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Effects of Atropine Treatment on Choroidal Thickness in Myopic Children
Luyao Ye1,2, Ya Shi1,2, Yao Yin1
1Shanghai Eye Disease Prevention and Treatment Center, Shanghai Eye Hospital, Shanghai, China.
Insights
One percent atropine increased choroidal thickness (ChT) in children, while 0.01% atropine decreased it. A short-term ChT increase with 1% atropine was linked to less eye elongation.
Area of Science:
- Ophthalmology
- Pediatric Ophthalmology
- Myopia Control
Background:
- Myopia is a growing public health concern in children.
- Effective myopia control strategies are crucial to prevent vision impairment.
- Choroidal thickness (ChT) and axial elongation are key indicators of myopia progression.
Purpose of the Study:
- To evaluate changes in choroidal thickness (ChT) after 6 months of 1% or 0.01% atropine treatment.
- To identify factors associated with eye elongation in pediatric myopia.
Main Methods:
- 207 myopic children (6-12 years) were randomized into two groups.
- Group A received 1% atropine (loading dose then weekly); Group B received 0.01% atropine daily for 6 months.
- Choroidal thickness and internal axial length were measured at baseline and follow-up visits.
Main Results:
- 1% atropine significantly increased ChT after 1 week, with stabilization over time; no significant change in axial length.
- 0.01% atropine led to decreased ChT and significant eye elongation after 6 months.
- Less ChT increase at 1 week, younger age, and peripapillary atrophy were associated with greater axial elongation in the 1% atropine group.
Conclusions:
- 1% atropine increases ChT, while 0.01% atropine decreases it after 6 months.
- Short-term ChT increase with 1% atropine is negatively associated with long-term eye elongation.
- Younger age and peripapillary atrophy are risk factors for myopia progression.
Purpose:
To examine the changes in choroidal thickness (ChT) after 6 months of 1% or 0.01% atropine treatment and the independent factors associated with eye elongation.
Methods:
A total of 207 myopic children aged 6 to 12 years were recruited and randomly assigned to groups A and B in a ratio of 1:1. Participants in group A received 1% atropine once a day for 1 week, and then once a week for 23 weeks. Participants in group B received 0.01% atropine once a day for 6 months. ChT and internal axial length (IAL) were measured at baseline, 1 week, 3 months, and 6 months.
Results:
In group A, the ChT significantly increased after a 1-week loading dose of 1% atropine (26 ± 14 µm; P < 0.001) and the magnitude of increase stabilized throughout the following weekly treatment. The internal axial length did not significantly change at the 6-month visit (-0.01 ± 0.11 mm; P = 0.74). In contrast, a decreased ChT (-5 ± 17 µm; P < 0.001) and pronounced eye elongation (0.19 ± 0.12 mm; P < 0.001) were observed in group B after 6 months. Multivariable regression analysis showed that less increase in ChT at the 1-week visit (P = 0.03), younger age (P < 0.001), and presence of peripapillary atrophy (P = 0.001) were significantly associated with greater internal axial length increase over 6 months in group A.
Conclusions:
One percent atropine could increase the ChT, whereas 0.01% atropine caused a decrease in ChT after 6 months of treatment. For participants receiving 1% atropine, the short-term increase in ChT was negatively associated with long-term eye elongation. Younger age and the presence of peripapillary atrophy were found to be risk factors for greater eye elongation.
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