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5 至 12 岁儿童 30 个月内近视进展和眼轴伸长相关的基线因素。

Baseline factors associated with myopia progression and axial elongation over 30 months in children 5 to 12 years of age.

机构信息

Department of Ophthalmology, Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.

Jaeb Center for Health Research, Tampa, Florida.

出版信息

Optom Vis Sci. 2024 Oct 1;101(10):619-626. doi: 10.1097/OPX.0000000000002187.

Abstract

PURPOSE

This study aimed to identify baseline factors associated with greater myopia progression and axial elongation in children with myopia.

METHODS

This study performed a post hoc analysis of data from a 30-month randomized trial of atropine 0.01% versus placebo in children 5 to <13 years old with baseline spherical equivalent refractive error (SER) of -1.00 to -6.00 D, astigmatism of ≤1.50 D, and anisometropia of <1.00 D SER. Data from atropine 0.01% and placebo groups were pooled given outcomes were similar. Baseline factors of age, SER, axial length, race, sex, parental myopia, and iris color were evaluated for association with changes in SER and with changes in axial length at 30 months (24 months on treatment and then 6 months off) using backward model selection.

RESULTS

Among 187 randomized participants, 175 (94%) completed 30 months of follow-up. The mean change in SER was greater among younger children (-0.19 D per 1 year younger; 95% confidence interval [CI], -0.25 to -0.14 D; p<0.001) and children with higher myopia (-0.14 D per 1 D more myopia at baseline; 95% CI, -0.23 to -0.05 D; p=0.002). The mean change in axial length was also greater among younger children (0.13 mm per 1 year younger; 95% CI, 0.10 to 0.15 mm; p<0.001) and children with higher baseline myopia (0.04 mm per 1 D more myopia; 95% CI, 0.002 to 0.08; p=0.04).

CONCLUSIONS

Younger children with higher myopia had greater myopic progression and axial elongation over 30 months than older children with lower myopia. Developing effective treatments to slow the faster myopic progression in younger children should be a target of further research.

摘要

目的

本研究旨在确定与近视儿童近视进展和眼轴伸长相关的基线因素。

方法

本研究对一项为期 30 个月的阿托品 0.01%与安慰剂治疗 5 至<13 岁儿童近视的随机试验进行了事后分析。纳入儿童的基线球镜等效屈光度(SER)为-1.00 至-6.00 D,散光≤1.50 D,双眼屈光参差<1.00 D SER。由于阿托品 0.01%和安慰剂组的结果相似,因此将两组的数据合并。使用向后模型选择评估年龄、SER、眼轴长度、种族、性别、父母近视和虹膜颜色等基线因素与 30 个月(治疗 24 个月,停药 6 个月)时 SER 变化和眼轴长度变化的相关性。

结果

在 187 名随机参与者中,175 名(94%)完成了 30 个月的随访。年龄较小的儿童 SER 变化更大(每年轻 1 岁,SER 变化-0.19 D;95%置信区间[CI],-0.25 至-0.14 D;p<0.001),基线近视程度较高的儿童 SER 变化也更大(每增加 1 D 基线近视,SER 变化-0.14 D;95%CI,-0.23 至-0.05 D;p=0.002)。年龄较小的儿童眼轴长度变化也更大(每年轻 1 岁,眼轴长度变化 0.13 mm;95%CI,0.10 至 0.15 mm;p<0.001),基线近视程度较高的儿童眼轴长度变化也更大(每增加 1 D 基线近视,眼轴长度变化 0.04 mm;95%CI,0.002 至 0.08;p=0.04)。

结论

与年龄较大、基线近视程度较低的儿童相比,近视程度较高的年龄较小的儿童在 30 个月内近视进展和眼轴伸长更快。进一步的研究应针对开发有效治疗方法以减缓年龄较小儿童的近视进展速度。

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