Evidence map›Paper›PMID 42549570›Full record

ArticleDiabetes & vascular disease research

Identification of circulating biomarkers and immune subtypes for diabetic retinopathy through multi-cohort integrative analysis.

Jiwei Zhang, Linglin Zhang, Zhihong Yu, Gaojie Yang, Liling Yu

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Article in Diabetes & vascular disease research. 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

5 authors.

Jiwei ZhangDepartment of Ophthalmology, The First People's Hospital of Lin'an District, Hangzhou, Zhejiang, China.ORCID 0009-0009-9585-6939
Linglin ZhangDepartment of Ophthalmology, The First People's Hospital of Lin'an District, Hangzhou, Zhejiang, China.ORCID 0009-0009-3023-4231
Zhihong YuDepartment of Ophthalmology, The First People's Hospital of Lin'an District, Hangzhou, Zhejiang, China.ORCID 0009-0000-4834-6404
Gaojie YangDepartment of Ophthalmology, The First People's Hospital of Lin'an District, Hangzhou, Zhejiang, China.ORCID 0009-0004-9957-3489
Liling YuDepartment of Ophthalmology, The First People's Hospital of Lin'an District, Hangzhou, Zhejiang, China.ORCID 0009-0007-0576-4228

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PurposeTo elucidate the dynamic molecular evolution and immune heterogeneity in diabetic retinopathy (DR) and identify diagnostic biomarkers.MethodsMulti-omics integrative analysis was performed on peripheral blood transcriptomic data from diabetic patients with and without DR. Techniques included differential expression analysis, immune infiltration profiling, unsupervised clustering, and LASSO regression for biomarker selection. Findings were validated in an independent high-glucose-treated endothelial cell model.ResultsDR progression exhibits staged molecular evolution from diabetes (immune suppression) to early DR (cell cycle inhibition, immune burst) and advanced DR (metabolic stress, persistent immune dysregulation). Six co-downregulated immune modules indicated systemic immune suppression. Patients were classified into three immune subtypes: vascular-inflammatory, metabolic disorder, and oxidative stress-tissue remodeling. A diagnostic model based on IK, PLBD2, FLNA, H6PD, and ZMAT2 achieved an AUC of 0.876 for distinguishing DR from diabetes alone.ConclusionThis study delineates the dynamic molecular landscape and immune heterogeneity of DR, providing a potential multi-gene diagnostic signature and a framework for patient stratification, which may facilitate early detection and personalized management.

Indexed as

Diabetic RetinopathyTranscriptomeBiomarkersEndothelial CellsFemaleGene Expression ProfilingHumansMaleMultiomicsPredictive Value of TestsBiomarkersbiomarkersdiabetic retinopathyimmune microenvironmentmolecular typingperipheral blood transcriptome

Identifiers

PMID42549570
PMCPMC13438248

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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.