1-125) and human MBP antigen preparations. Clinical follow ups were performed retrospectively by telephone interviews and documented neurological examination. Results: Using the Cox proportional hazards model there was no significant increased risk for developing CDMS in anti-MOG and anti-MBP positive patients compared with negative. However regarding the median of the time span between CIS and CDMS over the whole follow up, antibody positive patients (MOG/MBP+/+) developed significantly earlier relapses (median 5.5 months (range 3-20)) than the antibody negative ones (median 25.0 months (range 7-43); p < 0.006). On testing sera from 56 apparently healthy students, quite high frequencies of anti-MOG and anti-MBP antibodies (21% and 28% respectively) were detected. This limited specificity of anti-MOG and anti-MBP antibodies has been seen earlier and restricts their diagnostic relevance in MS despite their role as a predictor of relapses after a CIS. Conclusions: This study confirms previous data only in a subanalysis indicating that patients with positive anti-MOG/MBP antibodies develop earlier relapses than patients who are antibody negative. However, the authors could not verify that the presence of these antibodies anticipates the overall risk of developing CDMS-according to study criteria-after a first demyelinating event within the study period of 21-106 months (mean 60 (SD 25)).
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页码:739 / 742
页数:4
相关论文
共 23 条
[1]  
Archelos JJ, 2000, ANN NEUROL, V47, P694, DOI 10.1002/1531-8249(200006)47:6<694::AID-ANA2>3.3.CO
[2]  
2-N
[3]   Antimyelin antibodies as a predictor of clinically definite multiple sclerosis after a first demyelinating event [J].
Berger, T ;
Rubner, P ;
Schautzer, F ;
Egg, R ;
Ulmer, H ;
Mayringer, I ;
Dilitz, E ;
Deisenhammer, F ;
Reindl, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (02) :139-145
[4]   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
[5]  
DIEBLER G, 1972, PREP BIOCHEM, V2, P39
[6]   CRITERIA FOR AN INCREASED SPECIFICITY OF MRI INTERPRETATION IN ELDERLY SUBJECTS WITH SUSPECTED MULTIPLE-SCLEROSIS [J].
FAZEKAS, F ;
OFFENBACHER, H ;
FUCHS, S ;
SCHMIDT, R ;
NIEDERKORN, K ;
HORNER, S ;
LECHNER, H .
NEUROLOGY, 1988, 38 (12) :1822-1825
[7]   Correlation of clinical, magnetic resonance imaging, and cerebrospinal fluid findings in optic neuritis [J].
Jacobs, LD ;
Kaba, SE ;
Miller, CM ;
Priore, RL ;
Brownscheidle, CM .
ANNALS OF NEUROLOGY, 1997, 41 (03) :392-398
[8]   Elevated levels of antibody to myelin oligodendrocyte glycoprotein is not specific for patients with multiple sclerosis [J].
Karni, A ;
Bakimer-Kleiner, R ;
Abramsky, O ;
Ben-Nun, A .
ARCHIVES OF NEUROLOGY, 1999, 56 (03) :311-315
[9]   Similar low frequency of anti-MOG IgG and IgM in MS patients and healthy subjects [J].
Lampasona, V ;
Franciotta, D ;
Furlan, R ;
Zanaboni, S ;
Fazio, R ;
Bonifacio, E ;
Comi, G ;
Martino, G .
NEUROLOGY, 2004, 62 (11) :2092-2094
[10]   Heterogeneity of multiple sclerosis pathogenesis:: implications for diagnosis and therapy [J].
Lassmann, H ;
Brück, W ;
Lucchinetti, C .
TRENDS IN MOLECULAR MEDICINE, 2001, 7 (03) :115-121