MRC Biostatistics Unit, Cambridge Institute of Public Health, Forvie Site, Robinson Way, Cambridge Biomedical Campus, Cambridge, CB2 0SR, UK.
MRC Biostatistics Unit, Cambridge Institute of Public Health, Forvie Site, Robinson Way, Cambridge Biomedical Campus, Cambridge, CB2 0SR, UK.
J Clin Epidemiol. 2015 Jan;68(1):52-60. doi: 10.1016/j.jclinepi.2014.08.012. Epub 2014 Oct 7.
Estimation of between-study heterogeneity is problematic in small meta-analyses. Bayesian meta-analysis is beneficial because it allows incorporation of external evidence on heterogeneity. To facilitate this, we provide empirical evidence on the likely heterogeneity between studies in meta-analyses relating to specific research settings.
Our analyses included 6,492 continuous-outcome meta-analyses within the Cochrane Database of Systematic Reviews. We investigated the influence of meta-analysis settings on heterogeneity by modeling study data from all meta-analyses on the standardized mean difference scale. Meta-analysis setting was described according to outcome type, intervention comparison type, and medical area. Predictive distributions for between-study variance expected in future meta-analyses were obtained, which can be used directly as informative priors.
Among outcome types, heterogeneity was found to be lowest in meta-analyses of obstetric outcomes. Among intervention comparison types, heterogeneity was lowest in meta-analyses comparing two pharmacologic interventions. Predictive distributions are reported for different settings. In two example meta-analyses, incorporating external evidence led to a more precise heterogeneity estimate.
Heterogeneity was influenced by meta-analysis characteristics. Informative priors for between-study variance were derived for each specific setting. Our analyses thus assist the incorporation of realistic prior information into meta-analyses including few studies.
小样本荟萃分析中存在研究间异质性评估问题。贝叶斯荟萃分析具有优势,因为它允许纳入关于异质性的外部证据。为此,我们提供了关于特定研究环境中荟萃分析之间可能存在的异质性的经验证据。
我们的分析包括 Cochrane 系统评价数据库中的 6492 项连续性结局荟萃分析。我们通过对所有荟萃分析的研究数据进行标准化均数差尺度建模,研究了荟萃分析设置对异质性的影响。根据结局类型、干预比较类型和医学领域描述荟萃分析设置。获得了未来荟萃分析中预期的研究间方差的预测分布,可直接用作信息性先验。
在结局类型中,产科结局的荟萃分析中异质性最低。在干预比较类型中,两种药物干预比较的荟萃分析中异质性最低。报告了不同设置的预测分布。在两个示例荟萃分析中,纳入外部证据可得出更精确的异质性估计。
荟萃分析特征影响异质性。为每个特定设置生成了研究间方差的信息性先验。因此,我们的分析有助于将现实的先验信息纳入包括少量研究的荟萃分析中。