Evidence map›Paper›PMID 30575273›Full record

ArticleAging cell2019

Cell-free DNA as a biomarker of aging.

Yee Voan Teo, Miriam Capri, Cristina Morsiani, Grazia Pizza, Ana Maria Caetano Faria, Claudio Franceschi, Nicola Neretti

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

84 citing papers in PubMed, 146 citations in OpenAlex.

  1. A multi-analyte blood test for acute spinal cord injury.The Journal of clinical investigation · 2025
    Trial
  2. Article
  3. The long-lived immune system of centenarians.Nature reviews. Immunology · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Cancer-Like Fragmentomic Characteristics of Somatic Variants in Cell-Free DNA.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review

24 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

7 authors at 5 institutions in 4 countries.

Yee Voan TeoDepartment of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, Rhode Island.
Miriam CapriCIG Interdepartmental Centre "Galvani", University of Bologna, Bologna, Italy.
Cristina MorsianiDIMES-Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
Grazia PizzaDIMES-Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
Ana Maria Caetano FariaDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Claudio FranceschiIRCCS, Institute of Neurological Sciences of Bologna, Bologna, Italy.
Nicola NerettiDepartment of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, Rhode Island.
Brown University · USUniversity of Bologna · ITImperial College London · GBIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversidade Federal de Minas Gerais · BR

Funding

The Role of Somatic Transposition in Age-associated Genomic InstabilityR01AG050582 · NIA · BROWN UNIVERSITY · PI NERETTI, NICOLA, SEDIVY, JOHN M · 2017 to 2022
$2.2M
NIA NIH HHS R01 AG050582
6 · The paper itself

Abstract

Cell-free DNA (cfDNA) is present in the circulating plasma and other body fluids and is known to originate mainly from apoptotic cells. Here, we provide the first in vivo evidence of global and local chromatin changes in human aging by analyzing cfDNA from the blood of individuals of different age groups. Our results show that nucleosome signals inferred from cfDNA are consistent with the redistribution of heterochromatin observed in cellular senescence and aging in other model systems. In addition, we detected a relative cfDNA loss at several genomic locations, such as transcription start and termination sites, 5'UTR of L1HS retrotransposons and dimeric AluY elements with age. Our results also revealed age and deteriorating health status correlate with increased enrichment of signals from cells in different tissues. In conclusion, our results show that the sequencing of circulating cfDNA from human blood plasma can be used as a noninvasive methodology to study age-associated changes to the epigenome in vivo.

Indexed as

AdultAgedAged, 80 and overAgingBiomarkersCell-Free Nucleic AcidsDNA Transposable ElementsHumansLongevityNucleosomesBiomarkersCell-Free Nucleic AcidsDNA Transposable ElementsNucleosomesagingcell-free DNAepigenetics

Identifiers

PMID30575273
PMCPMC6351822
OpenAlexW2905772373

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.