TY - JOUR
T1 - Adjusting for misclassification of an exposure in an individual participant data meta-analysis
AU - de Jong, Valentijn M.T.
AU - Campbell, Harlan
AU - Maxwell, Lauren
AU - Jaenisch, Thomas
AU - Gustafson, Paul
AU - Debray, Thomas P.A.
N1 - Funding Information:
Horizon 2020 Framework Programme under ReCoDID grant agreement, Grant/Award Number: 825746; Canadian Institutes of Health Research, Institute of Genetics (CIHR‐IG), Grant/Award Number: 01886‐000 Funding information
Funding Information:
This project has received funding from the European Union's Horizon 2020 research, the Canadian Institutes of Health Research, Institute of Genetics (CIHR-IG) grant agreement No 01886-000 and innovation programme under ReCoDID grant agreement No 825746. We thank the IDAMS consortium for providing aggregate data on the diagnosis of dengue. We would like to thank the Editor in Chief, the Associate Editor, and the reviewers for their helpful comments that have substantially improved the manuscript.
Funding Information:
This project has received funding from the European Union's Horizon 2020 research, the Canadian Institutes of Health Research, Institute of Genetics (CIHR‐IG) grant agreement No 01886‐000 and innovation programme under ReCoDID grant agreement No 825746. We thank the IDAMS consortium for providing aggregate data on the diagnosis of dengue. We would like to thank the Editor in Chief, the Associate Editor, and the reviewers for their helpful comments that have substantially improved the manuscript.
Publisher Copyright:
© 2022 The Authors. Research Synthesis Methods published by John Wiley & Sons Ltd.
PY - 2023/3
Y1 - 2023/3
N2 - A common problem in the analysis of multiple data sources, including individual participant data meta-analysis (IPD-MA), is the misclassification of binary variables. Misclassification may lead to biased estimators of model parameters, even when the misclassification is entirely random. We aimed to develop statistical methods that facilitate unbiased estimation of adjusted and unadjusted exposure-outcome associations and between-study heterogeneity in IPD-MA, where the extent and nature of exposure misclassification may vary across studies. We present Bayesian methods that allow misclassification of binary exposure variables to depend on study- and participant-level characteristics. In an example of the differential diagnosis of dengue using two variables, where the gold standard measurement for the exposure variable was unavailable for some studies which only measured a surrogate prone to misclassification, our methods yielded more accurate estimates than analyses naive with regard to misclassification or based on gold standard measurements alone. In a simulation study, the evaluated misclassification model yielded valid estimates of the exposure-outcome association, and was more accurate than analyses restricted to gold standard measurements. Our proposed framework can appropriately account for the presence of binary exposure misclassification in IPD-MA. It requires that some studies supply IPD for the surrogate and gold standard exposure, and allows misclassification to follow a random effects distribution across studies conditional on observed covariates (and outcome). The proposed methods are most beneficial when few large studies that measured the gold standard are available, and when misclassification is frequent.
AB - A common problem in the analysis of multiple data sources, including individual participant data meta-analysis (IPD-MA), is the misclassification of binary variables. Misclassification may lead to biased estimators of model parameters, even when the misclassification is entirely random. We aimed to develop statistical methods that facilitate unbiased estimation of adjusted and unadjusted exposure-outcome associations and between-study heterogeneity in IPD-MA, where the extent and nature of exposure misclassification may vary across studies. We present Bayesian methods that allow misclassification of binary exposure variables to depend on study- and participant-level characteristics. In an example of the differential diagnosis of dengue using two variables, where the gold standard measurement for the exposure variable was unavailable for some studies which only measured a surrogate prone to misclassification, our methods yielded more accurate estimates than analyses naive with regard to misclassification or based on gold standard measurements alone. In a simulation study, the evaluated misclassification model yielded valid estimates of the exposure-outcome association, and was more accurate than analyses restricted to gold standard measurements. Our proposed framework can appropriately account for the presence of binary exposure misclassification in IPD-MA. It requires that some studies supply IPD for the surrogate and gold standard exposure, and allows misclassification to follow a random effects distribution across studies conditional on observed covariates (and outcome). The proposed methods are most beneficial when few large studies that measured the gold standard are available, and when misclassification is frequent.
KW - individual participant data
KW - measurement error
KW - meta-analysis
KW - misclassification
UR - http://www.scopus.com/inward/record.url?scp=85142155733&partnerID=8YFLogxK
U2 - 10.1002/jrsm.1606
DO - 10.1002/jrsm.1606
M3 - Article
AN - SCOPUS:85142155733
SN - 1759-2879
VL - 14
SP - 193
EP - 210
JO - Research Synthesis Methods
JF - Research Synthesis Methods
IS - 2
ER -