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Peripheral capillary non-perfusion in treatment-naïve proliferative diabetic retinopathy associates with postoperative disease activity 6 months after panretinal photocoagulation
  1. Thomas Lee Torp1,2,
  2. Ryo Kawasaki3,
  3. Tien Yin Wong4,
  4. Tunde Peto2,5,
  5. Jakob Grauslund1,2
  1. 1 Department of Ophthalmology, Odense University Hospital, Odense, Denmark
  2. 2 Department of Clinical Research, University of Southern Denmark, Odense, Denmark
  3. 3 Department of Vision Informatics, Osaka University Graduate School of Medicine, Osaka, Japan
  4. 4 Singapore National Eye Centre, Duke-NUS Medical School, National University of Singapore, Singapore
  5. 5 School of Medicine, Dentistry and Biomedical Sciences, Queen’s University Belfast, Belfast, UK
  1. Correspondence to Dr Thomas Lee Torp, Department of Ophthalmology, Odense University Hospital, Odense 5000, Denmark; thomas.lee.torp{at}rsyd.dk

Footnotes

  • Contributors JG conceived the aims and overall design of the study. TLT acquired the data and did the writing of the different sections, tables and figures. JG and TLT did the literature search and statistical analyses. All authors were involved in the study design, data analyses, data interpretation and revision of the paper. TLT and JG had access to the full raw dataset. The corresponding author had the final responsibility to submit for publication.

  • Funding This study was funded by The Region of Southern Denmark, The Velux Foundation.

  • Competing Interests None declared.

  • Patient consent Obtained.

  • Ethics approval Regional Scientific Ethics Committee (ID S-20140046).

  • Provenance and peer review Not commissioned; externally peer reviewed.

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Introduction

Diabetic retinopathy (DR) is a microvascular disease induced by metabolic disturbances in the retinal homeostasis leading to retinal hypoxia.1 Proliferative diabetic retinopathy (PDR) is a late complication, which remains an important cause of severe visual loss around the world.2 3 PDR is characterised by the formation of retinal neovascularisations, potentially resulting in vitreous haemorrhage or tractional retinal detachment.4 Panretinal laser photocoagulation (PRP) halves the risk of severe visual loss as demonstrated by the DRS study in the late 1970s.5 Since then, PRP has been the gold standard of treatment for PDR. Nevertheless, post-laser activity of PDR can be hard to predict, and some patients may require more PRP (number of treatment episodes and number of burns) than others. Non-invasive preoperative markers will need to provide more precise PRP treatment algorithms, optimising the balance between treatment efficacy and side effects like visual field loss, night blindness and diabetic macular oedema.

The vast majority of the retinal area is located outside the traditional seven fields of the ETDRS. The retinal periphery has important prognostic value when evaluating disease activity,6 7 and it has been demonstrated that the presence of peripheral retinal diabetic lesions are correlated with a 4.7-fold increase risk of developing PDR.8 Furthermore, the overall hypoxic state of the retina is driven by capillary occlusion and retinal non-perfusion, which is predominantly found in the retinal periphery in association with severe DR.8–10 Peripheral capillary non-perfusion (PCNP) can be assessed by ultra-widefield fluorescein angiography (UWFA) covering a 200-degree overview of the retina, as compared with the conventional image of 30–50 degrees. Retinal oximetry is another promising marker for retinal metabolism; several studies demonstrated increased retinal venular oxygen saturation in association with increased levels of DR.11–15 These non-invasive measurements of retinal function and metabolism may serve as risk factors for disease activity. To determine this, we aimed to test if PCNP and oxygen saturation could predict disease activity 6 months (6M) after PRP in treatment-naïve patients with PDR.

