Evidence map›Paper›PMID 38045345›Full record

ArticlemedRxiv : the preprint server for health sciences2024

LST-AI: a Deep Learning Ensemble for Accurate MS Lesion Segmentation.

Tun Wiltgen, Julian McGinnis, Sarah Schlaeger, Florian Kofler, CuiCi Voon, Achim Berthele, Daria Bischl, Lioba Grundl, Nikolaus Will, Marie Metz and 11 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Tun WiltgenDepartment of Neurology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Julian McGinnisDepartment of Neurology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Sarah SchlaegerDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Florian KoflerDepartment of Computer Science, Institute for AI in Medicine, Technical University of Munich, Munich, Germany.
CuiCi VoonDepartment of Neurology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Achim BertheleDepartment of Neurology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.ORCID 0000-0001-9650-6222
Daria BischlDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Lioba GrundlDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Nikolaus WillDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Marie MetzDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
David SchinzDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Dominik SeppDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Philipp PruckerDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Benita Schmitz-KoepDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Claus ZimmerDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Bjoern MenzeDepartment of Quantitative Biomedicine, University of Zurich, Zurich, Switzerland.
Daniel RueckertDepartment of Computer Science, Institute for AI in Medicine, Technical University of Munich, Munich, Germany.
Bernhard HemmerDepartment of Neurology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.ORCID 0000-0001-5985-6784
Jan KirschkeDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.ORCID 0000-0002-7557-0003
Mark MühlauDepartment of Neurology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Benedikt WiestlerDepartment of Diagnostic and Interventional Neuroradiology, School of Medicine, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.ORCID 0000-0002-2963-7772

Funding

Computational Imaging Biomarkers of Multiple SclerosisR01NS112161 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI VAN LEEMPUT, KOEN · 2019 to 2023
$1.5M
NINDS NIH HHS R01 NS112161
6 · The paper itself

Abstract

Automated segmentation of brain white matter lesions is crucial for both clinical assessment and scientific research in multiple sclerosis (MS). Over a decade ago, we introduced an engineered lesion segmentation tool, LST. While recent lesion segmentation approaches have leveraged artificial intelligence (AI), they often remain proprietary and difficult to adopt. As an open-source tool, we present LST-AI, an advanced deep learning-based extension of LST that consists of an ensemble of three 3D-UNets. LST-AI explicitly addresses the imbalance between white matter (WM) lesions and non-lesioned WM. It employs a composite loss function incorporating binary cross-entropy and Tversky loss to improve segmentation of the highly heterogeneous MS lesions. We train the network ensemble on 491 MS pairs of T1w and FLAIR images, collected in-house from a 3T MRI scanner, and expert neuroradiologists manually segmented the utilized lesion maps for training. LST-AI additionally includes a lesion location annotation tool, labeling lesion location according to the 2017 McDonald criteria (periventricular, infratentorial, juxtacortical, subcortical). We conduct evaluations on 103 test cases consisting of publicly available data using the Anima segmentation validation tools and compare LST-AI with several publicly available lesion segmentation models. Our empirical analysis shows that LST-AI achieves superior performance compared to existing methods. Its Dice and F1 scores exceeded 0.62, outperforming LST, SAMSEG (Sequence Adaptive Multimodal SEGmentation), and the popular nnUNet framework, which all scored below 0.56. Notably, LST-AI demonstrated exceptional performance on the MSSEG-1 challenge dataset, an international WM lesion segmentation challenge, with a Dice score of 0.65 and an F1 score of 0.63-surpassing all other competing models at the time of the challenge. With increasing lesion volume, the lesion detection rate rapidly increased with a detection rate of >75% for lesions with a volume between 10mm

Indexed as

Artificial IntelligenceDeep LearningLesion SegmentationMagnetic Resonance ImagingMultiple SclerosisWhite Matter Lesions

Identifiers

PMID38045345
PMCPMC10690346

What OpenQuestion holds

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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.