Ayer Amrita, Mills Claire, Donovan Catherine, Christenson Robert H, Ganz Peter, Dubin Ruth F
Division of Nephrology, San Francisco VA Medical Center, University of California, San Francisco, California, USA.
Division of Cardiology, Center for Vascular Excellence, Zuckerberg San Francisco General Hospital, University of California, San Francisco, California, USA.
Hemodial Int. 2019 Jan;23(1):58-68. doi: 10.1111/hdi.12675. Epub 2019 Feb 6.
Patients with end-stage renal disease (ESRD) have reduced endothelial function, but whether macro- and microvascular endothelial function correlate with baseline risk factors and cardiovascular outcomes in this population is not well understood.
Among 146 participants of the Cardiac, Endothelial Function and Arterial Stiffness in ESRD (CERES) study, we evaluated macro- and microvascular endothelial dysfunction as flow-mediated dilation (FMD) and velocity time integral (VTI), respectively. We examined cross-sectional correlations of baseline characteristics, inflammatory and cardiac markers with FMD and VTI. We followed participants for the composite outcome of cardiovascular hospitalization or all-cause death over fourteen months. Cox survival analyses were adjusted for demographics, comorbidities, medications, systolic blood pressure, inflammation, high-sensitivity troponin T (hs-TnT), and N-terminal pro B-type natriuretic peptide (NT-proBNP).
Impaired VTI was associated with older age and Black race (P < 0.05), as well as female gender, atherosclerosis, and hemodialysis (as opposed to peritoneal dialysis) (P < 0.2). Myocardial injury, measured as hs-TnT, inflammatory markers and NT-proBNP correlated with impaired VTI. In unadjusted analyses, VTI was significantly associated with the composite outcome (HR per SD VTI 0.65 [95%CI 0.45, 0.95]), but FMD was not (HR per SD FMD 0.97 [95%CI 0.69, 1.4]). When VTI was calculated as the ratio of (hyperemic VTI-baseline VTI)/baseline VTI, its association with the outcome persisted after multivariable adjustment.
Microvascular function was associated with higher rates of cardiovascular hospitalizations and all-cause mortality among individuals with ESRD on dialysis. Further research is needed to learn whether novel therapies that target microvascular endothelial function could improve outcomes in this high-risk population.
终末期肾病(ESRD)患者的内皮功能减退,但该人群中微血管和大血管内皮功能与基线危险因素及心血管结局之间的相关性尚不清楚。
在终末期肾病患者的心脏、内皮功能和动脉僵硬度(CERES)研究的146名参与者中,我们分别将微血管和大血管内皮功能障碍评估为血流介导的血管舒张(FMD)和速度时间积分(VTI)。我们研究了基线特征、炎症和心脏标志物与FMD和VTI之间的横断面相关性。我们对参与者进行了为期14个月的心血管住院或全因死亡复合结局随访。Cox生存分析针对人口统计学、合并症、药物治疗、收缩压、炎症、高敏肌钙蛋白T(hs-TnT)和N末端B型脑钠肽原(NT-proBNP)进行了校正。
VTI受损与年龄较大、黑人种族相关(P<0.05),还与女性、动脉粥样硬化和血液透析(而非腹膜透析)相关(P<0.2)。以hs-TnT、炎症标志物和NT-proBNP衡量的心肌损伤与VTI受损相关。在未校正的分析中,VTI与复合结局显著相关(每标准差VTI的风险比为0.65[95%置信区间0.45,0.95]),但FMD与复合结局无关(每标准差FMD的风险比为0.97[95%置信区间0.69,1.4])。当将VTI计算为(充血VTI-基线VTI)/基线VTI的比值时,其与结局的关联在多变量校正后仍然存在。
在接受透析的ESRD患者中,微血管功能与较高的心血管住院率和全因死亡率相关。需要进一步研究以了解针对微血管内皮功能的新型疗法是否能够改善这一高危人群的结局。