Journal of Diabetes Research
Volume 2019 (2019), Article ID 9548324, 12 pages
https://doi.org/10.1155/2019/9548324

Research Article

Adaptive Optics (rtx1) High-Resolution Imaging of Photoreceptors and Retinal Arteries in Patients with Diabetic Retinopathy

Anna Zaleska-Żmijewska,1,2 Zbigniew M. Wawrzyniak,³ Anna Dąbrowska,² and Jacek P. Szaflik1,2

¹Medical University of Warsaw, Department of Ophthalmology, Warsaw, Poland
²SPKSO Ophthalmic Teaching Hospital, Warsaw, Poland
³Warsaw University of Technology, Faculty of Electronics and Information Technology, Warsaw, Poland

Correspondence should be addressed to Anna Zaleska-Żmijewska; aniazaleska-zmijewska@wp.pl

Received 24 October 2018; Revised 5 January 2019; Accepted 30 January 2019; Published 17 March 2019

Academic Editor: Steven F. Abcouwer

Copyright © 2019 Anna Zaleska-Żmijewska et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Background. Diabetic retinopathy (DR) is the leading cause of impaired vision in patients with diabetes mellitus. An adaptive optics retinal camera (rtx1™; Imagine Eyes, France) was used to capture images of cones and retinal arteries from patients with DR. Objective. Cone parameters (density, interphotoreceptor distance, and regularity) and retinal artery parameters (wall thickness, lumen diameter, WLR, and WCSA) were analyzed in 36 patients with nonproliferative DR (NPDR; 22 with mild NPDR and 14 with moderate NPDR) and in 20 healthy volunteers (the control group). Results. Cone density at 2° eccentricities was significantly lower in the DR compared to the control group (/mm² vs. cells/mm², respectively). Cone density and regularity decreased with increasing severity of DR. The artery walls were significantly thicker in the DR group. The WLR and WCSA differed significantly between the DR and the control groups (WLR vs. ; WCSA vs. , respectively). Conclusions. Decreased cone regularity and density are seen in patients with mild and moderate NPDR. Abnormalities of retinal arterioles show signs of arteriolar dysfunction in DR. Retinal image analysis with the rtx1 offers a novel noninvasive measurement of early changes in the neural cells and retina vasculature in diabetic eyes.

1. Introduction

Diabetes is a chronic disease that causes complications in different organs, including the eye. Diabetic retinopathy (DR) is the leading cause of impaired vision worldwide [1]. It is estimated that the diabetes epidemic will result in a growing number of diabetic patients worldwide, increasing from 366 million in 2011 to 552 million in 2030 [2]. The prevalence of DR is therefore expected to be a serious problem in the near future. The development and progression of DR are closely associated with the type and duration of diabetes, glucose levels, and blood pressure [1]. DR typically develops over several years and may remain asymptomatic until vision-related complications occur; it can be classified into five stages, from no apparent retinopathy to proliferative retinopathy. The disease severity scale is based on the findings of the Wisconsin Epidemiologic Study of Diabetic Retinopathy (WESDR) and the Early Treatment Diabetic Retinopathy Study (ETDRS), which allowed experts to create the International Clinical Disease Severity Scale for DR [3].

The classic early hallmark of DR is microcirculatory impairment [4, 5]. Clinical diagnosis of DR traditionally relies on the detection of microangiopathy using ophthalmoscopy, conventional fundus photography, and intravenous fluorescein angiography. Histologic studies have shown that pericyte loss and basement membrane thickening consequent to prolonged hyperglycemia characterize the onset of DR. These early changes are not visible with classic clinical imaging modalities, however, and are thus considered subclinical.

Evidence suggests that neural dysfunction in diabetes may accompany or occur before the appearance of microvascular lesions [6]. Microvascular abnormalities seen in the early-to-moderate stages of DR include loss of pericytes, basement membrane thickening, arteriole wall thickening, and formation of microaneurysms [7]. Neural degenerative changes in the retina that are associated with diabetes involve apoptosis of several populations of retinal cells, including retinal ganglion cells, which are especially sensitive to hypoxia, as well as photoreceptors and bipolar cells [5]. Neurodegenerative changes in several retinal neural cells may participate in the occurrence of the earliest morphological alternations of the vascular elements (the neurodegenerative theory of DR) [5, 8]. Defects in the retinal glial cells as a result of hyperglycemia contribute to early changes in the photoreceptors and retinal microvasculature because support for neuronal and vascular homeostasis deteriorates [9]. Consequently, DR is a disease of both retinal neurons and microcirculation. Changes in the photoreceptor layer may be found in diabetic patients before the first clinical signs of retinopathy, but it is impossible to study such changes without special imaging techniques. Advances in retinal imaging devices and development of more sophisticated optical systems can allow the capture of en face images of photoreceptors. Innovative optical technologies permit early detection of tissue changes. The adaptive optics (AO) scanning laser ophthalmoscope (AOSLO) is one noninvasive method to visualize microcirculation and retinal structures. The AO technology has been used in several studies on patients with diabetes [10–18]. Lammer et al. used high-resolution AOSLO imaging to identify changes in the human retinal cone mosaic in individuals with diabetes and across a wide range of DR severity [18]. The absolute cone density did not change significantly in diabetic eyes in this cohort, but there was increasing irregularity of cone spacing in diabetes as well as with increasing severity of DR [18].

The rtx1™ (Imagine Eyes, Orsay, France) is a microscope that uses AO technology. It permits visualization of single retinal cells (photoreceptors) and the smallest blood vessels. The image resolution achieved by this technology is comparable to a histological resolution. The AO imaging system corrects aberrations that arise from various refractive surfaces within the eye. The rtx1 camera uses infrared illumination (wavelength of 850 nm) and has a lateral resolution of 1.6 microns at 850 nm. The field of view is , which corresponds to an approximately  mm square on the retinal surface, based on the axial length of the eye. The total image acquisition time is 4 s, during which 40 individual images can be acquired. The rtx1 microscope includes image acquisition and object recognition software for image analysis: AOdetect (for analysis of photoreceptors) and AOdetectArtery (for analysis of the retinal vasculature). The device allows the selection of any area of the retina for imaging, and measurements in the same spot can be repeated based on automatically saved coordinates [13, 16].

