Evidence map›Paper›PMID 34039610›Full record

ArticleScience advances2021

Disruption of paternal circadian rhythm affects metabolic health in male offspring via nongerm cell factors.

Maximilian Lassi, Archana Tomar, Gemma Comas-Armangué, Rebekka Vogtmann, Dorieke J Dijkstra, David Corujo, Raffaele Gerlini, Jonatan Darr, Fabienne Scheid, Jan Rozman and 10 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 29 citations in OpenAlex.

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  14. A single cell atlas of the mouse seminal vesicle.bioRxiv : the preprint server for biology · 2024
    Article
  15. Paternal impact on the developmental programming of sexual dimorphism.Frontiers in cell and developmental biology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 5 institutions in 5 countries.

Maximilian LassiInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.ORCID 0000-0002-2196-2378
Archana TomarInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.ORCID 0000-0001-5752-7020
Gemma Comas-ArmanguéInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.ORCID 0000-0001-6359-1053
Rebekka VogtmannDepartment of Gynecology and Obstetrics-University Hospital Essen - Essen, Germany.ORCID 0000-0002-8491-500X
Dorieke J DijkstraUniversity of Groningen, University Medical Center Groningen, Department of Obstetrics and Gynecology, Groningen, Netherlands.ORCID 0000-0001-6923-9237
David CorujoCancer and Leukemia Epigenetics and Biology Program, Josep Carreras Institute for Leukemia Research (IJC) Badalona, Spain.ORCID 0000-0001-7930-0935
Raffaele GerliniInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.
Jonatan DarrInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.
Fabienne ScheidInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.
Jan RozmanInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.ORCID 0000-0002-8035-8904
Antonio Aguilar-PimentelInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.ORCID 0000-0002-4694-7107
Omry KorenAzrieli Faculty of Medicine, Bar Ilan University, Safed, Israel.ORCID 0000-0002-7738-1337
Marcus BuschbeckCancer and Leukemia Epigenetics and Biology Program, Josep Carreras Institute for Leukemia Research (IJC) Badalona, Spain.ORCID 0000-0002-3218-4567
Helmut FuchsInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.ORCID 0000-0002-5143-2677
Susan MarschallInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.ORCID 0000-0001-5191-7060
Valerie Gailus-DurnerInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.ORCID 0000-0002-6076-0111
Martin Hrabe de AngelisInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany.ORCID 0000-0002-7898-2353
Torsten PlöschUniversity of Groningen, University Medical Center Groningen, Department of Obstetrics and Gynecology, Groningen, Netherlands.ORCID 0000-0002-9305-4045
Alexandra GellhausDepartment of Gynecology and Obstetrics-University Hospital Essen - Essen, Germany.ORCID 0000-0001-9506-4581
Raffaele TeperinoInstitute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health Neuherberg, Germany. raffaele.teperino@helmholtz-muenchen.de.ORCID 0000-0001-8815-1409
Helmholtz Zentrum München · DEEssen University Hospital · DEJosep Carreras Leukaemia Research Institute · ESUniversity Medical Center Groningen · NLBar-Ilan University · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circadian rhythm synchronizes each body function with the environment and regulates physiology. Disruption of normal circadian rhythm alters organismal physiology and increases disease risk. Recent epidemiological data and studies in model organisms have shown that maternal circadian disruption is important for offspring health and adult phenotypes. Less is known about the role of paternal circadian rhythm for offspring health. Here, we disrupted circadian rhythm in male mice by night-restricted feeding and showed that paternal circadian disruption at conception is important for offspring feeding behavior, metabolic health, and oscillatory transcription. Mechanistically, our data suggest that the effect of paternal circadian disruption is not transferred to the offspring via the germ cells but initiated by corticosterone-based parental communication at conception and programmed during in utero development through a state of fetal growth restriction. These findings indicate paternal circadian health at conception as a newly identified determinant of offspring phenotypes.

Indexed as

Circadian RhythmAnimalsMaleMicePhenotype

Identifiers

PMID34039610
PMCPMC8153725
OpenAlexW3165795642

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.