Atrial cardiomyopathy: from knowledge gaps to clinical impact

BACKGROUND: Atrial cardiomyopathy (AtCM) is increasingly recognised as an underlying atrial substrate contributing to atrial fibrillation (AF), heart failure (HF), and cardio-embolic stroke. However, diagnostic criteria, disease thresholds, and targeted treatment strategies remain poorly defined. OBJECTIVE: To describe the rationale, structure, and translational strategy of the EmbRACE (Electro-Molecular Basis and the theRapeutic management of Atrial Cardiomyopathy, fibrillation and associated outcomEs) network, a national consortium established to address key knowledge gaps in AtCM. METHODS: EmbRACE integrates mechanistic research, computational modelling, clinical trials, and implementation science within seven interconnected work packages. Human atrial tissue biobanking and deep phenotyping (WP1) enable molecular profiling of candidate pathways (WP2), which are validated in experimental models (WP3). Computational modelling and artificial intelligence (WP4) integrate multimodal clinical and biological data to derive composite AtCM phenotypes and severity frameworks. Substrate-targeting clinical trials evaluate AF ablation (RACE X; WP5), weight reduction using GLP‑1 agonists (DUTCH-WAIST; WP6), and optimised rate control using calcium channel antagonists (SMART-VERAPAF; WP6). Implementation science (WP7) focuses on guideline integration, decision-support tools, and governance of AI-based risk models. EmbRACE establishes a translational pipeline from mechanistic discovery to clinical application. By integrating tissue-level insights with multimodal risk modelling and interventional trials, the consortium aims to define clinically meaningful AtCM thresholds, to validate indirect markers, and to determine whether targeted treatment modifies disease progression and clinical outcomes. CONCLUSION: EmbRACE provides a multidisciplinary framework to transform AtCM from a theoretical construct into a clinically actionable entity, enabling earlier detection, improved risk stratification, and AtCM-directed therapy in cardiovascular prevention.

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Publication Details

Journal
Netherlands Heart Journal
Published
2026-10-15
DOI
https://doi.org/10.1007/s12471-026-02081-3
Citations
1
Primary Topic
Atrial Fibrillation Management and Outcomes
Type
article
Field-Weighted Citation Impact
4.57

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article

Atrial cardiomyopathy: from knowledge gaps to clinical impact

Jelle C L Himmelreich, Martin E W Hemels, Zarina Habibi, Sander van Doorn et al.
1 citations
Netherlands Heart Journal
Atrial Fibrillation Management and Outcomes
4.57
article

Atrial cardiomyopathy: from knowledge gaps to clinical impact

Jelle C L Himmelreich, Martin E W Hemels, Zarina Habibi, Sander van Doorn, Geert‐Jan Geersing, Jordi Heijman, Daniël A. Pijnappels, Ulrich Schotten, Ron Pisters, Robert G Tieleman, Monika Stoll, Michiel Rienstra, Joris R. de Groot, Fleur V.Y. Tjong, Nick L. van Vreeswijk
article en
1 citations

Abstract

BACKGROUND: Atrial cardiomyopathy (AtCM) is increasingly recognised as an underlying atrial substrate contributing to atrial fibrillation (AF), heart failure (HF), and cardio-embolic stroke. However, diagnostic criteria, disease thresholds, and targeted treatment strategies remain poorly defined. OBJECTIVE: To describe the rationale, structure, and translational strategy of the EmbRACE (Electro-Molecular Basis and the theRapeutic management of Atrial Cardiomyopathy, fibrillation and associated outcomEs) network, a national consortium established to address key knowledge gaps in AtCM. METHODS: EmbRACE integrates mechanistic research, computational modelling, clinical trials, and implementation science within seven interconnected work packages. Human atrial tissue biobanking and deep phenotyping (WP1) enable molecular profiling of candidate pathways (WP2), which are validated in experimental models (WP3). Computational modelling and artificial intelligence (WP4) integrate multimodal clinical and biological data to derive composite AtCM phenotypes and severity frameworks. Substrate-targeting clinical trials evaluate AF ablation (RACE X; WP5), weight reduction using GLP‑1 agonists (DUTCH-WAIST; WP6), and optimised rate control using calcium channel antagonists (SMART-VERAPAF; WP6). Implementation science (WP7) focuses on guideline integration, decision-support tools, and governance of AI-based risk models. EmbRACE establishes a translational pipeline from mechanistic discovery to clinical application. By integrating tissue-level insights with multimodal risk modelling and interventional trials, the consortium aims to define clinically meaningful AtCM thresholds, to validate indirect markers, and to determine whether targeted treatment modifies disease progression and clinical outcomes. CONCLUSION: EmbRACE provides a multidisciplinary framework to transform AtCM from a theoretical construct into a clinically actionable entity, enabling earlier detection, improved risk stratification, and AtCM-directed therapy in cardiovascular prevention.

Netherlands Heart Journal
University Medical Center Groningen (NL), Radboud University Nijmegen (NL), University of Groningen (NL), Utrecht University (NL), Medical University of Graz (AT), University of Münster (DE), Leiden University Medical Center (NL), Maastricht University Medical Centre (NL), Radboud University Medical Center (NL), University Medical Center Utrecht (NL), Maastricht University (NL), Amsterdam Neuroscience (NL), Martini Ziekenhuis (NL), Amsterdam Public Health (NL), Amsterdam University Medical Centers (NL), Rijnstate Hospital (NL), Amsterdam Cardiovascular Sciences (NL), University of Amsterdam (NL)
Dutch Cardiovascular Alliance, Hartstichting
Good health and well-being
Openalex Percentile: Top 4%
Atrial Fibrillation Management and Outcomes
4.57
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