Evidence map›Paper›PMID 39923192›Full record

ArticleJournal of neuroimaging : official journal of the American Society of Neuroimaging

Subject-Based Transfer Learning in Longitudinal Multiple Sclerosis Lesion Segmentation.

Sibaji Gaj, Bhaskar Thoomukuntla, Daniel Ontaneda, Kunio Nakamura

Abstract read
In one paragraph

Article in Journal of neuroimaging : official journal of the American Society of Neuroimaging. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Sibaji GajDepartment of Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0002-6997-5717
Bhaskar ThoomukuntlaDepartment of Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Daniel OntanedaMellen Center for Multiple Sclerosis and Research, Neurological Institute, Cleveland Clinic, Cleveland, Ohio, USA.
Kunio NakamuraDepartment of Biomedical Engineering, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio, USA.ORCID 0000-0002-7833-8138

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeAccurate and consistent lesion segmentation from magnetic resonance imaging is required for longitudinal multiple sclerosis (MS) data analysis. In this work, we propose two new transfer learning-based pipelines to improve segmentation performance for subjects in longitudinal MS datasets.

methodIn general, transfer learning is used to improve deep learning model performance for the unseen dataset by fine-tuning a pretrained model with a limited number of labeled scans from the unseen dataset. The proposed methodologies fine-tune the deep learning model for each subject using the first scan and improve segmentation performance for later scans for the same subject. We also investigated the statistical benefits of the proposed methodology by modeling lesion volume over time between progressors according to confirmed disability progression and nonprogressors for a large in-house dataset (937 MS patients, 3210 scans) using a linear mixed effect (LME) model.

resultsThe results show statistically significant improvement for the proposed methodology compared with the traditional transfer learning method using Dice (improvement: 2%), sensitivity (6%), and average volumetric difference (16%), as well as visual analysis for public and in-house datasets. The LME result showed that the proposed subject-wise transfer learning method had increased statistical power for the measurement of longitudinal lesion volume.

conclusionThe proposed method improved lesion segmentation performance and can reduce manual effort to correct the automatic segmentations for final data analysis in longitudinal studies.

Indexed as

BrainDeep LearningImage Interpretation, Computer-AssistedMagnetic Resonance ImagingMultiple SclerosisAdultDisease ProgressionFemaleHumansLongitudinal StudiesMaleMiddle Agedautomated segmentationdeep learningtransfer learningUNet

Identifiers

PMID39923192
PMCPMC11807364

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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 OpenQuestion graph.