Yan Huo , Le Chang , Ruisi Xie , Shiyao Zhang , Shu Yang , Haohan Zou , Shuangcheng Li , Yan Wang
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引用次数: 0
Abstract
Purpose
To explore scleral elastic modulus and its correlation with corneal biomechanics in vivo and in vitro, and to introduce a predictive model for non-destructive characterization of scleral and corneal elastic modulus.
Methods
In vivo biomechanical parameters of 21 rabbit eyes were measured using the Corvis ST. Uniaxial tensile tests on corneal and scleral (anterior, equatorial, and posterior sections) strips provided low-strain and high-strain tangent elastic modulus (LSTM and HSTM). Pearson's and Spearman's correlation analyses were used to examine the relationship. A multivariate linear regression model was used to characterize the elastic modulus in vivo. Transmission electron microscopy was used to elucidate the arrangement of collagen fibers in the anterior, equatorial, and posterior sclera.
Results
Twelve in vivo parameters significantly correlate with the corneal LSTM (P < 0.05), whereas no parameters are correlated with the corneal HSTM. SP-HC (Rho = 0.442) and HC Deflection Amp (HC DA, r = −0.605) correlated with anterior sclera LSTM. DA ratio 1 mm (r = 0.446) was correlated with the equatorial sclera LSTM. Integrated Radius (Rho = 0.483) and Radius (r = −0.473) were correlated with the equatorial sclera HSTM. The representative multivariate linear regression model indicated the follows:
Equatorial sclera LSTM = 0.22 + 0.114 ∗ DA Ratio 1 mm - 0.049 ∗ HC DA.
Conclusions
Biomechanical parameters, such as SP-A1 and SSI, correlate with the low-strain elasticity of the cornea, which primarily reflects the properties of the corneal ground matrix. Corvis ST may not be able to detect biomechanics changes in the cornea collagen structure. The scleral elastic modulus prediction model offers new insights into the non-destructive characterization of scleral biomechanics.
期刊介绍:
The primary goal of Experimental Eye Research is to publish original research papers on all aspects of experimental biology of the eye and ocular tissues that seek to define the mechanisms of normal function and/or disease. Studies of ocular tissues that encompass the disciplines of cell biology, developmental biology, genetics, molecular biology, physiology, biochemistry, biophysics, immunology or microbiology are most welcomed. Manuscripts that are purely clinical or in a surgical area of ophthalmology are not appropriate for submission to Experimental Eye Research and if received will be returned without review.