Lishinsky-Fischer Natan, Cnaany Yaacov, Nitzan Itay, Chowers Itay, Levy Jaime
Department of Ophthalmology, Hadassah Medical Organization and Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Ophthalmol Sci. 2025 Jul 23;5(6):100891. doi: 10.1016/j.xops.2025.100891. eCollection 2025 Nov-Dec.
To examine whether there is an association between age-related macular degeneration (AMD) and dementia using a large, multi-institutional clinical data.
A retrospective cohort study.
Patients with AMD, including both neovascular AMD (nvAMD) and non-neovascular AMD (non-nvAMD) types, along with matched controls who had a record of eye examination but no diagnosis of AMD.
Data were extracted from the 3 largest TriNetX networks (Global, United States, and Europe, Middle East, and Africa [EMEA]). Dementia diagnoses (Alzheimer disease [AD], vascular dementia, and unspecified dementia) and dementia-related medication use were compared between AMD and non-AMD groups. Diagnoses were identified using International Classification of Diseases, 10th Revision codes. Survival analyses were performed using Kaplan-Meier curves, and hazard ratios (HRs) were estimated using Cox proportional hazards models across 5-, 7-, and 10-year follow-up periods.
Hazard ratios for dementia subtypes in AMD patients versus non-AMD patients and in nvAMD patients versus non-nvAMD patients.
No significant association between AMD and AD was observed in the global network. In the United States, AMD was associated with a reduced risk of AD at 5 and 7 years (HR = 0.79 and 0.75; < 0.0001), but not at 10 years. In the EMEA cohort, a protective association emerged at 7 and 10 years (HR = 0.16 and 0.33; = 0.0063 and 0.0265). Vascular dementia showed no global association but was reduced in the United States at 5 and 7 years (HR = 0.73 and 0.79; < 0.0001 and 0.0003). Unspecified dementia was associated with increased risk globally (HR = 1.17-1.27; ≤ 0.0016), while the US data indicated a protective trend at 5 and 7 years. Dementia medication use was elevated in the global network at 7 years (HR = 1.27, < 0.0001), but lower in the United States across all time points ( < 0.01). The negative control outcome (appendicitis) showed no difference between groups. No significant differences in AD or vascular dementia were found between nvAMD and non-AMD patients, although unspecified dementia and dementia medication use were lower in the nvAMD group.
Age-related macular degeneration was not consistently positively associated with AD or vascular dementia across networks. Regional variation, particularly negative associations in the United States, suggests underlying health care or diagnostic differences.
Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
利用大型多机构临床数据研究年龄相关性黄斑变性(AMD)与痴呆症之间是否存在关联。
一项回顾性队列研究。
AMD患者,包括新生血管性AMD(nvAMD)和非新生血管性AMD(non-nvAMD)类型,以及有眼部检查记录但未诊断出AMD的匹配对照组。
从3个最大的TriNetX网络(全球、美国以及欧洲、中东和非洲[EMEA])提取数据。比较AMD组和非AMD组之间的痴呆症诊断(阿尔茨海默病[AD]、血管性痴呆和未特定的痴呆)以及与痴呆相关的药物使用情况。使用国际疾病分类第10版编码来识别诊断。使用Kaplan-Meier曲线进行生存分析,并在5年、7年和10年的随访期内使用Cox比例风险模型估计风险比(HR)。
AMD患者与非AMD患者以及nvAMD患者与non-nvAMD患者中痴呆症亚型的风险比。
在全球网络中未观察到AMD与AD之间存在显著关联。在美国,AMD在5年和7年时与AD风险降低相关(HR = 0.79和0.75;P < 0.0001),但在10年时无此关联。在EMEA队列中,在7年和10年时出现了保护性关联(HR = 0.16和0.33;P = 0.0063和0.0265)。血管性痴呆在全球范围内未显示出关联,但在美国5年和7年时有所降低(HR = 0.73和0.79;P < 0.0001和0.0003)。未特定的痴呆在全球范围内与风险增加相关(HR = 1.17 - 1.27;P ≤ 0.0016),而美国的数据表明在5年和7年时有保护趋势。在全球网络中,7年时痴呆药物使用增加(HR = 1.27,P < 0.0001),但在美国所有时间点均较低(P < 0.01)。阴性对照结果(阑尾炎)在组间无差异。nvAMD患者与非AMD患者在AD或血管性痴呆方面未发现显著差异,尽管nvAMD组中未特定的痴呆和痴呆药物使用较低。
年龄相关性黄斑变性在各网络中与AD或血管性痴呆并非始终呈正相关。区域差异,特别是在美国的负相关,表明存在潜在的医疗保健或诊断差异。
在本文末尾的脚注和披露中可能会发现专有或商业披露信息。