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A Latent Cardiomyocyte Regeneration Potential in Human Heart Disease
Tech Univ Dresden, Ctr Regenerat Therapies Dresden, Dresden, Germany..
Tech Univ Dresden, Informat Serv & High Performance Comp, Dresden, Germany..
Karolinska Inst, Dept Cell & Mol Biol, Stockholm, Sweden..
Tech Univ Dresden, Ctr Regenerat Therapies Dresden, Dresden, Germany.;Tech Univ Dresden, Informat Serv & High Performance Comp, Dresden, Germany.;Tech Univ Dresden, DRESDEN Concept Genome Ctr, Technol Platform Ctr Mol & Cellular Bioengn, Dresden, Germany..ORCID iD: 0000-0001-6466-2589
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2025 (English)In: Circulation, ISSN 0009-7322, E-ISSN 1524-4539, Vol. 151, no 3, p. 245-256Article in journal (Refereed) Published
Abstract [en]

BACKGROUND:

Cardiomyocytes in the adult human heart show a regenerative capacity, with an annual renewal rate of ≈0.5%. Whether this regenerative capacity of human cardiomyocytes is employed in heart failure has been controversial.

METHODS:

We determined cardiomyocyte renewal in 52 patients with advanced heart failure, 28 of whom received left ventricular assist device support. We measured the concentration of nuclear bomb test–derived 14C in cardiomyocyte genomic DNA and performed mathematical modeling to establish cardiomyocyte renewal in heart failure with and without LVAD unloading.

RESULTS:

We show that cardiomyocyte generation is minimal in end-stage heart failure patients at rates 18 to 50× lower compared with the healthy heart. However, patients receiving left ventricle support device therapy, who showed significant functional and structural cardiac improvement, had a >6-fold increase in cardiomyocyte renewal relative to the healthy heart.

CONCLUSIONS:

Our findings reveal a substantial cardiomyocyte regeneration potential in human heart disease, which could be exploited therapeutically.

Place, publisher, year, edition, pages
Wolters Kluwer, 2025. Vol. 151, no 3, p. 245-256
Keywords [en]
myocytes, cardiac, heart failure, heart-assist device, polyploidy, regeneration
National Category
Cardiology and Cardiovascular Disease Cell and Molecular Biology
Identifiers
URN: urn:nbn:se:uu:diva-551606DOI: 10.1161/CIRCULATIONAHA.123.067156ISI: 001422174900001PubMedID: 39569515Scopus ID: 2-s2.0-85210310672OAI: oai:DiVA.org:uu-551606DiVA, id: diva2:1941126
Funder
Karolinska InstituteSwedish Research CouncilSwedish Cancer SocietyKnut and Alice Wallenberg FoundationRagnar Söderbergs stiftelseÅke Wiberg FoundationAvailable from: 2025-02-27 Created: 2025-02-27 Last updated: 2025-02-27Bibliographically approved

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