Larner College of Medicine at the University of Vermont, Burlington, VT, USA.
University of Vermont, Burlington, VT, USA.
J Thromb Haemost. 2018 Sep;16(9):1743-1752. doi: 10.1111/jth.14235. Epub 2018 Aug 9.
Essentials Chronic kidney disease (CKD) is associated with procoagulant and inflammatory biomarkers. We studied the association of CKD and venous thromboembolism (VTE) in a case-cohort study. Factor VIII, D-dimer and C-reactive protein appeared to explain the association of CKD and VTE. Statin use was protective against VTE in those with and without CKD.
Background Chronic kidney disease (CKD) is associated with venous thromboembolism (VTE) risk via unknown mechanisms. Whether factors associated with reduced VTE risk in the general population might also be associated with reduced VTE risk in CKD patients is unknown. Objectives To determine whether thrombosis biomarkers attenuate VTE risk, and whether factors associated with reduced VTE risk are similarly effective in CKD patients. Methods Baseline biomarkers were measured in a cohort (294 VTE cases; 939 non-cases) from the Reasons for Geographic and Racial Differences in Stroke (REGARDS) study, a nationwide prospective cohort study of 30 239 persons aged ≥45 years with 4.3 years of follow-up. The hazard ratio (HR) of VTE per 10 mL min 1.73 m decrease in estimated glomerular filtration rate (eGFR), and the percentage attenuation of this HR by each biomarker, were calculated. Associations of protective factors (physical activity, lower body mass index [BMI], and aspirin, warfarin and statin use) with VTE were estimated in those with and without CKD. Results The HR for VTE with lower eGFR was 1.13 (95% confidence interval [CI] 1.02-1.25), and VTE risk was attenuated by 23% (95% CI 5-100) by D-dimer, by 100% (95% CI 50-100) by factor VIII, and by 15% (95% CI 2-84) by C-reactive protein. Normal BMI was associated with lower VTE risk in those without CKD (HR 0.47, 95% CI 0.32-0.70), but not in those with CKD (HR 1.07, 95% CI 0.51-2.22). Statin use, physical activity and warfarin use were associated with lower VTE risk in both groups. Conclusions Procoagulant and inflammatory biomarkers mediated the association of eGFR with VTE. Higher physical activity, statin use and warfarin use mitigated VTE risk in those with CKD and those without CKD, but normal BMI did not mitigate VTE risk in CKD patients.
慢性肾脏病(CKD)与静脉血栓栓塞(VTE)风险相关,但具体机制尚不清楚。一般人群中降低 VTE 风险的因素是否也与 CKD 患者的 VTE 风险降低相关,目前尚不清楚。目的:确定血栓形成生物标志物是否能减弱 VTE 风险,以及与降低 VTE 风险相关的因素在 CKD 患者中是否同样有效。方法:在一项全国性前瞻性队列研究——原因地理和种族差异在中风(REGARDS)研究中,对队列(294 例 VTE 病例;939 例非病例)进行了基线生物标志物测量。分析了肾小球滤过率(eGFR)每下降 10 mL min 1.73 m 时 VTE 的风险比(HR),以及每个生物标志物对该 HR 的衰减程度。在有或没有 CKD 的患者中,评估了保护性因素(体力活动、较低的 BMI 和阿司匹林、华法林和他汀类药物的使用)与 VTE 的相关性。结果:eGFR 较低时发生 VTE 的 HR 为 1.13(95%置信区间[CI]1.02-1.25),D-二聚体使 VTE 风险降低了 23%(95%CI5-100),因子 VIII 使 VTE 风险降低了 100%(95%CI50-100),C 反应蛋白使 VTE 风险降低了 15%(95%CI2-84)。在无 CKD 的患者中,正常 BMI 与较低的 VTE 风险相关(HR0.47,95%CI0.32-0.70),但在有 CKD 的患者中不相关(HR1.07,95%CI0.51-2.22)。他汀类药物的使用、体力活动和华法林的使用与两组的 VTE 风险降低相关。结论:促凝和炎症生物标志物介导了 eGFR 与 VTE 之间的关系。较高的体力活动、他汀类药物的使用和华法林的使用降低了 CKD 和无 CKD 患者的 VTE 风险,但正常 BMI 并未降低 CKD 患者的 VTE 风险。