Abstract
Purpose
To evaluate the topographic distribution of the choriocapillaris (CC) flow deficits in a population of healthy subjects.
Methods
Using a swept-source optical-coherence tomography angiography (SS-OCTA) device, two repeated volume 6 x 6 mm and 3 x 3 mm scans were acquired in healthy subjects at the Doheny—UCLA Eye Centers. The en-face CC angiogram was binarized and analyzed for percentage of flow deficits (FD%) using a grid of progressive, concentric rings covering a circular area with a diameter of 2.5 mm (in the 3 x 3 mm scans) and 5 mm (in the 6 x 6 mm scans). The FD% for each ring was plotted against the distance from the fovea. The linear trendline of the resulting curve was analyzed and the slope (m) and intercept (q) were computed.
Results
Seventy-five eyes of 75 subjects were enrolled and divided into three subgroups based on age (year ranges: 21–40, 41–60 and 61–80). For the entire cohort and within each subgroup, there was a significant association between distance from the fovea and FD% in both 3X3 mm and 6X6 mm scans, with flow deficits increasing with closer proximity to the foveal center. Age was a significant predictor for both m and q for both scan patterns, with older subjects showing a steeper slope.
Conclusions
In SS-OCTA images, the topographic distribution of CC flow deficits varies with distance from the fovea and age. In particular, the FD% tends to decrease from the fovea towards the periphery, with a steeper decline with advancing age. These normal trends may need to be accounted for in future studies of the CC in disease.
Introduction
The development of optical coherence tomography angiography (OCTA) has provided new insights into the retinal and choroidal microvasculature. allowing individual vascular plexi to be evaluated at extremely high resolution [1]. OCTA has thus opened the door for a precise correlation between vascular, structural and functional alterations in vivo in both a cross-sectional and longitudinal fashion.
Visualization and analysis of the choriocapillaris (CC) in particular, has been a topic of great interest with OCTA. The choriocapillaris represents an approximately 10-μm-thin layer of capillaries interconnected in a densely packed arrangement with very small intercapillary pillars located between the medium/large choroidal vessels and Bruch’s membrane [2]. Changes in CC are known to occur physiologically with increasing age and to be associated with a wide range of retinal diseases including age-related macular degeneration (AMD) and central serous chorioretinopathy (CSC), which are major causes of vision loss [3–6].
Imaging the CC in vivo is difficult because of the light scattering caused by overlying structures, in particular the retinal pigment epithelium (RPE)[7]. The introduction of swept-source (SS) OCTA has allowed a more reliable visualization of the CC thanks to greater sensitivity and the use of a longer wavelength which better penetrates deeper tissues and is less scattered by the RPE [8–11]. The high quality images provided by SS-OCTA can produce visualization of the CC which can resemble histology in many respects [10–12]. With typical processing approaches, OCTA images of the CC appear as grainy pictures where white pixels represents flow and black pixels represents areas of signal deficits where the flow is supposed to be absent or below the detecting threshold. A post-processing analysis of these images allows the quantification of the black pixels (flow deficits) within the CC. This type of analysis has been used in many studies as an indication of CC impairment in various retinal diseases [13]. Recently Spaide et al. measured the size and number of the flow deficits in subjects at different ages and in different diseases, and observed that these parameters are dependent on age and hypertension [5]. In previous studies, we have shown that choroid, as assessed by choroidal thickness, can show significant regional variation in normal individuals [14]. Thus, it is reasonable to hypothesize that the CC could also demonstrate significant regional variation (personal communication, Phil Rosenfeld). This hypothesis is supported by histologic studies which have demonstrated differences in the CC morphology in central compared to more peripheral regions [2]. These topographical variations in the CC may be significant confounders of studies which compare CC flow deficits within regions of interest in the macula [3,4,15,16]. To study the potential impact of these regional and age-related variations, we studied the topographical distribution of CC flow deficits in a cohort of normal subjects.
Methods
SS-OCTA images from healthy volunteers were obtained as part of a normative study conducted at the Doheny-UCLA Eye Centers between December 2017 and May 2018. Eligible subjects were healthy, with no systemic or eye-related conditions, and confirmed by examination. Any refractive error greater than 3 diopters and presence of significant media opacities which could impact the quality of the OCT images were exclusion criteria for this study. The study was advertised at the Doheny-UCLA Eye Centers to all staff members, visitors and family to participate and volunteers, if eligible, were consecutively recruited.
The study was performed in accordance with the Health Insurance Portability and Accountability Act and adhered to the principles of the Declaration of Helsinki. All subjects provided written informed consent to participate in this observational study. The informed consent form and research was approved by the institutional review board (IRB) of the University of California–Los Angeles (UCLA).
