Literature DB >> 34232432

Comparative analysis of the morphological and biomechanical properties of normal cornea and keratoconus at different stages.

Ying Wu1, Li-Li Guo2, Lei Tian3,4, Ze-Quan Xu1, Qian Li1, Jian Hu1, Yi-Fei Huang1, Li-Qiang Wang5.   

Abstract

PURPOSE: To compare the morphological and biomechanical properties of normal cornea and keratoconus at different stages.
METHODS: A total of 408 patients (517 eyes) with keratoconus were included in this study. According to the Topographic Keratoconus (TKC) grading method, keratoconus was divided into stage I (TKC = 1, 130 eyes), stage II (TKC = 1-2, 2, 164 eyes), stage III (TKC = 2-3, 3, 125 eyes) and stage IV (TKC = 3-4, 4, 98 eyes). A total of 158 normal subjects (158 eyes) were recruited as the normal group. The corneal morphological parameters and biomechanical parameters were obtained with Scheimpflug tomography (Pentacam) and corneal visualization Scheimpflug technology (Corvis ST), and the receiver operating characteristic (ROC) curves were drawn.
RESULTS: Each corneal morphological and most biomechanical parameters of the keratoconic eyes were significantly different from those of the normal eyes in this study (p < 0.001). ROC curve demonstrated that most parameters in this study showed high efficiency in diagnosing keratoconus (the area under the ROC (AUC) was > 0.9), with the Belin-Ambrósio deviation (BAD-D) and Tomographic and Biomechanical Index (TBI) showing higher efficiency. The efficiency of BAD-D and TBI was high in differentiating keratoconus at different stages (AUC > 0.963). The comparison of ROC curves of keratoconus at different stages did not reveal statistically significant differences for TBI.
CONCLUSION: BAD-D and TBI can effectively diagnose stage I keratoconus. Moreover, the efficiency of TBI is the same in diagnosing keratoconus at all stages, while the diagnostic efficiency of other parameters increases with the increase in keratoconus stages.
© 2021. The Author(s).

Entities:  

Keywords:  Corneal biomechanics; Corneal morphology; Corneal visualization Scheimpflug technology; Keratoconus

Mesh:

Year:  2021        PMID: 34232432      PMCID: PMC8536578          DOI: 10.1007/s10792-021-01929-4

Source DB:  PubMed          Journal:  Int Ophthalmol        ISSN: 0165-5701            Impact factor:   2.031


Introduction

Keratoconus is a chronic progressive disease, characterized by thinning of the central or para-central corneal stroma and protruding conical shape [1]. The majority of keratoconus patients are adolescents, and 90% of cases are binocular, often with asymmetric progression in both eyes [2, 3]. During keratoconus progression, the Bowman's membrane breaks, leading to the development of disproportion in the compositions of collagen fibers. The increase in protein kinase and other catabolic enzymes and the decrease in protein kinase inhibitor in cornea lead to the destruction of corneal stroma structure, causing instability of corneal biomechanical properties and the weakening of mechanical strength [4, 5]. Therefore, the diagnosis of keratoconus by analyzing corneal biomechanical properties has become a research hotspot. The ocular response analyzer (ORA) [6] and the corneal visualization Scheimpflug technology (Corvis ST) [7] are the only in vivo corneal biomechanical measurement equipment currently used in clinical practice. Both devices utilize the reaction of cornea under the action of fast air pulse to indirectly evaluate the biomechanical properties of cornea [8]. Although studies have reported that the corneal hysteresis (CH) and corneal resistance factor (CRF) of typical keratoconus measured by ORA are lower than those of normal cornea, their distributions mostly overlap; thus, their sensitivity and specificity in diagnosing keratoconus are relatively low [9]. And the limited corneal detection area of ORA results in poor diagnostic ability of CH and CRF in normal cornea and early keratoconus. The biomechanical parameters measured with early version of Corvis ST (1.00r30) have been proven to be significantly different between keratoconus and normal cornea. Among them, the maximum compression depth (DA) is efficient in diagnosing keratoconus, but could be easily affected by intraocular pressure (IOP); thus, its efficiency in diagnosing mild keratoconus is low [10]. With the update of Corvis ST software (1.5r1902), some new parameters have been incorporated [11], including the maximum value of the ratio between the deformation amplitude at the apex and at 2 mm from the central apex (DA Ratio 2), Ambrósio related thickness to the horizontal profile (ARTh), inverse of the radius of curvature during the concave phase of the deformation (Integrated Radius), stiffness parameter at first application (SPA1) and Corvis biomechanical index (CBI), as well as Tomographic and Biomechanical Index (TBI), which was obtained with combined use of Pentacam and Corvis ST. Studies have shown that these new parameters are highly efficient in diagnosing keratoconus [12-14]. However, there are few studies on the combined use of Pentacam and Corvis ST for keratoconus at different stages. The purpose of this study is to measure and compare the morphological and biomechanical properties of normal cornea and keratoconus at different stages. Moreover, the efficiency of corneal morphological and biomechanical parameters in diagnosing keratoconus at different stages was explored and compared the diagnostic efficacy among new parameters.

