Volume 30, Issue 5 pp. 521-528
Methodology Article

Constructing Causal Diagrams for Common Perinatal Outcomes: Benefits, Limitations and Motivating Examples with Maternal Antidepressant Use in Pregnancy

Gretchen Bandoli

Corresponding Author

Gretchen Bandoli

Department of Pediatrics, University of California, San Diego, La Jolla, CA

Correspondence:

Gretchen Bandoli, Department of Pediatrics, Center for Better Beginnings, 7910 Frost Street, Ste 370, San Diego, CA 92123, USA.

E-mail: [email protected]

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Kristin Palmsten

Kristin Palmsten

Department of Pediatrics, University of California, San Diego, La Jolla, CA

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Katrina F. Flores

Katrina F. Flores

Department of Pediatrics, University of California, San Diego, La Jolla, CA

Department of Family Medicine and Public Health, University of California, San Diego, La Jolla, CA

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Christina D. Chambers

Christina D. Chambers

Department of Pediatrics, University of California, San Diego, La Jolla, CA

Department of Family Medicine and Public Health, University of California, San Diego, La Jolla, CA

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First published: 10 May 2016
Citations: 29

Abstract

Background

Covariate selection to reduce bias in observational data analysis has primarily relied upon statistical criteria to guide researchers. This approach may lead researchers to condition on variables that ultimately increase bias in the effect estimates. The use of directed acyclic graphs (DAGs) aids researchers in constructing thoughtful models based on hypothesised biologic mechanisms to produce the least biased effect estimates possible.

Methods

After providing an overview of different relations in DAGs and the prevailing mechanisms by which conditioning on variables increases or reduces bias in a model, we illustrate examples of DAGs for maternal antidepressants in pregnancy and four separate perinatal outcomes.

Results

By comparing and contrasting the diagrams for maternal antidepressant use in pregnancy and spontaneous abortion, major malformations, preterm birth, and postnatal growth, we illustrate the different conditioning sets required for each model. Moreover, we illustrate why it is not appropriate to condition on the same set of covariates for the same exposure and different perinatal outcomes. We further discuss potential selection biases, overadjustment of mediators on the causal path, and sufficient sets of conditioning variables.

Conclusion

In our efforts to construct parsimonious models that minimise confounding and selection biases, we must rely upon our scientific knowledge of the causal mechanism. By structuring data collection and analysis around hypothesised DAGs, we ultimately aim to validly estimate the causal effect of interest.

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