Imaging biomarkers in diabetic macular oedema: Predicting vision beyond retinal thickness - Scorecard - MDSpire
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Imaging markers for diabetic macular oedema: Forecasting visual outcomes beyond retinal thickness

  • By

  • Enrico Borrelli

  • October 18, 2026

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Clinical Scorecard: Imaging biomarkers associated with visual outcomes in diabetic macular oedema

At a Glance

CategoryDetail
ConditionClinical topic addressed by the source article: Imaging markers for diabetic macular oedema
Key MechanismsStructural OCT features and OCTA measures of retinal capillary perfusion are associated with visual acuity and visual-acuity change during anti-VEGF treatment. The source also identifies diabetic macular ischaemia assessed by OCTA as a strong predictor of long-term visual outcomes.
Target PopulationPatients or participants described in the source article.
Care SettingAssessment of visual prognosis in DMO using retinal imaging.

Key Highlights

  • In the 60-eye post hoc analysis, mean visual acuity increased from 62.9 letters at baseline to 75.4 letters at week 52.
  • Baseline central subfield thickness (CSFT) independently predicted baseline visual acuity and week-52 visual acuity.
  • A composite of superficial perfusion density and vessel length density was independently associated with week-52 visual acuity.
  • Greater baseline volume of hyperreflective foci was independently associated with a smaller visual-acuity gain.
  • The source identifies diabetic macular ischaemia assessed with OCTA as one of the strongest predictors of long-term visual outcomes.
  • A meta-analysis of 27 studies and 75 candidate biomarkers found five associated with reduced visual acuity at two or more time points, with moderate certainty.

Guideline-Based Recommendations

Diagnosis

    Management

      Monitoring & Follow-up

      • The source notes that CSFT explains only a limited fraction of variation in visual acuity; it discusses visual outcomes alongside imaging features.
      • The source describes standardised OCTA acquisition and processing—including scan protocol, slab definitions, segmentation, projection-artefact removal, and binarisation thresholds—as prerequisites for comparable measurements.

      Risks

      • The featured analysis was limited by 60 eyes, discretionary OCTA acquisition, use of Heidelberg Spectralis scans, models accounting for 19%–32% of variance, and no adjustment for multiple comparisons.
      • OCTA vascular measurements may vary by device and analysis pipeline; thresholds may not transfer between centres unless acquisition and processing are reproduced.
      • The exclusion of deep vascular complex metrics from the models may reflect more consistent measurement of the superficial slab in oedematous eyes, rather than greater biological relevance.

      Patient & Prescribing Data

      Patients with DMO treated with anti-VEGF injections; the featured analysis used baseline imaging and week-52 visual-acuity data from 60 eyes.

      The article reports associations between baseline imaging biomarkers and visual outcomes, but does not provide prescribing instructions or validated biomarker-based treatment thresholds.

      Clinical Best Practices

      • The source describes limited concordance between CSFT and visual acuity and discusses structural and vascular imaging features in relation to visual outcomes.
      • The source notes that post hoc biomarker findings require validation and that evidential strength depends on the number of eyes included.
      • The source identifies standardised imaging acquisition and analysis as prerequisites for comparable OCTA measurements.
      • The source discusses prespecified imaging substudies as a way to develop exploratory signals into more reliable estimates.

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      Original Source(s)

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