June 2021
Volume 62, Issue 7
Open Access
Glaucoma  |   June 2021
Biomechanical Glaucoma Factor and Corneal Hysteresis in Treated Primary Open-Angle Glaucoma and Their Associations With Visual Field Progression
Author Affiliations & Notes
  • Shuichiro Aoki
    Department of Ophthalmology, Sapporo City General Hospital, Sapporo, Japan
    Department of Ophthalmology, the University of Tokyo Graduate School of Medicine, Tokyo, Japan
  • Atsuya Miki
    Department of Ophthalmology and Visual Science, Osaka University, Osaka, Japan
    Department of Innovative Visual Science, Osaka University Graduate School of Medicine, Osaka, Japan
  • Takashi Omoto
    Department of Ophthalmology, the University of Tokyo Graduate School of Medicine, Tokyo, Japan
  • Yuri Fujino
    Department of Ophthalmology, the University of Tokyo Graduate School of Medicine, Tokyo, Japan
    Department of Ophthalmology, Seirei Hamamatsu General Hospital, Hamamatsu, Japan
  • Masato Matsuura
    Department of Ophthalmology, the University of Tokyo Graduate School of Medicine, Tokyo, Japan
    Orthopic and Visual Science, Department of Rehabilitation, School of Allied Health Sciences, Kitasato University, Kanagawa, Japan
    Department of Ophthalmology, Saneikai Tsukazaki Hospital, Hyogo, Japan
  • Hiroshi Murata
    Department of Ophthalmology, the University of Tokyo Graduate School of Medicine, Tokyo, Japan
  • Ryo Asaoka
    Department of Ophthalmology, the University of Tokyo Graduate School of Medicine, Tokyo, Japan
    Department of Ophthalmology, Seirei Hamamatsu General Hospital, Hamamatsu, Japan
    Nanovision Research Division, Research Institute of Electronics, Shizuoka University, Shizuoka, Japan
    The Graduate School for the Creation of New Photonics Industries, Shizuoka, Japan
  • Correspondence: Ryo Asaoka, Department of Ophthalmology, the University of Tokyo Graduate School of Medicine, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan; rasaoka-tky@umin.ac.jp
Investigative Ophthalmology & Visual Science June 2021, Vol.62, 4. doi:https://doi.org/10.1167/iovs.62.7.4
  • Views
  • PDF
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Shuichiro Aoki, Atsuya Miki, Takashi Omoto, Yuri Fujino, Masato Matsuura, Hiroshi Murata, Ryo Asaoka; Biomechanical Glaucoma Factor and Corneal Hysteresis in Treated Primary Open-Angle Glaucoma and Their Associations With Visual Field Progression. Invest. Ophthalmol. Vis. Sci. 2021;62(7):4. https://doi.org/10.1167/iovs.62.7.4.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose: To investigate the relationship between biomechanical glaucoma factor (BGF) measured with Corvis ST and glaucomatous visual field (VF) progression, compared to corneal hysteresis (CH) measured with ocular response analyzer using a longitudinal dataset of primary open-angle glaucoma (POAG). The discriminative powers of BGF and CH were also compared using a cross-sectional dataset.

Methods: The longitudinal dataset included 166 POAG eyes. The rate of VF change during the follow-up period was evaluated using the mean of 52 pointwise total deviations in the Humphrey 24-2 field test. Variables associated with the VF progression rate were identified from BGF, CH, age, baseline VF severity, and intraocular pressure during the VF follow-up period by identifying the optimal model. The cross-sectional dataset included 68 POAG eyes and 68 healthy eyes. Using this dataset, the area under the curve (AUC) values of the receiver-operating curve were compared between CH and BGF.

Results: The optimal multivariate linear mixed model to describe the VF rate included age and CH, but not BGF. Between POAG and healthy eyes, CH was statistically different (P < 0.001), although this was not the case with BGF. The AUC values were 0.61 and 0.71 for BGF and CH, respectively (P = 0.027).

Conclusions: CH, but not BGF, was associated with VF progression in POAG patients under treatment. BGF was not useful to discriminate POAG between treated and normal eyes.

