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Role of monocarboxylate transporters in regulating metabolic homeostasis in the outer retina: Insight gained from cell-specific Bsg deletion.单羧酸转运蛋白在外网状层代谢稳态调控中的作用:来自细胞特异性 Bsg 缺失的见解。
FASEB J. 2020 Apr;34(4):5401-5419. doi: 10.1096/fj.201902961R. Epub 2020 Feb 28.
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Age-related macular degeneration.年龄相关性黄斑变性。
Lancet. 2018 Sep 29;392(10153):1147-1159. doi: 10.1016/S0140-6736(18)31550-2.
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EFFICACY OF ADJUVANT TOPICAL DORZOLAMIDE-TIMOLOL IN PATIENTS WITH NEOVASCULAR AGE-RELATED MACULAR DEGENERATION REFRACTORY TO ANTI-VASCULAR ENDOTHELIAL GROWTH FACTOR THERAPY.辅助局部多佐胺-噻吗洛尔治疗对血管内皮生长因子治疗抵抗的新生血管性年龄相关性黄斑变性患者的疗效。
Retina. 2019 Oct;39(10):1953-1958. doi: 10.1097/IAE.0000000000002293.
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Prevalence and causes of vision loss in high-income countries and in Eastern and Central Europe in 2015: magnitude, temporal trends and projections.2015 年高收入国家和东欧及中欧视力丧失的患病率及其病因:规模、时间趋势和预测。
Br J Ophthalmol. 2018 May;102(5):575-585. doi: 10.1136/bjophthalmol-2017-311258. Epub 2018 Mar 15.
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SYSTEMIC BETA-BLOCKERS AND RISK OF PROGRESSION TO NEOVASCULAR AGE-RELATED MACULAR DEGENERATION.系统β受体阻滞剂与新生血管性年龄相关性黄斑变性进展的风险。
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Characterizing Disease Burden and Progression of Geographic Atrophy Secondary to Age-Related Macular Degeneration.描述与年龄相关性黄斑变性相关的地图样萎缩的疾病负担和进展。
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Association between open-angle glaucoma and neovascular age-related macular degeneration: a case-control study.开角型青光眼与新生血管性年龄相关性黄斑变性之间的关联:一项病例对照研究。
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在美国保险理赔数据库中,眼部抗高血压药物与年龄相关性黄斑变性的发生和进展的关系。

Association of Ocular Antihypertensive Medications and the Development and Progression of Age-related Macular Degeneration in a U.S. Insurance Claims Database.

机构信息

Department of Ophthalmology and Visual Sciences, University of Michigan, Kellogg Eye Center, Ann Arbor, Michigan, USA.

Department of Ophthalmology, Stanford University, Byers Eye Institute, Palo Alto, California, USA.

出版信息

Curr Eye Res. 2021 Jul;46(7):995-1001. doi: 10.1080/02713683.2020.1849731. Epub 2020 Dec 9.

DOI:10.1080/02713683.2020.1849731
PMID:33174463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8187259/
Abstract

: To assess whether ocular antihypertensives are associated with the development and progression of age-related macular degeneration (AMD).: This retrospective, observational cohort study using healthcare claims data from a U.S. nationwide managed-care network between January 1, 2006 and December 31, 2016, included enrollees ≥40 years old with primary open-angle glaucoma with or without a diagnosis of nonexudative AMD at the index date. Hazard ratios (HR) for developing AMD or progressing from nonexudative to exudative AMD with exposure to ocular antihypertensive medications were analyzed.: Of 132 963 eligible enrollees, 118 174 (87.5%) had no diagnosis of AMD at baseline while 14 789 (12.5%) had adiagnosis of nonexudative AMD. Prostaglandin analog exposure had adecreased hazard of developing AMD among individuals without baseline disease (HR, 0.90; 95% CI, 0.87-0.94; < .0001), while topical alpha-agonist exposure demonstrated an increased hazard of AMD development (HR, 1.08; 95% CI, 1.03-1.14; = .004). Among patients with baseline nonexudative AMD, topical carbonic anhydrase inhibitor exposure was associated with adecreased hazard of progressing to exudative disease (HR, 0.84; 95% CI, 0.71-0.99; = .04) while topical alpha-agonists had increased hazard (HR, 1.17; 95% CI, 1.01-1.36; = .04).: Certain ocular antihypertensive medications may be associated with development or progression of AMD. Their role in AMD pathogenesis should be better understood as they are considered for therapeutics in this disease.

摘要

评估眼部降压药是否与年龄相关性黄斑变性(AMD)的发生和进展有关。这项回顾性观察队列研究使用了美国全国管理式医疗网络 2006 年 1 月 1 日至 2016 年 12 月 31 日的医疗保健索赔数据,纳入了索引日期时患有原发性开角型青光眼且伴有或不伴有非渗出性 AMD 诊断的≥40 岁患者。分析了暴露于眼部降压药物的情况下,发生 AMD 或从不渗出性 AMD 进展为渗出性 AMD 的风险比(HR)。在 132963 名合格的参保者中,118174 名(87.5%)基线时无 AMD 诊断,14789 名(12.5%)有非渗出性 AMD 诊断。在无基线疾病的个体中,前列腺素类似物暴露可降低发生 AMD 的风险(HR,0.90;95%CI,0.87-0.94;<0.0001),而局部α激动剂暴露则显示出 AMD 发展的风险增加(HR,1.08;95%CI,1.03-1.14;=0.004)。在基线有非渗出性 AMD 的患者中,局部碳酸酐酶抑制剂暴露与进展为渗出性疾病的风险降低相关(HR,0.84;95%CI,0.71-0.99;=0.04),而局部α激动剂的风险增加(HR,1.17;95%CI,1.01-1.36;=0.04)。某些眼部降压药物可能与 AMD 的发生或进展有关。在考虑将其用于治疗这种疾病时,应更好地了解它们在 AMD 发病机制中的作用。