Deo Rajat, Katz Ronit, de Boer Ian H, Sotoodehnia Nona, Kestenbaum Bryan, Mukamal Kenneth J, Chonchol Michel, Sarnak Mark J, Siscovick David, Shlipak Michael G, Ix Joachim H
Section of Electrophysiology, Division of Cardiovascular Medicine, University of Pennsylvania, Philadelphia, PA.
Kidney Research Institute, University of Washington, Seattle, WA.
Am J Kidney Dis. 2015 Jul;66(1):40-6. doi: 10.1053/j.ajkd.2014.10.025. Epub 2015 Jan 5.
Elevated fibroblast growth factor 23 (FGF-23) concentrations are associated with greater risk of cardiovascular events and mortality, especially among people with chronic kidney disease (CKD). Because individuals with CKD are at an increased risk of sudden cardiac death (SCD), we sought to understand whether FGF-23 level is a stronger risk factor for SCD versus non-SCD.
Cohort study.
SETTING & PARTICIPANTS: 3,244 participants 65 years or older in the community-based Cardiovascular Health Study.
Plasma FGF-23 concentrations.
We assessed SCD and non-SCD in these analyses. SCD was adjudicated rigorously and was defined as a sudden pulseless condition of cardiac origin in a previously stable person occurring out of hospital or in the emergency department.
We estimated associations of baseline FGF-23 concentrations with SCD and non-SCD using Cox proportional hazards models after adjustment for demographics, cardiovascular risk factors, comorbid conditions, and kidney function. We also tested whether associations differed by CKD status.
During a median follow-up of 8.1 years, there were 118 adjudicated SCD and 570 non-SCD events. After multivariable adjustment for demographics, cardiovascular risk factors, comorbid conditions, and parameters of kidney function, higher FGF-23 concentrations were an independent risk factor for non-SCD (HR [per doubling], 1.17; 95% CI, 1.06-1.30). However, elevated FGF-23 concentrations were not associated independently with SCD (HR [per doubling], 1.07; 95% CI, 0.85-1.35). In stratified analysis by CKD status (36.5% of cohort), doubling of FGF-23 concentrations was associated independently with non-SCD (adjusted HR, 1.26; 95% CI, 1.10-1.45). A similar magnitude of association was observed between FGF-23 level and SCD in the CKD subgroup; however, it was not significant (HR, 1.20; 95% CI, 0.89-1.62).
Limited power to detect moderate-sized effects between FGF-23 level and SCD in both the primary and stratified analyses.
In this population-based study, FGF-23 level elevations were associated independently with non-SCD. Among individuals with CKD, the associations between FGF-23 level and SCD and non-SCD were similar.
成纤维细胞生长因子23(FGF - 23)浓度升高与心血管事件和死亡风险增加相关,尤其是在慢性肾脏病(CKD)患者中。由于CKD患者发生心源性猝死(SCD)的风险增加,我们试图了解FGF - 23水平是否是SCD相对于非SCD的更强风险因素。
队列研究。
社区心血管健康研究中3244名65岁及以上的参与者。
血浆FGF - 23浓度。
我们在这些分析中评估了SCD和非SCD。SCD经过严格判定,定义为既往病情稳定的人在院外或急诊科发生的心脏源性突然无脉状态。
在对人口统计学、心血管危险因素、合并症和肾功能进行调整后,我们使用Cox比例风险模型估计基线FGF - 23浓度与SCD和非SCD之间的关联。我们还测试了关联是否因CKD状态而异。
在中位随访8.1年期间,有118例经判定的SCD事件和570例非SCD事件。在对人口统计学、心血管危险因素、合并症和肾功能参数进行多变量调整后,较高的FGF - 23浓度是发生非SCD的独立危险因素(风险比[每加倍],1.17;95%置信区间,1.06 - 1.30)。然而,FGF - 23浓度升高与SCD并无独立关联(风险比[每加倍],1.07;95%置信区间,0.85 - 1.35)。在按CKD状态分层分析中(队列的36.5%),FGF - 23浓度加倍与非SCD独立相关(调整后风险比,1.26;95%置信区间,1.10 - 1.45)。在CKD亚组中,FGF - 23水平与SCD之间观察到类似程度的关联;然而,并不显著(风险比,1.20;95%置信区间,0.89 - 1.62)。
在主要分析和分层分析中检测FGF - 23水平与SCD之间中等效应的能力有限。
在这项基于人群的研究中,FGF - 23水平升高与非SCD独立相关。在CKD患者中,FGF - 23水平与SCD和非SCD之间的关联相似。