Intraocular pressure (IOP) is a major contributor of glaucoma development and progression.1,2 However, visual field (VF) progression can be observed in 20% of patients with primary open-angle glaucoma (POAG), even after a 30% reduction in IOP.3 A wide range of VF progression rates in POAG eyes in the real-world setting cannot be fully explained based only on the IOP.4 Therefore, the variables related to VF progression in patients with glaucoma, other than IOP, must be examined. 
Corneal biomechanical properties are good examples of such variables and can be measured with two clinical devices currently. Corneal hysteresis (CH), measured using the ocular response analyzer (ORA; Reichert Inc., Depew, NY), reflects damping capacity of the cornea.5 Low CH is associated with the diagnosis,6 development,7 severity,8 and progression of glaucoma.9,10 Furthermore, a prospective study indicated the effect of IOP on rates of VF progression depended on CH.9 By contrast, the clinical application of an ultra-high-speed Scheimpflug camera provides detailed images of the corneal deformation induced by the application of an air jet in the corneal visualization Scheimpflug technology (Corvis ST, Oculus GmbH, Wetzlar, Germany). This yields a number of corneal dynamic response parameters; our previous studies suggested the usefulness of such parameters when analyzing the severity8 and VF progression11 of POAG. 
Very recently, a novel Corvis ST-related parameter (biomechanical glaucoma factor [BGF]) was developed to distinguish the eyes with normal tension glaucoma (NTG) from healthy eyes by calculating the optimal combination of Corvis ST parameters.12 However, the usefulness of BGF was merely validated through an internal cross-validation (three folds) in a single dataset (70 healthy individuals and 70 NTG patients). Moreover, the association of BGF with VF progression has not been investigated. In particular, the usefulness of BGF in a broader glaucoma subtype, such as POAG, has not yet been examined, and thus requires assistance in interpreting BGF in terms of biomechanical properties that are involved in disease pathogenesis. 
The present study aimed to evaluate relationships between rates of VF change and values of BGF and CH in POAG under treatment, using a longitudinal dataset. The discrimination abilities of BGF and CH between POAG and normal control eyes were also compared, using a cross-sectional dataset. 
Method
A total of 192 eyes of 134 POAG patients and 68 normal eyes of 68 people, obtained at the University of Tokyo Hospital, Osaka University, and Seirei Hamamatsu General Hospital, were included in this retrospective study. The Research Ethics Committees of the Graduate School of Medicine and Faculty of Medicine at the University of Tokyo, Osaka University, and Seirei Hamamatsu General Hospital approved this study. All participants signed a written informed consent for their clinical information to be stored in the hospital database and used for research. The present study was conducted according to the tenets of the Declaration of Helsinki. 
POAG was diagnosed using the following criteria: (1) typical glaucomatous changes in the optic nerve head (ONH), such as a rim notch with a rim width of ≦0.1 disc diameters or a vertical cup-to-disc ratio of >0.7, and/or a retinal nerve fiber layer defect with its edge at the ONH margin greater than a major retinal vessel; (2) glaucomatous VF defects compatible with the ONH changes that fulfill the Anderson-Patella criteria13 on two consecutive occasions; (3) the absence of systemic or ocular history or existing factors that could explain glaucomatous change or raised IOP. 
The healthy control group included participants with no abnormal eye-related findings except for clinically insignificant senile cataract and no history of ocular diseases. This healthy control group served as the normal control in the cross-sectional analysis, which is described later. 
Subjects were excluded if they presented systemic or ocular conditions that affect intraocular pressure or visual field. These include a history of systemic corticosteroid, narrow angle, clinically significant cataract, and ocular surgeries (except for uneventful intraocular lens implantation). Patients younger than 20 years old were also excluded. POAG eyes under topical medication were not excluded. 
Corvis ST and ORA measurements were conducted on the same day with a 15 minute interval between the two measurements. The order of the measurements was randomly determined. The axial length was measured using the IOLMaster, ver. 5.02 (Carl Zeiss Meditec, CA). IOP was measured with a Goldmann applanation tonometer throughout the observation period. VF was measured using the Humphrey Field Analyzer II (Carl Zeiss Meditec Inc., Dublin, CA) either with a 24-2 or 30-2 SITA-standard program. Reliable VF was defined as the fixation loss, false-positive results, and false-negative results less than 33%. 
Corvis ST Measurement
The principles of Corvis ST measurements were described thoroughly elsewhere.14 The high-speed Scheimpflug camera records 140 images of the cornea with a transient indentation in 30 ms after the application of an air impulse. The corneal response is characterized by two applanations during the inward and outward corneal movements, respectively; the highest concavity (HC) is defined as the maximal displacement of the corneal apex. Parameters provided by the current version of the Corvis ST software (software version 1.6r2036) include applanation length, velocity, and time of the two applanations; corneal deflection amplitude, radius, and time at HC; and several biomechanical indices calculated using the software. Some of the parameters relevant to BGF derivation are described below. Corvis ST measurements were conducted thrice, and the results were averaged. Only reliable Corvis ST measurements were used, based on the “OK” quality index displayed on the device monitor. 
BGF was calculated using the formula below:12 
\begin{eqnarray*}Beta = 34.128 + 2.64 \times DARatioProg - 0.641 \times HCTime - \\ \!\! 0.049 \times PachySlope - 0.202 \times bIOP - 0.036 \times CCT\end{eqnarray*}
 
\begin{equation*}BGF\; = \frac{{EXP\left( {Beta} \right)}}{{EXP\left( {Beta} \right) + 1}}\end{equation*}
 
