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The effect of glaucoma on central visual function.

机译:青光眼对中央视觉功能的影响。

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摘要

Glaucoma has traditionally been thought to affect peripheral visual function in its early stages and to spare central visual function until late in the disease process. The basis for this assumption has been the reliance on Goldmann-type perimetry, a rather sensitive method for assessing the peripheral visual function, and on Snellen-type visual acuity measurements, a rather insensitive method of assessing central visual function. This belief has persisted despite frequent complaints from patients with glaucoma that their central vision is disturbed. Over the past two decades, several investigations of central visual functions and their anatomic substrate have challenged this assumption. Histologic studies of the nerve fiber layer in eyes with glaucoma suggest that the number of ganglion cells subserving macular function is decreased even in early stages of the disease. In addition, afferent pupillary defects (a gross measurement of macular nerve fiber function) may also be present in eyes with early glaucoma. Several studies have demonstrated that color perception (largely mediated by the fovea) is defective in glaucoma. Furthermore, defects in color perception may even precede the development of visual field abnormalities. Seventy-eight percent of patients with early glaucomatous visual field defects were found to have a defect in color perception when tested with a desaturated D-15 color panel that tests only the central 1.5 degrees. In addition, both chromatic and achromatic foveal perception channels are defective in eyes with glaucoma and even in some eyes of those with suspected glaucoma. Contrast sensitivity has become recognized as an important component of visual function. Partial loss of contrast sensitivity may cause a degradation in the quality of perception even though the Snellen visual acuity remains normal. Although contrast sensitivity is not entirely a macular function, it has been shown that as little as 3 degrees of disturbance of the macula (eg, with macular degeneration or with an artificial central scotoma) will reduce the contrast sensitivity, suggesting that this modality is indeed mediated to a significant extent by this portion of the retina. Spatial contrast sensitivity appears to be reduced in patients with glaucoma. However, because of overlap and lack of a sharp cutoff measurement, present testing procedures fail to allow a clear distinction between the glaucomatous and normal populations. Although reduced temporal contrast sensitivity has been demonstrated in glaucomatous eyes by others, I undertook a systematic investigation of this function in a large group of patients with glaucoma and with suspected glaucoma.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:传统上认为青光眼在其早期阶段会影响周围的视觉功能,并在疾病过程的后期保留中央视觉功能。该假设的基础是依赖于戈德曼型视野检查法,一种相当灵敏的评估周围视觉功能的方法,以及依赖于斯内伦型视敏度测量,一种相当不灵敏的评估中央视觉功能的方法。尽管青光眼患者经常抱怨他们的中心视力受到干扰,但这种信念仍然存在。在过去的二十年中,对中央视觉功能及其解剖基底的几项研究对这一假设提出了挑战。对青光眼眼中神经纤维层的组织学研究表明,即使在疾病的早期阶段,支持黄斑功能的神经节细胞的数量也会减少。此外,患有早期青光眼的眼睛中也可能出现传入瞳孔缺损(黄斑神经纤维功能的总体测量值)。几项研究表明,青光眼的颜色感知(主要由中央凹介导)是有缺陷的。此外,色彩感知的缺陷甚至可能在视野异常发展之前。当使用仅测试中心1.5度的去饱和D-15彩色面板进行测试时,发现有78%的具有早期青光眼视野缺损的患者在色彩感知方面存在缺陷。此外,在青光眼的眼睛中,甚至在怀疑患有青光眼的人的某些眼睛中,彩色和无彩色中央凹感知通道均存在缺陷。对比度敏感度已被认为是视觉功能的重要组成部分。即使Snellen视敏度保持正常,对比度敏感性的部分丧失也可能导致感知质量下降。尽管对比敏感度不完全是一种黄斑功能,但已证明,低至3度的黄斑紊乱(例如,黄斑变性或人工中心性暗点)会降低对比敏感度,这表明这种方式的确是视网膜的这一部分在很大程度上介导了介导作用。青光眼患者的空间对比敏感性似乎降低。但是,由于重叠和缺乏精确的截止值测量,当前的测试程序无法清晰区分青光眼和正常人群。尽管其他人已经在青光眼中证明了时间对比敏感度的降低,但我对一大批青光眼和疑似青光眼患者进行了系统性研究(摘要截断了400字)

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