All participants underwent a complete ophthalmic examination, including best-corrected visual acuity (BCVA) using Early Treatment Diabetic Retinopathy Study (ETDRS) charts, slit lamp biomicroscopy, tonometry and SS-OCTA.
Imaging
Subjects underwent SS-OCTA imaging with the PLEX Elite 9000 device (Carl Zeiss Meditec Inc., Dublin, CA, USA) which uses a swept laser source with a central wavelength of 1050 nm (1000–1100 nm full bandwidth) and operates at 100,000 A-scans per second. This instrument employs a full-width at half-maximum axial resolution of approximately 5 μm in tissue, and a lateral resolution at the retinal surface estimated at approximately 14 μm. OCTA imaging of the macula was performed using two scan patterns: a 3 X 3 mm (300 A-scans x 300 B-scans) and a 6 X 6 mm (500 A-scans x 500 B-scans) scans centered on the fovea. The right eye of each subject was repeatedly imaged after pupil dilation to obtain two OCTA volume scan sets per area investigated with sufficient image quality (signal strength index (SSI)>7) that fulfilled the acceptance criteria of the Doheny Image Reading Center (DIRC), as previously reported [4,17].
The manufacturer’s fully-automated retinal layer segmentation algorithm was applied to the three-dimensional structural OCT data, in order to segment the CC slab as defined previously (10 μm thick starting 31 μm posterior to the RPE reference) [5]. This segmentation was then applied to OCTA flow intensity data to obtain vascular images. Maximum projection analyses of the flow intensity were performed to generate the en-face images of the CC plexus.
Quantitative image analysis
The CC en-face image was exported and analyzed using ImageJ software version 1.50 (National Institutes of Health, Bethesda, MD; available at http://rsb.info.nih.gov/ij/index.html) [18]. The CC en-face images were binarized for quantitative image analysis of the signal deficits using the Phansalkar method (radius, 15 pixels) as previously described [5,19,20]. The CC en face images were then processed with the ‘Analyze Particles’ command (size: 0-infinity, circularity 0–1) in order to count the flow deficits as a percentage of each analyzed area (FD%).
The analysis of the flow deficits was performed within a circular area with a diameter of 2.5 mm and 5 mm for the 3 X 3 mm and 6 X 6 mm, respectively. This roughly correspond to a circle measuring 854 pixels in diameter (note as the OCTA images were exported at a similar resolution, both the 3x3mm and 6x6mm en face OCTA CC images were composed of a similar number of pixels: 1024x1024). Starting from this outermost boundary, we constructed a grid of continuous concentric rings of progressively increasing width towards the fovea following these steps: (1) after delineating the outermost circle (radius: 427 pixel), we delineated an inner circle with a radius of 426 pixel, concentric to the first one and measured the area of the resulting ring (2678 pixel2) as:
(A) |
where r2 is the radius of the outer circle and r1 is the radius of the inner circle; (2) we progressively added inner concentric circles using the formula (A) such that the area of the resultant rings were within ±35% of the area of the outermost ring (2678 pixel2). It was necessary to increase the width of the more central rings in this way in order to maintain a somewhat similar area for the various concentric rings. If such an adjustment was not introduced and the ring width was instead maintained constant at all eccentricities, the innermost ring would only be composed of a few pixels which would reduce the reliability of subsequent flow deficits calculations. At the same time, we chose not to make all concentric rings of exactly the same area as the most central rings would be very wide and limit our ability to study differences in CC flow deficits as a function of distance from the foveal center. Using this “compromise” strategy, the size (area) of the rings varied from 1741 and 3615 pixel2 (i.e. 2678 ± 35%) (Fig 1).
The precise 35% threshold itself was arbitrarily chosen because it ensures the minimum possible fluctuation in ring areas. This can be explained through an example: with the choice of a threshold of 30% from the outermost ring (range of 1875–3482 pixel2), the delineation of progressively smaller concentric circles leads to the 1-pixel wide ring of 1880 pixel2. The subsequent 1-pixel ring would be under the 30% threshold; hence, we would have to widen the ring to 2-pixels. In this case, the resultant ring has an area of 3742 pixel2 which is over the upper limit of the chosen range. On the other hand with a threshold of 35% (range: 1741–3615 pixel2), when we reach the 1742 pixel2 ring, the widening of the subsequent ring to 2-pixels, results in an area of 3466 pixel2, which is still within the 35% range.
For each image we used the en face angiogram of the superficial plexus to identify the fovea and center the grid (Fig 1).