  • DARatioProg: “Deformation amplitude ratio progression” represents the increase ratio of the deformation amplitude from the corneal apex toward the periphery. Higher DARatioProg values indicate a stiffer cornea.12
  • HC time: “Highest concavity time” refers to the timing of the highest concavity.
  • PachySlope: “Pachymetry slope” represents the difference in corneal thickness from the corneal apex toward the periphery. A smaller PachySlope indicates a relatively thin cornea in the periphery compared with that in the central region.
  • CCT stands for “Central corneal thickness.”
  • bIOP: “Biomechanical IOP” is described as the corrected estimate of IOP obtained using the Corvis ST following the finite element method, adjusted for CCT and age variations.15
BGF ranges from 0 to 1; a higher value indicates a higher possibility of glaucoma.12 
ORA Measurement
Details of the ORA measurement are summarized elsewhere.16 The ORA records two applanation pressures, namely, prior to and following an indentation of the cornea after the application of a rapid air jet. Because of its viscoelastic property, the cornea dissipates a part of the energy given off the air jet, resulting in a delay in the outward corneal movement and thus causing the difference in the pressures at the inward and outward applanation. This difference is called CH.17 The ORA measurement was conducted thrice. Only the measurements with a quality index of >7.0 were used, and the average value was used in the analysis. 
Statistical Analysis
Longitudinal Analysis (VF Progression Analysis)
A longitudinal dataset comprising 166 eyes of 108 POAG patients was used to examine the association of BGF/CH with VF progression. POAG eyes were included in this dataset if they had at least eight reliable VFs, excluding the initial VF, for a minimum period of four years. Topical prostaglandin analogue use throughout the VF follow-up was also required to adjust for the potential influence of the therapeutics on corneal biomechanical measures, as was reported.1820 
We used the mean total deviation (mTD) of the 52 test points overlapping with the 24-2 HFA test to estimate the progression. The mTD progression rate was evaluated by linearly regressing mTD values against time using the latest eight VFs. Linear mixed models were used to investigate the relationship between the mTD progression rate and the BGF, CH, CCT, axial length, baseline age, baseline mTD at first VF, and mean IOP throughout the period where eight VFs were examined. As both eyes of patients were included in the longitudinal dataset and measurements would be highly correlated, each patient was regarded as having a random effect. This condition was modeled by fitting a linear model using the maximum likelihood method with a varying-intercept group effect. Then, model selection was used to identify the optimal linear mixed model for the mTD progression rate according to the second-order of the bias-corrected Akaike information criterion index (AICc), from all two7 patterns using the seven tested variables. The AIC is a well-known statistical measurement used in model selection. The AICc is a corrected version of the AIC, which provides an accurate estimation even when the sample size is small.21 The detail of AICc is described later in this section. 
Cross-Sectional Analysis (Comparison of CH and BGF Between Normal and Glaucoma Eyes)
For this purpose, a cross-sectional dataset was used, which comprised 68 eyes of 68 POAG patients (POAG group) and 68 eyes of 68 healthy people (normal group) who underwent Corvis ST and ORA measurements. One eye was randomly selected for the analysis if both eyes satisfied the inclusion criteria. The two groups were matched for number of eyes and age. The values of CH, BGF, and five Corvis ST parameters comprising BGF were compared between normal and POAG eyes. The discrimination ability of BGF was investigated through the area under the receiver operating characteristics curve (AUC) using a method by Delong et al.22 for a comparison with CH. To better understand the mechanism of BGF on the diagnosis of glaucoma, variables that were useful for discriminating POAG eyes from normal eyes were identified by selecting the optimal multivariate logistic regression model with AICc, among five parameters comprised BGF (DARatioProg, HC time, PachySlope, CCT and bIOP), where the logistic model was assumed to have a linear relationship between the predictor variables and log-odds of POAG involvement. 
In a multivariate regression model, the degrees of freedom decreases as the number of variables increases; hence, model selection methods should be used for better model fitting by removing redundant variables.23,24 A decrease in the AICc values suggests an improvement of the model; the relative likelihood that a model (modelx with AICcx) minimizes information loss compared with a model with the smallest AICc (modelmin with AICcmin) was calculated as exp ((AICcmin − AICcx)/2).25 
Holm's method was used to adjust the Pvalues for the problem of multiple testings.26 The statistical programming language “R” (R version 3.3.1; the foundation for Statistical Computing, Vienna, Austria) was used to conduct all statistical analyses. 
Results
VF Progression Analysis (Longitudinal Analysis)
The longitudinal dataset included 166 eyes of 108 patients. The demographics for this dataset are shown in Table 1. The univariate relationship between the mTD progression rate and various parameters are shown in Table 2. Age and CH were significantly related to the mTD progression rate (P = 0.025 and 0.027, respectively; linear mixed model), but BGF was not (P = 0.61). The optimal model for the mTD progression rate was as follows: mTD progression rate = −0.53 − 0.0065 × age + 0.062 × CH (AICc = 172.27). The relative likelihood that a null hypothesis (a model without covariates; AICc = 176.24) minimizes information loss compared with the optimal model was 0.083. 
Table 1.
 
