Age-dependent Transcriptional Programs Distinguish Pediatric from Adult Dilated Cardiomyopathy

<b>What Is New?:</b> This comparative transcriptomic analysis demonstrates that pediatric and adult dilated cardiomyopathy possess profoundly distinct biological signatures, with only 7.4% of differentially expressed disease-associated genes shared between the two age groups.Unlike adult dilated cardiomyopathy, which is driven by metabolic dysfunction and extensive remodeling of the β1-adrenergic receptor gene signaling network, pediatric disease is uniquely characterized by the activation of developmental pathways such as WNT/β-catenin and Notch signaling without significant pathological β1-adrenergic remodeling.<b>What Are the Clinical Implications?:</b> The absence of pathological β-adrenergic remodeling in pediatric hearts provides a molecular explanation for the limited clinical efficacy of β-blocker therapy in this population, underscoring the critical need to develop age-specific precision medicine strategies rather than continuing to extrapolate guideline-directed medical therapies from adult heart failure.

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Publication Details

Journal
medRxiv
Published
2026-03-20
DOI
https://doi.org/10.64898/2026.03.17.26348665
Primary Topic
Cardiac Fibrosis and Remodeling
Type
article
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article

Age-dependent Transcriptional Programs Distinguish Pediatric from Adult Dilated Cardiomyopathy

Sharon Graw, Carmen C. Sucharov, Matthew L. Stone, Bonnie Neltner et al.
medRxiv
Cardiac Fibrosis and Remodeling
article

Age-dependent Transcriptional Programs Distinguish Pediatric from Adult Dilated Cardiomyopathy

Sharon Graw, Carmen C. Sucharov, Matthew L. Stone, Bonnie Neltner, Obed Ofori Nyarko, Brian L. Stauffer, Anis Karimpour-Fard, Matthew Taylor, Shelley D Miyamoto, Luisa Mestroni, Zoe Lerouz
article en

Abstract

<b>What Is New?:</b> This comparative transcriptomic analysis demonstrates that pediatric and adult dilated cardiomyopathy possess profoundly distinct biological signatures, with only 7.4% of differentially expressed disease-associated genes shared between the two age groups.Unlike adult dilated cardiomyopathy, which is driven by metabolic dysfunction and extensive remodeling of the β1-adrenergic receptor gene signaling network, pediatric disease is uniquely characterized by the activation of developmental pathways such as WNT/β-catenin and Notch signaling without significant pathological β1-adrenergic remodeling.<b>What Are the Clinical Implications?:</b> The absence of pathological β-adrenergic remodeling in pediatric hearts provides a molecular explanation for the limited clinical efficacy of β-blocker therapy in this population, underscoring the critical need to develop age-specific precision medicine strategies rather than continuing to extrapolate guideline-directed medical therapies from adult heart failure.

medRxiv
Health and Hospital Corporation (US), University of Colorado Anschutz Medical Campus (US), University of Colorado Denver (US)
Good health and well-being
Openalex Percentile: Top 23%
Cardiac Fibrosis and Remodeling
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