Department of Ophthalmology, International University of Health and Welfare Hospital, Nasu-Shiobara, Tochigi, Japan.
Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Ophthalmology. 2018 Sep;125(9):1372-1383. doi: 10.1016/j.ophtha.2018.02.039. Epub 2018 Apr 7.
Posterior vitreous detachment (PVD) plays an important role in vitreoretinal interface disorders. Historically, observations of PVD using OCT have been limited to the macular region. The purpose of this study is to image the wide-angle vitreoretinal interface after PVD in normal subjects using montaged OCT images.
An observational cross-sectional study.
A total of 144 healthy eyes of 98 normal subjects aged 21 to 95 years (51.4±22.0 [mean ± standard deviation]).
Montaged images of horizontal and vertical OCT scans through the fovea were obtained in each subject.
Montaged OCT images.
By using wide-angle OCT, we imaged the vitreoretinal interface from the macula to the periphery. PVD was classified into 5 stages: stage 0, no PVD (2 eyes, both aged 21 years); stage 1, peripheral PVD limited to paramacular to peripheral zones (88 eyes, mean age 38.9±16.2 years, mean ± standard deviation); stage 2, perifoveal PVD extending to the periphery (12 eyes, mean age 67.9±8.4 years); stage 3, peripapillary PVD with persistent vitreopapillary adhesion alone (7 eyes, mean age 70.9±11.9 years); stage 4, complete PVD (35 eyes, mean age 75.1±10.1 years). All stage 1 PVDs (100%) were observed in the paramacular to peripheral region where the vitreous gel adheres directly to the cortical vitreous and retinal surface. After progression to stage 2 PVD, the area of PVD extends posteriorly to the perifovea and anteriorly to the periphery. Vitreoschisis was observed in 41.2% at PVD initiation (stage 1a).
Whereas prior work suggests that PVD originates in the perifoveal region and after the sixth decade, our observations demonstrate that (1) PVD first appears even in the third decade of life and gradually appears more extensively throughout life; (2) more than 40% of eyes without fundus diseases at their PVD initiation are associated with vitreoschisis; and (3) PVD is first noted primarily in the paramacular-peripheral region where vitreous gel adheres to the retinal surface and is noted to be more extensive in older ages to ultimately involve the fovea.
玻璃体后脱离(PVD)在玻璃体视网膜界面疾病中起着重要作用。历史上,使用 OCT 观察 PVD 仅限于黄斑区域。本研究的目的是使用 montaged OCT 图像在正常受试者中成像 PVD 后的广角玻璃体视网膜界面。
观察性横断面研究。
共有 98 名正常受试者的 144 只健康眼,年龄 21 至 95 岁(51.4±22.0 [平均值±标准差])。
在每个受试者中获得通过黄斑的水平和垂直 OCT 扫描的 montaged 图像。
montaged OCT 图像。
通过使用广角 OCT,我们从黄斑到周边成像了玻璃体视网膜界面。PVD 分为 5 个阶段:0 期,无 PVD(2 只眼,均为 21 岁);1 期,局限于旁黄斑至周边区域的周边 PVD(88 只眼,平均年龄 38.9±16.2 岁,平均±标准差);2 期,累及周边的中心凹旁 PVD(12 只眼,平均年龄 67.9±8.4 岁);3 期,伴有持续的玻璃体视乳头粘连的视乳头旁 PVD(7 只眼,平均年龄 70.9±11.9 岁);4 期,完全 PVD(35 只眼,平均年龄 75.1±10.1 岁)。所有 1 期 PVD(100%)均在玻璃体凝胶直接附着于皮质玻璃体和视网膜表面的旁黄斑至周边区域观察到。进展至 2 期 PVD 后,PVD 区向后扩展至中心凹后,向前扩展至周边。在 PVD 起始时(1a 期)观察到玻璃体后脱离裂孔的发生率为 41.2%。
虽然先前的研究表明 PVD 起源于中心凹旁区域,并在 60 岁以后,但我们的观察结果表明:(1)PVD 首先出现在 30 多岁,并且随着时间的推移逐渐更加广泛地出现;(2)在 PVD 起始时没有眼底疾病的超过 40%的眼与玻璃体后脱离裂孔有关;(3)PVD 首先主要在玻璃体凝胶附着于视网膜表面的旁黄斑-周边区域被注意到,并随着年龄的增长变得更加广泛,最终累及中心凹。