Baseline Demographics of the Longitudinal Dataset
Table 1.
 
Baseline Demographics of the Longitudinal Dataset
Table 2.
 
Univariate Relationship Between mTD Progression Rate and Various Parameters of the Longitudinal Dataset
Table 2.
 
Univariate Relationship Between mTD Progression Rate and Various Parameters of the Longitudinal Dataset
Comparison of CH and BGF Between Normal and Glaucoma Eyes
The cross-sectional dataset included 68 eyes of 68 POAG patients and 68 eyes of 68 healthy subjects. Forty-two eyes of 42 patients with POAG were derived from the longitudinal dataset. The baseline demographics of this dataset are shown in Table 3. The two groups were matched for age (P = 1). BGF was not significantly different between the two groups (P = 0.27). PachySlope and CH were significantly lower (P = 0.0014, 0.00018, respectively) in POAG eyes than in healthy eyes. Of the 68 POAG eyes, 64 were under some topical anti-IOP medication. In particular, 56, 40, and 32 POAG eyes were treated with topical prostaglandin analogue, beta blocker, and carbonic anhydrase inhibitor, respectively. 
Table 3.
 
Baseline Demographics of the Cross-Sectional Dataset
Table 3.
 
Baseline Demographics of the Cross-Sectional Dataset
The receiver operating characteristic curves of BGF and CH for discriminating POAG eyes from normal eyes are shown in Figure. The AUC value was 0.61 (95% confidence interval [CI]: 0.51–0.70) and 0.71 (95% CI: 0.62–0.80) for BGF and CH, respectively. The two AUC values were significantly different (P = 0.027 with Delong's method). 
Figure.
 
Receiver operating characteristic curves of BGF and CH for discriminating POAG eyes from normal eyes.
Figure.
 