Patients and methods

Study group A total of 408 keratoconus patients (517 eyes) and 158 normal subjects (158 eyes) who visited Chinese PLA General Hospital and Beijing Tongren Hospital from January 2018 to December 2019 were recruited. Given that most keratoconus cases develop binocularly and progress asymmetrically, patients diagnosed as binocular keratoconus were included in this study, and the right eye of all normal subjects were included. According to the Topographic Keratoconus (TKC) grading method, keratoconus cases were divided into stage I (130 eyes), stage II (164 eyes), stage III (125 eyes) and stage IV (98 eyes). The study protocol was approved by the Chinese PLA General Hospital, Beijing, China and the ethics committee of Beijing Tongren Hospital, Capital Medical University. Informed consent was obtained from all participants. Inclusion criteria Keratoconus group: the diagnosis of keratoconus was based on the Rabinowitz criteria [15]. 1. A history of myopia and astigmatism, decreased vision, corrected visual acuity < 1.0; at least one of the following signs was positive in slit lamp examination: corneal stromal thinning, conical corneal protrusion, Fleischer ring, Vogt's striae, epithelial or subepithelial scar; corneal topography showed that diopter was > 47D in the central area of anterior corneal surface; the diopter difference between areas 3 mm below and above the central corneal area was > 3D; the difference in diopter of anterior surface of central corneal area between right and left eyes was > 1D. 2. The central corneal diopter was > 46.5D, the diopter difference between areas 3 mm above and below was > 1.26D, and the corneal diopter difference between right and left eyes of the same patient was > 0.92D. Keratoconus grading method [16]: Based on the TKC grading method provided by Pentacam, keratoconus patients were divided into stage I (TKC = 1) group, stage II (TKC = 1–2, 2) group, stage III (TKC = 2–3, 3) group and stage IV (TKC = 3–4, 4) group. Normal group: subjects were matched based on age and gender of patients in the keratoconus group. The inclusion criteria of the normal group were: binocular anterior surface curvature < 46.5D; posterior surface curvature < 57.2D; thinnest corneal thickness (TCT) > 490 μm [17]. Exclusion criteria Patients with the following conditions were excluded: other ocular diseases, trauma, surgery history, systemic diseases that could affect the eyes; patients who wore soft contact lens should have stopped wearing them for > 2 weeks; patients who wore hard contact lens should have stopped wearing them for > 1 month. Examinations All the subjects received routine ophthalmic examinations, including uncorrected distant vision, slit lamp microscopy and fundus examination. Additionally, corneal morphological parameters were obtained with Pentacam and biomechanical parameters were obtained with Corvis ST. Pentacam (Oculus Optikgeräte GmbH, Wetzlar, Germany, software version 1.20r134) is a commonly used corneal tomography image analysis instrument. It uses Scheimpflug camera to scan from the anterior surface of cornea to the posterior surface of lens and obtains the morphological parameters of anterior segment by calculating and analyzing the data collected. Corvis ST (Oculus Optikgeräte GmbH, Wetzlar, Germany, software version 1.5r1902) records the compression deformation of cornea caused by the air pulse with a high-speed Scheimpflug-camera. The bi-directional applanation and maximum compression status during the deformation are specially monitored and analyzed, so that the parameters reflecting the corneal biomechanical characteristics can be obtained. Pentacam and Corvis ST were operated by the same trained and skilled technicians. The display of "OK" indicated good measurement quality, and the record data were saved. Table1 shows the parameters of Pentacam and Corvis ST included in this study.
Table 1

Corneal morphological and biomechanical parameters obtained with Pentacam and Corvis ST

ParametersParameters
PentacamA2VThe second velocity of applanation
K1Steepest keratometric readingHCTTime from the start until the highest concavity
K2Flattest keratometric readingPDPeak distance
Km F Mean keratometry from the anterior corneal surfaceRadiusCentral curvature radius at the highest concavity
KmaxMaximum keratometry from the anterior corneal surfaceA1DfLDeflection length of the first applanation
Astig FCentral astigmatism from the anterior corneal surfaceHC DfLDeflection length of the highest concavity
CCTCentral corneal thicknessA2 DfLDeflection length of the second applanation
TPPachymetry at the thinnest pointA1 DfADeflection amplitude of the first applanation
ISVIndex of surface varianceHC DfADeflection amplitude of the highest concavity
IVAIndex of vertical asymmetryA2 DfADeflection amplitude of the second applanation
KI Keratoconus indexDA Ratio 2 The maximal value of the ratio between the deformation amplitude at the apex and at 2 mm from the corneal apex
CKICentral keratoconus indexDA Ratio 1 The maximal value of the ratio between the deformation amplitude at the apex and at 1 mm from the corneal apex
IHA Index of height asymmetryARThAmbrósio relational thickness to the horizontal profile
IHDIndex of height decentrationbIOPBiomechanical-corrected intraocular pressure
BAD-DBelin-Ambrósio deviationIntegrated RadiusInverse of the radius of curvature during the concave phase of the deformation
Corvis ST
A1TFirst applanation timeSPA1Stiffness parameter at the first applanation
A1VFirst velocity of applanationCBI Corvis biomechanical index
A2TSecond applanation timeTBITomographic and Biomechanical Index
Corneal morphological and biomechanical parameters obtained with Pentacam and Corvis ST Analysis index (Table1). Statistical methods Statistical analysis and drawing were completed with R language. 4.0.5(https://www.r-project.org/) and SPSS 20 (IBM Corp., Armonk, NY, USA). Shapiro test was used to test the normality of corneal morphological and biomechanical indexes; the mean ± standard deviation was adopted to describe the normal distribution of measurement data; the median and quartile were used to describe the non-normal data. Parameters of keratoconus at different stages and normal cornea were compared between the keratoconus group and the normal group with Kruskal–Wallis test, with p < 0.05 considered as statistically significant. Pairwise comparison was conducted with post-hoc test, and as multiple comparisons were made, the test level was corrected to 0.017 according to Bonferroni principle (p < 0.017 was considered as statistically significant). Receiver operating characteristic (ROC) curve was used to explore the diagnostic ability of corneal morphological and biomechanical parameters for distinguishing keratoconus at different stages and normal cornea. Delong test was used to compare the areas under curves (AUCs) of different parameters and AUCs of the same parameter in keratoconus at different stages. In the pairwise comparison of ROC curve, the test level was corrected to 0.0023 and 0.005 according to Bonferroni principle.

