Can we really distinguish 'responders' from 'non-responders' to myopia control interventions?

IF 2.8 3区 医学 Q1 OPHTHALMOLOGY
Noel A Brennan, Alex D Nixon, Xu Cheng, Mark A Bullimore
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引用次数: 0

Abstract

Purpose: It is common to hear talk of 'responders' and 'non-responders' with respect to myopia control interventions. We consider the reality of distinguishing these sub-groups using data from the first year of the Low-concentration Atropine for Myopia Progression (LAMP) study.

Methods: The first year of the LAMP study was a robustly designed, placebo-controlled trial of three different low concentrations of atropine using a large sample size (N > 100 randomised to each group). The authors subsequently published mean axial elongation and myopia progression rates by age group. We used these data to calculate efficacy in terms of both absolute reduction in myopic progression and absolute reduction in axial elongation for each of the different atropine concentrations at each age group. We then compared these efficacy data to the overall progression for each of the two progression metrics.

Results: Plotting efficacy as a function of overall myopia progression and axial elongation for each of the different atropine concentrations demonstrates the invariant nature of efficacy, in terms of clinically meaningful reduction in progression, despite a substantial range of underlying overall progression. That is, faster progressors-the so-called non-responders-achieved similar reduction in axial elongation and myopia progression as the slower progressors-the so-called responders-within the various atropine treatment groups.

Conclusion: The use of the terms, responders and non-responders, during myopia progression interventions is not supported by evidence. Those designated as such may simply be slower or faster progressors, who, on average achieve the same benefit from treatment.

我们真的能区分近视控制干预措施的 "响应者 "和 "非响应者 "吗?
目的:在近视控制干预方面,"有反应者 "和 "无反应者 "的说法屡见不鲜。我们利用低浓度阿托品治疗近视进展(LAMP)研究第一年的数据,研究了区分这些亚组的实际情况:低浓度阿托品治疗近视进展(LAMP)研究的第一年是一项设计严谨的安慰剂对照试验,试验中使用了三种不同浓度的低浓度阿托品,样本量较大(每组随机样本数大于 100)。作者随后公布了各年龄组的平均轴伸长率和近视发展率。我们利用这些数据计算了各年龄组不同浓度阿托品的疗效,即近视度数加深的绝对减少量和轴伸长的绝对减少量。然后,我们将这些疗效数据与这两种进展指标的总体进展情况进行比较:结果:将每种不同浓度阿托品的疗效与总体近视度数和轴伸长率的函数关系绘制成图,表明尽管总体近视度数在很大程度上存在差异,但从临床意义上降低近视度数的角度来看,疗效是不变的。也就是说,在不同的阿托品治疗组中,近视进展较快者(即所谓的非反应者)与近视进展较慢者(即所谓的反应者)在轴伸长和近视进展方面的减幅相似:结论:在近视进展干预过程中使用有反应者和无反应者这两个术语并无证据支持。那些被称为反应者或无反应者的人可能只是近视进展较慢或较快的人,他们平均都能从治疗中获得相同的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.10
自引率
13.80%
发文量
135
审稿时长
6-12 weeks
期刊介绍: Ophthalmic & Physiological Optics, first published in 1925, is a leading international interdisciplinary journal that addresses basic and applied questions pertinent to contemporary research in vision science and optometry. OPO publishes original research papers, technical notes, reviews and letters and will interest researchers, educators and clinicians concerned with the development, use and restoration of vision.
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