Receiver operating characteristic curves of BGF and CH for discriminating POAG eyes from normal eyes.
An optimal multivariate logistic regression model to discriminate POAG eyes from healthy eyes, identified using AICc, where predictor variables were selected from five parameters comprising BGF, was: log(P/(1 − P)) = 2.39 − 0.061 × PachySlope, where P stands for the probability that an eye has POAG. This gives an explicit formula for P: P = 1/(1 + exp (2.39 − 0.061 × PachySlope )) (AICc = 177.85). The odds ratio of PachySlope was 0.94 (95% CI: [0.91, 0.97]). 
Discussion
In the present study, the relationship between BGF, in comparison to CH, and VF progression rate in POAG was examined using eight VFs from 166 eyes of 108 participants. Age and CH were included in the optimal model to determine the mTD progression rate. In addition, the differences in BGF and CH between POAG and normal eyes were investigated using a cross-sectional dataset. CH had a higher AUC value than that of BGF. 
BGF is a novel Corvis ST index that was constructed to distinguish eyes with OAG (NTG) from normal eyes.12 The reported AUC to distinguish glaucoma eyes from normal eyes was 0.81. The present study reported a relatively lower AUC value (0.61). CH is an established risk factor for glaucoma development and progression.510 In the present study, the AUC of CH was 0.71 and was significantly higher than that of BGF. Our results suggested that BGF is not useful in diagnosing POAG in the current population, which may be due to the broader background of glaucoma patients (POAG, not only NTG) in contrast to the original study in which BGF were developed,12 as discussed later. 
A multivariate analysis of the longitudinal dataset suggested that BGF was not significantly associated with glaucoma progression. This could be because BGF was derived from cross-sectional data.12 Age and CH were significantly associated with VF progression, which is consistent with the findings of several studies demonstrating the association of CH9,10 with glaucoma progression. Previous studies suggest that CH reflects the damping capacity of the cornea5,17,27; the eyes with higher CH may have an ONH structure that protects the optic nerve axons from external stress such as IOP, thus preventing glaucoma progression.2832 Furthermore, the correlation between CH and VF progression may be accounted for by the correlation between CH and (measured) IOP; that is, CH is correlated with a real IOP and also affects IOP measurement.33 The absence of IOP in the optimal linear mixed model does not indicate IOP is not associated with the progression of VF, because the effect of IOP may be masked by the inclusion of CH in the optimal model. In addition, the currently analyzed patients were under IOP-reduction treatment. Indeed, both progression rate and mean IOP in the longitudinal dataset were rather low: –0.26 ± 0.43 dB/year and 13.13 ± 2.07 mmHg, respectively. These values were even lower than those reported in several recent studies, which indicated the VF progression rate based on the data obtained in real-world settings. Heijl et al. reported a VF progression rate of −0.80 dB/year (mean IOP: 18.1–20.2 mmHg), obtained from 583 OAG patients.34 De Moraes et al. reported a −0.45 dB/year VF progression rate (mean IOP: 15.2 mmHg), obtained from 587 glaucoma patients.35 Low IOP and resulting slow VF progression could make less detectable the association of the investigated parameters. 
BGF was empirically derived from five Corvis ST measurements in NTG patients and normal controls; thus, it is not easy to interpret the medical mechanism. In particular, the relationship between the five Corvis ST variables and glaucoma remains inexplicable compared with that between CH and glaucoma. Analysis of the cross-sectional dataset revealed that lower PachySlope value was significantly correlated with the diagnosis of POAG. A lower PachySlope indicates more homogeneity in the thickness of the cornea, which is more common in eyes with NTG than in those with ocular hypertension.36 However, other variables, including CCT, DARatioProg, and HCtime, were not significantly different between the POAG and healthy control eyes. This is in disagreement with the study by Karin et al; the NTG population had lower CCT than that of the normal controls.12 It has been suggested that a thinner CCT increases the likelihood of conversion from ocular hypertension to glaucoma.1,2 CCT has a significant effect on the Goldmann applanation tonometry measurement, which leads to an underestimation of the IOP. Furthermore, a thin CCT has been reported as an independent risk factor for glaucoma development (even when correcting for an underestimation of