Evidence map›Paper›PMID 42045455›Full record

SynthesisEye (London, England)2026

Low-concentration atropine for management of myopia progression: does iris colour matter?

Gareth Lingham, James Loughman, Samantha Sy Lee, Michael X Repka, Eoin Kerin, Alicia Gómez Sánchez, Emmanuel Kobia-Acquah, Ernest Kyei Nkansah, Ian Flitcroft, David A Mackey

Abstract readMeta-Analysis
In one paragraph

Synthesis in Eye (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. 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

10 authors.

Gareth LinghamCentre for Ophthalmology and Visual Science (incorporating Lions Eye Institute), University of Western Australia, Perth, WA, Australia. gareth.lingham@lei.org.au.ORCID http://orcid.org/0000-0002-8957-0733
James LoughmanCentre for Eye Research Ireland, Sustainability and Health Research Hub, Technological University Dublin, Dublin, Ireland.
Samantha Sy LeeCentre for Ophthalmology and Visual Science (incorporating Lions Eye Institute), University of Western Australia, Perth, WA, Australia.ORCID http://orcid.org/0000-0001-6635-1098
Michael X RepkaWilmer Eye Institute, Baltimore, MD, USA.
Eoin KerinCentre for Eye Research Ireland, Sustainability and Health Research Hub, Technological University Dublin, Dublin, Ireland.ORCID http://orcid.org/0009-0004-8474-8856
Alicia Gómez SánchezCentre for Eye Research Ireland, Sustainability and Health Research Hub, Technological University Dublin, Dublin, Ireland.
Emmanuel Kobia-AcquahTransitions Optical Limited, Tuam, Ireland.
Ernest Kyei NkansahCentre for Eye Research Ireland, Sustainability and Health Research Hub, Technological University Dublin, Dublin, Ireland.
Ian Flitcroft *Centre for Eye Research Ireland, Sustainability and Health Research Hub, Technological University Dublin, Dublin, Ireland.ORCID http://orcid.org/0000-0002-7004-6026
David A Mackey *Centre for Ophthalmology and Visual Science (incorporating Lions Eye Institute), University of Western Australia, Perth, WA, Australia.

Funding

Health Research Board (HRB) MRCG 2016-03
6 · The paper itself

Abstract

backgroundTo investigate interactions between iris colour and low-concentration atropine on outcomes relevant to clinical myopia management

methodsA post-hoc, exploratory meta-analysis of three randomised clinical trials investigating atropine 0.01% or 0.05% eye drops vs placebo: the Western Australian Atropine Treatment of Myopia study, the Myopia Treatment Study and the Myopia Outcome Study of Atropine in Children. Iris colour was graded as brown or not brown (including blue/green/hazel). Change in accommodative amplitude, pupil diameter, spherical equivalent refraction (SER) and axial length were assessed using linear mixed models.

resultsIn participants (baseline ages 5-16 years) using atropine 0.01% (n = 396), pupil diameter change did not differ by iris colour (p ≥ 0.15), while accommodative amplitude decreased more in not brown vs brown iris colour groups at month 12 (adjusted difference = -1.07D, 95% CI: -2.02, -0.12, p = 0.03), but not at month 24 (p = 0.76). Change in pupil and accommodative outcomes with 0.05% atropine (n = 66) did not differ by iris colour (p ≥ 0.10). Among not brown iris colour participants, myopia progression was lower in the atropine 0.01% vs placebo group at 24 months (SER: +0.17D, 95% CI: 0.07, 0.26, p < 0.001; axial length: -0.09 mm, 95% CI: -0.12, -0.05, p < 0.001), but not among brown iris colour participants (SER: -0.08D, 95% CI: -0.20, 0.05; axial length: +0.03 mm, 95% CI: -0.02, 0.07).

conclusionChange in pupil diameter and accommodative amplitude with low-concentration atropine largely did not differ between iris colour groups. Among participants using 0.01% atropine eye drops, there was less 24-month myopia progression compared to placebo in participants with blue/green irides, but not with brown irides.

Indexed as

AtropineEye ColorMydriaticsMyopiaAccommodation, OcularAdolescentAxial Length, EyeChildChild, PreschoolDisease ProgressionFemaleHumansIrisMaleOphthalmic SolutionsPupilAtropineMydriaticsOphthalmic Solutions

Identifiers

PMID42045455
PMCPMC13342569

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.