Evidence map›Paper›PMID 28990592›Full record

ArticleInternational journal of obesity (2005)2018

Maternal and fetal genetic contribution to gestational weight gain.

N M Warrington, R Richmond, B Fenstra, R Myhre, R Gaillard, L Paternoster, C A Wang, R N Beaumont, S Das, M Murcia and 54 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of obesity (2005), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
7.7field-weighted citation impact, top 3% of its field
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

30 citing papers in PubMed, 50 citations in OpenAlex.

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  14. Selection bias, a caveat in gestational weight gain researchJournal of the Turkish German Gynecological Association · 2023
    Article
  15. [Cholesterol 7α-Hydroxylase Gene-204A/C Polymorphism in Normal and Gestational Diabetic Pregnancies].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2023
    Article
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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

64 authors at 20 institutions in 12 countries.

N M WarringtonUniversity of Queensland Diamantina Institute, Translational Research Institute, Brisbane, Queensland, Australia.
R RichmondMedical Research Council Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
B FenstraDepartment of Epidemiology Research, Statens Serum Institute, Copenhagen, Denmark.
R MyhreNorwegian Institute of Public Health, Oslo, Norway.
R GaillardThe Generation R Study Group, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
L PaternosterMedical Research Council Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
C A WangDivision of Obstetrics and Gynaecology, The University of Western Australia, Perth, Western Australia, Australia.
R N BeaumontInstitute of Biomedical and Clinical Science, University of Exeter Medical School, University of Exeter, Royal Devon and Exeter Hospital, Exeter, UK.
S DasDepartment of Public Health and Primary Care, School of Public Health, Imperial College London, London, UK.
M MurciaEpidemiology and Environmental Health Joint Research Unit, FISABIO-Universitat Jaume I-Universitat de València, Valencia, Spain.
S J BartonMRC Lifecourse Epidemiology Unit, Faulty of Medicine, University of Southampton, Southampton, UK.
A EspinosaSpanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Spain.
E ThieringInstitute of Epidemiology I, Helmholtz Zentrum München- German Research Center for Environmental Health, Neuherberg, Germany.
M AtalayInstitute of Biomedicine, School of Medicine, University of Eastern Finland, Kuopio, Finland.
N PitkänenResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Turku, Finland.
I NtallaWilliam Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
A E JonssonThe Novo Nordisk Foundation Center for Basic Metabolic Research, Section of Metabolic Genetics, and Department of Public Health, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
R FreathyMedical Research Council Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
V KarhunenCenter for Life Course Health Research, Faculty of Medicine, University of Oulu, Oulu, Finland.
C M T TieslerInstitute of Epidemiology I, Helmholtz Zentrum München- German Research Center for Environmental Health, Neuherberg, Germany.
C AllardCentre de Recherche du Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Canada.
A CrawfordMedical Research Council Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
S M RingMedical Research Council Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
M MelbyeDepartment of Epidemiology Research, Statens Serum Institute, Copenhagen, Denmark.
P MagnusNorwegian Institute of Public Health, Oslo, Norway.
F RivadeneiraThe Generation R Study Group, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.ORCID 0000-0001-9435-9441
L SkotteDepartment of Epidemiology Research, Statens Serum Institute, Copenhagen, Denmark.
T HansenThe Novo Nordisk Foundation Center for Basic Metabolic Research, Section of Metabolic Genetics, and Department of Public Health, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
J MarshDivision of Obstetrics and Gynaecology, The University of Western Australia, Perth, Western Australia, Australia.
M GuxensSpanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Spain.
J W HollowayHuman Development and Health, Faculty of Medicine, University of Southampton, Southampton, UK.
H GrallertInstitute of Epidemiology II, Research Unit of Molecular Epidemiology, Helmholtz Zentrum München Research Center for Environmental Health, Neuherberg, Germany.
V W V JaddoeThe Generation R Study Group, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
W L LoweDepartment of Medicine, Division of Endocrinology, Metabolism, and Molecular Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
T RoumeliotakiDepartment of Social Medicine, University of Crete, Crete, Greece.
A T HattersleyInstitute of Biomedical and Clinical Science, University of Exeter Medical School, University of Exeter, Royal Devon and Exeter Hospital, Exeter, UK.
V LindiInstitute of Biomedicine, School of Medicine, University of Eastern Finland, Kuopio, Finland.
K PahkalaResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Turku, Finland.
K PanoutsopoulouDepartment of Human Genetics, Wellcome Trust Sanger Institute, Hinxton, UK.
M StandlInstitute of Epidemiology I, Helmholtz Zentrum München- German Research Center for Environmental Health, Neuherberg, Germany.
C FlexederInstitute of Epidemiology I, Helmholtz Zentrum München- German Research Center for Environmental Health, Neuherberg, Germany.
L BouchardDepartment of Biochemistry, Faculty of medicine and life sciences, Université de Sherbrooke, Sherbrooke, Canada.
E Aagaard NohrPublic Health Division of Gipuzkoa, Basque Government, Vitoria-Gasteiz, Spain.
L Santa MarinaSpanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Spain.
M KogevinasSpanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Spain.ORCID 0000-0002-9605-0461
H NiinikoskiDepartment of Pediatrics, Turku University Hospital, Turku, Finland.
G DedoussisDepartment of Nutrition and Dietetics, Harokopio University of Athens, Athens, Greece.
J HeinrichInstitute of Epidemiology I, Helmholtz Zentrum München- German Research Center for Environmental Health, Neuherberg, Germany.
R M ReynoldsBritish Heart Foundation Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
T LakkaInstitute of Biomedicine, School of Medicine, University of Eastern Finland, Kuopio, Finland.
E ZegginiDepartment of Human Genetics, Wellcome Trust Sanger Institute, Hinxton, UK.ORCID 0000-0003-4238-659X
O T RaitakariResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Turku, Finland.
L ChatziDepartment of Social Medicine, University of Crete, Crete, Greece.
H M InskipMRC Lifecourse Epidemiology Unit, Faulty of Medicine, University of Southampton, Southampton, UK.
M BustamanteSpanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Spain.
M-F HivertDepartment of Population Medicine at Harvard Pilgrim Health Care Institute, Harvard Medical School, Boston, MA, USA.
M-R JarvelinCenter for Life Course Health Research, Faculty of Medicine, University of Oulu, Oulu, Finland.
T I A SørensenThe Novo Nordisk Foundation Center for Basic Metabolic Research, Section of Metabolic Genetics, and Department of Public Health, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
C PennellDivision of Obstetrics and Gynaecology, The University of Western Australia, Perth, Western Australia, Australia.
J F FelixThe Generation R Study Group, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.
B JacobssonDepartment of Obstetrics and Gynecology, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden.
F GellerDepartment of Epidemiology Research, Statens Serum Institute, Copenhagen, Denmark.
D M EvansUniversity of Queensland Diamantina Institute, Translational Research Institute, Brisbane, Queensland, Australia.
D A LawlorMedical Research Council Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Helmholtz Zentrum München · DEErasmus MC · NLStatens Serum Institut · DKUniversitat Pompeu Fabra · ESUniversity of Bristol · GBNorwegian Institute of Public Health · NOThe University of Western Australia · AUUniversity of Copenhagen · DKUniversity of Eastern Finland · FIUniversity of Exeter · GBUniversity of Turku · FIBritish Heart Foundation · GBTranslational Research Institute · AUWellcome Sanger Institute · GBBasque Government · ESBiogipuzkoa Health Research Institute · ESCentre Hospitalier Universitaire de Sherbrooke · CAHarokopio University of Athens · GRHarvard University · USImperial College London · GB

