Evidence map›Paper›PMID 36369345›Full record

ArticleScientific reports2022

Ensemble machine learning identifies genetic loci associated with future worsening of disability in people with multiple sclerosis.

Valery Fuh-Ngwa, Yuan Zhou, Phillip E Melton, Ingrid van der Mei, Jac C Charlesworth, Xin Lin, Amin Zarghami, Simon A Broadley, Anne-Louise Ponsonby, Steve Simpson-Yap and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. 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
1.3field-weighted citation impact, top 19% 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, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Artificial Intelligence and Multiple Sclerosis.Current neurology and neuroscience reports · 2024
    Review
  6. Observational
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

12 authors at 5 institutions in 1 country.

Valery Fuh-NgwaMenzies Institute for Medical Research, University of Tasmania, 17 Liverpool St, Hobart, TAS, 7000, Australia.
Yuan ZhouMenzies Institute for Medical Research, University of Tasmania, 17 Liverpool St, Hobart, TAS, 7000, Australia.
Phillip E MeltonMenzies Institute for Medical Research, University of Tasmania, 17 Liverpool St, Hobart, TAS, 7000, Australia.
Ingrid van der MeiMenzies Institute for Medical Research, University of Tasmania, 17 Liverpool St, Hobart, TAS, 7000, Australia.
Jac C CharlesworthMenzies Institute for Medical Research, University of Tasmania, 17 Liverpool St, Hobart, TAS, 7000, Australia.
Xin LinMenzies Institute for Medical Research, University of Tasmania, 17 Liverpool St, Hobart, TAS, 7000, Australia.
Amin ZarghamiMenzies Institute for Medical Research, University of Tasmania, 17 Liverpool St, Hobart, TAS, 7000, Australia.
Simon A BroadleyMenzies Health Institute Queensland and School of Medicine, Griffith University Gold Coast, G40 Griffith Health Centre, QLD 4222, Australia.
Anne-Louise PonsonbyDeveloping Brain Division, The Florey Institute for Neuroscience and Mental Health, Royal Children's Hospital, University of Melbourne Murdoch Children's Research Institute, Parkville, VIC, 3052, Australia.
Steve Simpson-YapNeuroepidemiology Unit, Melbourne School of Population & Global Health, The University of Melbourne, Melbourne, VIC, 3053, Australia.
Jeannette Lechner-ScottDepartment of Neurology, Hunter Medical Research Institute, Hunter New England Health, University of Newcastle, Callaghan, NSW, 2310, Australia.
Bruce V TaylorMenzies Institute for Medical Research, University of Tasmania, 17 Liverpool St, Hobart, TAS, 7000, Australia. bruce.taylor@utas.edu.au.
University of Tasmania · AUGriffith University · AUHunter Medical Research Institute · AUMurdoch Children's Research Institute · AUUniversity of Melbourne · AU

Funding

Henry Baldwin Trust and the Medical Research Future Fund EPCP000008National Health and Medical Research Council investigator grant L1 GNT1173155National Health and Medical Research Council of Australia APP1127819
6 · The paper itself

Abstract

Limited studies have been conducted to identify and validate multiple sclerosis (MS) genetic loci associated with disability progression. We aimed to identify MS genetic loci associated with worsening of disability over time, and to develop and validate ensemble genetic learning model(s) to identify people with MS (PwMS) at risk of future worsening. We examined associations of 208 previously established MS genetic loci with the risk of worsening of disability; we learned ensemble genetic decision rules and validated the predictions in an external dataset. We found 7 genetic loci (rs7731626: HR 0.92, P = 2.4 × 10

Indexed as

Multiple SclerosisGenetic LociHumansMachine LearningPrognosis

Identifiers

PMID36369345
PMCPMC9652373
OpenAlexW4308918288

What Socratic 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 Socratic graph.