Magnetic resonance active lesions as individual-level surrogate for relapses in multiple sclerosis

2010 ◽  
Vol 17 (5) ◽  
pp. 541-549 ◽  
Author(s):  
Maria Pia Sormani ◽  
Bettina Stubinski ◽  
Peter Cornelisse ◽  
Sanda Rocak ◽  
David Li ◽  
...  

Background: Use of quantitative magnetic resonance imaging (MRI) metrics as surrogates for clinical outcomes in multiple sclerosis (MS) trials is controversial. Objectives: We sought to validate, at the individual-patient level, the number of MRI active lesions, as a surrogate marker for relapses in MS. Methods: Individual-patient data from two large, placebo-controlled clinical trials of subcutaneous interferon β-1a in patients with relapsing–remitting or secondary progressive (SP) MS were analysed separately and as pooled data. The four Prentice criteria were applied to assess surrogacy for the number of new T2 MRI lesions. The predictive value of short-term treatment effects on this MRI marker for longer-term clinical relapses was also assessed. Results: All Prentice criteria were satisfied. The number of new T2 MRI lesions correlated with the number of relapses over the follow-up period. The proportion of treatment effect on relapses accounted for by the effect of treatment on new T2 MRI lesions over 2 years was 53% in patients with relapsing–remitting MS, 67% in patients with secondary progressive MS, and 62% in pooled data. In the pooled data, treatment effects on new lesions over 1 year mediated a good proportion (70%) of effects on relapses over the subsequent year. Conclusions: This study provides evidence that new T2 MRI lesion count is a surrogate for relapses in patients with MS treated with interferon or drugs with a similar mechanism of action. Short-term treatment effects on this MRI measure can predict longer-term effects on relapses.

Biomedicines ◽  
2022 ◽  
Vol 10 (1) ◽  
pp. 152
Author(s):  
Thomas Metzner ◽  
Deborah R. Leitner ◽  
Gudrun Dimsity ◽  
Felix Gunzer ◽  
Peter Opriessnig ◽  
...  

Background: Short-term effects of alirocumab on vascular function have hardly been investigated. Moreover, there is a scarce of reliable non-invasive methods to evaluate atherosclerotic changes of the vasculature. The ALIROCKS trial was performed to address these issues using standard ultrasound-based procedures and a completely novel magnetic resonance-based imaging technique. Methods: A total of 24 patients with an indication for treatment with PCSK9 antibodies were recruited. There were 2 visits to the study site, the first before initiation of treatment with alirocumab and the second after 10 weeks of treatment. The key outcome measures included the change of carotid vessel wall fractional anisotropy, a novel magnetic resonance-based measure of vascular integrity, and the changes of carotid intima-media thickness and flow-dependent dilatation of the brachial artery measured with ultrasound. Results: A total of 19 patients completed the trial, 2 patients stopped treatment, 3 patients did not undergo the second visit due to the COVID pandemic. All of them had atherosclerotic vascular disease. Their mean (standard deviation) LDL-cholesterol concentration was 154 (85) mg/dL at baseline and was reduced by 76 (44) mg/dL in response to alirocumab treatment (p < 0.001, n = 19). P-selectin and vascular endothelial growth factors remained unchanged. Flow-dependent dilatation of the brachial artery (+41%, p = 0.241, n = 18), carotid intima-media thickness (p = 0.914, n = 18), and fractional anisotropy of the carotid artery (p = 0.358, n = 13) also did not significantly change. Conclusion: Despite a nominal amelioration for flow-dependent dilatation, significant effects of short-term treatment with alirocumab on vascular function were not detectable. More work would be needed to evaluate, whether fractional anisotropy may be useful in clinical atherosclerosis research.


2019 ◽  
Vol 51 (4) ◽  
pp. 323-334 ◽  
Author(s):  
Ilana Berlowitz ◽  
Heinrich Walt ◽  
Christian Ghasarian ◽  
Fernando Mendive ◽  
Chantal Martin-Soelch

2014 ◽  
Vol 37 (2) ◽  
pp. 170-176 ◽  
Author(s):  
Sayeh Ehsani ◽  
Brian Nebbe ◽  
David Normando ◽  
Manuel O. Lagravere ◽  
Carlos Flores-Mir

2012 ◽  
Vol 17 (2) ◽  
pp. 463-473 ◽  
Author(s):  
Seida Erovic Ademovski ◽  
G. Rutger Persson ◽  
Edwin Winkel ◽  
Albert Tangerman ◽  
Peter Lingström ◽  
...  

2020 ◽  
Vol 78 (12) ◽  
pp. 789-796
Author(s):  
Ziya EKŞİ ◽  
Murat ÇAKIROĞLU ◽  
Cemil ÖZ ◽  
Ayse ARALAŞMAK ◽  
Hasan Hüseyin KARADELİ ◽  
...  

ABSTRACT Introduction: Magnetic resonance imaging (MRI) is the most important tool for diagnosis and follow-up in multiple sclerosis (MS). The discrimination of relapsing-remitting MS (RRMS) from secondary progressive MS (SPMS) is clinically difficult, and developing the proposal presented in this study would contribute to the process. Objective: This study aimed to ensure the automatic classification of healthy controls, RRMS, and SPMS by using MR spectroscopy and machine learning methods. Methods: MR spectroscopy (MRS) was performed on a total of 91 participants, distributed into healthy controls (n=30), RRMS (n=36), and SPMS (n=25). Firstly, MRS metabolites were identified using signal processing techniques. Secondly, feature extraction was performed based on MRS Spectra. N-acetylaspartate (NAA) was the most significant metabolite in differentiating MS types. Lastly, binary classifications (healthy controls-RRMS and RRMS-SPMS) were carried out according to features obtained by the Support Vector Machine algorithm. Results: RRMS cases were differentiated from healthy controls with 85% accuracy, 90.91% sensitivity, and 77.78% specificity. RRMS and SPMS were classified with 83.33% accuracy, 81.81% sensitivity, and 85.71% specificity. Conclusions: A combined analysis of MRS and computer-aided diagnosis may be useful as a complementary imaging technique to determine MS types.


1981 ◽  
Vol 115 (1) ◽  
pp. 143-144
Author(s):  
Janey H. Oakes ◽  
Peter A. Williamson

2016 ◽  
Vol 31 (suppl_1) ◽  
pp. i90-i91
Author(s):  
Niek F. Casteleijn ◽  
A. Lianne Messchendorp ◽  
Edwin M. Spithoven ◽  
Hedwig M. d'Agnolo ◽  
Joost P. Drenth ◽  
...  

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