Evidence map›Paper›PMID 41279958›Full record

ArticlebioRxiv : the preprint server for biology2025

The influence of captivity on cardiac structure and function across age, in rhesus macaques.

T G Dawkins, B A Curry, A Drane, V N Rivas, Y Ueda, J A Stern, D Philips, J Negron-Del Valle, Cayo Biobank Research Unit, J P Higham and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

13 authors.

T G DawkinsCentre for Heart, Lung, and Vascular Health, School of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, Canada.ORCID 0000-0001-5203-135X
B A CurryCentre for Heart, Lung, and Vascular Health, School of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, Canada.ORCID 0000-0002-5078-518X
A DraneFaculty of Medicine, Health & Life Sciences, Swansea University, Swansea, United Kingdom.ORCID 0000-0002-5208-917X
V N RivasDepartment of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, United States.ORCID 0000-0002-5016-3743
Y UedaCentre for Heart, Lung, and Vascular Health, School of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, Canada.ORCID 0000-0002-5577-3110
J A SternDepartment of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, United States.ORCID 0000-0001-5611-5745
D PhilipsSchool of Life Sciences, Arizona State University, Tempe, Arizona, United States.
J Negron-Del ValleSchool of Life Sciences, Arizona State University, Tempe, Arizona, United States.
Cayo Biobank Research Unit
J P HighamDepartment of Anthropology, New York University, New York, New York, United States.ORCID 0000-0002-1133-2030
N Snyder-MacklerSchool of Life Sciences, Arizona State University, Tempe, Arizona, United States.ORCID 0000-0003-3026-6160
L BrentCentre of Research in Animal Behaviour, University of Exeter, Exeter, United Kingdom.ORCID 0000-0002-1202-1939
R ShaveCentre for Heart, Lung, and Vascular Health, School of Health and Exercise Sciences, University of British Columbia Okanagan, Kelowna, Canada.ORCID 0000-0002-0283-037X

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
Training Program In Basic & Translational Cardiovascular ScienceT32HL086350 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Martin Cadeiras, David A. Liem · 2008 to 2026
$7.1M
UC Davis CTSC TL1 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility MentorshipTL1TR001861 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MEDICI, VALENTINA · 2016 to 2025
$4.7M
Social modifiers of the pace of aging across multiple domains and tissuesR01AG060931 · NIA · UNIVERSITY OF WASHINGTON · PI BRENT, LAUREN JOHANNA NICOLE, HIGHAM, JAMES P · 2019 to 2023
$3.6M
Impacts of hurricanes and social buffering on biological aging in a free-ranging animal modelR01AG084706 · NIA · NEW YORK UNIVERSITY · PI Lauren Johanna Nicole Brent, James P Higham · 2023 to 2026
$2.5M
NCATS NIH HHS TL1 TR001861NHLBI NIH HHS T32 HL086350NIA NIH HHS R01 AG060931NIA NIH HHS R01 AG084706NIH HHS P51 OD011107
6 · The paper itself

Abstract

Background: Captive non-human primates are widely used as models of human aging, yet the conditions they live in differ markedly from their naturalistic environment. Differences between captive and free-ranging environments may impact how the cardiovascular system adapts with age, potentially confounding studies of natural aging. This study characterized age-related cardiac phenotypes in free-ranging rhesus macaques and compared these patterns with their captive-housed counterparts to assess the influence of living environment on cardiac health across the lifespan. Methodology: We performed transthoracic echocardiography in a cross-sectional cohort of 133 free-ranging rhesus macaques ( Results: In our free-ranging cohort, older macaques had greater interventricular septal thickness and relative wall thickness (RWT) than young. Males exhibited larger left ventricular (LV) internal dimensions, wall thickness, LV mass, and LV volumes than females, but these differences were attenuated when indexed to body mass. Diastolic function was lower with advanced age in both sexes, reflected by a lower E/A ratio, reduced myocardial tissue velocities during early diastole (e') and greater myocardial tissue velocities during atrial contraction (a'). Compared with captive macaques, free-ranging animals exhibited better diastolic function, including a significantly higher E/A ratio, greater e', and lower a'. Captive macaques also had significantly greater relative wall thickness across age and between sexes. Conclusions and implications: Our study provides the first comprehensive characterization of age-related cardiac differences in free-ranging rhesus macaques, which show structural and functional cardiac differences similar to those observed with human aging. Captive macaques exhibited a more pronounced age-related cardiac phenotype than their free-ranging counterparts, including thicker left ventricular walls and lower diastolic function for a given age. These findings highlight the importance of considering the ecological context when interpreting animal models of cardiovascular aging.

Identifiers

PMID41279958
PMCPMC12633217

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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.