Vilupuru Abhiram S, Glasser Adrian
College of Optometry, University of Houston, Texas 77004, USA.
Optom Vis Sci. 2003 May;80(5):383-94. doi: 10.1097/00006324-200305000-00013.
Prior studies in humans measured time constants of biometric accommodative changes as a function of amplitude, and prior studies in monkeys used slit lamp videography to analyze dynamic lenticular accommodative movements. Neither of these studies related biometric changes to refractive changes. We wished to develop and test methodology to begin to test the hypothesis that ocular biometric changes are well correlated with accommodative refractive changes in rhesus monkeys.
Methodology is described to dynamically measure biometric accommodative changes with A-scan ultrasonography. Lens thickness, anterior chamber depth, and anterior segment length (anterior chamber depth plus lens thickness) were measured dynamically during Edinger-Westphal-stimulated accommodation in two eyes of one rhesus monkey. In addition, dynamic accommodative refractive changes were measured with infrared photorefraction. Functions were fit to the accommodative and disaccommodative responses to obtain time constants. Derivatives of these functions allow peak velocities to be determined for each amplitude. Dynamic changes in lens thickness and anterior chamber depth measured with A-scan biometry were compared with dynamic measures of accommodation using infrared photorefraction.
Lens thickness and anterior segment length increase and anterior chamber depth decreases during accommodation. The biometric changes are well correlated with the accommodative optical changes. Peak velocities of accommodative changes in lens thickness and anterior chamber depth increase with amplitude and peak velocities for disaccommodation were higher than those for accommodation.
Dynamic A-scan provides a method for dynamic analysis of the accommodative biometric changes during Edinger-Westphal-stimulated accommodation in monkeys, although the measurement resolution of this approach is limited.
先前对人类的研究测量了生物计量性调节变化的时间常数与调节幅度的函数关系,而先前对猴子的研究则使用裂隙灯摄像来分析晶状体的动态调节运动。这些研究均未将生物计量变化与屈光变化联系起来。我们希望开发并测试一种方法,以开始检验恒河猴眼生物计量变化与调节性屈光变化密切相关这一假设。
描述了一种使用A扫描超声动态测量生物计量性调节变化的方法。在一只恒河猴的两只眼睛进行动眼神经核刺激调节期间,动态测量晶状体厚度、前房深度和眼前节长度(前房深度加晶状体厚度)。此外,使用红外光屈光测量法测量动态调节性屈光变化。对调节和放松反应拟合函数以获得时间常数。这些函数的导数可确定每个幅度的峰值速度。将A扫描生物测量法测量的晶状体厚度和前房深度的动态变化与使用红外光屈光测量法的调节动态测量结果进行比较。
调节期间晶状体厚度和眼前节长度增加,前房深度减小。生物计量变化与调节性光学变化密切相关。晶状体厚度和前房深度调节变化的峰值速度随幅度增加,放松的峰值速度高于调节的峰值速度。
动态A扫描提供了一种在动眼神经核刺激猴子调节期间对调节性生物计量变化进行动态分析的方法,尽管这种方法测量分辨率有限。