One-stage dose-response meta-analysis for aggregated data

被引:264
作者
Crippa, Alessio [1 ]
Discacciati, Andrea [2 ]
Bottai, Matteo [2 ]
Spiegelman, Donna [3 ]
Orsini, Nicola [1 ]
机构
[1] Karolinska Inst, Dept Publ Hlth Sci, Solnavagen 1E, S-11365 Stockholm, Sweden
[2] Karolinska Inst, Inst Environm Med, Stockholm, Sweden
[3] Harvard TH Chan Sch Publ Hlth, Boston, MA USA
关键词
Meta-analysis; dose-response; mixed model; random-effects; flexible model; LINEAR MIXED-MODEL; MULTIVARIATE METAANALYSIS; TREND ESTIMATION; HETEROGENEITY; REGRESSION; ALCOHOL; DISEASE; 2-STAGE;
D O I
10.1177/0962280218773122
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
The standard two-stage approach for estimating non-linear dose-response curves based on aggregated data typically excludes those studies with less than three exposure groups. We develop the one-stage method as a linear mixed model and present the main aspects of the methodology, including model specification, estimation, testing, prediction, goodness-of-fit, model comparison, and quantification of between-studies heterogeneity. Using both fictitious and real data from a published meta-analysis, we illustrated the main features of the proposed methodology and compared it to a traditional two-stage analysis. In a one-stage approach, the pooled curve and estimates of the between-studies heterogeneity are based on the whole set of studies without any exclusion. Thus, even complex curves (splines, spike at zero exposure) defined by several parameters can be estimated. We showed how the one-stage method may facilitate several applications, in particular quantification of heterogeneity over the exposure range, prediction of marginal and conditional curves, and comparison of alternative models. The one-stage method for meta-analysis of non-linear curves is implemented in the dosresmeta R package. It is particularly suited for dose-response meta-analyses of aggregated where the complexity of the research question is better addressed by including all the studies.
引用
收藏
页码:1579 / 1596
页数:18
相关论文
共 37 条
[1]  
[Anonymous], BIOMETRICS
[2]   Flexible meta-regression functions for modeling aggregate dose-response data, with an application to alcohol and mortality [J].
Bagnardi, V ;
Zambon, A ;
Quatto, P ;
Corrao, G .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2004, 159 (11) :1077-1086
[3]  
Berkey CS, 1998, STAT MED, V17, P2537, DOI 10.1002/(SICI)1097-0258(19981130)17:22<2537::AID-SIM953>3.0.CO
[4]  
2-C
[5]   METAANALYSIS OF EPIDEMIOLOGIC DOSE-RESPONSE DATA [J].
BERLIN, JA ;
LONGNECKER, MP ;
GREENLAND, S .
EPIDEMIOLOGY, 1993, 4 (03) :218-228
[6]   Multivariate Dose-Response Meta-Analysis: The dosresmeta R Package [J].
Crippa, Alessio ;
Orsini, Nicola .
JOURNAL OF STATISTICAL SOFTWARE, 2016, 72 (CS1)
[7]   Dose-response meta-analysis of differences in means [J].
Crippa, Alessio ;
Orsini, Nicola .
BMC MEDICAL RESEARCH METHODOLOGY, 2016, 16
[8]   A new measure of between-studies heterogeneity in meta-analysis [J].
Crippa, Alessio ;
Khudyakov, Polyna ;
Wang, Molin ;
Orsini, Nicola ;
Spiegelman, Donna .
STATISTICS IN MEDICINE, 2016, 35 (21) :3661-3675
[9]   Coffee Consumption and Mortality From All Causes, Cardiovascular Disease, and Cancer: A Dose-Response Meta-Analysis [J].
Crippa, Alessio ;
Discacciati, Andrea ;
Larsson, Susanna C. ;
Wolk, Alicja ;
Orsini, Nicola .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2014, 180 (08) :763-775
[10]   Goodness of fit tools for dose-response meta-analysis of binary outcomes [J].
Discacciati, Andrea ;
Crippa, Alessio ;
Orsini, Nicola .
RESEARCH SYNTHESIS METHODS, 2017, 8 (02) :149-160