Abstract
purpose. To investigate relationships between acute intraocular pressure (IOP)–induced optic nerve head surface deformation and corneal hysteresis and thickness in glaucomatous and nonglaucomatous human eyes.
methods. This was a prospective experimental study of 100 subjects (38 with glaucoma, 62 without glaucoma). Data collected included spherical equivalent, optic disc diameter, central corneal thickness (CCT), axial length, cylinder, Goldmann IOP, Pascal IOP, and ocular pulse amplitude and ocular response analyzer (ORA) measurements of corneal hysteresis (CH). Elevation of IOP was induced in the right eye of each subject with a modified LASIK suction ring to an average of 64 mm Hg for less than 30 seconds. Heidelberg Retina Tomography II (HRT) was used to map the optic nerve surface before and during IOP elevation. Mean cup depth was calculated using built-in HRT data analysis software. Change in optic disc depth during IOP elevation was calculated for all right eyes, and tests for correlation with the parameters listed were performed.
results. Both CH and CCT were lower in the glaucoma group (8.8 mm Hg and 532 μm) than in the control group (9.6 mm Hg, P = 0.012; 551 μm, P = 0.011, respectively). There were no statistically significant differences in spherical equivalent, cylinder, axial length, optic disc size, or ocular pulse amplitude between the glaucoma and the control groups. There was no difference between the amount of IOP elevation between the two groups (P = 0.41), and the average difference in mean cup depth between baseline (mean cup depth, 247 μm) and during IOP elevation was 33 μm (29.8 μm in glaucoma and 36.1 μm in control; P = 0.5). Multiple variable analysis, controlling for age and sex, showed that CH was correlated with mean cup depth increase (P = 0.032). This relationship persisted (P = 0.032) after controlling for glaucoma status in addition to age and sex. Other factors, including CCT (P = 0.3), axial length (P = 0.9), ocular pulse amplitude (P = 0.22), and spherical equivalent (P = 0.38), were not significant in this model.
conclusions. In the glaucoma patients but not the control patients, CH but not CCT or other anterior segment parameters was associated with increased deformation of the optic nerve surface during transient elevations of IOP. (ClinicalTrials.gov number, NCT00328835.)
It has been known since Goldmann first described what is currently the gold standard for intraocular pressure (IOP) measurement
1 that the biomechanical characteristics of the cornea, especially central corneal thickness (CCT), play a role in the accuracy of IOP measurement. Particularly since the Ocular Hypertension Treatment Study (OHTS)
2 brought CCT back into the limelight, there has been much discussion
3 4 5 6 7 8 9 regarding the role that CCT has on the risk for glaucoma development or progression. Included in that discussion has been speculation that the biomechanical characteristics of the cornea might somehow reflect vulnerability of the optic nerve head to glaucoma, in addition to the well-described discrepancies between measured and true IOP. Corneal tissue properties may or may not be directly related to lamina tissue properties given that their embryological derivation is different, but there are also plausible connections.
First, corneal thickness might be associated with structural characteristics of the sclera and adjacent tissues and of the optic disc.
3 Thinner corneas have been shown not to be associated with myopia or thinner anterior sclera,
10 but there does seem to be a correlation between thinner corneas and larger optic discs.
3 Larger optic disc diameters may be associated with increased vulnerability to pressure-induced deformation; Sigal et al.
11 have described the importance of the peripapillary scleral stiffness and thickness and the optic canal diameter in determining lamina cribrosa strain. Bellezza et al.
12 examined monkey eyes with and without induced glaucoma and found plastic expansions of the anterior scleral canal at Bruch membrane and anterior laminar insertions in glaucomatous eyes but not in control eyes.
Second, the corneal tissue characteristics themselves, such as the ability to resist deformation, might reflect the constitution of the extracellular matrix (ECM). This is supported by suggestions that corneal hysteresis (CH) is lower in patients with Marfan syndrome, a systemic connective tissue disorder (Gatinel D, personal communication, 2008), and in pregnancy (Sousa AK, et al. IOVS 2007;48 ARVO E-Abstract 3144), which has hormonally mediated systemic effects on connective tissues.
Given that the cornea, sclera, peripapillary ring, and lamina cribrosa in an individual eye are essentially made from ECM constituents coded for by the same genes, it is plausible, but unproven, that their biomechanical characteristics might be similar. It has been speculated that an eye with a more deformable cornea, or one with less viscous damping, might also have an optic disc that is more vulnerable to glaucoma damage from raised IOP. Both the cornea
13 14 and the lamina
15 16 17 18 tend to become more rigid with age and to become stiffer, less resilient structures. Age-related stiffening of connective tissues is possibly similar in the cornea and lamina, and, because CH declines with age,
13 it is possible that the lamina and peripapillary sclera behave similarly.
