Cennamo Gilda, Di Maio Laura Giovanna, Montorio Daniela, Tranfa Fausto, Russo Camilla, Pontillo Giuseppe, Cocozza Sirio, Esposito Roberta, Di Risi Teodolinda, Imbriaco Massimo, Spinelli Letizia, Riccio Eleonora, Pisani Antonio
Eye Clinic, Public Health Department, University of Naples "Federico II", 80100 Naples, Italy.
Department of Neurosciences, Reproductive Sciences and Dentistry, University of Naples "Federico II", 80100 Naples, Italy.
J Clin Med. 2019 Apr 17;8(4):528. doi: 10.3390/jcm8040528.
Fabry disease (FD) is a X-linked recessive lysosomal storage disorder characterized by altered biodegradation of glycosphingolipids. It is a multisystem pathology, also involving ophthalmological systems that show modifications of the vessel wall due to glycosphingolipid deposits. Optical coherence tomography angiography (OCT-A) allows for an objective analysis of retinal microvasculature alterations, evaluating retinal vessel density in macular region.
A total of 54 FD patients (34 females, 20 males, mean age 44.1 ± 15.6 years) and 70 controls (36 females, 34 males, mean age 42.3 ± 15.6 years) were included in this study. We evaluated vessel density in different macular areas (whole image, fovea, and parafovea) of both the superficial capillary plexus (SCP) and of the deep capillary plexus (DCP).
In the SCP there was a significantly lower vascular density in patients compared with controls in whole image (49.95 ± 5.17% vs. 51.99 ± 2.52%; 0.001), parafovea (52.01 ± 6.69% vs. 54.30 ± 2.61%; 0.002), and fovea (22.38 ± 9.01% vs. 29.31 ± 5.84%; < 0.0001). In the DCP the vessel density was statistically increased in each macular area in patients compared with controls (54.82 ± 8.07% vs. 50.93 ± 5.46%; 0.005, 57.76 ± 7.26% vs. 53.59 ± 5.46%; 0.0001, and 39.75 ± 8.59% vs. 34.43 ± 8.68%; 0.0001 for whole image, parafovea, and fovea, respectively).
OCT-A analysis showed that the macular vessel density was significantly reduced in the SCP and increased in the DCP in FD patients compared with controls. These findings, which might be a consequence of the alteration of vascular wall occurring in FD, support the hypothesis that the evaluation of early retinal microvascular network changes could be a useful tool in the clinical evaluation of the disease.
法布里病(FD)是一种X连锁隐性溶酶体贮积症,其特征是糖鞘脂的生物降解改变。它是一种多系统疾病,也累及眼科系统,表现为糖鞘脂沉积导致血管壁改变。光学相干断层扫描血管造影(OCT-A)可以客观分析视网膜微血管改变,评估黄斑区视网膜血管密度。
本研究共纳入54例FD患者(34例女性,20例男性,平均年龄44.1±15.6岁)和70例对照者(36例女性,34例男性,平均年龄42.3±15.6岁)。我们评估了浅表毛细血管丛(SCP)和深部毛细血管丛(DCP)在不同黄斑区域(全图、中央凹和旁中央凹)的血管密度。
在SCP中,患者全图(49.95±5.17%对51.99±2.52%;P=0.001)、旁中央凹(52.01±6.69%对54.30±2.61%;P=0.002)和中央凹(22.38±9.01%对29.31±5.84%;P<0.0001)的血管密度显著低于对照者。在DCP中,患者各黄斑区域的血管密度与对照者相比均有统计学意义的增加(全图:54.82±8.07%对50.93±5.46%;P=0.005;旁中央凹:57.76±7.26%对53.59±5.46%;P=0.0001;中央凹:39.75±8.59%对34.43±8.68%;P=0.0001)。
OCT-A分析显示,与对照者相比,FD患者SCP中的黄斑血管密度显著降低,DCP中的黄斑血管密度增加。这些发现可能是FD中血管壁改变的结果,支持了早期视网膜微血管网络变化评估可能是该疾病临床评估有用工具的假说。