Abstract
Even after idiopathic macular hole (MH) surgery and with successful closure of MH, aniseikonia is a common postoperative symptom. We investigated the correlation of MH diameter, retinal displacement and retinal layer thicknesses with aniseikonia in 41 eyes of 41 patients undergoing MH surgery with internal limiting membrane peeling. Aniseikonia was measured with the New Aniseikonia Test. Retinal displacement (RD%) was defined as change of retinal distance between the temporal margin of the optic papilla and the intersection of the retinal vessels. Changes of thicknesses of the inner nuclear layer (INL%) and the outer retinal layer (OR%) were calculated. Aniseikonia improved postoperatively. Preoperative aniseikonia and their improvement at 6 months correlated with MH diameters (P = 0.004–0.046). Improvement of aniseikonia correlated with temporal RD% (P = 0.002–0.012). Improvement of vertical aniseikonia correlated with INL% at 2 weeks and with the nasal OR% at 1, 3, and 6 months (P = < 0.001–0.028). MH diameter and age were significant predictors for improvement of aniseikonia. The greater the temporal retina displacement, and the thinner the postoperative INL and OR, the greater the improvement of aniseikonia. MH diameter and age are strong predictors for improvement of aniseikonia after MH surgery.
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Recent advances in vitreoretinal surgical techniques for the repair of idiopathic macular hole (MH) have improved anatomical success rates and visual outcomes1,2,3,4. However, even in cases of successful and uncomplicated surgery, visual complaints such as metamorphopsia and aniseikonia are common symptoms before and after MH surgery.
Aniseikonia is a binocular condition perceived by both eyes as a difference in the size of ocular image. Aniseikonia may be caused by changes of the density of photoreceptor cells due to the elongation or contraction of the retina associated with retinal disease, resulting in changes in the size of the image5, however how aniseikonia is generated in patients with MH remains to be elucidated.
We previously reported that the temporal retinal displacement due to internal limiting membrane (ILM) peeling in MH surgery correlates with the basal diameter of the MH6, and that the retinal displacement correlates with changes in the inner nuclear layer thickness (INL), indirectly proving our hypothesis that retinal displacement is caused by contraction of the optic nerve fiber7. We showed that the degree of metamorphopsia correlates not only with changes in INL but also with MH diameter (MHD), and that photoreceptor displacement is the most important cause of metamorphopsia8.
As a step to elucidate the mechanism of aniseikonia in MH, we analyzed the relationship between the degree of aniseikonia, MHD, change of retinal thickness and retinal displacement before and after MH surgery. In addition, we identified predictors for pre- and postoperative aniseikonia and its improvement.
Methods
A consecutive series of patients with idiopathic MH who underwent pars plana vitrectomy and achieved successful closure of the MH in the Department of Ophthalmology, Teikyo University School of Medicine, University Hospital Mizonokuchi from June 2017 to June 2021 were enrolled in this retrospective study. This study was performed in accordance with the tenets of the Declaration of Helsinki and received approval from the Institutional Review Committee of the Teikyo University School of Medicine (No. 20-206). Due to the retrospective nature of this study and the anonymized nature of the image analysis and data, need to obtain informed consent was waived by the Institutional Review Board of Teikyo University School of Medicine. This research information was presented on our institutional website and all the patients were provided the opportunity to opt out of this study.
Patients who were followed up for at least 6 months postoperatively were included. Exclusion criteria included eyes with an axial length ≧ 27 mm, glaucoma, retinal vascular disease, uveitis, proliferative diabetic retinopathy, traumatic MH and secondary MH, a history of vitreoretinal diseases except MH or vitreoretinal surgery and eyes undergoing the inverted ILM flap technique. Eyes with anisometropia of more than 2.0 D at baseline and 6 months postoperatively, eyes that changed more than 2.0 D postoperatively, and eyes with diseases that can affect anisometropia such as MH, epiretinal membrane (ERM), rhegmatogenous retinal detachment (RRD) and cystoid macular edema in the fellow eye was excluded. The best-corrected visual acuity (BCVA) using a Landolt C chart were performed preoperatively and at 2 weeks and 1, 3 and 6 months postoperatively.