Results

There were 408 cases (517 eyes) in the keratoconus group (289 eyes from males and 228 eyes from females), with an average age of (22.56 ± 7.77) years (range: 13–45 years). There were 158 cases (158 eyes) in the normal group (99 males and 59 females), with an average age of (23.08 ± 4.61) years (range: 16–40 years). There were 130 eyes with stage I keratoconus, with an average age of (20.53 ± 8.50) years (range: 13–39 years), 164 eyes with stage II keratoconus, with an average age of (23.04 ± 8.2) years (range: 13–45 years), 125 eyes with stage III keratoconus, with an average age of (23.89 ± 6.73) years (range: 15–32 years), and 98 eyes with stage IV keratoconus, with an average age of (22.78 ± 6.76) years (range: 16–36 years). There was no significant difference in age between the keratoconus group and the normal group (p = 0.056). There was no significant difference in gender between the keratoconus group and the normal group (p = 0.133, chi-square test). Comparison between groups Among the corneal morphological and biomechanical parameters, except HCT and A2 DFL, there were significant differences in all other parameters among the six groups (all p < 0.001), as shown in Table 2. Significant differences were found in all other parameters between the normal group and the keratoconus group (all p < 0.017), except HCT, A1 DfL and A2 DfL. Significant differences were found in all other parameters between the normal group and the stage I keratoconus group (all p < 0.017), except HCT, PD, A1 DfL, A2 DfL, HC DfL and A2 DfA. Significant differences were found in all other parameters between the normal group and the stage II keratoconus group (all p < 0.017), except HCT, A1 DfL, A2 DfL and HC DfL. Significant differences were found in all other parameters between the normal group and the stage III and IV keratoconus groups (all p < 0.017), except HCT and A2 DfL.
Table 2

Differences in corneal morphological and biomechanical parameters between normal group and keratoconus group as well as KC at different stages. (skewed distribution, median and range of variation)

