Evidence map›Paper›PMID 39461952›Full record

ArticleNature communications2024

DINGO: increasing the power of locus discovery in maternal and fetal genome-wide association studies of perinatal traits.

Liang-Dar Hwang, Gabriel Cuellar-Partida, Loic Yengo, Jian Zeng, Jarkko Toivonen, Mikko Arvas, Robin N Beaumont, Rachel M Freathy, Gunn-Helen Moen, Nicole M Warrington and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Liang-Dar HwangInstitute for Molecular Bioscience, The University of Queensland, St Lucia, Australia. d.hwang@uq.edu.au.ORCID 0000-0002-5535-2199
Gabriel Cuellar-PartidaGilead Sciences, Inc, Foster City, CA, USA.
Loic YengoInstitute for Molecular Bioscience, The University of Queensland, St Lucia, Australia.ORCID 0000-0002-4272-9305
Jian ZengInstitute for Molecular Bioscience, The University of Queensland, St Lucia, Australia.
Jarkko ToivonenFinnish Red Cross Blood Service, Vantaa, Finland.ORCID 0000-0002-6843-5831
Mikko ArvasFinnish Red Cross Blood Service, Vantaa, Finland.ORCID 0000-0002-6902-8488
Robin N BeaumontDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.ORCID 0000-0003-0750-8248
Rachel M FreathyDepartment of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, UK.ORCID 0000-0003-4152-2238
Gunn-Helen MoenInstitute for Molecular Bioscience, The University of Queensland, St Lucia, Australia.
Nicole M WarringtonInstitute for Molecular Bioscience, The University of Queensland, St Lucia, Australia.ORCID 0000-0003-4195-775X
David M EvansInstitute for Molecular Bioscience, The University of Queensland, St Lucia, Australia. d.evans1@uq.edu.au.ORCID 0000-0003-0663-4621

Funding

Integrating genomic studies of gestational duration and birth weight to understand maternal and fetal causes of adverse pregnancy outcomes and links with later diseasesR01HD101669 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI FREATHY, RACHEL, JACOBSSON, BO · 2021 to 2024
$2.1M
Department of Education and Training | Australian Research Council (ARC) DE220101226Department of Education and Training | Australian Research Council (ARC) DE240100014Department of Education and Training | Australian Research Council (ARC) FT220100069Department of Health | National Health and Medical Research Council (NHMRC) 2008723Department of Health | National Health and Medical Research Council (NHMRC) 2017942Department of Health | National Health and Medical Research Council (NHMRC) GNT1157714NICHD NIH HHS R01 HD101669Wellcome TrustWellcome Trust (Wellcome) WT220390
6 · The paper itself

Abstract

Perinatal traits are influenced by fetal and maternal genomes. We investigate the performance of three strategies to detect loci in maternal and fetal genome-wide association studies (GWASs) of the same quantitative trait: (i) the traditional strategy of analysing maternal and fetal GWASs separately; (ii) a two-degree-of-freedom test which combines information from maternal and fetal GWASs; and (iii) a one-degree-of-freedom test where signals from maternal and fetal GWASs are meta-analysed together conditional on estimated sample overlap. We demonstrate that the optimal strategy depends on the extent of sample overlap, correlation between phenotypes, whether loci exhibit fetal and/or maternal effects, and whether these effects are directionally concordant. We apply our methods to summary statistics from a recent GWAS meta-analysis of birth weight. Both the two-degree-of-freedom and meta-analytic approaches increase the number of genetic loci for birth weight relative to separately analysing the scans. Our best strategy identifies an additional 62 loci compared to the most recently published meta-analysis of birth weight. We conclude that whilst the two-degree-of-freedom test may be useful for the analysis of certain perinatal phenotypes, for most phenotypes, a simple meta-analytic strategy is likely to perform best, particularly in situations where maternal and fetal GWASs only partially overlap.

Indexed as

Birth WeightFetusGenome-Wide Association StudyQuantitative Trait LociFemaleHumansPhenotypePolymorphism, Single NucleotidePregnancy

Identifiers

PMID39461952
PMCPMC11513127

What Socratic 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 Socratic graph.