A Review of Corneal Biomechanics and Scleral Stiffness in Topical Prostaglandin Analog Therapy for Glaucoma

被引:6
|
作者
Shen, Steven R. [1 ]
Fleming, Gloria P. [2 ]
Jain, Shelly Gupta [2 ]
Roberts, Cynthia J. [2 ,3 ]
机构
[1] Ohio State Univ, Coll Med, Columbus, OH 43212 USA
[2] Ohio State Univ, Dept Ophthalmol & Visual Sci, Columbus, OH 43212 USA
[3] Ohio State Univ, Dept Biomed Engn, Columbus, OH 43212 USA
关键词
Corneal biomechanics; prostaglandin analog; intraocular pressure; corneal hysteresis; Corvis ST; Ocular Response Analyzer; INTRAOCULAR-PRESSURE; MATRIX METALLOPROTEINASES; IN-VIVO; LATANOPROST; HYSTERESIS; PACHYMETRY; EXPRESSION; PARAMETERS; THICKNESS; 6-MONTH;
D O I
10.1080/02713683.2022.2099903
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose The mechanism of action underlying prostaglandin analog (PGA) therapy involves changes in the expression of different metalloproteases to increase permeability of the sclera and allow increased aqueous humor outflow through this alternative drainage pathway. This alteration of structure impacts cornea/scleral biomechanics and may introduce artifact into the measurement of intraocular pressure (IOP) in the clinical setting. Methods A literature search reviewing the impact of PGA therapy on corneal and scleral biomechanics was conducted including basic studies, clinical studies with treatment naive patients, and a clinical study examining the cessation of PGA therapy. Additional literature including engineering texts was added for greater clarity of the concepts underlying ocular biomechanics. Results One study with an animal model reported significant corneal stiffening with PGA treatment. Most longitudinal clinical studies examining the effects of initiation of PGA therapy in PGA naive subjects failed to report biomechanical parameters associated with stiffness using the Corvis ST and only included those parameters strongly influenced by IOP. One study reported a significant reduction in scleral stiffness with IOP as a co-variate, highlighting the need to account for the effects of IOP lowering when assessing clinical biomechanics. The report of cessation of PGA therapy on corneal biomechanics showed no change in corneal compensated IOP after 6 weeks, raising the question of reversibility of the PGA-induced structural alteration. Conclusions Given that the findings in several clinical studies may merely reflect a reduction in IOP, further studies are warranted using Corvis ST parameters associated with corneal and scleral stiffness. The gold standard for IOP measurement in the clinical setting is Goldmann applanation tonometry, a technique previously shown to be affected by corneal stiffness. Since PGA therapy has been reported to alter not only scleral biomechanics, but also corneal biomechanics, it is essential to consider alternative tonometry technologies in the clinic.
引用
收藏
页码:172 / 181
页数:10
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