OCT measurements
Retinal distances and thicknesses of retinal layers were measured as previously reported using Spectralis (Heidelberg Engineering, Inc., Heidelberg, Germany) before and after surgery7. The methods of measurement for retinal distances, minimum and basal MHDs and retinal layer thicknesses are shown in Fig. 1. INL% and outer retinal thickness (OR) % were calculated as rate of changes of OR and INL after surgery in each sector. Retinal displacement (RD%) was calculated as rate of change of retinal distance after surgery in each sector.
Aniseikonia measurement
The New Aniseikonia Test (NAT; Handaya Co., Tokyo, Japan) was used for quantitative evaluation of aniseikonia. The detailed procedure for NAT scoring is described in our previous reports9. Briefly, the degree of aniseikonia was measured by dissociating the two eyes using spectacles with a green filter in front of the right eye and a red filter in front of the left eye. The patients wore red–green spectacles and examined a book containing a pair of red and green semicircles at 40 cm distance. The diameter of the red semicircle on the left remains constant at 4 cm, while the size of the green semicircle on the right varies from 1 to 24% in 1% increments. The difference in the actual size of a pair of semicircles, in which the patient indicated two semicircles appear to be equal in size, represents the percentage of anisometropia. The NAT scores were examined for vertical and horizontal lines. Aniseikonia of more than + 2% was defined as macropsia and that of less than − 2%, as micropsia10,11.
Surgical procedures
Pars plana vitrectomy with 25-gauge instruments combined with ILM peeling, air–liquid exchange and 20% sulfur hexafluoride tamponade were performed by 3 surgeons (M.I., Y.I. and A.T.). ILMs were removed by staining with the 10% triamcinolone acetonide or 0.25% brilliant blue G. ILM peeling was performed in all quadrants. With all the surgeons, ILM was peeled to the edges of vascular arcade, close to the optic papillary margin on the nasal side, and to the same or greater area on the temporal side. Phakic eyes over 50 years of age underwent phacoemulsification with intraocular lens implantation simultaneously with vitrectomy. The surgical procedures were the same as the procedures previously reported in detail7.
Statistical analysis
The BCVA was analyzed on the logarithm of the minimal angle of resolution (logMAR) units for statistical analysis. A nonparametric test (the Shapiro–Wilk test) was chosen for evaluation, as our data did not follow a normal distribution. The Wilcoxon signed-rank test was performed to compare between preoperative and postoperative data. Correlations between NAT score, MHD, retinal thickness %, and RD% were determined using Spearman's rank correlation coefficient test. Multiple regression analysis was performed to identify predictors for NAT scores. SPSS software version 24.0 (SPSS, Chicago, Illinois, USA) was used for statistical analysis. A P value of < 0.05 was considered statistically significant.
Results
Forty-one eyes of 41 patients were included in this study. The average age of patients at the time of surgery was 65.1 ± 6.4 years (range 50–78 years) and 23 patients (56.1%) were women. The average preoperative spherical equivalent was − 1.0 ± 1.8 D and absolute difference of spherical equivalent between both eyes was 0.3 ± 0.8 D. The average spherical equivalent at 6 months was − 0.8 ± 2.0 D and difference of spherical equivalent between preoperative and 6 months was 0.2 ± 1.1 D. The staging of MH was classified as follows: 17 eyes (41.5%) as stage 2, 17 eyes (41.5%) as stage 3, and 7 eyes (17.0%) as stage 4. Phacoemulsification with intraocular lens implantation simultaneously with vitrectomy was performed for all eyes. TA was used for staining for 17 eyes and BBG was used for 24 eyes during ILM peeling. Two eyes in which ILM was completely detached during surgery were included in this study, although an inverted ILM flap technique had been originally scheduled because the minimum MHD was greater than 450 μm.
After evaluating the mean values of vertical and horizontal NAT scores, 12 eyes (29.3%) had micropsia, 28 eyes (68.3%) had no aniseikonia, and 1 eye (2.4%) had macropsia preoperatively. Four eye (9.8%) had micropsia, 30 eyes (73.2%) had no aniseikonia and 7 eyes (17.0%) had macropsia at 6 months postoperatively.
The average horizontal minimum MHD was 266.7 ± 117.4 μm (range 68–584 μm) and the horizontal basal MHD was 651.3 ± 245.1 μm (range 109–1108 μm), whereas the average vertical minimum MHD was 241.6 ± 105.3 μm (range 43–513 μm) and the vertical basal MHD was 577.4 ± 227.4 μm (range 109–983 μm). The demographics and ocular characteristics are provided in Table 1.
