Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, 243 Charles Street, Boston, MA, 02114, USA.
Department of Ophthalmology, Scheie Eye Institute, University of Pennsylvania, Philadelphia, PA, USA.
Graefes Arch Clin Exp Ophthalmol. 2021 Sep;259(9):2783-2793. doi: 10.1007/s00417-021-05243-8. Epub 2021 May 29.
The purpose of this study is to determine if statin therapy decreases the incidence of non-infectious uveitis (NIU) using a retrospective cohort study.
Patients enrolled in a national insurance plan who initiated statin (n = 711,734, statin cohort) or other lipid-lowering therapy (n = 148,044, non-statin cohort) were observed for NIU development. Incident NIU in the primary analysis was defined as a new diagnosis code for NIU followed by a second instance of a NIU code within 120 days. For the secondary outcome definition, a corticosteroid prescription or code for an ocular corticosteroid injection within 120 days of the NIU diagnosis code was used instead of the second NIU diagnosis code. Estimation of NIU incidence used multivariable Cox proportional hazards regression. The proportional hazards assumption was satisfied by creating two time periods of analysis, ≤ 150 and > 150 days. Subanalyses were performed by anatomic subtype.
Overall, the primary outcome occurred 541 times over 690,465 person-years in the statin cohort and 103 times over 104,301 person-years in the non-statin cohort. No associations were seen in the ≤ 150-day analyses (p > 0.20 for all comparisons). However, after 150 days, the statin cohort was less likely to develop any uveitis [hazard ratio (HR) = 0.70, 95% confidence interval (CI): 0.51-0.97, P = 0.03] in the primary outcome analysis, but did not meet significance for the secondary outcome (HR = 0.85, 95% CI: 0.63-1.15, P = 0.30). Similarly, in the anatomic subtype analysis, after 150 days, the statin cohort was less likely to develop anterior uveitis (HR = 0.67, 95% CI: 0.47-0.97, P = 0.03) in the primary analysis, but the association did not reach significance for the secondary outcome (HR = 0.82, 95% CI: 0.56-1.20, P = 0.31).
Our results suggest that statin therapy for > 150 days decreases the incidence of NIU.
本研究旨在通过回顾性队列研究,确定他汀类药物治疗是否会降低非感染性葡萄膜炎(NIU)的发生率。
本研究纳入了参加国家保险计划的患者,他们开始接受他汀类药物(n=711734,他汀类药物队列)或其他降脂治疗(n=148044,非他汀类药物队列),观察 NIU 的发展情况。主要分析中,新发 NIU 的定义为首次诊断为 NIU 后 120 天内再次出现 NIU 诊断代码。次要结局定义中,在 NIU 诊断代码后 120 天内使用皮质类固醇处方或眼部皮质类固醇注射代码代替第二次 NIU 诊断代码。使用多变量 Cox 比例风险回归估计 NIU 的发生率。通过创建两个分析时间段(≤150 天和>150 天)来满足比例风险假设。进行了解剖亚型的亚分析。
总体而言,在他汀类药物队列中,主要结局在 690465 人年中发生了 541 次,在非他汀类药物队列中发生了 103 次。在≤150 天的分析中未观察到相关性(所有比较的 P>0.20)。然而,在 150 天后,他汀类药物队列发生任何葡萄膜炎的可能性较低[风险比(HR)=0.70,95%置信区间(CI):0.51-0.97,P=0.03],但次要结局无统计学意义(HR=0.85,95%CI:0.63-1.15,P=0.30)。同样,在解剖亚型分析中,在 150 天后,他汀类药物队列发生前葡萄膜炎的可能性较低(主要分析 HR=0.67,95%CI:0.47-0.97,P=0.03),但次要结局无统计学意义(HR=0.82,95%CI:0.56-1.20,P=0.31)。
我们的结果表明,他汀类药物治疗>150 天可降低 NIU 的发生率。