Downie Laura E, Cheng Ada S, Vingrys Algis J
*BOptom, PhD, FAAO †BOptom, PhD ‡BScOptom, PhD, FAAO Department of Optometry and Vision Sciences, University of Melbourne, Victoria, Australia (all authors).
Optom Vis Sci. 2014 Aug;91(8):932-8. doi: 10.1097/OPX.0000000000000246.
To assess the effect of intermediate age-related macular degeneration (AMD) on foveal cone-contrast thresholds.
We measured L-M and S-cone-contrast thresholds in subjects with intermediate AMD (n = 10) and age-matched control subjects (n = 10). Monocular, foveal 3-degree Gaussian blobs (600-millisecond raised cosine) were presented at 16 cone ratios throughout L-, M-, and S-cone space, and threshold contours were modeled with probability summation between two independent detection mechanisms. The role that preretinal absorption plays in aging was also evaluated by simulation with FG15 and neutral-density filters.
Aging results in loss of neural sensitivity, not explained by lens changes. On average, intermediate AMD was associated with reduced sensitivity in both color and luminance channels (p < 0.05) that appeared to indicate greater involvement of S-cones. When data were normalized to age-expected values, the changes to cone sensitivity were shown to be consistent (∼200% loss) across L-M, M-L, and S-cone mechanisms. In comparison, the luminance (L + M) mechanism showed relative sparing (155% loss, p < 0.05).
Eyes with the same phenotype of intermediate AMD can have varying degrees of color threshold loss. Functional markers enhance the clinical definition of disease expression in AMD.
评估中度年龄相关性黄斑变性(AMD)对中央凹视锥细胞对比度阈值的影响。
我们测量了中度AMD患者(n = 10)和年龄匹配的对照受试者(n = 10)的L-M和S视锥细胞对比度阈值。在整个L、M和S视锥细胞空间中,以16种视锥细胞比例呈现单眼、中央凹3度高斯斑点(600毫秒升余弦),并通过两个独立检测机制之间的概率总和对阈值轮廓进行建模。还通过使用FG15和中性密度滤光片进行模拟,评估视网膜前吸收在衰老过程中所起的作用。
衰老导致神经敏感性丧失,这无法用晶状体变化来解释。平均而言,中度AMD与颜色和亮度通道的敏感性降低相关(p < 0.05),这似乎表明S视锥细胞受累程度更大。当数据归一化为年龄预期值时,视锥细胞敏感性的变化在L-M、M-L和S视锥细胞机制中显示出一致性(约200%丧失)。相比之下,亮度(L + M)机制显示出相对保留(155%丧失,p < 0.05)。
具有相同中度AMD表型的眼睛可能有不同程度的颜色阈值丧失。功能标志物增强了AMD疾病表达的临床定义。