Evidence map›Paper›PMID 29467291›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice.

Kan Xie, Devon P Ryan, Brandon L Pearson, Kristin S Henzel, Frauke Neff, Ramon O Vidal, Magali Hennion, Isabelle Lehmann, Melvin Schleif, Susanne Schröder and 18 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing 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

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

  1. Pooled it
  2. A Review of the Effects of Maternal and Paternal Obesity on Neurodevelopmental Disorders and Related Neurobiology in Rodent and Human Offspring.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2026
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  19. Dietary restriction in senolysis and prevention and treatment of disease.Critical reviews in food science and nutrition · 2024
    Review
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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

28 authors.

Kan XieMolecular and Cellular Cognition Lab, German Center for Neurodegenerative Diseases (DZNE), 53127 Bonn, Germany.
Devon P RyanMolecular and Cellular Cognition Lab, German Center for Neurodegenerative Diseases (DZNE), 53127 Bonn, Germany.
Brandon L PearsonMolecular and Cellular Cognition Lab, German Center for Neurodegenerative Diseases (DZNE), 53127 Bonn, Germany.
Kristin S HenzelMolecular and Cellular Cognition Lab, German Center for Neurodegenerative Diseases (DZNE), 53127 Bonn, Germany.
Frauke NeffInstitute of Pathology, Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
Ramon O VidalComputational Systems Biology Lab, German Center for Neurodegenerative Diseases (DZNE), 37077 Göttingen, Germany.
Magali HennionComputational Systems Biology Lab, German Center for Neurodegenerative Diseases (DZNE), 37077 Göttingen, Germany.
Isabelle LehmannMolecular and Cellular Cognition Lab, German Center for Neurodegenerative Diseases (DZNE), 53127 Bonn, Germany.
Melvin SchleifSelective Vulnerability of Neurodegenerative Diseases Lab, German Center for Neurodegenerative Diseases (DZNE), 53127 Bonn, Germany.
Susanne SchröderMolecular and Cellular Cognition Lab, German Center for Neurodegenerative Diseases (DZNE), 53127 Bonn, Germany.
Thure AdlerGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Birgit RathkolbGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.ORCID 0000-0003-1239-0547
Jan RozmanGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Anna-Lena SchützComputational Systems Biology Lab, German Center for Neurodegenerative Diseases (DZNE), 37077 Göttingen, Germany.
Cornelia PrehnGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Michel E MickaelComputational Systems Biology Lab, German Center for Neurodegenerative Diseases (DZNE), 37077 Göttingen, Germany.
Marco WeiergräberResearch Group Experimental Neuropsychopharmacology, Federal Institute for Drugs and Medical Devices, 53175 Bonn, Germany.
Jerzy AdamskiGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Dirk H BuschInstitute for Medical Microbiology, Immunology and Hygiene, Technische Universität München, 81675 Munich, Germany.
Gerhard EhningerDepartment of Internal Medicine I, University Hospital Carl Gustav Carus, Technical University Dresden, 01307 Dresden, Germany.
Anna MatyniaJules Stein Eye Institute, University of California, Los Angeles, CA 90095.
Walker S JacksonSelective Vulnerability of Neurodegenerative Diseases Lab, German Center for Neurodegenerative Diseases (DZNE), 53127 Bonn, Germany.
Eckhard WolfChair of Molecular Animal Breeding and Biotechnology, Gene Center, Ludwig-Maximilians-Universität München, 81377 Munich, Germany.ORCID 0000-0002-0430-9510
Helmut FuchsGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Valerie Gailus-DurnerGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Stefan BonnComputational Systems Biology Lab, German Center for Neurodegenerative Diseases (DZNE), 37077 Göttingen, Germany.ORCID 0000-0003-4366-5662
Martin Hrabě de AngelisGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Dan EhningerMolecular and Cellular Cognition Lab, German Center for Neurodegenerative Diseases (DZNE), 53127 Bonn, Germany; dan.ehninger@dzne.de.ORCID 0000-0001-7464-1335

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced age is not only a major risk factor for a range of disorders within an aging individual but may also enhance susceptibility for disease in the next generation. In humans, advanced paternal age has been associated with increased risk for a number of diseases. Experiments in rodent models have provided initial evidence that paternal age can influence behavioral traits in offspring animals, but the overall scope and extent of paternal age effects on health and disease across the life span remain underexplored. Here, we report that old father offspring mice showed a reduced life span and an exacerbated development of aging traits compared with young father offspring mice. Genome-wide epigenetic analyses of sperm from aging males and old father offspring tissue identified differentially methylated promoters, enriched for genes involved in the regulation of evolutionarily conserved longevity pathways. Gene expression analyses, biochemical experiments, and functional studies revealed evidence for an overactive mTORC1 signaling pathway in old father offspring mice. Pharmacological mTOR inhibition during the course of normal aging ameliorated many of the aging traits that were exacerbated in old father offspring mice. These findings raise the possibility that inherited alterations in longevity pathways contribute to intergenerational effects of aging in old father offspring mice.

Indexed as

Epigenesis, GeneticLongevityAge FactorsAgingAnimalsDNA MethylationFathersFemaleHumansLife ExpectancyMaleMechanistic Target of Rapamycin Complex 1MicePedigreePromoter Regions, GeneticSpermatozoaMechanistic Target of Rapamycin Complex 1agingepigeneticsintergenerational inheritancemTORsperm

Identifiers

PMID29467291
PMCPMC5877957

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Registered trials

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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.