Evidence map›Paper›PMID 42415123›Full record

ArticleBMC biology2026

Network-based machine learning to identify biomarkers for systemic lupus erythematosus.

Minhyuk Park, Donghyo Kim, Juhun Lee, Jaegyun Noh, Chan Johng Kim, Youngchul Oh, Chang-Hee Suh, Ji-Won Kim, Sin-Hyeog Im, Sanguk Kim and 1 more

Abstract read
In one paragraph

Article in BMC biology, 2026. 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

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

11 authors.

Minhyuk Park *ImmunoBiome Inc., Pohang, Republic of Korea.
Donghyo Kim *Department of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Juhun Lee *ImmunoBiome Inc., Pohang, Republic of Korea.
Jaegyun Noh *Department of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Chan Johng KimDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Youngchul OhDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Chang-Hee SuhDepartment of Rheumatology, Ajou University School of Medicine, Suwon, Republic of Korea.
Ji-Won KimDepartment of Rheumatology, Ajou University School of Medicine, Suwon, Republic of Korea.
Sin-Hyeog ImImmunoBiome Inc., Pohang, Republic of Korea. iimsh@postech.ac.kr.
Sanguk KimDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea. sukim@postech.ac.kr.
Inhae KimImmunoBiome Inc., Pohang, Republic of Korea. ihkim@immunobiome.co.kr.ORCID https://orcid.org/0000-0002-4134-3953

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSystemic lupus erythematosus (SLE) is a complex autoimmune disease, making accurate diagnosis and effective treatment challenging. Despite the critical need for reliable biomarkers, conventional differential gene expression (DGE) analyses often yield high false-positive rates and have limited ability to identify clinically actionable targets, leaving a significant gap in SLE precision medicine.

resultsTo address this, we developed NetSLE, a network-based machine learning framework that integrates diverse SLE-related prior knowledge with comprehensive biological networks. By effectively filtering out false positives from differentially expressed genes (DEGs), NetSLE identified a robust panel of 150 key biomarkers. Clinically, the NetSLE-derived biomarkers outperformed conventional markers and full transcriptomes in predicting disease activity across independent cohorts. Furthermore, they successfully identified experimentally validated drug repurposing candidates (e.g., lipid-modifying and antithrombotic agents) and enabled precise stratification of patients into distinct immunological subtypes (AS1 and AS2).

conclusionsNetSLE offers a translatable approach to overcome the limitations of traditional biomarker discovery. The clinically sized 150-gene panel provides a practical tool for enhancing diagnostic precision, guiding targeted treatments, and advancing personalized medicine in SLE.

Indexed as

BiomarkersLupus Erythematosus, SystemicMachine LearningHumansPrecision MedicineBiomarkersBiomarker discoveryDrug repurposingNetwork-based machine learningPatient stratificationPrecision medicineSystemic lupus erythematosus (SLE)

Identifiers

PMID42415123
PMCPMC13628947

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.