Evidence map›Paper›PMID 40341365›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2025

Biomarkers of Oxidative and Mitochondrial Stress Are Associated With Accelerated Pace of Aging at Midlife in a Birth Cohort.

Te-Rina J King-Hudson, Andree G Pearson, Caitlin Dunstan-Harrison, Mathew T Powell, Nicholas J Magon, Teagan S Edwards, Louise N Paton, Jeffry S Tang, Anthony J Kettle, John F Pearson and 8 more

Abstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. 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

18 authors.

Te-Rina J King-HudsonDepartment of Pathology and Biomedical Science, Mātai Hāora-Centre for Redox Biology and Medicine, University of Otago, Christchurch, New Zealand.
Andree G PearsonDepartment of Pathology and Biomedical Science, Mātai Hāora-Centre for Redox Biology and Medicine, University of Otago, Christchurch, New Zealand.
Caitlin Dunstan-HarrisonDepartment of Biochemistry, University of Otago, Dunedin, New Zealand.
Mathew T PowellDepartment of Biochemistry, University of Otago, Dunedin, New Zealand.
Nicholas J MagonDepartment of Pathology and Biomedical Science, Mātai Hāora-Centre for Redox Biology and Medicine, University of Otago, Christchurch, New Zealand.
Teagan S EdwardsDepartment of Pathology and Biomedical Science, Mātai Hāora-Centre for Redox Biology and Medicine, University of Otago, Christchurch, New Zealand.ORCID 0009-0003-4428-7082
Louise N PatonDepartment of Pathology and Biomedical Science, Mātai Hāora-Centre for Redox Biology and Medicine, University of Otago, Christchurch, New Zealand.
Jeffry S TangDepartment of Pathology and Biomedical Science, Mātai Hāora-Centre for Redox Biology and Medicine, University of Otago, Christchurch, New Zealand.
Anthony J KettleDepartment of Pathology and Biomedical Science, Mātai Hāora-Centre for Redox Biology and Medicine, University of Otago, Christchurch, New Zealand.
John F PearsonDepartment of Medicine, University of Otago, Christchurch, New Zealand.
Jesse KokauaDunedin Multidisciplinary Health and Development Research Unit, Department of Psychology, University of Otago, Dunedin, New Zealand.
Hayley GuineyDunedin Multidisciplinary Health and Development Research Unit, Department of Psychology, University of Otago, Dunedin, New Zealand.
Reremoana TheodoreDunedin Multidisciplinary Health and Development Research Unit, Department of Psychology, University of Otago, Dunedin, New Zealand.
Sandhya RamrakhaDunedin Multidisciplinary Health and Development Research Unit, Department of Psychology, University of Otago, Dunedin, New Zealand.ORCID 0000-0002-0383-9886
Richie PoultonDunedin Multidisciplinary Health and Development Research Unit, Department of Psychology, University of Otago, Dunedin, New Zealand.
Terrie E MoffittDepartment of Psychology and Neuroscience, Duke University, Durham, North Carolina, USA.
Elizabeth C LedgerwoodDepartment of Pathology and Biomedical Science, Mātai Hāora-Centre for Redox Biology and Medicine, University of Otago, Christchurch, New Zealand.
Mark B HamptonDepartment of Pathology and Biomedical Science, Mātai Hāora-Centre for Redox Biology and Medicine, University of Otago, Christchurch, New Zealand.ORCID 0000-0002-7349-3729

Funding

Is mental disorder a preventable cause of age-related disease? The Dunedin Study.R01AG032282 · NIA · DUKE UNIVERSITY · PI CASPI, AVSHALOM, MOFFITT, TERRIE E · 2009 to 2025
$9.5M
Science CoreP2CHD065563 · NICHD · DUKE UNIVERSITY · PI Giovanna M Merli · 2015 to 2026
$5.7M
Validating a 3rd-generation methylation measure of accelerated aging: DunedinPoAm4xR01AG073207 · NIA · DUKE UNIVERSITY · PI CASPI, AVSHALOM, MOFFITT, TERRIE E · 2022 to 2025
$2.9M
NIA NIH HHS R01 AG032282NIA NIH HHS R01AG032282, AG073207NIA NIH HHS R01 AG073207NICHD NIH HHS P2C HD065563
6 · The paper itself

Abstract

Oxidative stress and mitochondrial dysfunction are proposed to play prominent roles in the biology of aging. Human studies are limited and confounded by metabolic disturbances associated with age-related diseases. In this study, we have measured biomarkers of oxidative and mitochondrial stress in blood samples from up to 864 participants in the longitudinal Dunedin Multidisciplinary Health and Development Study at age 45. We then determined the correlation between these cross-sectional biomarkers and the longitudinal Pace of Aging, a composite score that represents whole-organism functional decline in each participant from 26 to 45 years old, and facial age at 45 years old. Protein carbonyls and allantoin were selected as biomarkers for oxidative stress, and GDF-15 as a marker of mitochondrial stress. Midlife levels of these biomarkers were low but varied across the population. GDF-15 showed the strongest associations with the Pace of Aging (β = 0.26, p < .0001) and facial age (β = 0.12, p = .001) in sex- and smoking-adjusted models. The Pace of Aging was also significantly associated with allantoin (β = 0.14, p < .0001) and protein carbonyls (β = 0.09, p = .005), and allantoin was associated with facial age (β = 0.08, p = .02). These associations remained when the limited number of participants with age-related disease were removed from the analyses. Our results provide evidence of increased oxidative stress and mitochondrial stress in faster-aging humans at midlife, well before the onset of age-related disease.

Indexed as

AgingMitochondriaOxidative StressAdultAllantoinBiomarkersCross-Sectional StudiesFemaleGrowth Differentiation Factor 15HumansLongitudinal StudiesMaleMiddle AgedProtein CarbonylationAllantoinBiomarkersGDF15 protein, humanGrowth Differentiation Factor 15AgingBiomarkersGDF-15MitochondriaOxidative stress

Identifiers

PMID40341365
PMCPMC12202046

What Socratic holds

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LicenceCC BY-NC-ND
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.