Decline in Estimated Glomerular Filtration Rate and Subsequent Risk of End-Stage Renal Disease and Mortality

被引:781
作者
Coresh, Josef [1 ]
Turin, Tanvir Chowdhury [2 ]
Matsushita, Kunihiro [1 ]
Sang, Yingying [1 ]
Ballew, Shoshana H. [1 ]
Appel, Lawrence J. [3 ]
Arima, Hisatomi [4 ]
Chadban, Steven J. [5 ,6 ]
Cirillo, Massimo [7 ]
Djurdjev, Ognjenka [8 ]
Green, Jamie A. [9 ]
Heine, Gunnar H. [10 ]
Inker, Lesley A. [11 ]
Irie, Fujiko [12 ]
Ishani, Areef [13 ,14 ]
Ix, Joachim H. [15 ]
Kovesdy, Csaba P. [16 ,17 ]
Marks, Angharad [18 ,19 ]
Ohkubo, Takayoshi [20 ,21 ,22 ]
Shalev, Varda [23 ,24 ]
Shankar, Anoop [25 ]
Wen, Chi Pang [26 ,27 ]
de Jong, Paul E. [28 ]
Iseki, Kunitoshi [29 ]
Stengel, Benedicte [30 ,31 ]
Gansevoort, Ron T. [28 ]
Levey, Andrew S. [11 ]
机构
[1] Johns Hopkins Bloomberg, Sch Publ Hlth, Baltimore, MD USA
[2] Univ Calgary, Dept Community Hlth Sci, Calgary, AB, Canada
[3] Johns Hopkins Med Inst, Baltimore, MD 21205 USA
[4] Univ Sydney, George Inst Global Hlth, Sydney, NSW 2006, Australia
[5] Royal Prince Alfred Hosp, Dept Nephrol & Transplantat, Sydney, NSW, Australia
[6] Univ Sydney, Sydney Med Sch, Sydney, NSW 2006, Australia
[7] Univ Salerno, Dept Med, I-84100 Salerno, Italy
[8] BC Prov Renal Agcy, Vancouver, BC, Canada
[9] Geisinger Med Ctr, Dept Nephrol, Danville, PA 17822 USA
[10] Saarland Univ Med Ctr, Dept Internal Med Nephrol & Hypertens 4, Hamburg, Germany
[11] Tufts Med Ctr, Div Nephrol, Boston, MA USA
[12] Ibaraki Prefectural Off, Dept Hlth & Welf, Mito, Ibaraki, Japan
[13] Univ Minnesota, Minneapolis VA Hlth Care Syst, Minneapolis, MN USA
[14] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA
[15] Univ Calif San Diego, San Diego, CA 92103 USA
[16] Memphis Vet Affairs, Med Ctr, Memphis, TN USA
[17] Univ Tennessee, Ctr Hlth Sci, Memphis, TN 38163 USA
[18] Univ Aberdeen, Div Appl Hlth Sci, Aberdeen, Scotland
[19] NHS Grampian, Aberdeen, Scotland
[20] Teikyo Univ, Sch Med, Dept Hyg & Publ Hlth, Tokyo 173, Japan
[21] Tohoku Univ, Grad Sch Pharmaceut Sci, Dept Planning Drug Dev & Clin Evaluat, Sendai, Miyagi 980, Japan
[22] Shiga Univ Med Sci, Dept Hlth Sci, Shiga, Japan
[23] Tel Aviv Univ, Dept Med Informat, Maccabi Healthcare Serv, IL-69978 Tel Aviv, Israel
[24] Tel Aviv Univ, Fac Med, IL-69978 Tel Aviv, Israel
[25] Virginia Commonwealth Univ, Sch Med, Dept Family Med & Populat Hlth, Richmond, VA 23284 USA
[26] China Med Univ Hosp, Taichung, Taiwan
[27] Inst Populat Hlth Sci, Natl Hlth Res Inst, Zhunan, Taiwan
[28] Univ Groningen, Univ Med Ctr Groningen, Dept Nephrol, Groningen, Netherlands
[29] Univ Hosp Ryukyus, Dialysis Unit, Okinawa, Japan
[30] Univ Paris Sud, Inserm U1018, CESP Ctr Res Epidemiol & Populat Hlth, Villejuif, France
[31] Univ Paris Sud, UMRS 1018, Villejuif, France
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2014年 / 311卷 / 24期
基金
美国国家卫生研究院;
关键词
KIDNEY-FUNCTION DECLINE; COLLABORATIVE METAANALYSIS; HIGHER ALBUMINURIA; ALL-CAUSE; ESTIMATED GFR; POPULATION; EQUATION;
D O I
10.1001/jama.2014.6634
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE The established chronic kidney disease (CKD) progression end point of end-stage renal disease (ESRD) or a doubling of serum creatinine concentration (corresponding to a change in estimated glomerular filtration rate [GFR] of -57% or greater) is a late event. OBJECTIVE To characterize the association of decline in estimated GFR with subsequent progression to ESRD with implications for using lesser declines in estimated GFR as potential alternative end points for CKD progression. Because most people with CKD die before reaching ESRD, mortality risk also was investigated. DATA SOURCES AND STUDY SELECTION Individual meta-analysis of 1.7 million participants with 12 344 ESRD events and 223 944 deaths from 35 cohorts in the CKD Prognosis Consortium with a repeated measure of serum creatinine concentration over 1 to 3 years and outcome data. DATA EXTRACTION AND SYNTHESIS Transfer of individual participant data or standardized analysis of outputs for random-effects meta-analysis conducted between July 2012 and September 2013, with baseline estimated GFR values collected from 1975 through 2012. MAIN OUTCOMES AND MEASURES End-stage renal disease (initiation of dialysis or transplantation) or all-cause mortality risk related to percentage change in estimated GFR over 2 years, adjusted for potential confounders and first estimated GFR. RESULTS The adjusted hazard ratios (HRs) of ESRD and mortality were higher with larger estimated GFR decline. Among participants with baseline estimated GFR of less than 60 mL/min/1.73m(2), the adjusted HRs for ESRD were 32.1 (95% CI, 22.3-46.3) for changes of -57% in estimated GFR and 5.4 (95% CI, 4.5-6.4) for changes of -30%. However, changes of -30% or greater (6.9%[95% CI, 6.4%-7.4%] of the entire consortium) were more common than changes of -57%(0.79% [95% CI, 0.52%-1.06%]). This association was strong and consistent across the length of the baseline period (1 to 3 years), baseline estimated GFR, age, diabetes status, or albuminuria. Average adjusted 10-year risk of ESRD (in patients with a baseline estimated GFR of 35 mL/min/1.73m(2)) was 99%(95% CI, 95%-100%) for estimated GFR change of -57%, was 83%(95% CI, 71%-93%) for estimated GFR change of -40%, and was 64%(95% CI, 52%-77%) for estimated GFR change of -30% vs 18%(95% CI, 15%-22%) for estimated GFR change of 0%. Corresponding mortality risks were 77%(95% CI, 71%-82%), 60%(95% CI, 56%-63%), and 50% (95% CI, 47%-52%) vs 32%(95% CI, 31%-33%), showing a similar but weaker pattern. CONCLUSIONS AND RELEVANCE Declines in estimated GFR smaller than a doubling of serum creatinine concentration occurred more commonly and were strongly and consistently associated with the risk of ESRD and mortality, supporting consideration of lesser declines in estimated GFR (such as a 30% reduction over 2 years) as an alternative end point for CKD progression.
引用
收藏
页码:2518 / 2531
页数:14
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