NL groupKCKC groupp
Stage I KCStage II KCStage III KCStage IV KC
K142.40(41.50–43.30)43.35(42.10–44.30)44.70(42.80–46.65)48.10(45.80–50.20)56.65(51.00–60.30)45.60(43.30–49.30) < 0.001
K243.95(43.00–44.90)45.85(44.70–47.20)48.00(45.60–49.80)52.60(50.30–55.30)60.35(55.40–65.30)48.90(46.30–53.80) < 0.001
Km43.20(42.40–44.00)44.65(43.30–45.70)46.20(44.20–48.10)50.00(48.30–52.60)58.75(53.80–62.80)47.20(44.60–51.30) < 0.001
Kmax44.40(43.70–45.60)47.65(45.70–48.90)52.25(50.05–54.65)60.90(57.90–63.30)73.00(67.30–80.00)54.00(49.10–62.30) < 0.001
Astig F1.20(0.80–1.90)2.60(1.50–3.40)3.05(2.00–4.45)4.20(2.90–6.00)4.00(2.20–6.60)3.30(2.00–4.80) < 0.001
CCT553.59(537.63–578.00)510.50(483.00–531.00)477.43(457.50–502.00)449.00(432.00–472.00)430.00(400.00–457.00)472.00(439.00–504.00) < 0.001
TP548.00(533.00–573.00)500.50(478.00–522.00)467.50(449.50–487.50)441.00(419.00–460.00)418.00(388.00–441.00)461.00(429.00–493.00) < 0.001
ISV17.00(14.00–22.00)37.00(33.00–41.00)62.50(52.00–74.00)101.00(94.00–112.00)156.50(142.00–175.00)75.00(46.00–112.00) < 0.001
IVA0.11(0.08–0.15)0.30(0.23–0.38)0.63(0.49–0.77)1.00(0.79–1.20)1.26(0.99–1.62)0.68(0.39–1.02) < 0.001
KI1.03(1.01–1.04)1.09(1.07–1.10)1.15(1.11–1.19)1.26(1.22–1.30)1.40(1.33–1.49)1.17(1.10–1.28) < 0.001
CKI1.01(1.00–1.01)1.02(1.01–1.02)1.04(1.02–1.07)1.10(1.07–1.14)1.19(1.15–1.25)1.05(1.02–1.12) < 0.001
IHA5.40(2.10–9.70)19.60(9.80–26.50)19.15(9.10–41.05)27.60(15.60–52.80)31.15(16.60–49.50)22.20(12.50–38.90) < 0.001
IHD0.01(0.01–0.01)0.03(0.02–0.04)0.08(0.06–0.10)0.15(0.12–0.17)0.23(0.18–0.27)0.10(0.05–0.16) < 0.001
BAD0.96(0.53–1.29)3.01(2.15–4.10)6.38(5.28–7.90)10.77(9.49–12.26)17.42(14.11–21.35)7.58(4.49–11.79) < 0.001
A1T7.40(7.24–7.59)7.19(7.01–7.33)7.02(6.87–7.17)6.96(6.79–7.13)6.92(6.73–7.08)7.02(6.87–7.21) < 0.001
A1V0.15(0.13–0.16)0.16(0.15–0.17)0.17(0.15–0.18)0.18(0.16–0.20)0.19(0.17–0.21)0.17(0.16–0.19) < 0.001
A2T21.81(21.52–22.04)21.96(21.73–22.19)22.07(21.85–22.35)22.16(21.90–22.37)22.22(21.86–22.42)22.12(21.83–22.35) < 0.001
A2V−0.27(−0.29–0.25)−0.29(−0.32–0.26)−0.32(−0.34–0.28)−0.34(−0.37–0.31)−0.38(−0.44–0.32)−0.32(−0.36–0.28) < 0.001
HCT16.86(16.63–17.13)16.86(16.63–17.33)16.86(16.63–17.19)16.86(16.40–17.09)16.86(16.63–17.09)16.86(16.63–17.09)0.763
PD5.17(4.96–5.28)5.14(5.01–5.35)5.23(5.03–5.40)5.24(5.13–5.38)5.24(5.07–5.41)5.21(5.06–5.38) < 0.001
Radius7.31(6.95–7.94)6.44(5.83–7.02)5.65(5.06–6.35)5.27(4.73–5.70)4.38(3.82–5.16)5.55(4.84–6.42) < 0.001
A1 DfL2.33(2.22–2.42)2.31(2.20–2.37)2.35(2.23–2.43)2.41(2.25–2.52)2.48(2.33–2.63)2.36(2.24–2.48) < 0.001
HC DfL6.70(6.34–6.96)6.60(6.28–6.85)6.67(6.20–6.96)6.53(6.25–6.78)6.29(5.90–6.63)6.54(6.18–6.83) < 0.001
A2 DfL2.80(2.56–3.42)2.78(2.37–3.48)2.85(2.45–3.52)2.81(2.48–3.62)3.01(2.48–3.64)2.86(2.44–3.55)0.353
A1 DfA0.10(0.09–0.10)0.10(0.09–0.10)0.10(0.10–0.11)0.11(0.10–0.12)0.13(0.12–0.14)0.11(0.10–0.12) < 0.001
HC DfA0.91(0.85–0.97)0.96(0.89–1.04)1.04(0.96–1.11)1.12(1.04–1.20)1.22(1.12–1.35)1.07(0.97–1.18) < 0.001
A2 DfA0.11(0.10–0.12)0.11(0.10–0.12)0.11(0.10–0.13)0.13(0.11–0.14)0.15(0.13–0.17)0.12(0.11–0.14) < 0.001
DA Ratio 24.06(3.85–4.30)4.62(4.34–5.29)5.31(4.76–6.01)6.13(5.70–6.80)7.25(6.10–8.81)5.67(4.79–6.52) < 0.001
DA Ratio 11.54(1.52–1.58)1.60(1.57–1.66)1.64(1.61–1.69)1.71(1.66–1.76)1.78(1.68–1.83)1.67(1.60–1.74) < 0.001
ARTh452.06(390.36–524.38)362.12(293.19–475.31)229.31(181.91–284.65)157.87(125.12–206.00)103.27(79.78–147.78)212.10(139.63–303.59) < 0.001
bIOP14.90(13.70–15.82)14.70(13.20–15.90)13.80(12.60–15.20)13.90(12.50–15.20)13.70(12.80–14.70)14.05(12.70–15.30) < 0.001
Integrated Radius7.75(7.31–8.35)9.33(8.44–10.42)10.90(9.74–12.39)12.41(11.30–13.74)14.82(12.08–17.55)11.31(9.56–13.24) < 0.001
SPA1107.21(96.17–117.78)80.64(68.54–98.19)63.45(51.04–73.65)48.13(42.24–58.98)38.45(28.48–48.23)58.84(43.91–75.02) < 0.001
CBI0.01(0.00–0.07)0.69(0.01–0.99)1.00(0.97–1.00)1.00(1.00–1.00)1.00(1.00–1.00)1.00(0.96–1.00) < 0.001
TBI0.14(0.02–0.26)1.00(0.98–1.00)1.00(1.00–1.00)1.00(1.00–1.00)1.00(1.00–1.00)1.00(1.00–1.00) < 0.001

KC keratoconus, NL normal cornea

Differences in corneal morphological and biomechanical parameters between normal group and keratoconus group as well as KC at different stages. (skewed distribution, median and range of variation) KC keratoconus, NL normal cornea ROC curve analysis ROC curve analysis showed that the area under the ROC curve (AUC) of BAD-D, DA Ratio 2, ARTh, Integrated Radius, SPA1, CBI and TBI in diagnosing keratoconus were all > 0.9 (Table 3). ROC curve analysis on normal cornea and keratoconus at different stages showed that the AUCs of BAD-D and TBI in distinguishing normal cornea from keratoconus at different stages were all > 0.96. The efficiency of DA Ratio 2, ARTh, Integrated Radius, SPA1 and CBI in diagnosing stage I keratoconus was relatively low, but the AUCs of all parameters increased with the increase in keratoconus stages. Figure 1 a-e shows the ROC curves of all parameters in diagnosing keratoconus, and keratoconus at different stages.
Table 3 

