Abstract
Purpose
To investigate the optical intensity in different compartments of subretinal fluid in acute Vogt-Koyanagi-Harada (VKH) disease by using spectral domain optical coherence tomography (SD-OCT).
Methods
Fifty acute VKH eyes and 25 cases with acute central serous chorioretinopathy (CSCR) were included in this retrospective comparative study. The optical intensities of subretinal fluid, vitreous humour and the entire scanned region displayed by SD-OCT were measured with Image J by three independent readers. In the VKH eyes with subretinal septa, the subretinal fluid was segmented into two types of compartments, supra-septa space and sub-septa space. Optical intensity ratios of different compartments of subretinal fluids divided by vitreous humour or the entire scanned region were compared.
Results
The measurement of optical intensity was highly reproducible (intraclass correlation coefficient> 0.9). The optical intensity of the supra-septa space divided by the vitreous humour was significantly higher compared to that of sub-septa space in VKH (mean difference = 4.27 ± 5.15, p <0.001). The optical intensity ratio of the supra-septa space (1.14 ± 0.12), but not subsepta space (1.05 ± 0.05) in VKH, was significantly higher compared to that of the subretinal space in VKH without the subretinal septa (1.07 ± 0.08), and the subretinal fluid in CSCR (1.08 ± 0.09). Similar results were found for the optical intensity ratios divided by the entire scan region.
Conclusion
The optical intensity in the supra-septa space of VKH is higher compared to the sub-septa space in VKH, subretinal space in VKH and CSCR, suggesting that the components in these spaces are different.
Introduction
Vogt-Koyanagi-Harada (VKH) disease is a common cause of bilateral panuveitis in darkly pigmented races. There is often involvement of other organs, including the ears, skin, and meninges.[1] The acute phase of VKH disease is characterized by diffuse choroidal inflammation and serous retinal detachment at the posterior pole.[2] With the introduction of optical coherence tomography (OCT), several microstructural changes have been identified in VKH disease, such as subretinal fluid, choroidal and retinal pigment epithelial (RPE) fold, fluctuation of the internal limiting membrane, subretinal septa, bulge of RPE, increased retinal thickness and choroidal thickness.[3–9]
In some cases, the subretinal space is separated into several compartments by subretinal septa on the cross sectional images of OCT.[10] There are arguments concerning the nature of these septa and compartments. At first, it was assumed that the septa are part of the outer retina and the supra-septa space is intra-retinal fluid [3], intra-retinal edema [11], or cystoid space [10]. Later, by using spectral domain OCT (SD-OCT), the septa was found to be continuous with the line representing the junction of the photoreceptor inner and outer segments (IS/OS) in the attached areas of the retina, suggested a splitting off of outer segments from the inner segments of the photoreceptor layer, and formation of a membranous structure through binding of these outer segments to each other, forming cysts in the supra-septa space within photoreceptor layer.[8, 12, 13] However, this hypothesis was questioned that intraretinal cysts or photoreceptor cleavage and vision cannot recover so rapidly or completely.[14, 15] On FFA, the subretinal compartments correspond to multilobular dye pooling, and there is no petaloid pattern. Therefore, it is assumed that the septa are fibrinous or proteinaceous subretinal exudates, whereas the supra-septa fluid is subretinal fluid segmented by a fibrous membrane.[16]
The purpose of this study is to investigate the component of fluids in different compartments of subretinal spaces in VKH by quantitatively comparing the optical intensities in these compartments on OCT images.
Patients and Methods
Subjects
This is a retrospective comparative study. The Institutional Review Board of the Joint Shantou International Eye Center approved this study and waived the informed consent due to the retrospective nature of this study. Our study complies with the Declaration of Helsinki. The patient records/information was anonymized and de-identified prior to analysis.
The patient database of Joint Shantou International Eye Center, Shantou University and the Chinese University of Hong Kong, from January 2012 to July 2013, was searched. The medical charts of patients diagnosed as having VKH disease or central serous chorioretinopathy, which was included as control, received further review. The patients received comprehensive ophthalmic examinations including best-corrected visual acuity (BCVA), intraocular pressure, slit lamp biomicroscopy of the anterior segment and retina with mydriasis, fundus fluorescein angiography and SD-OCT.
