Comparative performance of heterogeneity variance estimators in meta-analysis: a review of simulation studies

被引:103
作者
Langan, Dean [1 ]
Higgins, Julian P. T. [2 ]
Simmonds, Mark [1 ]
机构
[1] Univ York, Ctr Reviews & Disseminat, York YO10 5DD, N Yorkshire, England
[2] Univ Bristol, Sch Social & Community Med, Bristol, Avon, England
基金
英国医学研究理事会;
关键词
meta-analysis; heterogeneity; simulation; random effects; DerSimonian-Laird; RANDOM-EFFECTS MODEL; CLINICAL-TRIALS; INFERENCE; COMPONENT;
D O I
10.1002/jrsm.1198
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Random-effects meta-analysis methods include an estimate of between-study heterogeneity variance. We present a systematic review of simulation studies comparing the performance of different estimation methods for this parameter. We summarise the performance of methods in relation to estimation of heterogeneity and of the overall effect estimate, and of confidence intervals for the latter. Among the twelve included simulation studies, the DerSimonian and Laird method was most commonly evaluated. This estimate is negatively biased when heterogeneity is moderate to high and therefore most studies recommended alternatives. The Paule-Mandel method was recommended by three studies: it is simple to implement, is less biased than DerSimonian and Laird and performs well in meta-analyses with dichotomous and continuous outcomes. In many of the included simulation studies, results were based on data that do not represent meta-analyses observed in practice, and only small selections of methods were compared. Furthermore, potential conflicts of interest were present when authors of novel methods interpreted their results. On the basis of current evidence, we provisionally recommend the Paule-Mandel method for estimating the heterogeneity variance, and using this estimate to calculate the mean effect and its 95% confidence interval. However, further simulation studies are required to draw firm conclusions. Copyright (C) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:181 / 198
页数:18
相关论文
共 33 条
[1]   Meta-Analysis of Rare Binary Adverse Event Data [J].
Bhaumik, Dulal K. ;
Amatya, Anup ;
Normand, Sharon-Lise T. ;
Greenhouse, Joel ;
Kaizar, Eloise ;
Neelon, Brian ;
Gibbons, Robert D. .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 2012, 107 (498) :555-567
[2]  
Borenstein M, 2009, INTRO METAANALYSIS
[3]   Avoiding zero between-study variance estimates in random-effects meta-analysis [J].
Chung, Yeojin ;
Rabe-Hesketh, Sophia ;
Choi, In-Hee .
STATISTICS IN MEDICINE, 2013, 32 (23) :4071-4089
[4]   Characteristics of meta-analyses and their component studies in the Cochrane Database of Systematic Reviews: a cross-sectional, descriptive analysis [J].
Davey, Jonathan ;
Turner, Rebecca M. ;
Clarke, Mike J. ;
Higgins, Julian P. T. .
BMC MEDICAL RESEARCH METHODOLOGY, 2011, 11
[5]   METAANALYSIS IN CLINICAL-TRIALS [J].
DERSIMONIAN, R ;
LAIRD, N .
CONTROLLED CLINICAL TRIALS, 1986, 7 (03) :177-188
[6]   Random-effects model for meta-analysis of clinical trials: An update [J].
DerSimonian, Rebecca ;
Kacker, Raghu .
CONTEMPORARY CLINICAL TRIALS, 2007, 28 (02) :105-114
[7]   Valid inference in random effects meta-analysis [J].
Follmann, DA ;
Proschan, MA .
BIOMETRICS, 1999, 55 (03) :732-737
[8]  
Hardy RJ, 1996, STAT MED, V15, P619, DOI 10.1002/(SICI)1097-0258(19960330)15:6<619::AID-SIM188>3.0.CO
[9]  
2-A
[10]   Reducing the number of unjustified significant results in meta-analysis [J].
Hartung, J ;
Makambi, KH .
COMMUNICATIONS IN STATISTICS-SIMULATION AND COMPUTATION, 2003, 32 (04) :1179-1190