·Clinical Research· Current Issue· ·Achieve· ·Search Articles· ·Online Submission· ·About IJO· PMC
Citation: Teng MC, Poon YC, Hung
KC, Chang HW, Lai IC, Tsai JC, Lin PW, Wu CY, Chen CT, Wu PC.
Diagnostic capability of peripapillary retinal nerve fiber layer parameters in
time-domain versus spectral-domain optical coherence tomography for assessing
glaucoma in high myopia. Int J Ophthalmol 2017;10(7):1106-1112
Diagnostic capability of peripapillary retinal nerve fiber layer parameters in
time-domain versus spectral-domain optical coherence tomography for assessing
glaucoma in high myopia
Mei-Ching Teng1, Yi-Chieh Poon1,
Kuo-Chi Hung1, Hsueh-Wen Chang 2, Ing-Chou Lai1,
Jen-Chia Tsai1, Pei-Wen Lin1, Chien-Yun Wu1,
Chueh-Tan Chen1, Pei-Chang Wu1
1Department of Ophthalmology, Kaohsiung Chang Gung Memorial Hospital and
Chang Gung University College of Medicine, Niaosong
Dist., Kaohsiung City, Taiwan 83301, China
2Department of Biological Sciences,
National Sun Yat-Sen University, Kaohsiung City, Taiwan 80424, China
Correspondence to: Pei-Chang Wu. Department of Ophthalmology, Kaohsiung Chang Gung Memorial
Hospital, 2F No.123, Dapi Rd., Niaosong Dist., Kaohsiung City, Taiwan 83301,
China. wpc@adm.cgmh.org.tw
Received:
2016-07-26
Accepted: 2016-12-21
AIM: To
evaluate and compare the diagnostic capabilities of peripapillary retinal nerve
fiber layer (p-RNFL) parameters of Spectralis optical coherence tomography
(OCT) versus Stratus OCT to detect glaucoma in patients with high myopia.
METHODS: This
is a retrospective, cross-sectional study. Sixty highly myopic eyes of 60
patients were enrolled, with 30 eyes in the glaucoma group and 30 eyes in the
control group. All eyes received peripapillary imaging of the optic disc using
Stratus and Spectralis OCT. Areas under the receiver operating characteristic
curve (AUROC) and the sensitivity at specificity of >80% and >95% for p-RNFL
parameters obtained using the two devices to diagnose glaucoma were analysed
and compared.
RESULTS: In
Spectralis OCT, p-RNFL thickness parameters with the largest AUROC were the
temporal-inferior sector (0.974) and the inferior quadrant (0.951), whereas in
Stratus OCT, the best parameters were the 7-o’clock sector (0.918) and the
inferior quadrant (0.918). Compared to the Stratus OCT parameters, the
Spectralis OCT parameters demonstrated generally higher AUROC; however, the
difference was not statistically significant.
CONCLUSION: The
best p-RNFL parameters for diagnosing glaucoma in patients with high myopia
were the temporal-inferior sector on Spectralis OCT and the 7-o’clock sector on
Stratus OCT. There were no significant differences between the AUROCs for
Spectralis OCT and Stratus OCT, which suggest that the glaucoma diagnostic
capabilities of these two devices in patients with high myopia are similar.
KEYWORDS: diagnostic
capability; glaucoma; high myopia; optical coherence tomography; retinal nerve fiber
layer
DOI:10.18240/ijo.2017.07.14
Citation: Teng MC, Poon YC, Hung KC, Chang HW, Lai IC, Tsai
JC, Lin PW, Wu CY, Chen CT, Wu PC. Diagnostic capability of
peripapillary retinal nerve fiber layer parameters in time-domain versus
spectral-domain optical coherence tomography for assessing glaucoma in high
myopia. Int J Ophthalmol 2017;10(7):1106-1112
Glaucoma is an optic neuropathy that is characterised
by the selective loss of retinal ganglion cells and their axons, which
manifests as the loss of the retinal nerve fiber layer (RNFL)[1]. Numerous studies have shown that the extent of RNFL damage
correlates with the severity of functional deficit in the visual field (VF),
and that RNFL measurement by optical coherence tomography (OCT) has good
sensitivity for the detection of glaucoma[2-4].
High myopia is a known risk factor for open angle
glaucoma[5]. Clinical diagnosis of glaucoma in this group of patients is
often difficult because of the variation in the sizes, shapes, tilt of the
optic nerve head, and the presence of large peripapillary atrophy (PPA) in
these eyes. In high myopia, RNFL loss also occurs more frequently in a
generalized or diffuse pattern rather than in a localised pattern. These
characteristics of highly myopic eyes make it difficult to accurately determine
the cup-to-disc ratio and the extent of RNFL damage in susceptible patients[6-9].
