Abstract
Diabetic macular edema (DME) refractory to anti-VEGF drugs is a socioeconomic burden. In this retrospective study, we investigated the relationship between DME remission and hyperreflective walls in foveal cystoid spaces, a novel finding on spectral domain optical coherence tomography (SD-OCT) images in DME. In a cross-sectional study, we assessed the relationship between hyperreflective walls in foveal cystoid spaces and other OCT findings in 110 eyes of 110 DME patients. Hyperreflective walls were delineated in 27 of 171 foveal cystoid spaces. Eyes with hyperreflective walls in foveal cystoid spaces had poorer visual acuity and more severe photoreceptor disruption than did those without such findings (P = 0.008 and P < 0.001, respectively). In the other longitudinal study, we evaluated the relationship between this finding and the remission in 54 eyes of 51 DME patients treated with as-needed ranibizumab injections for 24 months. Foveal cystoid spaces with hyperreflective walls were often persistent, and the cumulative rates of DME remission among eyes with and without the hyperreflective walls were 7.7% (1 eye) and 48.8% (20 eyes) at 18 months (hazard ratio, 0.092; P = 0.025). We characterized hyperreflective walls in foveal cystoid spaces and designated them as a predictor of no DME remission under ranibizumab injections.
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Diabetic macular edema (DME) is a major cause of visual dysfunction in diabetic patients1. The breakdown of the blood-retinal barrier (BRB) leads to the accumulation of intracellular and extracellular fluids in the retinal parenchyma2. Two major clinical examinations, fluorescein angiography (FA) and spectral domain optical coherence tomography (SD-OCT), delineate the various patterns of vascular hyperpermeability and neuroglial impairment3. However, how the diversity in clinical findings influences the responsiveness to individual interventions remains poorly understood.
Structural analyses using OCT improve the qualities of medical management for diabetic patients. The measurement of central subfield (CSF) thickness provides an objective and quantitative diagnosis of center-involved DME. There are modest correlations between CSF thickness and visual acuity (VA) in DME4. The qualitative assessment of retinal morphologies on sectional OCT images allows us to understand the pathological mechanisms more precisely3,5. Macular thickening is composed of cystoid macular edema (CME), serous retinal detachment (SRD), and sponge-like retinal swelling on OCT images6. CME is associated with enlarged foveal avascular zone and the patterns of fluorescein pooling7,8. In addition, structural OCT revealed a few findings in cystoid spaces, e.g., high reflectance, heterogeneous reflectivity, and hyperreflective foci9,10. Some OCT findings are biomarkers to predict the early response to anti-vascular endothelial growth factor (VEGF) treatment or steroids for DME11,12,13,14. Hyperreflective intraretinal spots and subfoveal neuroretinal detachment decrease after anti-VEGF therapy15. This idea suggests the clinical feasibility of OCT parameters, although whether they are predictors of the long-term responses for DME remains largely unknown.
Among several therapeutic strategies, anti-VEGF drugs are the first-line treatment for DME16. Despite its significant efficacy, we need to consider the severe socioeconomic burden and higher cost-per-quality-adjusted life years of anti-VEGF treatment than those of other conventional therapies17. Major clinical trials using pro re nata (PRN) dosing revealed that the median treatment frequency is reduced in the second year and beyond, although some cases need frequent injections at later visits16,18. We should consider several possible explanations for the refractory disease, e.g., tachyphylaxis to these drugs, molecular mechanisms other than VEGF, and retinal degeneration19,20. These explanations might support the decision for additional therapeutic strategies to some extent, although clinical fundus findings in the refractory DME should be elucidated.
In this study, we characterized hyperreflective walls in foveal cystoid spaces, a novel OCT finding, and investigated whether this finding can predict DME refractory to anti-VEGF drugs.
Results
Characteristics of hyperreflective walls in foveal cystoid spaces
We retrospectively reviewed 110 eyes of 110 patients with treatment-naïve center-involving DME. Patient characteristics are shown in Table S1. Hyperreflective walls were delineated in 27 (15.8%) of 171 foveal cystoid spaces (Figs. 1, 2). Only seven (3.6%) of 192 parafoveal cystoid spaces had the walls. This OCT finding was often delineated in the whole bottom and sometimes in the top or septa (or lateral boundaries) and their thicknesses were 51μm (48–56). The relative reflectivity of the hyperreflective walls was 51.8 (44.0–58.5). Cystoid spaces with the hyperreflective walls had lower levels of OCT reflectivity (P = 0.036) and greater width (P = 0.004) than did those without such walls. Hyperreflective foci were delineated in cystoid spaces with the hyperreflective walls more frequently than those without such walls (P = 0.044; Table 1).