Several studies have demonstrated the use of the rtx1 in patients with diabetes [13, 17, 19–23]. Lombardo et al. showed with AO imaging lower cone density and abnormalities in the spatial arrangement of the parafoveal cones in DM1 patients, even when no signs of diabetic retinopathy were seen on fundoscopy [21]. The cone density decline was moderately associated with a disturbance in the glucose metabolism in diabetic patients [23]. Soliman et al. also found significantly lower cone density in patients with DR [20]. Results of AO imaging may predict anatomic or additional functional retinal outcomes in patients with diabetes.

Previous studies provided important insights into the status of photoreceptors in the eyes with DR; they did not study the status of the retinal circulation in relationship to photoreceptors. To our knowledge, there are no studies analyzing cones and retinal arteries together in the course of diabetes with the AO device and comparing these with blood test results. This study investigates the ability of an AO system to detect microvascular changes together with photoreceptor density and regularity deterioration in a cohort of diabetic subjects with mild to moderate nonproliferative DR (NPDR).

2. Methods

Retinal examinations with the rtx1 device were conducted between May and July 2018 at the Department of Ophthalmology, Second Faculty of Medicine, Medical University of Warsaw, located in the Ophthalmic University Hospital in Warsaw. The study protocol was approved by the Bioethical Commission of the Medical University of Warsaw. Each patient received both written and oral information explaining the objective and design of the study, the operating principles of the device, and the examination procedure. In accordance with the Declaration of Helsinki, written informed consent was obtained from all subjects who participated in the study.

2.1. Eligibility Criteria

The study group consisted of adult (>18 years, white European) patients recruited from Retina and Laser Services of the Ophthalmic University Hospital in Warsaw with confirmed diabetes mellitus (DM) according to the criteria of the American Diabetes Association [24] and age-matched normoglycemic healthy volunteers. Participants were divided into 2 groups: control (healthy subjects) and diabetic retinopathy (DR) study group. The control group included only healthy participants with the same exclusion criteria as the study group and a body mass index (BMI) lower than 25 kg/m². The study group consisted of patients with diagnosed DR and was subdivided into mild nonproliferative diabetic retinopathy (mild NPDR) and moderate nonproliferative diabetic retinopathy (moderate NPDR) subgroups according to the International Clinical Disease Severity Scale for DR [3].

All patients provided a medical history and current blood samples to verify inclusion and exclusion criteria. The blood tests were collected two days before the retinal imaging.

The inclusion criteria for the study group were

(i)diagnosis of nonproliferative diabetic retinopathy in the course of diabetes mellitus(ii)best-corrected visual acuity equal or better than 0.4 on Snellen chart(iii)central fixation

The inclusion criteria for the control group were

(i)glycemia and blood pressure within normal limits(ii)no treatment for diabetes mellitus, hypertension, and coronary heart disease(iii)no prescription medications including oral contraception(iv)body mass index (BMI) less than 25 kg/m²(v)best-corrected visual acuity equal or better than 0.4 on Snellen chart(vi)central fixation

The ophthalmic exclusion criteria for both groups were

(i)best-corrected visual acuity less than 0.4 on Snellen chart(ii)refractive errors for diopter or diopter cylindrical(iii)the presence or a history of glaucoma(iv)the presence of media opacities(v)a scar, subretinal fluid, or edema in the fovea(vi)and no central fixation

Eligibility for study participation was confirmed by comprehensive ocular examination.

2.2. Patient Characteristics

An initial group of 74 patients with DR who had been seen at the laser service at the Ophthalmic Hospital from January to May 2018 was selected. Of these, 42 patients with visual acuity better or equal to 0.4 on the Snellen chart and with a diagnosis of diabetic retinopathy were invited to participate in this study. A total of 36 patients were recruited to the study group (DR group) and met the inclusion criteria. The DR group included 14 women (39%) and 22 men (61%). The mild NPDR subgroup consisted of 22 patients (61%), and moderate NPDR was diagnosed in 14 patients. Most of the patients from the study group were treated with laser photocoagulations and were under control at least 2 times a year at the offices of an ophthalmologist or diabetologist. From the study group, 12 patients had had a diagnosis of diabetes for 5 to 10 years, and 24 patients had a history of the disease for more than 10 years. Most of the diabetic patients were treated with insulin injections (32 individuals; 89%) and only 4 patients received oral treatment. Patients were asked to fill out a questionnaire about their symptoms when DM was diagnosed, their lifestyle, and coexisting diseases. Information on participants’ sociodemographic characteristics, lifestyle risk factors, and medical history of diabetes and cardiovascular disease was obtained in a questionnaire (Table 1). Hypertension was defined as systolic blood  mmHg, diastolic blood  mmHg, or self-reported physician diagnosis of hypertension or current use of antihypertensive medications. Duration of diabetes was estimated by subtracting the year of diagnosis from the date of attendance at the research clinic. Smoking status was categorized as current, former, or never. BMI was calculated as weight in kilograms divided by the square of height in meters.

Table 1: Results of the questionnaire in the DR group () and the control group ().

No. of subjects/DR group (%)
No. of subjects/control group (%)

History of the and <10 years
12 (33)
0

History of the years
24 (67)
0

Elementary education
14 (39)
0

Secondary education
16 (44)
6 (30)

University education
6 (17)
14 (70)

Current cigarette smokers
11 (31)
2 (10)

Active lifestyle/sports
13 (36)
12 (60)

Diagnosis of DM after incidental blood test for glucose level
14 (39)
0

Diagnosis of DM after worrying symptoms
22 (61)
0

Family history of DM
21 (58)
4 (20)

Hypertension
33 (92)
0

Hypertension and coronary heart disease
4 (11)
0

Hypertension and neuropathy
8 (22)
0

Hypertension and nephropathy
2 (6)
0

Abbreviations: DR: diabetic retinopathy; DM: diabetes mellitus.

