Li Xuefei, Luo Shenglong, Lin Kuangching, Soha Hera, Shen Meixiao, Lu Fan, Wang Junjie
National Engineering Research Center of Ophthalmology and Optometry, Eye Hospital, Wenzhou Medical University, Wenzhou 325027, China.
National Clinical Research Center for Ocular Diseases, Eye Hospital, Wenzhou Medical University, Wenzhou 325027, China.
Bioengineering (Basel). 2025 Apr 13;12(4):412. doi: 10.3390/bioengineering12040412.
Myopia is a leading cause of visual impairment worldwide, and accumulating evidence suggests that biomechanics may be closely linked to its development. Understanding this relationship may help clarify the underlying mechanisms of myopia and guide treatment strategies. The aim of the study is to investigate the causal relationship between myopia and corneal biomechanics using the UK Biobank (UKB) database.
Data from 11,064 eyes in the UKB, including refraction results and Ocular Response Analyzer (ORA) measurements, were analyzed. Eyes were categorized by spherical equivalent (SE) into emmetropia, mild myopia, moderate myopia, and high myopia. One-way ANOVA assessed differences in corneal biomechanical parameters across the varying myopia groups, while Quantile Regression (QR) explored the relationship between these parameters and myopia severity across the different quantiles. A Mendelian randomization (MR) analysis was employed to explore the causal relationships.
Significant differences in corneal biomechanical parameters and intraocular pressure (IOP) were observed across the myopia levels ( < 0.001). High myopia was associated with lower corneal hysteresis (CH), a lower corneal resistance factor (CRF), and increased IOP. The QR analysis demonstrated that lower corneal biomechanics were associated with higher degrees of myopia, with the impact of corneal biomechanics becoming more pronounced as the myopia severity increased. The MR analysis indicated that low CH (OR = 0.9943, = 0.004) and CRF (OR = 0.9946, = 0.002) values were risk factors for myopia, while no causal effect was found when the myopia was treated as the exposure and corneal biomechanics as the outcome.
This study establishes a causal relationship where reduced corneal biomechanics contribute to myopia, while myopia itself does not directly affect biomechanics. Corneal biomechanics could serve as a biomarker for assessing high myopia risk. These findings offer new insights into high myopia's pathological mechanisms and targeted prevention.
近视是全球视力损害的主要原因,越来越多的证据表明生物力学可能与其发展密切相关。了解这种关系可能有助于阐明近视的潜在机制并指导治疗策略。本研究的目的是使用英国生物银行(UKB)数据库研究近视与角膜生物力学之间的因果关系。
分析了UKB中11064只眼睛的数据,包括屈光结果和眼反应分析仪(ORA)测量值。根据等效球镜度(SE)将眼睛分为正视、轻度近视、中度近视和高度近视。单向方差分析评估不同近视组角膜生物力学参数的差异,而分位数回归(QR)探索这些参数与不同分位数下近视严重程度之间的关系。采用孟德尔随机化(MR)分析来探索因果关系。
在不同近视水平下观察到角膜生物力学参数和眼压(IOP)存在显著差异(<0.001)。高度近视与较低的角膜滞后(CH)、较低的角膜阻力因子(CRF)和眼压升高有关。QR分析表明,较低的角膜生物力学与较高程度的近视有关,随着近视严重程度的增加,角膜生物力学的影响变得更加明显。MR分析表明,低CH(OR = 0.9943, = 0.004)和CRF(OR = 0.9946, = 0.002)值是近视的危险因素,而当将近视视为暴露因素,角膜生物力学视为结果时,未发现因果效应。
本研究建立了一种因果关系,即角膜生物力学降低导致近视,而近视本身并不直接影响生物力学。角膜生物力学可作为评估高度近视风险的生物标志物。这些发现为高度近视的病理机制和靶向预防提供了新的见解。