- 1Department of Ophthalmology, Shanghai General Hospital (Shanghai First People's Hospital), Shanghai Jiao Tong University School of Medicine, Shanghai, China
- 2National Clinical Research Center for Eye Diseases, Shanghai, China
- 3Shanghai Key Laboratory of Fundus Disease, Shanghai, China
- 4Shanghai Engineering Center for Visual Science and Photomedicine, Shanghai, China
- 5Department of Ophthalmology, Affiliated Hospital of Nantong University, Nantong, China
Purpose: To investigate the correlation between retinal capillary structure and macular function in patients with idiopathic epiretinal membrane (iERM) by using optical coherence tomography angiography (OCTA) and microperimetry.
Methods: This retrospective and observational study included 30 idiopathic ERM eyes of 30 consecutive patients. OCTA was performed to evaluate macular microvasculature including the superficial capillary plexus, deep capillary plexus, and foveal avascular zone. Best corrected visual acuity (BCVA) and microperimetry were measured at baseline and 3 months after surgery. Associations between macular microvasculature and visual function were assessed.
Results: Visual function including BCVA and macular sensitivity improved significantly at 3 months post-operatively (p < 0.001). At baseline, BCVA was positively correlated with foveal or parafoveal sensitivities and negatively correlated with central foveal thickness (p < 0.05). Pre-operative foveal sensitivity was significantly correlated with the vessel density of foveal or parafoveal superficial capillary plexus (p < 0.05). A multiple regression model revealed that pre-operative vessel density of foveal deep capillary plexus was an independent positive prognostic factor for post-operative BCVA (B = −0.020 ± 0.006, p = 0.006) and macular sensitivity (B = 0.200 ± 0.081, p = 0.027).
Conclusion: Integrated evaluation of iERM by using OCTA and microperimetry shows an association between microvasculature and macular sensitivity. Pre-operative vessel density of foveal deep capillary plexus assessed by OCTA may be a potentially valuable prognostic factor for iERM surgery.
Introduction
Idiopathic epiretinal membrane (iERM) is characterized by a semi-translucent fibrocellular proliferative membrane at the vitreoretinal interface (1). It occurs mostly in patients over 50 years old with an incidence ranging from 2.2 to 28.9% (2). The proliferation of various cell types such as glial cells, hyalocytes, fibroblasts, and the alterations of vitreous status contributes to the membrane formation (3, 4). An incomplete posterior vitreous detachment (PVD) may provide appropriate conditions for proliferation in the area between the vitreous and the retina (5). Additionally, the dysregulation of vitreous microRNAs (miRNAs) (miR-19b, miR-24, and miR-142-3p) has been reported to be correlated with the fibrosis in eyes affected by ERM (6). The anteroposterior and tangential traction caused by ERM on the inner retina and macular vasculature may induce functional and circulatory disturbance in foveal and/or perifoveal areas, which eventually lead to visual acuity impairment and metamorphopsia (7).
Optical coherence tomography (OCT) has been widely applied in the evaluation of different ocular diseases and in particular to detect any macular or optic disk change in different systemic or macular disorders (8–10), but does not allow detection and visualization of the retinal microvasculature (11). OCT angiography (OCTA) is a more recent development, which makes it possible to visualize the vascular network and blood flow by using an algorithm known as split-spectrum amplitude-decorrelation angiography (12, 13). Compared with fundus fluorescein angiography, OCTA has the advantage of higher resolution, less time-consuming, and non-invasive (14–16). Furthermore, OCTA can visualize blood vessels at various depth-resolved levels including the superficial capillary plexus (SCP), the deep capillary plexus (DCP), and can better delineate the complexities of the vessels at the edge of the foveal avascular zone (FAZ) (17, 18).
In the management of iERM, pars plana vitrectomy (PPV) has become a standard surgical technique. Particularly, recent advances in transconjunctival small-gauge vitrectomy and non-vitrectomizing vitreous technique have provided much potential improvement over conventional 20-gauge surgery such as less surgical-related complications, faster incision healing, better patient comfort, and earlier visual recovery (19, 20). Although best corrected visual acuity (BCVA) is regarded as the main outcome of functional recovery after PPV for ERM, it does not reveal many other functional changes related to macular pathologies. Microperimetry can provide further objective and quantitative information about macular function by evaluating retinal sensitivity in the area of interest (21, 22). It has already shown better efficacy and higher sensitivity compared with BCVA for ERM (23). Moreover, retinal sensitivity has a closer association with reading ability in patients with fundus diseases (24). Only one previous study integrated OCTA with microperimetry to assess iERM eyes (25). However, this study mainly focused on a 1-mm2 square foveal region and excluded parafoveal region. Besides, the associations of pre-operative OCTA parameters and post-operative visual function were not investigated.
