Evidence map›Paper›PMID 36722651›Full record

ArticlePaediatric and perinatal epidemiology2023

Bounding the average causal effect in Mendelian randomisation studies with multiple proposed instruments: An application to prenatal alcohol exposure and attention deficit hyperactivity disorder.

Elizabeth W Diemer, Alexandra Havdahl, Ole A Andreassen, Marcus R Munafò, Pal R Njolstad, Henning Tiemeier, Luisa Zuccolo, Sonja A Swanson

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Article in Paediatric and perinatal epidemiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Elizabeth W DiemerDepartment of Child and Adolescent Psychiatry, Erasmus MC, Rotterdam, the Netherlands.
Alexandra HavdahlMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Ole A AndreassenNORMENT, KG Jebsen Centre for Psychosis Research, Department of Clinical Science, University of Bergen, Bergen, Norway.
Marcus R MunafòMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Pal R NjolstadDepartment of Paediatric and Adolescent Medicine, Haukeland University Hospital, Bergen, Norway.
Henning TiemeierDepartment of Child and Adolescent Psychiatry, Erasmus MC, Rotterdam, the Netherlands.
Luisa ZuccoloMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Sonja A SwansonCAUSALab, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

Funding

Medical Research Council G0902144Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_19009Medical Research Council MC_UU_00011/7Wellcome Trust
6 · The paper itself

Abstract

backgroundAs large-scale observational data become more available, caution regarding causal assumptions remains critically important. This may be especially true for Mendelian randomisation (MR), an increasingly popular approach. Point estimation in MR usually requires strong, often implausible homogeneity assumptions beyond the core instrumental conditions. Bounding, which does not require homogeneity assumptions, is infrequently applied in MR.

objectivesWe aimed to demonstrate computing nonparametric bounds for the causal risk difference derived from multiple proposed instruments in an MR study where effect heterogeneity is expected.

methodsUsing data from the Norwegian Mother, Father and Child Cohort Study (n = 2056) and Avon Longitudinal Study of Parents and Children (n = 6216) to study the average causal effect of maternal pregnancy alcohol use on offspring attention deficit hyperactivity disorder symptoms, we proposed 11 maternal SNPs as instruments. We computed bounds assuming subsets of SNPs were jointly valid instruments, for all combinations of SNPs where the MR model was not falsified.

resultsThe MR assumptions were violated for all sets with more than 4 SNPs in one cohort and for all sets with more than 2 SNPs in the other. Bounds assuming one SNP was an individually valid instrument barely improved on assumption-free bounds. Bounds tightened as more SNPs were assumed to be jointly valid instruments, and occasionally identified directions of effect, though bounds from different sets varied.

conclusionsOur results suggest that, when proposing multiple instruments, bounds can contextualise plausible magnitudes and directions of effects. Computing bounds over multiple assumption sets, particularly in large, high-dimensional data, offers a means of triangulating results across different potential sources of bias within a study and may help researchers to better evaluate and emphasise which estimates are compatible with the most plausible assumptions for their specific setting.

Indexed as

Attention Deficit Disorder with HyperactivityPrenatal Exposure Delayed EffectsChildCohort StudiesFemaleHumansLongitudinal StudiesMendelian Randomization AnalysisPregnancyALSPACboundsinstrumental variablesMendelian randomisationMoBa

Identifiers

PMID36722651
PMCPMC10946905

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