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Additive risk versus additive relative risk models
1Department of Epidemiology, UCLA School of Public Health 90024-1772.
Epidemiology (Cambridge, Mass.)
|January 1, 1993
Summary
Additive risk models, not additive relative risk models, are crucial for assessing causal interaction (interdependence of effects). This is especially important in stratified studies where relative risk models may incorrectly imply no interaction when it exists.
Area of Science:
- Epidemiology
- Biostatistics
- Causal Inference
Background:
- Assessing causal interaction is vital in epidemiology for understanding the interplay of multiple risk factors.
- Nonadditivity is often used as a criterion for detecting causal interaction.
- The choice of statistical model (additive risk vs. additive relative risk) can impact the assessment of interaction.
Purpose of the Study:
- To clarify the distinction between additive risk models and additive relative risk models in the context of causal interaction.
- To demonstrate that additive relative risk models do not reliably indicate the absence of causal interaction in stratified studies.
- To establish the necessity of using additive risk models for a complete assessment of causal interaction.
Main Methods:
- Theoretical analysis of additive risk and additive relative risk models.
- Examination of causal models, including those proposed by Rothman.
- Consideration of implications for stratified studies and matched case-control studies.
Main Results:
- Additive relative risk models do not consistently correspond to the absence of causal interaction in stratified analyses.
- The presence of nonadditivity in relative risk models does not necessarily equate to causal interaction.
- Additive risk models are required for a comprehensive evaluation of causal interaction.
Conclusions:
- Researchers should utilize additive risk models for accurate assessment of causal interaction.
- Findings highlight potential misinterpretations of causal interaction when relying solely on additive relative risk models.
- Matched case-control studies may necessitate external data for fitting appropriate additive risk models.