The average BCVA was 0.57 ± 1.20 logMAR units preoperatively, 0.38 ± 0.22 logMAR units at 2 weeks, 0.21 ± 0.21 logMAR units at 1 month, 0.10 ± 0.20 logMAR units at 3 months, 0.09 ± 0.20 logMAR units at 6 months postoperatively. The average BCVA for all postoperative visits improved significantly (P value range P < 0.001–0.001). Preoperative BCVA correlated with the mean of vertical and horizontal NAT score at preoperatively, 1 month and 3 months postoperatively (r = − 0.359, P = 0.021, r = − 0.433, P = 0.004 and r = − 0.421, P = 0.007, respectively). Postoperative BCVA correlated with the mean of vertical and horizontal NAT score at 3 and 6 months (r = − 0.355, P = 0.023 and r = − 0.396, P = 0.010). In other words, the better the postoperative BCVA at 3 and 6 months, the smaller the degree of micropsia.
Time course of the average NAT scores
The average preoperative vertical NAT score was − 1.05 ± 2.00% which improved to − 0.02 ± 1.10% at 2 weeks (P < 0.001), − 0.12 ± 2.00% at 1 month (P = 0.001), 0.15 ± 1.83% at 3 months (P = 0.003) and 0.17 ± 1.71% at 6 months (P = 0.002). The average preoperative horizontal NAT score was − 1.22 ± 2.20%, which did not change to − 0.85 ± 2.07% at 2 weeks (P = 0.180) but improved to − 0.37 ± 2.34% at 1 month (P = 0.010), 0.17 ± 2.45% at 3 months (P = 0.001), and 0.32 ± 2.17%at 6 months (P < 0.001). The mean of vertical and horizontal the NAT scores after MH surgery are shown in Fig. 2. The mean of vertical and horizontal the NAT score was − 1.13 ± 1.94% which improved to − 0.43 ± 1.34% at 2 weeks (P = 0.004), − 0.24 ± 1.90% at 1 month (P = 0.001), 0.16 ± 1.98% at 3 months (P < 0.001) and 0.13 ± 1.81% at 6 months (P < 0.001).
Correlations of NAT scores with MHD
Correlations of NAT scores with the MHD are shown in Table 2. The preoperative NAT scores showed correlations with MHD (r and P value range r = − 0.428 to − 0.313, P = 0.005–0.046). Horizontal NAT scores at 2 weeks correlated with the horizontal minimum MHDs, and vertical NAT score at 1 month correlated with the vertical and horizontal basal MHDs (r and P value range r = − 0.416 to − 0.326, P = 0.007–0.038).
The difference in vertical and horizontal NAT scores at 2 weeks and 6 months correlated with the basal MHDs, respectively (r and P value range r = 0.322–0.438, P = 0.004–0.040). The difference in the horizontal NAT score at 3 months correlated with the vertical and horizontal basal MHDs (r = 0.416, P = 0.007 and r = 0.460, P = 0.002).
Correlations of NAT scores with retinal displacement
Correlations of NAT scores with RD% are shown in Table 3. The preoperative vertical NAT score correlated with the temporal RD% at all visits postoperatively (r and P value range r = 0.388–0.464, P = 0.002–0.012). The vertical NAT score at 6 months correlated with the nasal RD% at 6 months and the horizontal NAT score at 6 months correlated with the nasal RD% at 1 month and 6 months.
The difference in vertical NAT scores at 6 months correlated with the temporal RD% at 2 weeks, 1 month and 6 months (r and P value range r = 0.388–0.464, P = 0.002–0.012). The improvement of horizontal NAT scores at 6 months correlated with the temporal and superior RD% at 2 weeks (r = − 0.323, P = 0.039 and r = − 0.339, P = 0.030).
Correlations of the NAT scores with changes of retinal layer thickness
Preoperative vertical and horizontal NAT scores correlated with temporal INL% at 2 weeks and 1 month (r and P value range r = 0.343–0.411, P = 0.008–0.028), and preoperative vertical NAT score correlated with inferior INL% at 2 weeks (r = 0.405, P = 0.009) and temporal INL% at 6 months (r = 0.340, P = 0.030). Preoperative vertical NAT scores correlated with nasal OR% at 1 month (r = 0.530, P = 0.010), as well as horizontal NAT scores with inferior OR% at 2 weeks and 1, 3 months (r and P value range r = 0.371–0.457, P = 0.003–0.017).
