Early Change in Proteinuria as a Surrogate End Point for Kidney Disease Progression: An Individual Patient Meta-analysis

被引:101
作者
Inker, Lesley A. [1 ]
Levey, Andrew S. [1 ]
Pandya, Kruti [1 ]
Stoycheff, Nicholas [1 ]
Okparavero, Aghogho [1 ]
Greene, Tom [2 ]
机构
[1] Tufts Med Ctr, Div Nephrol, Boston, MA 02111 USA
[2] Univ Utah, Sch Med, Dept Med, Salt Lake City, UT USA
基金
美国国家卫生研究院;
关键词
Proteinuria; surrogate endpoint; kidney disease progression; disease trajectory; end-stage renal disease (ESRD); prognostic marker; BLOOD-PRESSURE CONTROL; CONVERTING ENZYME-INHIBITION; METHYLPREDNISOLONE PLUS CHLORAMBUCIL; IGA NEPHROPATHY; RENAL-DISEASE; RANDOMIZED-TRIAL; MYCOPHENOLATE-MOFETIL; CLINICAL-TRIALS; DOUBLE-BLIND; LONG-TERM;
D O I
10.1053/j.ajkd.2014.02.020
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: It is controversial whether proteinuria is a valid surrogate end point for randomized trials in chronic kidney disease. Study Design: Meta-analysis of individual patient-level data. Setting & Population: Individual patient data for 9,008 patients from 32 randomized trials evaluating 5 intervention types. Selection Criteria for Studies: Randomized controlled trials of kidney disease progression until 2007 with measurements of proteinuria both at baseline and during the first year of follow-up, with at least 1 further year of follow-up for the clinical outcome. Predictor: Early change in proteinuria. Outcomes: Doubling of serum creatinine level, end-stage renal disease, or death. Results: Early decline in proteinuria was associated with lower risk of the clinical outcome (pooled HR, 0.74 per 50% reduction in proteinuria); this association was stronger at higher levels of baseline proteinuria. Pooled estimates for the proportion of treatment effect on the clinical outcome explained by early decline in proteinuria ranged from -7.0% (95% CI, -40.6% to 26.7%) to 43.9% (95% CI, 25.3% to 62.6%) across 5 intervention types. The direction of the pooled treatment effects on early change in proteinuria agreed with the direction of the treatment effect on the clinical outcome for all 5 intervention types, with the magnitudes of the pooled treatment effects on the 2 end points agreeing for 4 of the 5 intervention types. The pooled treatment effects on both end points were simultaneously stronger at higher levels of proteinuria. However, statistical power was insufficient to determine whether differences in treatment effects on the clinical outcome corresponded to differences in treatment effects on proteinuria between individual studies. Limitations: Limited variety of interventions tested and low statistical power for many chronic kidney disease clinical trials. Conclusions: These results provide new evidence supporting the use of an early reduction in proteinuria as a surrogate end point, but do not provide sufficient evidence to establish its validity in all settings. (C) 2014 by the National Kidney Foundation, Inc.
引用
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页码:74 / 85
页数:12
相关论文
共 76 条
[1]  
Agodoa L, 2007, J HYPERTENS, V25, P951
[2]  
[Anonymous], METHODS METAANALYSIS
[3]   Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90,056 participants in 14 randomised trials of statins [J].
Baigent, C ;
Keech, A ;
Kearney, PM ;
Blackwell, L ;
Buck, G ;
Pollicino, C ;
Kirby, A ;
Sourjina, T ;
Peto, R ;
Collins, R ;
Simes, J .
LANCET, 2005, 366 (9493) :1267-1278
[4]   A perfect correlate does not a surrogate make [J].
Stuart G Baker ;
Barnett S Kramer .
BMC Medical Research Methodology, 3 (1) :1-5
[5]   Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy [J].
Brenner, BM ;
Cooper, ME ;
de Zeeuw, D ;
Keane, WF ;
Mitch, WE ;
Parving, HH ;
Remuzzi, G ;
Snapinn, SM ;
Zhang, ZX ;
Shahinfar, S .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (12) :861-869
[6]   The role of proteinuria in the progression of chronic renal failure [J].
Burton, C ;
Harris, KPG .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1996, 27 (06) :765-775
[7]  
Burzykowski T., 2005, EVALUATION SURROGATE
[8]   Criteria for the validation of surrogate endpoints in randomized experiments [J].
Buyse, M ;
Molenberghs, G .
BIOMETRICS, 1998, 54 (03) :1014-1029
[9]  
Buyse M, 2000, Biostatistics, V1, P49, DOI 10.1093/biostatistics/1.1.49
[10]   Cyclosporine in patients with steroid-resistant membranous nephropathy: A randomized trial [J].
Cattran, DC ;
Appel, GB ;
Hebert, LA ;
Hunsicker, LG ;
Pohl, MA ;
Hoy, WE ;
Maxwell, DR ;
Kunis, CL .
KIDNEY INTERNATIONAL, 2001, 59 (04) :1484-1490