Evidence map›Paper›PMID 39180122›Full record

ArticleBiology of sex differences2024

Sex-specific cardiac remodeling in aged rats after adolescent chronic stress: associations with endocrine and metabolic factors.

Carley Dearing, Ella Sanford, Nicolette Olmstead, Rachel Morano, Lawson Wulsin, Brent Myers

Abstract read
In one paragraph

Article in Biology of sex differences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Carley DearingBiomedical Sciences, Colorado State University, Fort Collins, CO, USA.
Ella SanfordBiomedical Sciences, Colorado State University, Fort Collins, CO, USA.
Nicolette OlmsteadBiomedical Sciences, Colorado State University, Fort Collins, CO, USA.
Rachel MoranoPsychiatry and Behavioral Neuroscience, University of Cincinnati, Cincinnati, OH, USA.
Lawson WulsinPsychiatry and Behavioral Neuroscience, University of Cincinnati, Cincinnati, OH, USA.
Brent MyersBiomedical Sciences, Colorado State University, Fort Collins, CO, USA. brent.myers@colostate.edu.

Funding

Cortical-Medullary Circuitry Preventing the Cardiovascular Consequences of Chronic StressR01HL150559 · NHLBI · COLORADO STATE UNIVERSITY · PI MYERS, BRENT PHILIP · 2020 to 2024
$1.9M
Veterinary Scholars Summer Research ProgramT35OD015130 · OD · COLORADO STATE UNIVERSITY · PI ZABEL, MARK D · 2012 to 2021
$654k
Sex differences and metabolic responses to chronic stressF30OD032120 · OD · COLORADO STATE UNIVERSITY · PI DEARING, CARLEY · 2021 to 2025
$227k
NHLBI NIH HHS R01 HL150559NIH HHS F30 OD032120NIH HHS HL150559NIH HHS OD032120NIH HHS T35 OD015130
6 · The paper itself

Abstract

backgroundCardiovascular disease is a leading cause of death worldwide. Rates of cardiovascular disease vary both across the lifespan and between sexes. While multiple factors, including adverse life experiences, impact the development and progression of cardiovascular disease, the potential interactions of biological sex and stress history on the aged heart are unknown. To this end, we examined sex- and stress-specific impacts on left ventricular hypertrophy (VH) after aging. We hypothesized that early-life chronic stress exposure impacts behavioral and physiologic responses that predict cardiac remodeling in a sex-specific manner.

methodsHistological analysis was conducted on hearts of male and female rats previously exposed to chronic variable stress during the late adolescent period (postnatal days 43-62). These animals were challenged with a forced swim test and a glucose tolerance test before aging to 15 months and again being challenged. Predictive analyses were then used to isolate factors that relate to cardiac remodeling among these groups.

resultsEarly-life chronic stress impacted cardiac remodeling in a sex-specific manner. Among rats with a history of chronic stress, females had increased concentric VH. However, there were few associations within the female groups among individual behavioral and physiologic parameters and cardiac remodeling. While males as a group did not have VH after chronic stress, they exhibited multiple individual associations with cardiac susceptibility. Passive coping in young males and active coping in aged males related to VH in a stress history-dependent manner. Moreover, baseline corticosterone positively correlated with VH in unstressed males, while chronically-stressed males had positive correlations between VH and visceral adiposity.

conclusionsThese results indicate that females as a group are uniquely susceptible to the effects of early-life stress on cardiac remodeling later in life. Conversely, males have more individual differences in vulnerability, where susceptibility to cardiac remodeling relates to endocrine, metabolic, and behavioral measures depending on stress history. These results ultimately support a framework for assessing cardiovascular risk based on biological sex and prior adverse experiences.

Indexed as

Sex CharacteristicsStress, PsychologicalVentricular RemodelingAgingAnimalsFemaleHypertrophy, Left VentricularMaleRatsRats, Sprague-DawleyAgingCardiac hypertrophyChronic variable stressCoping behaviorGlucose toleranceSex

Identifiers

PMID39180122
PMCPMC11342553

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LicenceCC BY
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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 Socratic graph.