# Investigating the eye in Down syndrome as a window to Alzheimer’s disease: the REVEAL protocol – a clinical cross-sectional study

**Authors:** Aoife Mary Louise Hunter, Sarah Atkinson, Elaine Murray, Kathryn Saunders, Tunde Peto, Lajos Csincsik, Jamie Mitchell, Henrik Zetterberg, André Strydom, Julie-Anne Little, Imre Lengyel

PMC · DOI: 10.1136/bmjopen-2024-098285 · BMJ Open · 2025-07-05

## TL;DR

This study explores eye changes in people with Down syndrome as a potential early sign of Alzheimer's disease, comparing them to individuals with mild cognitive impairment and healthy controls.

## Contribution

The study introduces a novel cross-sectional protocol to investigate eye biomarkers in Down syndrome as a proxy for Alzheimer's disease.

## Key findings

- Eye imaging and functional testing will profile retinal, choroidal, and lenticular status in participants.
- The study will compare blood and molecular markers between Down syndrome, MCI, and healthy control groups.
- Findings may reveal eye-related biomarkers linked to Alzheimer's disease risk in Down syndrome.

## Abstract

There is a need for early, non-invasive and inexpensive biomarkers for Alzheimer’s disease (AD), which could serve as a proxy measure in prevention and intervention trials that might eventually be suitable for mass screening. People with Down syndrome (DS) are the largest patient group whose condition is associated with a genetically determined increased risk of AD. The REVEAL study aims to examine changes in the structure and function of the eye in individuals with DS compared with those with mild cognitive impairment (MCI) and cognitively healthy control (HC) individuals. REVEAL will also explore whether these changes are connected to inflammatory markers previously associated with AD.

The protocol describes a cross-sectional, non-interventional, single-centre study recruiting three cohorts, including (1) participants with DS (target n=50; age range, 6–60 years), (2) participants with MCI (target n=50; age range, 50–80 years) and (3) HC participants (target n=50; age range, 50–80 years). The primary research objective is to profile retinal, choroidal and lenticular status using a variety of eye imaging modalities and retinal functional testing to determine potential associations with cognitive status. The REVEAL study will also measure and compare established blood markers for AD and proteomic and transcriptomic marker profiles between DS, MCI and HC groups. Between-group differences will be assessed with an independent sample t-test and χ2 tests for normally distributed or binary measures, respectively. Multivariate regression analysis will be used to analyse parameters across all three cohorts. Data collection began in October 2023 and is expected to end in October 2025.

The study gained a favourable opinion from Health and Social Care Research Ethics Committee A (REC reference 22/NI/0158; approved on 2 December 2022; Amendment 22/0064 Amend 1, 5 April 2023; Amendment 22/0064 Amend 2; 23 May 2024; Amendment 22/0064 Amend 3; 25 June 2024; Amendment 22/0064 Amend 4; 16 January 2025; Amendment 22.0064 Amend 5; 9 May 2025; Amendment 22.0064 Amend 6; 9 June 2025). The study has also been reviewed and approved by the School of Biomedical Sciences Research Ethics Filter Committee within Ulster University. Findings from the REVEAL study will be presented to academic audiences at international conferences and peer-reviewed publications in targeted high-impact journals after data collection and analysis are complete. Dissemination activities will also include presentations at public events.

## Linked entities

- **Diseases:** Alzheimer’s disease (MONDO:0004975), Down syndrome (MONDO:0008608)

## Full-text entities

- **Diseases:** MCI (MESH:D060825), AD (MESH:D000544), DS (MESH:D004314), inflammatory (MESH:D007249), cognitive impairment (MESH:D003072)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12228435/full.md

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Source: https://tomesphere.com/paper/PMC12228435