Structural changes at the optic nerve head are pivotal to the diagnosis of glaucoma and may be implicated in the pathogenesis of glaucoma. Biomechanical responses of the optic nerve head to elevations of IOP have been studied in several models, including monkey eyes,
12 19 human eyes,
20 and computer modeling techniques.
11 21 22 There are deformations of the lamina cribrosa in human and monkey eyes in response to transient IOP increase.
12 20 21 However, finite element analysis suggests that a significant proportion of the change measured by scanning laser ophthalmoscopy, such as Heidelberg Retina Tomography II (HRT), may be in the prelaminar tissues,
11 including the neuroretinal rim, rather than in the lamina.
Recently, the introduction of the ocular response analyser (ORA) has allowed the measurement of CH. Hysteresis of the cornea is correlated with CCT but only weakly.
13 CH has been associated with progressive visual field worsening
8 in glaucoma patients, and hysteresis is lower in patients who have glaucoma.
8
In this study, we investigated changes in optic disc cup depth in a large group of patients, with and without glaucoma, during a transient IOP rise and compared them with measurements of their CCT and CH.
One hundred patients older than 18 years of age who had attended a specialist appointment in the preceding 12 months were recruited from general ophthalmology and glaucoma clinics in Wellington, New Zealand. All had best-corrected visual acuities of at least 6/12. Patients were assigned to either the glaucoma or the control group based on their clinical findings on previous visits
(Table 1) . Those included in the glaucoma group had been diagnosed as having glaucoma by a glaucoma specialist (APW) and had documented glaucomatous optic disc appearance over at least two specialist visits. At study entry, the glaucoma group had a mean deviation (MD) of −3.2 ± 5.52 dB and a pattern SD (PSD) of 4.2 ± 1.9 dB on Humphrey Matrix perimetry. As a control group, we recruited patients with healthy eyes and others referred to our clinic as glaucoma suspects who had no evidence of glaucomatous optic neuropathy.
Patients with known or suspected ocular perfusion abnormalities were excluded from the study because of the potential effects of the high induced IOP on retinal circulation. Patients were also excluded if changes had been made to their treatment regimen or if they had undergone either intraocular surgery or laser trabeculoplasty within the preceding 3 months. Glaucoma patients with advanced disease, defined as any documented visual field defects within 5° of fixation, or inadequate control on maximal medical therapy requiring glaucoma filtration surgery, were excluded from the study.
More than half the patients in the control group were glaucoma suspects referred to our clinic with dysmorphic but nonglaucomatous disc appearances, visual fields within normal limits at study entry (MD, −0.5 ± 3.2, PSD, 3.0 ± 1.0; Humphrey matrix), IOP less than 20 mm Hg, and no documented disc changes on subsequent visits
(Table 1) . The rest of the control group consisted of patients with signs that might increase the risk for glaucoma, such as narrow angles and pseudoexfoliation, but normal optic discs at specialist review. Four patients in the control group were recruited from general ophthalmology clinics after being seen with problems unrelated to glaucoma
(Table 1) . None of the subjects whose right eyes were used as control eyes had glaucoma in the fellow eye.
Ethical review board approval was gained (CEN/05/08/063), and informed consent was obtained from all subjects. This trial adhered to the Declaration of Helsinki.
Transient IOP elevation was induced in the right eye of each subject by a modified laser-assisted in situ keratomileusis (LASIK) automated corneal shaper (Chiron; Hansa Research & Development, Miami, FL) after the administration of local anesthetic. Because LASIK suction rings can potentially produce IOPs in excess of 100 mm Hg, the rigid plastic tubing connecting the suction ring to the main pump had been punctured by two 18-gauge needles that were left in situ to reduce the potential intraluminal negative pressure produced and, therefore, limit the peak IOP elevation that could be generated. Elevation of IOP lasted up to a maximum of 30 seconds. IOP measurement during the procedure was obtained with a rebound tonometer (iCare; Tiolat, Helsinki, Finland). Measurements were taken with the rebound tonometer because technical difficulties made measurement with other available devices (including Goldmann IOP, Tono-Pen [Reichert Corp.], Pascal IOP, dynamic contour tonometer, and pneumotonometer) impossible. Because we did not have access to a rebound tonometer (iCare; Tiolat) at the beginning of the study, not all subjects had IOP readings taken during IOP elevation.
