Evidence map›Paper›PMID 39719411›Full record

ReviewJournal of the American Heart Association2025

Immunometabolism in the Aging Heart.

Kranti A Mapuskar, Barry London, Zeb R Zacharias, Jon C D Houtman, Bryan G Allen

Abstract readReview
In one paragraph

Review in Journal of the American Heart Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. The long-lived immune system of centenarians.Nature reviews. Immunology · 2026
    Review
  2. Multicellular senescence programs in the aged heart.Journal of molecular and cellular cardiology plus · 2026
    Review
  3. Review
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  5. The gut as a central hub for multi-organ crosstalk in aging.Cellular and molecular life sciences : CMLS · 2026
    Review
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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

5 authors.

Kranti A MapuskarDepartment of Radiation Oncology University of Iowa Hospitals and Clinic, University of Iowa Healthcare Iowa City IA USA.ORCID 0000-0002-7311-7184
Barry LondonHolden Comprehensive Cancer Center, Carver College of Medicine University of Iowa Hospitals and Clinic, University of Iowa Healthcare Iowa City IA USA.ORCID 0000-0003-1506-3947
Zeb R ZachariasHolden Comprehensive Cancer Center, Carver College of Medicine University of Iowa Hospitals and Clinic, University of Iowa Healthcare Iowa City IA USA.ORCID 0000-0001-9157-3469
Jon C D HoutmanHolden Comprehensive Cancer Center, Carver College of Medicine University of Iowa Hospitals and Clinic, University of Iowa Healthcare Iowa City IA USA.ORCID 0000-0002-5307-9854
Bryan G AllenDepartment of Radiation Oncology University of Iowa Hospitals and Clinic, University of Iowa Healthcare Iowa City IA USA.ORCID 0000-0002-4893-7105

Funding

Mechanisms of Arrhythmias Following Cardiac IrradiationR01HL152104 · NHLBI · UNIVERSITY OF IOWA · PI LONDON, BARRY · 2020 to 2023
$1.9M
Sex-dependent Impairment of Nitric Oxide Signaling and Mitochondrial Metabolism in Radiation-Induced Cardio-Pulmonary DysfunctionU01AI184289 · NIAID · UNIVERSITY OF IOWA · PI Bryan Allen, Barry London · 2024 to 2026
$1.6M
NHLBI NIH HHS R01 HL152104NIAID NIH HHS U01 AI184289
6 · The paper itself

Abstract

Structural, functional, and molecular-level changes in the aging heart are influenced by a dynamic interplay between immune signaling and cellular metabolism that is referred to as immunometabolism. This review explores the crosstalk between cellular metabolic pathways including glycolysis, oxidative phosphorylation, fatty acid metabolism, and the immune processes that govern cardiac aging. With a rapidly aging population that coincides with increased cardiovascular risk and cancer incidence rates, understanding the immunometabolic underpinnings of cardiac aging provides a foundation for identifying therapeutic targets to mitigate cardiac dysfunction. Aging alters the immune environment of the heart by concomitantly driving the changes in immune cell metabolism, mitochondrial dysfunction, and redox signaling. Shifts in these metabolic pathways exacerbate inflammation and impair tissue repair, creating a vicious cycle that accelerates cardiac functional decline. Treatment with cancer therapy further complicates this landscape, as aging-associated immunometabolic disruptions augment the susceptibility to cardiotoxicity. The current review highlights therapeutic strategies that target the immunometabolic axis to alleviate cardiac aging pathologies. Interventions include modulating metabolic intermediates, improving mitochondrial function, and leveraging immune signaling pathways to restore cardiac health. Advances in immunometabolism thus hold significant potential for translating preclinical findings into therapies that improve the quality of life for the aging population and underscore the need for approaches that address the immunometabolic mechanisms of cardiac aging, providing a framework for future research.

Indexed as

AgingMyocardiumAnimalsEnergy MetabolismHeartHumansSignal Transductioncardiac agingimmunometabolisminflammagingoxidative phosphorylation

Identifiers

PMID39719411
PMCPMC12054428

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.