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帕金森病患者的中央视力受损。

Foveal vision is impaired in Parkinson's disease.

机构信息

Department of Neurology, State University of New York Downstate Medical Center, 450 Clarkson Avenue, Box 1213, Brooklyn, NY 11203-2098, USA.

出版信息

Parkinsonism Relat Disord. 2013 Jan;19(1):1-14. doi: 10.1016/j.parkreldis.2012.07.012. Epub 2012 Sep 19.

Abstract

PURPOSE

The article aims to review foveal involvement in Parkinson's disease.

SCOPE

Clinical observations as well as electrophysiological and anatomical studies in animal models provide evidence that Parkinson's disease (PD) affects vision. The retina is the most distal locus of visual dysfunction in PD as shown by electroretinographic (ERG) and optical coherence tomographic (OCT) studies. Thinning of the retinal nerve fibre layer (RNFL) and the fovea has been reported in PD. This review summarises retinal physiology and foveal visual dysfunction in PD and quantification of retinal thinning as reported in different studies and using different instruments. At this point due to methodological diversity and relatively low number of subjects studied, a meta-analysis is not yet possible. Results obtained on one equipment are not yet transferable to another. The author also briefly alludes to some links of visual processing deficits beyond visual detection, such as visual discrimination, visual categorisation and visuospatial orientation in PD.

CONCLUSIONS

There are some promising results suggesting the potential applicability of ST-Oct as a biomarker in PD. Furthermore, these data raise some interesting neurobiological questions. However, there are identifiable pitfalls before OCT quantification may be used as a biomarker in PD. Analysis standardisation is needed on a larger than existing healthy and patient population. Furthermore, longitudinal studies are needed. The exact relationship between retinal foveal deficits and visuo-cognitive impairment in PD remains a challenging research question.

摘要

目的

本文旨在综述帕金森病(PD)的黄斑受累情况。

范围

临床观察以及动物模型的电生理和解剖研究均表明 PD 会影响视力。视网膜是 PD 患者视觉功能障碍的最远端部位,这可通过视网膜电图(ERG)和光学相干断层扫描(OCT)研究证实。已有研究报道 PD 患者的视网膜神经纤维层(RNFL)和黄斑变薄。本综述总结了 PD 中的视网膜生理学和黄斑视觉功能障碍,以及不同研究和使用不同仪器报告的视网膜变薄的量化情况。目前,由于方法学的多样性和研究对象相对较少,尚无法进行荟萃分析。在一种设备上获得的结果尚不能推广到另一种设备。作者还简要提到了 PD 中视觉处理缺陷的一些联系,例如视觉检测之外的视觉辨别、视觉分类和视空间定向。

结论

有一些有前途的结果表明,ST-Oct 作为 PD 的生物标志物具有潜在的适用性。此外,这些数据提出了一些有趣的神经生物学问题。然而,在 OCT 量化可作为 PD 的生物标志物之前,还存在一些明显的缺陷。需要在比现有健康人群和患者人群更大的范围内进行分析标准化。此外,还需要进行纵向研究。视网膜黄斑缺陷与 PD 中的视认知障碍之间的确切关系仍然是一个具有挑战性的研究问题。

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