All measurements were repeated by the same OCT grader (MN) on two different acquisitions in order to explore the “inter-scan” repeatability. Then, in order to rule out the possibility that the manual positioning of the grid on the fovea could affect the “inter-operator” repeatability, a second grader (EB) performed the analysis on one of the two acquisitions for each scan patterns.
Statistics
For each image we plotted the FD% (y-axis) with the distance from the fovea (x-axis) on Microsoft Excel 2013 software (Microsoft Corporation, Redmond, WA). We then obtained the linear trend line of the curve and reported the slope (m) and the intercept (q) from its equation (Fig 2).
Statistical analyses were performed using SPSS Statistics version 20 (IBM, Armonk, NY). An ANOVA test and an unpaired t-test were performed to investigate the differences in slopes and intercepts between the age groups and between genders, respectively. A linear regression analysis was used to investigate: (1) the association between distance from the fovea and FD% overall and within pre-specified age groups; (2) the association between age, sex and the slopes and the intercepts. Inter-scan and inter-operator repeatabilities were assessed by calculating the intraclass correlation coefficients (± 95% confidence interval [CI]) for m and q.
All data are presented as mean ± standard deviation. A p value ≤ 0.05 was considered to be statistically significant.
Results
A total of 75 eyes from 75 healthy subjects were enrolled in this study (mean age: 50 ± 17.15 years, range 23–80; 37 Females).
Overall, there was a significant association between distance from the fovea and FD% in both 3X3 mm and 6X6 mm scans as determined by the linear regression analysis. The regression coefficient was -0.08 (standard error (SE): 0.003) for an increase of 50 μm in distance from the foveal center in the 3x3 mm and -0.052 (SE: 0.003) for an increase of 100 μm distance from the foveal center in the 6X6 mm (Table 1).
Table 1. Univariate linear regression analysis of distance from the fovea versus percentage of flow deficits, for each optical coherence tomography angiography scan pattern.
Percentage of Flow Deficits | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Overall | Ages 21–40 | Ages 41–60 | Ages 61–80 | |||||||||
Unstandardized coefficient (standard error) | Standardized ß Coefficient | P value | Unstandardized coefficient (standard error) | Standardized ß Coefficient | P value | Unstandardized coefficient (standard error) | Standardized ß Coefficient | P value | Unstandardized coefficient (standard error) | Standardized ß Coefficient | P value | |
Distance from the fovea (50μm increase) (3X3 mm scan) | -0.08 (0.003) |
-0.872 | <0.001 | -0.016 (0.004) |
-0.264 | <0.001 | -0.081 (0.004) |
-0.741 | <0.001 | -0.143 (0.005) |
-0.880 | <0.001 |
Distance from the fovea (100μm increase) (6X6 mm scan) | -0.052 (0.003) |
-0.765 | <0.001 | -0.018 (0.004) |
-0.282 | <0.001 | -0.058 (0.004) |
-0.686 | <0.001 | -0.08 (0.005) |
-0.709 | <0.001 |
The linear regression analysis was performed using the entire cohort, and for the three age-based subgroups. In all situations, there is a significant association between the distance from the fovea and the percentage of flow deficits (FD%).
Age was a significant predictor for both m and q in each scan patterns while gender was not associated with either (Table 2). An unpaired t-test between genders revealed no significant differences for m and q in both 3X3 and 6X6 mm scan patterns (Table 3).
Table 2. Multivariate linear regression analysis between age and gender and the slopes (m) and intercepts (q) of trendlines of the curves plotted for percentage of flow deficits versus the distance from the fovea.
3X3 mm | 6X6 mm | |||||||
---|---|---|---|---|---|---|---|---|
Slope (m) | Intercept (q) | Slope (m) | Intercept (q) | |||||
Standardized ß Coefficient | P value | Standardized ß Coefficient | P value | Standardized ß Coefficient | P value | Standardized ß Coefficient | P value | |
Age | -0.450 | <0.001 | 0.409 | <0.001 | -0.430 | <0.001 | 0.346 | 0.002 |
Gender | 0.165 | 0.115 | -0.061 | 0.570 | 0.142 | 0.181 | 0.003 | 0.982 |
In this multivariate linear regression analysis, age is the only significant predictor for both m and q for both optical coherence tomography angiography scan patterns.
Table 3. Mean slopes and intercepts of the linear trendlines of the curves obtained by plotting the percentage of flow deficits versus the distance from the fovea.
