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Effect of Low-Dose Atropine on Choroidal Thickness in Children With Myopia Progression
Shrutakirty Parida1, Matuli Das2, Snehalata Dash3
1Pediatric Ophthalmology, Strabismus and Neuro-ophthalmology, Kalinga Institute of Medical Sciences, Bhubaneswar, IND.
Insights
Low-dose atropine (0.01%) significantly increased choroidal thickness in children with progressive myopia. This choroidal thickening correlated with slower myopia progression, indicating a potential therapeutic benefit.
Area of Science:
- Ophthalmology
- Pediatric Ophthalmology
- Myopia Control
Background:
- Progressive myopia is a growing concern in children.
- Choroidal thickness is a potential biomarker for myopia progression.
- Low-dose atropine is being investigated for myopia control.
Purpose of the Study:
- To evaluate the effect of 0.01% low-dose atropine on choroidal thickness in children with progressive myopia.
- To compare myopia progression rates between low-dose atropine and placebo groups.
- To assess changes in refractive error, axial length (AXL), and best-corrected visual acuity (BCVA).
Main Methods:
- A prospective, case-control interventional study.
- 87 children (5-16 years) with bilateral progressive myopia were randomized into two groups.
- Measurements included spherical equivalence, AXL, and choroidal thickness at baseline and 6 months; one group received low-dose atropine, the other placebo.
Main Results:
- Low-dose atropine significantly increased overall choroidal thickness at 3 and 6 months.
- The increase in choroidal thickness showed a significant correlation with slower myopia progression (spherical equivalence and AXL).
Conclusions:
- Low-dose atropine (0.01%) effectively induces choroidal thickening in children with progressive myopia.
- This choroidal thickening is associated with a reduced rate of myopia progression.
- Low-dose atropine demonstrates potential as a therapeutic intervention for myopia control.
Purpose:
The present study aims to evaluate the effect of low-dose atropine (0.01%) on choroidal thickness in children with progressive myopia. A secondary objective was to compare the rate of myopia progression between children treated with low-dose atropine (0.01%) and those receiving placebo eye drops (preservative-free carboxymethyl cellulose 0.5%) through changes in equivalent, axial length (AXL), and best-corrected visual acuity (BCVA).
Study Design:
A prospective case-control interventional study was conducted in the department of ophthalmology at a tertiary eye care center in eastern India.
Materials And Methods:
A total of 87 children aged 5-16 years with bilateral progressive myopia were recruited and randomly assigned into two groups. Spherical equivalence, AXL, and choroidal thickness (sub-foveal and at 1500 and 3000 microns nasal and temporal to the fovea) were documented at baseline,1 month,3 months, and 6 months.44 children in group A received treatment with once-daily dosing of atropine at bedtime, while 43 children in group B received a placebo eyedrop.
Results:
Children in group A showed a significant increase in overall choroidal thickness at 3 and 6 months (11+/-9.67) and (18+/-13.43) microns, respectively, which showed a significant correlation with the progression of myopia (in terms of spherical equivalence and AXL).
Conclusion:
Low-dose atropine induced a significant choroidal thickening effect, which was associated with slower progression of myopia in the treatment group.
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