Evidence map›Paper›PMID 41980431›Full record

ArticleHormones and behavior2026

Aging leads to altered physiological reactivity in response to repeated social separation stress in a nonhuman primate model.

Aaryn Mustoe, Jessica Greig, Addaline Alvarez, Clarissa Hinojosa, Jessica Duran, Alanna Melchor, Eden Comer, Yashfa Naseem, Juan-Pablo Arroyo, Hillary F Huber and 8 more

Abstract read
In one paragraph

Article in Hormones and behavior, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Aaryn MustoeSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA. Electronic address: amustoe@txbiomed.org.
Jessica GreigSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Addaline AlvarezSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Clarissa HinojosaSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Jessica DuranSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Alanna MelchorSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Eden ComerSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Yashfa NaseemSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Juan-Pablo ArroyoSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Hillary F HuberSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Donna Layne-ColonSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.
Ektoras LambrouDepartment of Biology, Trinity University, San Antonio, TX, USA.
Jessica CalleryDepartment of Biology, Trinity University, San Antonio, TX, USA.
Luis GiavedoniDepartment of Biology, Trinity University, San Antonio, TX, USA.
Kimberley A PhillipsSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA; Department of Psychology, Trinity University, San Antonio, TX, USA.
Emily S RothwellDepartment of Neurobiology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Adam B SalmonBarshop Institute for Longevity and Aging Studies and Department of Molecular Medicine, University of Texas Health San Antonio, San Antonio, TX, USA; Geriatric Research Education and Clinical Center, South Texas Veterans Healthcare Center, San Antonio, TX, USA.
Corinna N RossSouthwest National Primate Research Center, Texas Biomedical Research Institute, San Antonio, TX, USA.

Funding

The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
San Antonio OAIC - Research Education Component (REC)P30AG044271 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Adam Salmon, Elena Volpi · 2015 to 2026
$14.1M
Microbiome-mediated therapies for aging and healthspan in marmosetsR01AG065546 · NIA · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI REVELES, KELLY RENEE, ROSS, CORINNA NICOLE · 2020 to 2024
$3.4M
Development of Immunological Reagents for the Identification of New World Monkey BiomarkersR24OD030215 · OD · TRINITY UNIVERSITY · PI GIAVEDONI, LUIS DAVID · 2022 to 2025
$1.9M
Characterization of Marmosets as a Geroscience Model by the San Antonio MAPU34AG068482 · NIA · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI ROSS, CORINNA NICOLE, SALMON, ADAM · 2020 to 2022
$1.4M
NIA NIH HHS P30 AG044271NIA NIH HHS R01 AG065546NIA NIH HHS U34 AG068482NIH HHS P51 OD011133NIH HHS R24 OD030215
6 · The paper itself

Abstract

Social relationships are critical for maintaining physical health and psychological wellbeing. Since nearly 1 in 4 adults aged 65 years or older are socially isolated, there is a strong need to understand how repeated social stress negatively impacts health outcomes. Using a nonhuman primate model of social aging (i.e., marmosets), we examined whether individuals transitioning into old age ("peri-geri") or individuals who were already geriatric ("very-geri") showed differences in measures of hypothalamic-pituitary axis (HPA) activity, markers of metabolic function, and reunion social behavior in response to repeated social separation challenges (SSC). We found female marmosets, especially peri-geri females, had higher HPA reactivity and better HPA recovery than male marmosets, but this difference diminished in older, very-geri marmosets. HPA activity was correlated with multiple outcomes including locomotive behavior and grooming, changes in blood glucose levels, and neutrophil counts, but not estrogens. Marmosets who approached their partner more and were groomed less during reunions had higher cortisol levels the following day. Interestingly, we found two distinct HPA profiles among our marmosets with half showing strong HPA responses (reactors) and the other half showing little or no HPA response (non-reactors). Non-reactors had less weight gain/more weight loss; elevated levels of calcium, phosphorus, and white blood cells; and received less grooming and social contact time during reunion. Overall, old-aged marmosets who show attenuated HPA responses may have different vulnerabilities to negative health and behavioral outcomes during social stress, and male marmosets appear more likely to present with this HPA non-reactor phenotype earlier in aging.

Indexed as

AgingSocial IsolationStress, PsychologicalAnimalsBlood GlucoseCallithrixFemaleGroomingHydrocortisoneHypothalamo-Hypophyseal SystemMalePituitary-Adrenal SystemSocial BehaviorBlood GlucoseHydrocortisoneCortisolEstrogenInflammationMarmosetsMetabolismSocial agingStress reactivity

Identifiers

PMID41980431
PMCPMC13203376

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.