The control group consisted of 20 healthy volunteers, 13 women (65%) and 7 men (35%). Most of the participants in the control group were recruited from the hospital staff (nurses, doctors) and 4 were family members of the participants from the study group. Age and axial length were not significantly different between groups. The mean (±standard deviation) age in the control group and the DR group was 46.0 (±10.0) and 49.0 (±8.0), respectively (). The mean axial length of the right eye (OD-oculi dextri) in the control group was  mm and that of the left eye (OS-oculi sinistri) was  mm (Mann–Whitney test, ). The mean axial length of the OD in the DR group was  mm and that of the OS was  mm (-test, ). Because the eyes did not differ in terms of axial length, only the results obtained from the right eyes were included in further analyses. There were no significant differences between the eyes in both groups (-test for OD and for OS ). The characteristics of both groups are shown in Table 2.

Table 2: Overall and group characteristics ().

Total
Mild NPDR
Moderate NPDR
DR group
Control group

(%)
(%)
(%)
(%)
(%)

No. of subjects
56 (100)
22 (39)
14 (25)
36 (64)
20 (36)

Women
27 (48.2)
8 (36)
6 (43)
14 (39)
13 (65)

value

Age (years)

0.187†

AL (mm)

0.974†

BMI

<0.001‡

†-test; ‡Mann–Whitney test. Abbreviations: DR: diabetic retinopathy; SD: standard deviation; AL: mean axial length; BMI: body mass index.

2.3. Medical History of the DR Group and the Control Group

Recent results of blood parameters were analyzed, including fasting plasma glucose (FPG), glycated hemoglobin A1c (HbA1c), triglyceride (TG), total cholesterol, low-density lipoprotein cholesterol (LDL), high-density lipoprotein cholesterol (HDL), BMI, and the correlation between the chosen parameters and cone density and retinal artery parameters.

2.4. Image Acquisition with the rtx1™ Adaptive Optics (AO) Camera

An AO retinal camera (rtx1™; Imagine Eyes, Orsay, France) was used to acquire images of the parafoveal cones and retinal arterioles in patients from both groups. The imaging device has 3 main components: a high-resolution fundus camera, a Shack-Hartmann wavefront sensor, and a deformable mirror for real-time correction of the aberrations of the ocular wavefront. The rtx1™ uses en face reflectance imaging with flashed, noncoherent near-infrared illumination [13].

All subjects also had noncontact ocular biometry using the IOL Master (Carl Zeiss Meditec AG, Hennigsdorf, Germany).

2.5. rtx1 Examination Protocol and Parameter Evaluation

Each rtx1 examination captured scans of the 4 perifoveal areas of the retina, 2° (approximately 540–600 μm) off the center of the fovea (temporally, nasally, superiorly, and inferiorly) with a standardized  μm sampling window size (fixed by the manufacturer in the new model). Most of the examinations did not require dilation of the pupils. In cases in which the width of the pupil was less than 4 mm, one drop of 1% tropicamide was administered. None of the participants from the control group required pupil dilation. Seven (19.5%) patients with NPDR had the image acquisition after 1% tropicamide drop. Study participants were instructed to fixate on the yellow fixation cross in the camera. After finding the foveal reference point of the patient, eccentricities of 2° along the meridians were measured and used for further image analyses. In most of the cases, the acquisition of the best image of cones required at least 3 scans. In retinal artery imaging, one scan was enough. It took approximately only 2-5 seconds to reach a single scan.

The best sections of images captured were selected and analyzed using the image processing and recognition software AOdetect (for analysis of photoreceptors) and AOdetectArtery (for analysis of the retinal vasculature). The analyses of the photoreceptors included the mean (±standard deviation) cone density per square millimeter of the retinal surface and the morphology of the cones in terms of neighborhood (Voronoi domain), regularity, and cone spacing. The arithmetic average of 3 measurements of the selected cone images was taken for statistical analysis.

In the analyses of the retinal vessels, 3 measurements of the retinal arteriole with a size between 70 and 130 μm in the temporal superior quadrant were taken. The arithmetic average of these 3 values was taken. Measurements of the total vessel diameter (VD), the thickness of the two walls (wall 1, wall 2), and the lumen diameter (LD) were recorded, and the wall-to-lumen ratio (WLR) and the cross-sectional area of the vascular wall (WCSA) were then automatically calculated. VD resulted from a single arteriolar wall (WT) plus vessel lumen (LD) and single arteriolar wall thickness (WT): . WLR was calculated as . WCSA of the vascular wall was measured on the basis of VD and LD, and the value was obtained automatically from the AO artery detect software.

The area of the analyzed retina was chosen to avoid retinal vessels, hemorrhages, and laser scars during cone analysis and to avoid artery-venous crossing or close proximity of artery and vein during retinal artery analysis. We used automated cone and vessel parameter identification, in some cases with manual review of the artery profile.

2.6. Statistical Analyses

Descriptive analyses were conducted for all variables that were visually assessed for outliers. Three measurements of cone density in the four regions of interest (lower, upper, nasal, and temporal quadrants) were collected from each individual. The measurements were collected from the right eyes in a subset of the subjects. Kolmogorov–Smirnov and Shapiro–Wilk tests were used to determine if the parameters were normally distributed. Because the parameters were not normally distributed, we used the Mann–Whitney test to compare the DR and control groups.

The Pearson correlation coefficient () was calculated to examine the linear relationship between 2 continuous variables. Statistical analyses were generated with Dell™ Statistica™ 13.1 (data analysis software system), version 12 (http://www.tibco.com).

3. Results

The best-corrected visual acuity (BCVA) was 1.0 in the control group, and the mean BCVA was among patients with diabetes. Most of the patients from the DR group had a BCVA better than 0.4 (29; 81%). 19% of the participants with DR had BCVA equal to 0.4.