Previous studies on patients without high myopia have
shown that time-domain optical coherence tomography (TD-OCT), such as Stratus
OCT may have limited diagnostic capability for identifying localised RNFL
defects, particularly in the early stages of glaucoma[10-12]. Spectralis OCT, on the other hand, is a spectral-domain optical
coherence tomography (SD-OCT), with an acquisition speed of 40 000 A-scans/s,
which is 100 times faster than a Stratus OCT. Moreover, it has axial
resolutions that are almost twice as high (5-7 µm) as those of Stratus OCT
(approximately 8-10 µm) and has reduced speckle noise to drastically improve
the clarity of boundaries between inner retinal layers and to facilitate
visualization of small pathologic changes[13-17]. The improvements in the newer SD-OCT technology have been
shown to be useful in providing a better diagnostic performance in glaucoma
patients within the normative refractive range of between ±5 diopter (D) in
several studies. Nukada et al[18] reported that
Spectralis OCT had better diagnostic capability than single-scan TD-OCT for
detecting localised RNFL defects in perimetric glaucoma, while
Jeoung et al[19] recently also demonstrated that Spectralis OCT was better than TD-OCT
at detecting preperimetric localised RNFL defects.
However, it would be important to apply these technology
advantages towards not only a non-myopic or moderately myopic population, but
also towards a highly myopic population. High myopia has not only been shown to
be a risk factor for glaucoma[20-21], it is also currently a major public health concern
particularly in the east and southeast Asian countries. Population-based
studies have found the prevalence of high myopia to be 2.1%-4.2% in the general
population[22], and can be as high as 20% in high school graduates[23]. Yet, all of the
previous studies comparing SD-OCT to TD-OCT have been conducted on patients
with refractions of >-6 D, and not on highly myopic patients, and whether
the advantages of SD-OCT over TD-OCT in diagnosing glaucoma are also present in
patients with high myopia remains unclear. Therefore, the purpose of this study
is to evaluate and compare whether there are any differences in the diagnostic
capabilities of Spectralis SD-OCT and Stratus TD-OCT to detect glaucoma in
patients with high myopia.
This retrospective, cross-sectional study included
patients who presented to the Outpatient Department of Kaohsiung Chang Gung
Memorial Hospital, Kaohsiung, Taiwan, between May 2014 and April 2015. The
study was approved by the Ethics Committee of Chang Gung Memorial Hospital. The
methods applied in the study adhered to the tenets of the Declaration of
Helsinki for the use of human subjects in biomedical research. Informed consent
was obtained from all of the patients.
All of the patients enrolled in this study underwent a
complete ophthalmic examination, including best-corrected visual acuity,
refraction, slit-lamp biomicroscopy, gonioscopy, Goldmann applanation
tonometry, dilated stereoscopic examination of the optic disc, colour disc
photography and red-free fundus photography (TOPCON TRC-50EX, Japan), VF
examination by using Humphrey Field Analyzer Swedish interactive threshold
algorithm standard 30-2 test (Carl Zeiss Meditec, Dublin, CA, USA), and
peripapillary RNFL (p-RNFL) thickness measurement by using Stratus OCT (Model
3000, software version 4.0, Carl Zeiss Meditec, Dublin, CA, USA) and Spectralis
OCT (software version 5.6, Heidelberg Engineering, Dossenheim, Germany). OCT
imaging with the two devices was performed either on the same day or at
separate visits within a 6-month period.
The inclusion criteria were as follows: spherical
equivalent (SE) of ≤-6.0 D, best-corrected visual acuity of 20/40 or better, a
healthy anterior segment on slit-lamp biomicroscopy, open angles on gonioscopy,
clear ocular media, and reliable VF test results. The results of VF tests were
considered reliable when fixation losses were less than 20%, and false-positive
and false-negative rates were less than 15%, with reproducible VF result on at
least two reliable examinations. The OCT images with signal strength of at
least 7 on Stratus OCT and image quality of at least 20 on Spectralis OCT were
used for this study.
Patients were excluded if they had SE <-15.00 D, or
had large PPA that extended outside the peripapillary scanning circle on OCT.
In addition, patients with any evidence of intraocular surgery, laser history,
or evidence of eye trauma, uveal, retinal, or macular pathology, and those with
systemic diseases or neurological disorders that could produce VF defects that
might be confused with glaucoma were excluded. Patients with pseudoexfoliation
glaucoma, pigmentary glaucoma, or other secondary glaucomas were also excluded.
If both eyes of a patient were eligible for the study, only one eye was
randomly chosen for analysis.
In this study, the patients were categorised into two
groups: glaucoma group (GG) and control group (CG). The GG included patients
with glaucomatous VF defects confirmed by two reliable VF examinations that
corresponded with a glaucomatous disc appearance (notching or diffuse thinning
of the neuroretinal rim) and/or RNFL defects, irrespective of the level of
intraocular pressure (IOP). A glaucomatous VF defect was defined as a cluster
of three or more non-edge points with a probability of less than 5%, including
at least one point with a probability of less than 1% on a pattern deviation
map and glaucoma hemi-field test result outside normal limits.
The patients in the CG were age- and SE-matched to the
patients in the GG. The CG included highly myopic patients without any other
ocular diseases or ocular medications, had IOP <21 mm Hg, normal posterior
segment findings, and normal VF or any VF depressions that did not fulfil the
criteria for a glaucomatous VF defect.
