Kupersmith Mark J, Garvin Mona K, Wang Jui-Kai, Durbin Mary, Kardon Randy
New York Eye and Ear Infirmary and INN at Mount Sinai West Hospital New York, New York, United States.
Department of Electrical and Computer Engineering, The University of Iowa, Iowa City, Iowa, United States 3Department of Ophthalmology, Iowa University School of Medicine and Center for Prevention and Treatment of Visual Loss, Veterans Administration, Iow.
Invest Ophthalmol Vis Sci. 2016 Jul 1;57(8):3588-93. doi: 10.1167/iovs.15-18736.
Optical coherence tomography reveals retinal ganglion cell layer (GCL) and retinal nerve fiber layer (RNFL) thinning in chronic optic nerve injury. With acute optic nerve injury, as in acute nonarteritic anterior ischemic optic neuropathy (NAION), swelling obscures early demonstration of RNFL thinning, which might be used to evaluate therapies. We hypothesized that measurement of GCL plus inner plexiform layer (IPL) thickness and trajectory of thinning would show it is an earlier and more accurate biomarker of early permanent neuronal injury.
We prospectively studied 29 acute NAION eyes with standard automated perimetry and spectral domain (SD) optical coherence tomography for 6 months. We used a three-dimensional layer segmentation (method 1) and a commercial proprietary (method 2), to compute the combined thickness of macular GCL+IPL and method 2 to compute peripapillary RNFL thickness.
At presentation, the mean GCL+IPL thickness (78.7 μm ± 8.9) for NAION eyes, did not differ from unaffected fellow eyes (83 μm ± 6.4), using method 1 while method 2 (66.8 μm ± 18.7) failed in 34% of NAION eyes. At 1 to 2 months, 12% had RNFL loss compared to baseline, while 68% of NAION eyes had GCL+IPL thinning. The ganglion cell layer plus inner plexiform layer reduction was greatest at 1 to 2 months (19.6 μm ± 12.6) and was minimally worse after month 3. Ganglion cell layer plus inner plexiform layer thinning showed moderate to strong significant correlation with the visual acuity and mean deviation at each exam time. The retinal nerve fiber layer was not thinned until month 3.
Ganglion cell layer plus inner plexiform layer is acutely unaffected and provides a reliable measure of retinal neuronal structure using three-dimensional segmentation. Thinning develops within 1 to 2 months of onset, which is prior to RNFL swelling resolution. This suggests GCL+IPL measurement is better than the RNFL thickness to use as biomarker of early structural loss in NAION.
光学相干断层扫描显示慢性视神经损伤时视网膜神经节细胞层(GCL)和视网膜神经纤维层(RNFL)变薄。在急性视神经损伤中,如急性非动脉性前部缺血性视神经病变(NAION),肿胀会掩盖RNFL变薄的早期表现,而RNFL变薄可用于评估治疗效果。我们推测,测量GCL加内核层(IPL)厚度以及变薄轨迹将表明它是早期永久性神经元损伤的更早且更准确的生物标志物。
我们对29只急性NAION眼进行了为期6个月的前瞻性研究,采用标准自动视野计和光谱域(SD)光学相干断层扫描。我们使用三维层分割法(方法1)和一种商业专有方法(方法2)来计算黄斑区GCL+IPL的联合厚度,并使用方法2计算视乳头周围RNFL厚度。
就诊时,使用方法1,NAION眼的平均GCL+IPL厚度(78.7μm±8.9)与未受影响的对侧眼(83μm±6.4)无差异,而方法2(66.8μm±18.7)在34%的NAION眼中测量失败。在1至2个月时,与基线相比,12%的患者出现RNFL丢失,而68%的NAION眼出现GCL+IPL变薄。神经节细胞层加内核层的减少在1至2个月时最大(19.6μm±12.6),3个月后恶化程度最小。在每次检查时,神经节细胞层加内核层变薄与视力和平均偏差呈中度至强显著相关性。视网膜神经纤维层直到3个月时才变薄。
神经节细胞层加内核层在急性期未受影响,使用三维分割可提供可靠的视网膜神经元结构测量。变薄在发病后1至2个月内出现,早于RNFL肿胀消退。这表明GCL+IPL测量比RNFL厚度更适合作为NAION早期结构损伤的生物标志物。