Eyes with hyperreflective walls in foveal cystoid spaces had poorer logarithm of the minimum angle of resolution (logMAR) VA than did those without such findings, although there were no differences in CSF thicknesses (Table 2). There was no association of the hyperreflective walls with subretinal fluid, vitreoretinal abnormalities, and hyperreflective foci in the inner and outer retinal layers (Table 2). In contrast, the disrupted ellipsoid zone of photoreceptors (EZ) line and disorganization of the retinal inner layers (DRIL) extent were longer in eyes with hyperreflective walls in foveal cystoid spaces than in those without such walls (P < 0.001 and P = 0.032, respectively).
Course of hyperreflective walls in foveal cystoid spaces in eyes treated with anti-VEGF treatment
In the longitudinal study, we reviewed 54 eyes of 51 patients with center-involved DME after the exclusion of 75 eyes among 129 eyes that met the inclusion criteria (Table S2). Improvement of logMAR VA and decrease in CSF thickness were maintained until the 24-month visit (Figs. 3 and 4). Hyperreflective walls in foveal cystoid spaces, disrupted EZ line, and DRIL extent were decreased (Fig. S1).
We evaluated the course of hyperreflective walls in foveal cystoid spaces in eyes treated with ranibizumab injections. All 54 eyes had cystoid abnormalities at baseline and gradually decreased to 20 eyes (37.0%) at 24 months. In contrast, eyes with hyperreflective walls in foveal cystoid spaces persisted from 13 eyes at baseline to 19 and 13 eyes at 12- and 24-month visits, respectively (Fig. 3). Among 13 eyes with hyperreflective walls at baseline, 13 (100%) and 9 (69.2%) eyes had cystoid abnormalities at 12 and 24 months, respectively. In 41 eyes without pretreatment hyperreflective walls, cystoid abnormalities were delineated in only 19 (46.3%) and 11 (26.8%) eyes at 12 and 24 months (P < 0.001 in both comparisons at 12 and 24 months). The ratios of remission of cystoid abnormalities among eyes with and without hyperreflective walls at baseline increased to 7.7% (1 eye) and 46.3% (19 eyes) at 18 months (P = 0.048; Fig. 5A).
Hyperreflective walls in foveal cystoid spaces at baseline as a predictor of no DME remission until 18 months
There were no differences in VA improvement and the decrease in CSF thickness between eyes with and without the hyperreflective walls at baseline (Fig. 4B,D). LogMAR VA did not differ, whereas CSF thicknesses were greater in eyes with hyperreflective walls than in eyes without them at several time points (Fig. 4A,C). The ratios of eyes without center-involved DME were variable in eyes with the hyperreflective walls, compared to those without the walls (Fig. 5B). The cumulative rates of DME remission among eyes with and without the hyperreflective walls were 7.7% (1 eye) and 48.8% (20 eyes) at 18 months (Fig. 5C). According to multivariate analyses, the hyperreflective walls at baseline had significant higher risk of no remission until the 18-month visit (hazard ratio [HR], 0.092; 95% confidence interval [CI], 0.011–0.742; P = 0.025) (Table 3).
Discussion
In the cross-sectional study, we defined hyperreflective walls in foveal cystoid spaces as a novel structural OCT finding in DME. This OCT finding was delineated in the top or bottom of cystoid spaces or the septa between the spaces. Hyperreflective foci were frequently accompanied by hyperreflective walls. Since hyperreflective foci generally correspond to lipid-laden macrophages, inflammatory responses might contribute to the development of the hyperreflective walls. In the longitudinal study, foveal cystoid spaces with hyperreflective walls were persistent, whereas eyes with cystoid abnormalities were decreased under anti-VEGF treatment. This finding is consistent with poorer VA and more severe EZ disruption in eyes with hyperreflective walls. In particular, statistical analyses revealed that the hyperreflective walls in foveal cystoid spaces at baseline predicted unremitted DME under PRN intravitreal ranibizumab (IVR) injections.
