Advances in the genetics of refractive errors: Contributions from the <scp>CREAM</scp> consortium

The Consortium for Refractive Error and Myopia (CREAM) was established in 2011, bringing together an international team of researchers studying more than 30 cohorts. Since its establishment, CREAM has played a pivotal role in research investigating the genetics of myopia and other refractive errors, serving as a key driver of progress in the field. The aim of this review is to highlight the latest advances and insights from CREAM, with a focus on research carried out in the past 5 years. We performed a literature review of journal articles authored by the CREAM consortium since the year 2020, when the last review of CREAM consortium findings was published. Key discoveries from recent CREAM studies were the identification of SIX6, CRX, PER3, PDCD6IP, MAPT, CHST6, GRHL2, USH2A, P4HTM, COL4A4 and ATM as high-confidence candidate genes associated with myopia development. Variants in enhancers and lncRNA regions were shown to have potential regulatory effects on refractive error; the DDIT4 gene was highlighted as a potential hotspot for future analyses. A polygenic risk score for predicting high myopia with an area under the curve (AUC) accuracy of 0.78 was made openly available; prediction accuracy was close to that required for clinical use. A shared genetic architecture for refractive error and axial length was confirmed. Novel findings were the identification of rare, large-effect gene variants through targeted and whole exome sequencing and the development of a polygenic risk score for predicting children at risk of developing high myopia. Large-scale multi-ancestry genome-wide association studies of the myopia endophenotypes axial length and corneal curvature doubled the number of common genetic variants known to be associated with these traits. Nevertheless, much remains to be done to fulfil the promise of myopia genetics research for improving the detection of children at above-average risk of high myopia, and the prevention and treatment of myopia.

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Journal
Acta Ophthalmologica
Published
2025-11-13
DOI
https://doi.org/10.1111/aos.70025
Primary Topic
Ophthalmology and Visual Impairment Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Advances in the genetics of refractive errors: Contributions from the CREAM consortium

S. Li, Gareth Lingham, Virginie J. M. Verhoeven, Caroline C. W. Klaver et al.
Acta Ophthalmologica
Ophthalmology and Visual Impairment Studies
article

Advances in the genetics of refractive errors: Contributions from the CREAM consortium

S. Li, Gareth Lingham, Virginie J. M. Verhoeven, Caroline C. W. Klaver, Jeremy A. Guggenheim, Samantha Sze‐Yee Lee, David A. Mackey, Xi He, Louise Terry, Seang‐Mei Saw, Chi Pui Pang
article en

Abstract

The Consortium for Refractive Error and Myopia (CREAM) was established in 2011, bringing together an international team of researchers studying more than 30 cohorts. Since its establishment, CREAM has played a pivotal role in research investigating the genetics of myopia and other refractive errors, serving as a key driver of progress in the field. The aim of this review is to highlight the latest advances and insights from CREAM, with a focus on research carried out in the past 5 years. We performed a literature review of journal articles authored by the CREAM consortium since the year 2020, when the last review of CREAM consortium findings was published. Key discoveries from recent CREAM studies were the identification of SIX6, CRX, PER3, PDCD6IP, MAPT, CHST6, GRHL2, USH2A, P4HTM, COL4A4 and ATM as high-confidence candidate genes associated with myopia development. Variants in enhancers and lncRNA regions were shown to have potential regulatory effects on refractive error; the DDIT4 gene was highlighted as a potential hotspot for future analyses. A polygenic risk score for predicting high myopia with an area under the curve (AUC) accuracy of 0.78 was made openly available; prediction accuracy was close to that required for clinical use. A shared genetic architecture for refractive error and axial length was confirmed. Novel findings were the identification of rare, large-effect gene variants through targeted and whole exome sequencing and the development of a polygenic risk score for predicting children at risk of developing high myopia. Large-scale multi-ancestry genome-wide association studies of the myopia endophenotypes axial length and corneal curvature doubled the number of common genetic variants known to be associated with these traits. Nevertheless, much remains to be done to fulfil the promise of myopia genetics research for improving the detection of children at above-average risk of high myopia, and the prevention and treatment of myopia.

Acta Ophthalmologica
Lions Eye Institute (AU), Radboud University Nijmegen (NL), National University of Singapore (SG), Chinese University of Hong Kong (HK), The University of Western Australia (AU), University of Basel (CH), Singapore National Eye Center (SG), Erasmus MC (NL), Radboud University Medical Center (NL), Singapore Eye Research Institute (SG), Duke-NUS Medical School (SG), National University Health System (SG), Institute of Molecular and Clinical Ophthalmology Basel (CH), Cardiff University (GB), Erasmus University Rotterdam (NL)
UK Research and Innovation, HORIZON EUROPE Framework Programme, HORIZON EUROPE Health
Openalex Percentile: Top 55%
Ophthalmology and Visual Impairment Studies
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