Evidence map›Paper›PMID 39471746›Full record

ArticleMultiple sclerosis and related disorders2024

Artificial neural network-based prediction of multiple sclerosis using blood-based metabolomics data.

Nasar Ata, Insha Zahoor, Nasrul Hoda, Syed Mohammed Adnan, Senthilkumar Vijayakumar, Filious Louis, Laila Poisson, Ramandeep Rattan, Nitesh Kumar, Mirela Cerghet and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Multiple sclerosis and related disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Immune-responsive gene 1: The mitochondrial key to Th17 cell pathogenicity in CNS autoimmunity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Nasar AtaDepartment of Neurology, Henry Ford Health, Detroit, MI, 48202, USA.
Insha ZahoorDepartment of Neurology, Henry Ford Health, Detroit, MI, 48202, USA.
Nasrul HodaDepartment of Neurology, Henry Ford Health, Detroit, MI, 48202, USA.
Syed Mohammed AdnanFaculty of Engineering, Aligarh Muslim University, Aligarh, 202002, India.
Senthilkumar VijayakumarIEEE Senior Member, Dallas, TX, 75063, USA.
Filious LouisIEEE Senior Member, Dallas, TX, 75063, USA.
Laila PoissonPublic Health Services, Henry Ford Health, Detroit, MI, 48202, USA.
Ramandeep RattanWomen's Health Services, Henry Ford Health, Detroit, MI, 48202, USA.
Nitesh KumarDepartment of Microbiology, Jaipur National University, Jaipur, 302017, India.
Mirela CerghetDepartment of Neurology, Henry Ford Health, Detroit, MI, 48202, USA.
Shailendra GiriDepartment of Neurology, Henry Ford Health, Detroit, MI, 48202, USA. Electronic address: sgiri1@hfhs.org.

Funding

Novel Regulation and Targeting of Macrophages Metabolism in Neuroinflammatory DisordersR01AI144004 · NIAID · HENRY FORD HEALTH SYSTEM · PI GIRI, SHAILENDRA · 2019 to 2023
$1.9M
Endogenous metabolite restricts GM-CSF signaling pathway in pathogenic macrophages to ameliorate CNS AutoimmunityR01NS112727 · NINDS · HENRY FORD HEALTH SYSTEM · PI GIRI, SHAILENDRA · 2019 to 2023
$1.6M
NIAID NIH HHS R01 AI144004NINDS NIH HHS R01 NS112727
6 · The paper itself

Abstract

Multiple sclerosis (MS) remains a challenging neurological condition for diagnosis and management and is often detected in late stages, delaying treatment. Artificial intelligence (AI) is emerging as a promising approach to extracting MS information when applied to different patient datasets. Given the critical role of metabolites in MS profiling, metabolomics data may be an ideal platform for the application of AI to predict disease. In the present study, a machine-learning (ML) approach was used for a detailed analysis of metabolite profiles and related pathways in patients with MS and healthy controls (HC). This approach identified unique alterations in biochemical metabolites and their correlation with disease severity parameters. To enhance the efficiency of using metabolic profiles to determine disease severity or the presence of MS, we trained an AI model on a large volume of blood-based metabolomics datasets. We constructed this model using an artificial neural network (ANN) architecture with perceptrons. Data were divided into training, validation, and testing sets to determine model accuracy. After training, accuracy reached 87 %, sensitivity was 82.5 %, specificity was 89 %, and precision was 77.3 %. Thus, the developed model seems highly robust, generalizable with a wide scope and can handle large amounts of data, which could potentially assist neurologists. However, a large multicenter cohort study is necessary for further validation of large-scale datasets to allow the integration of AI in clinical settings for accurate diagnosis and improved MS management.

Indexed as

MetabolomicsMultiple SclerosisNeural Networks, ComputerAdultFemaleHumansMachine LearningMaleMiddle AgedANNArtificial intelligenceMachine learningMetabolomicsMultiple sclerosis

Identifiers

PMID39471746
PMCPMC11649459

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.