We could not determine what type of histological lesions correspond to the hyperreflective walls in foveal cystoid spaces in this study. Several histological publications demonstrated Henle’s fibers or Müller cells in the lateral walls and photoreceptor cells in the bottom walls21. A recent surgical publication documented that fibrinogen-rich cystoid spaces resected during vitrectomy are encapsulated by collagen fibrils in DME22. The clear boundaries of hyperreflective walls may allow us to speculate that collagenous capsules correspond to hyperreflective walls in cystoid spaces and contribute to refractoriness to anti-VEGF treatment. Another possible explanation is that cystoid spaces might be surrounded by gliotic tissues23. In this study, most cystoid spaces with hyperreflective walls were accompanied by hyperreflective foci. Hyperreflective foci may correspond to lipid-laden macrophages and suggest inflammatory responses2,10. These macrophages could promote fibrotic/gliotic scar formation of cystoid spaces24. The third possibility is fibrin deposition, as in the case of intraretinal and subretinal deposits in chorioretinal vascular diseases22. The hyperreflective walls at the bottom of cystoid spaces might correspond to the compressed retina layers, although we carefully confirmed the different reflectivity between the wall and nearby retinal parenchyma. Further investigation should elucidate the correspondence between histological and OCT findings.
Cystoid abnormalities sometimes relapsed in the second year, although most serous retinal detachment (SRD) was resolved until 12 months (Data not shown). Since SRD development is mediated via BRB breakdown, anti-VEGF drugs might decrease vascular hyperpermeability and subsequently resolve SRD25,26. In contrast, the pathophysiological mechanisms in foveal cystoid spaces are complicated; extravasation, ischemia, degeneration, vitreoretinal traction, intracytoplasmic swelling of Müller cells7,21,27. Anti-VEGF treatment can neither repair capillary nonperfusion nor neurodegeneration or do not remove vitreoretinal traction. This may partly explain the refractoriness of foveal cystoid spaces. Additionally, the current study designated hyperreflective walls in foveal cystoid spaces as a novel predictor of unremitted DME. The OCT reflectivity was lower in cystoid spaces with hyperreflective walls. It may allow us to speculate that the hyperreflective walls correspond to capsules of fibrotic tissues or fibrin deposits and maintain the structure of cystoid spaces even under anti-VEGF treatment. Another possibility is that some of cystoid spaces with hyperreflective walls correspond to cystoid macular degeneration as in the case of neovascular age-related macular degeneration, because such cystoid spaces sometimes had concave and straight border in this study28,29.
Frequent injections of expensive anti-VEGF drugs are the first-line treatment for DME.17 We speculate that remission induction is one of important factors to reduce a socioeconomic burden in this chronic disease. In this study, we designated hyperreflective walls in foveal cystoid spaces at baseline as a predictor of no DME remission until 18 months under PRN IVR injections. Since eyes without the hyperreflective walls often reached remission, they may be suitable for anti-VEGF treatment among several therapeutic strategies. In contrast, most eyes with hyperreflective walls in foveal cystoid spaces did not reach remission until 18 months, which might encourage us to consider the switch to or the combination with other interventions for such cases30,31. Future studies should elucidate whether other regimens, e.g., treat-and-extend or monthly regimens, of anti-VEGF injections allow eyes with the hyperreflective walls to achieve remission.
In the cross-sectional study, hyperreflective walls in foveal cystoid spaces were associated with visual impairment in DME. In the longitudinal study, VA did not differ in eyes with and without such OCT finding. The discrepancy might be dependent on the differences in participants. Although the former study included cases with good VA, some patients with good VA did not wish to receive anti-VEGF treatment and were not included into the longitudinal study. We may speculate that VA was not associated with the hyperreflective walls in DME cases with VA reduction.