Thus, in this study, we explored the associations between macular sensitivity and microvascular characteristics in both the foveal and parafoveal regions before and after iERM surgery and to identify the potential prognostic factors indicative of functional recovery.
Methods
This retrospective and observational study recruited 30 eyes of 30 consecutive patients diagnosed iERM at the Shanghai General Hospital between June 2019 and December 2019 were included. All the patients underwent 23-gauge PPV with ERM/internal limiting membrane (ILM) peeling and fluid-air exchange. Cataract surgery was performed at the time of vitrectomy in all the phakic eyes. All the patients were followed-up for at least 3 months after surgery. The study was compliant with the tenets of the Declaration of Helsinki and was approved by the Ethics Committee of Shanghai General Hospital.
At baseline, all the patients underwent comprehensive ophthalmological examinations including medical history, Snellen BCVA, slit-lamp biomicroscopy, OCTA, and microperimetry. Post-operative visual function including BCVA and microperimetry was also performed at 3 months after surgery.
Patient Eligibility
Inclusion criteria were as follows: (1) patients with iERM and (2) follow-up at least 3 months. Exclusion criteria were as follows: (1) ERM secondary to other retinal disease, (2) severe cataract or glaucoma, (3) high myopia with a refractive error of more than −6.00 diopters or an axial length longer than 26 mm, (4) retinal vascular disease, (5) a history of previous vitreoretinal surgery, or (6) uncontrolled systemic disease.
Optical Coherence Tomography Angiography Measurement
Optical coherence tomography angiography was conducted by using the AngioVue Imaging System (RTVue XR Avanti, Optovue Incorporation, Fremont, California, USA), which operates at an A-scan rate of 70,000 scans/s with an 840 nm wavelength. The split-spectrum amplitude-decorrelation angiography algorithm was utilized to record the vascular signals. Based on the default software (version 2015.100.0.35, Optovue Incorporation, Fremont, California, USA), the SCP and the DCP of OCTA images were segmented automatically. The boundary of the SCP was set from 3 μm below the ILM to 16 μm below the inner plexiform layer (IPL). The boundary of DCP was set from 16 to 69 μm below the IPL. Two masked ophthalmologists (authors YXT and SX) reviewed the accuracy of segmentation with a senior retinal specialist (author FJY) consulted in the event of discrepancy. If the automatically segmentation was not proper, manual correction of the segmentation was performed by embedded software in the AngioVue Imaging System (RTVue XR Avanti, Optovue Incorporation, Fremont, California, USA). Vessel density (VD) was defined as the percentage of an area occupied by vessels and calculated automatically by the software on OCTA. Each OCTA scan covered the areas of 1 mm × 1 mm and 3 mm × 3 mm to detect the vasculature of the SCP and DCP in the fovea and parafovea that correspond to the Early Treatment Diabetic Retinopathy Study (ETDRS) macular fields. The central foveal thickness (CFT) was defined as the mean thickness in the central circular area. The FAZ was defined as the area without capillary network in the macula and was measured automatically. Poor quality images with segmentation errors, motion artifacts, or low signal strength index (<50) were excluded. iERM was defined with OCTA B-scans as a thin hyperreflective band anterior to the ILM with focal areas of macular attachments or globally adherent to the retinal surface (26). A staging system reported by Govetto et al. was used to classify iERM (27).
Microperimetry Evaluation
Following our previous study described (28), MP-1 microperimetry (NIDEK, NAVIS Software version 3.6.4, Gamagori, Japan) was conducted in a dark room with pupil dilation (1% tropicamide) and with the contralateral eye patched. Macular sensitivity was tested at the central 10° with 40 points arranged in three concentric circles (2, 6, and 10°). The Goldmann III stimuli (10 candela/m2) were randomly presented for a duration of 200 ms on a 1.27 candela/m2 background. Sensitivity (dB, decibels) was assessed by using a 4-2-1 automated staircase strategy ranging from 0 to 20 dB in 2 dB steps. The mean overall macular sensitivity was calculated as the mean threshold of 40 points within the 10° central field. The mean foveal and perifoveal sensitivities were calculated from points within 2° of the center and points within the region from 2 to 10°, respectively.
