TY - JOUR
T1 - An automated optical coherence tomography to finite element analysis pipeline reveals key morphological determinants of optic nerve head biomechanics in glaucoma
AU - Li, Qi
AU - Zhan, Bohan
AU - Liu, Tingting
AU - Han, Yingxiang
AU - Xin, Sanfeng
AU - Chen, Zengsheng
AU - Tun, Tin Aung
AU - Wang, Xiaofei
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to The Royal College of Ophthalmologists 2025.
PY - 2026/2
Y1 - 2026/2
N2 - Background: Glaucoma, the leading cause of irreversible blindness, is closely linked to optic nerve head (ONH) damage, particularly within the lamina cribrosa (LC). Prior biomechanical studies have either relied on manual OCT‑based modelling, which is accurate but labour-intensive, or on idealised “standard” eye models, which allow high‑volume analysis but lack anatomical realism. To bridge this gap, we developed an automated pipeline that converts routine OCT into patient‑specific finite element (FE) models and quantifies biomechanical and morphological determinants. Methods: We analysed OCT volumes from 154 healthy and 170 glaucomatous eyes using automated segmentation of the retina, choroid, sclera, and lamina cribrosa, followed by patient-specific ONH reconstruction and finite-element simulation of LC strain under an intraocular pressure of 15 mmHg. We quantified eight morphological parameters. A Random Forest regression combined with SHAP analysis was used to determine morphological predictors of LC strain. Results: LC depth showed the strongest linear association with LC strain (r = −0.31). Other parameters with smaller associations included BMO radius (r = 0.17), pre-lamina volume (r = −0.14) and mean choroidal thickness (r = −0.12). After adjusting for age and gender, glaucomatous eyes exhibited significantly lower LC strain than healthy eyes (coefficient = 0.0018, p = 0.011), suggesting potential tissue remodelling. SHAP ranked pre-lamina depth, LC curvature, BMO radius, and LC depth as the most influential predictors despite modest explained variance. Conclusions: This study presents a scalable, image-based biomechanical framework enables high-throughput, patient-specific assessment and offers new opportunities to identify morphological biomarkers for glaucoma risk stratification and disease monitoring.
AB - Background: Glaucoma, the leading cause of irreversible blindness, is closely linked to optic nerve head (ONH) damage, particularly within the lamina cribrosa (LC). Prior biomechanical studies have either relied on manual OCT‑based modelling, which is accurate but labour-intensive, or on idealised “standard” eye models, which allow high‑volume analysis but lack anatomical realism. To bridge this gap, we developed an automated pipeline that converts routine OCT into patient‑specific finite element (FE) models and quantifies biomechanical and morphological determinants. Methods: We analysed OCT volumes from 154 healthy and 170 glaucomatous eyes using automated segmentation of the retina, choroid, sclera, and lamina cribrosa, followed by patient-specific ONH reconstruction and finite-element simulation of LC strain under an intraocular pressure of 15 mmHg. We quantified eight morphological parameters. A Random Forest regression combined with SHAP analysis was used to determine morphological predictors of LC strain. Results: LC depth showed the strongest linear association with LC strain (r = −0.31). Other parameters with smaller associations included BMO radius (r = 0.17), pre-lamina volume (r = −0.14) and mean choroidal thickness (r = −0.12). After adjusting for age and gender, glaucomatous eyes exhibited significantly lower LC strain than healthy eyes (coefficient = 0.0018, p = 0.011), suggesting potential tissue remodelling. SHAP ranked pre-lamina depth, LC curvature, BMO radius, and LC depth as the most influential predictors despite modest explained variance. Conclusions: This study presents a scalable, image-based biomechanical framework enables high-throughput, patient-specific assessment and offers new opportunities to identify morphological biomarkers for glaucoma risk stratification and disease monitoring.
UR - https://www.scopus.com/pages/publications/105023328986
U2 - 10.1038/s41433-025-04146-w
DO - 10.1038/s41433-025-04146-w
M3 - 文章
AN - SCOPUS:105023328986
SN - 0950-222X
VL - 40
SP - 238
EP - 244
JO - Eye (Basingstoke)
JF - Eye (Basingstoke)
IS - 2
ER -