Meta-analysis of a continuous outcome combining individual patient data and aggregate data: a method based on simulated individual patient data

被引:2
作者
Yamaguchi, Yusuke [1 ]
Sakamoto, Wataru [2 ]
Goto, Masashi [3 ]
Staessen, Jan A. [4 ,5 ]
Wang, Jiguang [6 ]
Gueyffier, Francois [7 ]
Riley, Richard D. [8 ]
机构
[1] Osaka Univ, Grad Sch Engn Sci, Div Math Sci, Toyonaka, Osaka 5608531, Japan
[2] Okayama Univ, Grad Sch Environm & Life Sci, Div Human Ecol, Kita Ku, Okayama 7008530, Japan
[3] Biostat Res Assoc, NPO, Toyonaka, Osaka 5600085, Japan
[4] Univ Leuven, Dept Cardiovasc Dis, Div Hypertens & Cardiovasc Rehabil, Studies Coordinating Ctr, B-3000 Leuven, Belgium
[5] Maastricht Univ, Dept Epidemiol, NL-6200 MD Maastricht, Netherlands
[6] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Ctr Epidemiol Studies & Clin Trials, Shanghai 200025, Peoples R China
[7] INSERM, CIC201, F-69000 Lyon, France
[8] Univ Birmingham, Birmingham B15 2TT, W Midlands, England
基金
英国医学研究理事会;
关键词
meta-analysis; individual patient data; treatment-covariate interaction; statistical simulation; META-REGRESSION; ECOLOGICAL INFERENCE; RANDOMIZED-TRIALS; BLOOD-PRESSURE; LEVEL; HETEROGENEITY;
D O I
10.1002/jrsm.1119
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
When some trials provide individual patient data (IPD) and the others provide only aggregate data (AD), meta-analysis methods for combining IPD and AD are required. We propose a method that reconstructs the missing IPD for AD trials by a Bayesian sampling procedure and then applies an IPD meta-analysis model to the mixture of simulated IPD and collected IPD. The method is applicable when a treatment effect can be assumed fixed across trials. We focus on situations of a single continuous outcome and covariate and aim to estimate treatment-covariate interactions separated into within-trial and across-trial effect. An illustration with hypertension data which has similar mean covariates across trials indicates that the method substantially reduces mean square error of the pooled within-trial interaction estimate in comparison with existing approaches. A simulation study supposing there exists one IPD trial and nine AD trials suggests that the method has suitable type I error rate and approximately zero bias as long as the available IPD contains at least 10% of total patients, where the average gain in mean square error is up to about 40%. However, the method is currently restricted by the fixed effect assumption, and extension to random effects to allow heterogeneity is required. Copyright (c) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:322 / 351
页数:30
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