There are several limitations in this retrospective and preliminary study with small sample sizes. In particular, the retrospective nature is a serious concern in predicting treatment responses in a longitudinal study. Since most patients were referred to our institute without enough information of DME duration, we could not evaluate the disease chronicity. The sectional OCT images were acquired and averaged using a specific SD-OCT machine and its equipped software. Whether this OCT finding is delineated on a single scan image using other OCT devices remains to be elucidated. Three-dimensional analyses would improve the localization of hyperreflective walls. Since several OCT findings were subjectively assessed in this study, future studies should develop procedures to evaluate them objectively. We selected the PRN dosing of IVR injections, although further studies have to confirm the generalizability to other regimens, other anti-VEGF drugs, or other interventions. All participants were Asian in a single institute; thus, we should plan to confirm the reproducibility in other races in prospective multicenter studies.
We documented hyperreflective walls in foveal cystoid spaces as a novel OCT finding and characterized its clinical relevance in DME. This OCT finding may be designated as a predictor of no DME remission under as-needed ranibizumab injections.
Methods
Patients
We prepared two datasets, i.e., a cross-sectional study for the characterization of foveal cystoid spaces and a longitudinal study, to evaluate the clinical relevance of OCT findings in eyes treated with anti-VEGF drugs. We retrospectively reviewed treatment-naïve center-involved DME accompanied with foveal cystoid spaces on which OCT images of sufficient quality were obtained. The inclusion criteria were 1. center-involved DME, 2. the presence of cystoid abnormalities at the foveal center, and 3. written informed consent. The exclusion criteria were as follows: 1. severe media opacity affecting visual function or image acquisition, 2. any other chorioretinal diseases, 3. any previous treatment for DME or macular diseases, 4. cataract surgery within 3 months, and 5. any intraocular surgery other than cataract surgery within 12 months. If both eyes met these criteria, we selected right eyes.
In another independent study, we retrospectively reviewed patients with center-involved DME who received IVR injections for 24 months or longer. The participants in the longitudinal study did not at all overlap with those in the cross-sectional study. The inclusion criteria at baseline were adults ≥ 20 years with diabetes mellitus, visual impairment due to center-involved DME, the presence of cystoid abnormalities at the foveal center, and written informed consent. The exclusion criteria at baseline were media opacity affecting VA, other chorioretinal diseases, angiogenic complications (neovascular glaucoma, vitreous hemorrhage, or tractional retinal detachment), any past intervention for DME (anti-VEGF therapy, focal/grid photocoagulation, vitreoretinal surgery, and intraocular or periocular corticosteroids), retinal photocoagulation within 6 months, intraocular surgery other than cataract extraction, and cataract surgery within the previous 3 months. We additionally excluded eyes that met the following criteria: 1. drop-out during 24-month follow-up due to patient’s inconvenience or desire to terminate treatment, 2. patient’s desire or doctor’s discretion to switch to other treatment during 12-month follow-up, and 3. patient’s desire or doctor’s discretion to switch to vitrectomy or intraocular or periocular corticosteroids.
All research and measurements were performed in accordance with the tenets of the Declaration of Helsinki and under the approval of the study protocol by the Kyoto University Graduate School and Faculty of Medicine, Ethics Committee. Written informed consent was obtained from all participants before study enrollment.
OCT
Best-corrected decimal VA was measured and converted to logMAR VA. After comprehensive ophthalmic examination, SD-OCT images were obtained using Spectralis OCT (Heidelberg Engineering, Heidelberg, Germany) and the raster scan mode and cross-hair mode (30-degree) of the manufacturer’s software were applied as previously described32. Subsequently, two-dimensional maps were created, and the mean retinal thickness in the CSF was measured using the equipped software. We then determined center-involved DME according to the definition in a recent publication33.
