使用全身性β受体阻滞剂的患者中老年相关性黄斑变性进展的风险

IF 0.9
Frontiers in ophthalmology Pub Date : 2025-04-14 eCollection Date: 2025-01-01 DOI:10.3389/fopht.2025.1535791
Brady Hogan, Nihaal Mehta, Anne Strong Caldwell, A Itzam Marin, Zafar S Gill, Andres Liske-Cervantes, Marc T Mathias, Niranjan Manoharan, Alan G Palestine, Talisa E de Carlo Forest, Naresh Mandava, Anne M Lynch, Jennifer L Patnaik
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引用次数: 0

摘要

目的:本研究旨在确定长期使用系统性β受体阻滞剂是否会影响中晚期老年性黄斑变性(AMD)的进展。方法:这项前瞻性队列研究利用了uchalth Sue Anschutz-Rodgers眼科中心科罗拉多大学年龄相关性黄斑变性登记处的数据。2014年10月至2021年11月期间纳入的中度AMD (iAMD)患者。在入组时,记录患者人口统计资料和用药史。在入组时和每次随访时评估β受体阻滞剂的使用情况。参与者被要求每年返回进行影像学检查,由两名玻璃体视网膜专家使用多模态成像将图像分类为中度AMD或转化为晚期非新生血管(NNV) AMD或新生血管(NV) AMD。利用Kaplan-Meier曲线分析每个晚期AMD表型和总体转化的转化时间,并按β受体阻滞剂状态分层。从中度到晚期AMD (NNV或NV)的进展通过多模态成像确定,包括光学相干断层扫描、彩色眼底摄影和眼底后极自身荧光。结果:共有292例患者纳入研究,其中22.6%使用全体性β受体阻滞剂,36.6% (n = 107)在至少一只眼睛中从iAMD进展为晚期AMD。入组时服用β受体阻滞剂的患者更有可能转化为NV性AMD(风险比:1.92 [95% CI: 1.04, 3.55], p值= 0.036),但在调整年龄和治疗高血压后,这种关联不再显著。在向晚期NNV或任何晚期AMD的转化方面,两组间无显著差异(均p < 0.05)。结论:在调整分析中,全体性β受体阻滞剂的使用与从iAMD发展为晚期NV或NNV型AMD的风险无显著相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Risk of progression in intermediate age-related macular degeneration among patients using systemic beta-blockers.

Risk of progression in intermediate age-related macular degeneration among patients using systemic beta-blockers.

Purpose: This study aims to determine whether systemic beta-blocker use over time influences the progression from intermediate to advanced age-related macular degeneration (AMD).

Methods: This prospective cohort study utilized data from the University of Colorado Age-Related Macular Degeneration Registry at the UCHealth Sue Anschutz-Rodgers Eye Center. Patients with intermediate AMD (iAMD) enrolled between October 2014 and November 2021. At enrollment, patient demographics and medication history were recorded. Beta-blocker use was assessed at enrollment and at each follow-up visit. Participants were asked to return annually for imaging, and images were classified as either intermediate AMD or conversion to advanced non-neovascular (NNV) AMD or neovascular (NV) AMD by two vitreoretinal specialists using multimodal imaging. Time to conversion was analyzed using Kaplan-Meier curves for each advanced AMD phenotype and for overall conversion, stratified by beta-blocker status. Progression from intermediate to advanced AMD (NNV or NV) was determined using multimodal imaging, including optical coherence tomography, color fundus photography, and fundus autofluorescence of the posterior pole.

Results: A total of 292 patients were included in the study, with 22.6% using a systemic beta-blocker and 36.6% (n = 107) progressing from iAMD to advanced AMD in at least one eye. Patients on a beta-blocker at enrollment were more likely to convert to NV AMD (HR: 1.92 [95% CI: 1.04, 3.55], p-value = 0.036), but this association was no longer significant after adjusting for age and treated hypertension. No significant differences were observed in conversion to advanced NNV or any advanced AMD between groups (all p > 0.05).

Conclusions: In adjusted analyses, systemic beta-blocker use was not significantly associated with the risk of progression from iAMD to advanced NV or NNV AMD.

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