Evidence map›Paper›PMID 34211149›Full record

ArticleNature human behaviour2021

Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour.

Melinda C Mills, Felix C Tropf, David M Brazel, Natalie van Zuydam, Ahmad Vaez, eQTLGen Consortium, BIOS Consortium, Human Reproductive Behaviour Consortium, Tune H Pers, Harold Snieder and 5 more

Erratum issuedAbstract read
In one paragraph

Article in Nature human behaviour, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 86 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed, 2 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

86 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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26 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Melinda C Mills *Leverhulme Centre for Demographic Science, University of Oxford, Oxford, United Kingdom. melinda.mills@nuffield.ox.ac.uk.ORCID http://orcid.org/0000-0003-1704-0001
Felix C Tropf *Leverhulme Centre for Demographic Science, University of Oxford, Oxford, United Kingdom.ORCID http://orcid.org/0000-0003-2445-515X
David M Brazel *Leverhulme Centre for Demographic Science, University of Oxford, Oxford, United Kingdom.ORCID http://orcid.org/0000-0001-5361-2498
Natalie van ZuydamThe Beijer Laboratory and Department of Immunology, Genetics and Pathology, Uppsala University and SciLifeLab, Uppsala, Sweden.
Ahmad VaezDepartment of Epidemiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.ORCID http://orcid.org/0000-0001-9048-3795
eQTLGen Consortium
BIOS Consortium
Human Reproductive Behaviour Consortium
Tune H PersThe Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-0207-4831
Harold SniederDepartment of Epidemiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.ORCID http://orcid.org/0000-0003-1949-2298
John R B PerryMRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0001-6483-3771
Ken K OngMRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.ORCID http://orcid.org/0000-0003-4689-7530
Marcel den Hoed *The Beijer Laboratory and Department of Immunology, Genetics and Pathology, Uppsala University and SciLifeLab, Uppsala, Sweden.ORCID http://orcid.org/0000-0001-8081-428X
Nicola Barban *Department of Statistical Sciences, University of Bologna, Bologna, Italy.ORCID http://orcid.org/0000-0002-4362-4652
Felix R Day *MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom. felix.day@mrc-epid.cam.ac.uk.ORCID http://orcid.org/0000-0003-3789-7651

Funding

European Research Council 615603European Research Council 835079European Research Council 865356Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MC_UU_00006/2Medical Research Council MC_UU_12015/2Medical Research Council MR/T030852/1
6 · The paper itself

Abstract

Age at first sexual intercourse and age at first birth have implications for health and evolutionary fitness. In this genome-wide association study (age at first sexual intercourse, N = 387,338; age at first birth, N = 542,901), we identify 371 single-nucleotide polymorphisms, 11 sex-specific, with a 5-6% polygenic score prediction. Heritability of age at first birth shifted from 9% [CI = 4-14%] for women born in 1940 to 22% [CI = 19-25%] for those born in 1965. Signals are driven by the genetics of reproductive biology and externalising behaviour, with key genes related to follicle stimulating hormone (FSHB), implantation (ESR1), infertility and spermatid differentiation. Our findings suggest that polycystic ovarian syndrome may lead to later age at first birth, linking with infertility. Late age at first birth is associated with parental longevity and reduced incidence of type 2 diabetes and cardiovascular disease. Higher childhood socioeconomic circumstances and those in the highest polygenic score decile (90%+) experience markedly later reproductive onset. Results are relevant for improving teenage and late-life health, understanding longevity and guiding experimentation into mechanisms of infertility.

Indexed as

Polymorphism, Single NucleotideAdolescentAge FactorsCoitusFemaleGenetic Association StudiesHumansMaleParturitionReproduction

Identifiers

PMID34211149
PMCPMC7612120

What Socratic holds

Textmetadata
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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.