ArticleJournal of the Royal Statistical Society. Series B, Statistical methodology2012
Semiparametric tests for sufficient cause interaction.
Article in Journal of the Royal Statistical Society. Series B, Statistical methodology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- SUFFICIENT CAUSE INTERACTIONS FOR CATEGORICAL AND ORDINAL OUTCOMES.Statistica Sinica · 2021Article
- Invited Commentary: The Continuing Need for the Sufficient Cause Model Today.American journal of epidemiology · 2017Article
- Invited commentary: Some advantages of the relative excess risk due to interaction (RERI)--towards better estimators of additive interaction.American journal of epidemiology · 2014Article
- Causation and causal inference for genetic effects.Human genetics · 2012Review
- Inference for additive interaction under exposure misclassification.Biometrika · 2012Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
A sufficient cause interaction between two exposures signals the presence of individuals for whom the outcome would occur only under certain values of the two exposures. When the outcome is dichotomous and all exposures are categorical, then under certain no confounding assumptions, empirical conditions for sufficient cause interactions can be constructed based on the sign of linear contrasts of conditional outcome probabilities between differently exposed subgroups, given confounders. It is argued that logistic regression models are unsatisfactory for evaluating such contrasts, and that Bernoulli regression models with linear link are prone to misspecification. We therefore develop semiparametric tests for sufficient cause interactions under models which postulate probability contrasts in terms of a finite-dimensional parameter, but which are otherwise unspecified. Estimation is often not feasible in these models because it would require nonparametric estimation of auxiliary conditional expectations given high-dimensional variables. We therefore develop 'multiply robust tests' under a union model that assumes at least one of several working submodels holds. In the special case of a randomized experiment or a family-based genetic study in which the joint exposure distribution is known by design or Mendelian inheritance, the procedure leads to asymptotically distribution-free tests of the null hypothesis of no sufficient cause interaction.
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