Recent qualitative studies have reported the clinical relevance of the photoreceptor status on OCT images,
17,19 –21 although the mechanisms of photoreceptor degeneration are still poorly defined. The present study showed for the first time several associations between the characteristics of the cystoid spaces and photoreceptor changes beneath them in DME. Our findings suggested that the cystoid spaces might affect the pathogenesis in the photoreceptors, in addition to the signal transduction system, and that the cystoid spaces might be a therapeutic target for improving the photoreceptor function. It had been speculated that the cystoid spaces disturb light transmission at the fovea, and in the present study we showed other mechanisms for the visual dysfunction associated with the cystoid spaces. However, we evaluated the retinal sections using cross-hair mode, which suggests the limited quality of information, compared with the full delineation by three-dimensional scan mode. Because the present study was cross-sectional and retrospective in nature, another longitudinal study should be planned.
We first investigated the photoreceptor status seen on SD-OCT (Spectralis; Heidelberg Engineering) that is represented by the ELM, IS/OS, and COST lines. Compared with the reproducible and clear delineation of the ELM and IS/OS lines, COST lines were often blurred or diminished, even in vivo. Although further advances in OCT technology would facilitate accurate evaluation of the interface between the RPE and photoreceptors, the present study focused on the ELM and IS/OS lines, both of which might represent individual properties.
30 SD-OCT improves visualization of each retinal layer with reduced speckle noise, and both lines appeared continuously in the physiologic eyes, which enabled us to differentiate the fragmented lines more precisely.
We therefore investigated the transverse length or the OCT reflectivity of the continuous ELM and IS/OS lines. The reflectivity levels of the ELM lines were relatively homogeneous, and their presence could be clearly determined. However, the continuous IS/OS lines had varying reflectivity, and it was difficult to differentiate fragmented IS/OS lines from RPE hyperplasia, hyperreflective foci, or degenerative processes in the neuroglial tissue.
26,31,32 All these conditions might be associated with photoreceptor damage, which prompted us to categorize them as disrupted IS/OS, and would correspond to the absent or discontinuous IS/OS lines reported previously.
19,20 We also evaluated the transverse length of the discontinuous IS/OS, which should depend on the signal intensity, which might have led us to reach erroneous conclusions compared with the clinical relevance in the qualitative analyses. These situations encouraged us to introduce a novel classification for quantitative analyses. However, the reflectivity levels of the continuous IS/OS lines varied, which led us to subdivide them further into faint and intact lines. For the objective evaluation, we performed additional quantification of the IS/OS reflectivity, which also showed differential levels of OCT reflectivity compared with that of ELM lines.
Several mechanisms might lead to photoreceptor changes. Breakdown of the BRB associated with diabetes might increase extravasation of the blood constituents (water, ions, proteins, lipids) and inflammatory cells and concomitantly exacerbate the pathomorphologic changes in the macula.
3,4,33 SRDs might decrease the metabolism of the photoreceptor cells, resulting in their degradation. We recently found that hyperreflective foci in the outer retinal layers were associated with photoreceptor damage.
34 The Early Treatment Diabetic Retinopathy Study (ETDRS) reported that foveal hard exudates led to subretinal fibrosis and visual impairment,
35 which might depend on photoreceptor degradation, as in AMD. In addition to those possible mechanisms, the present study found that disrupted or faint IS/OS lines were beneath the cystoid spaces more frequently, suggesting that the cystoid spaces might be an additional mechanism contributing to exacerbation of photoreceptor damage.
Enlarged cystoid spaces can extend from the inner retinal layers to the OPL in macular edema associated with retinal vascular diseases.
13 We identified such cystoid spaces extending from the INL to OPL in 18 eyes in the present study; these cystoid spaces had larger transverse length of the disrupted IS/OS or ELM, but not that of the faint IS/OS. Extended cystoid spaces might represent degeneration of the neuroglial components in signal transduction, which could lead to retrograde degeneration of the photoreceptor cells. Otherwise, the degenerative changes in the glia and Müller cells might result in disruption of the ELM, which is the heterophilic adherens junction between the Müller cells and photoreceptors and is a barrier for macromolecules.
30 Concomitantly, blood constituents or inflammatory cells might migrate into the outer retinal layers and exacerbate photoreceptor degeneration, which possibly is supported by the association between the hyperreflective foci in the outer retinal layers and the disrupted photoreceptors.
31 Furthermore, because Müller cells function as living optical fibers,
36 their damage might lead to the reduced transparency of the retina, which explains the reflectivity error in outer retinal layers and visual dysfunction. On the contrary, we had to consider the possibility that photoreceptor degeneration might contribute to the pathogenesis of CME, because retinitis pigmentosa, whose primary lesions are in photoreceptors and RPE, is sometimes accompanied with cystoid spaces.
37 Another explanation might be that a longer duration or more severe DME might result in both extended cystoid spaces and photoreceptor damage.
The present study also showed that decreased OCT reflectivity was specifically associated with IS/OS lines but not ELM or RPE lines beneath the cystoid spaces in the OPL. The classic speculation regarding the disturbed light transmission through the cystoid spaces might be supported by the signal reduction in some areas with cystoid spaces on OCT images. In other words, we could not completely exclude the possibility that faint IS/OS line might correspond to an optical artifact. However, previous studies have reported that OCT reflectivity levels in the outer segments increase after light exposure and are associated with retinal function.
27,28 Those authors speculated that light-evoked cell swelling and shrinkage and membrane depolarization might result in optical changes in the outer segments (i.e., scattering or transmission). Instead of light exposure, blood constituents or waste in the cystoid spaces might change the cellular metabolism with concomitant cellular swelling or shrinkage, or local imbalance of ions might affect membrane depolarization, although we could not find a definite association between VA and a faint IS/OS line. Further longitudinal analysis might identify factors predictive of photoreceptor degeneration at least in part.
FA has provided important information regarding DME, and several recent publications have reported interesting associations between FA and OCT findings,
12,16,25,29 which encouraged us to investigate whether patterns of fluorescein pooling are related to photoreceptor characteristics seen on OCT images. Although we could not find a relationship between fluorescein pooling and OCT reflectivity of the ELM or IS/OS, the descent of the ELM to the RPE occurred more frequently in eyes with single-lobulated pooling than in those with multi-lobulated pooling. This suggested that a single-lobulated cystoid space might compress the surrounding retinal parenchyma, resulting in the descent of the ELM, and support the finding that these eyes often have enlarged cystoid spaces. However, it is unclear what determines the patterns of fluorescein pooling. Some eyes with a descended ELM had continuous IS/OS lines beneath the cystoid spaces and others did not, and the transverse length of the disrupted IS/OS beneath the descended ELM was much longer. This suggested that distortion of the photoreceptor layer might contribute partly to visual impairment. Another possible explanation might be that persistent multi-lobulated cystoid spaces might result in a single-lobulated cystoid space, with progression of the atrophic changes in the outer retinal layers. A longitudinal study would elucidate whether these mechanical changes exacerbate photoreceptor degeneration beneath the cystoid spaces.
The present study found a significant association between cystoid spaces and photoreceptor degeneration beneath them in the DME, suggesting that the cystoid spaces in the OPL might be an important mechanism in photoreceptor damage and visual disturbance.