3x3 SCAN | 6x6 SCAN | |||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Overall | Gender | Age range | Overall | Gender | Age range | |||||||||||
Males | Females | p-value* | 21–40 | 41–60 | 61–80 | p-value** | Males | Females | p-value* | 21–40 | 41–60 | 61–80 | p-value** | |||
Slope (m) | -0.0017 (0.0024) | -0.0021 (0.0024) | -0.0012 (0.0024) | 0.138 | -0.0003 (0.0019) | -0.0016 (0.0024) | -0.003 (0.002) | <0.001 | -0.0005 (0.00069) | -0.00071 (0.0006) | -0.0004 (0.0006) | 0.201 | -0.0002 (0.0004) | -0.0006 (0.0009) | -0.0009 (0.0004) | 0.001 |
Intercept (q) | 13.68 (4.08) | 13.96 (4.404) | 13.4 (3.76) | 0.559 | 11.63 (3.67) | 13.66 (3.85) | 15.77 (3.76) | 0.001 | 20.66 (2.76) | 20.67 (3.41) | 20.66 (1.91) | 0.987 | 19.55 (1.57) | 20.7 (3.65) | 21.89 (2.3) | 0.011 |
Data are presented separately for the two optical coherence tomography angiography scan patterns (3X3 and 6X6 mm) and for the entire population and subgroups divided by gender and age range. All data are presented as means (standard deviation). P-value*: unpaired t-test; p-value**: one-way ANOVA.
Age groups
We divided the population in three pre-specified sub-groups based on the age range: (1) 21–40 years (25 subjects, 12 Females); (2) 41–60 years (25 subjects, 13 Females); (3) 61–80 years (25 subjects, 12 Females).
Plots of the mean FD% versus the corresponding distance from the foveal center for the overall population and for each age groups are shown in Fig 3.
In the 3X3 mm scan there was a significant association between distance from the fovea and FD% in all three groups. For an increase of 50 μm from the fovea, the regression coefficients were -0.016 (SE: 0.004), -0.081 (SE: 0.004) and -0.143 (SE: 0.005) for the groups between 21–40 years, 41–60 years and 61–80 years of age, respectively (all p<0.001) (Table 1).
The mean m in the youngest group was -0.0003 ± 0.0019, while in the group between 41–60 years it was -0.0016 ± 0.0024 and in the oldest group m it was -0.003 ± 0.002 (one-way ANOVA (F(2,74) = 9.823, p<0.001) (Table 3).
The mean q in the youngest group was 11.63 ± 3.67, while in the group between 41–60 years it was 13.66 ± 3.85 and in the oldest group the q was 15.77 ± 3.76 (one-way ANOVA (F(2,74) = 7.544, p = 0.001) (Table 3).
In the 6X6 mm scan there was a significant association between distance from the fovea and FD% in all three groups. For an increase of 100 μm from the fovea, the regression coefficients were -0.018 (SE: 0.004), -0.058 (SE: 0.004) and -0.08 (SE: 0.005) for the groups between 21–40 years, 41–60 years and 61–80 years of age, respectively (all p<0.001) (Table 1).
The mean m in the youngest group was -0.0002 ± 0.0004, while in the group between 41–60 years it was -0.0006 ± 0.0009, and in the oldest group m was -0.0009 ± 0.0004 (one-way ANOVA (F(2,74) = 7.748, p = 0.001) (Table 3).
The mean q in the youngest group was 19.55 ± 1.57, while in the group between 41–60 years it was 20.7 ± 3.65 and in the oldest group the q was 21.89 ± 2.3 (one-way ANOVA (F(2,74) = 4.848, p = 0.011) (Table 3).
Repeatability
For 3 X 3 mm acquisitions, the inter-scan repeatability demonstrated an ICC of 0.858 (95% CI 0.810–0.914) for m and 0.863 (95% CI 0.847–0.912) for q. The inter-operator repeatability was 0.991 (95% CI 0.976–0.996) and 0.997 (95% CI 0.996–0.999) for m and q respectively.
For 6 X 6 mm scans, the inter-scan repeatability had an ICC of 0.831 (95% CI 0.801–0.856) for m and 0.814 (95% CI 0.784–0.865) for q. The inter-operator repeatability was 0.990 (95% CI 0.975–0.996) and 0.999 (95% CI 0.996–0.999) for m and q respectively.
Discussion
In this study, we developed a strategy to analyze the topographical distribution of flow deficits in OCTA en face images of the choriocapillaris in a continuous fashion throughout the macula. Our analysis approach uses a series of thin concentric rings spreading from the fovea towards the periphery with a width between 1 pixel and 28 pixels. By plotting the FD% calculated in each ring versus the distance from the fovea we obtained a detailed profile of the topographic distribution of the flow deficits in the CC. This curve resembles a sinusoid with irregular peaks and cycles. The shape of the curve is not surprising when one considers the structure of the CC, which is a dense net of capillaries. Of course, while a regular mesh would generate a more “regular” curve (Fig 4, box A), the relatively irregular CC mesh, together with the limitations of the methodologies used (e.g. resolution, magnification), yield a more irregular curve for the OCTA image (Fig 4, box C).
