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New research · Ophthalmology
Current eye research · 4d
ReviewCurrent eye research · 2026

Cross-Compartment Proteomic Signatures in Human Diabetic Retinopathy: A Systematic Review and Meta-Analysis.

Soumya Behera, Nibedita Sahoo, Subhangi Sahu
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OphthalmologyReview

Proteins are consistently elevated in eye fluid samples from diabetic retinopathy patients

Cross-Compartment Proteomic Signatures in Human Diabetic Retinopathy: A Systematic Review and Meta-Analysis.

Soumya Behera … Subhangi Sahu
Current eye research · 2026
Background

Diabetic retinopathy (diabetic retinopathy) is a leading cause of preventable blindness, with complex molecular pathophysiology spanning multiple biological compartments.

Purpose

This systematic review and meta-analysis aimed to synthesize proteomic findings from human diabetic retinopathy studies to identify consistent cross-compartment molecular signatures and evaluate their clinical translation potential.

Methods

Following a prespecified PRISMA protocol, we searched databases and registries to September 2025.

n = 28 studies
Results

protein levels ran higher in eye fluid from diabetic retinopathy patients than controls

Log2FC 1.49 (95% CI 0.72 to 2.27)
null 0
0.72
2.27
CI excludes the null - significant
More results

Twenty-eight studies contributed data.

Fibrinogen chains (FGA, FGB, FGG) were robustly upregulated across compartments and exceeded complement proteins ( β = +1.41; p < 0.001).

More results

Qualitative evidence highlighted vitronectin, RBP4, prothrombin, and afamin as additional stage-specific candidates, while tear- and urine-based markers showed potential for noninvasive screening.

“
Conclusion

This first integrated systematic review and meta-analysis of multicompartment proteomic studies in diabetic retinopathy shows consistent upregulation of fibrinogen chains across ocular compartments, highlights vitronectin and stage-specific proteins as additional candidates, and establishes a rigorous evidence base to guide biomarker validation and clinical translation.

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