# Correlation between tear cytokine profiles and corneal injury degree in patients with dry eye syndrome

**Authors:** Lei Cao, Cuiyu Wang, Kai Zhang, Zhida You, Yingxin Chen

PMC · DOI: 10.3389/fimmu.2026.1756076 · 2026-03-19

## TL;DR

This study finds that specific tear cytokines correlate with the severity of corneal injury in dry eye syndrome patients, offering potential for predicting and managing the condition.

## Contribution

Identifies key cytokines as independent risk factors and develops predictive models for corneal injury severity in dry eye syndrome.

## Key findings

- IL-1β, IL-6, IL-8, and TNF-α are independent risk factors for moderate corneal injury with a combined model AUC of 0.865.
- IL-1β, IL-6, and IL-8 are independent risk factors for severe corneal injury with a combined model AUC of 0.885.
- Ordered logistic regression confirms these cytokines as risk factors across all injury severity grades.

## Abstract

Dry eye syndrome (DES) is a very common ocular surface disorder that is closely related to corneal damage. However, the relationship between tear cytokines in patients with DES and the severity of corneal damage remains unclear.

Patients with DES of different corneal injury degrees (mild, moderate, severe) were enrolled. The baseline data of each group of patients were compared. The levels of tears cytokines were detected by the multiplex Luminex assay. The Kruskal-Wallis H test and the Mann-Whitney U test were used to compare the levels of cytokines. Independent risk factors were screened out using the logistic regression method, and their predictive effects were evaluated by the ROC curve analysis. Ordered logistic regression analysis confirmed the association between key cytokines and the severity of corneal injury.

There were no significant differences in baseline data among the three groups (all P > 0.05). IL-1β, IL-6, IL-8, and TNF-α were identified as independent risk factors for moderate corneal injury, with the combined model achieving an AUC of 0.865. IL-1β, IL-6, and IL-8 were independent risk factors for severe corneal injury, and the combined model had an AUC of 0.885. The ordered logistic regression analysis further confirmed that IL-1β, IL-6, TNF-α and IL-8 were independent risk factors for the aggravation of corneal injury severity across all grades.

IL-1β, IL-6, TNF-α and IL-8 play key roles in injury progression. The targeted combined models can efficiently predict the progression of corneal injury degree, providing reliable evidence for clinical graded management and individualized intervention.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta), IL6 (interleukin 6), CXCL8 (C-X-C motif chemokine ligand 8), TNF (tumor necrosis factor)
- **Diseases:** dry eye syndrome (MONDO:0006733)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** ocular surface disorder (MESH:D010534), DES (MESH:D015352), corneal damage (MESH:D065306)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13043374/full.md

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Source: https://tomesphere.com/paper/PMC13043374