Testa Francesco, Melillo Paolo, Rossi Settimio, Marcelli Vincenzo, de Benedictis Antonella, Colucci Raffaella, Gallo Beatrice, Brunetti-Pierri Raffaella, Donati Simone, Azzolini Claudio, Marciano Elio, Simonelli Francesca
a Eye Clinic, Multidisciplinary Department of Medical , Surgical and Dental Sciences, University of Campania Luigi Vanvitelli , Naples , Italy.
b Audiology Unit, Department of Neuroscience , Reproductive and Odontostomatologic Science, University of Naples Federico II , Naples , Italy.
Ophthalmic Genet. 2018 Jan-Feb;39(1):17-21. doi: 10.1080/13816810.2017.1329445. Epub 2017 Jul 13.
To investigate the prevalence of macular abnormalities in patients affected by Usher syndrome (USH), by comparing the clinical findings between two types (i.e., USH1 and USH2).
A retrospective study was performed by reviewing optical coherence tomography (OCT) in 134 USH patients to determine the presence of macular abnormalities, including cystoid macular edema (CME), epiretinal membrane (ERM), vitreo-macular traction syndrome (VMT), and macular hole (MH).
Macular abnormalities were observed in 126/268 (47.0%) examined eyes. The most frequent abnormality was ERM observed in 51 eyes (19%), followed by CME observed in 42 eyes (15.7%). Moreover, CME was significantly (p < 0.05) associated with younger age (CME: 30.1 ± 11.1 years; without CME: 36.9 ± 14.9 years), whereas VMT and full thickness MH were associated with older age (p < 0.05). Moreover, a significantly (p < 0.05) decreased best-corrected visual acuity was associated with MH compared to eyes without MH. Finally, CME was more frequent in USH1 compared to USH2.
Our study, for the first time in the literature, showed the distribution of all macular abnormalities assessed by SD-OCT in a large USH cohort, comparing USH1 and USH2 patients. We observed that ocular abnormalities are highly prevalent in USH patients compared to general population, with ERM and CME being the most common alterations. Based on these findings, OCT screening in USH patients is recommended for early detection of macular changes and early treatment.
通过比较两种类型(即USH1和USH2)的临床发现,研究患有Usher综合征(USH)患者黄斑异常的患病率。
进行一项回顾性研究,通过回顾134例USH患者的光学相干断层扫描(OCT)来确定黄斑异常的存在,包括黄斑囊样水肿(CME)、视网膜前膜(ERM)、玻璃体黄斑牵引综合征(VMT)和黄斑裂孔(MH)。
在268只受检眼中,有126只(47.0%)观察到黄斑异常。最常见的异常是51只眼(19%)观察到的ERM,其次是42只眼(15.7%)观察到的CME。此外,CME与较年轻的年龄显著相关(p<0.05)(CME:30.1±11.1岁;无CME:36.9±14.9岁),而VMT和全层MH与年龄较大相关(p<0.05)。此外,与无MH的眼相比,MH与最佳矫正视力显著下降相关(p<0.05)。最后,与USH2相比,CME在USH1中更常见。
我们的研究首次在文献中展示了在一个大型USH队列中通过SD-OCT评估的所有黄斑异常的分布情况,比较了USH1和USH2患者。我们观察到,与普通人群相比,USH患者的眼部异常非常普遍,ERM和CME是最常见的改变。基于这些发现,建议对USH患者进行OCT筛查,以早期发现黄斑变化并尽早治疗。