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Prognosis of a second clinical event from baseline MRI in patients with a CIS: a multicenter study using a machine learning approach

  • Diagnostic Neuroradiology
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Abstract

Purpose

To predict the occurrence of a second clinical event in patients with a CIS suggestive of MS, from baseline magnetic resonance imaging (MRI), by means of a pattern recognition approach.

Methods

Two hundred sixty-six patients with a CIS were recruited from four participating centers. Over a follow-up of 3 years, 130 patients had a second clinical episode and 136 did not. Grey matter and white matter T1-hypointensities masks segmented from 3D T1-weighted images acquired on 3 T scanners were used as features for the classification approach. Differences between CIS that remained CIS and those that developed a second event were assessed at a global level and at a regional level, arranging the regions according to their contribution to the classification model.

Results

All classification metrics were around or even below 50% for both global and regional approaches. Accuracies did not change when T1-hypointensity maps were added to the model; just the specificity was increased up to 80%. Among the 30 regions with the largest contribution, 26 were grey matter and 4 were white matter regions. For grey matter, regions contributing showed either a larger or a smaller volume in the group of patients that remained CIS, compared to those with a second event. The volume of T1-hypointensities was always larger for the group that presented a second event.

Conclusions

Prediction of a second clinical event in CIS patients from baseline MRI seems to present a highly heterogeneous pattern, leading to very low classification accuracies. Adding the T1-hypointensity maps does not seem to improve the accuracy of the classification model.

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Acknowledgements

We thank C. Cavallo for English writing support.

Funding

We would like to acknowledge funding received from the “Red Española de Esclerosis Múltiple (REEM)” (RD07/0060; RD12/0032) and the project, PI18/00823, which are sponsored by the Fondo de Investigación Sanitaria (FIS), the Instituto de Salud Carlos III and the Ministry of Economy and Competitiveness in Spain, as well as the “Ajuts per Donar Suport als Grups de Recerca de Catalunya (2009 SGR 0793)”, which is sponsored by the “Agència de Gestió d’Ajuts Universitaris i de Recerca” (AGAUR) of the Generalitat de Catalunya in Spain.

Instituto de Salud Carlos III,PI18/00823,Deborah Pareto

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Authors and Affiliations

Authors

Corresponding author

Correspondence to Deborah Pareto.

Ethics declarations

Ethics approval

The study was approved by the local ethics committee, under the standards of the 1964 Declaration of Helsinki.

Consent to participate

All patients signed an informed consent for participation.

Conflict of interest

DP has received speaking honoraria from Novartis and Sanofi-Genzyme and a research contract from Biogen.

AG-V has nothing to disclose.

SG has nothing to disclose.

GG-E has nothing to disclose.

MR received speaker honoraria from Biogen Idec, Novartis, Genzyme, Teva, Merck Serono, Roche, Celgene and Bayer and receives research support from the Italian Ministry of Health, MS Society of Canada and Fondazione Italiana Sclerosi Multipla.

MF: Editor-in-Chief of the Journal of Neurology received compensation for consulting services and/or speaking activities from Bayer, Biogen Idec, Merck-Serono, Novartis, Roche, Sanofi Genzyme, Takeda, and Teva Pharmaceutical Industries; and receives research support from Biogen Idec, Merck-Serono, Novartis, Roche, Teva Pharmaceutical Industries, Italian Ministry of Health, Fondazione Italiana Sclerosi Multipla, and ARiSLA (Fondazione Italiana di Ricerca per la SLA).

MK has received funding for travel and speaker honoraria from Bayer Schering Pharma, Novartis Genzyme, Merck Serono, Biogen Idec and Teva Pharmaceutical Industries Ltd. and serves on scientific advisory boards for Biogen Idec, Merck Serono and Roche.

CH received funding for travel and speaker honoraria from Bayer, Biogen, Genzyme, Merck, Novartis, Roche, Shire, and Teva Pharmaceutical Industries Ltd./sanofi-aventis, research support from Biogen, Merck, and Teva Pharmaceutical Industries Ltd./sanofi-aventis and serving on scientific advisory boards for Bayer, Biogen, Merck, Novartis, Roche and Teva Pharmaceutical Industries Ltd./sanofi- Aventis.

SL received compensation for consulting services and speaker honoraria from Biogen Idec, Novartis, TEVA, Genzyme, Sanofi, Roche, and Merck.

MT has received speaking honoraria and travel expenses for scientific meetings with Amirall, Bayer, Biogen Idec, Genzyme, Merck Serono, Novartis, Sanofi-Aventis, Roche, and Teva.

JSG is Director of Revista de Neurología and serves on the Editorial Board of MSJ. In the last 36 months he has received compensation for serving on scientific advisory boards or on speaker’s bureaus from Biogen, Merck, Almirall, Novartis, Teva, Roche, Celgene, and Genzyme.

ÀR has served on scientific advisory boards for Novartis, Sanofi-Genzyme, Icometrix, Bayer SyntheticMR, and OLEA Medical and has received speaking honoraria from Bayer, Sanofi-Genzyme, Bracco, Merck-Serono, Teva Pharmaceutical Industries Ltd, Novartis, Roche, and Biogen Idec.

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Pareto, D., Garcia-Vidal, A., Groppa, S. et al. Prognosis of a second clinical event from baseline MRI in patients with a CIS: a multicenter study using a machine learning approach. Neuroradiology 64, 1383–1390 (2022). https://doi.org/10.1007/s00234-021-02885-7

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  • DOI: https://doi.org/10.1007/s00234-021-02885-7

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