Optical Coherence Tomography Measurements For Stratus OCT, a scan circle with a diameter of 3.46 mm was manually
positioned with the optic disc at its centre; the fast RNFL scan protocol was
used for measurement. This protocol consisted ofthree consecutive peripapillary
scans, with each image consisting of 400 A-scans. The device’s built-in
software calculated the mean p-RNFL thickness of average, four quadrants
(superior, inferior, nasal, and temporal), and 12 clock-hour sectors. The
p-RNFL thickness profiles were plotted in a clockwise direction for right eyes
and an anticlockwise direction for left eyes. Thus, the 3-o’clock sector of the
peripapillary scan represented the nasal optic disc side of both eyes.
For Spectralis OCT, a scan circle with a diameter of
3.46 mm was manually positioned with the optic disc at its centre while the
eye-tracking system was activated. This enabled real-time three-dimensional
tracking of eye movements with real-time averaging of multiple B-scans acquired
at an identical location of the retina to reduce speckle noise. For this study,
100 images were acquired at the scan circle under high-resolution settings (40
000 A-scans) and were averaged automatically by the software. The device’s
built-in software calculated the mean p-RNFL thickness of global average four
quadrants (superior, inferior, nasal, and temporal) and sectors
(nasal-superior, temporal-superior, temporal-inferior, and nasal-inferior). The
same experienced operators performed all of the OCT scans under standardised
mesopic lighting conditions.
Statistical Analysis Comparisons between the GG and CG were performed using the independent t-test
for continuous variables and Chi-square test for categorical variables. The
comparison of average and four quadrants p-RNFL thickness measurements obtained
using the two OCT devices were analysed using paired t-tests. To
evaluate the diagnostic ability of the p-RNFL thickness parameters in diagnosing
glaucoma, area under the receiver operating characteristics curve (AUROC)
values were calculated. The AUROC was calculated using the standard formula[24]. An AUROC
of 1.0 represented perfect discrimination, whereas an AUROC of 0.5 represented
chance discrimination. AUROC values of comparable parameters obtained using the
two devices were compared using Chi-square tests. The sensitivities were
calculated at specificities >80% and >95%. All analyses were performed using
SPSS Version 21.0 (SPSS Inc., Chicago, IL, USA) and SAS 9.3 for Windows (SAS
Institute Inc., Cary, NC, USA). A P value of <0.05 was considered
statistically significant.
The study enrolled 60 highly myopic eyes from 60
Chinese patients (32 females and 28 males). Mean age was 41.0±9.8y (range: 21
to 63y); mean SE was -8.3±2.2 D (range: -6.00 to -15.00 D). Thirty eyes of 30
patients were categorized into the GG and 30 eyes of 30 patients into the CG.
The characteristics of participants in both groups are summarised in Table 1.
There was a slight female predominance in the CG, but there was no significant
difference between the two groups in laterality, mean age, and SE.
Table 1 Demographic data of study subjects
n=30
Parameters |
Glaucoma group |
Control group |
2P |
Age (a)1 |
42.4±8.6 |
39.7±10.9 |
0.292 |
Sex ratio (M:F) |
18:12 |
10:20 |
0.038 |
Laterality (right:left) |
12:18 |
14:16 |
0.602 |
Spherical equivalent (Diopters)1 |
-8.8±2.5 |
-7.9±2.1 |
0.148 |
Mean deviation (dB)1 |
-6.4±4.1 |
-3.0±1.9 |
0.0004 |
Pattern standard deviation (dB)1 |
6.9±4.5 |
3.4±2.2 |
0.001 |
1Values are expressed as mean±standard deviation; 2Continuous
data were analysed using the independent t-test and categorical data by
using the Chi-square test.
Table 2 shows the mean p-RNFL thickness measured by
Stratus OCT and Spectralis OCT. For both study groups, the average and quadrant
p-RNFL thickness measured by Spectralis OCT was thinner than that measured by
Stratus OCT, and the difference was more pronounced in the glaucoma group than
in the control group.
Table 2 The mean peripapillary retinal nerve fibre
layer thickness measured by Stratus and Spectralis OCT
Groups |
Location |
Thickness parameter (µm) |
Mean difference1 |
2P |
|
Stratus1 |
Spectralis1 |
||||
Glaucoma group (n=30) |
Average |
73.1±14.2 |
63.6±14.7 |
9.5±7.3 |
<0.0001 |
Superior |
93.6±20.8 |
83.9±23.2 |
9.7±12.5 |
0.0007 |
|
Temporal |
62.8±23.6 |
60.9±25.2 |
1.9±11.7 |
0.419 |
|
Inferior |
74.5±19.5 |
66.0±18.7 |
8.4±10.1 |
0.0002 |
|
Nasal |
59.4±14.2 |
43.7±15.7 |
15.7±11.0 |
<0.0001 |
|
Control group (n=30) |
Average |
91.5±12.6 |
86.1±10.6 |
5.4±10.7 |
0.054 |
Superior |
111.8±28.5 |
102.1±19.1 |
9.7±20.8 |
0.072 |
|
Temporal |
97.6±13.7 |
93.5±24.2 |
4.1±18.2 |
0.364 |
|
Inferior |
107.7±11.6 |
106.0±12.4 |
1.7±7.7 |
0.377 |
|
Nasal |
52.9±10.0 |
38.2±17.6 |
14.8±17.3 |
0.003 |
1All values are expressed as mean±standard deviation; 2Comparison
between the thicknesses measured using two devices was performed using the
paired t-test.