In addition, we qualitatively evaluated the OCT findings of medium or large foveal cystoid spaces (≥250 μm in horizontal width, as defined in a previous publication5) in the central 1 mm of the retinal sections. We excluded smaller cysts, because the structural characterization is difficult in such cysts. We first determined the foveal center where inner retinal layers were absent and the central 1 mm areas in each OCT image. We evaluated the OCT findings, heterogeneous or homogenous reflectivity and hyperreflective foci in cystoid spaces within 1 mm in the vertical sectional images9. The height and width of each cystoid space were measured using the caliper of the manufacturer’s software. The OCT reflectivity was calculated in each foveal cystoid space as previously described9. Briefly, the margin of cystoid spaces was traced and the mean reflectivity level in the area encircled was quantified using image processing software (Photoshop, Adobe Systems, San Jose, CA). We compared it to the reflectivity levels of the vitreous cavity (as 0) and never fiber layer (NFL) (as 100) and calculated the relative reflectivity as arbitrary unit (AU) according to the formula:
We defined a hyperreflective wall in foveal cystoid spaces as a novel OCT finding. We selected cystoid spaces with medium or large size (≥250 μm in horizontal width5) within central 1 mm areas on sectional OCT images. We first determined the smooth contour of round or oval-shaped cystoid spaces (Fig. 1). The walls of cystoid spaces are usually composed of surrounding parenchyma or thin lines with high reflectance due to the optical differences at the boundaries (Fig. 2B,C). ‘Plot profile’ function in ImageJ version 1.52 software (NIH, Bethesda, MD) demonstrated the differences in reflectivity levels between cystoid spaces and retinal parenchyma (right column in Fig. 2). Parts of cystoid spaces were sometimes outlined by thick bands (≥ 40μm) which had higher reflectivity levels than nearby parenchyma (Figs. 1D and 2A). This OCT finding was defined and referred to as hyperreflective walls in foveal cystoid spaces in this study, after the discrimination of hyperreflective deposits within round or oval-shaped cystoid spaces (Fig. 1C). Eyes with this OCT finding in either horizontal and/or vertical sectional images were defined as eyes with hyperreflective walls in foveal cystoid spaces.
We quantitatively evaluated the reflectivity levels and thicknesses of the hyperreflective walls. Using the caliper of the manufacturer’s software, we manually measured the thicknesses at three different places and calculated the mean thicknesses. The reflectivity of hyperreflective walls were quantified using Photoshop as in the case of that of cystoid spaces. We manually traced the margin of hyperreflective walls and measured the mean reflectivity in the areas encircled. The relative reflectivity levels were calculated according to the formula as described above.
We investigated whether parafoveal cystoid spaces were accompanied with hyperreflective walls in the cross-sectional study. Cystoid spaces between 0.5 and 1.5 mm from the foveal center were determined as parafoveal cystoid spaces on the vertical sectional images. We evaluated the hyperreflective walls in parafoveal cystoid spaces with 250 μm or more horizontal width, as in the case of walls in foveal cystoid spaces.
We further evaluated the DRIL and EZ disruption on the sectional OCT images as described previously5,34. Briefly, DRIL was determined as the horizontal extent where any boundaries between the ganglion cell layer-inner plexiform layer complex, inner nuclear layer, and outer plexiform layer were not identified5. The horizontal length of DRIL extent was measured using the caliper of the manufacturer’s software. The disrupted EZ line was defined as the horizontal length (%) of absent EZ line, after the exclusion of faint or intact EZ line34. Further, hyperreflective foci in the inner or outer retinal layers were defined as those between the inner limiting membrane and external limiting membrane (ELM) or those between the ELM and retinal pigment epithelium (RPE), as described previously35. Two independent retinal specialists evaluated qualitative and quantitative OCT findings.
Post-hoc analyses in clinical trials reported that reduced macular thickness was maintained in the second year despite the significant decrease in the treatment frequency of IVR injections16,18. We therefore investigated the remission of DME under PRN dosing. The absence of macular thickening at each time point does not necessarily mean the resolution or remission of DME, because we often observe the relapsing DME under PRN dosing. We speculated that cases without DME for 6 or more months may be determined as remission of DME. In the current study, eyes without center-involved DME from any time point (from 1-month to 18-month visit) to the 24-month visit were defined as those in DME remission at that time point as described previously36. The absence of cystoid abnormalities from any time point to 24-month visit was defined as remission of cystoid abnormalities in the similar manner.
Intervention
IVR injections were performed according to a PRN regimen following three loading doses as described in the RESTORE study16. Ranibizumab (0.5 mg) was administered 3.5 mm posterior to the limbus after disinfection. As-needed injections at monthly visits were performed according to the retreatment criteria of the RESTORE study. At the 12-month visit and later, intravitreal aflibercept (IVA) injections, panretinal photocoagulation, or macular photocoagulation were also performed at the doctor’s discretion.
