Evidence map›Paper›PMID 40325212›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2025

Identification of markers predicting clinical course in patients with Behcet disease by combination of machine learning and unbiased clustering analysis.

Kinya Tsubota, Yoshihiko Usui, Hiroyuki Shimizu, Hiroshi Goto

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In one paragraph

Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Kinya TsubotaDepartment of Ophthalmology, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-Ku, Tokyo, 160-0023, Japan. tsubnkin@hotmail.co.jp.ORCID http://orcid.org/0000-0002-7680-3745
Yoshihiko UsuiDepartment of Ophthalmology, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-Ku, Tokyo, 160-0023, Japan.
Hiroyuki ShimizuDepartment of Ophthalmology, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-Ku, Tokyo, 160-0023, Japan.
Hiroshi GotoDepartment of Ophthalmology, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-Ku, Tokyo, 160-0023, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBehçet's disease (BD) is a multisystem inflammatory disorder with diverse clinical manifestations. Identifying biomarkers predictive of clinical outcomes, such as tumor necrosis factor (TNF) inhibitor initiation and ocular inflammatory attack frequency, is critical for improving management. This study aimed to identify biomarkers predicting the clinical course of BD using peripheral blood test data and unbiased clustering combined with machine learning.

methodsA retrospective cohort study of 238 BD patients diagnosed at Tokyo Medical University Hospital (2004-2020) was conducted. Unsupervised hierarchical clustering was applied to peripheral blood data, dividing patients into distinct groups. Machine learning techniques were used to explore biomarkers predicting the clinical course.

resultsCluster analysis identified four groups: Group A (low C-reactive protein), Group B (high angiotensin-converting enzyme), Group C (high anti-streptolysin O), and Group D (low neutrophil count). Group C had a higher rate of TNF inhibitor initiation (47%, p = 0.04), while Group D had fewer ocular inflammation attacks per year (1.4, p = 0.04). Logistic regression analysis identified red blood cell count (p < 0.01) and monocyte percentage (p = 0.02) as predictive biomarkers for TNF inhibitor initiation. Machine learning further confirmed mean corpuscular hemoglobin concentration (MCHC) as a significant predictor of TNF inhibitor initiation. Additionally, multiple regression analysis identified the neutrophil/lymphocyte ratio as a predictor of the number of inflammatory attacks per year (p = 0.02).

conclusionsUnsupervised clustering of blood test data identified distinct BD clinical phenotypes. Monocyte percentage may predict TNF inhibitor initiation, while neutrophil/lymphocyte ratio may predict ocular inflammation frequency, highlighting pathophysiologic heterogeneity in BD.

Indexed as

Behcet SyndromeBiomarkersMachine LearningAdultCluster AnalysisC-Reactive ProteinFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRetrospective StudiesBiomarkersC-Reactive ProteinBehçet’s diseaseMachine learningMonocyte percentageNeutrophil/lymphocyte ratioTNF inhibitorUnsupervised hierarchical clustering

Identifiers

PMID40325212
PMCPMC12513920

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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.