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IJE Advance Access originally published online on August 27, 2007
International Journal of Epidemiology 2007 36(5):1111-1118; doi:10.1093/ije/dym157
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Published by Oxford University Press on behalf of the International Epidemiological Association © The Author 2007; all rights reserved.

Estimating interaction on an additive scale between continuous determinants in a logistic regression model

Mirjam J Knol1,2,*, Ingeborg van der Tweel3, Diederick E Grobbee1, Mattijs E Numans1 and Mirjam I Geerlings1

1Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, The Netherlands.
2Department of Pharmaco-Epidemiology and Pharmacotherapy, Utrecht Institute of Pharmaceutical Sciences, Utrecht University, The Netherlands.
3Centre for Biostatistics, Utrecht University, The Netherlands.

*Corresponding author. Str. 6.131, Julius Center, University Medical Center Utrecht, PO Box 85500, 3508 GA Utrecht, The Netherlands. E-mail: m.j.knol{at}umcutrecht.nl


   Abstract

Background To determine the presence of interaction in epidemiologic research, typically a product term is added to the regression model. In linear regression, the regression coefficient of the product term reflects interaction as departure from additivity. However, in logistic regression it refers to interaction as departure from multiplicativity. Rothman has argued that interaction estimated as departure from additivity better reflects biologic interaction. So far, literature on estimating interaction on an additive scale using logistic regression only focused on dichotomous determinants. The objective of the present study was to provide the methods to estimate interaction between continuous determinants and to illustrate these methods with a clinical example.

Methods and results From the existing literature we derived the formulas to quantify interaction as departure from additivity between one continuous and one dichotomous determinant and between two continuous determinants using logistic regression. Bootstrapping was used to calculate the corresponding confidence intervals. To illustrate the theory with an empirical example, data from the Utrecht Health Project were used, with age and body mass index as risk factors for elevated diastolic blood pressure.

Conclusions The methods and formulas presented in this article are intended to assist epidemiologists to calculate interaction on an additive scale between two variables on a certain outcome. The proposed methods are included in a spreadsheet which is freely available at: http://www.juliuscenter.nl/additive-interaction.xls.


Keywords Interaction, biologic, additive, continuous, effect-modification, relative excess risk

Accepted 3 July 2007


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