Department of Medicine, Division of Cardiology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada; Duke Clinical Research Institute, Durham, NC.
Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC.
Am Heart J. 2021 Jan;231:36-44. doi: 10.1016/j.ahj.2020.10.055. Epub 2020 Oct 21.
Statins failed to reduce cardiovascular (CV) events in trials of patients on dialysis. However, trial populations used criteria that often excluded those with atherosclerotic heart disease (ASHD), in whom statins have the greatest benefit, and included outcome composites with high rates of nonatherosclerotic CV events that may not be modified by statins. Here, we study whether statin use associates with lower atherosclerotic CV risk among patients with known ASHD on dialysis, including in those likely to receive a kidney transplant, a group excluded within trials but with lower competing mortality risks.
Using data from the United States Renal Data System including Medicare claims, we identified adults initiating dialysis with ASHD. We matched statin users 1:1 to statin nonusers with propensity scores incorporating hard matches for age and kidney transplant listing status. Using Cox models, we evaluated associations of statin use with the primary composite of fatal/nonfatal myocardial infarction and stroke (including within prespecified subgroups of younger age [<50 years] and waitlisting status); secondary outcomes included all-cause mortality and the composite of all-cause mortality, nonfatal myocardial infarction, or stroke.
Of 197,716 patients with ASHD, 47,562 (24%) were consistent statin users from which we created 46,186 matched pairs. Over a median 662 days, statin users had similar risk of fatal/nonfatal myocardial infarction or stroke overall (hazard ratio [HR] 1.00, 95% CI 0.97-1.02), or in subgroups (age< 50 years [HR = 1.05, 95% CI 0.95-1.17]; waitlisted for kidney transplant [HR 0.99, 95% CI 0.97-1.02]). Statin use was modestly associated with lower all-cause mortality (HR 0.96, 95% CI 0.94-0.98; E value = 1.21) and, similarly, a modest lower composite risk of all-cause mortality, nonfatal myocardial infarction, or stroke over the first 2 years (HR 0.90, 95% CI 0.88-0.91) but attenuated thereafter (HR 0.98, 95% CI 0.96-1.01).
Our large observational analyses are consistent with trials in more selected populations and suggest that statins may not meaningfully reduce atherosclerotic CV events even among incident dialysis patients with established ASHD and those likely to receive kidney transplants.
他汀类药物未能降低透析患者的心血管(CV)事件。然而,试验人群使用的标准通常排除了那些有动脉粥样硬化性心脏病(ASHD)的患者,他汀类药物对这些患者的益处最大,并且包括高非动脉粥样硬化性 CV 事件发生率的复合结局,这些事件可能不受他汀类药物的影响。在这里,我们研究了在已知患有 ASHD 的透析患者中,他汀类药物的使用是否与较低的动脉粥样硬化性 CV 风险相关,包括那些可能接受肾移植的患者,这是试验中排除的一组,但具有较低的竞争死亡率风险的患者。
使用包括医疗保险索赔在内的美国肾脏数据系统的数据,我们确定了开始透析时患有 ASHD 的成年人。我们使用包含年龄和肾移植清单状态硬匹配的倾向评分对他汀类药物使用者和他汀类药物非使用者进行了 1:1 匹配。使用 Cox 模型,我们评估了他汀类药物使用与致命/非致命性心肌梗死和中风的主要复合指标(包括年龄<50 岁和等待名单状态的预先指定亚组)之间的关联;次要结局包括全因死亡率和全因死亡率、非致命性心肌梗死或中风的复合指标。
在 197716 名患有 ASHD 的患者中,有 47562 名(24%)是持续使用他汀类药物的患者,我们从中创建了 46186 对匹配。在中位 662 天的时间内,他汀类药物使用者的致命/非致命性心肌梗死或中风总体风险相似(风险比 [HR] 1.00,95%CI 0.97-1.02),或在亚组中(年龄<50 岁 [HR=1.05,95%CI 0.95-1.17];等待肾移植 [HR 0.99,95%CI 0.97-1.02])。他汀类药物的使用与全因死亡率的降低适度相关(HR 0.96,95%CI 0.94-0.98;E 值=1.21),同样,在最初 2 年内,全因死亡率、非致命性心肌梗死或中风的复合风险也适度降低(HR 0.90,95%CI 0.88-0.91),但此后减弱(HR 0.98,95%CI 0.96-1.01)。
我们的大型观察性分析与更具选择性的人群的试验一致,并表明他汀类药物可能并不能显著降低动脉粥样硬化性 CV 事件,即使在有明确 ASHD 且可能接受肾移植的新发生透析患者中也是如此。