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Record W2938667012 · doi:10.1101/602516

Within-family studies for Mendelian randomization: avoiding dynastic, assortative mating, and population stratification biases

2019· preprint· en· W2938667012 on OpenAlexfundno aff
Ben Brumpton, Eleanor Sanderson, Fernando Pires Hartwig, Sean Harrison, Gunnhild Åberge Vie, Yoonsu Cho, Laura D Howe, Amanda Hughes, Dorret I. Boomsma, Alexandra Havdahl, John L. Hopper, Michael C. Neale, Michel G. Nivard, Nancy L. Pedersen, Chandra A. Reynolds, Elliot M. Tucker–Drob, Andrew D. Grotzinger, Laurence J Howe, Tim Morris, Shuai Li, Wei‐Min Chen, Johan Hå‌kon Bjø‌rngaard, Kristian Hveem, Cristen J. Willer, David M. Evans, Jaakko Kaprio, Bjørn Olav Åsvol, George Davey Smith, Bjørn Olav Åsvold, Gibran Hemani, Neil M Davies

Bibliographic record

VenuebioRxiv (Cold Spring Harbor Laboratory) · 2019
Typepreprint
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenetic Associations and Epidemiology
Canadian institutionsnot available
FundersEconomic and Social Research CouncilMedical Research CouncilFakultet for medisin og helsevitenskap, Norges Teknisk-Naturvitenskapelige UniversitetNorwegian Institute of Public HealthNational Institutes of HealthFaculty of Medicine and Health, University of SydneyKarolinska InstitutetIstituto Superiore di SanitàUniversity of MelbourneUniversity of ExeterQIMR Berghofer Medical Research InstituteSt. Olavs Hospital Universitetssykehuset i TrondheimNorges ForskningsrådAcademy of FinlandStiftelsen Kristian Gerhard JebsenNorges Teknisk-Naturvitenskapelige UniversitetUniversité LavalSchool of Public Health, University of MichiganUniversidad de MurciaWellcome TrustHelse Midt-NorgeUniversity of Bristol
KeywordsMendelian randomizationAssortative matingPopulation stratificationPopulationMendelian inheritanceCausal inferenceDemographyRandomizationOffspringBiologyGeneticsEconometricsGenotypeBioinformaticsGenetic variantsClinical trialMathematicsGenePregnancySingle-nucleotide polymorphism

Abstract

fetched live from OpenAlex

Estimates from Mendelian randomization studies of unrelated individuals can be biased due to uncontrolled confounding from familial effects. Here we describe methods for within-family Mendelian randomization analyses and use simulation studies to show that family-based analyses can reduce such biases. We illustrate empirically how familial effects can affect estimates using data from 61,008 siblings from the Nord-Trøndelag Health Study and UK Biobank and replicated our findings using 222,368 siblings from 23andMe. Both Mendelian randomization estimates using unrelated individuals and within family methods reproduced established effects of lower BMI reducing risk of diabetes and high blood pressure. However, while Mendelian randomization estimates from samples of unrelated individuals suggested that taller height and lower BMI increase educational attainment, these effects were strongly attenuated in within-family Mendelian randomization analyses. Our findings indicate the necessity of controlling for population structure and familial effects in Mendelian randomization studies.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.116
metaresearch head score (Gemma)0.264
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesMetaresearch
Consensus categoriesnone
DomainCandidate signal: Methods · Consensus signal: none
Study designCandidate signal: Theoretical or conceptual · Consensus signal: Theoretical or conceptual
GenreCandidate signal: Methods · Consensus signal: Methods
Teacher disagreement score0.884
Threshold uncertainty score0.615

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.1160.264
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0030.002
Bibliometrics0.0020.003
Science and technology studies0.0020.004
Scholarly communication0.0020.003
Open science0.0030.002
Research integrity0.0020.003
Insufficient payload (model declined to judge)0.0030.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.037
GPT teacher head0.290
Teacher spread0.253 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

Study designTheoretical or conceptual
DomainMethods
GenreMethods

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations77
Published2019
Admission routes1
Has abstractyes

Explore more

Same venuebioRxiv (Cold Spring Harbor Laboratory)→Same topicGenetic Associations and Epidemiology→French-language works237,207→