The results of the blood test revealed significant differences between groups in the levels of white blood cells (WBC), total cholesterol, LDL cholesterol, FPG, and HbA1c. The results of the blood parameters for both groups are presented in Table 3.

Table 3: The results of the blood parameters in both groups (): DR group (mild NPDR, ; moderate NPDR, ) and control group ().

Blood parameters
†

†
value†
Control vs. DR
value for NPDR

Control
Mild NPDR
Moderate NPDR
DR

WBC (k)

0.008
0.823‡

RBC (M)

0.838
0.068†

HGB (g/dl)

0.342
0.025†

HCT (%)

0.619
0.017†

PLT (k)

0.054
0.441†

FPG (mg/dl)

<0.001
0.314†

HBA1C (%)

<0.001
0.520†

Total cholesterol (mg/dl)

0.030
0.283†

HDL (mg/dl)

0.155
0.503†

LDL (mg/dl)

0.010
0.253†

TG (mg/dl)

0.163
0.891‡

†-test; ‡Mann–Whitney test. Abbreviations: SD: standard deviation; DR: diabetic retinopathy; NPDR: nonproliferative diabetic retinopathy; FPG: fasting plasma glucose; HbA1c: glycated hemoglobin A1c; TG: triglyceride; LDL: low-density lipoprotein cholesterol; HDL: high-density lipoprotein cholesterol; WBC: white blood cells; RBC: red blood cells; HGB: hemoglobin; HCT: hematocrit; PLT: platelets.

3.1. Cone Parameters

Figure 1 shows an image of the parafoveal cone mosaic and Voronoi distribution at the 600 μm eccentricity (equal to 2°) taken from a healthy patient (upper) and from a patient with mild NPDR (lower).

Figure 1: Image of the retina cones captured with the rtx1 adaptive optics retinal camera degree square, visualization of cone mosaic, in a healthy patient from the control group (a1, a2) and a patient from the DR group (mild NPDR) (b1, b2).

Figure 2 shows irregular cone morphology taken from an eye with mild NPDR from the DR group.

Figure 2: Image of the retinal cones mosaic with inset of window with Voronoi representation in four quadrants captured with the rtx1 adaptive optics retinal camera, visualization of irregular cone morphology; a patient from the DR group, mild NPDR at 2° eccentricities.

The cone density was significantly lower in the DR group of patients compared to the control group at the 2° retinal eccentricities in all 4 analyzed locations. The results of cone density for all quadrants are presented in Table 4. The average (±SD) cone density, the mean of the cone density values in the 4 quadrants, in the control and DR groups were cells/mm² and cells/mm², respectively (; Table 4). The cone density decreased as the severity of DR increased ( cells/mm² in mild NPDR, cells/mm² in moderate NPDR; 0.26). We also observed a higher standard deviation in the DR group compared to the control group (Table 4).

Table 4: The mean cone density in 4 retinal quadrants at 2° eccentricities in both groups () and the DR group (mild NPDR, ; moderate NPDR, ).

Quadrants
Mean (±SD) cone density, cone/mm²
DR groupa
Mean (±SD) cone density, cone/mm²
Control groupb
value

T

<0.001†

N

<0.001†

S

<0.001†

I

<0.001†

4 quadrants

<0.001†

Mild NPDR group
Moderate NPDR group

4 quadrants

0.260†

†-test; ‡Friedman ANOVA test; a value ‡for all quadrants (in column) ; b value ‡for all quadrants (in column) .  = value for all quadrants for whole group (in columns) . Abbreviations: SD: standard deviation; DR: diabetic retinopathy; NPDR: nonproliferative diabetic retinopathy; T: temporal; N: nasal; S: superior; I: inferior.

The interphotoreceptor spacing was significantly higher in all locations in the DR group compared to controls (Table 5).

Table 5: The mean (±SD) spacing, Voronoi, and cone regularity in the control group and the DR group (divided into 2 subgroups: mild NPDR and moderate NPDR) in 4 quadrants.

Cone parameters in quadrants
The DR group
The control group
value†

Spacing_ T (mm)

<0.001‡

Spacing_ N (mm)

<0.001‡

Spacing_ S (mm)

<0.001‡

Spacing_ I (mm)

<0.001‡

Spacing_4Q (mm)
a
b
<0.001‡

Voronoi N%6_T (%)

<0.001†

Voronoi N%6_N (%)

0.011†

Voronoi N%6_S (%)

0.008†

Voronoi N%6_I (%)

0.066†

Voronoi %6_4Q (%)
c
d
<0.001†

Regularity_T (%)

0.007†

Regularity_N (%)

0.005‡

Regularity_S (%)

0.003†

Regularity_I (%)

0.073‡

Regularity_4Q (%)
e
f
<0.001‡

For the DR subgroups
Mild NPDR group
Moderate NPDR group

Spacing_4Q (mm)

0.214‡

Voronoi %6_4Q (%)

0.505†

Regularity_4Q (%)

0.417‡

†-test; ‡Mann–Whitney test; §Friedman ANOVA test; a value §for all quadrants (in column) ; b value §for all quadrants (in column) . c value §for all quadrants (in column) ; d value §for all quadrants (in column) . c value §for all quadrants (in column) ; d value §for all quadrants (in column) . Abbreviations: SD: standard deviation; T: temporal; N: nasal; S: superior; I: inferior; 4Q: for all quadrants (T, N, S, I); regularity: the summary of the percentage of pentagonal, hexagonal, and heptagonal cones in analyzed image; Voronoi_%6 tiles: percentage of hexagonal cones in analyzed image; spacing: interphotoreceptor distance.

Cone packing regularity was assessed through the analysis of Voronoi domains. The mean percentage (±SD) of cones with hexagonal Voronoi tiles (N%6) in the control and DR groups was and , respectively (; Table 5). Significant differences in cone regularity, which means the summary of the percentage of pentagonal (N%5), hexagonal (N%6), and heptagonal (N%7) cones, were found in the temporal, nasal, and superior quadrants (; Table 5). In the inferior quadrant, the regularity was also lower in the DR group (Table 5).