The right eye of each patient was imaged before and during IOP elevation using HRT II. Three scans were averaged, combined into a single mean topography image, using the standard HRT data acquisition process. Imaging was performed with an eyelid speculum in place before and during IOP elevation to control for refractive or ocular distortion effects from the speculum. Artificial tears (Bion Tears; Alcon, Fort Worth, TX) were used to lubricate the cornea and to maximize image quality.
Contour lines were drawn by an experienced operator using the built-in HRT II software for each of the 200 scans (100 right eyes before and during IOP elevation). A masked operator drew the contour lines at an interval of some hours after image acquisition. The automated contour line import function in HRT II scales the contour line in proportion to the scaling inherent in sequential image alignment. Given that we were examining changes to the optic nerve as a response to raised IOP and that there would likely have been a differential between stretch of the optic nerve head and that of the surrounding retinal features, contour lines were placed manually for each image. The contour line was drawn, the average optic disc depth was recorded, and the contour line was deleted before the image window was closed so that the previous image was not visible, and then the same procedure was performed on subsequent images.
Results from this study suggest that optic disc surface compliance may have a relationship with corneal hysteresis, a parameter of ocular biomechanics that is easily and noninvasively measurable at the front of the eye. Optic disc compliance was not associated with CCT in this study. If optic disc compliance, as measured by the amount of deepening of the optic cup during an acute rise in pressure, is associated with increased risk for glaucoma, it is possible that CHmight provide further information about glaucoma risk and pathogenesis. It is possible that CH had a relationship to change in mean optic disc depth in this study because it represents properties of the rest of the eye rather than just the cornea.
The relationship between hysteresis and optic nerve surface compliance observed in this study occurred only in patients with glaucoma, suggesting that glaucoma patients have altered ocular tissue biomechanics.
Nicolela et al.
26 described 23 glaucoma patients in whom topography was performed before and after glaucoma medication was stopped in one eye, and they did not detect a change in stereometric or topographic change analysis parameters with an IOP shift of 5 mm Hg. This might have been too small an IOP change to deform the optic nerve surface, or the number of patients might have been too small to detect a very small change.
Lesk et al.
27 lowered IOP in 32 patients with glaucoma or ocular hypertension through medication, laser trabeculoplasty, or trabeculectomy by a mean of 35% and split the cohort in half on the basis of CCT. Patients with thin CCT had larger decreases in Goldmann-measured IOP than the patients with thick CCT (mean 38% vs. 30%;
P = 0.09) and also had statistically significant differences in the change in mean (−36 ± 32 vs. −4 ± 36 μm;
P = 0.003) and maximum (−73 ± 107 vs. −4 ± 89 μm;
P = 0.02) cup depth. CH was not assessed. Those results suggested that thicker corneas are associated with a less compliant optic nerve surface, a finding not replicated in our study. Possible explanations include the fundamentally different nature of the intervention, raising the IOP in our study compared with lowering it in the Lesk et al.
27 study, the possibility that a few patients in the Lesk et al.
27 study with postintervention low IOP might have had distorted topography results, and the possible overestimation of IOP in eyes with thicker corneas. If the latter, the measured IOP would have changed less, because of the larger contribution of corneal stiffness to the measurement, and subsequent changes in the optic cup would have been correspondingly smaller.
The task of outlining the optic nerve head in the HRT software was subjective; we attempted to minimize the impact of this by using a relatively large number of subjects. Similarly the relatively high topography standard deviations for the baseline tests, as well as the raised pressure tests, reflected the decision to standardize scans as much as possible by performing all imaging with the speculum in place. Again, the large number of subjects should have minimized the impact of this. It is possible that the method of raising IOP might itself have altered the structural characteristics of the eye during IOP elevation, though the built-in image alignment algorithm in the HRT software would have compensated for minor changes in image refraction.
We also drew the contour lines separately rather than using the automated contour line import function between image series to eliminate the possibility that errors in the automated importing of the contour line could affect the results. In particular, this allowed us to control for possible changes in disc size, which would not have been possible using the automated contour line alignment.
The control cohort had similar numbers of male and female patients, but the glaucoma cohort of the study group had a strong sex bias toward male patients. Some studies have found a correlation between male sex and higher CCT values,
28 29 but others have not.
