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证据表明,正视化对近视的遗传和环境风险因素都有缓冲作用。

Evidence That Emmetropization Buffers Against Both Genetic and Environmental Risk Factors for Myopia.

机构信息

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出版信息

Invest Ophthalmol Vis Sci. 2020 Feb 7;61(2):41. doi: 10.1167/iovs.61.2.41.

Abstract

PURPOSE

To test the hypothesis that emmetropization buffers against genetic and environmental risk factors for myopia by investigating whether risk factor effect sizes vary depending on children's position in the refractive error distribution.

METHODS

Refractive error was assessed in participants from two birth cohorts: Avon Longitudinal Study of Parents and Children (ALSPAC) (noncycloplegic autorefraction) and Generation R (cycloplegic autorefraction). A genetic risk score for myopia was calculated from genotypes at 146 loci. Time spent reading, time outdoors, and parental myopia were ascertained from parent-completed questionnaires. Risk factors were coded as binary variables (0 = low, 1 = high risk). Associations between refractive error and each risk factor were estimated using either ordinary least squares (OLS) regression or quantile regression.

RESULTS

Quantile regression: effects associated with all risk factors (genetic risk, parental myopia, high time spent reading, low time outdoors) were larger for children in the extremes of the refractive error distribution than for emmetropes and low ametropes in the center of the distribution. For example, the effect associated with having a myopic parent for children in quantile 0.05 vs. 0.50 was as follows: ALSPAC: age 15, -1.19 D (95% CI -1.75 to -0.63) vs. -0.13 D (-0.19 to -0.06), P = 0.001; Generation R: age 9, -1.31 D (-1.80 to -0.82) vs. -0.19 D (-0.26 to -0.11), P < 0.001. Effect sizes for OLS regression were intermediate to those for quantiles 0.05 and 0.50.

CONCLUSIONS

Risk factors for myopia were associated with much larger effects in children in the extremes of the refractive error distribution, providing indirect evidence that emmetropization buffers against both genetic and environmental risk factors.

摘要

目的

通过研究风险因素效应大小是否取决于儿童的屈光不正分布位置,来检验正视化是否可以缓冲近视的遗传和环境风险因素这一假说。

方法

在两个出生队列中评估参与者的屈光不正:阿冯纵向父母与子女研究(ALSPAC)(非睫状肌麻痹自动折射)和世代研究(cycloplegic autorefraction)。近视的遗传风险评分是根据 146 个基因座的基因型计算得出的。阅读时间、户外活动时间和父母近视情况均由家长填写问卷获得。风险因素编码为二分类变量(0=低风险,1=高风险)。使用普通最小二乘法(OLS)回归或分位数回归来估计屈光不正与每个风险因素之间的关联。

结果

分位数回归:与所有风险因素(遗传风险、父母近视、阅读时间长、户外活动时间少)相关的效应在屈光不正分布的极端值处的儿童中比在分布中心的正视者和低度远视者中更大。例如,对于处于第 0.05 分位数和第 0.50 分位数的儿童,与近视父母相关的效应如下:在 ALSPAC 中,年龄 15 岁时,-1.19 D(95%CI -1.75 至 -0.63)与-0.13 D(-0.19 至 -0.06),P=0.001;在 Generation R 中,年龄 9 岁时,-1.31 D(-1.80 至 -0.82)与-0.19 D(-0.26 至 -0.11),P<0.001。OLS 回归的效应大小介于第 0.05 分位数和第 0.50 分位数之间。

结论

近视的风险因素与屈光不正分布极端值处的儿童的效应关系更大,这为正视化可以缓冲遗传和环境风险因素提供了间接证据。

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