Evidence map›Paper›PMID 36052758›Full record

ArticleAging cell2022

Umbilical cord plasma concentrate has beneficial effects on DNA methylation GrimAge and human clinical biomarkers.

James Clement, Qi Yan, Megha Agrawal, Ramon E Coronado, John A Sturges, Markus Horvath, Ake T Lu, Robert T Brooke, Steve Horvath

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

  1. Trial
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  3. Review
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  7. Article
  8. Review
  9. Quantification of Epigenetic Aging in Public Health.Annual review of public health · 2025
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Young Plasma Rejuvenates Blood DNA Methylation Profile, Extends Mean Lifespan, and Improves Physical Appearance in Old Rats.The journals of gerontology. Series A, Biological sciences and medical sciences · 2024
    Article
  17. Article
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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

9 authors at 6 institutions in 2 countries.

James ClementBetterhumans Inc., Gainesville, Florida, USA.
Qi YanEpigenetic Clock Development Foundation, Torrance, California, USA.
Megha AgrawalBetterhumans Inc., Gainesville, Florida, USA.
Ramon E CoronadoTransplant Department, UT Health San Antonio, San Antonio, Texas, USA.
John A SturgesJohn A Sturges, M.D., Coeur d'Alene, Idaho, USA.
Markus HorvathEpigenetic Clock Development Foundation, Torrance, California, USA.
Ake T LuDepartment of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, California, USA.
Robert T BrookeEpigenetic Clock Development Foundation, Torrance, California, USA.
Steve HorvathDepartment of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, California, USA.ORCID 0000-0002-4110-3589
Epigenetix (United States) · USUniversity of California, Los Angeles · USBetter Education Inc · USCrown College · USNorth Idaho College · USUniversity of Ferrara · IT

Funding

Validation and optimization of epigenetic clocksU01AG060908 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RITZ, BEATE R. · 2018 to 2022
$3.4M
NIA NIH HHS U01 AG060908
6 · The paper itself

Abstract

Plasma transfusions are standard treatments to replace missing proteins in people with rare genetic diseases. Prior studies have demonstrated that heterochronic parabiosis has beneficial effects on several tissues of old animals receiving young blood. Human clinical trials are currently underway to investigate whether the infusion of plasma or plasma-derived factors from young donors can be used to mitigate human age-related conditions. Here, we use data from a safety study (n = 18, mean age 74) to investigate whether human umbilical cord plasma concentrate (hereinafter Plasma Concentrate) injected weekly (1 ml intramuscular) into elderly human subjects over a 10-week period affects different biomarkers, including epigenetic age measures, standard clinical biomarkers of organ dysfunction, mitochondrial DNA copy number (mtDNA-CN), and leukocyte telomere length. This study shows that treatment with plasma concentrate is safe. More than 20 clinical biomarkers were significantly and beneficially altered following the treatments. For example, creatinine was significantly decreased (p = 0.0039), while estimated glomerular filtration rate (eGFR) was increased (p = 0.0044), indicating the treatment may improve biomarkers of kidney function. Three of four immunoglobulin biomarkers decreased, while telomere length and mtDNA-CN were not significantly affected by the treatment. The treatment reduced DNA methylation-based GrimAge by an average of 0.82 years (p = 0.0093), suggests a reduction in morbidity and mortality risk. By contrast, no significant results could be observed for epigenetic clocks that estimate chronological age. Our results support the view that plasma concentrate contains youth-promoting factors.

Indexed as

DNA MethylationDNA, MitochondrialAdolescentAgedAgingBiomarkersCreatinineEpigenesis, GeneticHumansInfantUmbilical CordBiomarkersCreatinineDNA, Mitochondrialclinical trialepigenetic clocksexosome treatmentumbilical cord plasmayoung plasma

Identifiers

PMID36052758
PMCPMC9577957
OpenAlexW4294218735

What OpenQuestion holds

Textmetadata
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.