Improvement of vertical NAT scores at 6 months correlated with INL% in the 4 sectors at 2 weeks (nasal: r = − 0.356, P = 0.022, temporal: r = − 0.582, P < 0.001, superior: r = − 0.422, P = 0.006 and inferior: r = − 0.448, P = 0.003), with that in temporal and inferior sectors at 1 month (r = − 0.560, P < 0.001 and r = − 0.485, P = 0.001), with that in the superior at 3 months (r = − 0.440, P = 0.004), and with the nasal OR% at 1, 3, and 6 months (r and P value range r = − 0.451 to − 0.342, P = 0.003–0.028). Improvement of horizontal NAT scores at 6 months correlated with INL% in temporal and superior sectors at 2 weeks, with that in temporal and inferior at 1 month, and with that in inferior at 3 months (r and P value range r = − 0.457 to − 0.310, P = 0.003–0.049).
In other words, the larger the postoperative change of INL in 4 sectors, especially in the temporal sector, and the larger the postoperative change of OR in nasal sector, the greater the improvement of vertical aniseikonia after MH surgery. Furthermore, the larger the change of INL in 3 sectors except for the nasal, the greater the improvement in horizontal aniseikonia after surgery.
Correlations of age with retinal displacement
Age correlated with the temporal and inferior RD% at 2 weeks (r = 0.308, P = 0.049 and r = 0.316, P = 0.044) and the nasal and inferior at 6 months (r = 0.474, P = 0.002 and r = 0.312, P = 0.047), suggesting that the older the patient, the smaller retinal displacement.
Multivariate analysis to identify factors associated with NAT scores
The results of stepwise multiple regression analysis to identify predictors for NAT scores are shown in Tables 4 and 5. The dependent factor was the average of the vertical and horizontal NAT scores at baseline, 6 months and differences at 6 months postoperatively. The independent factors were age, sex, MHD, preoperative INL and OR, INL%, OR%, and RD% at 6 months. Preoperative retinal thicknesses, changes of retinal thickness and RD% were analyzed for each of the four sectors. The average of the vertical and horizontal basal MHDs was used for the analysis.
The significant predictors for the preoperative NAT score were the basal MHDs and inferior OR%, and that for the postoperative NAT score at 6 months were age. MHD and age were significant predictors for improvement of NAT scores at 6 months. The older the patient, the poorer improvement of aniseikonia and the greater postoperative micropsia.
Discussion
Our results showed that aniseikonia improved with time after MH surgery. Preoperative aniseikonia correlated with MHD, and improvement of postoperative aniseikonia also correlated with MHD. Preoperative aniseikonia and improvement of postoperative aniseikonia correlated with postoperative temporal retinal displacement. Improvement of postoperative vertical aniseikonia correlated with changes of temporal INL and nasal OR, indicating that the larger postoperative thinning of temporal INL and nasal OR, the greater the improvement of vertical aniseikonia. MHD were predictors for preoperative aniseikonia. MHD and age were predictors for the improvement of aniseikonia.
Recently, the relationship between aniseikonia and retinal diseases such as ERM9,10,11,12,13,14,15, MH16, RRD17,18, and branch retinal vein occlusion (BRVO)19 has been reported. Okamoto et al.16 reported that 55% of MH patients had micropsia and that the degree of preoperative aniseikonia was related to the defect length of the external limiting membrane and diameter of the MH, while postoperative aniseikonia at 12 months did not correlate with any preoperative parameters. Our results that early postoperative aniseikonia correlates with MHD are different from the previous report16 probably due to the difference of the times of examination of aniseikonia. Because reconstruction of retinal tissues continues after surgery, aniseikonia shortly after surgery is affected by the size of MH.
Contraction of the inner retina of ERM causes centripetal migration of retinal photoreceptor cells, resulting in aniseikonia, which is mainly perceived as macropsia. The reason why contraction of the inner retina causes metamorphopsia and aniseikonia remains to be elucidated however a reasonable explanation is that if the inner retinal layer is displaced from the photoreceptor layer, Müller cells, which act as optic fibers to transfer photons from the retinal surface to the photoreceptor cells20,21, reach the photoreceptor cells far from the original location9,22. Following closure of the MH, changes of INL correlated with changes in aniseikonia, and retinal displacement caused INL thinning in eyes with larger MH, indicating that dislocated Müller cells play a significant role in the generation of aniseikonia.