Surgical Procedure
A standard three-port 23-gauge PPV was conducted by the same surgeon by using the Constellation Vision System (Alcon, Fort Worth, Texas, USA). After core vitrectomy, the posterior hyaloid was removed from the retina with the assistance of triamcinolone acetonide (TA) (2.5 mg/ml) and a complete vitrectomy was performed at the peripheral vitreous base. The macular ERM was removed by using intraocular forceps and indocyanine green solution (1.5 mg/ml) was applied to stain the ILM within the arcade. The ILM was peeled around the macula to a region of approximately three optic disk diameters. Abundant fluid-air exchange was slowly conducted by using sterilized air. If air leakage occurred through any of the three incisions, a transscleral suture was applied. All the patients were required to maintain a face-down position for at least 3 days after surgery.
Statistical Analysis
Continuous parameters were presented as mean and SD. The BCVA was converted to the logarithm of the minimum angle of resolution (logMAR). The significant difference in logMAR BCVA before and after surgery was analyzed by using the Wilcoxon signed-rank test. Pre- and post-operative retinal sensitivities were analyzed by using the paired t-test. The Pearson correlation analysis was used to analyze the associations between OCTA parameters and post-operative visual outcomes. The multiple linear regression analysis was performed to assess the influence of variables on post-operative visual function. All the statistical analyses were performed by using the Statistical Package for the Social Sciences (SPSS) software (version 21.0, SPSS Incorporation, Chicago, Illinois, USA). p < 0.05 was considered to be statistically significant.
Results
General Characteristics
This study reviewed the records of 30 iERM eyes from 30 consecutive patients. Three eyes were excluded due to unstable fixation during microperimetry and two eyes were excluded due to low quality of OCTA images. Data from 25 eyes (stage 2: 4 eyes; stage 3: 17 eyes; and stage 4: 4 eyes) of 25 patients (8 males and 17 females) were, therefore, included in analysis. The mean age of the sample was 67.00 ± 8.18 years (range: 55–82 years). The mean axial length (AL) and intraocular pressure (IOP) were 23.12 ± 0.52 mm and 14.20 ± 2.42 mm Hg, respectively. Four eyes (16.0%) were pseudophakic at baseline. The mean pre-operative logMAR BCVA of included eyes was 0.62 ± 0.23 (Table 1). At 3 months post-operatively, the mean logMAR BCVA had increased to 0.39 ± 0.18 (t = 5.986, p < 0.001).
Optical Coherence Tomography Angiography and Microperimetry Analysis Outcomes
At baseline, VD of the SCP and the DCP, measured by using OCTA, was 44.54 ± 6.45% and 43.54 ± 6.65%, respectively. The mean VD was 38.38 ± 8.55% for the foveal SCP and 44.98 ± 6.58% for the parafoveal SCP. The mean VD was 35.68 ± 6.53% for foveal DCP and 44.85 ± 7.81% for parafoveal DCP. The mean area of FAZ was 0.08 ± 0.06 mm2 in the eyes with iERM. The mean CFT of included eyes was 467.44 ± 87.84 μm (Table 2).
The mean macular sensitivity (within 10° of center) was 10.16 ± 1.79 dB at baseline and increased to 11.72 ± 2.14 dB at 3 months after surgery (t = −3.684, p = 0.001). The mean foveal sensitivity (within 2° of center) improved from 7.61 ± 2.07 pre-operatively to 9.16 ± 3.22 dB post-operatively (t = −3.006, p = 0.006). The mean parafoveal sensitivity (in the region 2° to 10° of center) improved from 10.79 ± 1.89 pre-operatively to 12.36 ± 2.05 dB post-operatively (t = −3.585, p = 0.001) (Table 2). Representative case is shown in Figure 1.
Figure 1. Representative OCTA and microperimetry images. (A) OCTA images of a 63-year-old female with iERM (lower row) compared with the normal eye (upper row). (B) The microperimetry results from this patient by MP-1 examination before and 3 months after surgery showed improvement.
Association of OCTA and Microperimetry Parameters in iERM
At baseline, the VD of foveal and the parafoveal SCP was each significantly correlated with foveal sensitivity (r = −0.596, p = 0.002 and r = −0.438, p = 0.029, respectively). Statistically significant correlations were also found between pre-operative sensitivity and the baseline logMAR BCVA at the fovea and parafovea (r = −0.747, p < 0.001 and r = −0.771, p < 0.001, respectively). Thus, the VD of the SCP reflected the retinal sensitivity in fovea, but not in parafovea. No significant association was found between the SCP and BCVA (p > 0.05) indicating that microperimetry may be a more sensitive indicator of changes in the SCP parameters. The mean pre-operative CFT was associated with the mean baseline FAZ and the logMAR BCVA (r = −0.444, p = 0.026 and r = 0.457, p = 0.022, respectively) (Figure 2). We did not find any significant correlation between VD of the DCP with foveal or parafoveal sensitivity or the logMAR BCVA at baseline (p > 0.05).