30 We controlled for sex in addition to age and glaucoma status in our model; therefore, it is unlikely that the sex bias in the glaucoma group had a tangible influence on the results.
Although the amount of suction applied was constant and a single device was used throughout, we have no way of knowing whether the IOP responses were uniform across the eyes. In addition, when IOP was measured, this was measured using an external device, so true IOP was not known. IOP was transiently raised to high levels—approximately 64 mm Hg—in this study. We might have achieved similar deformations at lower IOPs, but the design and methods of the study made investigation of a dose–response relationship impossible. It is also unknown whether the corneal biomechanical properties might have influenced the magnitude of IOP elevation obtained by the method used. The duration of IOP elevation in this study was less than 1 minute, which might not have allowed enough time for the response to raised IOP to fully equilibrate, described in ex vivo studies,
22 31 to take up to several minutes. Our inclusion of glaucomatous eyes made us reluctant to adopt an approach with more sustained IOP elevations.
Early glaucoma in experimental monkeys produced an
increased compliance of the optic nerve head in the monkey glaucoma model described by Bellezza.
12 This may represent an initial response. Previously, Burgoyne et al.
19 had demonstrated that in a similar model, optic disc compliance initially increased for 1 to 2 weeks before decreasing again to the original level. In a study
37 before that, IOP-induced optic nerve deformation was noted in the nonglaucomatous monkey model over much longer periods, usually more than 10 minutes.
If the optic nerve head were more rigid, a given applied force would produce less lamina movement, which ought to be seen through the methods used in this study as decreased surface compliance. If optic nerve head rigidity were related to cross-linking between collagen fibrils in the laminae, then one might expect greater stiffness to be associated with lower hysteresis and the findings of this study would be consistent with this hypothesis. We did not find a link between CH and cup change in the control eyes; hence, one might speculate that glaucoma-related changes to the ocular tissues might result in a stiffer, but less viscoelastic, material.
The importance of the measurable biomechanical parameters of the cornea, such as CH, remains to be fully elucidated. The ability for the sclerocorneal shell to dampen brief IOP fluctuations, such as the 10 mm Hg spike from blinking
38 or perhaps significantly larger pressures from eye rubbing or Valsalva, may protect eyes with glaucoma from sudden pressure spikes. From this study and others,
8 it appears that CH in particular may have relevance to glaucoma that is separate from that of CCT.
Supported by the Capital Vision Research Trust, and, in part, by the Department of Health’s National Institute for Health Research Biomedical Research Centre, Moorfields Eye Hospital and UCL Institute of Ophthalmology. The views expressed in this publication are those of the authors and not necessarily those of the Department of Health.
Submitted for publication December 5, 2007; revised February 16, 2008; accepted June 5, 2008.
Disclosure:
A.P. Wells, Reichert Ophthalmic Instruments (F);
D.F. Garway-Heath, None;
A. Poostchi, None;
T. Wong, None;
K.C.Y. Chan, None;
N. Sachdev, None
The publication costs of this article were defrayed in part by page charge payment. This article must therefore be marked “
advertisement” in accordance with 18 U.S.C. §1734 solely to indicate this fact.
Corresponding author: Anthony P. Wells, Capital Eye Specialists, L2/148 Cuba Street, Wellington, New Zealand;
[email protected].
| Glaucoma | Control | P |
Subjects (n) | 38 | 62 | — |
Male/female | 29/9 | 32/30 | 0.01 |
Age (y) | 61.8 ± 12.8 | 59.8 ± 10.1 | 0.38 |
Diagnosis (n) | POAG/NTG (29) | Glaucoma suspect (37) | — |
| PXF glaucoma (4) | Narrow angle (8) | — |
| NAG (3) | PXF (6) | — |
| PDS (2) | OHTN (3) | — |
| — | Narrow angle/OHTN/previous PI (3) | — |
| — | Cataract/other (6) | — |
Treatment | Medication (28) | YAG PI (9) | — |
| SLT (9) | Cataract extraction (5) | — |
| Cataract extraction (6) | Medication (4) | — |
| YAG PI (4) | — | — |
Right eye IOP (mm) | 17.1 ± 4.5 | 17.4 ± 4.3 | 0.75 |
Elevated level | 66.6 ± 11.8 | 63.2 ± 14.1 | 0.39 |
Left eye IOP (mm Hg) | 18.2 ± 4.8 | 17.6 ± 3.8 | 0.46 |
The authors thank Reichert Ophthalmic Instruments, Andrew Logan, Bausch & Lomb, and Designs for Vision New Zealand for supporting this study
GoldmannH, SchmidtT. Über applanationstonometrie. Ophthalmologica. 1957;134:221–242.