Table 3 shows the AUROC values and sensitivities at
fixed specificities for the p-RNFL average and quadrant parameters in
Spectralis OCT and Stratus OCT. The parameters of Spectralis OCT demonstrated
generally higher AUROC values than did the parameters of Stratus OCT; however,
the difference was not statistically significant. Both OCT devices had the
largest AUROC at the inferior quadrant, and the value was higher in Spectralis
OCT (0.951) than in Stratus OCT (0.918), but there was no significant
difference (P=0.157). For Stratus OCT, the sensitivity of the inferior
quadrant parameter was 91.3% at a specificity of 82.1% and 60.9% at a
specificity of 96.4%. For Spectralis OCT, the sensitivity of the inferior
quadrant parameter was 87.5% at a specificity of 85.2%, and 58.3% at a
specificity of 96.4%.
Table 3 Areas under the receiver operating
characteristic curves and sensitivities at fixed specificities for the average and
quadrant parameters in Spectralis and Stratus OCT
Parameters |
AUROC (SE) |
P |
Sensitivity/Specificity |
||||
Specificity >80.0% |
Specificity >95% |
||||||
Spectralis |
Stratus |
Spectralis |
Stratus |
Spectralis |
Stratus |
||
Average |
0.893 (0.049) |
0.840 (0.061) |
0.301 |
75.0/81.5 |
78.3/82.1 |
29.2/96.3 |
47.8/96.4 |
Superior |
0.744 (0.078) |
0.704 (0.092) |
0.584 |
50.0/81.5 |
52.2/82.1 |
16.7/100.0 |
34.8/96.4 |
Temporal |
0.933 (0.035) |
0.815 (0.074) |
0.09 |
75.0/81.5 |
82.6/85.7 |
45.8/96.3 |
60.9/96.4 |
Inferior |
0.951 (0.030) |
0.918 (0.041) |
0.157 |
87.5/85.2 |
91.3/82.1 |
58.3/96.4 |
60.9/96.4 |
Nasal |
0.575 (0.092) |
0.597 (0.089) |
0.828 |
8.3/81.5 |
4.3/89.3 |
8.3/92.6 |
4.3/96.4 |
AUROC: Area under the receiver operating
characteristic curve; SE: Standard error. AUROC values of comparable parameters
obtained using the two devices were compared using Chi-square tests.
Table 4 indicates the AUROC values and sensitivities
at fixed specificities for the p-RNFL sector parameters in Spectralis OCT and
p-RNFL clock-hour parameters in Stratus OCT. In Spectralis OCT, the parameter
with the highest AUROC was the temporal-inferior sector (0.974), with a
sensitivity of 95.8% at 85.2% specificity and 66.7% at 96.3% specificity. In
Stratus OCT, the parameter with the highest AUROC was the 7-o’clock sector
(0.918), with a sensitivity of 91.3% at 82.1% specificity and 73.9% at 96.4%
specificity. The AUROC for the best parameter from Spectralis OCT was higher
than that for the best parameter from Stratus OCT (0.974 vs 0.918, P=0.120),
but the difference was not statistically significant.
Table 4 Areas under the receiver operating
characteristic curves and sensitivities at fixed specificities for the sector
parameters in Spectralis and Stratus OCT
Parameters |
AUROC (SE) |
Sensitivity/Specificity |
|
Specificity >80.0% |
Specificity >95% |
||
Spectralis OCT (sectors) |
|
|
|
Temporal-superior |
0.885 (0.052) |
62.5/81.5 |
41.7/96.3 |
Nasal-superior |
0.502 (0.094) |
4.2/81.5 |
0/96.3 |
Nasal-inferior |
0.648 (0.089) |
37.5/81.5 |
25.0/96.3 |
Temporal-inferior |
0.974 (0.020) |
95.8/85.2 |
66.7/96.3 |
Stratus OCT (clock hours) |
|
|
|
12 superior |
0.627 (0.098) |
43.5/82.1 |
39.1/96.4 |
11 |
0.842 (0.061) |
73.9/82.1 |
56.5/96.4 |
10 |
0.779 (0.080) |
78.3/82.1 |
47.8/96.4 |
9 temporal |
0.772 (0.074) |
60.9/82.1 |
21.7/96.6 |
8 |
0.840 (0.060) |
69.6/82.1 |
39.1/96.4 |
7 |
0.918 (0.042) |
91.3/82.1 |
73.9/96.4 |
6 inferior |
0.878 (0.053) |
87.0/82.1 |
34.8/96.4 |
5 |
0.551 (0.093) |
17.4/82.1 |
13.0/96.4 |
4 |
0.584 (0.090) |
13.0/82.1 |
0/96.4 |
3 nasal |
0.689 (0.084) |
8.7/85.7 |
0/96.4 |
2 |
0.634 (0.089) |
17.4/82.1 |
4.3/96.4 |
1 |
0.513 (0.099) |
30.4/82.1 |
17.4/96.4 |
AUROC: Area under the receiver operating
characteristic curves; OCT: Optical coherence tomography; SE: Standard error.
