TY - JOUR

T1 - Survivor bias in Mendelian randomization analysis

AU - Vansteelandt, Stijn

AU - Dukes, Oliver

AU - Martinussen, Torben

N1 - © The Author 2017. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

PY - 2018

Y1 - 2018

N2 - Mendelian randomization studies employ genotypes as experimental handles to infer the effect of genetically modified exposures (e.g. vitamin D exposure) on disease outcomes (e.g. mortality). The statistical analysis of these studies makes use of the standard instrumental variables framework. Many of these studies focus on elderly populations, thereby ignoring the problem of left truncation, which arises due to the selection of study participants being conditional upon surviving up to the time of study onset. Such selection, in general, invalidates the assumptions on which the instrumental variables analysis rests. We show that Mendelian randomization studies of adult or elderly populations will therefore, in general, return biased estimates of the exposure effect when the considered genotype affects mortality; in contrast, standard tests of the causal null hypothesis that the exposure does not affect the mortality rate remain unbiased, even when they ignore this problem of left truncation. To eliminate "survivor bias" or "truncation bias" from the effect of exposure on mortality, we next propose various simple strategies under a semi-parametric additive hazard model. We examine the performance of the proposed methods in simulation studies and use them to infer the effect of vitamin D on all-cause mortality based on the Monica10 study with the genetic variant filaggrin as instrumental variable.

AB - Mendelian randomization studies employ genotypes as experimental handles to infer the effect of genetically modified exposures (e.g. vitamin D exposure) on disease outcomes (e.g. mortality). The statistical analysis of these studies makes use of the standard instrumental variables framework. Many of these studies focus on elderly populations, thereby ignoring the problem of left truncation, which arises due to the selection of study participants being conditional upon surviving up to the time of study onset. Such selection, in general, invalidates the assumptions on which the instrumental variables analysis rests. We show that Mendelian randomization studies of adult or elderly populations will therefore, in general, return biased estimates of the exposure effect when the considered genotype affects mortality; in contrast, standard tests of the causal null hypothesis that the exposure does not affect the mortality rate remain unbiased, even when they ignore this problem of left truncation. To eliminate "survivor bias" or "truncation bias" from the effect of exposure on mortality, we next propose various simple strategies under a semi-parametric additive hazard model. We examine the performance of the proposed methods in simulation studies and use them to infer the effect of vitamin D on all-cause mortality based on the Monica10 study with the genetic variant filaggrin as instrumental variable.

U2 - 10.1093/biostatistics/kxx050

DO - 10.1093/biostatistics/kxx050

M3 - Journal article

C2 - 29028924

VL - 19

SP - 426

EP - 443

JO - Biostatistics

JF - Biostatistics

SN - 1465-4644

IS - 4

ER -