BACKGROUND: Mendelian randomization uses a carefully selected gene as an instrumental-variable (IV) to test or estimate an association between a phenotype and a disease. Classical IV analysis assumes linear relationships between the variables, but disease status is often binary and modelled by a logistic regression. When the linearity assumption between the variables does not hold the IV estimates will be biased. The extent of this bias in the phenotype-disease log odds ratio of a Mendelian randomization study is investigated. METHODS: Three estimators termed direct, standard IV and adjusted IV, of the phenotype-disease log odds ratio are compared through a simulation study which incorporates unmeasured confounding. The simulations are verified using formulae relating marginal and conditional estimates given in the Appendix. RESULTS: The simulations show that the direct estimator is biased by unmeasured confounding factors and the standard IV estimator is attenuated towards the null. Under most circumstances the adjusted IV estimator has the smallest bias, although it has inflated type I error when the unmeasured confounders have a large effect. CONCLUSIONS: In a Mendelian randomization study with a binary disease outcome the bias associated with estimating the phenotype-disease log odds ratio may be of practical importance and so estimates should be subject to a sensitivity analysis against different amounts of hypothesized confounding.
BACKGROUND: Mendelian randomization uses a carefully selected gene as an instrumental-variable (IV) to test or estimate an association between a phenotype and a disease. Classical IV analysis assumes linear relationships between the variables, but disease status is often binary and modelled by a logistic regression. When the linearity assumption between the variables does not hold the IV estimates will be biased. The extent of this bias in the phenotype-disease log odds ratio of a Mendelian randomization study is investigated. METHODS: Three estimators termed direct, standard IV and adjusted IV, of the phenotype-disease log odds ratio are compared through a simulation study which incorporates unmeasured confounding. The simulations are verified using formulae relating marginal and conditional estimates given in the Appendix. RESULTS: The simulations show that the direct estimator is biased by unmeasured confounding factors and the standard IV estimator is attenuated towards the null. Under most circumstances the adjusted IV estimator has the smallest bias, although it has inflated type I error when the unmeasured confounders have a large effect. CONCLUSIONS: In a Mendelian randomization study with a binary disease outcome the bias associated with estimating the phenotype-disease log odds ratio may be of practical importance and so estimates should be subject to a sensitivity analysis against different amounts of hypothesized confounding.
Authors: Paul M McKeigue; Harry Campbell; Sarah Wild; Veronique Vitart; Caroline Hayward; Igor Rudan; Alan F Wright; James F Wilson Journal: Int J Epidemiol Date: 2010-03-25 Impact factor: 7.196
Authors: Aaron P Thrift; Nicholas J Shaheen; Marilie D Gammon; Leslie Bernstein; Brian J Reid; Lynn Onstad; Harvey A Risch; Geoffrey Liu; Nigel C Bird; Anna H Wu; Douglas A Corley; Yvonne Romero; Stephen J Chanock; Wong-Ho Chow; Alan G Casson; David M Levine; Rui Zhang; Weronica E Ek; Stuart MacGregor; Weimin Ye; Laura J Hardie; Thomas L Vaughan; David C Whiteman Journal: J Natl Cancer Inst Date: 2014-09-30 Impact factor: 13.506
Authors: Simon M Collin; Chris Metcalfe; Tom M Palmer; Helga Refsum; Sarah J Lewis; George Davey Smith; Angela Cox; Michael Davis; Gemma Marsden; Carole Johnston; J Athene Lane; Jenny L Donovan; David E Neal; Freddie C Hamdy; A David Smith; Richard M Martin Journal: Int J Mol Epidemiol Genet Date: 2011-11-28