Evidence map›Paper›PMID 41102684›Full record

SynthesisBMC medical research methodology2025

Meta-analysis models relaxing the random-effects normality assumption: methodological systematic review and simulation study.

Kanella Panagiotopoulou, Theodoros Evrenoglou, Christopher H Schmid, Silvia Metelli, Anna Chaimani

Abstract readSystematic Review
In one paragraph

Synthesis in BMC medical research methodology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Kanella PanagiotopoulouCenter of Research in Epidemiology and Statistics (CRESS), Université Paris Cité, Inserm, Paris, France. kanellapanag@gmail.com.
Theodoros EvrenoglouInstitute of Medical Biometry and Statistics, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg im Breisgau, Germany.
Christopher H SchmidDepartment of Biostatistics, School of Public Health, Brown University, Providence, RI, USA.
Silvia MetelliCenter of Research in Epidemiology and Statistics (CRESS), Université Paris Cité, Inserm, Paris, France.
Anna ChaimaniCenter of Research in Epidemiology and Statistics (CRESS), Université Paris Cité, Inserm, Paris, France.

Funding

Agence Nationale de la Recherche ANR-22-CE36-0013-01
6 · The paper itself

Abstract

backgroundRandom-effects meta-analysis is widely used for synthesizing the studies of a systematic review assuming a normal distribution for the study-specific effects. However, this assumption might not always be plausible. Alternative options have been suggested but not used in published meta-analyses.

methodsWe conducted a systematic review to identify articles that proposed alternative meta-analysis models assuming non-normal distributions for the random effects, such as skewed or semi-parametric distributions. Subsequently, we performed a simulation study to evaluate the performance of the identified models and to compare them with the normal model. We considered 22 scenarios varying the amount of random-effects variance, the number of included studies, and the shape of the true distribution: normal, skew-normal, and mixture of two normal distributions. For each scenario, we generated 1000 meta-analyses datasets. To investigate additional aspects of the alternative models, we also applied them at three extracted simulated datasets representing three scenarios with different true distributions.

resultsWe identified in total 27 articles suggesting 24 alternative models that can be classified into three broad categories: models based on long-tail and skewed distributions, on mixtures of distributions, and on Dirichlet process priors (DP). We compared 15 models in our simulation study implemented in the Frequentist or Bayesian framework. Results revealed small differences in bias between the different models but larger differences in the level of coverage probability. Scenarios with large random-effects variance, lead to more inaccurate estimates of the mean of the random-effects distribution. However, mixture and semi-parametric models revealed latent underlying clustering of studies and assisted to form subgroups of common characteristics. The three simulated datasets demonstrated similar patterns with the simulation study for the bias of the mean of the random-effects distribution.

conclusionFocusing only on the mean of the random-effects distribution in meta-analysis can be misleading when substantial heterogeneity is suspected or outliers are present. In such cases, identifying the factors that differentiate the studies and looking at the prediction intervals can be very informative. Based on our simulation, investigators could have the normal model as their starting point and consider alternative models as sensitivity analysis in view of seemingly non-normal data.

Indexed as

Meta-Analysis as TopicModels, StatisticalBayes TheoremComputer SimulationData Interpretation, StatisticalHumansResearch DesignEvidence synthesisHeterogenous studiesOutliersSemi-parametric modelsSkewed data

Identifiers

PMID41102684
PMCPMC12532406

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.