Evidence map›Paper›PMID 37649987›Full record

ArticleFrontiers in neuroinformatics2023

Decision trees to evaluate the risk of developing multiple sclerosis.

Manuela Pasella, Fabio Pisano, Barbara Cannas, Alessandra Fanni, Eleonora Cocco, Jessica Frau, Francesco Lai, Stefano Mocci, Roberto Littera, Sabrina Rita Giglio

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
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

10 authors at 2 institutions in 1 country.

Manuela PasellaDepartment of Electrical and Electronic Engineering, University of Cagliari, Cagliari, Italy.
Fabio PisanoDepartment of Electrical and Electronic Engineering, University of Cagliari, Cagliari, Italy.
Barbara CannasDepartment of Electrical and Electronic Engineering, University of Cagliari, Cagliari, Italy.
Alessandra FanniDepartment of Electrical and Electronic Engineering, University of Cagliari, Cagliari, Italy.
Eleonora CoccoDepartment of Medical Science and Public Health, Centro Sclerosi Multipla, University of Cagliari, Cagliari, Italy.
Jessica FrauDepartment of Medical Science and Public Health, Centro Sclerosi Multipla, University of Cagliari, Cagliari, Italy.
Francesco LaiUnit of Oncology and Molecular Pathology, Department of Biomedical Sciences, University of Cagliari, Cagliari, Italy.
Stefano Mocci *Medical Genetics, Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.
Roberto Littera *AART-ODV (Association for the Advancement of Research on Transplantation), Cagliari, Italy.
Sabrina Rita Giglio *Medical Genetics, Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.
University of Cagliari · ITATS Sardegna (Italy) · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Multiple sclerosis (MS) is a persistent neurological condition impacting the central nervous system (CNS). The precise cause of multiple sclerosis is still uncertain; however, it is thought to arise from a blend of genetic and environmental factors. MS diagnosis includes assessing medical history, conducting neurological exams, performing magnetic resonance imaging (MRI) scans, and analyzing cerebrospinal fluid. While there is currently no cure for MS, numerous treatments exist to address symptoms, decelerate disease progression, and enhance the quality of life for individuals with MS. Methods: This paper introduces a novel machine learning (ML) algorithm utilizing decision trees to address a key objective: creating a predictive tool for assessing the likelihood of MS development. It achieves this by combining prevalent demographic risk factors, specifically gender, with crucial immunogenetic risk markers, such as the alleles responsible for human leukocyte antigen (HLA) class I molecules and the killer immunoglobulin-like receptors (KIR) genes responsible for natural killer lymphocyte receptors. Results: The study included 619 healthy controls and 299 patients affected by MS, all of whom originated from Sardinia. The gender feature has been disregarded due to its substantial bias in influencing the classification outcomes. By solely considering immunogenetic risk markers, the algorithm demonstrates an ability to accurately identify 73.24% of MS patients and 66.07% of individuals without the disease. Discussion: Given its notable performance, this system has the potential to support clinicians in monitoring the relatives of MS patients and identifying individuals who are at an increased risk of developing the disease.

Indexed as

decision treeshuman leukocyte antigenimmunogenetic risk markerslikelihood of multiple sclerosis developmentmachine learningmultiple classifiermultiple sclerosis

Identifiers

PMID37649987
PMCPMC10465164
OpenAlexW4385855768

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.