Dose-response meta-analysis of differences in means

被引:135
作者
Crippa, Alessio [1 ]
Orsini, Nicola [1 ]
机构
[1] Karolinska Inst, Dept Publ Hlth Sci, Stockholm, Sweden
来源
BMC MEDICAL RESEARCH METHODOLOGY | 2016年 / 16卷
关键词
Meta-analysis; Dose-response; Mean differences; Random-effects; MULTIVARIATE METAANALYSIS; SCHIZOAFFECTIVE DISORDER; REGRESSION-MODELS; TREND ESTIMATION; SCHIZOPHRENIA; ARIPIPRAZOLE; STRATEGY; EFFICACY; PLACEBO; SAFETY;
D O I
10.1186/s12874-016-0189-0
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Meta-analytical methods are frequently used to combine dose-response findings expressed in terms of relative risks. However, no methodology has been established when results are summarized in terms of differences in means of quantitative outcomes. Methods: We proposed a two-stage approach. A flexible dose-response model is estimated within each study (first stage) taking into account the covariance of the data points (mean differences, standardized mean differences). Parameters describing the study-specific curves are then combined using a multivariate random-effects model (second stage) to address heterogeneity across studies. Results: The method is fairly general and can accommodate a variety of parametric functions. Compared to traditional non-linear models (e.g. E-max, logistic), spline models do not assume any pre-specified dose-response curve. Spline models allow inclusion of studies with a small number of dose levels, and almost any shape, even non monotonic ones, can be estimated using only two parameters. We illustrated the method using dose-response data arising from five clinical trials on an antipsychotic drug, aripiprazole, and improvement in symptoms in shizoaffective patients. Using the Positive and Negative Syndrome Scale (PANSS), pooled results indicated a non-linear association with the maximum change in mean PANSS score equal to 10.40 (95 % confidence interval 7.48, 13.30) observed for 19.32 mg/day of aripiprazole. No substantial change in PANSS score was observed above this value. An estimated dose of 10.43 mg/day was found to produce 80 % of the maximum predicted response. Conclusion: The described approach should be adopted to combine correlated differences in means of quantitative outcomes arising from multiple studies. Sensitivity analysis can be a useful tool to assess the robustness of the overall dose-response curve to different modelling strategies. A user-friendly R package has been developed to facilitate applications by practitioners.
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页数:10
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共 40 条
[31]  
Pinheiro JC, 2006, STAT BIOL HEALTH, P146
[32]   Aripiprazole, an antipsychotic with a novel mechanism of action, and risperidone vs placebo in patients with schizophrenia and schizoaffective disorder [J].
Potkin, SG ;
Saha, AR ;
Kujawa, MJ ;
Carson, WH ;
Ali, M ;
Stock, E ;
Stringfellow, J ;
Ingenito, G ;
Marder, SR .
ARCHIVES OF GENERAL PSYCHIATRY, 2003, 60 (07) :681-690
[33]   Multivariate meta-analysis for data consortia, individual patient meta-analysis, and pooling projects [J].
Ritz, John ;
Demidenko, Eugene ;
Spiegelman, Donna .
JOURNAL OF STATISTICAL PLANNING AND INFERENCE, 2008, 138 (07) :1919-1933
[34]  
Royston P, 2000, STAT MED, V19, P1831, DOI 10.1002/1097-0258(20000730)19:14<1831::AID-SIM502>3.0.CO
[35]  
2-1
[36]   A new strategy for meta-analysis of continuous covariates in observational studies [J].
Sauerbrei, Willi ;
Royston, Patrick .
STATISTICS IN MEDICINE, 2011, 30 (28) :3341-3360
[37]   Meta-analysis of individual patient data from randomized trials: a review of methods used in practice [J].
Simmonds, MC ;
Higgins, JPT ;
Stewart, LA ;
Tierney, JF ;
Clarke, MJ ;
Thompson, SG .
CLINICAL TRIALS, 2005, 2 (03) :209-217
[38]   Meta-Analysis of Clinical Dose-Response in a Large Drug Development Portfolio [J].
Thomas, Neal ;
Sweeney, Kevin ;
Somayaji, Veena .
STATISTICS IN BIOPHARMACEUTICAL RESEARCH, 2014, 6 (04) :302-317
[39]  
Ting N., 2006, Dose finding in drug development
[40]   Publication Bias in Antipsychotic Trials: An Analysis of Efficacy Comparing the Published Literature to the US Food and Drug Administration Database [J].
Turner, Erick H. ;
Knoepflmacher, Daniel ;
Shapley, Lee .
PLOS MEDICINE, 2012, 9 (03)