Gao Audrey, Tuz-Zahra Fatima, Vig Viha, Zeng Rebecca, Tripodis Yorghos, Stein Thor D, Alosco Michael L, Ness Steven, Chen Xuejing, Siegel Nicole, Subramanian Manju L
Department of Ophthalmology, Boston University Chobanian & Avedisian School of Medicine, Boston, Massachusetts.
Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts.
Ophthalmol Retina. 2025 Aug 16. doi: 10.1016/j.oret.2025.08.010.
Vascular disease is associated with increased incidence of dementia and has the potential to be an indicator of underlying cognitive disease. The goal of this study is to investigate the association between retinal vascular occlusions and neurodegenerative disorders that lead to dementia, including all-cause dementia, Alzheimer disease (AD), and vascular dementia (VD).
Retrospective longitudinal cohort study.
This study consists of 502 133 participants from the UK Biobank, aged 40 to 69 years at recruitment. There are 1463 individuals with retinal vascular occlusion and 500 670 individuals without.
Individuals were categorized as having retinal vein occlusion (RVO), retinal artery occlusion (RAO), and any retinal vascular occlusion (both RVO and RAO). Prevalence and incidence of all-cause dementia, AD, and VD were calculated. The patients with RVO were then matched on age, sex, education, and employment score on a 1:3 ratio to controls. Univariate and multivariate Cox proportional hazards models on the matched participants were used to determine associations over time to all-cause dementia, AD, and VD, with added adjustments for diabetes, hypertension, and smoking status.
Prevalence and hazard ratios (HRs) of all-cause dementia, AD, and VD.
The prevalence of all-cause dementia and AD is significantly increased among patients with RVO, RAO, and any retinal vascular occlusion, whereas the prevalence of VD is significantly increased in RVO and any retinal vascular occlusion. In the matched analysis, increased risk for all-cause dementia was seen in patients with any retinal vascular occlusion (HR, 1.52; confidence interval [CI], 1.11-2.07, P = 0.01) and RVO (HR, 1.38; CI, 1.01-1.90, P = 0.04). When adjusting for covariates, RVO did not show increased risk of all-cause dementia, AD, and VD.
Any retinal vascular occlusions and RVO are associated with increased risk of all-cause dementia, and individuals with RVO also have higher risk of VD. After adjusting for shared risk factors, there is no association between dementia and retinal vascular occlusions. Findings from this study are both consistent and in conflict with prior reports, and indicate that the connection between retinal vascular occlusions and neurodegenerative diseases causing dementia may be due to their shared pathogenesis and risk factors.
FINANCIAL DISCLOSURE(S): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
血管疾病与痴呆发病率增加相关,有可能作为潜在认知疾病的一个指标。本研究的目的是调查视网膜血管阻塞与导致痴呆的神经退行性疾病之间的关联,包括全因性痴呆、阿尔茨海默病(AD)和血管性痴呆(VD)。
回顾性纵向队列研究。
本研究包括来自英国生物银行的502133名参与者,招募时年龄在40至69岁之间。有1463名个体患有视网膜血管阻塞,500670名个体未患。
个体被分类为患有视网膜静脉阻塞(RVO)、视网膜动脉阻塞(RAO)以及任何视网膜血管阻塞(RVO和RAO两者)。计算全因性痴呆、AD和VD的患病率和发病率。然后将RVO患者按年龄、性别、教育程度和就业得分以1:3的比例与对照组进行匹配。对匹配的参与者使用单变量和多变量Cox比例风险模型来确定随时间与全因性痴呆、AD和VD的关联,并额外调整糖尿病、高血压和吸烟状况。
全因性痴呆、AD和VD的患病率及风险比(HRs)。
RVO、RAO以及任何视网膜血管阻塞患者中全因性痴呆和AD的患病率显著增加,而RVO和任何视网膜血管阻塞患者中VD的患病率显著增加。在匹配分析中,任何视网膜血管阻塞患者(HR,1.52;置信区间[CI],1.11 - 2.0, P = 0.01)和RVO患者(HR,1.38;CI,1.0, P = 0.04)全因性痴呆风险增加。在调整协变量后,RVO在全因性痴呆、AD和VD方面未显示出增加的风险。
任何视网膜血管阻塞和RVO与全因性痴呆风险增加相关,RVO个体患VD的风险也更高。在调整共同风险因素后,痴呆与视网膜血管阻塞之间无关联。本研究结果与先前报告既有一致之处也有冲突之处,表明视网膜血管阻塞与导致痴呆的神经退行性疾病之间的联系可能归因于它们共同的发病机制和风险因素。
在本文末尾的脚注和披露中可能会找到专有或商业披露信息。