Evidence map›Paper›PMID 40578003›Full record

ArticlePsychoneuroendocrinology2025

Saliva and blood cell-free mtDNA reactivity to acute psychosocial stress.

Caroline Trumpff, David Shire, Jeremy Michelson, Natalia Bobba-Alves, Temmie Yu, Richard P Sloan, Robert-Paul Juster, Michio Hirano, Martin Picard

Abstract read
In one paragraph

Article in Psychoneuroendocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Caroline TrumpffDivision of Behavioral Medicine, Department of Psychiatry, Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States.
David ShireDivision of Behavioral Medicine, Department of Psychiatry, Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States.
Jeremy MichelsonDivision of Behavioral Medicine, Department of Psychiatry, Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States.
Natalia Bobba-AlvesDivision of Behavioral Medicine, Department of Psychiatry, Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States.
Temmie YuDivision of Behavioral Medicine, Department of Psychiatry, Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States.
Richard P SloanDivision of Behavioral Medicine, Department of Psychiatry, Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States.
Robert-Paul JusterDepartment of Psychiatry and Addiction, University of Montreal, Pavillon Roger-Gaudry, 2900 boulevard Édouard-Montpetit, Montréal, Québec H3T 1J4, Canada.
Michio HiranoH. Houston Merritt Center for Neuromuscular and Mitochondrial Disorders, Columbia Translational Neuroscience Initiative, Department of Neurology, Columbia University Irving Medical Center, 630 West 168th Street, New York, NY 10032, United States.
Martin PicardDivision of Behavioral Medicine, Department of Psychiatry, Columbia University Irving Medical Center, 1051 Riverside Drive, New York, NY 10032, United States; H. Houston Merritt Center for Neuromuscular and Mitochondrial Disorders, Columbia Translational Neuroscience Initiative, Department of Neurology, Columbia University Irving Medical Center, 630 West 168th Street, New York, NY 10032, United States; Robert N. Butler Columbia Aging Center, Columbia University Mailman School of Public Health, 722 West 168th Street, 4th Floor Suite 410, MSPH Box 25, New York, NY 10032, United States; New York State Psychiatric Institute, 1051 Riverside Drive, New York, NY 10032, United States. Electronic address: martin.picard@columbia.edu.

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
The North American Mitochondrial Disease Consortium (NAMDC)U54NS078059 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HAAS, RICHARD H · 2011 to 2023
$17.5M
Mitochondrial regulation of stress reactivity in humansR01MH122706 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PICARD, MARTIN · 2020 to 2024
$3.8M
Transduction of Psychological Stress into Systematic Inflammation by Mitochondrial DNA SignalingR01MH119336 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI KAUFMAN, BRETT A, MARSLAND, ANNA L · 2019 to 2023
$3.4M
Mitochondrial Energetics, Circuits and Cognitive Decline in the Aging Human BrainRF1AG076821 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PICARD, MARTIN · 2022 to 2022
$2.4M
Psychobiological regulation and molecular characterization of cell-free mitochondrial DNA in humansR01MH137190 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Martin Picard, Caroline Trumpff · 2024 to 2026
$2.4M
Mitochondrial Regulation of Stress Reactivity in HumansR21MH113011 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PICARD, MARTIN · 2017 to 2018
$440k
Psychobiological Regulation of Cell-Free Mitochondrial DNA in Human SalivaR21MH123927 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PICARD, MARTIN · 2021 to 2022
$405k
NCATS NIH HHS UL1 TR001873NCI NIH HHS P30 CA013696NIA NIH HHS RF1 AG076821NIMH NIH HHS R01 MH119336NIMH NIH HHS R01 MH122706NIMH NIH HHS R01 MH137190NIMH NIH HHS R21 MH113011NIMH NIH HHS R21 MH123927NINDS NIH HHS U54 NS078059
6 · The paper itself

Abstract

Human blood contains cell-free mitochondrial DNA (cf-mtDNA) that dynamically increases in concentration in response to acute mental stress. Like other neuroendocrine stress markers, we previously found that cf-mtDNA is also detectable in saliva, calling for studies examining saliva cf-mtDNA reactivity to mental stress. In the present study, participants from the MiSBIE (Mitochondrial Stress, Brain Imaging, and Epigenetics) study (n = 68, 66 % women), were exposed to a brief socio-evaluative stressor, which induced a striking 280 % or 2.8-fold increase in saliva cf-mtDNA concentration within 10 min (g=0.55, p < 0.0001). In blood drawn concurrently with saliva sampling, stress increased cf-mtDNA by an average 32 % at 60 min in serum (g=0.20), but not in anticoagulated plasma where cf-mtDNA decreased by 19 % at 60 min (g=0.25). Examining the influence of mitochondrial health on cf-mtDNA reactivity in participants with rare mitochondrial diseases (MitoD), we report that a subset of MitoD participants exhibit markedly blunted saliva cf-mtDNA stress reactivity, suggesting that bioenergetic defects within mitochondria may influence the magnitude of saliva, and possibly blood cf-mtDNA responses. Our results document robust saliva cf-mtDNA stress reactivity and provide a methodology to examine the psychobiological regulation of cell-free mitochondria in future studies.

Indexed as

Cell-Free Nucleic AcidsDNA, MitochondrialSalivaStress, PsychologicalAdultFemaleHumansMaleMiddle AgedMitochondriaMitochondrial DiseasesYoung AdultCell-Free Nucleic AcidsDNA, MitochondrialAcute psychological stressCell-free mitochondrial DNA (cf-mtDNA)EnergyMitochondrionRepeated measuresSaliva

Identifiers

PMID40578003
PMCPMC12276903

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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.