Hamilton Glaucoma Center, Department of Ophthalmology, University of California, La Jolla, California 92093-0946, USA.
Ophthalmology. 2013 Apr;120(4):736-44. doi: 10.1016/j.ophtha.2012.09.039. Epub 2012 Dec 12.
To estimate retinal ganglion cell (RGC) losses associated with the earliest development of visual field defects in glaucoma.
Observational cohort study.
The study group included 53 eyes of 53 patients with suspected glaucoma who were followed as part of the Diagnostic Innovations in Glaucoma (DIGS) study. These eyes had normal standard automated perimetry (SAP) visual fields at baseline and developed repeatable (3 consecutive) abnormal test results during a median follow-up of 6.7 years. An age-matched control group of 124 eyes of 124 healthy subjects recruited from the general population was included.
Estimates of RGC counts were obtained using a previously published model that combines estimates of RGC numbers from SAP sensitivity thresholds and retinal nerve fiber layer (RNFL) thickness measurements with spectral domain optical coherence tomography (SD-OCT). For eyes converting to glaucoma, estimates of RGC counts were obtained at the time (within ± 3 months) of the first abnormal visual field, representing the time of earliest detection of visual field losses.
Estimates of RGC counts in eyes converting to glaucoma versus healthy eyes.
The average RGC count estimate in the eyes with early visual field defects was 652057 ± 115829 cells, which was significantly lower than the average of 910 584 ± 142 412 cells found in healthy eyes (P < 0.001). Compared with the average number of RGCs in the healthy group, glaucomatous eyes had an average RGC loss of 28.4%, ranging from 6% to 57%, at the time of the earliest visual field defect on SAP. Retinal ganglion cell counts performed significantly better than the SD-OCT average RNFL thickness parameter in discriminating glaucomatous from healthy eyes with receiver operating characteristic curve areas of 0.95 ± 0.02 versus 0.88 ± 0.03, respectively (P = 0.001).
Glaucomatous eyes with the earliest detectable visual field loss on automated perimetry may already show substantial loss of RGCs. Empirical estimates of RGC counts combining structural and functional tests agreed closely with previous histologic reports on the number of RGCs associated with early visual fields defects on SAP.
评估青光眼最早发生视野缺损时相关的视网膜神经节细胞(RGC)损失。
观察性队列研究。
研究组包括 53 例疑似青光眼患者的 53 只眼,这些患者作为诊断性青光眼创新研究(DIGS)的一部分进行了随访。这些眼在基线时标准自动视野计(SAP)视野正常,在中位随访 6.7 年内发展为 3 次重复(连续 3 次)异常测试结果。纳入了一组年龄匹配的 124 名健康受试者的 124 只眼作为对照组,这些受试者来自普通人群。
使用先前发表的模型估算 RGC 计数,该模型结合了 SAP 敏感性阈值和视网膜神经纤维层(RNFL)厚度测量值的 RGC 数量估算值,以及光谱域光学相干断层扫描(SD-OCT)。对于转为青光眼的眼,在首次异常视野时(±3 个月内)获得 RGC 计数的估计值,这代表最早检测到视野损失的时间。
转为青光眼的眼与健康眼的 RGC 计数估计值。
早期视野缺损眼的平均 RGC 计数估计值为 652057±115829 个细胞,明显低于健康眼的平均 910584±142412 个细胞(P<0.001)。与健康组的平均 RGC 数量相比,青光眼眼在 SAP 最早出现视野缺陷时,平均 RGC 损失 28.4%,范围为 6%至 57%。在区分青光眼眼和健康眼方面,RGC 计数的受试者工作特征曲线下面积明显优于 SD-OCT 平均 RNFL 厚度参数,分别为 0.95±0.02 与 0.88±0.03(P=0.001)。
在自动视野计上最早检测到视野损失的青光眼眼可能已经出现了大量的 RGC 损失。结合结构和功能测试的 RGC 计数经验估计值与 SAP 早期视野缺陷相关的 RGC 数量的先前组织学报告非常吻合。