Evidence map›Paper›PMID 34587296›Full record

SynthesisBiometrics2023

Accounting for post-randomization variables in meta-analysis: A joint meta-regression approach.

Qinshu Lian, Jing Zhang, James S Hodges, Yong Chen, Haitao Chu

Abstract readMeta-Analysis
In one paragraph

Synthesis in Biometrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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.

Qinshu LianDivision of Biostatistics, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0001-9570-5000
Jing ZhangDepartment of Epidemiology and Biostatistics, University of Maryland, College Park, Maryland.
James S HodgesDivision of Biostatistics, University of Minnesota, Minneapolis, Minnesota.
Yong ChenDepartment of Biostatistics, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0003-0835-0788
Haitao ChuDivision of Biostatistics, University of Minnesota, Minneapolis, Minnesota.ORCID 0000-0003-0932-598X

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR002494 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, WEISDORF, DANIEL J · 2018 to 2022
$34.9M
Prevention of Lower Urinary Tract Symptoms in Women: Bladder Health Scientific and Data Coordinating Center (PLUS-SDCC) (U01)U01DK106786 · NIDDK · UNIVERSITY OF MINNESOTA · PI HARLOW, BERNARD L, RUDSER, KYLE · 2015 to 2019
$8.4M
Prevention of Lower Urinary Tract Symptoms (PLUS) Research Consortium Scientific and Data Coordinating CenterU24DK106786 · NIDDK · UNIVERSITY OF MINNESOTA · PI MCGWIN, GERALD, RUDSER, KYLE · 2020 to 2024
$7.1M
Transforming mental health delivery through behavioral economics and implementation scienceP50MH113840 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI MANDELL, DAVID S · 2017 to 2020
$6.6M
Dynamic learning for post-vaccine event prediction using temporal information in VAERSR01AI130460 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI CHEN, YONG, TAO, CUI · 2017 to 2021
$3.4M
Machine Learning Prediction of Cancer SusceptibilityR01LM009012 · NLM · UNIVERSITY OF PENNSYLVANIA · PI MOORE, JASON H. · 2006 to 2014
$3.3M
Biomedical Computing and Informatics Strategies for Infectious Disease ResearchR01AI116794 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI MOORE, JASON H. · 2016 to 2020
$2.9M
A General Framework to Account for Outcome Reporting Bias in Systematic ReviewsR01LM012607 · NLM · UNIVERSITY OF PENNSYLVANIA · PI CHEN, YONG · 2017 to 2020
$1.4M
Statistical Methods and Software for Multivariate Meta-analysisR01LM012982 · NLM · UNIVERSITY OF MINNESOTA · PI LIN, LIFENG, SIEGEL, LIANNE · 2019 to 2022
$1.3M
Training in Biostatistics for Heart, Lung and Blood Disease ResearchT32HL129956 · NHLBI · UNIVERSITY OF MINNESOTA · PI NEATON, JAMES DENNIS · 2016 to 2020
$1.1M
Joint Meta-Regression Methods Accounting for Postrandomization VariablesR21LM012744 · NLM · UNIVERSITY OF MINNESOTA · PI CHU, HAITAO · 2017 to 2018
$376k
NCATS NIH HHS UL1 TR002494NHLBI NIH HHS T32 HL129956NIAID NIH HHS R01 AI116794NIAID NIH HHS R01 AI130460NIDDK NIH HHS U01 DK106786NIDDK NIH HHS U24 DK106786NIMH NIH HHS P50 MH113840NLM NIH HHS R01 LM009012NLM NIH HHS R01 LM012607NLM NIH HHS R01 LM012982NLM NIH HHS R21 LM012744
6 · The paper itself

Abstract

Meta-regression is widely used in systematic reviews to investigate sources of heterogeneity and the association of study-level covariates with treatment effectiveness. Existing meta-regression approaches are successful in adjusting for baseline covariates, which include real study-level covariates (e.g., publication year) that are invariant within a study and aggregated baseline covariates (e.g., mean age) that differ for each participant but are measured before randomization within a study. However, these methods have several limitations in adjusting for post-randomization variables. Although post-randomization variables share a handful of similarities with baseline covariates, they differ in several aspects. First, baseline covariates can be aggregated at the study level presumably because they are assumed to be balanced by the randomization, while post-randomization variables are not balanced across arms within a study and are commonly aggregated at the arm level. Second, post-randomization variables may interact dynamically with the primary outcome. Third, unlike baseline covariates, post-randomization variables are themselves often important outcomes under investigation. In light of these differences, we propose a Bayesian joint meta-regression approach adjusting for post-randomization variables. The proposed method simultaneously estimates the treatment effect on the primary outcome and on the post-randomization variables. It takes into consideration both between- and within-study variability in post-randomization variables. Studies with missing data in either the primary outcome or the post-randomization variables are included in the joint model to improve estimation. Our method is evaluated by simulations and a real meta-analysis of major depression disorder treatments.

Indexed as

Random AllocationBayes TheoremHumansSystematic Reviews as TopicTreatment OutcomeBayesian methodjoint modelingmeta-regressionmissing datapost-randomization variable

Identifiers

PMID34587296
PMCPMC8960477

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.