# Age-Related Associations of Foveal Structural Parameters in Healthy Adults: A Comparative Analysis of Biological and Chronological Age

**Authors:** Anait S. Khalatyan, Yusef Yusef, Khadishat K. Altemirova, Liubov V. Machekhina, Alexandra A. Melnitskaya, Irina D. Strazhesko

PMC · DOI: 10.3390/vision10010016 · Vision · 2026-03-03

## TL;DR

This study found that the foveal bulge decreases with age and is a sensitive marker of aging in the eye, but biological age does not add value over chronological age in predicting these changes.

## Contribution

The foveal bulge is identified as a sensitive qualitative marker of age-related changes in the eye.

## Key findings

- The core geometry of the foveal pit showed no significant dependence on either biological or chronological age.
- Foveal bulge prevalence declined significantly with both chronological and biological age.
- Biological age does not provide additional predictive value over chronological age for foveal structural parameters.

## Abstract

Background: This research compared the relationship between foveal optical coherence tomography (OCT) parameters and two age measures—biological and chronological—in healthy adults. Methods: This cross-sectional study analyzed swept-source optical coherence tomography (OCT) data from 308 eyes of 154 healthy adults aged 22–89 years. Parameters assessed: foveal thickness, foveal pit depth and diameter, pit slope steepness, and the presence or absence of the foveal bulge. Biological age was calculated using the PhenoAge algorithm. Results: The core geometry of the foveal pit showed no significant dependence on either type of age (all p ≥ 0.66). In contrast, the foveal bulge prevalence declined significantly with age (adjusted p = 0.011 for chronological age, p = 0.005 for biological age; OR per year ≈0.95, 95% CI 0.92–0.98 for both age models). Model-predicted prevalence decreased from approximately 93% in younger adults to 60–68% in the 60–74-year-old group. Conclusion: The foveal architecture remains structurally stable throughout adulthood. The foveal bulge emerges as a sensitive qualitative marker of age-related changes. Biological age does not provide additional predictive value over chronological age for foveal structural parameters under physiological aging conditions.

## Full-text entities

- **Genes:** PLXNA2 (plexin A2) [NCBI Gene 5362] {aka OCT, PLXN2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** cataract (MESH:D002386), diabetic retinopathy (MESH:D003930), injury to (MESH:D014947), infection (MESH:D007239), glaucoma (MESH:D005901), oncological disease (MESH:D000072716), metabolic, cardiovascular, or neurodegenerative diseases (MESH:D019636), rheumatoid arthritis (MESH:D001172), mitochondrial dysfunction (MESH:D028361), diabetes mellitus (MESH:D003920), retinal vascular occlusion (MESH:D015356), psychiatric disorders (MESH:D001523), uveitis (MESH:D014605), Eye Diseases (MESH:D005128), hypermetropia (MESH:D006956), optic neuropathy (MESH:D009901), age-related macular degeneration (MESH:D008268), dementia (MESH:D003704), autoimmune diseases (MESH:D001327), systemic lupus erythematosus (MESH:D008180), chronic systemic inflammation (MESH:D007249), Systemic diseases (MESH:D034721), respiratory (MESH:D012131), myopia (MESH:D009216), choroidal atrophy (MESH:C535810), fever (MESH:D005334), hypertension (MESH:D006973)
- **Chemicals:** creatinine (MESH:D003404), glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13030814/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC13030814/full.md

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Source: https://tomesphere.com/paper/PMC13030814