Adhi Mehreen, Badaro Emmerson, Liu Jonathan J, Kraus Martin F, Baumal Caroline R, Witkin Andre J, Hornegger Joachim, Fujimoto James G, Duker Jay S, Waheed Nadia K
New England Eye Center, Tufts University School of Medicine, Boston, Massachusetts; Departments of Electrical Engineering and Computer Science and Research Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, Massachusetts.
Department of Ophthalmology, Federal University of Brazil, Sao Paulo, Brazil.
Am J Ophthalmol. 2016 Feb;162:140-149.e1. doi: 10.1016/j.ajo.2015.10.025. Epub 2015 Nov 6.
To analyze the vitreoretinal interface in diabetic eyes using 3-dimensional wide-field volumes acquired using high-speed, long-wavelength swept-source optical coherence tomography (SSOCT).
Prospective cross-sectional study.
Fifty-six diabetic patients (88 eyes) and 11 healthy nondiabetic controls (22 eyes) were recruited. Up to 8 SSOCT volumes were acquired for each eye. A registration algorithm removed motion artifacts and merged multiple SSOCT volumes to improve signal. Vitreous visualization was enhanced using vitreous windowing method.
Of 88 diabetic eyes, 20 eyes had no retinopathy, 21 eyes had nonproliferative diabetic retinopathy (NPDR) without macular edema, 20 eyes had proliferative diabetic retinopathy (PDR) without macular edema, and 27 eyes had diabetic macular edema (DME) with either NPDR or PDR. Thick posterior hyaloid relative to healthy nondiabetic controls was observed in 0 of 20 (0%) diabetic eyes without retinopathy, 4 of 21 (19%) eyes with NPDR, 11 of 20 (55%) eyes with PDR, and 11 of 27 (41%) eyes with DME (P = .0001). Vitreoschisis was observed in 6 of 22 (27%) healthy nondiabetic eyes, 9 of 20 (45%) diabetic eyes without retinopathy, 10 of 21 (48%) eyes with NPDR, 13 of 20 (65%) eyes with PDR, and 17 of 27 (63%) eyes with DME (P = .007). While no healthy nondiabetic controls and diabetic eyes without retinopathy had adhesions/pegs between detached posterior hyaloid and retina, 1 of 21 (4%), 11 of 20 (55%), and 11 of 27 (41%) eyes with NPDR, PDR, and DME, respectively, demonstrated this feature (P = .0001).
SSOCT with motion-correction and vitreous windowing provides wide-field 3-dimensional information of vitreoretinal interface in diabetic eyes. This may be useful in assessing progression of retinopathy, planning diabetic vitreous surgery, and predicting treatment outcomes.
使用高速、长波长扫频源光学相干断层扫描(SSOCT)获取的三维宽视野容积分析糖尿病患者眼内的玻璃体视网膜界面。
前瞻性横断面研究。
招募了56例糖尿病患者(88只眼)和11例健康非糖尿病对照者(22只眼)。每只眼最多获取8个SSOCT容积。一种配准算法去除运动伪影并合并多个SSOCT容积以改善信号。使用玻璃体开窗法增强玻璃体可视化。
在88只糖尿病眼中,20只眼无视网膜病变,21只眼有非增殖性糖尿病视网膜病变(NPDR)且无黄斑水肿,20只眼有增殖性糖尿病视网膜病变(PDR)且无黄斑水肿,27只眼有糖尿病性黄斑水肿(DME)合并NPDR或PDR。在无视网膜病变的20只糖尿病眼中,0只(0%)观察到相对于健康非糖尿病对照者的厚后玻璃体;在有NPDR的21只眼中,4只(19%);在有PDR的20只眼中,11只(55%);在有DME的27只眼中,11只(41%)(P = 0.0001)。在22只健康非糖尿病眼中,6只(27%)观察到玻璃体劈裂;在无视网膜病变的20只糖尿病眼中,9只(45%);在有NPDR的21只眼中,10只(48%);在有PDR的20只眼中,13只(65%);在有DME的27只眼中,17只(63%)(P = 0.007)。在健康非糖尿病对照者和无视网膜病变的糖尿病眼中,未观察到脱离的后玻璃体与视网膜之间有粘连/钉状物,但在有NPDR、PDR和DME的眼中,分别有21只中的1只(4%)、20只中的11只(55%)和27只中的11只(41%)出现此特征(P = 0.0001)。
具有运动校正和玻璃体开窗功能的SSOCT可提供糖尿病患者眼内玻璃体视网膜界面的宽视野三维信息。这可能有助于评估视网膜病变的进展、规划糖尿病玻璃体手术以及预测治疗结果。