Yin Wenhui, Shen Yonghui, Li Lin, Zhang Min, Liang Chunyu, Feng Ye, Yang Peizeng
Department of Ophthalmology, The First Affiliated Hospital of Zhengzhou University, Henan Province Eye Hospital, Henan International Joint Research Laboratory for Ocular Immunology and Retinal Injury Repair, Zhengzhou, Henan Province, PR China.
Department of Ophthalmology, The First Affiliated Hospital of Zhengzhou University, Henan Province Eye Hospital, Henan International Joint Research Laboratory for Ocular Immunology and Retinal Injury Repair, Zhengzhou, Henan Province, PR China.
Photodiagnosis Photodyn Ther. 2025 Jun;53:104592. doi: 10.1016/j.pdpdt.2025.104592. Epub 2025 Apr 16.
This study aimed to investigate retinal and choroidal changes at different stages of Vogt-Koyanagi-Harada (VKH) syndrome and analyze their association with visual prognosis.
This retrospective study comprised 22 healthy controls and 81 VKH patients. Patients were categorized into three groups: the initial-onset, recurrent and quiescent groups. Swept-source optical coherence tomography angiography (SS-OCTA) was used to evaluate the vascular density (VD) and perfusion area (PA) of the superficial, intermediate, and deep retinal capillary plexus (SCP, ICP and DCP), as well as the choroidal vascular index (CVI) and volume (CVV). Best-corrected visual acuity (BCVA) was assessed. Statistical analyses were used to assess the relationship between vascular parameters and visual outcomes.
Compared to the control group, patients in the initial-onset stage showed decreased ICP-PA, choriocapillaris perfusion area (CCPA), and CVI (all p < 0.05), while CVV increased (p = 0.01). The PA of retinal capillaries, CVV, and CVI in patients in recurrent or quiescent stage were lower than in the control group (all p < 0.05), and patients in recurrent stage had lower DCP-PA than in the quiescent stage (p = 0.03). The VD of the deep vascular complex, the PA of DCP, and ICP exhibited a negative correlation with BCVA across all VKH groups (all p < 0.05). Binary logistic regression analysis showed that disease course, recurrence, and SCP-PA were positively associated with irreversible complications.
The retinal and choroidal vascular systems in VKH show dysfunction throughout various stages, with recurrent inflammation intensifying microcirculatory damage. Monitoring these changes may aid to predict visual prognosis and guide intervention strategies for VKH patients.
本研究旨在探讨伏格特-小柳-原田(VKH)综合征不同阶段的视网膜和脉络膜变化,并分析它们与视力预后的关系。
这项回顾性研究包括22名健康对照者和81名VKH患者。患者被分为三组:初发组、复发组和静止组。使用扫频光学相干断层扫描血管造影(SS-OCTA)评估浅表、中间和深层视网膜毛细血管丛(SCP、ICP和DCP)的血管密度(VD)和灌注面积(PA),以及脉络膜血管指数(CVI)和体积(CVV)。评估最佳矫正视力(BCVA)。采用统计分析评估血管参数与视力结果之间的关系。
与对照组相比,初发阶段的患者ICP-PA、脉络膜毛细血管灌注面积(CCPA)和CVI降低(均p<0.05),而CVV增加(p=0.01)。复发或静止期患者的视网膜毛细血管PA、CVV和CVI低于对照组(均p<0.05),复发期患者的DCP-PA低于静止期(p=0.03)。在所有VKH组中,深层血管复合体的VD、DCP的PA和ICP与BCVA呈负相关(均p<0.05)。二元逻辑回归分析表明,病程、复发和SCP-PA与不可逆并发症呈正相关。
VKH患者的视网膜和脉络膜血管系统在各个阶段均表现出功能障碍,反复炎症会加剧微循环损伤。监测这些变化可能有助于预测VKH患者的视力预后并指导干预策略。