Department of Ophthalmology and Visual Science, Pritzker School of Medicine, The University of Chicago, Chicago, Illinois, United States.
The Center for Health and the Social Sciences, The University of Chicago, Chicago, Illinois, United States.
Invest Ophthalmol Vis Sci. 2023 Aug 1;64(11):22. doi: 10.1167/iovs.64.11.22.
To investigate if metformin use is associated with decreased odds of developing new non-neovascular ("dry") age-related macular degeneration (AMD).
Case-control study examining 194,135 cases with diagnoses of new-onset AMD between 2008 and 2017 and 193,990 matched controls in the Merative MarketScan Research Databases. The diabetic subgroup included 49,988 cases and 49,460 controls. Multivariable conditional logistic regressions identified the risks of exposures on the development of dry AMD. Main outcome measures were odds ratios (ORs) of developing dry AMD with metformin use.
In multivariable conditional logistic regression, any metformin use was associated with decreased odds of developing dry AMD (OR = 0.97; 95% confidence interval [CI], 0.95-0.99). This protective effect was noted for cumulative 2-year doses of metformin of 1 to 270 g (OR = 0.93; 95% CI, 0.90-0.97) and 271 to 600 g (OR = 0.92; 95% CI, 0.89-0.96). In a diabetic subgroup, metformin use below 601 g per 2 years decreased the odds of developing dry AMD (1-270 g: OR = 0.95; 95% CI, 0.91-0.99; 271-600 g: OR = 0.92; 95% CI, 0.89-0.96). Unlike in diabetic patients with diabetic retinopathy, diabetic patients without diabetic retinopathy had decreased odds of developing dry AMD with any metformin use (OR = 0.97; 95% CI, 0.94-0.998) and cumulative two-year doses of 1 to 270 g (OR 0.96; 95% CI, 0.91-0.998) and 271 to 600 g (OR = 0.92; 95% CI, 0.88-0.96).
Metformin use was associated with decreased odds of developing dry AMD. The protective effect was observed for cumulative 2-year doses below 601 g. In diabetics, this association persisted, specifically in those without diabetic retinopathy. Therefore, metformin may be a strategy to prevent development of dry AMD.
研究二甲双胍的使用是否与新发生的非新生性(“干性”)年龄相关性黄斑变性(AMD)的几率降低有关。
这项病例对照研究在 Merative MarketScan 研究数据库中,检查了 2008 年至 2017 年间新确诊为 AMD 的 194135 例病例和 193990 名匹配对照者,并对其中的糖尿病亚组进行了研究,该亚组包括 49988 例病例和 49460 名对照者。多变量条件逻辑回归确定了暴露于干性 AMD 发展的风险。主要观察指标为二甲双胍使用后发展为干性 AMD 的优势比(OR)。
在多变量条件逻辑回归中,任何剂量的二甲双胍使用与发展干性 AMD 的几率降低相关(OR=0.97;95%置信区间[CI],0.95-0.99)。在累积 2 年的二甲双胍剂量为 1 至 270g(OR=0.93;95%CI,0.90-0.97)和 271 至 600g(OR=0.92;95%CI,0.89-0.96)时,这种保护作用是明显的。在糖尿病亚组中,2 年内二甲双胍用量低于 601g/每年降低了发展干性 AMD 的几率(1-270g:OR=0.95;95%CI,0.91-0.99;271-600g:OR=0.92;95%CI,0.89-0.96)。与患有糖尿病性视网膜病变的糖尿病患者不同,无糖尿病性视网膜病变的糖尿病患者使用任何剂量的二甲双胍(OR=0.97;95%CI,0.94-0.998)和累积两年剂量为 1 至 270g(OR=0.96;95%CI,0.91-0.998)和 271 至 600g(OR=0.92;95%CI,0.88-0.96),发展干性 AMD 的几率均降低。
二甲双胍的使用与干性 AMD 发病几率降低有关。这种保护作用在 601g 以下的累积 2 年剂量中观察到。在糖尿病患者中,这种关联仍然存在,特别是在没有糖尿病性视网膜病变的患者中。因此,二甲双胍可能是预防干性 AMD 发展的一种策略。