Diagnosing glaucoma in myopic eyes can be challenging,
mainly because of the morphologic changes in the optic disc, such as PPA
related to myopia, and atypical VF defects such as an enlarged blind spot,
temporal peripheral defect, or generalised reduction in sensitivity. Thus, true
glaucomatous eyes can sometimes be misdiagnosed with conventional diagnostic
tools such as fundus examinations or VF testing. With improvements in
technology, ophthalmic imaging, such as OCT, has been found to be important
adjunct to clinical diagnosis of glaucoma[9,25-26].
Compared to the older TD-OCT, the newer SD-OCT
technology in Spectralis OCT offers the advantages of multiple B-scan
averaging, in which studies have shown to be able to improve the clarity of
boundaries between inner retinal layers[15-16], and may provide a significant advantage over the older
time-domain technology in diagnosing glaucoma. Nukada et al[18] reported
that Spectralis OCT had a better diagnostic capability than single-scan Stratus
OCT to detect localised RNFL defects in patients with perimetric glaucoma.
Jeoung et al[19] also demonstrated that Spectralis OCT was better than Stratus OCT in
detecting preperimetric localised RNFL defects. Both of these studies found
that with the use of technology to reduce speckle noise, Spectralis OCT has an
improved capability to detect localised RNFL defects before disruption of its
reflectivity, and proposed that a device having higher accuracy to detect the
RNFL would have higher diagnostic performance in detecting RNFL defects[18-19]; however, all of these studies have excluded patients with a
refraction of <-6 D. In an era of growing prevalence in high myopia[23], it would
be important to also assess whether these technological advances may provide an
advantage in this group of patients. While none of the previous studies have
directly compared whether SD-OCT would also offer a diagnostic advantage over
TD-OCT in the diagnosis of glaucoma in patients with high myopia, our studys
pecifically compared the glaucoma diagnostic capabilities of Spectralis OCT and
Stratus OCT in highly myopic patients (Table 1).
In the present study, we found that the thickness
measurements of p-RNFL in patients with high myopia from Spectralis OCT were
generally thinner than that measured by Stratus OCT, and the difference in
thickness was more pronounced in the GG (Table 2). Our results are consistent
with a previous study that also found the average RNFL thickness in patients
with open-angle glaucoma to be lower when measured using Spectralis OCT than
using Stratus OCT[27]. This difference in thickness measurements obtained using
the two devices might be explained by the differences in their segmentation
algorithms. The RNFL thickness is generated in Spectralis OCT by setting its
posterior border to the bottom part of the RNFL, whereas in Stratus OCT, the
posterior border of the RNFL is set to be the top layer of the ganglion cell
layer, thereby resulting in a possibly thicker measurement on Stratus OCT.
Although no studies have directly compared the
glaucoma diagnostic capabilities of Spectralis SD-OCT versus Stratus TD-OCT in
patients with high myopia, several studies have evaluated the diagnostic
performances of various SD-OCT devices in highly myopic patients. Shoji et
al[28] evaluated the diagnostic capability of p-RNFL parameters in patients
with high myopia [SE=-8.9±3.1 D; mean deviation (MD)=-8.1±7.7 dB] using RTVue
SD-OCT and found that the largest AUROC was obtained for average p-RNFL
thickness (0.826), followed by the inferior quadrant (0.811). Kim et al[29] also performed a
similar study using RTVue SD-OCT in patients with high myopia (SE=-9.25±3.70 D;
MD=-8.56±5.82 dB) and found that the parameter with the largest AUROC was the
inferior p-RNFL thickness (0.881), followed by the average p-RNFL thickness
(0.825). In the study by Akashi et al[30] p-RNFL in patients
with high myopia (SE=-7.87±1.34 D; MD= -7.36±6.52 dB) was measured using Cirrus
SD-OCT, RTVue SD-OCT, and 3D OCT; they found that the largest AUROC values were
the average p-RNFL thickness (0.969, 0.975, and 0.957, respectively) and
inferior p-RNFL thickness (0.944, 0.953, and 0.964, respectively). Using Cirrus
SD-OCT, Choi et al[31] also found that in
patients with high myopia (SE= -8.70±3.11 D; MD=-7.44±4.85 dB), the p-RNFL
parameter with the largest AUROC was the inferior RNFL thickness (0.906),
followed by the average RNFL thickness (0.899) and the 7-o’clock sector
(0.840). Our results are consistent with the previous studies regarding the
diagnostic capability of SD-OCT in highly myopic glaucoma, and found that
Spectralis OCT also demonstrated good to excellent diagnostic capability for
glaucoma in patients with high myopia (Tables 3, 4). In our study, the SD-OCT
p-RNFL parameters with the best ability for discriminating highly myopic
patients with and without glaucoma were the temporal-inferior sector (0.974)
and the inferior quadrant (0.951).