In addition to dislocated Müller cells, the density of photoreceptor cells seems to be critical for generation of metamorphopsia and aniseikonia. As discussed in our previous publication, simultaneous stimulation of the overlapping photoreceptors which were elevated from retinal pigment epithelium may cause a sense of distortion and micropsia in MH8.
Earlier, we reported that the degree of aniseikonia significantly correlated with the distance of retinal displacement after ERM surgery9, although aniseikonia was unlikely to improve9,10. Prolonged persistent macular traction by ERM disrupts the alignment of Müller cells and photoreceptor cells, resulting in permanent changes that are less likely to become normal after surgery23, causing the perception of residual aniseikonia after surgery. On the other hand, metamorphopsia and aniseikonia in MH improve in many cases postoperatively, although patients with large MH still complain of them even after successful surgery.
In our present analysis, we found that improvement of aniseikonia was poorer with older age, and that postoperative retinal displacement was smaller with older age. Metamorphopsia is less likely to improve in older patients with ERM as shown in our recent publication24. In rats, Müller cells were reported to respond to age-related photoreceptor degeneration by increasing expression of glial fibrillary acidic protein, the intermediate filament protein25. These findings suggest that, in humans also, the retina becomes less flexible with age, and consequently recovery of visual function is likely to be delayed.
Interestingly, 17% of patients experienced macropsia after MH surgery. We considered that the presence of macropsia after surgery was due to the afferent migration of the photoreceptor cells around the hole during closure of the MH, and the deviation of Müller cells was attributable to thinning of the INL and displacement of the inner retinal layer (Fig. 3).
The limitations of this study were retrospective study, relatively small number of cases and short follow-up period. The accuracy of the NAT score may be affected by the subject’s visual acuity, and we may need to interpret data from those with low BCVA carefully. Furthermore, areas of ILM peeling were not measured. The possibility of bias due to differences of the area of peeled ILM among surgeons was not completely excluded. The manual measurement points for each retinal thickness were not always identical and changed with tangential migration of the retina after MH surgery.
In conclusion, the aniseikonia in patients with MH improves after surgery. The larger the MHD, the greater the temporal retinal displacement, and the thinner the INL and OR postoperatively, then the greater the improvement of aniseikonia. The changes of photoreceptor density and thinning of the inner retinal layer appear to generate sensations of aniseikonia after MH surgery. In addition to MHD, age is a clinical biomarker for improvement of aniseikonia after MH surgery.
Data availability
The datasets generated and analyzed during the current study are available from the corresponding author on reasonable requests.
References
Wendel, R. T. et al. Vitreous surgery for macular holes. Ophthalmology 100, 1671–1676 (1993).
Brooks, H. L. Jr. Macular hole surgery with and without internal limiting membrane peeling. Ophthalmology 107, 1939–1948 (2000).
Christensen, U. C. et al. Value of internal limiting membrane peeling in surgery for idiopathic macular hole stage 2 and 3: A randomised clinical trial. Br. J. Ophthalmol. 93, 1005–1015 (2009).
Lois, N. et al. Internal limiting membrane peeling versus no peeling for idiopathic full-thickness macular hole: A pragmatic randomized controlled trial. Investig. Ophthalmol. Vis. Sci. 52, 1586–1592 (2011).
Benegas, N. M., Egbert, J., Engel, W. K. & Kushner, B. J. Diplopia secondary to aniseikonia associated with macular disease. Arch. Ophthalmol. 117, 896–899 (1999).
Ishida, M. et al. Retinal displacement toward optic disc after internal limiting membrane peeling for idiopathic macular hole. Am. J. Ophthalmol. 157, 971–977 (2014).
Takeyama, A. et al. Retinal displacement and intraretinal structural changes after idiopathic macular hole surgery. Jpn. J. Ophthalmol. 66, 173–182 (2022).
Takeyama, A. et al. Predictors for metamorphopsia in eyes undergoing macular hole surgery. Sci. Rep. 16, 810. https://doi.org/10.1038/s41598-023-28031-2 (2023).
Ichikawa, Y., Imamura, Y. & Ishida, M. Associations of aniseikonia with metamorphopsia and retinal displacements after epiretinal membrane surgery. Eye (London) 32, 400–405 (2018).
