Pulse Pressure and Cardiovascular and Kidney Outcomes by Age in the Chronic Renal Insufficiency Cohort (CRIC)

医学 肾脏疾病 危险系数 内科学 比例危险模型 肾功能 混淆 队列 血压 心脏病学 脉冲压力 置信区间
作者
Clara Fischman,Raymond R. Townsend,Debbie L. Cohen,Mahboob Rahman,Jiang He,Stephen P. Juraschek,Andrew M. South,Lawrence J. Appel,Paul E. Drawz,Jordana B. Cohen,Amanda H. Anderson,Jing Chen,Laura M. Dember,Alan S. Go,James P. Lash,Panduranga S. Rao,Vallabh O. Shah,Mark L. Unruh
出处
期刊:American Journal of Hypertension [Oxford University Press]
被引量:2
标识
DOI:10.1093/ajh/hpae136
摘要

Abstract BACKGROUND Wide pulse pressure (PP) is associated with cardiovascular events and the progression of chronic kidney disease (CKD) to kidney failure. PP naturally widens with age, but it is unclear whether the risks associated with greater PP are the same across all ages. METHODS We used Cox proportional hazards models to investigate the association of PP with (i) atherosclerotic cardiovascular disease (ASCVD) events or death and (ii) a 50% reduction in estimated glomerular filtration rate or kidney failure in the chronic renal insufficiency cohort (CRIC). We evaluated the association of time-updated PP with these outcomes, accounting for time-updated confounders using inverse probability weighting. RESULTS Among 5,621 participants with CKD, every 10-mmHg greater PP was associated with a 6% higher risk of an ASCVD event or death (hazard ratio [HR] = 1.06, 95% CI 1.04, 1.08) and 17% higher risk of the composite kidney outcome (HR = 1.17, 95% CI 1.16, 1.18). Greater PP was associated with a higher risk of ASCVD events or death among participants in the lowest age tertile (21–61 years), but a higher risk of the composite kidney outcome in the oldest age tertile (71–79 years). While wide PP in participants that experienced the primary outcomes was predominantly driven by elevated SBP, PP remained significantly associated with the composite kidney outcome across all ages and with ASCVD events or death in the first age tertile when SBP was added to the Cox regression model. CONCLUSIONS Our findings suggest that the mechanism by which PP is associated with adverse outcomes may differ by age.
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