Suh Min Hee, Zangwill Linda M, Manalastas Patricia Isabel C, Belghith Akram, Yarmohammadi Adeleh, Medeiros Felipe A, Diniz-Filho Alberto, Saunders Luke J, Weinreb Robert N
Hamilton Glaucoma Center, Shiley Eye Institute, and the Department of Ophthalmology, University of California, San Diego, La Jolla, California; Department of Ophthalmology, Haeundae Paik Hospital, Inje University College of Medicine, Busan, South Korea.
Hamilton Glaucoma Center, Shiley Eye Institute, and the Department of Ophthalmology, University of California, San Diego, La Jolla, California.
Ophthalmology. 2016 Dec;123(12):2509-2518. doi: 10.1016/j.ophtha.2016.09.002. Epub 2016 Oct 18.
To investigate factors associated with dropout of the parapapillary deep retinal layer microvasculature assessed by optical coherence tomography angiography (OCTA) in glaucomatous eyes.
Cross-sectional study.
Seventy-one eyes from 71 primary open-angle glaucoma (POAG) patients with β-zone parapapillary atrophy (βPPA) enrolled in the Diagnostic Innovations in Glaucoma Study.
Parapapillary deep-layer microvasculature dropout was defined as a complete loss of the microvasculature located within the deep retinal layer of the βPPA from OCTA-derived optic nerve head vessel density maps by standardized qualitative assessment. Circumpapillary vessel density (cpVD) within the retinal nerve fiber layer (RNFL) also was calculated using OCTA. Choroidal thickness and presence of focal lamina cribrosa (LC) defects were determined using swept-source optical coherence tomography.
Presence of parapapillary deep-layer microvasculature dropout. Parameters including age, systolic and diastolic blood pressure, axial length, intraocular pressure, disc hemorrhage, cpVD, visual field (VF) mean deviation (MD), focal LC defects βPPA area, and choroidal thickness were analyzed.
Parapapillary deep-layer microvasculature dropout was detected in 37 POAG eyes (52.1%). Eyes with microvasculature dropout had a higher prevalence of LC defects (70.3% vs. 32.4%), lower cpVD (52.7% vs. 58.8%), worse VF MD (-9.06 dB vs. -3.83 dB), thinner total choroidal thickness (126.5 μm vs. 169.1 μm), longer axial length (24.7 mm vs. 24.0 mm), larger βPPA (1.2 mm vs. 0.76 mm), and lower diastolic blood pressure (74.7 mmHg vs. 81.7 mmHg) than those without dropout (P < 0.05, respectively). In the multivariate logistic regression analysis, higher prevalence of focal LC defects (odds ratio [OR], 6.27; P = 0.012), reduced cpVD (OR, 1.27; P = 0.002), worse VF MD (OR, 1.27; P = 0.001), thinner choroidal thickness (OR, 1.02; P = 0.014), and lower diastolic blood pressure (OR, 1.16; P = 0.003) were associated significantly with the dropout.
Systemic and ocular factors including focal LC defects more advanced glaucoma, reduced RNFL vessel density, thinner choroidal thickness, and lower diastolic blood pressure were factors associated with the parapapillary deep-layer microvasculature dropout in glaucomatous eyes. Longitudinal studies are required to elucidate the temporal relationship between parapapillary deep-layer microvasculature dropout and systemic and ocular factors.
研究青光眼患者中,光学相干断层扫描血管造影(OCTA)评估的视乳头旁深层视网膜微血管层缺失的相关因素。
横断面研究。
71例原发性开角型青光眼(POAG)合并β区视乳头旁萎缩(βPPA)患者的71只眼睛,这些患者均参与了青光眼诊断创新研究。
视乳头旁深层微血管层缺失定义为,通过标准化定性评估,从OCTA衍生的视神经乳头血管密度图中,βPPA深层视网膜层内的微血管完全缺失。视网膜神经纤维层(RNFL)内的视乳头周围血管密度(cpVD)也使用OCTA进行计算。使用扫频光学相干断层扫描确定脉络膜厚度和局限性筛板(LC)缺陷的存在。
视乳头旁深层微血管层缺失的存在情况。分析包括年龄、收缩压和舒张压、眼轴长度、眼压、视盘出血、cpVD、视野(VF)平均偏差(MD)、局限性LC缺陷、βPPA面积和脉络膜厚度等参数。
在37只POAG眼中检测到视乳头旁深层微血管层缺失(52.1%)。微血管层缺失的眼睛LC缺陷患病率更高(70.3%对32.4%),cpVD更低(52.7%对58.8%),VF MD更差(-9.06 dB对-3.83 dB),总脉络膜厚度更薄(126.5μm对169.1μm),眼轴长度更长(24.7mm对24.0mm),βPPA更大(1.2mm对0.76mm),舒张压更低(74.7mmHg对81.7mmHg),均与无缺失的眼睛相比(P均<0.05)。在多因素逻辑回归分析中,局限性LC缺陷患病率更高(比值比[OR],6.27;P = 0.012)、cpVD降低(OR,1.27;P = 0.002)、VF MD更差(OR,1.27;P = 0.001)、脉络膜厚度更薄(OR,1.02;P = 0.014)和舒张压更低(OR,1.16;P = 0.003)与缺失显著相关。
全身和眼部因素,包括局限性LC缺陷、更严重的青光眼、RNFL血管密度降低、脉络膜厚度更薄和舒张压更低,是青光眼患者视乳头旁深层微血管层缺失的相关因素。需要进行纵向研究以阐明视乳头旁深层微血管层缺失与全身和眼部因素之间的时间关系。