[CrossRef] [PubMed]GordonMO, BeiserJA, BrandtJD, et al. The Ocular Hypertension Treatment Study: baseline factors that predict the onset of primary open-angle glaucoma. Arch Ophthalmol. 2002;120(6)714–720.discussion 829–830
[CrossRef] [PubMed]PakravanM, ParsaA, SanagouM, ParsaCF. Central corneal thickness and correlation to optic disc size: a potential link for susceptibility to glaucoma. Br J Ophthalmol. 2007;91(1)26–28.
[CrossRef] [PubMed]HongS, KimCY, SeongGJ, HongYJ. Central corneal thickness and visual field progression in patients with chronic primary angle-closure glaucoma with low intraocular pressure. Am J Ophthalmol. 2007;143(2)362–363.
[CrossRef] [PubMed]RogersDL, CantorRN, CatoiraY., et al. Central corneal thickness and visual field loss in fellow eyes of patients with open-angle glaucoma. Am J Ophthalmol. 2007;143(1)159–161.
[CrossRef] [PubMed]ChauhanBC, HutchisonDM, LeBlancRP, et al. Central corneal thickness and progression of the visual field and optic disc in glaucoma. Br J Ophthalmol. 2005;89(8)1008–1012.
[CrossRef] [PubMed]MedeirosFA, SamplePA, ZangwillLM, et al. Corneal thickness as a risk factor for visual field loss in patients with preperimetric glaucomatous optic neuropathy. Am J Ophthalmol. 2003;136(5)805–813.
[CrossRef] [PubMed]CongdonNG, BromanAT, Bandeen-RocheK, et al. Central corneal thickness and corneal hysteresis associated with glaucoma damage. Am J Ophthalmol. 2006;141(5)868–875.
[CrossRef] [PubMed]JonasJB, StrouxA, VeltenI, et al. Central corneal thickness correlated with glaucoma damage and rate of progression. Invest Ophthalmol Vis Sci. 2005;46(4)1269–1274.
[CrossRef] [PubMed]OliveiraC, TelloC, LiebmannJ, RitchR. Central corneal thickness is not related to anterior scleral thickness or axial length. J Glaucoma. 2006;15(3)190–194.
[CrossRef] [PubMed]SigalIA, FlanaganJG, TertineggI, EthierCR. Finite element modeling of optic nerve head biomechanics. Invest Ophthalmol Vis Sci. 2004;45(12)4378–4387.
[CrossRef] [PubMed]BellezzaAJ, RintalanCJ, ThompsonHW, et al. Deformation of the lamina cribrosa and anterior scleral canal wall in early experimental glaucoma. Invest Ophthalmol Vis Sci. 2003;44(2)623–637.
[CrossRef] [PubMed]KotechaA, ElsheikhA, RobertsCR, et al. Corneal thickness- and age-related biomechanical properties of the cornea measured with the ocular response analyzer. Invest Ophthalmol Vis Sci. 2006;47(12)5337–5347.
[CrossRef] [PubMed]ElsheikhA, WangD, BrownM, et al. Assessment of corneal biomechanical properties and their variation with age. Curr Eye Res. 2007;32(1)11–19.
[CrossRef] [PubMed]AlbonJ, FarrantS, AkhtarS, et al. Connective tissue structure of the tree shrew optic nerve and associated ageing changes. Invest Ophthalmol Vis Sci. 2007;48(5)2134–2144.
[CrossRef] [PubMed]AlbonJ, KarwatowskiWS, AveryN, et al. Changes in the collagenous matrix of the aging human lamina cribrosa. Br J Ophthalmol. 1995;79(4)368–375.
[CrossRef] [PubMed]AlbonJ, PurslowPP, KarwatowskiWS, EastyDL. Age related compliance of the lamina cribrosa in human eyes. Br J Ophthalmol. 2000;84(3)318–323.
[CrossRef] [PubMed]AlbonJ, KarwatowskiWS, EastyDL, et al. Age related changes in the non-collagenous components of the extracellular matrix of the human lamina cribrosa. Br J Ophthalmol. 2000;84(3)311–317.