OCTA has already been shown to generate images which are consistent with histology [10–12] and our method seems to support this contention mathematically. Obtaining a continuous function of the topographical distribution of the flow deficits in the en-face angiograms allowed us to verify the association between the FD% and the distance from the fovea. This association is statistically significant and should be taken into consideration when two different regions of the CC are compared. In a population of subjects between 21 and 80 years, increasing the distance from the fovea leads to a physiological decrease of FD% which, according to our results, can be estimated to be approximately 0.8% for every 500 μm in the 3 x 3 mm and 0.25% for every 500 μm in the 6 x 6 mm.
Furthermore, we demonstrated that this increase is age-dependent: in older subjects, the impact of the distance from the fovea on FD% is greater, with a decrease of 1.4% and 0.8% for every 500 μm from the foveal center, in the 3 x 3 mm and 6 x 6 mm, respectively, for subjects between 61 and 80 years of age. These results, together with the analysis of the intercepts and slopes of the trendlines for the subjects, confirms that older individuals tend to have more flow deficits, and this age-dependent difference is greatest closer to the foveal center (Fig 5). It is important to note that this behavior was noted in both the 3x3mm and 6x6mm scan patterns, despite differences in resolution between the scan patterns.
It has already been demonstrated that the increasing age leads to a generalized reduction in the vessel density in all retinal vascular layers. The physiologic mechanism for this is not known, in particular for why this effect appears more pronounced centrally. Ramrattan et al. demonstrated in histologic samples that CC density decreases with age together with a significant increase in Bruch’s membrane (BM) thickness [21]. Whether these changes are uniform within the macula, however, was not specified and, to the best of our knowledge, never been investigated. An inhomogeneous thickening of BM, if more prominent under the fovea, could lead to an increased signal drop off on OCTA at the level of the CC, hence to an overestimation of the flow deficits in this zone.
Alternatively, it is possible that the CC under the fovea could be subjected to more stress to “recycle” the metabolites produced by the overlying RPE and photoreceptors, whose number/density is higher in this area. The foveal RPE cells are more tightly packed being smaller in diameter and taller compared to surrounding regions. This higher level of stress may be toxic for the CC leading to a faster impairment of the flow under the fovea with ageing. It is possible that after a “critical point”, the CC impairment under the fovea could lead to progressive pathological alterations at the level of the RPE (e.g. due to hypoxia and accumulation of metabolic debris) which may explaining the preference of some pathologies (e.g. age-related macular degeneration) to feature more pathology (e.g. regular drusen, macular neovascularization, or atrophy) near the center. If this hypothesis could be validated in future studies, it is possible that the monitoring of CC flow as an individual ages could prove to be useful tool to identify patients at risk for reaching this “critical tipping point”. Regardless, these regional differences in the CC that are accentuated by age must be taken into account in any studies comparing potential CC abnormalities in different parts of the macula. To address these regional differences, in a recent study evaluating CC flow deficits surround geographic atrophy lesions,[16] we compared regions at equal distances from the foveal center.
Our study is not without limitations, including a relatively small sample size. However, our study also has several strengths including its prospective design, the use of SS-OCTA, the use of two graders and repeat scan acquisitions to evaluate repeatability, and the use of two separate scan patterns (3x3 mm and 6x6 mm) which are the ones most commonly used in present CC studies in the literature. Considering the two angiograms had the same dimension (1024x1024 pixels), each ring of the grid covered a wider area when applied to the 6x6 mm scans compared to the 3x3 mm ones. This could potentially lead to a lower sensitivity in detecting small difference in flow deficits across the grid when using the wider pattern. However, the overall distribution of the flow deficits and their trend with respect to distance from the fovea, which are the main parameters of relevance in this study, were not significantly impacted by this. In summary, our study demonstrates that the distribution of flow deficits in the CC angiograms is regionally dependent and that aging seems to contribute to an increase of flow deficits, particularly as one approaches the fovea. These findings should be taken into account when assessing the CC in the setting of disease, particularly when studies are evaluating different macular regions or including subjects of varying ages.
Data Availability
All relevant data are within the manuscript and its Supporting Information files.
Funding Statement
The authors received no specific funding for this work.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
All relevant data are within the manuscript and its Supporting Information files.