Thomas Doneal, Platt Robert, Benedetti Andrea
Department of Epidemiology, Biostatistics & Occupational Health, McGill University, Montreal, Canada.
Department of Medicine, McGill University, Montreal, Canada.
BMC Med Res Methodol. 2017 Feb 16;17(1):28. doi: 10.1186/s12874-017-0307-7.
Individual patient data meta-analyses (IPD-MA) are often performed using a one-stage approach-- a form of generalized linear mixed model (GLMM) for binary outcomes. We compare (i) one-stage to two-stage approaches (ii) the performance of two estimation procedures (Penalized Quasi-likelihood-PQL and Adaptive Gaussian Hermite Quadrature-AGHQ) for GLMMs with binary outcomes within the one-stage approach and (iii) using stratified study-effect or random study-effects.
We compare the different approaches via a simulation study, in terms of bias, mean-squared error (MSE), coverage and numerical convergence, of the pooled treatment effect (β ) and between-study heterogeneity of the treatment effect (τ ). We varied the prevalence of the outcome, sample size, number of studies and variances and correlation of the random effects.
The two-stage and one-stage methods produced approximately unbiased β estimates. PQL performed better than AGHQ for estimating τ with respect to MSE, but performed comparably with AGHQ in estimating the bias of β and of τ . The random study-effects model outperformed the stratified study-effects model in small size MA.
The one-stage approach is recommended over the two-stage method for small size MA. There was no meaningful difference between the PQL and AGHQ procedures. Though the random-intercept and stratified-intercept approaches can suffer from their underlining assumptions, fitting GLMM with a random-intercept are less prone to misfit and has good convergence rate.
个体患者数据荟萃分析(IPD-MA)通常采用单阶段方法——一种用于二元结局的广义线性混合模型(GLMM)形式。我们比较了(i)单阶段与两阶段方法,(ii)在单阶段方法中用于二元结局GLMM的两种估计程序(惩罚拟似然法-PQL和自适应高斯埃尔米特求积法-AGHQ)的性能,以及(iii)使用分层研究效应或随机研究效应的情况。
我们通过模拟研究比较不同方法,涉及合并治疗效应(β)的偏倚、均方误差(MSE)、覆盖率和数值收敛性,以及治疗效应的研究间异质性(τ)。我们改变了结局的患病率、样本量、研究数量以及随机效应的方差和相关性。
两阶段和单阶段方法产生的β估计值大致无偏。在估计τ的MSE方面,PQL比AGHQ表现更好,但在估计β和τ的偏倚方面与AGHQ相当。在小样本量的荟萃分析中,随机研究效应模型优于分层研究效应模型。
对于小样本量的荟萃分析,推荐使用单阶段方法而非两阶段方法。PQL和AGHQ程序之间没有显著差异。尽管随机截距和分层截距方法可能受其潜在假设的影响,但采用随机截距拟合GLMM不太容易出现拟合不佳的情况,且具有良好的收敛速度。