Materials and methods

We carried out a 6M prospective, interventional study of 33 treatment-naïve eyes with PDR treated at Odense University Hospital, Denmark, between August 2014 and October 2015. We excluded patients with clinical significant macular oedema, previous PRP and treatment-requiring cataract, age <18 years or those pregnant. We only included one eye from each patient in order to avoid possible intereye correlations.16

The study was registered at the Regional Scientific Ethics Committee (ID S-20140046), the Danish Data Protection Agency (ID 14/16546), ClinicalTrials.gov (ID NCT02157350) and conducted in accordance with the criteria of Helsinki II Declaration and good clinical practice. The patient sample presented in this study is part of a bigger cohort, and data regarding retinal oxygen saturation and vascular geometry have previously been published.17 18

Baseline examinations

All patients provided a full medical history and underwent a thorough eye examination including mydriatic (tropicamide 10 mg/mL and phenylephrine 10%) slit-lamp examination, intraocular pressure (Goldmann applanation tonometry), optical coherence tomography (OCT) by 3D OCT-2000 Spectral domain OCT (Topcon, Tokyo, Japan), retinal oximetry (Oxymap model T1; Oxymap, software V.2.5.1, Reykjavik, Iceland) and blood pressure on the upper arm after 10 min in rest (Omron 705CP, Hoofdrop, The Netherlands), and Haemoglobin A1c (HbA1c) was analysed centrally by wash solution resin photometry, ion exchange HPLC-UV (Tosoh G8; normal range <48 mmol/mol). The baseline examinations were supplemented by UWFA and imaging (Optomap; OPTOS 200Tx, Optos PLC, Dunfermline, Scotland, UK), and the diagnosis of PDR was verified by a retinal specialist (JG) before the patient was included in the study.

PRP was given in two sessions by a navigated laser system (NAVILAS; OD-OS GmbH, Berlin, Germany) with a NAVILAS 34 mm or 38 mm contact lens in local anaesthesia (oxybuprocain hydrochloride 0.4%). All treatments were given by certified personnel (TLT and JG), and a treatment summary was automatically provided by the laser system after each session.

Follow-up examinations

Follow-up examinations were performed 6M after PRP, and baseline (BL) examinations were repeated. At 6M, patients were divided into two groups depending on the activity of PDR: active or inactive PDR. Active PDR was defined as either the formation of new retinal proliferations, or increased area of one or more proliferations, or increased area of fluorescein leakage as given by UWFA. Patients were also seen 3 months (3M) after PRP, and rescue laser treatment was given if indicated (n=2).

Retinal peripheral capillary non-perfusion

The retinal areas of PCNP were assessed by UWFA images 1 min after fluorescein injection, and a macular centred grading grid was placed on the image using a Matlab add-on program.19 The grader was allowed to adjust brightness/contrast when grading the different zones.

The grading grid divided the retinal UWFA image into 12 different zones, four in each retinal quadrant (superior, temporal, inferior and nasal) (figure 1). Zones were numbered 1 (innermost) through 4 (outermost). Each zone was manually categorised (graded) depending on the area of PCNP: 0 (no PCNP), 1 (1–25% PCNP), 2 (26–50% PCNP), 3 (51–75% PCNP), 4 (76–100% PCNP) or 5 (ungradable) (figure 2). Given that zones 1–4 differed in size, that the superior zone 4 was often ungradable due to eyelid interference and that zone 1 usually contained hyperfluorescent NVE, we used zone 3 as a marker for PCNP. The overall capillary density decreases towards the periphery of the retina, and thereby the difference in zone size was less important. But in order to get a global score that was as uniform as possible, the global PCNP score was assessed by averaging the four equally sized quadrants of zone 3. When evaluating the global PCNP score (continuous data), the focal grading scale (categorical) could not be used. Therefore, we used a moderated scale in order to assess the global PCNP score properly. The global PCNP score was evaluated according to the following moderated scale: 0–0.5 (close to no CNP), >0.5–1.5 (1%–25%), >1.5–2.5 (26%–50%), >2.5–3.5 (51%–75%) and >3.5–4.0 (76%–100%).

Figure 1

Ultra-widefield fluorescein angiography (OPTOS) of left eye with overlaid grading grid dividing the retinal into 12 zones, each graded according to area of capillary non-perfusion (CNP) (no CNP, 1%–25%, 26%–50%, 51%–75%, 76%–100% or ungradable).

Figure 2

Baseline ultra-widefield fluorescein angiography (OPTOS) of patients with treatment-naïve proliferative diabetic retinopathy. (A) Patient with subsequent disease inactivity 6 months after panretinal photocoagulation (PRP). Zone 3 graded as no capillary non-perfusion. (B) Patient with subsequent disease inactivity 6 months after PRP. Zone 3 graded as 76%–100% capillary non-perfusion.