Statistics
The results are shown as the median (interquartile range [IQR]). After testing the normal distribution using the Shapiro-Wilk test, parametric and nonparametric data were compared using Student’s t-test and the Mann-Whitney U-test, respectively. The differences in the sampling distributions were assessed using Fisher’s exact test. The Kappa coefficient or intraclass correlation coefficient (ICC) were employed to evaluate the concordance in the qualitative and quantitative factors, respectively. Cox proportional hazard model were applied to investigate whether DME remission was predicted by baseline factors. Multivariate analyses were employed in a stepwise forward manner. P < 0.05 was considered statistically significant. SPSS version 24.0 was used for statistical analyses (SPSS, Inc., Chicago, IL, USA).
References
Yau, J. W. et al. Global prevalence and major risk factors of diabetic retinopathy. Diabetes Care. 35, 556–564 (2012).
Antonetti, D. A., Klein, R. & Gardner, T. W. Diabetic retinopathy. N Engl J Med. 366, 1227–1239 (2012).
Murakami, T. & Yoshimura, N. Structural changes in individual retinal layers in diabetic macular edema. J Diabetes Res. 2013, 920713 (2013).
Browning, D. J. et al. Relationship between optical coherence tomography-measured central retinal thickness and visual acuity in diabetic macular edema. Ophthalmology. 114, 525–536 (2007).
Sun, J. K. et al. Disorganization of the retinal inner layers as a predictor of visual acuity in eyes with center-involved diabetic macular edema. JAMA Ophthalmol. 132, 1309–1316 (2014).
Otani, T., Kishi, S. & Maruyama, Y. Patterns of diabetic macular edema with optical coherence tomography. Am J Ophthalmol. 127, 688–693 (1999).
Murakami, T. et al. Foveal cystoid spaces are associated with enlarged foveal avascular zone and microaneurysms in diabetic macular edema. Ophthalmology. 118, 359–367 (2011).
Otani, T. & Kishi, S. Correlation between optical coherence tomography and fluorescein angiography findings in diabetic macular edema. Ophthalmology. 114, 104–107 (2007).
Horii, T. et al. Relationship between Fluorescein Pooling and Optical Coherence Tomographic Reflectivity of Cystoid Spaces in Diabetic Macular Edema. Ophthalmology. 119, 1047–1055 (2012).
Bolz, M. et al. Optical coherence tomographic hyperreflective foci: a morphologic sign of lipid extravasation in diabetic macular edema. Ophthalmology. 116, 914–920 (2009).
Horii, T. et al. Optical coherence tomographic reflectivity of cystoid spaces is related to recurrent diabetic macular edema after triamcinolone. Retina. 35, 264–271 (2015).
Murakami, T. et al. Association between characteristics of foveal cystoid spaces and short-term responsiveness to ranibizumab for diabetic macular edema. Jpn J Ophthalmol. 62, 292–301 (2018).
Shimura, M., Yasuda, K., Yasuda, M. & Nakazawa, T. Visual outcome after intravitreal bevacizumab depends on the optical coherence tomographic patterns of patients with diffuse diabetic macular edema. Retina. 33, 740–747 (2013).
Bressler, S. B. et al. Factors associated with changes in visual acuity and central subfield thickness at 1 year after treatment for diabetic macular edema with ranibizumab. Arch Ophthalmol. 130, 1153–1161 (2012).
Vujosevic, S. et al. Diabetic macular edema with neuroretinal detachment: OCT and OCT-angiography biomarkers of treatment response to anti-VEGF and steroids. Acta Diabetol. 57, 287–296 (2020).
Elman, M. J. et al. Intravitreal Ranibizumab for diabetic macular edema with prompt versus deferred laser treatment: 5-year randomized trial results. Ophthalmology. 122, 375–381 (2015).
Smiddy, W. E. Clinical applications of cost analysis of diabetic macular edema treatments. Ophthalmology. 119, 2558–2562 (2012).
Schmidt-Erfurth, U. et al. Three-year outcomes of individualized ranibizumab treatment in patients with diabetic macular edema: the RESTORE extension study. Ophthalmology. 121, 1045–1053 (2014).
Funatsu, H. et al. Increased levels of vascular endothelial growth factor and interleukin-6 in the aqueous humor of diabetics with macular edema. Am J Ophthalmol. 133, 70–77 (2002).
Barber, A. J. et al. Neural apoptosis in the retina during experimental and human diabetes. Early onset and effect of insulin. J Clin Invest. 102, 783–791 (1998).
