Molnar Amber O, Bota Sarah E, Garg Amit X, Harel Ziv, Lam Ngan, McArthur Eric, Nesrallah Gihad, Perl Jeffrey, Sood Manish M
Division of Nephrology, McMaster University, Hamilton, Ontario, Canada; Division of Nephrology, University of Ottawa, Ottawa, Ontario, Canada; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada;
Institute for Clinical Evaluative Sciences, Ontario, Canada; Department of Epidemiology and Biostatistics and.
J Am Soc Nephrol. 2016 Sep;27(9):2825-32. doi: 10.1681/ASN.2015050535. Epub 2016 Jan 28.
New staging systems for CKD account for both reduced eGFR and albuminuria; whether each measure associates with greater risk of hemorrhage is unclear. In this retrospective cohort study (2002-2010), we grouped 516,197 adults ≥40 years old by eGFR (≥90, 60 to <90, 45 to <60, 30 to <45, 15 to <30, or <15 ml/min per 1.73 m(2)) and urine albumin-to-creatinine ratio (ACR; >300, 30-300, or <30 mg/g) to examine incidence of hemorrhage. The 3-year cumulative incidence of hemorrhage increased 20-fold across declining eGFR and increasing urine ACR groupings (highest eGFR/lowest ACR: 0.5%; lowest eGFR/highest ACR: 10.1%). Urine ACR altered the association of eGFR with hemorrhage (P<0.001). In adjusted models using the highest eGFR/lowest ACR grouping as the referent, patients with eGFR=15 to <30 ml/min per 1.73 m(2) had adjusted relative risks of hemorrhage of 1.9 (95% confidence interval [95% CI], 1.5 to 2.4) with the lowest ACR and 3.7 (95% CI, 3.0 to 4.5) with the highest ACR. Patients with the highest eGFR/highest ACR had an adjusted relative risk of hemorrhage of 2.3 (95% CI, 1.8 to 2.9), comparable with the risk for patients with the lowest eGFR/lowest ACR. The associations attenuated but remained significant after adjustment for anticoagulant and antiplatelet use in patients ≥66 years old. The risk of hemorrhage differed by urine ACR in high risk subgroups. Our data show that declining eGFR and increasing albuminuria each independently increase hemorrhage risk. Strategies to reduce hemorrhage events among patients with CKD are warranted.
慢性肾脏病(CKD)的新分期系统兼顾了估算肾小球滤过率(eGFR)降低和蛋白尿情况;目前尚不清楚这两项指标是否均与出血风险增加相关。在这项回顾性队列研究(2002 - 2010年)中,我们根据eGFR(≥90、60至<90、45至<60、30至<45、15至<30或<15 ml/min/1.73 m²)和尿白蛋白与肌酐比值(ACR;>300、30 - 300或<30 mg/g),将516,197名年龄≥40岁的成年人进行分组,以研究出血发生率。随着eGFR下降和尿ACR升高,3年累积出血发生率增加了20倍(eGFR最高/ACR最低组:0.5%;eGFR最低/ACR最高组:10.1%)。尿ACR改变了eGFR与出血之间的关联(P<0.001)。在以eGFR最高/ACR最低分组作为参照的校正模型中,eGFR为15至<30 ml/min/1.73 m²的患者,ACR最低时出血的校正相对风险为1.9(95%置信区间[95%CI],1.5至2.4),ACR最高时为3.7(95%CI,3.0至4.5)。eGFR最高/ACR最高的患者出血校正相对风险为2.3(95%CI,1.8至2.9),与eGFR最低/ACR最低的患者风险相当。在对66岁及以上患者使用抗凝剂和抗血小板药物进行校正后,这些关联减弱但仍具有显著性。在高风险亚组中,出血风险因尿ACR而异。我们的数据表明,eGFR下降和蛋白尿增加均独立增加出血风险。有必要采取策略降低CKD患者的出血事件。