Diabetes complications

Multimodal Exploratory Analysis of Persistent Diabetic Macular Edema: Integrating Aqueous Humour Metabolomics, Clinical and OCT Features

Diabetes Obes MetabPublished Prospective cohort study with nested case-control comparison

Authors' conclusion

PDME is characterized by elevated BMI, serum triglyceride, low SRF incidence, but a higher rate of DRIL and vitreoretinal interface abnormality. Purine metabolism and DNA repair pathways were associated with treatment response and correlated with OCT structural changes.

Study context

Population
DME patients treated with monthly anti-VEGF injections over 3 months146 eyes
Participants
103 patients
Comparison
Persistent diabetic macular edema (pDME) vs non-pDME after monthly anti-VEGF injections over 3 months
Outcome
Clinical, OCT and aqueous humour metabolomic features of pDME vs non-pDME
Methodological detailsexploratory, untargeted metabolomics, multimodal
  • Exploratory
  • Untargeted metabolomics
  • Multimodal

Main finding

As reported in the abstract

Differentially expressed metabolites
405
Purine metabolism pathway enrichment
p = 0.001, Q = 0.024
DNA repair pathway enrichment
p < 0.001, Q = 0.013
LOOCV AUC for pDME: metabolomic markers (purine score) vs clinical vs OCT features
0.963 vs. 0.716 and 0.505

Observational data: associations, not effects.

Further findings

Associations of OCT features with metabolomic scores

Estimate
Vitreoretinal interface abnormalityOR (purine metabolism) 5.820 (95% CI 1.136–29.811)
Vitreoretinal interface abnormalityOR (DNA repair score) 3.790 (95% CI 1.096–13.109)
DRILOR (DNA repair score) 0.214 (95% CI 0.046–0.990)
OutcomepDMEnon-pDMEP value
BMI25.2023.27P = 0.004
Triglyceride1.801.50P = 0.003
OCT features
P = 0.026
OCT features
P = 0.009
OCT features
P = 0.019

Original publication

Multimodal Exploratory Analysis of Persistent Diabetic Macular Edema: Integrating Aqueous Humour Metabolomics, Clinical and OCT Features. Diabetes Obes Metab. Published 20 September 2026. doi:10.1111/dom.71173

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