The mean percentage of hexagonal cones was significantly lower in both DR subgroups, but there were no significant differences between the mild NPDR () and the moderate NPDR subgroups () (; Table 5). There were also no significant differences in the other analyzed parameters of cone morphology (spacing and regularity) between the mild NPDR and moderate NPDR subgroups (Table 5).

Most of the patients with diabetes were overweight, described as and <29.9, or obese, with . There were no significant differences in all analyzed cone and vessel parameters depending on BMI values (Table 6). We observed decreasing cone density and increasing cone spacing with higher BMI values (Table 6).

Table 6: Characteristics of cone parameters in the DR group depending on BMI ().

Parameter
Mean ()
Mean ()
Mean ()
value KW

Cone density (1/mm²)
20250
17132
18788
0.172

Spacing (μm)
7.7
8.6
8.1
0.204

KW: ANOVA rank Kruskal–Wallis test. Abbreviations: spacing: interphotoreceptor distance; BMI: body mass index.

3.2. Retinal Artery Parameters

A representative image from the retinal artery analysis is shown in Figure 3 (a1, a2). An example of microvascular changes in a diabetic patient is shown in Figure 3 (b1, b2), with increased WLR and thickening of arteriole walls.

Figure 3: Image of the retinal artery of a patient (WLR 0.250) from the control group (a1, a2) and from the DR group with diabetes and hypertension (WLR 0.360) (b1, b2) captured with the rtx1 adaptive optics retinal camera obtained automatically, with wall and lumen visualization using AOdetectArtery.

The mean lumen and total diameter of the analyzed retinal artery were not significantly different between both groups (). The mean of both artery walls (wall1, wall 2) was significantly thicker in the DR group than in controls (). The mean WLR and WCSA values also differed significantly between the DR group and the control group (for WLR vs. , ; for WCSA vs. , respectively, ; Table 7).

Table 7: Characteristics of retinal artery parameters in the DR group depending on BMI ().

Parameter
m ()
m ()
m ()
value KW

Lumen (μm)
96.5
97.0
101.8
0.725

Total diameter (μm)
123.8
128.2
136.6
0.323

Wall 1 (μm)
13.4
15.0
15.3
0.855

Wall 2 (μm)
13.9
16.2
19.6
0.059

WCSA (μm²)
4715
5527
6529
0.189

WLR (1)
0.285
0.332
0.343
0.554

KW-ANOVA rank Kruskal–Wallis test.

The lumen of the artery decreased and WLR and WCSA increased with increasing severity of DR, but there were no significant differences in all analyzed vessel parameters between the mild and moderate NPDR subgroups (Table 8).

Table 8: Characteristics of retinal artery parameters in the DR (mild NPDR, ; moderate NPDR, ) and control groups ( and ).

Parameters
Mean (±SD)
Mean† (±SD)
Mean† (±SD)
Mean (±SD)
value
Control vs. DR
value† NPDR

Control group
Mild NPDR group
Moderate NPDR
DR group

Lumen (μm)

0.580†
0.685

Total diameter (μm)

0.113†
0.658

WALL_1 (μm)

<0.001†
0.834

WALL_2 (μm)

<0.001‡
0.295

WLR (1)

<0.001†
0.245

WCSA (μm²)

<0.001‡
0.796

†-test; ‡Mann–Whitney test. Abbreviations: SD: standard deviation; WLR: wall-to-lumen ratio; WCSA: wall cross-sectional area.

As with the cone analysis relative to BMI values for the DR group, the analysis of retinal artery parameters revealed no significant differences in all analyzed vessel parameters based on BMI, but increasing values of all artery parameters with greater values of BMI (Table 7).

3.3. Correlation between Cone and Artery Parameters and Blood Parameters in the DR Group

We observed a tendency for lower values of red blood cells, hemoglobin, and hematocrit in the DR group, and the values of the two last parameters differed significantly between the two subgroups mild and moderate NPDR (Table 3).

No correlations were found between cone and artery parameters and any of the blood parameters (). There were also no correlations between cone and artery parameters and the results of the questionnaire (duration of diabetes diagnosis, cigarettes smoking, physical activity, and education level).

4. Discussion

In this study, we analyzed retinal photoreceptor (cone) morphology and retinal microvasculature with the new rtx1 device in a selected group of patients with DR and age-matched healthy volunteers; the rtx1 is a microscope with AO technology, which provides detailed visualization of retinal microstructures that, until recently, was only feasible in histological studies [13]. Limitations in the currently available imaging instruments focused the investigation on the microvascular changes caused by diabetes. The in vivo evaluation of the structure of neuronal retinal cells was not previously possible, but AO now offers a noninvasive method. We chose patients with diagnosed DR and good visual acuity, better than or equal to 0.400 on the Snellen chart. Most of the studied images were taken from patients with previous or current laser treatment, so we expected some difficulties in image acquisition. The areas of the retina selected for analysis were outside of the areas of retinal edema and laser scars. We selected the best image from several taken and made 3 measurements of cone mosaics and retinal arteries and the average value was analyzed.

Our results indicate that individuals with DR demonstrate decreased parafoveal cone density and signs of dysfunction in the retinal arterioles. Other authors presented similar results for patients with diabetes [13, 17, 20, 21, 23]. Lombardo et al. showed 6% lower cone density and differences in the percentage of hexagonal cones even in diabetic eyes without DR [21]. Soliman and coworkers also included patients with different stages of DR and found significantly lower cone density compared to the control group [20]. In our study, cone density at about 600 μm off the fovea was in the control group, while in diabetic patients it was . The cone density, described by Soliman et al., at the same location as ours, was comparable to our results in both the control and diabetic groups ( vs. ) [20]. We compared cone parameters across the 4 meridians and observed no significant differences. These results are similar to measures by other authors [20, 25].

