Evidence map›Paper›PMID 40856652›Full record

ArticleInvestigative ophthalmology & visual science2025

Revisiting the Trans-Ancestry Genetic Correlation of Refractive Error.

Rosie Clark, Xi He, Thu Nga Nguyen, Thanh Huyen Bui, Hannah Noor, Cathy Williams, Louise Terry, Jeremy A Guggenheim, UK Biobank Eye and Vision Consortium

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Rosie ClarkSchool of Optometry & Vision Sciences, Cardiff University, Cardiff, United Kingdom.
Xi HeSchool of Optometry & Vision Sciences, Cardiff University, Cardiff, United Kingdom.
Thu Nga NguyenSchool of Optometry & Vision Sciences, Cardiff University, Cardiff, United Kingdom.
Thanh Huyen BuiSchool of Optometry & Vision Sciences, Cardiff University, Cardiff, United Kingdom.
Hannah NoorSchool of Optometry & Vision Sciences, Cardiff University, Cardiff, United Kingdom.
Cathy WilliamsCentre for Academic Child Health, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Louise TerrySchool of Optometry & Vision Sciences, Cardiff University, Cardiff, United Kingdom.
Jeremy A GuggenheimSchool of Optometry & Vision Sciences, Cardiff University, Cardiff, United Kingdom.
UK Biobank Eye and Vision Consortium

Funding

Wellcome Trust
6 · The paper itself

Abstract

Purpose: The prevalence of myopia varies significantly across the globe. This may be a consequence of differences in exposure to lifestyle risk factors or differences in genetic susceptibility across ancestry groups. "Trans-ancestry genetic correlation" quantifies the similarity in genetic predisposition to a trait or disease between different populations. We estimated the trans-ancestry genetic correlation of refractive error across Europeans, South Asians, East Asians, and Africans using recently developed approaches. Methods: Two methods were applied: (1) trans-ancestry genetic correlation with unbalanced data resources (TAGC-UDR) and (2) trans-ancestry bivariate genomic-relatedness-based restricted maximum-likelihood (TAB-GREML). TAGC-UDR analyses were carried out for UK Biobank participants of European (n = 3500), East Asian (n = 972), South Asian (n = 4303), and African (n = 3877) ancestry. TAB-GREML analyses were carried out for participants of European (n = 10,000), South Asian (n = 4303), and African (n = 3877) ancestry. Results: TAGC-UDR analyses suggested the trans-ancestry genetic correlation of refractive error was in the range 0.7-1.0 for the European versus African, European versus East Asian, and European versus South Asian ancestry pairs. The TAB-GREML estimates were consistent with the TAGC-UDR findings. Precision of the estimates was limited, reflecting the modest sample sizes of the non-European samples. Conclusions: These results support and extend previous work suggesting that genetic susceptibility to refractive error is largely shared across Europeans, Africans, and South Asians. This suggests geographical differences in myopia prevalence are mostly driven by lifestyle factors or rare genetic variants not considered in the current work.

Indexed as

Asian PeopleGenetic Predisposition to DiseaseMyopiaRefractive ErrorsWhite PeopleAdultBlack PeopleFemaleHumansMaleMiddle AgedPolymorphism, Single NucleotidePrevalenceUnited Kingdom

Identifiers

PMID40856652
PMCPMC12395803

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.