Evidence map›Paper›PMID 37758804›Full record

ArticleScientific reports2023

Assessing robustness of quantitative susceptibility-based MRI radiomic features in patients with multiple sclerosis.

Cristiana Fiscone, Leonardo Rundo, Alessandra Lugaresi, David Neil Manners, Kieren Allinson, Elisa Baldin, Gianfranco Vornetti, Raffaele Lodi, Caterina Tonon, Claudia Testa and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
–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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Observational
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. 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

12 authors.

Cristiana Fiscone *Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Leonardo Rundo *Department of Information and Electrical Engineering and Applied Mathematics, University of Salerno, Fisciano, Italy.
Alessandra LugaresiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
David Neil MannersDepartment for Life Quality Sciences, University of Bologna, Bologna, Italy.
Kieren AllinsonDepartment of Histopathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge, United Kingdom.
Elisa BaldinEpidemiology and Statistics Unit, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy.
Gianfranco VornettiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Raffaele LodiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Caterina TononDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Claudia TestaDepartment of Physics and Astronomy, University of Bologna, Bologna, Italy. claudia.testa@unibo.it.
Mauro CastelliNOVA Information Management School (NOVA IMS), Universidade NOVA de Lisboa, Campus de Campolide, 1070-312, Lisbon, Portugal.
Fulvio ZaccagnaDepartment of Imaging, Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple Sclerosis (MS) is an autoimmune demyelinating disease characterised by changes in iron and myelin content. These biomarkers are detectable by Quantitative Susceptibility Mapping (QSM), an advanced Magnetic Resonance Imaging technique detecting magnetic properties. When analysed with radiomic techniques that exploit its intrinsic quantitative nature, QSM may furnish biomarkers to facilitate early diagnosis of MS and timely assessment of progression. In this work, we explore the robustness of QSM radiomic features by varying the number of grey levels (GLs) and echo times (TEs), in a sample of healthy controls and patients with MS. We analysed the white matter in total and within six clinically relevant tracts, including the cortico-spinal tract and the optic radiation. After optimising the number of GLs (n = 64), at least 65% of features were robust for each Volume of Interest (VOI), with no difference (p > .05) between left and right hemispheres. Different outcomes in feature robustness among the VOIs depend on their characteristics, such as volume and variance of susceptibility values. This study validated the processing pipeline for robustness analysis and established the reliability of QSM-based radiomics features against GLs and TEs. Our results provide important insights for future radiomics studies using QSM in clinical applications.

Indexed as

Autoimmune DiseasesMultiple SclerosisHumansMagnetic Resonance ImagingPatientsReproducibility of Results

Identifiers

PMID37758804
PMCPMC10533494

What Socratic holds

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Registered trials

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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.