Evidence map›Paper›PMID 40397236›Full record

ArticleMolecular biology reports2025

Expression of thrombomodulin in pterygium: implications for inflammation and disease progression.

Yu-Kuei Lee, Chun-Chieh Lai, I-Chen Peng, Yi-Hsun Huang

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Article in Molecular biology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yu-Kuei LeeDepartment of Ophthalmology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Chun-Chieh LaiDepartment of Ophthalmology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
I-Chen PengDepartment of Ophthalmology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Yi-Hsun HuangDepartment of Ophthalmology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan. jackhyh@gmail.com.ORCID https://orcid.org/0000-0002-4150-5481

Funding

National Cheng Kung University Hospital NCKUH-11405011National Science and Technology Council 111-2314-B-006-072-MY3
6 · The paper itself

Abstract

backgroundPterygium is a chronic inflammatory condition of conjunctiva. Thrombomodulin (TM) is a glycoprotein involved in the regulation of inflammation. This study investigated TM expression in primary and recurrent pterygium compared to normal conjunctiva, along with its role in pterygium pathogenesis and potential as a therapeutic target for inflammation control. METHODS AND

resultsPterygium (10 primary, 10 recurrent) and normal conjunctiva specimens were collected from 20 patients who underwent pterygium excision. TM expression was analyzed using immunofluorescence, western blotting, and real-time quantitative polymerase chain reaction (RT-PCR). Inflammatory markers, including interleukin-6 (IL-6), high mobility group box 1 (HMGB1), vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), and matrix metalloproteinase-1 (MMP-1), were measured. The results showed significantly lower TM expression in pterygium tissues (p < 0.01), with higher TM levels in the head region compared to the body, suggesting a localized inflammatory response. Additionally, macrophage marker F4/80 and neutrophil marker NIMP-R14 were elevated in pterygium tissues. Western blot and RT-PCR confirmed significantly reduced TM expression (p < 0.0001) in primary and recurrent pterygium, with recurrent cases showing even lower levels (p < 0.05). Elevated IL-6, HMGB1, VEGF, bFGF, and MMP-1 levels suggest a strong association between TM downregulation and increased inflammation.

conclusionsTM downregulation in pterygium (particularly in recurrent cases) may contribute to chronic inflammation and disease progression. Upregulation of TM at the pterygium head may represent a localized protective response against inflammation. TM supplementation should be explored as a novel therapeutic strategy to mitigate inflammation in pterygium.

Indexed as

InflammationPterygiumThrombomodulinAdultAgedBiomarkersConjunctivaDisease ProgressionFemaleFibroblast Growth Factor 2HMGB1 ProteinHumansInterleukin-6MaleMatrix Metalloproteinase 1Middle AgedBiomarkersFibroblast Growth Factor 2HMGB1 ProteinInterleukin-6Matrix Metalloproteinase 1THBD protein, humanThrombomodulinVascular Endothelial Growth Factor AVEGFA protein, humanConjunctivaInflammationPterygiumThrombomodulin

Identifiers

PMID40397236

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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.