The decline in cone density was observed in mild NPDR and moderate NPDR subgroups, but the differences were not significant. These results are also similar to those obtained by Soliman et al. [20]. Lammer and coworkers did not find any differences in cone density and spacing between healthy and diabetic patients [18]. They also did not notice any significant association between severity of DR and cone density and morphology [18]. Their study used adaptive optics scanning laser ophthalmoscopy (AOSLO), which may be the cause of some of the differences when comparing their results to the rtx1 analyses, while the AO technology in AOSLO is similar; the imaging modality is quite different. AOSLO rejects the scattered light greatly improving image contrast and providing more accurate cone counting. They also used a 6 mm pupil which will improve lateral resolution.

Although the absolute cone density did not change in diabetic eyes in this study, the authors observed increasing irregularity of cone spacing in the study group [18].

In our study, the interphotoreceptor distance increased significantly in the DR group compared to the control group. We also found decreasing hexagonal mosaics of cones (Voronoi 6 tiles) with increased severity of DR. The increased spacing and decreased regularity of cones in the DR group may be a result of shadowing artefacts from intraretinal pathologies, such as edema of retinal cells anterior to the photoreceptors, presence of intraretinal cysts, hemorrhages, hard exudates, and extracellular fluid accumulation [13, 18, 23, 26]. All of these pathologies may affect the reliability of our assessment of the cone mosaic. Probably as a result of this situation, there was high standard deviation in the DR group for the cone parameters compared to the healthy eyes in our study. Analyzing the retina images, we found that cone spacing regularity was disturbed by dark patches, which was also described by other authors [13, 18]. The dark patches may be caused by cone pathology, leading to decreased cone reflectance [18]. The decreased regularity and rearrangement of the cone mosaic found in our patients with DR were also described by other authors [13, 18, 21, 26]. This may support the neurodegenerative theory of DR development, in which neural cells, such as cones, degenerate in the course of diabetes [5, 8, 21, 26, 27]. Retinal neurodegeneration is also supposed to participate in microvascular changes in diabetes [5, 8].

Recently published studies of prediabetic patients or patients with diabetes but without signs of DR showed no differences in cone density and mosaic, however [22, 28]. Our findings from a previous study indicated that cone density was not affected by impaired glucose tolerance [22].

Although pathologies occur in retinal neural cells during diabetes, the clinically observed intraretinal microvascular changes serve as a basis for the classification of DR from nonproliferative to proliferative stages. Photography taken from the eyes with severe DR shows a full spectrum of microvascular abnormalities [3, 4, 7]. Recently, advances in high-resolution imaging techniques, such as AO and optical coherence tomography angiography (OCTA), have expanded our ability to visualize the living human retinal vasculature noninvasively [11–14, 19, 22].

The mean lumen and total diameter of the analyzed retinal artery were not significantly different between the control and DR groups (). Both artery walls were significantly thicker in the DR group than in controls (). The mean WLR and WCSA values also differed significantly between the DR group and the control group. The lumen of the artery decreased and the WLR and WCSA increased with increasing severity of DR, but there were no significant differences in all analyzed vessel parameters between the mild and moderate NPDR subgroups. Arterial remodeling is best characterized by increased WLR, and an overall increase in WLR can result from wall thickening, narrowing of the lumen, or a combination of both. Our results are similar to those obtained by other authors, who also described narrowing of the arteriole lumen and thickening of the arteriole walls in diabetes even without signs of retinopathy [29–35]. The results of the AusDiab study also confirmed that wider arteriolar wall caliber is a specific and effective indicator of diabetic microvascular dysfunction independent of blood pressure, glycemic control, and other retinopathy risk factors and serves as a “prepathology” marker for DR [30]. In diabetes, the lumen of retinal arterioles is narrowed due to the growth of smooth muscle cells and vascular fibrosis, a consequence of which is seen as an increased wall-to-lumen ratio [32]. Burns et al., using nonconfocal AOSLO, demonstrated results similar to ours, showing microvascular remodeling with significantly larger arteriolar wall thickness in the diabetic group compared to the controls [36]. These results support our findings of an increased WLR ratio in diabetic patients due to changes in retinal artery walls. In contrast to our results, according to the Rotterdam Study and the Blue Mountain Eye Study, a decreased arteriovenous ratio was found to depend on venular dilatation rather than arteriolar narrowing in patients with diabetes [37, 38]. The limitation of these findings is the coexistence of hypertension in the majority of diabetic patients, which may also have a strong impact on the arterial remodeling.

We analyzed the correlation of cone and retinal artery parameters with blood test results and no correlation was found. Soliman et al. presented similar results [20].

In our cohort, most of the diabetic patients were overweight, described as and <29.9, or obese, with . There were no significant differences in all analyzed cone and vessel parameters depending on BMI values. We observed decreased cone density and increased cone spacing with greater values of BMI. The analysis of the retinal artery revealed increasing thickness of the walls, WLR, and WCSA at greater BMI values. None of these results reached the level of significance, however. To the best of our knowledge, there are no papers analyzing both cones and arteries in terms of BMI values.

Analysis of the questionnaires did not yield any correlations with cone and artery parameters. Some authors found a relationship between decreases in cone density and the duration of the disease, but others did not find such correlations [18, 20, 21].

To our knowledge, there are no studies analyzing cones and retinal arteries together in the course of diabetes with the AO devices. In some publications, primary attention is paid to changes in photoreceptors during DR, as a result of the neurodegeneration theory of DR. Others suggest a primary role for microvascular changes in DR development. The results of our work and that of other authors confirm that both cone density and retinal arterioles show early pathological changes in patients with nonproliferative diabetic retinopathy [7, 10–13, 17–23, 33, 36].

