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Statin use and the risk of progression to vision threatening diabetic retinopathy

机译:使用他汀类药物和进展为视力威胁糖尿病视网膜病变的风险

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Abstract Purpose This study aims to assess the effect of statins on progression from nonproliferative diabetic retinopathy (NPDR) to vision‐threatening diabetic retinopathy (VTDR), proliferative diabetic retinopathy (PDR) or diabetic macular edema (DME). Methods Two cohort studies using a U.S. medical claims database from 2002 to 2019 including NPDR patients 18?years or older. A risk factor analysis performed a time‐updating cox regression model assessing statin usage. A second new‐user active comparator design analysis replicating a previously published study. Main outcomes included a new diagnosis of VTDR (composite of either PDR or DME) or DME and PDR individually for the risk factor study and included additional outcomes of new DR, NPDR, vitreous hemorrhage (VH) and tractional retinal detachment (TRD) for the new user study. Results Risk factor analysis included 66?617 statin users with NPDR at baseline and 83?365 nonstatin users. Of these, 27?325 (18.2) progressed to VTDR, 4086 (2.71) progressed to PDR, and 22?750 (15.1) progressed to DME. After multivariable analysis, no protective effect of statin use was found for progression to VTDR, PDR, or DME (HR?=?1.01–3, p?>0.33 for all comparisons). Replicated new user design analysis also showed no protective effect for statins on risk of development of DR (HR?=?1.03, 95 CI: 0.99–1.07, p?=?0.13), PDR (HR?=?0.89, 95 CI: 0.79–1.02, p?=?0.09), DME (HR?=?0.94, 95 CI: 0.86–1.03, p?=?0.21), VH (HR?=?1.00, 95 CI: 0.86–1.16, p?=?0.99), and TRD (HR?=?1.11, 95 CI: 0.89–1.38, p?=?0.36). Conclusion Statin use was found not to be protective for progression of DR regardless of study methodology. These results suggest that the specifics of the population studied rather than differing study methodology are important in assessing the effect of statins on DR progression.
机译:摘要 目的 本研究旨在评估他汀类药物对从非增殖性糖尿病视网膜病变(NPDR)进展为威胁视力的糖尿病视网膜病变(VTDR)、增殖性糖尿病视网膜病变(PDR)或糖尿病性黄斑水肿(DME)的影响。方法 2002 年至 2019 年使用美国医疗索赔数据库进行的两项队列研究,包括 18 岁或以上的 NPDR 患者。危险因素分析执行了时间更新的 cox 回归模型,评估他汀类药物的使用情况。第二个新用户有源比较器设计分析,复制了先前发表的研究。主要结局包括危险因素研究的新诊断VTDR(PDR或DME的复合)或DME和PDR的单独诊断,以及新用户研究的新DR、NPDR、玻璃体出血(VH)和牵引性视网膜脱离(TRD)的额外结局。结果 危险因素分析包括66?617例基线NPDR他汀类药物使用者和83?365例非他汀类药物使用者。其中,27?325例(18.2%)进展为VTDR,4086例(2.71%)进展为PDR,22?750例(15.1%)进展为DME。经过多变量分析,未发现他汀类药物使用对进展为 VTDR、PDR 或 DME 的保护作用(所有比较均为 HR?=?1.01–3,p?>0.33)。重复的新用户设计分析也显示,他汀类药物对DR(HR?=?1.03,95%CI:0.99-1.07,p?=?0.13)、PDR(HR?=?0.89,95%CI:0.79-1.02,p?=?0.09)、DME(HR?=?0.94,95% CI:0.86-1.03,p?=?0.21)、VH(HR?=?1.00,95% CI:0.86-1)的发生风险没有保护作用。16,p?=?0.99)和TRD(HR?=?1.11,95%CI:0.89–1.38,p?=?0.36)。结论 无论研究方法如何,他汀类药物的使用均对DR的进展没有保护作用。这些结果表明,在评估他汀类药物对 DR 进展的影响时,研究人群的具体情况而不是不同的研究方法很重要。

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