Figure 2. Associations of visual function and OCTA parameters in iERM eyes at baseline. Scatterplots show the statistically significant correlation between preoperative foveal sensitivity and vessel density (VD) of foveal or parafoveal SCP (r = −0.596, P = 0.002; r = −0.438, P = 0.029). Preoperative BCVA was significantly correlated with foveal or parafoveal sensitivity, CFT (r = −0.747, P < 0.001; r = −0.771, P < 0.001; r = 0.457, P = 0.022). FAZ area was significantly correlated with CFT (r = −0.444, P = 0.026).
Predictors for Post-operative Visual Functional Recovery
To explore the predictive factors for visual functional recovery after iERM surgery, correlations between the post-operative logMAR BCVA or retinal sensitivity and pre-operative ocular variables were analyzed (Figure 3). The logMAR BCVA at 3 months after surgery was significantly correlated with pre-operative overall macular or foveal sensitivity (r = −0.443, p = 0.026 and r = −0.632, p = 0.001, respectively), baseline VD of the foveal DCP (r = −0.734, p < 0.001), and the CFT (r = 0.544, p = 0.005). The foveal sensitivity at 3 months after surgery was significantly correlated with pre-operative foveal sensitivity (r = 0.602, p = 0.001) and baseline VD of the foveal DCP (r = 0.599, p = 0.002). The parafoveal sensitivity at 3 months after surgery was correlated with pre-operative foveal sensitivity (r = 0.546, p = 0.005) and baseline VD of the foveal DCP (r = 0.586, p = 0.002). There was no correlation between post-operative visual function and pre-operative FAZ (p > 0.05).
Figure 3. Associations of postoperative visual function and preoperative parameters. Scatterplots show the statistically significant correlation between postoperative logMAR BCVA and preoperative macular or foveal sensitivity, vessel density (VD) of foveal SCP and CFT (r = −0.443, P = 0.026; r = −0.632, P = 0.001; r = −0.734, P < 0.001; r = 0.544, P = 0.005). Postoperative foveal or parafoveal sensitivity was significantly correlated with preoperative foveal sensitivity and vessel density of foveal DCP (r = 0.602, P = 0.001; r = 0.599, P = 0.002; r = 0.546, P = 0.005; r = 0.586, P = 0.002).
Based on these findings, the multiple linear regression model, adjusted for age and gender, was applied to screen the prognostic factors for visual functional recovery after iERM surgery. We found that pre-operative VD of the foveal DCP was an independent predictor for the post-operative logMAR BCVA (B = −0.020 ± 0.006, p = 0.006) and mean macular sensitivity (B = 0.200 ± 0.081, p = 0.027) at 3 months after surgery (Table 3).
Table 3. Multiple linear regression model of post-operative logMAR BCVA or macular sensitivity and baseline ocular parameters.
Discussion
We have provided a novel report on the association between microvasculature and macular sensitivity both the foveally and parafoveally before and after surgery for iERM. Our findings included: (1) The VD of foveal or the parafoveal SCP was negatively correlated with foveal sensitivity in iERM eyes, but not with BCVA and (2) Pre-operative VD of the foveal DCP was an independent positive prognostic factor for post-operative visual function including BCVA and macular sensitivity.
The relationship between morphology and function is an interesting and meaningful topic. However, few studies focused on morpho-functional evaluation by combining the OCTA and microperimetry. The correlation between VD and post-operative retinal function has been reported in full-thickness macular holes (29). For iERM, only one study investigated the post-operative VD of the SCP, the DCP, and retinal sensitivity (25). However, in contrast with this study, no OCTA-based pre-operative predictors were identified for ERM surgeries. A possible explanation for this discrepancy is the shape and range of macular region measured in the two studies. This study used a circular shape including the foveal and parafoveal regions, while the previous study (25) used a square shape excluding the parafoveal region. According to former study, 1° apart from fovea is approximately equal to 300 μm in human eyes with normal AL (30). Using this metric, the diameters of 2, 6, and 10° in the microperimetry are around 600, 1,800, and 3,000 μm. In the OCTA, the foveal circle has a diameter of 1,000 μm and the parafoveal area is an annulus with inner diameter of 1,000 μm and an outer diameter of 3,000 μm. These dimensions allow 2° retinal sensitivity in the microperimetry to be fully covered by foveal VD in the OCTA and the 6 and 10° dimensions are fully covered by the parafoveal vessel density. Thus, the foveal and parafoveal VD have a well-geographical correspondence with 2, 6, and 10° retinal sensitivity, respectively.
