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Leber 遗传性视神经病变和显性视神经萎缩的视网膜神经节细胞复合体的光相干断层扫描。

Optical Coherence Tomography of the Retinal Ganglion Cell Complex in Leber's Hereditary Optic Neuropathy and Dominant Optic Atrophy.

机构信息

a Department of Ophthalmology , Doheny Eye Center , Los Angeles , CA , USA.

b Department of Ophthalmology, David Geffen School of Medicine , University of California Los Angeles , Los Angeles , CA , USA.

出版信息

Curr Eye Res. 2019 Jun;44(6):638-644. doi: 10.1080/02713683.2019.1567792. Epub 2019 Feb 4.

DOI:10.1080/02713683.2019.1567792
PMID:30649972
Abstract

: Mitochondrial optic neuropathies such as Leber's Hereditary Optic Neuropathy (LHON) and Dominant Optic Atrophy (DOA) have been shown to produce an optic neuropathy secondary to retinal ganglion cell loss with thinning of the retinal ganglion cell complex (RGCC). : We performed a retrospective analysis assessing the thicknesses of the peripapillary retinal nerve fiber layer (pRNFL) along with the macular retinal ganglion cell-inner plexiform layer (RGC-IPL) using optical coherence tomography (OCT). We compared these changes among acute and chronic LHON, DOA, and normal healthy control patients. : Patients with chronic LHON exhibited statistically significant thinning of the RNFL in the superior, nasal, and inferior quadrants of the retina. In acute LHON, the RNFL was relatively thicker in all but the temporal quadrant when compared with respective quadrants in normal eyes; however, statistical significance was not achieved. In DOA, the RNFL was thinnest in the superior and inferior quadrants of the retina, measuring between acute and chronic LHON thickness values. In chronic LHON and DOA, both the pRNFL and RGC-IPL were significantly thinner in all four retinal quadrants relative to controls. : This article represents the first comparative study of the RGCC between LHON and DOA. Our findings demonstrated significant thickness reductions in pRNFL and macular RGC-IPL in patients with LHON and DOA, with different specific patterns consistent with the general patterns of thinning classically observed. This study suggests the usefulness of the RGCC as a potential biomarker for assessing disease in patients with LHON and DOA.

摘要

: 线粒体视神经病变,如莱伯遗传性视神经病变(LHON)和显性视神经萎缩(DOA),已被证明会导致视网膜神经节细胞(RGC)丢失引起的视神经病变,视网膜神经节细胞复合体(RGCC)变薄。 : 我们进行了一项回顾性分析,使用光学相干断层扫描(OCT)评估了视盘周围视网膜神经纤维层(pRNFL)和黄斑视网膜神经节细胞-内丛状层(RGC-IPL)的厚度。我们比较了急性和慢性 LHON、DOA 以及正常健康对照组患者之间的这些变化。 : 慢性 LHON 患者的视网膜上、鼻侧和下象限的 RNFL 厚度明显变薄。与正常眼相比,急性 LHON 患者除颞侧象限外,所有象限的 RNFL 相对较厚;然而,未达到统计学意义。在 DOA 中,视网膜上、下象限的 RNFL 最薄,介于急性和慢性 LHON 厚度值之间。在慢性 LHON 和 DOA 中,与对照组相比,pRNFL 和黄斑 RGC-IPL 在所有四个视网膜象限均明显变薄。 : 本文代表了 LHON 和 DOA 之间 RGCC 的首次比较研究。我们的研究结果表明,LHON 和 DOA 患者的 pRNFL 和黄斑 RGC-IPL 厚度明显减少,具有不同的特定模式,与经典观察到的变薄模式一致。这项研究表明,RGCC 作为评估 LHON 和 DOA 患者疾病的潜在生物标志物具有一定的价值。

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