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Comparison of time-resolved autofluorescence in the eye-ground of healthy subjects and patients suffering from age-related macular degeneration

机译:健康受试者眼地及患有年龄相关性黄斑变性的患者的时间分辨自发荧光的比较

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Age-related macular degeneration (AMD) is the most frequent cause for blindness for person older than 65 years in western countries. Besides the subjective pain, it is also an economic problem in the ageing population. As the pathomechanism is unknown, no curative treatment is possible. International research for discovering of early age-related alterations at the fundus is directed on in vivo measurements of autofluorescence. One way is the measurement of fluorescence spectra. Unfortunately, any selective excitation of fluorophores is excluded by the absorption edge of the ocular media at 400 nm. Furthermore, the shape of fluorescence spectra is influenced by the spectral absorption of layers in front of the emitting fluorophore. Weakly emitting fluorophores are covered by intensive emitting substances. The most serious limitation in fluorescence measurements of the living human fundus is the maximal permissible exposure. For that reason, fluorescence spectra of the fundus can not be detected with a high spatial resolution. The detection of dynamic fluorescence provides substance-specific lifetimes Ti, amplitudes Ai, and information about the relative contribution Qi of components in fluorescence images. As these parameters are calculated for each image point, diagrams of Ti vs. Tj, Ai vs. Aj, and Qi vs. Qj can be drawn, in which specific clusters appear for healthy subjects or AMD - patients. The projection of lifetime - clusters onto corresponding axis represents histogram of the considered lifetime. The slope in the correlation between Ai and Aj can also be used as a discriminating mark. Considering image lines as intersection through characteristic anatomical structures (optic disc, macula) profiles of Ti, Ai, or Qi show changes of these parameters (e.g. depigmentation) as function of location, which might be specific for AMD.
机译:与年龄相关的黄斑变性(AMD)是西方人65岁的人最常见的失明原因。除了主观痛苦之外,它也是老龄化人口的经济问题。随着土地机制未知的,没有疗效治疗。发现对眼底的早期相关改动的国际研究是针对自发荧光的体内测量。一种方法是荧光光谱的测量。不幸的是,荧光团的任何选择性激发被400nm的眼介质的吸收边缘排除在外。此外,荧光光谱的形状受发射荧光团前面的层的光谱吸收的影响。弱发射荧光团被密集的发射物质覆盖。活人底的荧光测量最严重的限制是最大的允许暴露。因此,不能以高空间分辨率检测眼底的荧光光谱。动态荧光的检测提供了特定于物质的寿命Ti,巨大AI和关于荧光图像中组分的相对贡献Qi的信息。由于针对每个图像点计算这些参数,可以绘制Ti与TJ,AI与AJ和Qi与QJ的图表,其中特定群集出现为健康受试者或AMD患者。寿命 - 簇的投影到相应的轴上表示所考虑的寿命的直方图。 AI和AJ之间的相关性的斜率也可以用作辨别标记。考虑通过TI,AI或QI的特征解剖结构(光盘,黄斑)曲线作为交叉点的图像线,显示了这些参数(例如,揭示)的变化作为位置的功能,这可能是AMD的特定。

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