Wu Jing, Zhang Cong, Wang Jingying
Ophthalmology Department, The University of Hong Kong-Shenzhen Hospital, ShenZhen, Guangdong, China.
Ophthalmology Department, The Shapingba Hospital, Chongqing University, Peoples Hospital of Shapingba District, Chonqing, China.
BMC Ophthalmol. 2025 Aug 28;25(1):490. doi: 10.1186/s12886-025-04278-3.
Primary refractive error screening parameters are commonly employed in clinical and community settings before cycloplegic assessment of myopia, however, their utility in identifying premyopia and myopia intervention candidates remains underexplored. This study aimed to develop a nomogram based on these routinely measured parameters to support clinical decision-making for premyopia and myopia prevention.
Pediatric patients (aged 4-17 years) from two medical centers in China were enrolled in this retrospective cohort study. A predictive model for the candidates of premyopia and myopia intervention was developed using logistic regression with multiple imputations. The model included the following primary screening parameters: age, gender, uncorrected visual acuity (UCVA), average corneal curvature (ACC), non-cycloplegic spherical equivalent refraction (NCSER), axial length (AL), and the axial length to average corneal radius of curvature (AL/ACRC) ratio. The efficacy of the model was assessed using the area under the receiver operating characteristic (ROC) curve, calibration curves, and decision curve analysis (DCA). R was employed to conduct all statistical analyses.
A total of 1006 participants (507 females, 499 boys) were enrolled, with 87.4% demonstrating cycloplegic spherical equivalent refraction (CSER) ≤ + 0.75D. In multivariate logistic regression, UCVA, NCSER, AL, and AL/ACRC were identified as independent predictors. These predictors were incorporated into a nomogram to predict the candidates for premyopia and myopia intervention. The nomogram exhibited exceptional discrimination in the derivation set (AUC = 0.971, 95% CI: 0.957-0.984), whereas in the external validation set, the AUC was 0.921 (95% CI: 0.866-0.976) when a cutoff of 0.851 in derivation set was employed. Calibration was verified through the calibration curve and Hosmer-Lemeshow tests (P = 0.99 and P = 0.96, respectively), and the decision curve analysis demonstrated robust clinical utility for threshold probabilities of 0.10-1.00 in the derivation set and 0.20-1.00 in the external validation set.
The nomogram derived from the parameters of primary refractive error screening has the potential to preliminarily predict premyopia and myopia intervention candidates, thereby facilitating clinical decision-making in the context of premyopia and myopia prevention.
在对近视进行睫状肌麻痹验光评估之前,临床和社区环境中通常会使用原发性屈光不正筛查参数,然而,它们在识别近视前期和近视干预候选者方面的效用仍未得到充分探索。本研究旨在基于这些常规测量参数开发一种列线图,以支持近视前期和近视预防的临床决策。
本回顾性队列研究纳入了来自中国两个医疗中心的儿科患者(4至17岁)。使用多重插补的逻辑回归建立了近视前期和近视干预候选者的预测模型。该模型包括以下主要筛查参数:年龄、性别、未矫正视力(UCVA)、平均角膜曲率(ACC)、非睫状肌麻痹等效球镜度(NCSER)、眼轴长度(AL)以及眼轴长度与平均角膜曲率半径之比(AL/ACRC)。使用受试者操作特征(ROC)曲线下面积、校准曲线和决策曲线分析(DCA)评估模型的有效性。使用R进行所有统计分析。
共纳入1006名参与者(507名女性,499名男性),其中87.4%的人睫状肌麻痹等效球镜度(CSER)≤ +0.75D。在多变量逻辑回归中,UCVA、NCSER、AL和AL/ACRC被确定为独立预测因素。这些预测因素被纳入列线图,以预测近视前期和近视干预候选者。该列线图在推导集中表现出出色的辨别力(AUC = 0.971,95% CI:0.957 - 0.984),而在外部验证集中,当采用推导集中0.851的截断值时,AUC为0.921(95% CI:0.866 - 0.976)。通过校准曲线和Hosmer-Lemeshow检验验证了校准(P分别为0.99和0.96),决策曲线分析表明,在推导集中阈值概率为0.10 - 1.00,在外部验证集中为0.20 - 1.00时,具有强大的临床实用性。
从原发性屈光不正筛查参数得出的列线图有可能初步预测近视前期和近视干预候选者,从而有助于在近视前期和近视预防背景下的临床决策。