IOP).37 The current population has a CCT that is similar to that of the healthy controls, probably due to the broader glaucoma subtype with different baseline IOP before treatment was administered. This may have weakened the relationship between BGF and POAG. DARatioProg and HCtime should be influenced not only by corneal biomechanical properties like stiffness itself12 but true IOP, as was suggested from the reported influence of IOP on Corvis ST dynamic corneal response parameters.38,39 Thus, Karin et al. claimed that BGF should include bIOP for adjustment.12 In the current dataset, POAG eyes indeed had a similar bIOP value of 13.06 mmHg compared with that in their report (13.5 mmHg for NTG eyes); however, it should be noted the current POAG population was already under IOP-reduction treatments, and the unavailable baseline IOP would have been higher. The lowered IOP, together with changes in other biomechanical measures such as DARatioProg and HCtime, may have weakened the potential relationship between BGF and POAG. To summarize, a broader range of the glaucoma population was being treated to induce lower IOP, which could have masked the possible BGF difference between POAG eyes and normal eyes. Our findings should be corroborated in a future study that compares untreated POAG and NTG cases to shed light on a potential different pathogeneses that occur between NTG and broader POAG. 
The present study has some limitations. Our population probably included both POAG and NTG patients. We could not distinguish them because the baseline IOP value was not available; many of the patients who referred to our hospitals from other clinics had already undergone IOP-reduction therapy. However, most of the cases analyzed were NTG cases due to the mean IOP level (13.13 mmHg) in the longitudinal dataset being considerably low. This is a glaucoma subtype common in Japanese individuals. A representative survey of the prevalence of glaucoma in Japan reported that 92% of POAG cases was NTG.40 Another limitation of the present study is the effect of anti-glaucoma eye drops on the corneal biomechanical properties. Of the POAG population that were included in the cross-sectional study, 82.4% (56 out of 68 eyes) used a prostaglandin analogue, which was similar to a previous report (82%).12 Anti-IOP agents can alter the cornea's biomechanical properties4143; in particular, clinical studies have demonstrated that chronic use of a topical prostaglandin analogue significantly affects CH.1820 This implies that there are similar effects on Corvis ST-related parameters, such as BGF, because it also uses air jet applications. We conducted this study to compare BGF with CH using POAG patients under treatment, following a method used in a previous study12; however, a future study should investigate the usefulness of BGF in diagnosing glaucoma using untreated patients. Moreover, due to the high prevalence of myopia in Japan,44 the current population included a relatively large proportion of myopic eyes (Table 1 and 3). Myopic eyes reportedly exhibited a different response to ORA and the Corvis ST measurement4547; thus, the effect of the refraction status should be investigated in a future study. 
In conclusion, CH was significantly associated with VF progression in POAG eyes undergoing treatment, but BGF was not. CH had a higher AUC value than BGF. The discriminative power of BGF should be validated further with treatment-naïve cases. 
Acknowledgments
The authors thank Enago (www.enago.jp) for the English language review. 
Supported by the Translational Research program; Strategic Promotion for practical application of Innovative medical Technology, TR-SPRINT, from the Japan Agency for Medical Research and Development, AMED, Grants 18KK0253 and 17K11418 from the Ministry of Education, Culture, Sports, Science, and Technology of Japan and Japan Science and Technology Agency (JST) CREST JPMJCR1304. 
Disclosure: S. Aoki, None; A. Miki, Santen Pharmaceuticals (F, R), Sensimed (F), Nitto Medic (R), Pfizer Japan (R), Otsuka Pharmaceuticals (R), Novartis Pharma (R), Topcon (R), SEED (R), Senju Pharmaceutical (R), Kowa Pharmaceuticals (R); T. Omoto, None; Y. Fujino, None; M. Matsuura, None; H. Murata, None; R. Asaoka, OCULUS (F), Reichert (F), KOWA (F), HAAG-STREIT (F), NIDEK (F), CenterVue (F) 
References
Kass MA, Heuer DK, Higginbotham EJ, et al. The Ocular Hypertension Treatment Study: a randomized trial determines that topical ocular hypotensive medication delays or prevents the onset of primary open-angle glaucoma. Arch Ophthalmol. 2002; 120: 701–713; discussion 829-30. [CrossRef] [PubMed]
