Evidence map›Paper›PMID 36675783›Full record

ArticleJournal of personalized medicine2023

Combining Clinical and Genetic Data to Predict Response to Fingolimod Treatment in Relapsing Remitting Multiple Sclerosis Patients: A Precision Medicine Approach.

Laura Ferrè, Ferdinando Clarelli, Beatrice Pignolet, Elisabetta Mascia, Marco Frasca, Silvia Santoro, Melissa Sorosina, Florence Bucciarelli, Lucia Moiola, Vittorio Martinelli and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.8field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 2 countries.

Laura FerrèNeurology and Neurorehabilitation Unit, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Ferdinando ClarelliLaboratory of Human Genetics of Neurological Disorders, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Beatrice PignoletCentre Hospitalier Universitaire de Toulouse, CEDEX 9, 31059 Toulouse, France.
Elisabetta MasciaLaboratory of Human Genetics of Neurological Disorders, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Marco FrascaAnacletoLab, Dipartimento di Informatica, Università degli Studi di Milano, 20133 Milan, Italy.ORCID 0000-0002-4170-0922
Silvia SantoroLaboratory of Human Genetics of Neurological Disorders, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Melissa SorosinaLaboratory of Human Genetics of Neurological Disorders, IRCCS San Raffaele Hospital, 20132 Milan, Italy.ORCID 0000-0003-4376-2550
Florence BucciarelliCentre Hospitalier Universitaire de Toulouse, CEDEX 9, 31059 Toulouse, France.
Lucia MoiolaNeurology and Neurorehabilitation Unit, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Vittorio MartinelliNeurology and Neurorehabilitation Unit, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Giancarlo ComiVita-Salute San Raffaele University, 20132 Milan, Italy.
Roland LiblauInstitut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity), INSERM UMR1291-CNRS UMR5051-Université Toulouse III, CEDEX 3, 31024 Toulouse, France.
Massimo FilippiNeurology and Neurorehabilitation Unit, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Giorgio ValentiniAnacletoLab, Dipartimento di Informatica, Università degli Studi di Milano, 20133 Milan, Italy.ORCID 0000-0002-5694-3919
Federica EspositoNeurology and Neurorehabilitation Unit, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Vita-Salute San Raffaele University · ITCentre National de la Recherche Scientifique · FRUniversity of Milan · IT

Funding

Fondazione Italiana Sclerosi Multipla project 2013/R/13
6 · The paper itself

Abstract

A personalized approach is strongly advocated for treatment selection in Multiple Sclerosis patients due to the high number of available drugs. Machine learning methods proved to be valuable tools in the context of precision medicine. In the present work, we applied machine learning methods to identify a combined clinical and genetic signature of response to fingolimod that could support the prediction of drug response. Two cohorts of fingolimod-treated patients from Italy and France were enrolled and divided into training, validation, and test set. Random forest training and robust feature selection were performed in the first two sets respectively, and the independent test set was used to evaluate model performance. A genetic-only model and a combined clinical-genetic model were obtained. Overall, 381 patients were classified according to the NEDA-3 criterion at 2 years; we identified a genetic model, including 123 SNPs, that was able to predict fingolimod response with an AUROC= 0.65 in the independent test set. When combining clinical data, the model accuracy increased to an AUROC= 0.71. Integrating clinical and genetic data by means of machine learning methods can help in the prediction of response to fingolimod, even though further studies are required to definitely extend this approach to clinical applications.

Indexed as

fingolimodgenetic markersmachine learningmultiple sclerosisprecision medicinepredictive model

Identifiers

PMID36675783
PMCPMC9861774
OpenAlexW4313890904

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.