Hamilton Glaucoma Center and Shiley Eye Institute, Viterbi Family Department of Ophthalmology, University of California, San Diego, La Jolla, California.
Hamilton Glaucoma Center and Shiley Eye Institute, Viterbi Family Department of Ophthalmology, University of California, San Diego, La Jolla, California; Department of Ophthalmology, University of São Paulo, São Paulo, Brazil.
Ophthalmology. 2020 Aug;127(8):1043-1052. doi: 10.1016/j.ophtha.2019.12.030. Epub 2020 Jan 13.
To characterize the change rate of ganglion cell complex (GCC) thickness and macular vessel density in healthy, preperimetric glaucoma and primary open-angle glaucoma (POAG) eyes.
Prospective, longitudinal study.
One hundred thirty-nine eyes (23 healthy eyes, 36 preperimetric glaucoma eyes, and 80 POAG eyes) of 94 patients who had at least 3 visits were included from the Diagnostic Innovations in Glaucoma Study. The mean follow-up was 2.0 years for healthy eyes, 2.6 years for preperimetric glaucoma eyes, and 2.6 years for POAG eyes.
OCT angiography (OCTA)-based vessel density and OCT-based structural thickness of the same 3×3-mm GCC scan slab were evaluated. The dynamic range-based normalized rates of vessel density and thickness change were calculated and compared within each diagnostic group. The association between the rates of thickness and vessel density change and potential factors were evaluated.
The rates of GCC thinning and macular vessel density loss.
Significant rates of GCC thinning and macular vessel density decrease were detectable in all diagnostic groups (all P < 0.05). In healthy eyes and preperimetric glaucoma eyes, the normalized rates of GCC thinning and macular vessel density decrease were comparable (all P > 0.1). In contrast, the normalized rate (mean, 95% confidence interval) of macular vessel density decrease in the POAG eyes (-7.12 [-8.36, -5.88]%/year) was significantly faster than GCC thinning (-2.13 [-3.35, -0.90]%/year; P < 0.001). In the POAG group, more than two thirds of the eyes showed faster macular vessel density decrease than GCC thinning; faster macular vessel density decrease rate was associated significantly with worse glaucoma severity (P = 0.037). The association between GCC thinning rate and glaucoma severity was not significant (P = 0.586). Intraocular pressure during follow-up significantly affected the rate of GCC thinning in all groups (all P < 0.05) but showed no association with the rate of macular vessel density decrease.
Both GCC thinning and macular vessel density decrease were detectable over time in all diagnostic groups. In POAG eyes, macular vessel density decrease was faster than GCC thinning and was associated with severity of disease. Macular vessel density is useful for evaluating glaucoma progression, particularly in more advanced disease.
描述健康眼、前期青光眼和原发性开角型青光眼(POAG)眼中神经节细胞复合体(GCC)厚度和黄斑血管密度的变化率。
前瞻性、纵向研究。
该研究纳入了来自诊断性青光眼创新研究中的 94 名患者的 139 只眼(23 只健康眼、36 只前期青光眼眼和 80 只 POAG 眼),这些患者至少接受了 3 次随访。健康眼的平均随访时间为 2.0 年,前期青光眼眼为 2.6 年,POAG 眼为 2.6 年。
评估基于 OCT 血管造影(OCTA)的血管密度和基于 OCT 的相同 3×3-mm GCC 扫描板的结构厚度。在每个诊断组内计算并比较了基于动态范围的血管密度和厚度变化率的标准化率。评估了厚度和血管密度变化率与潜在因素之间的关系。
GCC 变薄和黄斑血管密度损失的速率。
所有诊断组均检测到明显的 GCC 变薄和黄斑血管密度下降(均 P<0.05)。在健康眼和前期青光眼眼中,GCC 变薄和黄斑血管密度下降的标准化率相当(均 P>0.1)。相比之下,POAG 眼黄斑血管密度下降的标准化率(平均值,95%置信区间)为-7.12[-8.36,-5.88]%/年,明显快于 GCC 变薄(-2.13[-3.35,-0.90]%/年;P<0.001)。在 POAG 组中,超过三分之二的眼显示出比 GCC 变薄更快的黄斑血管密度下降;更快的黄斑血管密度下降率与更严重的青光眼严重程度显著相关(P=0.037)。GCC 变薄率与青光眼严重程度之间的关联不显著(P=0.586)。随访期间的眼内压在所有组中均显著影响 GCC 变薄率(均 P<0.05),但与黄斑血管密度下降率无关。
在所有诊断组中,随时间推移均可检测到 GCC 变薄和黄斑血管密度下降。在 POAG 眼中,黄斑血管密度下降速度快于 GCC 变薄,与疾病严重程度相关。黄斑血管密度有助于评估青光眼进展,尤其是在更严重的疾病中。