Naimark David M J, Grams Morgan E, Matsushita Kunihiro, Black Corri, Drion Iefke, Fox Caroline S, Inker Lesley A, Ishani Areef, Jee Sun Ha, Kitamura Akihiko, Lea Janice P, Nally Joseph, Peralta Carmen Alicia, Rothenbacher Dietrich, Ryu Seungho, Tonelli Marcello, Yatsuya Hiroshi, Coresh Josef, Gansevoort Ron T, Warnock David G, Woodward Mark, de Jong Paul E
Division of Nephrology, Sunnybrook Health Sciences Centre and Institute of Health Policy Management and Evaluation, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada;
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland; Division of Nephrology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland;
J Am Soc Nephrol. 2016 Aug;27(8):2456-66. doi: 10.1681/ASN.2015060688. Epub 2015 Dec 11.
A single determination of eGFR associates with subsequent mortality risk. Prior decline in eGFR indicates loss of kidney function, but the relationship to mortality risk is uncertain. We conducted an individual-level meta-analysis of the risk of mortality associated with antecedent eGFR slope, adjusting for established risk factors, including last eGFR, among 1.2 million subjects from 12 CKD and 22 other cohorts within the CKD Prognosis Consortium. Over a 3-year antecedent period, 12% of participants in the CKD cohorts and 11% in the other cohorts had an eGFR slope <-5 ml/min per 1.73 m(2) per year, whereas 7% and 4% had a slope >5 ml/min per 1.73 m(2) per year, respectively. Compared with a slope of 0 ml/min per 1.73 m(2) per year, a slope of -6 ml/min per 1.73 m(2) per year associated with adjusted hazard ratios for all-cause mortality of 1.25 (95% confidence interval [95% CI], 1.09 to 1.44) among CKD cohorts and 1.15 (95% CI, 1.01 to 1.31) among other cohorts during a follow-up of 3.2 years. A slope of +6 ml/min per 1.73 m(2) per year also associated with higher all-cause mortality risk, with adjusted hazard ratios of 1.58 (95% CI, 1.29 to 1.95) among CKD cohorts and 1.43 (95% CI, 1.11 to 1.84) among other cohorts. Results were similar for cardiovascular and noncardiovascular causes of death and stronger for longer antecedent periods (3 versus <3 years). We conclude that prior decline or rise in eGFR associates with an increased risk of mortality, independent of current eGFR.
估算肾小球滤过率(eGFR)的单次测定结果与后续死亡风险相关。既往eGFR下降表明肾功能丧失,但其与死亡风险的关系尚不确定。我们在慢性肾脏病预后协作组的12个慢性肾脏病队列和22个其他队列中的120万名受试者中,进行了一项个体水平的荟萃分析,以研究与既往eGFR斜率相关的死亡风险,并对包括末次eGFR在内的既定风险因素进行了校正。在3年的前期阶段,慢性肾脏病队列中12%的参与者以及其他队列中11%的参与者的eGFR斜率<-5 ml/(min·1.73 m²)/年,而分别有7%和4%的参与者的eGFR斜率>5 ml/(min·1.73 m²)/年。与每年1.73 m²的斜率为0 ml/min相比,每年1.73 m²的斜率为-6 ml/min与慢性肾脏病队列全因死亡率的校正风险比为1.25(95%置信区间[95%CI],1.09至1.44),在其他队列中为1.15(95%CI,1.01至1.31),随访时间为3.2年。每年1.73 m²的斜率为+6 ml/min也与更高的全因死亡风险相关,慢性肾脏病队列中的校正风险比为1.58(95%CI,1.29至1.95),其他队列中为1.43(95%CI,1.11至1.84)。心血管及非心血管死因的结果相似,且在更长的前期阶段(3年与<3年)更为显著。我们得出结论,既往eGFR的下降或上升与死亡风险增加相关,且独立于当前的eGFR。