ROC curve analysis of normal group and keratoconus at different stages

ParametersAUC (95% CI)CutoffSensitivity, %Specificity, %
KC group vs. NL group
BAD-D0.9891.5950.9591
DA Ratio 20.9214.7420.7680.975
ARTh0.9328.60.7830.981
Integrated Radius0.939.0240.820.949
SP-A10.9479.130.8020.981
CBI0.9160.5160.8451
TBI0.9930.5150.9671
Stage I KC group vs. NL group
BAD-D0.9631.59511
DA Ratio 20.8114.350.7460.816
ARTh0.712356.90.4920.93
Integrated Radius0.8538.5730.7380.842
SPA10.81898.750.7850.703
CBI0.7610.5160.5691
TBI0.9790.5150.9671
Stage II KC group vs. NL group
BAD-D0.9961.670.9761
DA Ratio 20.9354.5230.860.905
ARTh0.926328.60.8230.981
Integrated Radius0.9379.180.8480.962
SPA10.96585.660.9390.918
CBI0.9460.5160.8961
TBI0.9970.5740.9881
Stage III KC group vs. NL group
BAD-D13.0211
DA Ratio 20.9834.9030.9440.994
ARTh0.985313.40.9760.987
Integrated Radius0.9809.4230.9360.987
SPA10.98977.220.9440.981
CBI0.9750.7180.9521
TBI0.9970.710.9841
Stage IV KC group vs. NL group
BAD-D13.3211
DA Ratio 20.9644.8060.860.905
ARTh0.995258.10.8230.981
Integrated Radius0.9589.6960.8480.962
SPA10.99872.270.9390.918
CBI0.9960.7010.8961
TBI0.9970.5660.9881

KC keratoconus, NL normal cornea, AUC area under the receiver operating characteristic curve

Fig. 1

ROC curves of the different groups a NL group vs. KC group, b NL group vs. stage I KC group, c NL group vs. stage II KC group, d NL group vs. stage III KC group, e NL group vs. stage IV KC group

ROC curve analysis of normal group and keratoconus at different stages KC keratoconus, NL normal cornea, AUC area under the receiver operating characteristic curve ROC curves of the different groups a NL group vs. KC group, b NL group vs. stage I KC group, c NL group vs. stage II KC group, d NL group vs. stage III KC group, e NL group vs. stage IV KC group Comparison of ROC curves of different parameters in keratoconus at the same stage Comparison of the ROC curves between the normal group and the keratoconus group showed that the ROC curves of both BAD-D and TBI were statistically different from those of DA Ratio 2, Integrated Radius, SPA1 and CBI. In addition, the AUCs of BAD-D and TBI were greater than those of other parameters. Therefore, the diagnostic efficiency of BAD-D and TBI were higher than that of other parameters. However, no significant difference was found in the AUCs of BAD-D and TBI (p = 0.232). Hence, efficiency of BAD-D and TBI was the highest among all parameters in diagnosing keratoconus. The ROC curves of the normal group and the stage I keratoconus group showed that BAD-D and TBI were the most effective among the seven parameters, while ARTh and CBI showed the lowest efficiency. The ROC curves of the normal group and the stage II keratoconus group showed that BAD-D and TBI were the most effective among the seven parameters, while the other parameters showed the same efficiency in the diagnosis of stage II keratoconus. The ROC curves of the normal group and the stage III and IV keratoconus groups showed no significant difference among the seven parameters in diagnosing keratoconus, indicating the same diagnostic efficiency (Table 4).
Table 4

Comparison of ROC curves of different parameters among groups

Two curves under comparisonD 0P 0D 1P 1D 2P 2D 3P 3D 4P 4
BAD-DDA Ratio 27.164 < 0.0016.073 < 0.0014.425 < 0.0011.8030.0712.0800.037
ARTh8.381 < 0.0018.849 < 0.0014.494 < 0.0011.6490.0981.0030.316
Integrate6.602 < 0.0014.976 < 0.0014.170 < 0.0012.0940.0362.5340.011
SP-A15.973 < 0.0016.029 < 0.0013.1700.00152.0870.0361.3270.185
CBI7.478 < 0.0017.030 < 0.0013.495 < 0.0012.1060.0350.9960.319
TBI − 1.1940.232 − 1.8030.071 − 0.5180.6041.3860.1660.9930.321
DA Ratio 2ARTh2.0140.0443.2380.0010.6720.501 − 0.2740.784 − 1.7400.082
Integrate − 1.2060.228 − 2.1570.031 − 0.1180.9050.5210.6020.3340.738
SP-A1 − 2.2540.024 − 0.3010.763 − 0.3010.763 − 1.1260.260 − 2.0090.044
CBI0.5280.5972.0050.045 − 2.8430.0050.6500.516 − 1.7750.075
TBI − 7.325 < 0.001 − 6.527 < 0.001 − 4.524 < 0.001 − 1.6200.105 − 1.8720.061
ARThIntegrate − 2.6290.009 − 4.732 < 0.001 − 0.6880.4910.4500.6522.1300.033
SP-A1 − 2.3110.021 − 3.539 < 0.001 − 2.8480.044 − 0.4580.646 − 0.8270.408
CBI − 2.3920.0172.5470.011 − 1.7840.0740.9810.326 − 1.0090.313
TBI − 8.549 < 0.001 − 8.766 < 0.001 − 4.589 < 0.001 − 1.6820.092 − 0.9850.324
IntegrateSP-A1 − 1.1130.2661.4710.141 − 2.1300.033 − 1.4580.145 − 2.4600.014
CBI1.3420.1803.2710.001 − 0.5900.5540.4040.686 − 2.2320.026
TBI − 6.801 < 0.001 − 5.538 < 0.001 − 4.294 < 0.001 − 1.8360.066 − 2.3310.019
SP-A1CBI2.9830.0032.3890.0171.7700.0761.3580.1750.7170.472
TBI − 6.506 < 0.001 − 6.843 < 0.001 − 3.2730.001 − 1.4890.1360.5170.605
CBITBI − 7.610 < 0.001 − 7.339 < 0.001 − 3.592 < 0.001 − 1.9980.046 − 0.9230.355

