Evidence map›Paper›PMID 32056197›Full record

SynthesisBiometrics2020

Relative efficiency of using summary versus individual data in random-effects meta-analysis.

Ding-Geng Chen, Dungang Liu, Xiaoyi Min, Heping Zhang

Abstract readMeta-Analysis
In one paragraph

Synthesis in Biometrics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 3 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

8 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
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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

4 authors.

Ding-Geng ChenSchool of Social Work & Department of Biostatistics, University of North Carolina, Chapel Hill, North Carolina.
Dungang LiuDepartment of Operations, Business Analytics, and Information Systems, Lindner College of Business, University of Cincinnati, Cincinnati, Ohio.ORCID 0000-0001-5340-9465
Xiaoyi MinDepartment of Mathematics and Statistics, Georgia State University, Atlanta, Georgia.
Heping ZhangDepartment of Biostatistics, Yale University, New Haven, Connecticut.ORCID 0000-0002-0688-4076

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Analysis of Big Data Squared in Biomedical StudiesR01MH116527 · NIMH · YALE UNIVERSITY · PI ZHANG, HEPING · 2018 to 2022
$2.3M
Analysis of Genomic and Complex DataR01HG010171 · NHGRI · YALE UNIVERSITY · PI ZHANG, HEPING · 2019 to 2022
$1.4M
National Science Foundation DMS-1722544NCATS NIH HHS UL1 TR001863NHGRI NIH HHS R01 HG010171NIH HHS R01 HG010171NIH HHS R01 MH116527NIMH NIH HHS R01 MH116527South Africa Medical Research Council 114613
6 · The paper itself

Abstract

Meta-analysis is a statistical methodology for combining information from diverse sources so that a more reliable and efficient conclusion can be reached. It can be conducted by either synthesizing study-level summary statistics or drawing inference from an overarching model for individual participant data (IPD) if available. The latter is often viewed as the "gold standard." For random-effects models, however, it remains not fully understood whether the use of IPD indeed gains efficiency over summary statistics. In this paper, we examine the relative efficiency of the two methods under a general likelihood inference setting. We show theoretically and numerically that summary-statistics-based analysis is at most as efficient as IPD analysis, provided that the random effects follow the Gaussian distribution, and maximum likelihood estimation is used to obtain summary statistics. More specifically, (i) the two methods are equivalent in an asymptotic sense; and (ii) summary-statistics-based inference can incur an appreciable loss of efficiency if the sample sizes are not sufficiently large. Our results are established under the assumption that the between-study heterogeneity parameter remains constant regardless of the sample sizes, which is different from a previous study. Our findings are confirmed by the analyses of simulated data sets and a real-world study of alcohol interventions.

Indexed as

Data Interpretation, StatisticalHumansdivide and conquerevidence synthesisindividual participant dataliterature reviewone-stage IPDtwo-stage IPD

Identifiers

PMID32056197
PMCPMC7955582

What OpenQuestion holds

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Registered trials

None linked

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.