4.1. Study Limitations

We have identified several possible limitations of this study and the presence of some sources of bias: the high variability of cone density seen in both groups (twice as high in the DR group) and the study size and inclusion criteria (patients with good visual acuity and diabetic retinopathy). Due to our inclusion criteria, we did not check the retinas of patients at more severe stages of DR, but we decided to limit the study group because of the difficulty in obtaining good quality AO images in the eyes with many retinal changes. We wanted to be sure that the results obtained from the rtx1 would be as reliable as possible. There was also an imbalanced sex distribution across the study groups. We decided to process the study in accordance with the results of the clinical study conducted by Park et al., which found no significant differences in cone density between sexes [25]. Another limitation of this study is the inclusion of the eyes previously treated for DR; the vasculature in such eyes may not reflect the natural course of the disease, in terms of both photoreceptor mosaic and microcirculation. Lastly, imbalanced sex distribution across the study groups, small size groups, and defective AO imaging the resolution of rtx1 camera, which was used in the present study, insufficient to assess the density of extremely tightly packed cones very close to the fovea, are possible sources of bias.

This study was designed as an exploratory study without an a priori sample size calculation, and finally, high effects in outcomes of interest were observed (Tables 4, 6, and 7). Prospective studies with well-powered sample sizes are now warranted to confirm our study results. In particular, the control group seemed to be relatively small because of restricted exclusion criteria; however, sufficient statistical power (>0.80 and the post hoc tested power for the conducted study was equal to.999) to detect the DR incidence effect is relatively high.

5. Conclusions

In conclusion, the AO retinal imaging accurately identified the cone mosaic and retinal microvasculature in patients with diabetic retinopathy. Decreases in regularity of retinal cone arrangement and densities are consistently associated with the presence of diabetic retinopathy and increasing severity of the disease. There is a trend towards lower cone density in mild to moderate nonproliferative diabetic retinopathy. Abnormalities of the retinal arterioles found in rtx1 examinations should be considered microvascular signs of arteriolar dysfunction. These changes may be a strong risk factor for cardiovascular changes, which are also more common in this group of patients.

Further analysis on a large cohort of patients would be helpful to understand the potential of AO-based imaging biomarkers in patients with different stages of diabetic retinopathy, as well as other vascular disorders.

Analyzing microvascular changes as well as photoreceptor abnormalities could become the key for improved clinical classification of diabetic patients, better understanding of the mechanisms of diabetic retinopathy, and better patient monitoring using this technology.

Data Availability

The AO-RTX-DR data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

References

D. Pascolini and S. P. Mariotti, “Global estimates of visual impairment: 2010,” British Journal of Ophthalmology, vol. 96, no. 5, pp. 614–618, 2012.

D. R. Whiting, L. Guariguata, C. Weil, and J. Shaw, “IDF diabetes atlas: global estimates of the prevalence of diabetes for 2011 and 2030,” Diabetes Research and Clinical Practice, vol. 94, no. 3, pp. 311–321, 2011.

C. P. Wilkinson, Ferris FL 3rd, R. E. Klein et al., “Proposed international clinical diabetic retinopathy and diabetic macular edema disease severity scales,” Ophthalmology, vol. 110, no. 9, pp. 1677–1682, 2003.

J. M. Tarr, K. Kaul, M. Chopra, E. M. Kohner, and R. Chibber, “Pathophysiology of diabetic retinopathy,” ISRN Ophthalmology, vol. 2013, Article ID 343560, 13 pages, 2013.

R. Simó, C. Hernández, and European Consortium for the Early Treatment of Diabetic Retinopathy (EUROCONDOR), “Neurodegeneration in the diabetic eye: new insights and therapeutic perspectives,” Trends in Endocrinology and Metabolism, vol. 25, no. 1, pp. 23–33, 2014.

D. A. Antonetti, A. J. Barber, S. K. Bronson et al., “Diabetic retinopathy: seeing beyond glucose-induced microvascular disease,” Diabetes, vol. 55, no. 9, pp. 2401–2411, 2006.

T. M. Curtis, T. A. Gardiner, and A. W. Stitt, “Microvascular lesions of diabetic retinopathy: clues towards understanding pathogenesis?” Eye, vol. 23, no. 7, pp. 1496–1508, 2009.

A. J. Barber, “A new view of diabetic retinopathy: a neurodegenerative disease of the eye,” Progress in Neuro-Psychopharmacology and Biological Psychiatry, vol. 27, no. 2, pp. 283–290, 2003.

D. G. Puro, “Diabetes-induced dysfunction of retinal Müller cells,” Transactions of the American Ophthalmological Society, vol. 100, pp. 339–352, 2002.

J. Tam, K. P. Dhamdhere, P. Tiruveedhula et al., “Disruption of the retinal parafoveal capillary network in type 2 diabetes before the onset of diabetic retinopathy,” Investigative Ophthalmology & Visual Science, vol. 52, no. 12, pp. 9257–9266, 2011.

T. Y. P. Chui, T. J. Gast, and S. A. Burns, “Imaging of vascular wall fine structure in the human retina using adaptive optics scanning laser ophthalmoscopy,” Investigative Ophthalmology & Visual Science, vol. 54, no. 10, p. 7115, 2013.

S. Arichika, A. Uji, T. Murakami et al., “Retinal hemorheologic characterization of early-stage diabetic retinopathy using adaptive optics scanning laser ophthalmoscopy,” Investigative Ophthalmology & Visual Science, vol. 55, no. 12, pp. 8513–8522, 2014.

M. Lombardo, S. Serrao, N. Devaney, M. Parravano, and G. Lombardo, “Adaptive optics technology for high-resolution retinal imaging,” Sensors, vol. 13, no. 1, pp. 334–366, 2013.

P. Godara, A. M. Dubis, A. Roorda, J. L. Duncan, and J. Carroll, “Adaptive optics retinal imaging: emerging clinical applications,” Optometry and Vision Science, vol. 87, no. 12, pp. 930–941, 2010.

Y. Kitaguchi, K. Bessho, T. Yamaguchi, N. Nakazawa, T. Mihashi, and T. Fujikado, “In vivo measurements of cone photoreceptor spacing in myopic eyes from images obtained by an adaptive optics fundus camera,” Japanese Journal of Ophthalmology, vol. 51, no. 6, pp. 456–461, 2007.

M. N. Muthiah, C. Gias, F. K. Chen et al., “Cone photoreceptor definition on adaptive optics retinal imaging,” British Journal of Ophthalmology, vol. 98, no. 8, pp. 1073–1079, 2014.