Visual prognostic factors of ERM surgery are varied and inconsistent in previous study with duration of symptoms, central bouquet (CB) alteration staging, and existence of pseudoholes having been reported as possible predictive factors (31, 32). In long-term prognosis, BCVA at baseline, but not classification of CB, appeared to be a strong predictor for BCVA improvement following surgery (26). The CFT has been identified as a significant predictor in some study (31), but not others (33, 34). In this study, we found that the CFT was associated with post-operative visual function, but the multiple linear regression analysis showed that it was not a significant predictor for the post-operative logMAR BCVA or macular sensitivity.
The inner retinal changes play a relatively important role in the pathology of ERM as the tangential traction imposed by the membrane occurs at the inner interface of the retina (35). Consistent with this, inner retinal deformation has been found to be the sole factor associated with significant long-term improvement in vision (36). These findings suggest that OCTA, which reflects inner retinal vessel flow (including the SCP and the DCP), could help in identify new prognostic factors for ERM surgical outcomes. This newly developed technique has the advantages of safety and speed of en face or transverse images of retinal vessel vasculature without dye injection.
Based on our observations, while the VD of foveal or the parafoveal SCP was negatively corrected with visual function at baseline, pre-operative VD of the foveal DCP but not the SCP was an independent positive prognostic factor for post-operative BCVA and macular sensitivity at 3 months after surgery. There are several possible explanations for this phenomenon: (1) Prior to surgery, greater distortion by the membrane leads to more of the vascular network being pulled into the central macular region. Outer retinal damage is derived from inner retinal change through tangential inward traction at the fovea and retrograde transneuronal degeneration (37); (2) After surgical removal of the ERM and ILM by microincision vitrectomy with gas tamponade, the traction force was alleviated and a flattening force was imposed and the vessels in the foveal returning to their original location. This process is reversible in most cases and could explain why the pre-operative SCP is not a prognostic factor for iERM surgery; and (3) The DCP vessels are close to the outer nuclear layer and photoreceptors, acting as the most important source of blood delivery to the outer retina. Due to edema, ischemia, and distortion in the pathological process, the flow of the DCP decreased, exacerbating damage to the outer retina and causing irreversible photoreceptor dysfunction. Lin et al. found that the tractional forces of ERM not only distorted the SCP, but also affected the DCP (38). Other studies also observed the defect of cone outer segment tips and abnormal microfolds of photoreceptor layer in eyes with ERM (36, 39). These findings indicate that tractional forces initiated from the inner retina could reach as far as the photoreceptor layer. It seems feasible that changes in VD of the DCP are secondary to tractional forces. The decreased VD of the DCP indicated a reduced blood supply to the outer retina, which further exacerbated the pathological progress of iERM.
The pre-operative FAZ area is reportedly correlated with post-operative FAZ area in the patients with ERM (40), but the relationship between the pre-operative FAZ and the post-operative logMAR BCVA was not explored in this study. Our multiple linear regression model showed that the FAZ area is not a significant predictor of the post-operative logMAR BCVA or macular sensitivity.
This study was limited by its relatively small sample. In addition, some patients underwent cataract surgery at the same time as ERM surgery, potentially introducing differences in outcomes within the group. However, previous study has shown that parameters are similar in patients with or without cataract surgery at each follow-up time point (1 month to 2 years) after iERM surgery (25).
In conclusion, this study investigated the morpho-functional relationships in iERM eyes and found correlations between retinal sensitivity and vessel density. Higher pre-operative VD of the foveal DCP is a prognostic factor for better visual function recovery after iERM surgery. Thus, it is useful to measure VD of the DCP by OCTA while evaluating surgical management and prognosis of iERM eyes.
Data Availability Statement
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.
Ethics Statement
The studies involving human participants were reviewed and approved by Ethics Committee of Shanghai General Hospital. The patients/participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.
Author Contributions
JF, PH, and XS contributed to the study design and protocol. XY conducted the examinations. MX, JF, and PH prepared and reviewed the manuscript. YW and YZ collected and did the statistical analysis of the data. All authors contributed to the article and approved the submitted version.
