Optical coherence tomography angiography measured area of retinal neovascularization is predictive of treatment response and progression of disease in patients with proliferative diabetic retinopathy

Anna Stage Vergmann, Kristian Tølbøl Sørensen, Thomas Lee Torp, Ryo Kawasaki, Tien Wong, Tunde Peto, Jakob Grauslund, Anna Stage Vergmann, Kristian Tølbøl Sørensen, Thomas Lee Torp, Ryo Kawasaki, Tien Wong, Tunde Peto, Jakob Grauslund

Abstract

Background: The purpose of this study was to evaluate the area of retinal neovascularization in patients with treatment-naïve proliferative diabetic retinopathy (PDR) as measured by optical coherence tomography angiography (OCT-A) as a marker of subsequent treatment response after panretinal photocoagulation (PRP), and to examine if this area correlated with area of retinal neovascularization as measured by fluorescein angiography (FA).

Methods: En face OCT-A scans (4.5 × 4.5 mm) of neovascularizations were obtained at baseline (BL) before PRP and at month (M) 3 and M6 after treatment. Progression of PDR were defined as lesion growth (assessed by ophthalmoscopy and wide-field fundus photo) or increasing leakage by Optos ultra-widefield FA, and patients were divided into two groups; progression or non-progression. Mann-Whitney U test and Wilcoxon signed-rank test were used to analyse differences between groups and between time points. Areas of retinal neovascularizations (OCT-A and FA) were calculated by algorithms developed in Python (version 3.6.8, The Python Software Foundation, USA).

Results: Of 21 eyes included, 14 had progression of disease. Median OCT-A area did not differ between the two groups (progression vs. non-progression) at BL (76.40 ± 162.03 vs. 72.62 ± 94.15, p = 0.43) but were statistically significantly larger in the progression group at M6 (276.69 ± 168.78 vs. 61.30 ± 70.90, p = 0.025). Median FA area did not differ in the progression vs. the non-progression group at BL (111.42 ± 143.08 vs. 60.80 ± 54.83, p = 0.05) or at M6 (200.12 ± 91.81 vs. 123.86 ± 162.16, p = 0.62). Intraclass correlation between area by OCT-A and FA was -5.99 (95% CI: -35.28-0.993), p = 0.71.

Conclusions: In this study of patients with treatment-naïve PDR, we showed that increasing area of retinal neovascularizations measured by OCT-A at M6 indicated progression of disease after PRP treatment. Our results suggest that area by OCT-A reflects disease activity and that it can be used as an indicator to monitor the progression of PDR over time, and to evaluate treatment response six months after PRP. Trial registration https://ichgcp.net/clinical-trials-registry/NCT03113006" title="See in ClinicalTrials.gov">NCT03113006). Registered April 13, 2017.

Keywords: Diabetic retinopathy; Fluorescein angiography; Optical coherence tomography angiography; Proliferative diabetic retinopathy.

Conflict of interest statement

The authors have no competing interests or financial conflicts to disclose.

Figures

Fig. 1
Fig. 1
Optical coherence tomography angiography measured area of neovascularization
Fig. 2
Fig. 2
Scatter plot between area (mm2) measured by optical coherence tomography angiography (OCT-A) and fluorescein angiography