Recent studies on non-highly myopic patients that have
directly compared between the Cirrus SD-OCT and Stratus TD-OCT foundthat
glaucoma detection capabilities were significantly better for SD-OCT[18-19], although some of the earlier studies have suggested
otherwise[12,32]. In the current study on highly myopic patients, which
compared the glaucoma diagnostic performance of Spectralis SD-OCT and Stratus
TD-OCT, we foundthat on Spectralis OCT, the temporal-inferior sector
(AUROC=0.974) and the inferior quadrant (AUROC=0.951) parameters performed the
best, whereas for Stratus OCT, the 7-o’clock sector (AUROC=0.918) and inferior
quadrant (AUROC=0.918) performed the best. Spectralis OCT had generally higher
AUROC values than Stratus OCT, although the differences were not statistically
significant.
However, the patient population in the study design
may affect the comparison between these two OCT devices. Our study evaluated
only highly myopic controls and patients with mild to moderate glaucoma
(MD=-6.4±4.1 dB). RNFL thickness has been shown to be increasingly thinned as
myopia increases[33], and since the patients in our glaucoma group only had mild
to moderate glaucoma, the RNFL thickness differences in the control group
versus the glaucoma group may not be pronounced enough to highlight a
significant difference in diagnostic capabilities of these two devices. In
addition to the thickness of RNFL, glaucoma severity may also affect its
reflectivity[18,34]. As the reflectivity of RNFL
decreases with worsening glaucoma, differentiation between the border of the
RNFL and the ganglion cell layer may be increasingly difficult, and may result
in misidentification of the RNFL layer by the OCT segmentation software.
Therefore, in patients with moderate to severe glaucoma and markedly reduced
reflectivity of RNFL, the reduced speckle noise technology in Spectralis OCT
may have a greater advantage in having a better visualization of the boundaries
between the inner retinal layers over Stratus OCT[18], and thus possibly
offering a better diagnostic capability.
Two additional explanations might account for the lack
of diagnostic advantage of Spectralis OCT over Stratus OCT in patients with
high myopia. First, small, focal, and narrow RNFL defects <10° may be masked
by the averaging of the thickness values in the sectors or quadrants; thus, if
the RNFL defects were very narrow, then they would likely be difficult to
detect using either device. Jeoung et al’s[10,12,19] previous studies found that for localised defects with
angular widths <10°, the sensitivities of Spectralis and Stratus OCT were
similar at 46.2% and 38.5%, respectively; however, when the defects had angular
widths of 20° to 30°, the sensitivity was 81.8% for Spectralis OCT and 63.6%
for Stratus OCT. A second possible explanation for the lack of differences
between the diagnostic capabilities of these two devices is that the present
study included only highly myopic eyes. Glaucomatous RNFL damage may appear as
both localised defects and diffuse RNFL atrophy, but the latter is more common
in high myopia. Compared with localised RNFL defects, diffuse RNFL atrophy may
be more difficult to detect[7-8]. A
previous study by Kim et al[35] also
found that the Stratus and Cirrus OCT devices did not differ significantly in
their capability to detect diffuse RNFL atrophy. The results of our study
suggest that even with the advances and improvements in SD-OCT imaging
technology, the glaucoma diagnostic capabilities of these two devices are
similar in patients with high myopia.
Our study has some limitations. First, the differences
in the sensitivity of imaging devices would depend on the severity of
glaucomatous damage, referral source for study patients, and criteria used to
define glaucoma. In this study, the definition of glaucoma was based on both
functional deterioration in glaucomatous VF defects as well as structural
changes in the optic disc and RNFL. The diagnostic accuracy of OCT has been
evaluated only for perimetric glaucoma. Some eyes with very early optic nerve
structural abnormality or with functional damage not apparent on VF testing may
have been categorised in the control group, thereby affecting our results.
Furthermore, since the results of our study showed that the glaucoma diagnostic
capability of Stratus OCT and Spectralis OCT appear to be similar in highly
myopic patients with mild to moderate glaucoma, it would be important in a
future study to include highly myopic glaucoma patients at different glaucoma
stages to clarify whether Spectralis OCT would perform better than Stratus OCT
in patients with more severe glaucoma and decreased RNFL reflectivity. Second,
we excluded patients with large PPA that extended outside the measurement circle
of the OCT in order to decrease the number of scans with artefacts. Exclusion
of these patients could have created a potential selection bias, as PPA is
considered an optic disc characteristic of myopia. However, we undertook a
within-patient comparison to ensure this selection bias did not alter the
conclusions.
In conclusion, this study found that the peripapillary
RNFL thickness parameters with the highest AUROC for diagnosing glaucoma in
patients with high myopia were the temporal-inferior sector on Spectralis
SD-OCT and the 7-o’clock sector on Stratus TD-OCT. These parameters could be
useful in distinguishing highly myopic patients with and without glaucoma.
