Tran H, Grimm J, Wang B, Smith M A, Gogola A, Nelson S, Tyler-Kabara E, Schuman J, Wollstein G, Sigal I A
Department of Ophthalmology, University of Pittsburgh, 203 Lothrop St., Pittsburgh, PA, USA 15213.
Department of Bioengineering, University of Pittsburgh, 3700 O'Hara St., Pittsburgh, PA, USA 15213.
Proc SPIE Int Soc Opt Eng. 2017 Feb;10067. doi: 10.1117/12.2257360.
Although it is well documented that abnormal levels of either intraocular (IOP) or intracranial pressure (ICP) can lead to potentially blinding conditions, such as glaucoma and papilledema, little is known about how the pressures actually affect the eye. Even less is known about potential interplay between their effects, namely how the level of one pressure might alter the effects of the other. Our goal was to measure in-vivo the pressure-induced stretch and compression of the lamina cribrosa due to acute changes of IOP and ICP. The lamina cribrosa is a structure within the optic nerve head, in the back of the eye. It is important because it is in the lamina cribrosa that the pressure-induced deformations are believed to initiate damage to neural tissues leading to blindness. An eye of a rhesus macaque monkey was imaged in-vivo with optical coherence tomography while IOP and ICP were controlled through cannulas in the anterior chamber and lateral ventricle, respectively. The image volumes were analyzed with a newly developed digital image correlation technique. The effects of both pressures were highly localized, nonlinear and non-monotonic, with strong interactions. Pressure variations from the baseline normal levels caused substantial stretch and compression of the neural tissues in the posterior pole, sometimes exceeding 20%. Chronic exposure to such high levels of biomechanical insult would likely lead to neural tissue damage and loss of vision. Our results demonstrate the power of digital image correlation technique based on non-invasive imaging technologies to help understand how pressures induce biomechanical insults and lead to vision problems.
尽管有充分的文献记载,眼内压(IOP)或颅内压(ICP)异常可导致潜在的致盲疾病,如青光眼和视乳头水肿,但对于这些压力如何实际影响眼睛却知之甚少。关于它们影响之间的潜在相互作用,即一种压力水平如何改变另一种压力的影响,了解得更少。我们的目标是在活体中测量由于IOP和ICP的急性变化导致的筛板压力诱导的拉伸和压缩。筛板是眼球后部视神经头内的一种结构。它很重要,因为据信在筛板中,压力诱导的变形会引发对神经组织的损伤,导致失明。在分别通过前房和侧脑室的插管控制IOP和ICP时,用光学相干断层扫描对恒河猴的一只眼睛进行活体成像。用一种新开发的数字图像相关技术分析图像体积。两种压力的影响都高度局部化、非线性且非单调,具有强烈的相互作用。与基线正常水平相比的压力变化导致后极神经组织的大量拉伸和压缩,有时超过20%。长期暴露于如此高水平的生物力学损伤可能会导致神经组织损伤和视力丧失。我们的结果证明了基于非侵入性成像技术的数字图像相关技术在帮助理解压力如何诱导生物力学损伤并导致视力问题方面的能力。