Funding
This study was supported by the Shanghai Public Health System's Talent Development Plan (GWV-10.2-YQ09) and the Bethune-Langmu Eye Research Fund (BJ-LM2018001J).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1. Romano MR, Cennamo G, Schiemer S, Rossi C, Sparnelli F, Cennamo G. Deep and superficial OCT angiography changes after macular peeling: idiopathic vs diabetic epiretinal membranes. Graefes Arch Clin Exp Ophthalmol. (2017) 255:681–9. doi: 10.1007/s00417-016-3534-4
2. Yoon YH, Joe SG, Hwang JU, Yang HS. Insights into epiretinal membranes: presence of ectopic inner foveal layers and a new optical coherence tomography staging scheme. Am J Ophthalmol. (2017) 177:226–7. doi: 10.1016/j.ajo.2017.01.033
3. Bringmann A, Wiedemann P. Involvement of Muller glial cells in epiretinal membrane formation. Graefes Arch Clin Exp Ophthalmol. (2009) 247:865–83. doi: 10.1007/s00417-009-1082-x
4. Zhao F, Gandorfer A, Haritoglou C, Scheler R, Schaumberger MM, Kampik A, et al. Epiretinal cell proliferation in macular pucker and vitreomacular traction syndrome: analysis of flat-mounted internal limiting membrane specimens. Retina. (2013) 33:77–88. doi: 10.1097/IAE.0b013e3182602087
5. Pietras-Baczewska A, Nowomiejska K, Brzozowska A, Toro MD, Załuska W, Sztanke M, et al. antioxidant status in the vitreous of eyes with rhegmatogenous retinal detachment with and without proliferative vitreoretinopathy, macular hole and epiretinal membrane. Life. (2021) 11:453. doi: 10.3390/life11050453
6. Russo A, Ragusa M, Barbagallo C, Longo A, Avitabile T, Uva MG, et al. miRNAs in the vitreous humor of patients affected by idiopathic epiretinal membrane and macular hole. PLoS ONE. (2017) 12:e0174297. doi: 10.1371/journal.pone.0174297
7. Nelis P, Alten F, Clemens CR, Heiduschka P, Eter N. Quantification of changes in foveal capillary architecture caused by idiopathic epiretinal membrane using OCT angiography. Graefes Arch Clin Exp Ophthalmol. (2017) 255:1319–24. doi: 10.1007/s00417-017-3640-y
8. Ceravolo I, Oliverio GW, Alibrandi A, Bhatti A, Trombetta L, Rejdak R, et al. The application of structural retinal biomarkers to evaluate the effect of intravitreal ranibizumab and dexamethasone intravitreal implant on treatment of diabetic macular edema. Diagnostics. (2020) 10:413. doi: 10.3390/diagnostics10060413
9. Chisari CG, Toro MD, Cimino V, Rejdak R, Luca M, Rapisarda L, et al. Retinal nerve fiber layer thickness and higher relapse frequency may predict poor recovery after optic neuritis in MS patients. J Clin Med. (2019) 8:2022. doi: 10.3390/jcm8112022
10. Reibaldi M, Avitabile T, Longo A, Uva MG, Bonfiglio V, Russo A, et al. Correlation of preoperative retinal pigment epithelium status with foveal microstructure in repaired macular holes. Ophthalmologica. (2014) 232:194–9. doi: 10.1159/000364883
11. Spaide RF, Fujimoto JG, Waheed NK, Sadda SR, Staurenghi G. Optical coherence tomography angiography. Prog Retin Eye Res. (2018) 64:1–55. doi: 10.1016/j.preteyeres.2017.11.003
12. Jia Y, Tan O, Tokayer J, Potsaid B, Wang Y, Liu JJ, et al. Split-spectrum amplitude-decorrelation angiography with optical coherence tomography. Opt Express. (2012) 20:4710–25. doi: 10.1364/OE.20.004710
13. Brinkmann MP, Kibele NX, Prasuhn M, Kakkassery V, Toro MD, Ranjbar M, et al. Evaluating retinal and choroidal perfusion changes after isometric and dynamic activity using optical coherence tomography angiography. Diagnostics. (2021) 11:808. doi: 10.3390/diagnostics11050808
14. Koman-Wierdak E, Nowomiejska K, Brzozowska A, Nowakowska D, Toro MD, Bonfiglio V, et al. Kinetic and static perimetry after 16 years and additional OCT-A analysis in eyes with long-lasting optic disc drusen. PLoS ONE. (2021) 16:e0247399. doi: 10.1371/journal.pone.0247399
15. Carnevali A, Giannaccare G, Gatti V, Battaglia C, Randazzo G, Yu AC, et al. Retinal microcirculation abnormalities in patients with systemic sclerosis: an explorative optical coherence tomography angiography study. Rheumatology. (2021). doi: 10.1093/rheumatology/keab258. [Epub ahead of print].
