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Retinal sublayer changes in cases with Alzheimer’s disease and depression
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Retinal sublayer changes in cases with Alzheimer’s disease and depression

Graefe's Archive for Clinical and Experimental Ophthalmology·July 8
OphthalmologyConfirms priorSafety signalAlzheimer'S DiseaseDepressionCross-Sectional StudyOptical Coherence TomographyOlder Adult

Summary

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What was studied

This cross-sectional study compared peripapillary RNFL (pRNFL) and macular layer thickness (via Heidelberg OCT) between 50 elderly adults with mild-to-moderate Alzheimer's disease (AD) and 50 age-matched healthy controls (HCs), while also assessing depression severity (PHQ-9) and cognition (MMSE) in both groups.

Key findings

AD patients had significant thinning in supra-temporal pRNFL (127.45 vs. 136.38 µm, P=0.010), infra-temporal pRNFL (127.99 vs. 139.46 µm, P=0.003), GCL volume (0.981 vs. 1.043 mm³, P<0.001), IPL volume (0.834 vs. 0.872 mm³, P=0.001), and GCC (2.671 vs. 2.832 mm³, P<0.001). Depression severity independently correlated with lower GCL volume (ρ=−0.260, P=0.009), and an AD × depression interaction showed that co-existing depression worsened GCL thinning beyond AD alone (β=−0.213, P=0.020).

Study limitations

- Cross-sectional design prevents causal inference or tracking of retinal changes over time. - Depression was assessed by PHQ-9 only; no clinical diagnosis of major depressive disorder was confirmed. - Sample limited to mild-to-moderate AD; findings may not generalize to severe AD or other dementias.

Clinical implications

OCT-measured inner retinal thinning (GCL, IPL, pRNFL) is meaningful in AD patients, but co-existing depression adds further thinning—so clinicians should account for both conditions when using OCT to screen for glaucoma or monitor neurodegeneration in elderly patients. Reliable visual field testing is also harder in AD, making OCT interpretation even more context-dependent.

Caveats

  • Depression was measured dimensionally by PHQ-9 score rather than confirmed as a clinical diagnosis of major depressive disorder; the 'depression group' represents a spectrum of severity rather than a distinct diagnostic cohort.
  • Interaction finding (AD × depression on GCL) is exploratory and from a stepwise regression; replication in larger samples is needed before clinical application.
  • The study was conducted at a single center (Shiraz University of Medical Sciences); ethnic and geographic generalizability is uncertain.

Related Questions

Explore related topics

How does OCT retinal thinning compare between Alzheimer's disease and glaucoma in elderly patients?Can peripapillary RNFL or GCL thickness on OCT serve as early biomarkers for Alzheimer's disease?How does comorbid depression affect retinal nerve fiber layer thickness in neurodegenerative disease?

Publication Details

Year
2026
Journal
Graefe's Archive for Clinical and Experimental Ophthalmology
Sample Size
n=100
Source
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