However, there were no significant differences between the AUROCs for
Spectralis SD-OCT and Stratus OCT, which suggest that the glaucoma diagnostic
capabilities of these two devices in patients with high myopia are similar.
Foundation: Supported by Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan,
China (No.CMRPG8C0541).
Conflicts of Interest: Teng MC, None; Poon YC, None; Hung KC, None; Chang
HW, None; Lai IC, None; Tsai JC, None; Lin PW, None; Wu
CY, None; Chen CT, None; Wu PC, None.
1 Weinreb RN, Khaw PT. Primary open-angle glaucoma. Lancet 2004;363(9422):1711-1720. [CrossRef]
2 Leung CK, Chan WM, Yung WH, Ng AC, Woo J, Tsang MK, Tse RK. Comparison
of macular and peripapillary measurements for the detection of glaucoma: an
optical coherence tomography study. Ophthalmology
2005;112(3):391-400. [CrossRef] [PubMed]
3 Hoffmann EM, Medeiros FA, Sample PA, Boden C, Bowd C, Bourne RR,
Zangwill LM, Weinreb RN. Relationship between patterns of visual field loss and
retinal nerve fiber layer thickness measurements. Am J Ophthalmol 2006;141(3):463-471. [CrossRef] [PubMed]
4 Medeiros FA, Zangwill LM, Bowd C, Weinreb RN. Comparison of the GDx
VCC scanning laser polarimeter, HRT II confocal scanning laser ophthalmoscope,
and stratus OCT optical coherence tomograph for the detection of glaucoma. Arch Ophthalmol 2004;122(6):827-837. [CrossRef] [PubMed]
5 Chen SJ, Lu P, Zhang WF, Lu JH. High myopia as a risk factor in
primary open angle glaucoma. Int J
Ophthalmol 2012;5(6):750-753. [PMC free article] [PubMed]
6 Chang RT, Singh K. Myopia and glaucoma: diagnostic and therapeutic
challenges. Curr Opin Ophthalmol 2013;24(2):96-101.
[CrossRef] [PubMed]
7 Tuulonen A, Airaksinen PJ. Initial glaucomatous optic disk and retinal
nerve fiber layer abnormalities and their progression. Am J Ophthalmol 1991;111(4):485-490. [CrossRef]
8 Jonas JB, Dichtl A. Optic disc morphology in myopic primary open-angle
glaucoma. Graefes Arch Clin Exp
Ophthalmol 1997;235(10):627-633. [CrossRef] [PubMed]
9 Hsu CH, Chen RI, Lin SC. Myopia and glaucoma: sorting out the
difference. Curr Opin Ophthalmol 2015;26(2):90-95.
[CrossRef] [PubMed]
10 Jeoung JW, Park KH, Kim TW, Khwarg SI, Kim DM. Diagnostic ability of
optical coherence tomography with a normative database to detect localized
retinal nerve fiber layer defects. Ophthalmology
2005;112(12):2157-2163. [CrossRef]
11 Kim TW, Park UC, Park KH, Kim DM. Ability of Stratus OCT to identify
localized retinal nerve fiber layer defects in patients with normal standard
automated perimetry results. Invest
Ophthalmol Vis Sci 2007;48(4):1635-1641. [CrossRef] [PubMed]
12 Jeoung JW, Park KH. Comparison of Cirrus OCT and Stratus OCT on the
ability to detect localized retinal nerve fiber layer defects in preperimetric
glaucoma. Invest Ophthalmol Vis Sci 2010;51(2):938-945.
[CrossRef] [PubMed]
13 Hangai M, Yamamoto M, Sakamoto A, Yoshimura N. Ultrahigh-resolution
versus speckle noise-reduction in spectral-domain optical coherence tomography.
Opt Express 2009;17(5):4221-4235. [CrossRef]
14 Mumcuoglu T, Wollstein G, Wojtkowski M, Kagemann L, Ishikawa H,
Gabriele ML, Srinivasan V, Fujimoto JG, Duker JS, Schuman JS. Improved
visualization of glaucomatous retinal damage using high-speed
ultrahigh-resolution optical coherence tomography. Ophthalmology 2008;115(5):782-789. [CrossRef] [PMC free article] [PubMed]
15 Sander B, Larsen M, Thrane L, Hougaard JL, Jorgensen TM. Enhanced
optical coherence tomography imaging by multiple scan averaging. Br J Ophthalmol 2005;89(2):207-212. [CrossRef] [PMC free article] [PubMed]
16 Sakamoto A, Hangai M, Yoshimura N. Spectral-domain optical coherence
tomography with multiple B-scan averaging for enhanced imaging of retinal
diseases. Ophthalmology 2008;115(6):1071-1078.