Tso, M. O. Pathology of cystoid macular edema. Ophthalmology. 89, 902–915 (1982).
Imai, H., Otsuka, K., Tetsumoto, A., Miki, A. and Nakamura, M. Effectiveness of En Bloc Removal of Fibrinogen-Rich Component of Cystoid Lesion for the Treatment of Cystoid Macular Edema. Retina. (2018).
Mizutani, M., Gerhardinger, C. & Lorenzi, M. Muller cell changes in human diabetic retinopathy. Diabetes. 47, 445–449 (1998).
Wynn, T. A. & Ramalingam, T. R. Mechanisms of fibrosis: therapeutic translation for fibrotic disease. Nat Med. 18, 1028–1040 (2012).
Murakami, T. et al. Association between Perifoveal Hyperfluorescence and Serous Retinal Detachment in Diabetic Macular Edema. Ophthalmology. 120, 2596–2603 (2013).
Sophie, R., Lu, N. & Campochiaro, P. A. Predictors of Functional and Anatomic Outcomes in Patients with Diabetic Macular Edema Treated with Ranibizumab. Ophthalmology. 122, 1395–1401 (2015).
Dodo, Y. et al. Diabetic Neuroglial Changes in the Superficial and Deep Nonperfused Areas on Optical Coherence Tomography Angiography. Invest Ophthalmol Vis Sci. 58, 5870–5879 (2017).
Querques, G. et al. Cystoid macular degeneration in exudative age-related macular degeneration. Am J Ophthalmol. 152(100-107), e102 (2011).
Lai, T. T., Hsieh, Y. T., Yang, C. M., Ho, T. C. & Yang, C. H. Biomarkers of optical coherence tomography in evaluating the treatment outcomes of neovascular age-related macular degeneration: a real-world study. Sci Rep. 9, 529 (2019).
Photocoagulation for diabetic macular edema. Early Treatment Diabetic Retinopathy Study report number 1. Early Treatment Diabetic Retinopathy Study research group. Arch Ophthalmol. 103, 1796–1806 (1985).
Jonas, J. B. & Sofker, A. Intraocular injection of crystalline cortisone as adjunctive treatment of diabetic macular edema. Am J Ophthalmol. 132, 425–427 (2001).
Murakami, T. et al. Integrative understanding of macular morphologic patterns in diabetic retinopathy based on self-organizing map. Invest Ophthalmol Vis Sci. 55, 1994–2003 (2014).
Chalam, K. V. et al. Retinal Thickness in People with Diabetes and Minimal or No Diabetic Retinopathy: Heidelberg Spectralis Optical Coherence Tomography. Invest Ophthalmol Vis Sci. 53, 8154–8161 (2012).
Murakami, T. et al. Optical coherence tomographic reflectivity of photoreceptors beneath cystoid spaces in diabetic macular edema. Invest Ophthalmol Vis Sci. 53, 1506–1511 (2012).
Uji, A. et al. Association between hyperreflective foci in the outer retina, status of photoreceptor layer, and visual acuity in diabetic macular edema. Am J Ophthalmol. 153(710-717), e711 (2012).
Yoshitake, T. et al. Predictor of Early Remission of Diabetic Macular Edema under As-Needed Intravitreal Ranibizumab. Sci Rep. 9, 7599 (2019).
Acknowledgements
This work was supported by Grant-in-Aid for Scientific Research of the Japan Society for the Promotion of Science (grant number; 18K19610, 17K11423) and Novartis Pharma K.K., Tokyo, Japan.
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N.T. wrote the manuscript; T.M., A.U., Y.D., Y.M., and A.T. analyzed data; T.M., A.U., and A.T. prepared figures; T.M., A.U., Y.D., Y.M., and A.T. provided conception and design of research. T.M., A.U., Y.D., Y.M., and A.T. edited the manuscript. All authors reviewed the manuscript.
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Terada, N., Murakami, T., Uji, A. et al. Hyperreflective Walls in Foveal Cystoid Spaces as a Biomarker of Diabetic Macular Edema Refractory to Anti-VEGF Treatment. Sci Rep 10, 7299 (2020). https://doi.org/10.1038/s41598-020-64332-6
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DOI: https://doi.org/10.1038/s41598-020-64332-6
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