Evidence map›Paper›PMID 40768637›Full record

ArticleAging and disease2025

Burn Injuries Accelerate Biological Aging and Increase the Epigenetically Inferred Risk of Mortality and Frailty.

Fadi Khalaf, Serena Yang, Dalia Barayan, Diana Julia Tedesco, Michael Chong, Guillaume Paré, Marc G Jeschke

Abstract read
In one paragraph

Article in Aging and disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Fadi KhalafDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Serena YangDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Dalia BarayanDavid Braley Research Institute, Hamilton, Ontario, Canada.
Diana Julia TedescoDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Michael ChongDavid Braley Research Institute, Hamilton, Ontario, Canada.
Guillaume ParéDavid Braley Research Institute, Hamilton, Ontario, Canada.
Marc G JeschkeDepartment of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.

Funding

Adverse outcomes of aged mice are associated with adipose tissue failure after burnR01AG080040 · NIA · HAMILTON HEALTH SCIENCES CORPORATION · PI Marc Gerhard Jeschke · 2023 to 2026
$1.3M
NIA NIH HHS R01 AG080040
6 · The paper itself

Abstract

Biological aging is closely associated with heightened disease risk, frailty, and mortality. Interestingly, physical traumas, such as burn injuries, exhibit physiological effects that resemble those of aging. However, the impact of burn injuries on biological aging remains underexplored, creating a gap in the literature that could inform better prognosis and outcomes. We conducted a prospective cohort study to investigate the effects of burn injuries on various epigenetic clocks, including HorvathAge, GrimAge, PhenoAge, and DunedinPoAm, using whole blood. The study included 59 burn patients and 25 healthy controls and was validated using a murine model of thermal injury. Our study demonstrates that burn injuries accelerate biological aging and the rate of aging, with these effects persisting for up to 28 days post-injury. The extent of biological aging was positively correlated with burn size, with severe burns resulting in an acceleration of 13-14 years in biological age as measured by GrimAge and PhenoAge-double the acceleration observed with chronic long-term smoking. This acceleration occurred irrespective of age or sex, though older patients were the most vulnerable to the aging effects of burn injuries. The role of burns as an accelerator of aging was further confirmed in mice, which exhibited the equivalent of 3-6 human years of accelerated aging (8 mouse months, or 7 human days) after the injury, reinforcing the chronic nature of the effect. Additionally, burn injuries increased epigenetically inferred risks of frailty and mortality in humans, highlighting their long-term and enduring consequences. Collectively, our findings identify burn injuries as the most significant and chronic accelerant of biological aging reported to date. To our knowledge, this study is one of the first to link burn injuries-or any form of physical trauma-to accelerated cellular and biological aging.

Indexed as

AgingBurnsEpigenesis, GeneticFrailtyAdultAgedAged, 80 and overAnimalsFemaleHumansMaleMiceMiddle AgedProspective StudiesRisk Factors

Identifiers

PMID40768637
PMCPMC13256645

What Socratic 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 Socratic graph.