D: Statistics of Delong test; 0: NL group vs. KC group; 1. NL group vs. stage I KC group; 2: NL group vs. stage II KC group; 3: NL group vs. stage III KC group; 4: NL group vs. stage IV KC group

Due to multiple comparisons, the test level was corrected according to Bonferroni principle, and p < 0.0023 was considered as statistically significant

Comparison of ROC curves of different parameters among groups D: Statistics of Delong test; 0: NL group vs. KC group; 1. NL group vs. stage I KC group; 2: NL group vs. stage II KC group; 3: NL group vs. stage III KC group; 4: NL group vs. stage IV KC group Due to multiple comparisons, the test level was corrected according to Bonferroni principle, and p < 0.0023 was considered as statistically significant Comparison of ROC curves of the same parameter in keratoconus at different stages There was no significant difference in the ROC curves of TBI in keratoconus at different stages, and no significant difference was found in pairwise comparison, which indicated that TBI had the same efficiency in diagnosing keratoconus at all stages. Moreover, statistically significant difference was found in the ROC curves of the other six parameters for diagnosing stage I keratoconus and keratoconus at other stages, indicating that these parameters had lower ability in diagnosing stage I keratoconus than keratoconus at other stages (Table 5).
Table 5

Comparison of ROC curves of the same parameter in diagnosing keratoconus at different stages

parameterD0P0D1P1D2P2D3P3D4P4D5P5
BAD-D − 2.9890.003 − 3.401 < 0.001 − 3.401 < 0.001 − 1.4680.138 − 1.4680.138NANA
DA Ratio 2 − 4.509 < 0.001 − 5.965 < 0.001 − 4.756 < 0.001 − 2.7310.006 − 1.2720.2040.9360.35
ARTh − 5.902 < 0.001 − 8.1039 < 0.001 − 8.620 < 0.001 − 3.1940.0015 − 4.008 < 0.001 − 0.9530.341
Integrated Radius − 3.0690.002 − 5.087 < 0.001 − 3.718 < 0.001 − 2.4890.013 − 0.9810.3271.1480.251
SP-A1 − 5.458 < 0.001 − 6.670 < 0.001 − 7.144 < 0.001 − 2.1470.032 − 3.271 < 0.001 − 1.6030.110
CBI − 5.343 < 0.001 − 6.339 < 0.001 − 7.435 < 0.001 − 1.5150.13 − 3.1920.0015 − 1.6420.102
TBI − 2.3890.017 − 2.2820.023 − 2.2490.0250.1820.8550.080.936 − 0.0720.94

D: Statistics of Delong test; 0: stage I KC group vs. stage II KC group; 1: stage I KC group vs. stage III KC group; 2: stage I KC group vs. stage IV KC group; 3: stage II KC group vs. stage III KC group; 4: stage II KC group vs. stage IV KC group; 5: stage III KC group vs. stage IV KC group

Due to multiple comparisons, the test level was corrected according to Bonferroni principle, and p < 0.005 was considered as statistically significant

Comparison of ROC curves of the same parameter in diagnosing keratoconus at different stages D: Statistics of Delong test; 0: stage I KC group vs. stage II KC group; 1: stage I KC group vs. stage III KC group; 2: stage I KC group vs. stage IV KC group; 3: stage II KC group vs. stage III KC group; 4: stage II KC group vs. stage IV KC group; 5: stage III KC group vs. stage IV KC group Due to multiple comparisons, the test level was corrected according to Bonferroni principle, and p < 0.005 was considered as statistically significant

