Assessing the Validity of Surrogate Outcomes for ESRD: A Meta-Analysis

被引:40
作者
Jun, Min [1 ,4 ]
Turin, Tanvir Chowdhury [2 ,3 ]
Woodward, Mark [4 ,5 ]
Perkovic, Vlado [4 ]
Heerspink, Hiddo J. Lambers [6 ]
Manns, Braden J. [1 ,2 ]
Tonelli, Marcello [2 ]
Hemmelgarn, Brenda R. [1 ,2 ]
机构
[1] Univ Calgary, Dept Med, Div Nephrol, Calgary, AB, Canada
[2] Univ Calgary, Dept Community Hlth Sci, Calgary, AB, Canada
[3] Univ Calgary, Dept Family Med, Calgary, AB, Canada
[4] Univ Sydney, George Inst Global Hlth, Sydney, NSW 2006, Australia
[5] Univ Oxford, George Inst Global Hlth, Nuffield Dept Populat Hlth, Oxford, England
[6] Univ Groningen, Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Groningen, Netherlands
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2015年 / 26卷 / 09期
基金
澳大利亚国家健康与医学研究理事会; 加拿大健康研究院; 英国医学研究理事会;
关键词
CHRONIC KIDNEY-DISEASE; TYPE-2; DIABETIC-NEPHROPATHY; RENIN-ANGIOTENSIN SYSTEM; CHRONIC RENAL-DISEASE; DOUBLE-BLIND; END-POINTS; CARDIOVASCULAR OUTCOMES; PROTEINURIA REDUCTION; OVERT NEPHROPATHY; CONTROLLED TRIAL;
D O I
10.1681/ASN.2014040396
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
Validation of current and promising surrogate outcomes for ESRD in randomized controlled trials (RCTs) has been limited. We conducted a systematic review and meta-analysis of RCTs to further inform the ability of surrogate outcomes for ESRD to predict the efficacy of various interventions on ESRD. MEDLINE, EMBASE, and CENTRAL (from inception through September 2013) were searched. All RCTs in adults with proteinuria, diabetes, or CKD stages 1-4 or renal transplant recipients reporting ESRD events and a surrogate outcome (change in proteinuria or doubling of serum creatinine [DSCR]) for ESRD during a year follow-up were included. Two reviewers abstracted trial characteristics and outcome data independently. To assess the correlation between the surrogate outcomes and ESRD, we determined the treatment effect ratio (TER), defined as the ratio of the treatment effects on ESRD and the effects on the change in surrogate outcomes. TERs close to 1 indicate greater agreement between ESRD and the surrogate, and these ratios were pooled across interventions. We identified 27 trials (97,458 participants; 4187 participants with ESRD). Seven trials reported the effects on change in proteinuria and showed consistent effects for proteinuria and ESRD (TER, 0.82; 95% confidence interval, 0.59 to 1.16), with minimal heterogeneity. Twenty trials reported on DSCR. Treatment effects on DSCR were consistent with the effects on ESRD (TER, 0.98; 95% confidence interval, 0.85 to 1.14), with moderate heterogeneity. In conclusion, DSCR is generally a good surrogate for ESRD, whereas data on proteinuria were limited. Further assessment of the surrogacy of proteinuria using prospective RCTs is warranted.
引用
收藏
页码:2289 / 2302
页数:14
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