[CrossRef] [PubMed]BurgoyneCF, QuigleyHA, ThompsonHW, et al. Early changes in optic disc compliance and surface position in experimental glaucoma. Ophthalmology. 1995;102(12)1800–1809.
[CrossRef] [PubMed]Azuara-BlancoA, HarrisA, CantorLB, et al. Effects of short term increase of intraocular pressure on optic disc cupping. Br J Ophthalmol. 1998;82(8)880–883.
[CrossRef] [PubMed]SigalIA, FlanaganJG, EthierCR. Factors influencing optic nerve head biomechanics. Invest Ophthalmol Vis Sci. 2005;46(11)4189–4199.
[CrossRef] [PubMed]SigalIA, FlanaganJG, TertineggI, EthierCR. Reconstruction of human optic nerve heads for finite element modeling. Technol Health Care. 2005;13(4)313–329.
[CrossRef] [PubMed]LuceDA. Determining in vivo biomechanical properties of the cornea with an ocular response analyzer. J Cataract Refract Surg. 2005;31(1)156–162.
[CrossRef] [PubMed]IlievME, GoldblumD, KatsoulisK, et al. Comparison of rebound tonometry with Goldmann applanation tonometry and correlation with central corneal thickness. Br J Ophthalmol. 2006;90(7)833–835.
[CrossRef] [PubMed]Martinez-de-la-CasaJM, Garcia-FeijooJ, CastilloA, Garcia-SanchezJ. Reproducibility and clinical evaluation of rebound tonometry. Invest Ophthalmol Vis Sci. 2005;46(12)4578–4580.
[CrossRef] [PubMed]NicolelaMT, SoaresAS, CarrilloMM, ChauhanBC, LeBlancRP, ArtesPH. Effect of moderate intraocular pressure changes on topographic measurements with confocal scanning laser tomography in patients with glaucoma. Arch Ophthalmol. 2006;124(5)633–640.
[CrossRef] [PubMed]LeskMR, HafezAS, DescovichD. Relationship between central corneal thickness and changes of optic nerve head topography and blood flow after intraocular pressure reduction in open-angle glaucoma and ocular hypertension. Arch Ophthalmol. 2006;124(11)1568–1572.
[CrossRef] [PubMed]MigliorS, PfeifferN, TorriV, et al. Predictive factors for open-angle glaucoma among patients with ocular hypertension in the European Glaucoma Prevention Study. Ophthalmology. 2007;114(1)3–9.
[CrossRef] [PubMed]TomidokoroA, AraieM, IwaseA, GroupTS. Corneal thickness and relating factors in a population-based study in Japan: the Tajimi study. Am J Ophthalmol. 2007;144(1)152–154.
[CrossRef] [PubMed]AltinokA, SenE, YaziciA, et al. Factors influencing central corneal thickness in a Turkish population. Curr Eye Res. 2007;32(5)413–419.
[CrossRef] [PubMed]DownsJC, SuhJK, ThomasKA, et al. Viscoelastic material properties of the peripapillary sclera in normal and early-glaucoma monkey eyes. Invest Ophthalmol Vis Sci. 2005;46(2)540–546.
[CrossRef] [PubMed]HerndonLW. Measuring intraocular pressure-adjustments for corneal thickness and new technologies. Curr Opin Ophthalmol. 2006;17(2)115–119.
[CrossRef] [PubMed]LeskeMC, HeijlA, HymanL, et al. Predictors of long-term progression in the early manifest glaucoma trial. Ophthalmology. 2007;114(11)1965–1972.
[CrossRef] [PubMed]RidleyF. The intraocular pressure and drainage of the aqueous humor. Br J Exp Pathol. 1930;11:217.
WooSL, KobayashiAS, SchlegelWA, LawrenceC. Nonlinear material properties of intact cornea and sclera. Exp Eye Res. 1972;14(1)29–39.
[CrossRef] [PubMed]JohnsonCS, MianSI, MoroiS, et al. Role of corneal elasticity in damping of intraocular pressure. Invest Ophthalmol Vis Sci. 2007;48(6)2540–2544.
[CrossRef] [PubMed]HeickellA, BellezzaA, ThompsonH, BurgoyneC. Optic disc surface compliance testing using confocal scanning laser tomography in the normal monkey eye. J Glaucoma. 2001;10(5)369–382.
[CrossRef] [PubMed]ColemanDJ, TrokelS. Direct-recorded intraocular pressure variations in a human subject. Arch Ophthalmol. 1969;82(5)637–640.
[CrossRef] [PubMed]