Evidence map›Paper›PMID 39217176›Full record

ArticleNature communications2024

scEpiAge: an age predictor highlighting single-cell ageing heterogeneity in mouse blood.

Marc Jan Bonder, Stephen J Clark, Felix Krueger, Siyuan Luo, João Agostinho de Sousa, Aida M Hashtroud, Thomas M Stubbs, Anne-Katrien Stark, Steffen Rulands, Oliver Stegle and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–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

12 citing papers in PubMed.

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  12. Time is encoded by methylation changes at clustered CpG sites.bioRxiv : the preprint server for biology · 2024
    Article
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.

Marc Jan BonderDivision of Computational Genomics and Systems Genetics, German Cancer Research Center, Heidelberg, Germany. bonder.m.j@gmail.com.ORCID 0000-0002-8431-3180
Stephen J ClarkAltos Labs, Cambridge Institute of Science, Cambridge, UK. sclark@altoslabs.com.ORCID 0000-0002-6183-491X
Felix KruegerAltos Labs, Cambridge Institute of Science, Cambridge, UK.ORCID 0000-0002-5513-3324
Siyuan LuoLaboratory of Nutrition and Metabolic Epigenetics, Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland.ORCID 0009-0007-6404-3244
João Agostinho de SousaLaboratory of Nutrition and Metabolic Epigenetics, Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland.ORCID 0000-0001-8124-6624
Aida M HashtroudMax Planck Institute for the Physics of Complex Systems, Dresden, Germany.
Thomas M StubbsEpigenetics Programme, The Babraham Institute, Cambridge, UK.ORCID 0000-0002-2990-7381
Anne-Katrien StarkImmunology Programme, The Babraham Institute, Cambridge, UK.
Steffen RulandsMax Planck Institute for the Physics of Complex Systems, Dresden, Germany.
Oliver StegleDivision of Computational Genomics and Systems Genetics, German Cancer Research Center, Heidelberg, Germany.ORCID 0000-0002-8818-7193
Wolf ReikAltos Labs, Cambridge Institute of Science, Cambridge, UK. wreik@altoslabs.com.ORCID 0000-0003-0216-9881
Ferdinand von MeyennLaboratory of Nutrition and Metabolic Epigenetics, Department of Health Sciences and Technology, ETH Zurich, Zurich, Switzerland. ferdinand.vonmeyenn@hest.ethz.ch.ORCID 0000-0001-9920-3075

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 803491EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 950349RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BBS/E/B/000C0421RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BBS/E/B/000C0422Wellcome TrustWellcome Trust (Wellcome) 210754/Z/18/Z
6 · The paper itself

Abstract

Ageing is the accumulation of changes and decline of function of organisms over time. The concept and biomarkers of biological age have been established, notably DNA methylation-based clocks. The emergence of single-cell DNA methylation profiling methods opens the possibility of studying the biological age of individual cells. Here, we generate a large single-cell DNA methylation and transcriptome dataset from mouse peripheral blood samples, spanning a broad range of ages. The number of genes expressed increases with age, but gene-specific changes are small. We next develop scEpiAge, a single-cell DNA methylation age predictor, which can accurately predict age in (very sparse) publicly available datasets, and also in single cells. DNA methylation age distribution is wider than technically expected, indicating epigenetic age heterogeneity and functional differences. Our work provides a foundation for single-cell and sparse data epigenetic age predictors, validates their functionality and highlights epigenetic heterogeneity during ageing.

Indexed as

AgingDNA MethylationEpigenesis, GeneticSingle-Cell AnalysisTranscriptomeAnimalsCellular SenescenceEpigenomicsFemaleGene Expression ProfilingMaleMiceMice, Inbred C57BL

Identifiers

PMID39217176
PMCPMC11366017

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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.