[CrossRef] [PubMed]
17 Byeon SH, Chu YK, Lee H, Lee SY, Kwon OW. Foveal ganglion cell layer
damage in ischemic diabetic maculopathy: correlation of optical coherence
tomographic and anatomic changes. Ophthalmology
2009; 116(10):1949-1959. [CrossRef] [PubMed]
18 Nukada M, Hangai M, Mori S, Nakano N, Nakanishi H, Ohashi-Ikeda H,
Nonaka A, Yoshimura N. Detection of localized retinal nerve fiber layer defects
in glaucoma using enhanced spectral-domain optical coherence tomography. Ophthalmology 2011;118(6):1038-1048. [CrossRef] [PubMed]
19 Jeoung JW, Kim TW, Weinreb RN, Kim SH, Park KH, Kim DM. Diagnostic
ability of spectral-domain versus time-domain optical coherence tomography in
preperimetric glaucoma. J Glaucoma 2014;
23(5):299-306. [CrossRef] [PubMed]
20 Mitchell P, Hourihan F, Sandbach J, Wang JJ. The relationship between
glaucoma and myopia: the Blue Mountain Eye Study. Ophthalmology 1999;106(10):2010-2015. [CrossRef]
21 Xu L, Wang Y, Wang S, Wang Y, Jonas JB. High myopia and glaucoma
susceptibility - the Beijing Eye Study. Ophthalmology
2007;114(2):216-220. [CrossRef] [PubMed]
22 Verkicharla PK, Ohno-Matsui K, Saw SM. Current and predicted
demographics of high myopia and an update of its associated pathological
changes. Ophthalmic Physiol Opt 2015;35(5):465-475.
[CrossRef] [PubMed]
23 Lin LL, Shih YF, Hsiao CK, Chen CJ. Prevalence of myopia in Taiwanese
schoolchildren: 1983 to 2000. Ann Acad
Med Singap 2004;33(1):27-33. [PubMed]
24 Obuchowski NA. ROC analysis. AJR
Am J Roentgenol 2005;184(2): 364-372. [CrossRef] [PubMed]
25 Grewal DS, Tanna AP. Diagnosis of glaucoma and detection of glaucoma
progression using spectral domain optical coherence tomography. Curr Opin Ophthalmol 2013;24(2):150-161.
[CrossRef] [PubMed]
26 Bussel II, Wollstein G, Schuman JS. OCT for glaucoma diagnosis,
screening and detection of glaucoma progression. Br J Ophthalmol 2014;98(Suppl 2):ii15-19. [CrossRef] [PMC free article] [PubMed]
27 Toteberg-Harms M, Sturm V, Knecht PB, Funk J, Menke MN. Repeatability
of nerve fiber layer thickness measurements in patients with glaucoma and
without glaucoma using spectral-domain and time-domain OCT. Graefes Arch Clin Exp Ophthalmol 2012;250(2):279-287.
[CrossRef] [PubMed]
28 Shoji T, Nagaoka Y, Sato H, Chihara E. Impact of high myopia on the
performance of SD-OCT parameters to detect glaucoma. Graefes Arch Clin Exp Ophthalmol
2012;250(12):1843-1849. [CrossRef] [PubMed]
29 Kim NR, Lee ES, Seong GJ, Kang SY, Kim JH, Hong S, Kim CY. Comparing
the ganglion cell complex and retinal nerve fibre layer measurements by Fourier
domain OCT to detect glaucoma in high myopia. Br J Ophthalmol 2011;95(8):1115-1121. [CrossRef] [PubMed]
30 Akashi A, Kanamori A, Nakamura M, Fujihara M, Yamada Y, Negi A. The
ability of macular parameters and circumpapillary retinal nerve fiber layer by
three SD-OCT instruments to diagnose highly myopic glaucoma. Invest Ophthalmol Vis Sci 2013;54(9):6025-6032.
[CrossRef] [PubMed]
31 Choi YJ, Jeoung JW, Park KH, Kim DM. Glaucoma detection ability of
ganglion cell-inner plexiform layer thickness by spectral-domain optical
coherence tomography in high myopia. Invest
Ophthalmol Vis Sci 2013;54(3):2296-2304. [CrossRef] [PubMed]
32 Sehi M, Grewal DS, Sheets CW, Greenfield DS. Diagnostic ability of
fourier-domain vs time-domain optical coherence tomography for glaucoma
detection. Am J Ophthalmol 2009;148(4):597-605.
[CrossRef] [PMC free article] [PubMed]
33 Oner V, Aykut V, Tas M, Alakus MF, Iscan Y. Effect of refractive
status on peripapillary retinal nerve fibre layer thickness: a study by RTVue
spectral domain optical coherence tomography. Br J Ophthalmol 2013;97(1):75-79. [CrossRef] [PubMed]
34 van der Schoot J, Vermeer KA, de Boer JF, Lemij HG. The effect of
glaucoma on the optical attenuation coefficient of the retinal nerve fiber
layer in spectral domain optical coherence tomography images. Invest Ophthalmol Vis Sci 2012;53(4):2424-2430.
[CrossRef] [PubMed]
35 Kim KE, Kim SH, Jeoung JW, Park KH, Kim TW, Kim DM. Comparison of
ability of time-domain and spectral-domain optical coherence tomography to
detect diffuse retinal nerve fiber layer atrophy. Jpn J Ophthalmol 2013;57(6):529-539. [CrossRef] [PubMed]