Heijl A, Leske MC, Bengtsson B, Hyman L, Bengtsson B, Hussein M. Reduction of intraocular pressure and glaucoma progression: results from the Early Manifest Glaucoma Trial. Arch Ophthalmol. 2002; 120: 1268–1279. [CrossRef] [PubMed]
The effectiveness of intraocular pressure reduction in the treatment of normal-tension glaucoma. Collaborative Normal-Tension Glaucoma Study Group. Am J Ophthalmol. 1998; 126: 498–505. [CrossRef] [PubMed]
Fujino Y, Asaoka R, Murata H, et al. Evaluation of glaucoma Pprogression in large-scale clinical data: The Japanese Archive of Multicentral Databases in Glaucoma (JAMDIG). Invest Ophthalmol Vis Sci. 2016; 57: 2012–2020. [CrossRef] [PubMed]
Roberts CJ. Concepts and misconceptions in corneal biomechanics. J Cataract Refract Surg. 2014; 40: 862–869. [CrossRef] [PubMed]
Detry-Morel M, Jamart J, Hautenauven F, Pourjavan S. Comparison of the corneal biomechanical properties with the ocular response analyzer (ORA) in African and Caucasian normal subjects and patients with glaucoma. Acta Ophthalmol. 2012; 90: e118–e124. [CrossRef] [PubMed]
Susanna CN, Diniz-Filho A, Daga FB, et al. A prospective longitudinal study to investigate corneal hysteresis as a risk factor for predicting development of glaucoma. Am J Ophthalmol. 2018; 187: 148–152. [CrossRef] [PubMed]
Hirasawa K, Matsuura M, Murata H, et al. Association between corneal biomechanical properties with ocular response analyzer and also CorvisST tonometry, and glaucomatous visual field everity. Transl Vis Sci Technol. 2017; 6: 18. [CrossRef] [PubMed]
Medeiros FA, Meira-Freitas D, Lisboa R, Kuang TM, Zangwill LM, Weinreb RN. Corneal hysteresis as a risk factor for glaucoma progression: a prospective longitudinal study. Ophthalmology. 2013; 120: 1533–1540. [CrossRef] [PubMed]
De Moraes CV, Hill V, Tello C, Liebmann JM, Ritch R. Lower corneal hysteresis is associated with more rapid glaucomatous visual field progression. J Glaucoma. 2012; 21: 209–13. [CrossRef] [PubMed]
Matsuura M, Hirasawa K, Murata H, Nakakura S, Kiuchi Y, Asaoka R. The usefulness of CorvisST tonometry and the cular response analyzer to assess the progression of glaucoma. Sci Rep. 2017; 7: 40798. [CrossRef] [PubMed]
Pillunat KR, Herber R, Spoerl E, Erb C, Pillunat LE. A new biomechanical glaucoma factor to discriminate normal eyes from normal pressure glaucoma eyes. Acta Ophthalmol. 2019; 97: e962–e967. [PubMed]
Anderson DR, Patella VM. Automated Static Perimetry, 2nd ed. St.Louis: Mosby; 1999.
Koprowski R. Automatic method of analysis and measurement of additional parameters of corneal deformation in the Corvis tonometer. Biomed Eng Online. 2014; 13: 150. [CrossRef] [PubMed]
Joda AA, Shervin MM, Kook D, Elsheikh A. Development and validation of a correction equation for Corvis tonometry. Comput Methods Biomech Biomed Engin. 2016; 19: 943–953. [CrossRef] [PubMed]
Matsuura M, Hirasawa K, Murata H, et al. The relationship between Corvis ST tonometry and ocular response analyzer measurements in eyes with glaucoma. PLoS One. 2016; 11: e0161742. [CrossRef] [PubMed]
Dupps WJ, Jr. Hysteresis: new mechanospeak for the ophthalmologist. J Cataract Refract Surg. 2007; 33: 1499–1501. [CrossRef] [PubMed]
Tsikripis P, Papaconstantinou D, Koutsandrea C, Apostolopoulos M, Georgalas I. The effect of prostaglandin analogs on the biomechanical properties and central thickness of the cornea of patients with open-angle glaucoma: a 3-year study on 108 eyes. Drug Des Devel Ther. 2013; 7: 1149–1156. [PubMed]
Bolívar G, Sánchez-Barahona C, Teus M, et al. Effect of topical prostaglandin analogues on corneal hysteresis: author's reply. Acta Ophthalmol. 2017; 95: e152. [CrossRef] [PubMed]
Meda R, Wang Q, Paoloni D, Harasymowycz P, Brunette I. The impact of chronic use of prostaglandin analogues on the biomechanical properties of the cornea in patients with primary open-angle glaucoma. Br J Ophthalmol. 2017; 101: 120–125. [CrossRef] [PubMed]
Burnham KP, Anderson DR. Multimodel inference. Sociol Methods Res. 2016; 33: 261–304. [CrossRef]
DeLong ER, DeLong DM, Clarke-Pearson DL. Comparing the areas under two or more correlated receiver operating characteristic curves: a nonparametric approach. Biometrics. 1988; 44: 837–845. [CrossRef] [PubMed]
Tibshirani RJ, Taylor J. Degrees of freedom in lasso problems. Ann Stat. 2012; 40: 1198–1232. [CrossRef]
Mallows CL. Some Comments on C p. Technometrics. 1973; 15: 661–675.
Burnham KP, Anderson DR. Multimodel inference understanding AIC and BIC in model selection. Sociol Methods Res. 2004; 33: 261–304. [CrossRef]
Holm S. A Simple sequentially rejective multiple test procedure. Scand J Stat. 1979; 6: 65–70.
Luce D, Taylor D. Determining in vivo biomechanical properties of the cornea with an ocular response analyzer. J Cataract Refract Surg. 2005; 31: 156–162. [CrossRef] [PubMed]