Retinal oxygen saturation

Retinal oxygen saturation was performed using the Oxymap T1, with the procedure described previously.20 21 In brief, one 50-degree optic disc centred image was taken, with a flash intensity of 50. Two rings were semiautomatically placed on the image. The inner ring was manually placed around the optic disc, with an antireflective margin of 20–30 pixels from the edge of the optic and outwards to the ring. The outer ring was automatically placed three disc diameters from the inner ring. One larger arteriole and venule in each quadrant was measured, tracing from the inner ring not exceeding the outer ring (figure 3). The vessel length had to be between 50 and 200 pixels. If the first branching point occurred before the vessel reached 50 pixels in length, the first branch vessel was chosen for measurement. All measurements were done on the same vessel segment at each time point. In order to assess the global retinal oxygen saturation, the mean retinal arteriolar and venular oxygen saturation of all four quadrants was used.

Figure 3

Oxymap T1 image showing traced vessels with overlaying colour map indicating oxygen saturation by colour in the left eye. Between the blue rings, the oxygen saturation is measured in traced vessels, seen as white lines on either side of the vessels. Retinal vessels covered in white areas are excluded vessel segments.

Statistical analyses

All statistical calculations were performed using STATA V.14.2 (StataCorp, College Station, Texas, USA), and p values under 0.05 were considered statistically significant. Categorical data are presented as percentage and continuous data as median with IQR. Differences between patients with inactive and active PDR were compared by the Mann-Whitney U test for continuous data and χ2 test for categorical data. The correlation between retinal oxygen saturation and PCNP were tested using the non-parametric test of Cuzick, and specific group comparisons were made by usage of the Mann-Whitney U test. Twenty per cent (n=21) of the UWFA images were re-graded and showed a substantial intragrader agreement on areas of PCNP in zone 3 (kappa=0.66).22

Results

We examined 33 eyes, and of those 69.6% were men and 21.2% were active smokers. At baseline, the median with IQR age and duration of diabetes were 51.6±23.4 and 20.0±15.0 years, respectively. HbA1c was 63.0±17.0 mmol/mol and the blood pressure was 152±37/82±24 mm Hg. The global PCNP was 51%–75% (2.3), and the retinal global arteriolar and venular oxygen saturation was 95.7%±6.9% and 67.2%±13.4%, respectively. At 6M follow-up, 30.3% (n=10) had active PDR. At BL, patients who had inactive PDR and active PDR at 6M did not differ according to BL sex, smoking, age, duration of diabetes, HbA1c, blood pressure, laser energy delivered at baseline or retinal oximetry image quality (table 1). Furthermore, we found no correlation between retinal oxygen saturation and the area of PCNP at any time points when performing a test for trend across ordered groups (data not shown).

Table 1

Baseline characteristics according to activity of proliferative diabetic retinopathy 6 months after panretinal laser photocoagulation

Baseline

At BL, patients with active PDR at 6M were found to have a significantly larger area of PCNP than those with inactive PDR (51%–75% (3.3±1.3) vs 26%–50% (2.0±2.3), p=0.03) (table 2). No differences were found in retinal oxygen saturation between the two groups.

Table 2

Retinal oximetry and peripheral capillary non-perfusion results at baseline and 6 months follow-up.

Six months’ follow-up

At 6M, similar to BL, patients with active PDR had a larger area of PCNP as compared with patients with inactive PDR (51%–75% (2.9±1.3) vs 26%–50% (2.0±1.6), p=0.03) (table 2). Moreover, when performing a Wilcoxon matched-pairs test on patients with active PDR, we found a statistically significant decrease in retinal arteriolar oxygen saturation from BL to 6M (93.4%±6.4% vs 93.3±7.2%, p=0.02).

Discussion

In this prospective, interventional study, we found patients with active PDR 6M after PRP to have a larger area of PCNP at baseline and 6M, as compared with patients with inactive PDR. Furthermore, it was found that increasing retinal vascular arteriolar oxygen saturation after PRP trended towards a lower risk of active PDR (p=0.05), although patients with active PDR was found to decrease in retinal arteriolar oxygen saturation from BL to 6M.