L. Mariotti, N. Devaney, G. Lombardo, and M. Lombardo, “Analysis of cone mosaic reflectance properties in healthy eyes and in eyes with nonproliferative diabetic retinopathy over time,” Investigative Ophthalmology & Visual Science, vol. 58, no. 10, pp. 4057–4067, 2017.

J. Lammer, S. G. Prager, M. C. Cheney et al., “Cone photoreceptor irregularity on adaptive optics scanning laser ophthalmoscopy correlates with severity of diabetic retinopathy and macular edema,” Investigative Ophthalmology & Visual Science, vol. 57, no. 15, pp. 6624–6632, 2016.

M. Lombardo, M. Parravano, S. Serrao, P. Ducoli, M. Stirpe, and G. Lombardo, “Analysis of retinal capillaries in patients with type 1 diabetes and nonproliferative diabetic retinopathy using adaptive optics imaging,” Retina, vol. 33, no. 8, pp. 1630–1639, 2013.

M. K. Soliman, M. A. Sadiq, A. Agarwal et al., “High-resolution imaging of parafoveal cones in different stages of diabetic retinopathy using adaptive optics fundus camera,” PLoS One, vol. 11, no. 4, article e0152788, 2016.

M. Lombardo, M. Parravano, S. Serrao, L. Ziccardi, D. Giannini, and G. Lombardo, “Investigation of adaptive optics imaging biomarkers for detecting pathological changes of the cone mosaic in patients with type 1 diabetes mellitus,” PLoS One, vol. 11, no. 3, article e0151380, 2016.

A. Zaleska-Żmijewska, P. Piątkiewicz, B. Śmigielska et al., “Retinal photoreceptors and microvascular changes in prediabetes measured with adaptive optics (rtx1™): a case-control study,” Journal of Diabetes Research, vol. 2017, Article ID 4174292, 9 pages, 2017.

M. Lombardo, M. Parravano, G. Lombardo et al., “Adaptive optics imaging of parafoveal cones in type 1 diabetes,” Retina, vol. 34, no. 3, pp. 546–557, 2014.

S. Genuth, K. G. Alberti, P. Bennett et al., “Follow-up report on the diagnosis of diabetes mellitus,” Diabetes Care, vol. 26, no. 11, pp. 3160–3167, 2003.

S. P. Park, J. K. Chung, V. Greenstein, S. H. Tsang, and S. Chang, “A study of factors affecting the human cone photoreceptor density measured by adaptive optics scanning laser ophthalmoscope,” Experimental Eye Research, vol. 108, pp. 1–9, 2013.

D. Scoles, B. P. Higgins, R. F. Cooper et al., “Microscopic inner retinal hyper-reflective phenotypes in retinal and neurologic disease,” Investigative Ophthalmology & Visual Science, vol. 55, no. 7, pp. 4015–4029, 2014.

E. L. Fletcher, J. A. Phipps, and J. L. Wilkinson-Berka, “Dysfunction of retinal neurons and glia during diabetes,” Clinical and Experimental Optometry, vol. 88, no. 3, pp. 132–145, 2005.

W. Tan, T. Wright, D. Rajendran et al., “Cone–photoreceptor density in adolescents with type 1 diabetes,” Investigative Ophthalmology & Visual Science, vol. 56, no. 11, p. 6339, 2015.

T. A. Gardiner, D. B. Archer, T. M. Curtis, and A. W. Stitt, “Arteriolar involvement in the microvascular lesions of diabetic retinopathy: implications for pathogenesis,” Microcirculation, vol. 14, no. 1, pp. 25–38, 2007.

S. L. Rogers, G. Tikellis, N. Cheung et al., “Retinal arteriolar caliber predicts incident retinopathy. The Australian Diabetes, Obesity and Lifestyle (AusDiab) study,” Diabetes Care, vol. 31, no. 4, pp. 761–763, 2008.

T. Y. Wong, R. Klein, A. R. Sharrett et al., “Retinal arteriolar narrowing and risk of diabetes mellitus in middle-aged persons,” Journal of the American Medical Association, vol. 287, no. 19, pp. 2528–2533, 2002.

A. C. Clermont and S. E. Bursell, “Retinal blood flow in diabetes,” Microcirculation, vol. 14, no. 1, pp. 49–61, 2007.

S. E. Bursell, A. C. Clermont, B. T. Kinsley, D. C. Simonson, L. M. Aiello, and H. A. Wolpert, “Retinal blood flow changes in patients with insulin-dependent diabetes mellitus and no diabetic retinopathy,” Investigative Ophthalmology & Visual Science, vol. 37, no. 5, pp. 886–897, 1996.

R. Klein et al., “The relations of retinal vessel caliber to the incidence and progression of diabetic retinopathy. XIX. The Wisconsin Epidemiologic Study of Diabetic Retinopathy,” Archives of Ophthalmology, vol. 122, no. 1, pp. 76–83, 2004.

G. T. Feke, S. M. Buzney, H. Ogasawara et al., “Retinal circulatory abnormalities in type 1 diabetes,” Investigative Ophthalmology & Visual Science, vol. 35, no. 7, pp. 2968–2975, 1994.

S. A. Burns, A. E. Elsner, T. Y. Chui et al., “In vivo adaptive optics microvascular imaging in diabetic patients without clinically severe diabetic retinopathy,” Biomedical Optics Express, vol. 5, no. 3, pp. 961–974, 2014.

M. K. Ikram, J. A. M. J. L. Janssen, A. M. E. Roos et al., “Retinal vessel diameters and risk of impaired fasting glucose or diabetes: the Rotterdam study,” Diabetes, vol. 55, no. 2, pp. 506–510, 2006.

A. Kifley, J. J. Wang, S. Cugati, T. Y. Wong, and P. Mitchell, “Retinal vascular caliber and the long-term risk of diabetes and impaired fasting glucose: the Blue Mountains Eye Study,” Microcirculation, vol. 15, no. 5, pp. 373–377, 2008.