16. Carnevali A, Mastropasqua R, Gatti V, Vaccaro S, Mancini A, D'Aloisio R, et al. Optical coherence tomography angiography in intermediate and late age-related macular degeneration: review of current technical aspects and applications. Appl Sci. (2020) 10:8865. doi: 10.3390/app10248865
17. Bonfiglio V, Ortisi E, Scollo D, Reibaldi M, Russo A, Pizzo A, et al. Vascular changes after vitrectomy for rhegmatogenous retinal detachment: optical coherence tomography angiography study. Acta Ophthalmol. (2020) 98:e563–9. doi: 10.1111/aos.14315
18. Wiest MRJ, Toro MD, Nowak A, Baur J, Fasler K, Hamann T, et al. Globotrioasylsphingosine levels and optical coherence tomography angiography in fabry disease patients. J Clin Med. (2021) 10:1093. doi: 10.3390/jcm10051093
19. Reibaldi M, Longo A, Avitabile T, Bonfiglio V, Toro MD, Russo A, et al. Transconjunctival nonvitrectomizing vitreous surgery versus 25-gauge vitrectomy in patients with epiretinal membrane: a prospective randomized study. Retina. (2015) 35:873–9. doi: 10.1097/IAE.0000000000000459
20. Reibaldi M, Rizzo S, Avitabile T, Longo A, Toro MD, Viti F, et al. Iatrogenic retinal breaks in 25-gauge vitrectomy under air compared with the standard 25-gauge system for macular diseases. Retina. (2014) 34:1617–22. doi: 10.1097/IAE.0000000000000112
21. Wrzesińska D, Nowomiejska K, Nowakowska D, Toro MD, Bonfiglio V, Reibaldi M, et al. Secondary vitrectomy with internal limiting membrane plug due to persistent full-thickness macular hole OCT-angiography and microperimetry features: case series. J Ophthalmol. (2020) 2020:2650873. doi: 10.1155/2020/2650873
22. Wrzesińska D, Nowomiejska K, Nowakowska D, Brzozowska A, Avitabile T, Reibaldi M, et al. Vertical and horizontal M-Charts and microperimetry for assessment of the visual function in patients after vitrectomy with ILM peeling due to stage 4 macular hole. J Ophthalmol. (2019) 2019:4975973. doi: 10.1155/2019/4975973
23. Romano MR, Cennamo G, Cesarano I, Cardone D, Nicoletti G, Mastropasqua R, et al. Changes of tangential traction after macular peeling: correlation between en-face analysis and macular sensitivity. Curr Eye Res. (2017) 42:780–8. doi: 10.1080/02713683.2016.1231322
24. Pearce E, Sivaprasad S, Chong NV. Factors affecting reading speed in patients with diabetic macular edema treated with laser photocoagulation. PLoS ONE. (2014) 9:e105696. doi: 10.1371/journal.pone.0105696
25. Osada U, Kunikata H, Yasuda M, Hashimoto K, Nishiguchi KM, Nakazawa T. Association of retinal vessel density with retinal sensitivity in surgery for idiopathic epiretinal membrane. Graefes Arch Clin Exp Ophthalmol. (2020) 258:1911–20. doi: 10.1007/s00417-020-04754-0
26. Brinkmann MP, Michels S, Brinkmann C, Toro MD, Johansen NG, Rommel F, et al. Influences of central bouquet alterations on the visual outcome in eyes receiving epiretinal membrane surgery. Appl Sci. (2021) 11:926. doi: 10.3390/app11030926
27. Govetto A, Lalane RA III, Sarraf D, Figueroa MS, Hubschman JP. insights into epiretinal membranes: presence of ectopic inner foveal layers and a new optical coherence tomography staging scheme. Am J Ophthalmol. (2017) 175:99–113. doi: 10.1016/j.ajo.2016.12.006
28. Huang P, Wang H, Chen F, Chen J, Hu Y, Sun J, et al. Functional evaluation with microperimetry in large idiopathic macular holes treated by a free internal limiting membrane flap tamponade technique. BMC Ophthalmol. (2020) 20:302. doi: 10.1186/s12886-020-01573-z