Funding

Metabolomic and Epigenomic Mechanisms in Developmental Overnutrition.R01DK103246 · NIDDK · UNIVERSITY OF BRISTOL · PI LAWLOR, DEBORAH ANNE · 2014 to 2018
$2.2M
British Heart Foundation RG/15/17/31749Cancer Research UK 19169European Research Council 648916Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_UP_A620_1017Medical Research Council MC_UU_12011/4Medical Research Council MC_UU_12013/4Medical Research Council MC_UU_12013/5Medical Research Council MR/J012165/1NIDDK NIH HHS R01 DK103246Wellcome Trust 088806
6 · The paper itself

Abstract

backgroundClinical recommendations to limit gestational weight gain (GWG) imply high GWG is causally related to adverse outcomes in mother or offspring, but GWG is the sum of several inter-related complex phenotypes (maternal fat deposition and vascular expansion, placenta, amniotic fluid and fetal growth). Understanding the genetic contribution to GWG could help clarify the potential effect of its different components on maternal and offspring health. Here we explore the genetic contribution to total, early and late GWG. PARTICIPANTS AND

methodsA genome-wide association study was used to identify maternal and fetal variants contributing to GWG in up to 10 543 mothers and 16 317 offspring of European origin, with replication in 10 660 mothers and 7561 offspring. Additional analyses determined the proportion of variability in GWG from maternal and fetal common genetic variants and the overlap of established genome-wide significant variants for phenotypes relevant to GWG (for example, maternal body mass index (BMI) and glucose, birth weight).

resultsApproximately 20% of the variability in GWG was tagged by common maternal genetic variants, and the fetal genome made a surprisingly minor contribution to explain variation in GWG. Variants near the pregnancy-specific beta-1 glycoprotein 5 (PSG5) gene reached genome-wide significance (P=1.71 × 10

conclusionsWe found a modest contribution of maternal common variants to GWG and some overlap of maternal BMI, glucose and type 2 diabetes variants with GWG. These findings suggest that associations between GWG and later offspring/maternal outcomes may be due to the relationship of maternal BMI and diabetes with GWG.

Indexed as

FemaleFetusGenome-Wide Association StudyGestational Weight GainHumansPregnancy

Identifiers

PMID28990592
PMCPMC5784805
OpenAlexW2600809019

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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.