Evidence map›Paper›PMID 41181297›Full record

ArticleClinical ophthalmology (Auckland, N.Z.)2025

Markedly Lower Rates of Age-Related Macular Degeneration in Malta Compared to European Countries: Results from The Malta Eye Study, Indicating Possible Divergent Genetic Ancestry?

David Agius, Julian J Mamo, Neville Calleja, Daniel Cassar, Xeniya Marku, Maria Christina Nappa, Michaela Zammit, Maria Elena Pace, Francis Carbonaro

Abstract read
In one paragraph

Article in Clinical ophthalmology (Auckland, N.Z.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

David AgiusDepartment of Surgery, University of Malta, Msida, Malta.ORCID 0000-0002-8485-1915
Julian J MamoDepartment of Public Health, University of Malta, Msida, Malta.
Neville CallejaDepartment of Public Health, University of Malta, Msida, Malta.
Daniel CassarDepartment of Ophthalmology, Mater Dei Hospital, Msida, Malta.
Xeniya MarkuDepartment of Ophthalmology, Mater Dei Hospital, Msida, Malta.ORCID 0000-0002-7149-4787
Maria Christina NappaDepartment of Medicine, Mater Dei Hospital, Msida, Malta.
Michaela ZammitDepartment of Medicine, Mater Dei Hospital, Msida, Malta.ORCID 0009-0000-9715-6105
Maria Elena PaceMedical School, University of Malta, Msida, Malta.
Francis CarbonaroDepartment of Surgery, University of Malta, Msida, Malta.ORCID 0000-0002-7583-1955

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To estimate the prevalence of age-related macular degeneration (ARMD) in a nationally representative sample of older adults from Malta, evaluate associations with established risk factors, and compare rates with those reported in other European populations, where substantial variation has been observed. Patients and Methods: A population-based cross-sectional study was conducted involving 1794 participants aged 50-80 years from Malta (1% of the represented population), recruited as part of The Malta Eye Study. Standardized ophthalmic examinations were performed, including retinal imaging graded for ARMD according to Age-Related Eye Disease Study criteria and optical coherence tomography scans. Data on demographics, medical history, behavioural risk factors, and ocular characteristics were collected via structured questionnaires. Associations were assessed using multivariable logistic regression. DNA samples were also collected for future genetic analyses. Results: The overall prevalence of ARMD was 6.5% (95% CI 5.4-7.8%), with early ARMD accounting for 5.6% (95% CI 4.6-6.7%) and late ARMD for 0.4% (95% CI 0.2-0.8%). Multivariate analysis showed that ARMD prevalence increased significantly with age (OR per year 1.08; 95% CI 1.05-1.11, p<0.001) and in the male sex (OR 1.57; 95% CI 1.01-2.44, p=0.043). The other traditional ARMD risk factors did not show significant associations in this cohort. Compared to other European populations, ARMD prevalence was notably lower. Conclusion: This study reports a relatively low prevalence of ARMD compared to other European settings, with age and male sex emerging as the only significant risk factors. The absence of association with other traditional risk factors may reflect underlying genetic differences or distinct gene-environment interactions. As DNA samples were collected, further investigation incorporating genetic data is warranted to better understand ARMD susceptibility in this population.

Indexed as

ageinggene–environment interactionmacular degenerationpopulation-based studyprevalencerisk factors

Identifiers

PMID41181297
PMCPMC12577580

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