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口服咖啡因代谢物 7-甲基黄嘌呤与丹麦儿童近视进展减缓有关。

Oral administration of caffeine metabolite 7-methylxanthine is associated with slowed myopia progression in Danish children.

机构信息

Trier Research Laboratories, Ojenlage Klaus Trier ApS, Hellerup, Denmark

Shenzhen Eye Hospital, Jinan University, Guangzhou, Guangdong, China.

出版信息

Br J Ophthalmol. 2023 Oct;107(10):1538-1544. doi: 10.1136/bjo-2021-320920. Epub 2022 Aug 22.

Abstract

PURPOSE

Myopia is associated with an increased risk of permanent vision loss. The caffeine metabolite 7-methylxanthine (7-MX), licensed in Denmark since 2009 as a treatment to reduce the rate of childhood myopia progression, is the only orally administered therapy available. The purpose of the current study was to assess the rate of myopia progression in children taking 7-MX.

METHODS

Longitudinal cycloplegic refraction and axial length data for 711 myopic children from Denmark treated with varying doses of oral 7-MX (0-1200 mg per day) were analysed using linear mixed models.

RESULTS

The median age at baseline was 11.1 years (range 7.0 -15.0 years). Children were followed for an average of 3.6 years (range 0.9-9.1 years) and the average myopia progression was 1.34 dioptres (D) (range -6.50 to +0.75 D). Treatment with 7-MX was associated with a reduced rate of myopia progression (p<0.001) and axial elongation (p<0.002). Modelling suggested that, on average, an 11-year-old child taking 1000 mg 7-MX daily would develop -1.43 D of myopia over the next 6 years, compared with -2.27 D if untreated. Axial length in this child would increase by 0.84 mm over 6 years when taking a daily dose of 1000 mg of 7-MX, compared with 1.01 mm if untreated. No adverse effects of 7-MX therapy were reported.

CONCLUSIONS

Oral intake of 7-MX was associated with reduced myopia progression and reduced axial elongation in this sample of myopic children from Denmark. Randomised controlled trials are needed to determine whether the association is causal.

摘要

目的

近视与永久性视力丧失风险增加有关。自 2009 年以来,咖啡因代谢物 7-甲基黄嘌呤(7-MX)在丹麦获得许可,作为一种降低儿童近视进展速度的治疗方法,是唯一可口服的治疗方法。本研究的目的是评估服用 7-MX 的儿童近视进展的速度。

方法

使用线性混合模型分析来自丹麦的 711 名近视儿童的纵向睫状肌麻痹折射和眼轴长度数据,这些儿童接受了不同剂量的口服 7-MX(每天 0-1200 毫克)治疗。

结果

基线时的中位年龄为 11.1 岁(范围为 7.0-15.0 岁)。儿童平均随访 3.6 年(范围 0.9-9.1 年),平均近视进展为 1.34 屈光度(D)(范围为-6.50 至+0.75 D)。7-MX 治疗与近视进展速度降低(p<0.001)和眼轴伸长(p<0.002)相关。建模表明,平均而言,11 岁每天服用 1000 毫克 7-MX 的儿童在接下来的 6 年内会发展出-1.43 D 的近视,而未接受治疗的儿童则会发展出-2.27 D 的近视。在每天服用 1000 毫克 7-MX 的情况下,该儿童的眼轴在 6 年内会增加 0.84 毫米,而未接受治疗的情况下会增加 1.01 毫米。没有报告 7-MX 治疗的不良反应。

结论

在本丹麦近视儿童样本中,口服 7-MX 与近视进展速度降低和眼轴伸长减少相关。需要进行随机对照试验来确定这种关联是否具有因果关系。

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