Peripapillary retinal nerve fibre layer thinning, perfusion changes and optic neuropathy in carriers of Leber hereditary optic neuropathy-associated mitochondrial variants

IF 2 Q2 OPHTHALMOLOGY
Clare Quigley, Kirk A J Stephenson, Paul F Kenna, Lorraine Cassidy
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Abstract

Background We investigated Leber hereditary optic neuropathy (LHON) families for variation in peripapillary retinal nerve fibre layer thickness and perfusion, and associated optic nerve dysfunction. Method A group of LHON-affected patients (n=12) and their asymptomatic maternal relatives (n=16) underwent examination including visual acuity (VA), visual-evoked-potential and optic nerve imaging including optical coherence tomography (OCT) and OCT angiography of the peripapillary retinal nerve fibre layer (RNFL). A control sample was also examined (n=10). The software imageJ was used to measure perfusion by assessing vessel density (VD), and statistical software ‘R’ was used to analyse data. Results The LHON-affected group (n=12) had significantly reduced peripapillary VD (median 7.9%, p=0.046). Overall, the LHON asymptomatic relatives (n=16) had no significant change in peripapillary VD (p=0.166), though three eyes had VD which fell below the derived normal range at 6% each, with variable VA from normal to blindness; LogMAR median 0, range 0–2.4. In contrast, RNFL thickness was significantly reduced in the LHON-affected group (median 51 µm, p=0.003), and in asymptomatic relatives (median 90 µm, p=0.01), compared with controls (median 101 µm). RNFL thinning had greater specificity compared with reduced perfusion for optic nerve dysfunction in asymptomatic carriers (92% vs 66%). Conclusion Overall, reduced peripapillary retinal nerve fibre layer perfusion was observed in those affected by LHON but was not reduced in their asymptomatic relatives, unlike RNFL thinning which was significantly reduced in both groups versus controls. The presence of RNFL changes was associated with signs of optic neuropathy in asymptomatic relatives. All data relevant to the study are included in the article or uploaded as supplementary information.
莱伯遗传性视神经病变相关线粒体变体携带者视网膜周围神经纤维层变薄、灌注变化和视神经病变
背景 我们调查了 Leber 遗传性视神经病变(LHON)家族的视网膜周围神经纤维层厚度和灌注的变化以及相关的视神经功能障碍。方法 对一组受 LHON 影响的患者(12 人)及其无症状的母系亲属(16 人)进行检查,包括视敏度(VA)、视觉诱发电位和视神经成像,包括视网膜周围神经纤维层(RNFL)的光学相干断层扫描(OCT)和 OCT 血管造影。还对一个对照样本(n=10)进行了检查。使用 imageJ 软件通过评估血管密度(VD)来测量灌注,并使用统计软件 "R "来分析数据。结果 受LHON影响组(12人)的毛细血管密度明显降低(中位数为7.9%,P=0.046)。总体而言,LHON 无症状亲属(n=16)的毛细血管周围 VD 无明显变化(p=0.166),但有三只眼睛的 VD 低于推导出的正常范围,每只眼睛为 6%,VA 从正常到失明不等;LogMAR 中位数为 0,范围为 0-2.4。相反,与对照组(中位数 101 µm)相比,LHON 受影响组(中位数 51 µm,p=0.003)和无症状亲属(中位数 90 µm,p=0.01)的 RNFL 厚度显著降低。与灌注减少相比,RNFL 变薄对无症状携带者视神经功能障碍的特异性更高(92% 对 66%)。结论 总体而言,在 LHON 患者中观察到毛细血管周围视网膜神经纤维层灌注减少,但在其无症状亲属中却没有减少,这与 RNFL 变薄不同,两组患者的 RNFL 变薄与对照组相比均显著减少。RNFL变化的出现与无症状亲属的视神经病变迹象有关。与该研究相关的所有数据均包含在文章中或作为补充信息上传。
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来源期刊
BMJ Open Ophthalmology
BMJ Open Ophthalmology OPHTHALMOLOGY-
CiteScore
3.40
自引率
4.20%
发文量
104
审稿时长
20 weeks
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