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[遗传性视网膜疾病中视网膜色素上皮和光感受器装置的形态学和功能指标]

[Morphological and functional indicators of retinal pigment epithelium and photoreceptor apparatus in inherited retinal diseases].

作者信息

Sheremet N L, Ronzina I A, Mikaelyan A A, Zhorzholadze N V, Plyukhova A A, Kiselev S L

机构信息

Research Institute of Eye Diseases, Moscow, Russia.

Vavilov Institute of General Genetics, Moscow, Russia.

出版信息

Vestn Oftalmol. 2020;136(4. Vyp. 2):183-192. doi: 10.17116/oftalma2020136042183.

Abstract

PURPOSE

To evaluate the relationship between the morphological and functional parameters of retinal pigment epithelium (RPE) and photoreceptors (PR) in inherited retinal diseases (IRD).

MATERIAL AND METHODS

The study included 52 patients (104 eyes), 23 of them with Stargardt Disease (STGD), 19 with cone-rod dystrophy (CRD), 10 with retinitis pigmentosa/pigmentary abiotrophy (RP) of comparable disease durations. All patients underwent standard and additional ophthalmological examination: fundus autofluorescence (AF), spectral optical coherence tomography (OCT), computer perimetry (CP), electro-oculography (EOG), Ganzfeld electroretinography (gERG).

RESULTS

Comparison of the groups of IRD patients and groups according to the degree of RPE damage with the control group revealed an increase in differences in the EOG and gERG indicators as the area and depth of damage to the RPE and PR progressed. The patterns of changes in RPE and PR, the frequency of their occurrence with IRD in this patient sample are described. A moderate correlation was found between the amount of RPE loss and EOG light rise, as well as between the defect of the ellipsoid zone and the amplitude of α- and β-waves, the latency of β-wave of the gERG. Some patients showed a mismatch between a small defect of the ellipsoid zone and RPE with significant damage to the visual field and reduction of the EOG and gERG indicators. The obtained electrophysiological indicators revealed pathological changes in RPE and PR, more significant and widespread in some cases than it was shown with visualization methods. Weak and moderate correlations between visual acuity, and RPE damage and light sensitivity index with loss of ellipsoid zone were calculated.

CONCLUSIONS

Modern methods of retinal examination can help obtain complete and versatile picture of morphological and functional state of the retina in IDR that supplement each other. EOG and gERG have capability to determine the degree of RPE and PR functions impairment including those cases when morphological studies are not sufficiently informative.

摘要

目的

评估遗传性视网膜疾病(IRD)中视网膜色素上皮(RPE)和光感受器(PR)的形态学与功能参数之间的关系。

材料与方法

该研究纳入了52例患者(104只眼),其中23例患有斯塔加特病(STGD),19例患有视锥视杆营养不良(CRD),10例患有视网膜色素变性/色素性营养障碍(RP),且疾病持续时间相近。所有患者均接受了标准及额外的眼科检查:眼底自发荧光(AF)、光谱光学相干断层扫描(OCT)、电脑视野计检查(CP)、眼电图(EOG)、全视野视网膜电图(gERG)。

结果

将IRD患者组以及根据RPE损伤程度划分的组与对照组进行比较,结果显示随着RPE和PR损伤面积及深度的进展,EOG和gERG指标的差异增大。描述了该患者样本中RPE和PR的变化模式及其在IRD中的发生频率。发现RPE损失量与EOG光反应升高之间、椭圆体带缺陷与gERG的α波和β波振幅、β波潜伏期之间存在中度相关性。一些患者的椭圆体带和RPE小缺陷与视野严重受损以及EOG和gERG指标降低之间存在不匹配。所获得的电生理指标显示RPE和PR存在病理变化,在某些情况下比可视化方法所显示的更为显著和广泛。计算了视力、RPE损伤以及椭圆体带缺失的光敏感度指数之间的弱和中度相关性。

结论

现代视网膜检查方法有助于全面、多维度地了解IRD中视网膜的形态学和功能状态,这些方法相互补充。EOG和gERG能够确定RPE和PR功能受损程度,包括形态学研究信息不足的情况。

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