Absence of cerebrospinal fluid oligoclonal bands is associated with delayed disability progression in relapsing-remitting MS patients treated with interferon-β
To assess the role of CSF oligoclonal bands (OB) in determining the clinical outcome in patients with relapsing-remitting multiple sclerosis (RRMS) treated with IFN-β, we carried out a retrospective, multicentre, observational study recruiting 209 RRMS patients from six MS centres from northern, cen...
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Veröffentlicht in: | Journal of the neurological sciences 2006-05, Vol.244 (1), p.97-102 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | To assess the role of CSF oligoclonal bands (OB) in determining the clinical outcome in patients with relapsing-remitting multiple sclerosis (RRMS) treated with IFN-β, we carried out a retrospective, multicentre, observational study recruiting 209 RRMS patients from six MS centres from northern, central and southern areas of Italy under treatment with IFN-β-1a i.m., IFN-β-1a s.c. and IFN-β-1b s.c. Twenty-two of 209 patients (10.6%) showed no OB in CSF. The patients without had, at disease onset, significantly higher frequency of visual disturbances (
p
=
0.02) and less sensory involvement (
p
=
0.04) than those with OB. A statistical trend (
p
=
0.056) towards a longer time to reach sustained disability progression during treatment was found in patients without compared to those with OB. Thirty-six of 187 (19%) patients with OB worsened by at least 1 EDSS point compared to none of 22 (0%) OB-negative patients (
p
=
0.017). The delaying of disability progression in OB-negative patients during treatment was significantly dependent only on the number of baseline MRI T2-weighted lesions (
p
=
0.012) that was found to be significantly lower in OB-negative than in OB-positive patients (
p
=
0.04). The absence of OB and low number of baseline T2-weighted lesions in this cohort of MS patients are favourable prognostic factors influencing the clinical response to IFN-β treatment in RRMS patients. |
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ISSN: | 0022-510X 1878-5883 |
DOI: | 10.1016/j.jns.2006.01.004 |