Diagnosis of VKH was based on the criteria defined by the International Committee in 2001 [1]. Diagnosis of acute CSCR was based on typical angiographic findings of focal neurosensory retinal detachment or retinal pigment epithelium (RPE) detachment with leakage at the level of the RPE, as seen on fluorescein angiography [17] without any sign of other diseases, such as uveitis, polypoidal choroidal vasculopathy, choroidal neovascularization, optic disc pitting or retinal vasculopathy. Patients with symptoms lasting longer than 3 months were excluded in this study.
Spectral domain optical coherence tomography
SD-OCT examinations were performed with a Cirrus HD-OCT (Carl Zeiss, Germany). The macula was scanned with the standard fovea-centered five line raster scan protocol. The single B-scan that contained the largest volume of subretinal fluid was chosen. The grayscale images were exported as bitmap files, which is an uncompressed format. No further image manipulation was performed on the OCT data. Only the OCT image with an signal strength ≥6 were included according to the manual of Cirrus OCT.
Optical intensity measurement
Optical intensity measurements were carried out with Image J software (National Institutes of Health, Bethesda, MD; available at http://rsb.info.nih.gov/ij/index.html) with a method modified from the literature.[18, 19] Four different types of regions of interest were defined with the largest possible area, including the supra-septa space (Fig 1A and 1B.) and sub-septa space (Fig 1B.) in VKH eyes with subretinal septa, subretinal space in CSCR and VKH eyes without subretinal septa, vitreous humour, and the entire B scan region (Fig 1C). The mean pixel intensities were calculated by the Image J software. Interpreting the exported B scan picture as 8-bit grayscale images resulted in 256 levels of gray, ranging from 0 to 255.To test the intra-observer reproducibility, the measurements were performed three separate times by Reader 1 (D.L.). To test the inter-observer reproducibility, the measurements were performed by three independent masked readers (D.L., M.L. and X.L.).
Statistical analysis
The software SPSS (version 17.0; SPSS, Inc., Chicago, IL) was used to conduct statistical analysis. The intraclass correlation coefficients (ICC) were determined by a two-way mixed effects model for measurements of absolute agreement. The optical intensity is affected by many factors, such as OCT signal strength and media opacity. We calculated the optical intensity ratio of the subretinal space divided by the vitreous humour [18, 19]or the entire scanned region [20] for normalization. The optical intensity ratio of the supra-septa or sub-septa space in VKH eyes with subretinal septa was compared to that of the subretinal space in VKH eyes without subretinal septa and CSCR eyes by one-way analysis of variance and the Student-Newman-Keuls test. The optical intensities of sub-septa and supra-septa space in the same eyes were compared by a paired t-test because they were affected by the same level of signal strength or media opacity. Pearson correlation between optical intensity ratios and the best-corrected visual acuity at presentation or at the last follow-up was assessed. P values of less than 0.05 were considered statistically significant. SPSS (version 22.0, IBM Inc. Chicago, IL) software was used to perform statistical analysis and Sigmaplot (version 12.0, Systat Inc. Chicago, IL) software was used to draw statistical plots.
Results
In total, 50 eyes of 30 patients with acute VKH and 25 eyes of 25 patients with acute CSCR were included in this study. The demographic information and optical intensity of each included subjects were listed in S1 Table. Ten of 85 eyes were excluded because image quality was unacceptable (signal strength < 6). Table 1 shows the demographic information, including age, gender and BCVA of the included subjects. There was a predominance of men in the CSCR group, but not in the VKH group (82.1% in CSCR vs. 46.7% in VKH, p = 0.004, chi square test). There was no significant difference of age of patients between the two diseases (p = 0.847, Student’s t test). BCVA was significantly worse in VKH than in CSCR group (0.77± 0.42 vs. 0.32 ± 0.23 LogMAR, p < 0.001, Student’s t test). Serous retinal detachment presented in all cases with VKH and all cases with CSCR, whereas subretinal septa only presented in 70% (35/50) cases with VKH, but not in CSCR. The measurement of optical intensities had high intra-observer repeatability and inter-observer reproducibility in all regions (all ICC > 0.927, Table 2).