Discussion

Keratoconus is a type of corneal ectatic disorder, which can lead to serious decline of corneal optical performance and gradual decrease in asymmetric binocular vision. As the absolute contraindication of keratorefractive surgery, its exact preoperative diagnosis is especially important. Despite the fact that the clinical diagnosis of moderate and advanced keratoconus is not difficult, the diagnosis of early keratoconus still remains a challenge [18]. Early keratoconus is considered as one of the most important independent risk factors for iatrogenic keratoectasis. At present, the main auxiliary diagnostic methods for the diagnosis of keratoconus are corneal topography, but this method has certain limitations for the diagnosis of early keratoconus [19, 20]. Studies have shown that the changes of corneal biomechanical characteristics may occur before the typical corneal morphological changes [5, 21]. In this study, the morphological and biomechanical characteristics of normal cornea and keratoconus at different stages were analyzed, as well as the diagnostic efficiency of different parameters in the diagnosis of keratoconus at different stages. Several studies have shown that there are significant differences in corneal morphological parameters between the normal cornea and keratoconus [16, 22]. This study also showed significant differences in all corneal morphological parameters between the normal cornea and keratoconus at different stages. For instance, the corneal curvature, ISV, IVA, KI, CKI, IHA, and IHD of the keratoconus group were significantly higher than those of the normal group, but the thickness was significantly less than that of normal group. Numerous studies have found that the ability of corneal morphological parameters to diagnose keratoconus is high [23-26]. In the Pentacam corneal topographic map, combining the anterior and posterior surface height map, cornea thickness spatial profile (CTSP) and percentage thickness increase (PTI), constitutes the Belin/Ambrosio Enhanced Ectasia Display (Belin-Ambrósio deviation [BAD-D]) software. BAD-D in this software is calculated based on a regression analysis that weights differently the parameters, which can effectively diagnose keratoconus [27]. Renato Ambrósio et al. [27] found that the AUC of BAD-D in detecting keratoconus was 1.00, with a critical value of 2.11, sensitivity of 1, and specificity of 1. In this study, BAD-D could effectively detect keratoconus, which was similar to previous reports [26]. In addition, BAD-D could effectively diagnose keratoconus at different stages (all AUC > 0.96). The AUC of BAD-D in distinguishing stage I keratoconus from normal cornea was 0.963, with a critical value of 1.595, and sensitivity and specificity of 1 respectively. Stage I keratoconus represents a relatively early stage of the disease, suggesting that BAD-D can be effective in the diagnosis of early keratoconus; and the diagnostic efficiency of BAD-D increases with the increase in keratoconus stages. Progression of keratoconus leads to the destruction of corneal stroma structure, causing instability of corneal biomechanical properties and weakening of mechanical strength [4]. Roberts and Dupps suggested that the underlying cause of corneal ectasia or keratoconus is the abnormal biomechanical properties of the cornea, while the morphological changes of the cornea are secondary manifestations [28]. With the recent development of corneal biomechanics in vivo, measuring the biomechanical properties of keratoconus has become a hotspot in ophthalmology. The current study found significant differences in most biomechanical parameters between the normal cornea and keratoconus as well as between the normal cornea and keratoconus at different stages. During the first and second applanation status, the applanation time and length of the keratoconus group were shorter than those of the normal group, and the applanation velocity was greater than that of the normal group. The easier deformation in the keratoconus group was due to the weaker matrical collagen fibers and thinner cornea. The results showed that HC DfL, HC DfA and PD of the keratoconus group were larger than those of the normal group, while the central curvature radius of the keratoconus group was smaller than that of the normal group. These findings indicated that the mechanical strength of cornea is weakened in keratoconus, leading to increased deformation amplitude (DA) under the same external force. Previous biomechanical studies found that the maximum DA was the most effective parameter in diagnosing keratoconus, with an AUC of 0.882, but there was significant overlap between the keratoconus group and the control group [10]. Salomao et al. found significant statistical differences in corneal biomechanical parameters between the normal cornea and keratoconus, but the AUCs of the parameters overlapped between 0.673 and 0.852 [29]. With the update of Corvis ST software, new biomechanical parameters have been proposed such as DA Ratio 2, Integrated Radius, ARTh, SPA1 and CBI. CBI is a combination of dynamic corneal deformation parameters such as DA ratio, A1V, ARTh and SPA1. Studies have shown that some new parameters have high efficiency in the diagnosis of keratoconus [30, 31]. In this study, these new parameters could effectively diagnose keratoconus (all AUC > 0.9), which was similar to previous reports [30]. According to DeLong curve analysis, DA Ratio 2, Integrated Radius and SPA1 had higher diagnostic efficiency than ARTh and CBI. In contrast, Pratik et al. found that CBI was more efficient than SPA1 in diagnosing keratoconus [14]. Sedaghat et al. [32] also found that the AUC of CBI was higher than other biomechanical parameters. This difference in our findings may be due to the included sample size or differences in the degree of keratoconus. In the present study, DA Ratio 2, Integrated Radius, ARTh, SPA1 and CBI had relatively low efficiency in distinguishing normal and stage I keratoconus, with ARTh and CBI showing the lowest efficiency in diagnosing stage I keratoconus. Among them, the AUC of CBI in diagnosing stage I keratoconus was 0.761, indicating that the ability of CBI to diagnose early keratoconus was relatively low, which was similar to the report of Pratik et al. [10]. However, with the increase in keratoconus stages, the diagnostic efficiency of these biomechanical parameters also increased, and the efficiency of each parameter in the diagnosis was same in keratoconus III or IV stages. Recently, Ambrosio et al. used artificial intelligence methods, including random forest analysis and combining corneal morphological parameters of Pentacam with biomechanical parameters of Corvis to develop a new parameter—TBI, which was applied in keratoconus study [13]. They found that TBI had higher diagnostic efficiency (AUC = 1) than parameters obtained with Pentacam and Corvis ST alone in the detection of corneal ectasia, with a critical value of 0.79, and the sensitivity and specificity of 1, respectively. In this study, TBI could effectively distinguish keratoconus from normal cornea (AUC = 0.993), with a critical value of 0.515, and sensitivity of 0.967, and specificity of 1. This difference from the previous threshold may be due to the different degree of keratoconus among the enrolled patients. In graded keratoconus, the efficiency of TBI in the diagnosis of keratoconus in each stage was high (AUC > 0.97). Among them, the AUC of TBI for differentiating normal cornea and stage I keratoconus was 0.979, indicating that TBI could effectively diagnose early keratoconus. Finally, according to DeLong curve analysis, the efficiency of TBI in diagnosing keratoconus in each stage was the same. In this study, according to DeLong curve analysis, BAD-D and TBI had the same efficiency in diagnosing keratoconus, which was higher than other parameters. In contrast, Salomao et al. [33] found that the efficiency of TBI in diagnosing keratoconus was higher than BAD-D. Moreover, the diagnostic efficiency of TBI was the same for keratoconus at all stages. This study included a large sample size, divided keratoconus into different grades for analysis, and focused on the diagnostic ability of some new parameters for different stages of keratoconus. The limitations of this study were that it was a cross-sectional study, and the enrolled patients were not followed-up. In addition, forme fruste keratoconus was not included in this study; further studies should be conducted in order to explore methods for the diagnosis of more early keratoconus. In summary, the morphological and biomechanical parameters of cornea in this study could effectively distinguish normal cornea from keratoconus, with BAD-D and TBI being the most efficient parameters. BAD-D and TBI showed high efficiency in the diagnosis of keratoconus of different grades, and the diagnostic efficiency of TBI was the same for keratoconus at all stages. Except for TBI, the efficiency of other parameters in diagnosing keratoconus increased with the increase in keratoconus stages.
  32 in total