Earlier studies have shown that the retinal areas of non-perfusion increased with increased severity of DR,23 and that it plateaus at the stage of severe non-PDR.9 In our study, all patients (who by protocol had treatment-naïve PDR) had retinal areas of CNP at baseline. Furthermore, at BL, patients with active PDR had significantly larger areas of PCNP than patients with inactive PDR. This would indicate that patients with a lower retinal hypoxic load received sufficient PRP, while the same amount of treatment could be insufficient in patients with a higher hypoxic load. A successful response to the PRP treatment is not fully understood, but one hypothesis is that the retinal laser scars has a positive effect on the haemodynamic mechanisms of the retinal circulation, thereby reducing the hypoxic load and preventing progression of PDR.24

We found the same difference in area of PCNP between the two groups at 6M, as found at BL. After PRP treatment, patients with active PDR were still seen to have larger areas of PCNP as compared with patients with inactive PDR. Traditionally, CNP is regarded an irreversible feature of DR,25 but reperfusion of occluded retinal capillary beds has been reported.26 The results found in our study did not show expansion in areas of PCNP in patients with active PDR or reduction in areas of PCNP in patients with inactive PDR from BL to 6M. Optical coherence tomography angiography (OCT-A) is a novel non-invasive technique for imaging the microvasculature of the retina and choroid by detection of moving erythrocytes through different retinal segments . OCT-A would benefit greatly in trying to quantify the amount of retinal PCNP and might confirm the finding of this study. OCT-A has for the past couple of years advanced from 50-degree fundus images to widefield images, although the technique remains subject to known imaging complications such as retinal variations in illumination and artefacts.

The retinal oxygen saturation has in the literature been reported to be affected by PRP treatment. Conflicting changes in the retinal vascular oxygen saturation have been reported. One study found lower venular oxygen saturation in patients earlier treated with PRP,14 and another study reported that the arteriolar oxygen saturation was seen to decrease 3M after PRP treatment,27 although these studies did not test responder versus non-responders. The results found in our study, although statistically significant, were not found to be clinical relevant.

The findings of this study should be interpreted in the context of the following limitations. Although adjustment of the UWFA image contrast was possible, a trend towards overestimation of CNP areas next to leaky areas may occur because of the sharp change in contrast colour. The moderated PCNP scale has a tendency to underestimate the degree of global PCNP; this was done deliberately in order to counterbalance the potential overestimation of CNP areas due to the mentioned contrast colour issue. Furthermore, grading UWFA images was challenging, especially in the superior and inferior quadrants, and therefore the far periphery in these quadrants may be under-represented because of covering eyelids.

Detecting predictive markers of disease activity has proven difficult, and no preoperative markers have to our knowledge been identified. Taking the DRS and ETDRS study into account, the reduction in risk of severe visual loss was found to be >50% after standard PRP treatment, still leaving almost half of the treated patients at risk. The possible predictive power of the area of PCNP gives food to thought. Standard PRP treatment was in this study found to be insufficient when dealing with larger retinal areas of PCNP in patients with PDR. An individualised treatment approach might be preferable. This might be achieved by additional PRP at an early stage, more intense follow-up during the first 6 months after PRP and maybe a lower threshold for vitrectomy or intravitreal anti-vascular endothelial growth factor intervention in severe cases of unsuccessful PRP treatment.

In summary, in patients with PDR, after PRP treatment, those with active PDR at 6M had larger areas of PCNP at BL as compared with those who have inactive PDR. Thus, PCNP may be used as a predictive marker at BL for PDR activity after PRP treatment, paving the possibility for individually titrated PRP treatment.

References

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Footnotes

  • Contributors JG conceived the aims and overall design of the study. TLT acquired the data and did the writing of the different sections, tables and figures. JG and TLT did the literature search and statistical analyses. All authors were involved in the study design, data analyses, data interpretation and revision of the paper. TLT and JG had access to the full raw dataset. The corresponding author had the final responsibility to submit for publication.

  • Funding This study was funded by The Region of Southern Denmark, The Velux Foundation.

  • Competing Interests None declared.

  • Patient consent Obtained.

  • Ethics approval Regional Scientific Ethics Committee (ID S-20140046).

  • Provenance and peer review Not commissioned; externally peer reviewed.

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