Miyahara E, Pokorny J, Smith V C, Szewczyk E, McCartin J, Caldwell K, Klerer A
Department of Psychology, California State University, Fullerton, 92834-6846, USA.
Vis Neurosci. 2004 May-Jun;21(3):465-9. doi: 10.1017/s0952523804213177.
An automated, computerized color-vision test was designed to diagnose congenital red-green color-vision defects. The observer viewed a yellow appearing CRT screen. The principle was to measure increment thresholds for three different chromaticities, the background yellow, a red, and a green chromaticity. Spatial and temporal parameters were chosen to favor parvocellular pathway mediation of thresholds. Thresholds for the three test stimuli were estimated by four-alternative forced-choice (4AFC), randomly interleaved staircases. Four 1.5-deg, 4.2 cd/m2 square pedestals were arranged as a 2 x 2 matrix around the center of the display with 15-minute separations. A trial incremented all four squares by 1.0 cd/m2 for 133 ms. One randomly chosen square included an extra increment of a test chromaticity. The observer identified the different appearing square using the cursor. Administration time was approximately 5 minutes. Normal trichromats showed clear Sloan notch as defined by log (deltaY/deltaR), whereas red-green color defectives generally showed little or no Sloan notch, indicating that their thresholds were mediated by their luminance system, not by the chromatic system. Data from 107 normal trichromats showed a mean Sloan notch of 0.654 (SD = 0.123). Among 16 color-vision defectives tested (2 protanopes, 1 protanomal, 6 deuteranopes, & 7 deuteranomals), the Sloan notch was between -0.062 and 0.353 for deutans and was < -0.10 for protans. A sufficient number of color-defective observers have not yet been tested to determine whether the test can reliably discriminate between protans and deutans. Nevertheless, the current data show that the test can work as a quick diagnostic procedure (functional trichromatism or dichromatism) of red-green color-vision defect.
设计了一种自动化的计算机化色觉测试,用于诊断先天性红绿色觉缺陷。观察者观看呈现黄色的阴极射线管(CRT)屏幕。其原理是测量三种不同色度(背景黄色、红色和绿色色度)的增量阈值。选择空间和时间参数以利于由小细胞通路介导阈值。通过四选一强制选择(4AFC)、随机交错的阶梯法估计三种测试刺激的阈值。四个1.5度、4.2坎德拉每平方米的方形基座围绕显示器中心排列成2×2矩阵,间隔15分钟。一次试验中,所有四个方块的亮度在133毫秒内增加1.0坎德拉每平方米。随机选择的一个方块包含测试色度的额外增量。观察者使用光标识别出外观不同的方块。测试时间约为5分钟。正常三色视者呈现出由log(deltaY/deltaR)定义的清晰的斯隆缺口,而红绿色觉缺陷者通常几乎没有或没有斯隆缺口,这表明他们的阈值是由亮度系统介导的,而非色度系统。107名正常三色视者的数据显示,斯隆缺口的平均值为0.654(标准差=0.123)。在测试的16名色觉缺陷者(2名红色盲、1名红色弱、6名绿色盲和7名绿色弱)中,绿色盲的斯隆缺口在-0.062至0.353之间,红色盲的斯隆缺口小于-0.10。尚未对足够数量的色觉缺陷观察者进行测试,以确定该测试是否能可靠地区分红色盲和绿色盲。然而,目前的数据表明,该测试可作为红绿色觉缺陷的快速诊断程序(功能性三色视或二色视)。