Harrington Síofra, Moore Michael, Loughman James, Flitcroft Ian, O'Dwyer Veronica
School of Physics, Clinical & Optometric Sciences, Technological University Dublin, Dublin, Ireland.
Centre for Eye Research Ireland, Sustainability & Health Research Centre, Technological University Dublin, City Campus, Dublin, Ireland.
Ophthalmic Physiol Opt. 2025 Jul;45(5):1080-1089. doi: 10.1111/opo.13525. Epub 2025 May 14.
Early detection of myopia is essential to delay its onset and progression. Pre-myopia, defined by an inadequate hyperopic reserve, increases myopia risk in childhood. However, effective screening methods remain limited. This study aimed to develop practical non-cycloplegic screening methods for pre-myopia and myopia in 6- to 7-year-olds to support earlier interventions.
This cross-sectional study of 621 Irish schoolchildren (mean age: 7.12 ± 0.45 years; 51.8% boys) assessed uncorrected distance visual acuity (UDVA). Cycloplegic spherical equivalent refraction (SER) classified refractive status (myopia: SER ≤ -0.50D; pre-myopia: SER > -0.50 ≤ 0.75D). Pre- and post-cycloplegic SER were measured using the Welch Allyn Spot Vision Screener and Dong-Yang Rekto-ORK 11, respectively. Axial length (AL) and corneal radius (CR) were measured with the Zeiss IOLMaster and parental myopia history via questionnaire. Logistic regression and ROC curves evaluated non-cycloplegic screening methods.
Pre-myopia prevalence was 24.3% (95% confidence intervals (CI): 29.3-36.2), and myopia prevalence was 3.3% (CI: 2.5-5.5). UDVA screening had an area under the curve (AUC) (CI) = 0.72 (0.59-0.86) and 0.42 (0.36-0.47) for detecting myopia and pre-myopia, respectively. For pre-myopia discrimination, non-cycloplegic SER, AL, AL/CR and parental myopia had AUCs of 0.67 (0.62-0.72), 0.67 (0.62-0.72), 0.69 (0.64-0.74) and 0.59 (0.53-0.64), respectively. The best method combined non-cycloplegic SER and AL/CR (AUC = 0.72 (0.67-0.76)). Including UDVA or parental myopia did not improve results. For myopia detection, AUCs were non-cycloplegic SER:0.84 (0.72-0.97), AL:0.88 (0.82-0.95), AL/CR:0.84 (0.75-0.94) and parental myopia:0.62 (0.48-0.75). The best method combined AL and non-cycloplegic SER 0.94 (0.90-0.99). Adding parental myopia did not improve the AUC = 0.93 (0.87-0.99) but adding UDVA achieved an AUC = 0.95 (0.90-0.99).
While UDVA alone provided acceptable discrimination for myopia, it was insufficient for screening pre-myopia. Non-cycloplegic SER alone had relatively poor discrimination for pre-myopia, but its performance improved when combined with the AL/CR ratio. The best results for myopia discrimination were achieved by combining non-cycloplegic SER, axial length and UDVA measures.
早期发现近视对于延缓其发病和进展至关重要。近视前期,即远视储备不足,会增加儿童近视风险。然而,有效的筛查方法仍然有限。本研究旨在开发针对6至7岁儿童近视前期和近视的实用非散瞳筛查方法,以支持更早的干预措施。
这项对621名爱尔兰学童(平均年龄:7.12±0.45岁;51.8%为男孩)的横断面研究评估了未矫正的远视力(UDVA)。散瞳等效球镜度(SER)用于分类屈光状态(近视:SER≤-0.50D;近视前期:SER>-0.50≤0.75D)。散瞳前后的SER分别使用Welch Allyn Spot Vision Screener和Dong-Yang Rekto-ORK 11进行测量。眼轴长度(AL)和角膜半径(CR)分别使用蔡司IOLMaster进行测量,并通过问卷询问父母的近视病史。逻辑回归和ROC曲线评估非散瞳筛查方法。
近视前期患病率为24.3%(95%置信区间(CI):29.3 - 36.2),近视患病率为3.3%(CI:2.5 - 5.5)。UDVA筛查检测近视和近视前期的曲线下面积(AUC)(CI)分别为0.72(0.59 - 0.86)和0.42(0.36 - 0.47)。对于近视前期的鉴别,非散瞳SER、AL、AL/CR和父母近视的AUC分别为0.67(0.62 - 0.72)、0.67(0.62 - 0.72)、0.69(0.64 - 0.74)和0.59(0.53 - 0.64)。最佳方法是将非散瞳SER和AL/CR相结合(AUC = 0.72(0.67 - 0.76))。纳入UDVA或父母近视并未改善结果。对于近视检测,非散瞳SER的AUC为0.84(0.72 - 0.97),AL为0.88(0.82 - 0.95),AL/CR为0.84(0.75 - 0.94),父母近视为0.62(0.48 - 0.75)。最佳方法是将AL和非散瞳SER相结合,AUC为0.94(0.90 - 0.99)。添加父母近视并未改善AUC = 0.93(0.87 - 0.99),但添加UDVA后AUC达到0.95(0.90 - 0.99)。
虽然单独的UDVA对近视有可接受的鉴别能力,但对于筛查近视前期是不够的。单独的非散瞳SER对近视前期的鉴别能力相对较差,但与AL/CR比值相结合时其性能有所改善。通过结合非散瞳SER、眼轴长度和UDVA测量,可获得最佳的近视鉴别结果。