Choroidal thickness and peripapillary RNFL in relation to axial length and progression in myopic children.

IF 4.8 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in Bioengineering and Biotechnology Pub Date : 2026-04-22 eCollection Date: 2026-01-01 DOI:10.3389/fbioe.2026.1777062
Zixun Wang, Xiaoxue Hu, Xiaoling Zhang, Yuhang Wang, Zhiqing Li, Zheng Guo
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引用次数: 0

Abstract

Background: Axial length (AL) elongation is a key structural hallmark of myopia progression in children. Identifying early ocular structural characteristics associated with AL growth may help improve risk stratification, although robust predictive models remain limited.

Purpose: To explore cross-sectional associations between baseline ocular structural parameters and AL, and to preliminarily evaluate the predictive potential of these parameters for rapid AL progression in myopic children.

Methods: A total of 463 myopic children were retrospectively followed for 1 year. Baseline assessments included cycloplegic refraction, ocular biometry, and optical coherence tomography (OCT)-derived measurements of choroidal thickness (ChT) and retinal nerve fiber layer (RNFL). Rapid AL progression was defined as an AL increase of >0.2 mm over 1 year. Cross-sectional correlations between baseline AL, ChT, and RNFL parameters were analyzed. Least absolute shrinkage and selection operator (Lasso) regression with 10-fold cross-validation was used for feature selection, followed by the development and validation of a logistic regression model. Model performance was assessed using the area under the receiver operating characteristic curve (AUC), calibration analysis, and decision curve analysis (DCA).

Results: At baseline, AL showed significant cross-sectional associations with ChT and multiple RNFL parameters, with the strongest correlations observed for ChT and nasal-inferior RNFL thickness (RNFL[NI]). Lasso regression retained age, baseline AL, ChT, and RNFL[NI] as candidate predictors of rapid AL progression. In the validation set, the final model demonstrated modest discriminative performance (AUC = 0.703, 95% CI: 0.598-0.801) with acceptable calibration. Decision curve analysis indicated limited but consistent net clinical benefit across a range of threshold probabilities.

Conclusion: This study provides exploratory evidence that posterior segment structural parameters are associated with AL and may be useful for predicting subsequent AL progression in myopic children. Although the model's predictive performance was modest, the findings support the hypothesis that OCT-derived biomarkers could contribute to future risk-stratification strategies, warranting further validation and refinement.

近视儿童脉络膜厚度和乳头周围RNFL与眼轴长度和进展的关系。
背景:轴长(AL)伸长是儿童近视进展的关键结构标志。识别与AL生长相关的早期眼部结构特征可能有助于改善风险分层,尽管可靠的预测模型仍然有限。目的:探讨基线眼结构参数与AL的横断面相关性,并初步评价这些参数对近视儿童AL快速进展的预测潜力。方法:对463例近视儿童进行1年的回顾性随访。基线评估包括睫状体屈光、眼部生物测量和光学相干断层扫描(OCT)衍生的脉络膜厚度(ChT)和视网膜神经纤维层(RNFL)测量。AL快速进展被定义为1年内AL增加>.2 mm。分析基线AL、ChT和RNFL参数的横断面相关性。最小绝对收缩和选择算子(Lasso)回归与10倍交叉验证用于特征选择,其次是逻辑回归模型的开发和验证。采用受试者工作特征曲线下面积(AUC)、校准分析和决策曲线分析(DCA)对模型性能进行评估。结果:基线时,AL与ChT和多个RNFL参数具有显著的横断面相关性,其中ChT与鼻下RNFL厚度(RNFL[NI])的相关性最强。Lasso回归保留了年龄、基线AL、ChT和RNFL[NI]作为AL快速进展的候选预测因子。在验证集中,最终模型在可接受的校准下表现出适度的判别性能(AUC = 0.703, 95% CI: 0.598-0.801)。决策曲线分析表明,在阈值概率范围内,净临床获益有限但一致。结论:本研究为后段结构参数与AL相关提供了探索性证据,并可用于预测近视儿童AL的后续进展。尽管该模型的预测性能不高,但研究结果支持oct衍生生物标志物可能有助于未来风险分层策略的假设,需要进一步验证和完善。
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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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