Chou Chien-Chih, Lu Yi-An, Weng Chien-Hsiang, Lin Hui-Ju, Wang I-Jong, Jou Tzuu-Shuh, Wang Chun-Yuan, Tsai Fuu-Jen, Cheng Yih-Dih, Hsu Tzu-Ju, Hung Yu-Tung, Huang Yu-Han, Tien Peng-Tai
School of Medicine, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Department of Ophthalmology, Taichung Veterans General Hospital, Taichung, Taiwan.
Eye (Lond). 2024 Dec;38(18):3511-3518. doi: 10.1038/s41433-024-03348-y. Epub 2024 Sep 28.
To estimate the risk of Alzheimer's disease (AD) associated with long-term use of topical glaucoma medications among middle-aged and older glaucoma patients, and compare the AD risk among various glaucoma subtypes.
This nationwide population-based cohort study utilized insurance claims data from Taiwan's National Health Insurance Research Database between 2008 and 2019. Participants were adults aged 45 years or older either with a diagnosis of glaucoma or without. Those with glaucoma must have received single antiglaucomatous medication (including α2-adrenergic agonists, cholinergic agonists, beta-blockers, prostaglandin analogs, and pilocarpine) for over 90 days. Those with pre-existing AD diagnoses prior to the index date were excluded.
A total of 202,000 participants were included in the study, with 101,000 in each group (glaucoma and control groups). Glaucoma patients on topical alpha-2 adrenergic agonist monotherapy exhibited a significantly higher AD risk (aHR 1.15, 95% CI = 1.01-1.31) compared to those on beta-blockers. Glaucoma was further categorized into primary open-angle glaucoma (POAG), normal-tension glaucoma (NTG), primary angle-closure glaucoma (PACG), and unspecified glaucoma. Irrespective of the type of glaucoma, individuals with glaucoma had a significantly higher risk of AD compared to those without glaucoma (POAG: aHR 1.23, 95% CI = 1.08-1.40; NTG: aHR 1.49, 95% CI = 1.19-1.85; PACG: aHR 1.35, 95% CI = 1.19-1.52; unspecified glaucoma: aHR 1.36, 95% CI = 1.23-1.50).
Topical alpha-2 adrenergic agonists might pose increased AD risk in individuals with glaucoma compared to beta-blockers. Accordingly, their utilization should be undertaken judiciously, especially in middle-aged and older populations. Our findings also indicate glaucoma may increase the risk of AD regardless of glaucoma subtype.
评估中老年青光眼患者长期使用局部青光眼药物与患阿尔茨海默病(AD)的风险,并比较不同青光眼亚型的AD风险。
这项基于全国人口的队列研究利用了2008年至2019年台湾国民健康保险研究数据库中的保险理赔数据。参与者为45岁及以上的成年人,有或无青光眼诊断。患有青光眼的患者必须接受单一抗青光眼药物(包括α2肾上腺素能激动剂、胆碱能激动剂、β受体阻滞剂、前列腺素类似物和毛果芸香碱)治疗超过90天。在索引日期之前已确诊AD的患者被排除。
共有202,000名参与者纳入研究,每组各101,000名(青光眼组和对照组)。与使用β受体阻滞剂的青光眼患者相比,局部使用α2肾上腺素能激动剂单药治疗的青光眼患者患AD的风险显著更高(校正风险比[aHR]为1.15,95%置信区间[CI]=1.01-1.31)。青光眼进一步分为原发性开角型青光眼(POAG)、正常眼压性青光眼(NTG)、原发性闭角型青光眼(PACG)和未明确的青光眼。无论青光眼类型如何,与无青光眼者相比,青光眼患者患AD的风险显著更高(POAG:aHR 1.23,95%CI=1.08-1.40;NTG:aHR 1.49,95%CI=1.19-1.85;PACG:aHR 1.35,95%CI=1.19-1.52;未明确的青光眼:aHR 1.36,95%CI=1.23-1.50)。
与β受体阻滞剂相比,局部使用α2肾上腺素能激动剂可能会增加青光眼患者患AD的风险。因此,应谨慎使用,尤其是在中老年人群中。我们的研究结果还表明,无论青光眼亚型如何,青光眼都可能增加患AD的风险。