29. Bacherini D, Savastano MC, Dragotto F, Finocchio L, Lenzetti C, Bitossi A, et al. Morpho-functional evaluation of full-thickness macular holes by the integration of optical coherence tomography angiography and microperimetry. J Clin Med. (2020) 9:229. doi: 10.3390/jcm9010229
30. Sborgia G, Niro A, Tritto T, Albano V, Sborgia L, Sborgia A, et al. Microperimetric biofeedback training after successful inverted flap technique for large macular hole. J Clin Med. (2020) 9:556. doi: 10.3390/jcm9020556
31. Sheales MP, Kingston ZS, Essex RW. Associations between preoperative OCT parameters and visual outcome 3 months postoperatively in patients undergoing vitrectomy for idiopathic epiretinal membrane. Graefes Arch Clin Exp Ophthalmol. (2016) 254:1909–17. doi: 10.1007/s00417-016-3326-x
32. Govetto A, Bhavsar KV, Virgili G, Gerber MJ, Freund KB, Curcio CA, et al. Tractional Abnormalities of the central foveal bouquet in epiretinal membranes: clinical spectrum and pathophysiological perspectives. Am J Ophthalmol. (2017) 184:167–80. doi: 10.1016/j.ajo.2017.10.011
33. Mitamura Y, Hirano K, Baba T, Yamamoto S. Correlation of visual recovery with presence of photoreceptor inner/outer segment junction in optical coherence images after epiretinal membrane surgery. Br J Ophthalmol. (2009) 93:171–5. doi: 10.1136/bjo.2008.146381
34. Shiono A, Kogo J, Klose G, Takeda H, Ueno H, Tokuda N, et al. Photoreceptor outer segment length: a prognostic factor for idiopathic epiretinal membrane surgery. Ophthalmology. (2013) 120:788–94. doi: 10.1016/j.ophtha.2012.09.044
35. Kim JY, Kim DY, Kim KT, Song J, Chae JB, Kim JG. Visual prognostic factors of epiretinal membrane surgery in patients with Pseudophakia. Ophthalmologica. (2020) 243:43–50. doi: 10.1159/000502748
36. Jeon S, Jung B, Lee WK. Long-term prognostic factors for visual improvement after epiretinal membrane removal. Retina. (2019) 39:1786–93. doi: 10.1097/IAE.0000000000002211
37. Cho KH, Park SJ, Woo SJ, Park KH. Correlation between inner-retinal changes and outer-retinal damage in patients with idiopathic epiretinal membrane. Retina. (2018) 38:2327–35. doi: 10.1097/IAE.0000000000001875
38. Lin TC, Chung YC, Lin CY, Lee FL, Chen SJ. Focal Nonperfusion of deep retinal capillary plexus in eyes with epiretinal membranes revealed by optical coherence tomography angiography. Ophthalmic Surg Lasers Imaging Retina. (2016) 47:404–9. doi: 10.3928/23258160-20160419-02
39. Yamaguchi M, Nakao S, Kaizu Y, Kobayashi Y, Nakama T, Arima M, et al. High-resolution imaging by adaptive optics scanning laser ophthalmoscopy reveals two morphologically distinct types of retinal hard exudates. Sci Rep. (2016) 6:33574. doi: 10.1038/srep33574
Keywords: microperimetry, epiretinal membrane, vessel density, prognostic factors, OCT angiography
Citation: Feng J, Yang X, Xu M, Wang Y, Shi X, Zhang Y and Huang P (2021) Association of Microvasculature and Macular Sensitivity in Idiopathic Macular Epiretinal Membrane: Using OCT Angiography and Microperimetry. Front. Med. 8:655013. doi: 10.3389/fmed.2021.655013
Received: 18 January 2021; Accepted: 14 October 2021;
Published: 16 November 2021.
Edited by:
Mario Damiano Toro, Medical University of Lublin, PolandReviewed by:
Andrea Govetto, ASST Fatebenefratelli Sacco, ItalyMaximilian Wiest, University Hospital Zürich, Switzerland
Copyright © 2021 Feng, Yang, Xu, Wang, Shi, Zhang and Huang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xiang Shi, ZHJzaGkyMDEyJiN4MDAwNDA7Zm94bWFpbC5jb20=; Peirong Huang, cGVpcm9uZ19odWFuZyYjeDAwMDQwOzEyNi5jb20=
†These authors have contributed equally to this work