Table 1. Demographic and clinical data of included subjects.
Variable | VKH | CSCR | P value | Statistics |
---|---|---|---|---|
N | 30 | 25 | ||
Age, year (range) | 43.5±11.9 (21–76) | 43.1±6.1 (25–62) | 0.847 | Student’s t test |
Gender (male: female) | 14:16 | 21: 4 | 0.004 | Chi-square test |
BCVA (LogMAR) | 0.77±0.42 | 0.32±0.23 | <0.001 | Student’s t test |
BCVA and age is presented as mean ± standard deviation. VKH: Vogt-Koyanagi-Harada disease; CSCR: central serous chorioretinopathy; BCVA: best corrected visual acuity; LogMAR: logarithm of the minimum angle of resolution
Table 2. Repeatability and reproducibility of optical intensity measurements.
Intra-observer ICC (95%CI) | Inter-observer ICC (95%CI) | |
---|---|---|
Vitreous | 0.999 (0.998–1.000) | 0.993 (0.986–0.997) |
Sub-septa fluid in VKH | 0.997 (0.995–0.998) | 0.992 (0.984–0.996) |
Supra-septa fluid in VKH | 0.994 (0.986–0.996) | 0.927 (0.836–0.974) |
Subretinal fluid in VKH | 0.999 (0.998–1.000) | 0.907 (0.797–0.965) |
Subretinal fluid in CSCR | 1.000 (1.000–1.000) | 0.945 (0.896–0.973) |
entire region | 1.000 (1.000–1.000) | 0.981 (0.964–0.991) |
ICC, intraclass correlation coefficient; CI, confidence interval; VKH: Vogt-Koyanagi-Harada disease; CSCR: central serous chorioretinopathy.
The optical intensity of supra-septa space was significantly higher compared to that of sub-septa space in VKH (mean difference = 4.27 ± 5.15, p <0.001, paired t test, Fig 2). The optical intensity ratio of supra-septa space divided by vitreous humour in VKH eyes (1.14 ± 0.12) was significantly higher compared to that of the subretinal space in VKH without subretinal septa (1.07 ± 0.08), and the subretinal fluid in CSCR (1.08 ± 0.09), with p = 0.019 (Fig 3A). There was no statistically significant difference between the sub-septa space in VKH with subretinal septa (1.05 ± 0.05) and subretinal space in VKH without subretinal septa or CSCR (p = 0.116, Fig 3A). Similarly, the optical intensity ratio of supra-septa space divided by the entire scanned region in VKH (0.87 ± 0.97) was significantly higher compared to that of the subretinal space in VKH without subretinal septa (0.81 ± 0.05), and the subretinal fluid in CSCR (0.81 ± 0.05) (p = 0.001, Fig 3B). There was no statistically significant difference between the sub-septa space in VKH with subretinal septa (0.80 ± 0.05) and subretinal space in VKH without subretinal septa or CSCR, with p = 0.669 (Fig 3B). There is no statistical significant correlation between the optical intensity ratios and the best-corrected visual acuity at presentation or at the last follow-up (all p > 0.05).
Discussion
In this study we quantitatively investigate the optical intensity of different compartments of the subretinal space in VKH, using a measurement with high repeatability and reproducibility. The results show that the optical intensity of supra-septa space in VKH is higher than that of the sub-septa space in VKH with subretinal septa, subretinal space in VKH without septa or CSCR. There is no statistical difference in the optical intensity of sub-septa space in VKH with septa, sub-retinal space in VKH without septa and CSCR.
