Dad Taimur, Tighiouart Hocine, Joseph Alin, Bostom Andrew, Carpenter Myra, Hunsicker Lawrence, Kusek John W, Pfeffer Marc, Levey Andrew S, Weiner Daniel E
Tufts Medical Center and Tufts University School of Medicine, Boston, MA.
Tufts Medical Center and Tufts University School of Medicine, Boston, MA; The Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA; Tufts Clinical and Translational Science Institute, Tufts University, Boston, MA.
Am J Kidney Dis. 2016 Aug;68(2):277-286. doi: 10.1053/j.ajkd.2016.01.019. Epub 2016 Mar 2.
Cardiovascular disease (CVD) is the leading cause of death in kidney transplant recipients. Whether aspirin may reduce the risk for CVD, death, and kidney failure outcomes is uncertain.
Post hoc cohort analysis of FAVORIT, a randomized trial examining the effect of homocysteine-lowering vitamins on CVD in kidney transplant recipients.
SETTING & PARTICIPANTS: Prevalent adult kidney transplant recipients with hyperhomocysteinemia and stable kidney function from the United States, Canada, and Brazil participating in FAVORIT, with no known history of CVD.
Aspirin use, with aspirin users matched to nonusers using a propensity score.
Incident CVD events, kidney failure, all-cause mortality, a composite of CVD events or mortality, and a composite of kidney failure or mortality. Cox proportional hazards models with a robust variance to account for the correlation in outcomes within matched pairs were sequentially adjusted for demographic, clinical, and laboratory characteristics to assess the association between aspirin use and events.
981 aspirin users were matched to 981 nonusers. During a 4-year mean follow up, there were 225 CVD events, 200 deaths, 126 kidney failure events, 301 composite kidney failure or mortality events, and 324 composite CVD or mortality events. Adjusted models showed no significant difference associated with aspirin use in risk for CVD events, all-cause mortality, kidney failure, composite of kidney failure or mortality, or composite of primary CVD events or mortality (HRs of 1.20 [95% CI, 0.92-1.58], 0.92 [95% CI, 0.69-1.23], 1.19 [95% CI, 0.81-1.74], 1.03 [0.82-1.31], and 1.11 [95% CI, 0.88-1.38], respectively).
We did not examine dose or continued use of aspirin after randomization. CVD history is dependent on participant report at baseline. Aspirin use was non-randomly assigned.
Aspirin use is not associated with reduced risk for incident CVD, all-cause mortality, or kidney failure in stable kidney transplant recipients with no history of CVD.
心血管疾病(CVD)是肾移植受者的主要死因。阿司匹林是否可降低CVD、死亡和肾衰竭结局的风险尚不确定。
对FAVORIT进行事后队列分析,FAVORIT是一项随机试验,研究降低同型半胱氨酸的维生素对肾移植受者CVD的影响。
来自美国、加拿大和巴西的患有高同型半胱氨酸血症且肾功能稳定的成年肾移植受者,参与FAVORIT研究,且无CVD病史。
阿司匹林使用情况,使用倾向评分将阿司匹林使用者与非使用者进行匹配。
新发CVD事件、肾衰竭、全因死亡率、CVD事件或死亡率的复合指标,以及肾衰竭或死亡率的复合指标。采用具有稳健方差的Cox比例风险模型来考虑匹配对中结局的相关性,并依次对人口统计学、临床和实验室特征进行调整,以评估阿司匹林使用与事件之间的关联。
981名阿司匹林使用者与981名非使用者进行了匹配。在平均4年的随访期间,发生了225例CVD事件、200例死亡、126例肾衰竭事件、301例肾衰竭或死亡率的复合事件以及324例CVD或死亡率的复合事件。调整后的模型显示,在CVD事件风险、全因死亡率、肾衰竭、肾衰竭或死亡率的复合指标,或原发性CVD事件或死亡率的复合指标方面,阿司匹林使用与之无显著差异(风险比分别为1.20[95%置信区间,0.92 - 1.58]、0.92[95%置信区间,0.69 - 1.23]、1.19[95%置信区间,0.81 - 1.74]、1.03[0.82 - 1.31]和1.11[95%置信区间,0.88 - 1.38])。
我们未研究随机分组后阿司匹林的剂量或持续使用情况。CVD病史依赖于参与者在基线时的报告。阿司匹林的使用并非随机分配。
对于无CVD病史的稳定肾移植受者,使用阿司匹林与降低新发CVD、全因死亡率或肾衰竭的风险无关。