1.  A new method for grading the severity of keratoconus: the Keratoconus Severity Score (KSS).

Authors:  Timothy T McMahon; Loretta Szczotka-Flynn; Joseph T Barr; Robert J Anderson; Mary E Slaughter; Jonathan H Lass; Sudha K Iyengar
Journal:  Cornea       Date:  2006-08       Impact factor: 2.651

Review 2.  Identification of biomechanical properties of the cornea: the ocular response analyzer.

Authors:  Naim Terai; Frederik Raiskup; Michael Haustein; Lutz E Pillunat; Eberhard Spoerl
Journal:  Curr Eye Res       Date:  2012-05-04       Impact factor: 2.424

Review 3.  Keratoconus.

Authors:  Y S Rabinowitz
Journal:  Surv Ophthalmol       Date:  1998 Jan-Feb       Impact factor: 6.048

4.  Diagnostic Ability of Corneal Shape and Biomechanical Parameters for Detecting Frank Keratoconus.

Authors:  Mohammad-Reza Sedaghat; Hamed Momeni-Moghaddam; Renato Ambrósio; Hamid-Reza Heidari; Nasim Maddah; Zeynab Danesh; Fatemeh Sabzi
Journal:  Cornea       Date:  2018-08       Impact factor: 2.651

Review 5.  Scheimpflug imaging for laser refractive surgery.

Authors:  Renato Ambrósio; Bruno F Valbon; Fernando Faria-Correia; Isaac Ramos; Allan Luz
Journal:  Curr Opin Ophthalmol       Date:  2013-07       Impact factor: 3.761

6.  Incidence and characteristics of unilateral keratoconus classified on corneal topography.

Authors:  Rui Hua Wei; Shao Zhen Zhao; Li Lim; Donald T H Tan
Journal:  J Refract Surg       Date:  2011-05-10       Impact factor: 3.573

7.  Corneal deformation measurement using Scheimpflug noncontact tonometry.

Authors:  Ying Hon; Andrew K C Lam
Journal:  Optom Vis Sci       Date:  2013-01       Impact factor: 1.973

8.  Detection of Keratoconus With a New Biomechanical Index.

Authors:  Riccardo Vinciguerra; Renato Ambrósio; Ahmed Elsheikh; Cynthia J Roberts; Bernardo Lopes; Emanuela Morenghi; Claudio Azzolini; Paolo Vinciguerra
Journal:  J Refract Surg       Date:  2016-12-01       Impact factor: 3.573

9.  Changes in collagen orientation and distribution in keratoconus corneas.

Authors:  Keith M Meek; Stephen J Tuft; Yifei Huang; Paulvinder S Gill; Sally Hayes; Richard H Newton; Anthony J Bron
Journal:  Invest Ophthalmol Vis Sci       Date:  2005-06       Impact factor: 4.799

10.  Repeatability and comparison of new Corvis ST parameters in normal and keratoconus eyes.

Authors:  Kaili Yang; Liyan Xu; Qi Fan; Dongqing Zhao; Shengwei Ren
Journal:  Sci Rep       Date:  2019-10-25       Impact factor: 4.379

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  1 in total

1.  Detection ability of corneal biomechanical parameters for early diagnosis of ectasia.

Authors:  Mohammad-Reza Sedaghat; Hamed Momeni-Moghaddam; Javad Heravian; Atiyeh Ansari; Helia Shayanfar; Majid Moshirfar
Journal:  Eye (Lond)       Date:  2022-08-29       Impact factor: 4.456

  1 in total

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