References

    1. Cheung N, Mitchell P, Wong TY. Diabetic retinopathy. Lancet. 2010;376(9735):124–136. doi: 10.1016/S0140-6736(09)62124-3.
    1. Wong TY, Cheung CMG, Larsen M, Sharma S, Simó R. Diabetic retinopathy. Nat Rev Dis Prim. 2016;2(1):16012. doi: 10.1038/nrdp.2016.12.
    1. Fluorescein Angiographic Risk Factors for Progression of Diabetic Retinopathy: ETDRS Report Number 13. Ophthalmology. 1991;98(5):834–40.
    1. Kwiterovich KA, Maguire MG, Murphy RP, Schachat AP, Bressler NM, Bressler SB, et al. Frequency of adverse systemic reactions after fluorescein angiography: results of a Prospective Study. Ophthalmology. 1991;98(7):1139–1142. doi: 10.1016/S0161-6420(91)32165-1.
    1. Torp T, Frydkjær-Olsen U, Hansen R, Peto T, Grauslund J. Intra- and intergrader reliability of semiautomatic measurements of fundus fluorescein angiography leakage in proliferative diabetic retinopathy. Eur J Ophthalmol. 2015;25(3):e7–e30. doi: 10.5301/ejo.5000612.
    1. Spaide RF, Fujimoto JG, Waheed NK, Sadda SR, Staurenghi G. Optical coherence tomography angiography. Prog Retin Eye Res. 2018;64:1–55. doi: 10.1016/j.preteyeres.2017.11.003.
    1. Spaide RF, Klancnik JM, Jr, Cooney MJ. Retinal vascular layers imaged by fluorescein angiography and optical coherence tomography angiography. JAMA Ophthalmol. 2015;133(1):45–50. doi: 10.1001/jamaophthalmol.2014.3616.
    1. Kuehlewein L, Bansal M, Lenis TL, Iafe NA, Sadda SR, Bonini Filho MA, et al. Optical coherence tomography angiography of type 1 neovascularization in age-related macular degeneration. Am J Ophthalmol. 2015;160(4):739–48.e2. doi: 10.1016/j.ajo.2015.06.030.
    1. Enders C, Baeuerle F, Lang GE, Dreyhaupt J, Lang GK, Loidl M, et al. Comparison between findings in optical coherence tomography angiography and in fluorescein angiography in patients with diabetic retinopathy. Ophthalmologica. 2020;243(1):21–26. doi: 10.1159/000499114.
    1. Johannesen SK, Viken JN, Vergmann AS, Grauslund J. Optical coherence tomography angiography and microvascular changes in diabetic retinopathy: a systematic review. Acta Ophthalmol. 2019;97(1):7–14. doi: 10.1111/aos.13859.
    1. Fawzi AA, Fayed AE, Linsenmeier RA, Gao J, Yu F. Improved macular capillary flow on optical coherence tomography angiography after panretinal photocoagulation for proliferative diabetic retinopathy. Am J Ophthalmol. 2019;206:217–227. doi: 10.1016/j.ajo.2019.04.032.
    1. Ishibazawa A, Nagaoka T, Yokota H, Takahashi A, Omae T, Song Y-S, et al. Characteristics of retinal neovascularization in proliferative diabetic retinopathy imaged by optical coherence tomography angiography. Invest Ophthalmol Vis Sci. 2016;57(14):6247–6255. doi: 10.1167/iovs.16-20210.
    1. de Carlo TE, Bonini Filho MA, Baumal CR, Reichel E, Rogers A, Witkin AJ, et al. Evaluation of preretinal neovascularization in proliferative diabetic retinopathy using optical coherence tomography angiography. Ophthalmic Surg Lasers Imaging Retina. 2016;47(2):115–119. doi: 10.3928/23258160-20160126-03.
    1. Vergmann AS, Nguyen TT, Lee Torp T, Kawasaki R, Wong TY, Peto T, et al. Efficacy and side effects of individualized panretinal photocoagulation. Ophthalmology Retina. 2020;4:642. doi: 10.1016/j.oret.2020.02.006.
    1. Topcon. Topcon DRI OCT Triton, Swept Source OCT : Topcon (Tokyo, Japan).
    1. Quigley HA, Brown AE, Morrison JD, Drance SM. The size and shape of the optic disc in normal human eyes. Arch Ophthalmol. 1990;108(1):51–57. doi: 10.1001/archopht.1990.01070030057028.
    1. Holmen IC, Konda MS, Pak JW, McDaniel KW, Blodi B, Stepien KE, et al. Prevalence and severity of artifacts in optical coherence tomographic angiograms. JAMA Ophthalmol. 2020;138(2):119–126. doi: 10.1001/jamaophthalmol.2019.4971.
    1. Russell JF, Shi Y, Hinkle JW, Scott NL, Fan KC, Lyu C, et al. Longitudinal wide-field swept-source OCT angiography of neovascularization in proliferative diabetic retinopathy after panretinal photocoagulation. Ophthalmol Retina. 2019;3(4):350–361. doi: 10.1016/j.oret.2018.11.008.
    1. Schwartz R, Khalid H, Sivaprasad S, Nicholson L, Anikina E, Sullivan P, et al. Objective evaluation of proliferative diabetic retinopathy using OCT. Ophthalmol Retina. 2020;4(2):164–174. doi: 10.1016/j.oret.2019.09.004.
    1. Koo TK, Li MY. A Guideline of selecting and reporting intraclass correlation coefficients for reliability research. J Chiropr Med. 2016;15(2):155–163. doi: 10.1016/j.jcm.2016.02.012.
    1. Enders C, Baeurle F, Lang GE, Dreyhaupt J, Trick S, Kilani A, et al. Darstellung von retinalen Neovaskularisationen mit der optischen Kohärenztomografie-Angiografie im Vergleich mit der Fluoreszeinangiografie. Klin Monatsbl Augenheilkd. 2019;236(11):1325–1330. doi: 10.1055/a-0983-2271.

Source: PubMed

3
Předplatit