Okamoto, F., Sugiura, Y., Okamoto, Y., Hiraoka, T. & Oshika, T. Time course of changes in aniseikonia and foveal microstructure after vitrectomy for epiretinal membrane. Ophthalmology 121, 2255–2260 (2014).
Chung, H. et al. Relationship between vertical and horizontal aniseikonia scores and vertical and horizontal OCT images in idiopathic epiretinal membrane. Investig. Ophthalmol. Vis. Sci. 56, 6542–6548 (2015).
Hirata, A. et al. Relationship between the morphology of the foveal avascular zone and the degree of aniseikonia before and after vitrectomy in patients with unilateral epiretinal membrane. Graefes Arch. Clin. Exp. Ophthalmol. 257, 507–515 (2019).
Moon, B. G., Yang, Y. S., Chung, H. & Sohn, J. Correlation between macular microstructures and aniseikonia after idiopathic epiretinal membrane removal. Retina 40, 1160–1168 (2020).
Kim, B. H., Kim, D. I., Bae, K. W. & Park, U. C. Influence of postoperative ectopic inner foveal layer on visual function after removal of idiopathic epiretinal membrane. PLoS ONE 16, e0259388. https://doi.org/10.1371/journal.pone.0259388 (2021).
Tanikawa, A., Shimada, Y. & Horiguchi, M. Comparison of visual acuity, metamorphopsia, and aniseikonia in patients with an idiopathic epiretinal membrane. Jpn. J. Ophthalmol. 62, 280–285 (2018).
Okamoto, F. et al. Aniseikonia and foveal microstructure in patients with idiopathic macular hole. Ophthalmology 123, 1926–1932 (2016).
Okamoto, F., Sugiura, Y., Okamoto, Y., Hiraoka, T. & Oshika, T. Aniseikonia and foveal microstructure after retinal detachment surgery. Investig. Ophthalmol. Vis. Sci. 17, IOVS-14-14618. https://doi.org/10.1167/iovs.14-14618 (2014).
Murakami, T. et al. Changes in aniseikonia and influencing-factors following successful macula-off retinal detachment surgery. Sci. Rep. 12(9), 11588. https://doi.org/10.1038/s41598-019-48112-5 (2019).
Morikawa, S. et al. Aniseikonia following intravitreal ranibizumab treatment for branch retinal vein occlusion. Jpn. J. Ophthalmol. 65, 672–679 (2021).
Franze, K. et al. Müller cells are living optical fibers in the vertebrate retina. Proc. Natl. Acad. Sci. U.S.A. 104, 8287–8292 (2007).
Labin, A. M., Safuri, S. K., Ribak, E. N. & Perlman, I. Müller cells separate between wavelengths to improve day vision with minimal effect upon night vision. Nat. commun. 5, 4319. https://doi.org/10.1038/ncomms5319 (2014).
Ichikawa, Y., Imamura, Y. & Ishida, M. Inner nuclear layer thickness, a biomarker of metamorphopsia in epiretinal membrane, correlates with tangential retinal displacement. Am. J. Ophthalmol. 193, 20–27 (2018).
Ooto, S. et al. High-resolution imaging of the photoreceptor layer in epiretinal membrane using adaptive optics scanning laser ophthalmoscopy. Ophthalmology 118, 873–881 (2011).
Watanabe, A. et al. One-year outcomes of metamorphopsia and retinal displacement after epiretinal membrane surgery. Retina 42, 1756–1761 (2022).
Fan, W., Lin, N., Sheedlo, H. J. & Turner, J. E. Müller and RPE cell response to photoreceptor cell degeneration in aging Fischer rats. Exp. Eye Res. 63, 9–18 (1996).
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M.I., Y.I. and A.T. contributed to the design of the study. T.F., T.I., Y.K., and A.T. contributed to data collection, analysis and interpretation. A.T. drafted the manuscript and A.T., Y.I., and M.I. revised it. All authors approved the final version to be submitted for publishing.
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Takeyama, A., Imamura, Y., Fujimoto, T. et al. Aniseikonia and retinal morphological changes in eyes undergoing macular hole surgery. Sci Rep 14, 59 (2024). https://doi.org/10.1038/s41598-023-51032-0
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DOI: https://doi.org/10.1038/s41598-023-51032-0
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