Evidence map›Paper›PMID 42535174›Full record

ArticleFrontiers in genetics2026

Integrated multi-omics analysis identifies candidate eRNA-associated signatures shared between osteoarthritis and type 2 diabetes.

Danni Huang, Junying Wu, Jinhua Chen, Qian Wu, Shengnan Wang

Abstract read
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Article in Frontiers in genetics, 2026. 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Danni HuangDivision of Orthopaedics and Traumatology, Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong Province, China.
Junying WuDepartment of Endocrinology and Metabolism, Jiangmen Central Hospital, Jiangmen, Guangdong Province, China.
Jinhua ChenDepartment of Orthopedics, The Third Hospital of Xiamen, Xiamen, Fujian Province, China.
Qian Wu *Division of Spine Surgery, Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong Province, China.
Shengnan Wang *Division of Orthopaedics and Traumatology, Department of Orthopaedics, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Osteoarthritis (OA) and type 2 diabetes mellitus (T2DM) frequently coexist and share inflammatory and metabolic disturbances, but the immune-epigenetic features that may overlap between these conditions remain incompletely defined. Enhancer RNAs (eRNAs) are increasingly recognized as regulators of enhancer activity and transcriptional programs, whereas eRNA-associated signatures shared between OA-related and T2DM-related datasets remain largely unexplored. Methods: Transcriptomic datasets from OA joint tissues and controls (63 OA, 35 controls) were analyzed together with an independent T2DM dataset of CD14 Results: We identified 473 annotated dysregulated eRNA-associated features in OA, with associated genes enriched in skeletal development, extracellular matrix remodeling, and PI3K-Akt signaling. CIBERSORT-based and pathway analyses suggested immune-associated transcriptional alterations and inflammatory pathway activation in OA. Integrative analysis prioritized TOB1 as a candidate eRNA-associated feature related to JUN, Conclusion: TOB1 was prioritized as a candidate eRNA-associated signal related to JUN,

Indexed as

CCNL1enhancer RNAs (eRNAs)immune signaturesmulti-omicsosteoarthritistype 2 diabetes mellitus

Identifiers

PMID42535174
PMCPMC13423288

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