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Very Preterm Infant Retinal Microanatomy at 36 Weeks’ Postmenstrual Age and 2-Year Neurodevelopment

JAMA Ophthalmology·June 4Open Access
OphthalmologyLimited evidenceNeurodevelopmental ImpairmentRetinopathy Of PrematurityVery Preterm BirthProspective Cohort StudyOptical Coherence TomographyNeonate

Summary

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What was studied

This prospective longitudinal cohort study (BabySTEPS, n=72 very preterm infants, mean GA 27.6 weeks) evaluated whether bedside OCT measures of retinal microanatomy at 36 weeks' postmenstrual age (PMA) — including RNFL thickness, choroidal thickness, inner retinal thickness, and macular edema — predicted neurodevelopmental outcomes (BSID-III, CBCL, M-CHAT-R) at 2 years' corrected age.

Key findings

Greater RNFL thickness was independently associated with higher BSID-III Motor scores (+7.50 points per 10-µm increase; P<.001) and Cognitive scores (+3.71 points; P=.02), lower autism risk (M-CHAT-R: −0.64 per 10 µm; P=.03), and fewer internalizing behavior problems (CBCL: −2.25 per 10 µm; P=.04). Adding RNFL thickness to standard infant factors boosted Motor score prediction from R²=0.36 to 0.53 (gain +0.17). Greater choroidal thickness also predicted better Motor scores (+4.84 points per 100 µm; P=.03) but added no incremental value beyond RNFL alone.

Study limitations

- Single-center study using a **research-only OCT device** not yet commercially available, limiting immediate clinical translation. - 26 of 98 surviving infants (26.5%) were lost to follow-up; those lost were slightly less preterm and heavier, potentially underestimating impairment burden. - Multiple comparisons were not adjusted, raising the risk of false-positive associations for secondary behavioral outcomes.

Clinical implications

Bedside OCT RNFL thickness measured during routine ROP examinations at ~36 weeks PMA may serve as an early, low-stress biomarker to flag very preterm infants most at risk for motor and cognitive delays — enabling earlier enrollment in developmental therapies. Pending independent validation and a commercially available device, clinicians should consider RNFL thickness data as a supplement to, not replacement for, standard neurodevelopmental risk assessment.

Related Questions

Explore related topics

Can bedside OCT retinal imaging in the NICU predict neurodevelopmental outcomes in preterm infants?What retinal biomarkers are associated with autism risk or cognitive delay in very preterm infants?How does RNFL thickness in preterm infants compare to brain MRI for predicting 2-year developmental outcomes?

Publication Details

Year
2026
Journal
JAMA Ophthalmology
Sample Size
n=72
Source
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