Literature DB >> 17945260

Effect of intravenous methylprednisolone on the number, size and confluence of plaques in relapsing-remitting multiple sclerosis.

Robert Zivadinov1, Marino Zorzon, Roberto De Masi, Davide Nasuelli, Giuseppe Cazzato.   

Abstract

The aim of the present study was to evaluate whether intravenous methylprednisolone (IVMP) pulses affect the confluence and enlargement of T2 lesions in the long term in patients with relapsing-remitting (RR) multiple sclerosis (MS). Of 88 RR MS patients, randomly assigned to regular pulses of IVMP (1 g/day for 5 days with an oral prednisone taper) or IVMP on the same dose schedule only for relapses, and followed up without other disease-modifying drug therapy for 5 years, 81 patients completed the trial as planned. Pulsed IVMP was given every 4 months for 3 years, and then every 6 months for the subsequent 2 years. Calculations were performed for number, size and lesion volume (LV) of T2- and confluent T2-lesions. At study entry, the number, size and LV of T2- and confluent T2-lesions were well matched in the two study arms. At the end of the study, patients who received IVMP pulses every 4-6 months for 5 years had significantly fewer confluent T2 lesions (105 vs. 270, p<0.0001), lower confluent T2-LV (5.4 ml vs. 17.4 ml, p<0.00001), fewer large T2 lesions (>10 mm) (165 vs. 541, p<0.00001), and lower T2-LV/N degrees T2 lesion index (0.52 vs. 1.1, p=0.007) when compared to patients who received IVMP only for relapses. There were more small T2 lesions (1082 vs. 288, p<0.000001) in the IVMP pulsed arm. Patients who received higher total doses of IVMP showed the smallest changes in confluent T2-LV during the study. This study suggests that treatment with pulses of IVMP may prevent the confluence of T2 lesions, which may in turn contribute to slower progression of disability in the long term. However, pulsed IVMP treatment did not significantly slow down accumulation of overall T2-LV and there were more smaller T2 lesions in the IVMP pulsed arm at the end of the study.

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Year:  2007        PMID: 17945260     DOI: 10.1016/j.jns.2007.09.025

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  9 in total

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Authors:  M Shuhaibar; M J McKenna; M Au-Yeong; J M T Redmond
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2.  Multiple sclerosis lesion segmentation from brain MRI using U-Net based on wavelet pooling.

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Review 4.  Cuprizone-induced demyelination as a tool to study remyelination and axonal protection.

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5.  An Automated Statistical Technique for Counting Distinct Multiple Sclerosis Lesions.

Authors:  J D Dworkin; K A Linn; I Oguz; G M Fleishman; R Bakshi; G Nair; P A Calabresi; R G Henry; J Oh; N Papinutto; D Pelletier; W Rooney; W Stern; N L Sicotte; D S Reich; R T Shinohara
Journal:  AJNR Am J Neuroradiol       Date:  2018-02-22       Impact factor: 3.825

6.  Inhibition of CD40-TRAF6 interactions by the small molecule inhibitor 6877002 reduces neuroinflammation.

Authors:  Suzanne A B M Aarts; Tom T P Seijkens; Pascal J H Kusters; Susanne M A van der Pol; Barbara Zarzycka; Priscilla D A M Heijnen; Linda Beckers; Myrthe den Toom; Marion J J Gijbels; Louis Boon; Christian Weber; Helga E de Vries; Gerry A F Nicolaes; Christine D Dijkstra; Gijs Kooij; Esther Lutgens
Journal:  J Neuroinflammation       Date:  2017-05-12       Impact factor: 8.322

7.  Multiple sclerosis, relapses, and the mechanism of action of adrenocorticotropic hormone.

Authors:  Amy Perrin Ross; Aliza Ben-Zacharia; Colleen Harris; Jennifer Smrtka
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8.  Quantitative MRI analysis in children with multiple sclerosis: a multicenter feasibility pilot study.

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Journal:  Medicina (Kaunas)       Date:  2022-03-03       Impact factor: 2.430

  9 in total

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