OCT is not only valuable in providing morphological images, but also quantitative measurement of the optical intensity (also referred to as optical density, reflectivity) of normal and pathological tissue. It has been reported that the optical intensity of the intraretinal or subretinal spaces with exudation, such as diabetic macular edema, retinitis pigmentosa, and CSCR, are higher than that of the vitreous humour. While the optical intensity of the intraretinal or subretinal spaces without exudation, including cone dystrophy and idiopathic perifoveal telangiectasia are lower compared to that of vitreous humour,[21] it has been shown that the optical intensity ratio of the subretinal space divided by the vitreous humour is significantly higher in patients with age-related macular degeneration, diabetic macular edema, CSCR, and postoperative macular edema, than in those with retinal detachment and retinoschisis.[19] In another study, it was reported the optical intensity ratio is not only increased in age-related macular degeneration, but also correlates with BCVA after anti-angiogenic therapy.[18] Furthermore, the optical intensity of intraretinal or subretinal space in diabetic macular edema is found to be correlated with visual acuity [22], fluorescein pooling,[23] and intravitreal concentration of vascular endothelial growth factor[24].These results suggest that the optical intensity of the intraretinal or subretinal spaces can be used as a biomarker and provide insight to the pathogenesis of retinal diseases.
Although the composition of the intra/sub-retinal spaces is still not well understood, a higher optical intensity signal may be an indication of increased component of the fluids being scanned, whereas a low optical intensity signal reflects a relatively clear fluid composition with fewer particles.[21] In current study, no significant difference in optical intensity is found between the sub-septa space or subretinal space between VKH and CSCR. The subretinal fluid of both VKH and CSCR are exudates from the choroidal vasculature through the breakdown of retinal pigment epithelium. Therefore, the composition of subretinal fluid coming from the serous retinal detachment space in these two diseases might be similar. So it is not surprising to find similar optical intensity of serous retinal detachment space in the two diseases.
The prevalence of subretinal septa in acute VKH has been reported to be 40–43% by time domain OCT [3, 10], and 85% by spectral domain OCT.[12]In our study, subretinal septa was found in 70% VKH eyes with spectral domain OCT, which is consistent with the literature. On the OCT image of VKH, the supra-septa fluid seems to be mildly reflective, whereas areas of sub-septa fluid are not reflective.[3] However, this result is based on qualitative observation. Our study quantitatively measures the optical intensity for VKH and finds that the optical intensity of the supra-septa space is higher compared to that of the sub-septa space.
The nature of the subretinal septa and the components of the supra-septa space fluid in acute VKH remains unknown and controversial. There are two hypotheses. In the first, the septa result from a splitting off of outer segments, from the inner segments of the photoreceptor layer, and formation of a membranous structure through the binding of these outer segments to each other, while the supra-septa space forms cysts within the photoreceptor layer.[8, 12, 13] The other hypothesis states that the septa are fibrinous or proteinaceous subretinal exudates that form on the RPE. Additional serous exudation through the RPE detaches the fibrin membrane from the RPE, forming septa that divide the subretinal space into multiple compartments.[16] Our study finds that the optical intensity in the supra-septa space is significantly higher compared to that of sub-septa space, suggesting that components of the supra-septa fluid are different from sub-septa fluid, and there are more particles in supra-septa fluid. This finding supports the hypothesis that subretinal septa is splitting off of outer segments from the inner segments, possibly due to the death of photoreceptors results in cell debris increased in the supra-septa space. Our study does not support the hypothesis that fibrinous or proteinaceous subretinal exudates dividing the subretinal space into multiple compartments, which should have similar optical intensity in this case.
Our study is a retrospective study and there may be sampling bias. A prospective study including more subjects is needed to confirm our results. In addition, there is only one time point in our study. Further study with longitudinal follow-up is needed to investigate the change in optical intensity of subretinal fluid in response to treatment. In summary, the present study finds significantly increased optical intensity in the supra-septa space compared to sub-septa space in VKH, subretinal space in VKH and CSCR, suggesting that the components in these spaces are different.
Supporting Information
Acknowledgments
This study was supported in part by the National Nature Science Foundation of China (81170853) and Medical Scientific Research Foundation of Guangdong Province (B2013290). We would like to thank Dr. Chien-Fu Lin for copy-editing.
Data Availability
All relevant data are within the paper and its Supporting Information files.
Funding Statement
This study was supported by the National Nature Science Foundation of China (www.nsfc.gov.cn/ #81170853) and Medical Scientific Research Foundation of Guangdong Province (B2013288). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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Supplementary Materials
Data Availability Statement
All relevant data are within the paper and its Supporting Information files.