Evidence map›Paper›PMID 35932451›Full record

ArticleHuman molecular genetics2023

Evaluating and implementing block jackknife resampling Mendelian randomization to mitigate bias induced by overlapping samples.

Si Fang, Gibran Hemani, Tom G Richardson, Tom R Gaunt, George Davey Smith

Abstract read
In one paragraph

Article in Human molecular genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Mendelian randomization.Nature reviews. Methods primers · 2022
    Article
  15. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Si FangPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol BS8 2BN, UK.ORCID 0000-0003-4934-1212
Gibran HemaniPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol BS8 2BN, UK.
Tom G RichardsonPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol BS8 2BN, UK.
Tom R GauntPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol BS8 2BN, UK.
George Davey SmithPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol BS8 2BN, UK.

Funding

British Heart Foundation AA/18/1/34219British Heart Foundation AA/18/7/34219Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MC_UU_00011/1Medical Research Council MC_UU_00011/4Medical Research Council MC_UU_00032/1Wellcome Trust 108902Wellcome Trust 108902/Z/15/ZWellcome Trust 208806Wellcome Trust 208806/Z/17/Z
6 · The paper itself

Abstract

Participant overlap can induce overfitting bias into Mendelian randomization (MR) and polygenic risk score (PRS) studies. Here, we evaluated a block jackknife resampling framework for genome-wide association studies (GWAS) and PRS construction to mitigate overfitting bias in MR analyses and implemented this study design in a causal inference setting using data from the UK Biobank. We simulated PRS and MR under three scenarios: (1) using weighted SNP estimates from an external GWAS, (2) using weighted SNP estimates from an overlapping GWAS sample and (3) using a block jackknife resampling framework. Based on a P-value threshold to derive genetic instruments for MR studies (P < 5 × 10-8) and a 10% variance in the exposure explained by all SNPs, block-jackknifing PRS did not suffer from overfitting bias (mean R2 = 0.034) compared with the externally weighted PRS (mean R2 = 0.040). In contrast, genetic instruments derived from overlapping samples explained a higher variance (mean R2 = 0.048) compared with the externally derived score. Overfitting became considerably more severe when using a more liberal P-value threshold to construct PRS (e.g. P < 0.05, overlapping sample PRS mean R2 = 0.103, externally weighted PRS mean R2 = 0.086), whereas estimates using jackknife score remained robust to overfitting (mean R2 = 0.084). Using block jackknife resampling MR in an applied analysis, we examined the effects of body mass index on circulating biomarkers which provided comparable estimates to an externally weighted instrument, whereas the overfitted scores typically provided narrower confidence intervals. Furthermore, we extended this framework into sex-stratified, multivariate and bidirectional settings to investigate the effect of childhood body size on adult testosterone levels.

Indexed as

Genome-Wide Association StudyMendelian Randomization AnalysisAdultBody Mass IndexHumansPolymorphism, Single NucleotideRisk Factors

Identifiers

PMID35932451
PMCPMC9840213

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.