# Expression of aqueous cytokines and their correlation with retinal morphological biomarkers in nAMD patients

**Authors:** Jingxin Zeng, Wenwen Shang, Pengfei Ren, Xiao Ke, Yonghao Zhao, Guina Liu, Jie Liu, Fang Lu, Xiaoshuang Jiang

PMC · DOI: 10.1371/journal.pone.0342259 · PLOS One · 2026-02-11

## TL;DR

This study found that specific cytokines in the eye fluid of nAMD patients correlate with retinal changes and vision outcomes, suggesting potential new treatment targets.

## Contribution

The study identifies elevated cytokine levels and their associations with retinal biomarkers and visual outcomes in nAMD patients.

## Key findings

- nAMD patients had higher levels of CA-1, PPK/PK, ICAM-1, VCAM-1, and MCP-1 compared to cataract patients.
- Elevated MCP-1 and retinal fibrosis were linked to worse visual outcomes in nAMD patients.
- Baseline best-corrected visual acuity was a strong predictor of future visual prognosis in nAMD.

## Abstract

Neovascular age-related macular degeneration (nAMD) is characterized by pathological neovascularization in the macula, leading to irreversible central vision loss. This study aimed to evaluate cytokine profiles in the aqueous humor of nAMD patients and explore correlation between specific cytokines, clinical characteristics, and retinal morphological features.

Our protocol was registered on Chinese Clinical Trial Registry (ChiCTR) under registration number ChiCTR2500106190 and approved by the Biomedical Research Ethics Committee of West China Hospital, Sichuan University (ID: 20231375). A total of 94 patients with nAMD and 34 cataract patients as the control group were enrolled. Aqueous humor samples were collected before anti-VEGF treatment or cataract surgery, and analyzed using cytometric bead array (CBA) for cytokines (MCP-1, ICAM-1, VCAM-1, CA-1, β-FGF, PPK/PK, and VEGF). Retinal structural biomarkers were assessed using optical coherence tomography (OCT), with statistical analysis performed to evaluate correlations between cytokine levels and retinal morphology.

Compared to cataract patients, nAMD patients exhibited elevated levels of CA-1, PPK/PK, ICAM-1, VCAM-1, and MCP-1 (P < 0.05). Baseline best-corrected visual acuity (BCVA) was reduced in nAMD patients with intraretinal fluid (IRF) or pigmentation compared to those without (P < 0.05). Visit BCVA also deteriorated in patients with fibrosis (P < 0.05). Additionally, central foveal thickness (CTR) was significantly thinner in patients with PED or SRF (P < 0.05). Visit BCVA demonstrated positive correlations with baseline BCVA (r = 0.689, P < 0.001). In contrast, the presence of fibrosis and elevated MCP-1 concentration was associated with a poorer visual outcome. In correlation analysis, β-FGF exhibited a negative correlation with CA-1, PPK, ICAM-1. VCAM-1 and MCP-1.

In this cross-sectional study, the presence of IRF was significantly associated with reduced BCVA in nAMD patients. Baseline BCVA emerged as a critical predictor of visual prognosis in nAMD. Notably, retinal fibrosis development and elevated MCP-1 level linked to worse clinical outcomes, underscoring their potential as therapeutic targets. While recent anti-VEGF injections decreased VEGF levels in aqueous humor of nAMD patients, the impact of these agents on other cytokines remain unclear, suggesting a need for adjunct therapies to address multifaceted pathogenic pathways.

## Linked entities

- **Proteins:** CCL2 (C-C motif chemokine ligand 2), ICAM1 (intercellular adhesion molecule 1), VCAM1 (vascular cell adhesion molecule 1), CA1 (carbonic anhydrase 1), FGF2 (fibroblast growth factor 2), VEGFA (vascular endothelial growth factor A)
- **Diseases:** cataract (MONDO:0005129)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, KLKB1 (kallikrein B1) [NCBI Gene 3818] {aka KLK3, PKK, PKKD, PPK}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, SRF (serum response factor) [NCBI Gene 6722] {aka MCM1}, FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, CA1 (carbonic anhydrase 1) [NCBI Gene 759] {aka CA-I, CAB, Car1, HEL-S-11}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}
- **Diseases:** retinal fibrosis (MESH:D012173), PED (OMIM:612126), pigmentation (MESH:D010859), fibrosis (MESH:D005355), Neovascular age-related macular degeneration (MESH:D008268), cataract (MESH:D002386), vision loss (MESH:D014786), IRF (MESH:D006949)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12893568/full.md

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Source: https://tomesphere.com/paper/PMC12893568