TY - JOUR
T1 - Quantifying microvascular density and morphology in diabetic retinopathy using spectral-domain optical coherence tomography angiography
AU - Kim, Alice Y.
AU - Chu, Zhongdi
AU - Shahidzadeh, Anoush
AU - Wang, Ruikang K.
AU - Puliafito, Carmen A.
AU - Kashani, Amir H.
N1 - Publisher Copyright:
© 2016, Association for Research in Vision and Ophthalmology Inc. All rights reserved.
PY - 2016
Y1 - 2016
N2 - PURPOSE. To quantify changes in retinal microvasculature in diabetic retinopathy (DR) by using spectral-domain optical coherence tomography angiography (SD-OCTA). METHODS. Retrospective, cross-sectional, observational study of healthy and diabetic adult subjects with and without DR. Retinal microvascular changes were assessed by using SDOCTA images and an intensity-based optical microangiography algorithm. A semiautomated program was used to calculate indices of microvascular density and morphology in nonsegmented and segmented SD-OCTA images. Microvascular density was quantified by using skeleton density (SD) and vessel density (VD), while vessel morphology was quantified as fractal dimension (FD) and vessel diameter index (VDI). Statistical analyses were performed by using the Student’s t-test or analysis of variance with post hoc Tukey honest significant difference tests for multiple comparisons. RESULTS. Eighty-four eyes with DR and 14 healthy eyes were studied. Spearman’s rank test demonstrated a negative correlation between DR severity and SD, VD, and FD, and a positive correlation with VDI (ρ = -0.767, -0.7166, -0.768, and +0.5051, respectively; P < 0.0001). All parameters showed high reproducibility between graders (ICC = 0.971, 0.962, 0.937, and 0.994 for SD, VD, FD, and VDI, respectively). Repeatability (j) was greater than 0.99 for SD, VD, FD, and VDI. CONCLUSIONS. Vascular changes in DR can be objectively and reliably characterized with SD, VD, FD, and VDI. In general, decreasing capillary density (SD and VD), branching complexity (FD), and increasing average vascular caliber (VDI) were associated with worsening DR. Changes in capillary density and morphology were significantly correlated with diabetic macular edema.
AB - PURPOSE. To quantify changes in retinal microvasculature in diabetic retinopathy (DR) by using spectral-domain optical coherence tomography angiography (SD-OCTA). METHODS. Retrospective, cross-sectional, observational study of healthy and diabetic adult subjects with and without DR. Retinal microvascular changes were assessed by using SDOCTA images and an intensity-based optical microangiography algorithm. A semiautomated program was used to calculate indices of microvascular density and morphology in nonsegmented and segmented SD-OCTA images. Microvascular density was quantified by using skeleton density (SD) and vessel density (VD), while vessel morphology was quantified as fractal dimension (FD) and vessel diameter index (VDI). Statistical analyses were performed by using the Student’s t-test or analysis of variance with post hoc Tukey honest significant difference tests for multiple comparisons. RESULTS. Eighty-four eyes with DR and 14 healthy eyes were studied. Spearman’s rank test demonstrated a negative correlation between DR severity and SD, VD, and FD, and a positive correlation with VDI (ρ = -0.767, -0.7166, -0.768, and +0.5051, respectively; P < 0.0001). All parameters showed high reproducibility between graders (ICC = 0.971, 0.962, 0.937, and 0.994 for SD, VD, FD, and VDI, respectively). Repeatability (j) was greater than 0.99 for SD, VD, FD, and VDI. CONCLUSIONS. Vascular changes in DR can be objectively and reliably characterized with SD, VD, FD, and VDI. In general, decreasing capillary density (SD and VD), branching complexity (FD), and increasing average vascular caliber (VDI) were associated with worsening DR. Changes in capillary density and morphology were significantly correlated with diabetic macular edema.
KW - Diabetic retinopathy
KW - Optical coherence tomography angiography
KW - Quantitative analysis
KW - Vessel density
KW - Vessel morphology
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U2 - 10.1167/iovs.15-18904
DO - 10.1167/iovs.15-18904
M3 - Article
C2 - 27409494
AN - SCOPUS:84978518688
SN - 0146-0404
VL - 57
SP - OCT362-OCT370
JO - Investigative Ophthalmology and Visual Science
JF - Investigative Ophthalmology and Visual Science
IS - 9
ER -