de Boer Irene, Steenmeijer Sylvie R, Pelzer Nadine, Al-Nofal Mays, Dijkman Greet, Notting Irene C, Terwindt Gisela M
Departments of Neurology (IB, NP, GMT) and Ophthalmology (SRS, MA, GD, ICN), Leiden University Medical Center, Leiden, the Netherlands.
J Neuroophthalmol. 2022 Mar 1;42(1):e130-e136. doi: 10.1097/WNO.0000000000001336. Epub 2021 Jul 27.
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (RVCL-S) is a monogenic small vessel disease caused by mutations in TREX1. Several organs, including retina and brain, are affected. Analyzing retinal anatomy is increasingly used as a biomarker for ophthalmological and neurological disorders (due to the shared embryological origin of retina and brain). Optical coherence tomography (OCT) provides a noninvasive cross-sectional visualization of optic disc and macula. We aimed to use OCT to investigate retinal layer thickness in RVCL-S.
Cross-sectional, 17 TREX1 mutation carriers (34 eyes) and 9 controls (18 eyes) underwent comprehensive ophthalmologic assessment followed by spectral domain OCT for measuring peripapillary retinal nerve fiber layer (pRNFL) thickness and total macular volume (TMV). Secondary outcomes included measuring thickness of individual macular retinal layers and peripapillary sectors. Findings were analyzed using generalized estimating equations to account for intereye correlation.
TREX1 mutation carriers had decreased pRNFL thickness (median [interquartile range] 76 [60-99] vs 99 [87-108] µm, P < 0.001) and TMV (8.1 [7.4-8.5] vs 8.7 [8.4-8.8] mm3, P = 0.006) compared with controls. With the exception of the temporal sector, the thickness of all peripapillary sectors was decreased in TREX1 mutation carriers. Ganglion cell layer (30 [22-37] vs 39 [36-41] µm, P < 0.001) and inner plexiform layer (27 [24-34] vs 34 [31-35], P = 0.001) were thinner in TREX1 mutation carriers. Notably, in 9 of 12 eyes with normal funduscopic examination, retinal thinning was already detected.
RVCL-S, which may serve as a vascular retinopathy model, is associated with retinal thinning in the peripapillary and macular area. OCT findings can potentially serve as early biomarkers for RVCL-S and other vascular retinopathies.
伴有脑白质脑病及全身表现的视网膜血管病变(RVCL-S)是一种由TREX1基因突变引起的单基因小血管疾病。包括视网膜和脑在内的多个器官会受到影响。分析视网膜解剖结构越来越多地被用作眼科和神经疾病的生物标志物(因为视网膜和脑有着共同的胚胎起源)。光学相干断层扫描(OCT)可对视盘和黄斑进行无创横断面成像。我们旨在利用OCT研究RVCL-S患者的视网膜层厚度。
对17名TREX1基因突变携带者(34只眼)和9名对照者(18只眼)进行横断面研究,先进行全面的眼科评估,然后采用光谱域OCT测量视乳头周围视网膜神经纤维层(pRNFL)厚度和黄斑总体积(TMV)。次要观察指标包括测量黄斑各视网膜层厚度和视乳头周围各象限厚度。采用广义估计方程分析结果,以考虑两眼之间的相关性。
与对照组相比,TREX1基因突变携带者的pRNFL厚度降低(中位数[四分位间距]76[60 - 99]μm对99[87 - 108]μm,P<0.001),TMV降低(8.1[7.4 - 8.5]对8.7[8.4 - 8.8]mm³,P = 0.006)。除颞侧象限外,TREX1基因突变携带者视乳头周围各象限厚度均降低。TREX1基因突变携带者的神经节细胞层(30[22 - 37]μm对39[36 - 41]μm,P<0.001)和内丛状层(27[24 - 34]μm对34[31 - 35]μm,P = 0.001)更薄。值得注意的是,在12只眼底检查正常的眼中,有9只已检测到视网膜变薄。
RVCL-S可作为一种视网膜血管病变模型,与视乳头周围和黄斑区视网膜变薄有关。OCT检查结果可能成为RVCL-S及其他视网膜血管病变的早期生物标志物。