Evidence map›Paper›PMID 28351387›Full record

ArticleGenome biology2017

Dietary restriction protects from age-associated DNA methylation and induces epigenetic reprogramming of lipid metabolism.

Oliver Hahn, Sebastian Grönke, Thomas M Stubbs, Gabriella Ficz, Oliver Hendrich, Felix Krueger, Simon Andrews, Qifeng Zhang, Michael J Wakelam, Andreas Beyer and 2 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 150 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
150citing papers in PubMed, 1 pooled it
11.4field-weighted citation impact, top 1% 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

150 citing papers in PubMed, 1 synthesis or guideline pooled it, 243 citations in OpenAlex.

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  14. Influence of farnesoid X receptor (Frontiers in veterinary science · 2026
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90 more citing papers are in PubMed but not listed here.

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

12 authors at 6 institutions in 2 countries.

Oliver HahnMax Planck Institute for Biology of Ageing, 50931, Cologne, Germany.
Sebastian GrönkeMax Planck Institute for Biology of Ageing, 50931, Cologne, Germany.
Thomas M StubbsEpigenetics Programme, The Babraham Institute, Cambridge, CB22 3AT, UK.
Gabriella FiczBarts Cancer Institute, Queen Mary University of London, London, EC1M 6BQ, UK.
Oliver HendrichMax Planck Institute for Biology of Ageing, 50931, Cologne, Germany.
Felix KruegerBioinformatics Group, The Babraham Institute, Cambridge, CB22 3AT, UK.
Simon AndrewsBioinformatics Group, The Babraham Institute, Cambridge, CB22 3AT, UK.
Qifeng ZhangInositide Lab, The Babraham Institute, Cambridge, CB22 3AT, UK.
Michael J WakelamInositide Lab, The Babraham Institute, Cambridge, CB22 3AT, UK.
Andreas BeyerCellular Networks and Systems Biology, CECAD, University of Cologne, Joseph-Stelzmann-Str. 26, Cologne, 50931, Germany. andreas.beyer@uni-koeln.de.
Wolf ReikEpigenetics Programme, The Babraham Institute, Cambridge, CB22 3AT, UK. wolf.reik@babraham.ac.uk.
Linda PartridgeMax Planck Institute for Biology of Ageing, 50931, Cologne, Germany. Partridge@age.mpg.de.
Babraham Institute · GBMax Planck Institute for Biology of Ageing · DECologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases · DEQueen Mary University of London · GBUniversity College London · GBUniversity of Cologne · DE

Funding

Biotechnology and Biological Sciences Research Council BBS/E/B/000C0413Biotechnology and Biological Sciences Research Council BBS/E/B/000C0417European Research Council 268739Medical Research Council MR/M004821/1Wellcome Trust
6 · The paper itself

Abstract

backgroundDietary restriction (DR), a reduction in food intake without malnutrition, increases most aspects of health during aging and extends lifespan in diverse species, including rodents. However, the mechanisms by which DR interacts with the aging process to improve health in old age are poorly understood. DNA methylation could play an important role in mediating the effects of DR because it is sensitive to the effects of nutrition and can affect gene expression memory over time.

resultsHere, we profile genome-wide changes in DNA methylation, gene expression and lipidomics in response to DR and aging in female mouse liver. DR is generally strongly protective against age-related changes in DNA methylation. During aging with DR, DNA methylation becomes targeted to gene bodies and is associated with reduced gene expression, particularly of genes involved in lipid metabolism. The lipid profile of the livers of DR mice is correspondingly shifted towards lowered triglyceride content and shorter chain length of triglyceride-associated fatty acids, and these effects become more pronounced with age.

conclusionsOur results indicate that DR remodels genome-wide patterns of DNA methylation so that age-related changes are profoundly delayed, while changes at loci involved in lipid metabolism affect gene expression and the resulting lipid profile.

Indexed as

DietDNA MethylationEpigenesis, GeneticAgingAnimalsChromatinFatty AcidsFemaleGene Expression RegulationGene Expression Regulation, EnzymologicLipid MetabolismLiverMiceTime FactorsTranscription, GeneticChromatinFatty Acids

Identifiers

PMID28351387
PMCPMC5370449
OpenAlexW2599323298

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.