Aoki S, Murata H, Nakakura S, et al. Correlation between elastic energy stored in an eye and visual field progression in glaucoma. PLoS One. 2018; 13: e0204451. [CrossRef] [PubMed]
Uysal BS, Yulek F, Nalcacioglu P, Sarac O, Yorgun MA, Cagil N. Can corneal biomechanical properties give clues about elasticity of optic nerve scleral component in nonarteritic anterior ischemic optic neuropathy? J Neuroophthalmol. 2016; 36: 285–289. [CrossRef] [PubMed]
Lanzagorta-Aresti A, Perez-Lopez M, Palacios-Pozo E, Davo-Cabrera J. Relationship between corneal hysteresis and lamina cribrosa displacement after medical reduction of intraocular pressure. Br J Ophthalmol. 2017; 101: 290–294. [PubMed]
Wells AP, Garway-Heath DF, Poostchi A, Wong T, Chan KC, Sachdev N. Corneal hysteresis but not corneal thickness correlates with optic nerve surface compliance in glaucoma patients. Invest Ophthalmol Vis Sci. 2008; 49: 3262–3268. [CrossRef] [PubMed]
Perez-Bartolome F, Martinez de la Casa JM, Camacho Bosca I, et al. Correlating corneal biomechanics and ocular biometric properties with lamina cribrosa measurements in healthy subjects. Semin Ophthalmol. 2018; 33: 223–230. [CrossRef] [PubMed]
Touboul D, Roberts C, Kérautret J, et al. Correlations between corneal hysteresis, intraocular pressure, and corneal central pachymetry. J Cataract Refract Surg. 2008; 34: 616–622. [CrossRef] [PubMed]
Heijl A, Buchholz P, Norrgren G, Bengtsson B. Rates of visual field progression in clinical glaucoma care. Acta Ophthalmol. 2013; 91: 406–412. [CrossRef] [PubMed]
De Moraes CG, Juthani VJ, Liebmann JM, et al. Risk factors for visual field progression in treated glaucoma. Arch Ophthalmol. 2011; 129: 562–568. [CrossRef] [PubMed]
Jordan JF, Joergens S, Dinslage S, Dietlein TS, Krieglstein GK. Central and paracentral corneal pachymetry in patients with normal tension glaucoma and ocular hypertension. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie. 2006; 244: 177–182.
Francis BA, Varma R, Chopra V, Lai MY, Shtir C, Azen SP. Intraocular pressure, central corneal thickness, and prevalence of open-angle glaucoma: the Los Angeles Latino Eye Study. Am J Ophthalmol. 2008; 146: 741–746. [CrossRef] [PubMed]
Roberts CJ, Liu J. Corneal Biomechanics: From Theory to Practice. Amsterdam: Kugler Publications; 2017.
Kling S, Marcos S. Contributing factors to corneal deformation in air puff measurements. Invest Ophthalmol Vis Sci. 2013; 54: 5078–5085. [CrossRef] [PubMed]
Suzuki Y, Iwase A, Araie M, et al. Risk factors for open-angle glaucoma in a Japanese population: the Tajimi Study. Ophthalmology. 2006; 113: 1613–1617. [CrossRef] [PubMed]
Zhong Y, Shen X, Yu J, Tan H, Cheng Y. The comparison of the effects of latanoprost, travoprost, and bimatoprost on central corneal thickness. Cornea. 2011; 30: 861–864. [CrossRef] [PubMed]
Nielsen CB, Nielsen PJ. Effect of alpha- and beta-receptor active drugs on corneal thickness. Acta Ophthalmol (Copenh). 1985; 63: 351–354. [CrossRef] [PubMed]
Sawada A, Yamamoto T. Switching efficacy on intraocular pressure from latanoprost to bimatoprost in eyes with open angle glaucoma: implication to the changes of central corneal thickness. Jpn J Ophthalmol. 2014; 58: 423–428. [CrossRef] [PubMed]
Ueda E, Yasuda M, Fujiwara K, et al. Trends in the prevalence of myopia and myopic maculopathy in a Japanese population: the Hisayama Study. Invest Ophthalmol Vis Sci. 2019; 60: 2781–2786. [CrossRef] [PubMed]
Wong YZ, Lam AK. The roles of cornea and axial length in corneal hysteresis among emmetropes and high myopes: a pilot study. Curr Eye Res. 2015; 40: 282–289. [CrossRef] [PubMed]
Chansangpetch S, Panpruk R, Manassakorn A, et al. Impact of myopia on corneal biomechanics in glaucoma and nonglaucoma patients. Invest Ophthalmol Vis Sci. 2017; 58: 4990–4996. [CrossRef] [PubMed]
Wu W, Dou R, Wang Y. Comparison of corneal biomechanics between low and high myopic eyes-A Meta-analysis. Am J Ophthalmol. 2019; 207: 419–425. [CrossRef] [PubMed]
Figure.
 
Receiver operating characteristic curves of BGF and CH for discriminating POAG eyes from normal eyes.
Figure.
 
Receiver operating characteristic curves of BGF and CH for discriminating POAG eyes from normal eyes.
Table 1.
 
Baseline Demographics of the Longitudinal Dataset
Table 1.
 
Baseline Demographics of the Longitudinal Dataset
Table 2.
 
Univariate Relationship Between mTD Progression Rate and Various Parameters of the Longitudinal Dataset
Table 2.
 
Univariate Relationship Between mTD Progression Rate and Various Parameters of the Longitudinal Dataset
Table 3.
 
Baseline Demographics of the Cross-Sectional Dataset
Table 3.
 
Baseline Demographics of the Cross-Sectional Dataset
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×