Published on 26.08.2026
Presentation
The Paris Cardiomyopathy Center, coordinated by Prof. Karim Wahbi, Prof. Albert Hagège, and Prof. Damien Bonnet, conducts clinical and translational research dedicated to genetic cardiomyopathies, with the aim of developing precision medicine strategies tailored to patients.
Systematic genetic sequencing, combined with the inclusion of patients in national and international registries backed by DNA banks and biobanks (among those coordinated by our team, REMY/GEREMY for hypertrophic cardiomyopathy (HCM), OPALE or DMD-Heart-Registry for dilated cardiomyopathies (DCM) linked to LMNA variants and DMD), studies of genotype-phenotype correlations, and the identification of prognostic factors for arrhythmias and heart failure, as well as relevant biomarkers for clinical trials.
1. Hôpital Cochin
2. HEGP
3. Hopital Necker Enfants Malades
Our team runs three rare disease reference centers within the AP-HP:
- Hôpital Européen Georges Pompidou (HEGP): hypertrophic cardiomyopathies,
- Hôpital Cochin: dilated cardiomyopathies, neuromuscular and metabolic cardiomyopathies,
- Hôpital Necker Enfants Malades: pediatric and neonatal cardiomyopathies.
These centers monitor more than 2,000 patients per year, with complementary expertise by age and theme, ensuring a smooth transition from childhood to adulthood.
Structural projectsSystematic genetic sequencing, combined with the inclusion of patients in national and international registries backed by DNA banks and biobanks (among those coordinated by our team, REMY/GEREMY for hypertrophic cardiomyopathy (HCM), OPALE or DMD-Heart-Registry for dilated cardiomyopathies (DCM) linked to LMNA variants and DMD), studies of genotype-phenotype correlations, and the identification of prognostic factors for arrhythmias and heart failure, as well as relevant biomarkers for clinical trials.
- European LMNA-CMD Registry: improving cardiac risk stratification and developing new prognostic biomarkers in LMNA-related dilated cardiomyopathies.
- Development of biomarkers for innovative therapies in Duchenne muscular dystrophy (DMD)
- Genotype-phenotype studies, risk stratification, and identification of modifier genes in pediatric and adult hypertrophic cardiomyopathy
- Assessment of myocardial stiffness in hypertrophic cardiomyopathy
- Cohort analysis using cardiac MRI, advanced echocardiography, and biobanks (plasma, serum, DNA, cardiac tissue from transplants or assist devices).
- Translational research on animal models (mice, rats, dogs) to evaluate gene therapies such as microdystrophin for DMD or MAPK inhibitors for LMNA.
- International clinical trials: myosin inhibitors (mavacamten/aficamten), AAV9 gene therapy (TN-201), prophylactic nebivolol.
- Integration of innovative technologies such as:
- 18F-FAPI nuclear imaging to detect active myocardial fibrosis,
- Deep proteomics using Imagine's Proteograph platform,
- Shear wave imaging for routine measurement of myocardial stiffness,
- OMICs analyses to identify modifier genes and predictive biomarkers.
1. Hôpital Cochin
- Pr Karim WAHBI (Cardiologie)
- Dr Youssef Ed Demri (Cardiologie)
- Dr Leslie Motte (Cardiologie)
- Nejette LALLOUCHE (Cheffe de projet CRMR)
- Pierre David HAVOUIS (Infirmier Coordinateur (IDEC))
- Mohammed El Hachmi (Conseiller en Génétique / Doctorant)
- Dr Gauthier Giordano (Doctorant)
- Mohammed Jaber (Etudiant en Master 2)
- Kahina Zimouche (TEC/ARC)
- Ny Lalasoa (TEC/ARC)
- Pauline Ben Soussan (TEC/ARC)
- Nassima Saci (TEC/ARC)
- Mohammed Dembele (Biostatisticien)
2. HEGP
- Pr Albert Hagège (Cardiologie)
- Pr. Nadia Aissaoui (Médecine Intensive et Réanimation)
- Pr. Emmanuel Messas (Cardiologie)
- Dr. Tania Puscas Muresan (Cardiologie)
- Tanguy Mareau (Conseiller en génétique)
- Anne Bachet (ARC)
- Vola Ranaivoarisoa
3. Hopital Necker Enfants Malades
- Pr Damien Bonnet (Cardiologie médicale pédiatrique)
- Dr Diala Khraiche (Cardiologie médicale pédiatrique)
- Dr Elena Panaioli (Cardiologie médicale pédiatrique)
- Dr Alexis Barat (Cardiologie médicale pédiatrique)
- Dr Pauline Pinon (Cardiologie)
- Dr Lorenzo Ridolfi (Cardiologie médicale pédiatrique)
- Victor Waldman (Cardiologie médicale pédiatrique)
- Dr Elise Daire
- Alain Camacho (ARC)
- Julia Tamburro (ARC)
- Aurélie Le Moel (IDE spécialisée)
- Alexandra Flouris (Psychologue)
- Roxana Borghese (Conseiller en génétique prénatal)
Scientific Publications
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2025
Electrocardiogram vs Electrophysiological Study and Major Conduction Delays i..., American Medical Association (AMA)
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2025
Mavacamten in Symptomatic Nonobstructive Hypertrophic Cardiomyopathy, Massachusetts Medical Society
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2025
Location of LMNA Variants and Clinical Outcomes in Cardiomyopathy, American Medical Association (AMA)
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2024
Aficamten for Symptomatic Obstructive Hypertrophic Cardiomyopathy, Massachusetts Medical Society
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2023
2023 ESC Guidelines for the management of cardiomyopathies, Oxford University Press (OUP)
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2022
Cardiac Outcomes in Adults With Mitochondrial Diseases, Elsevier BV
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2021
Association between prophylactic angiotensin-converting enzyme inhibitors and..., Oxford University Press (OUP)
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2019
Development and Validation of a New Risk Prediction Score for Life-Threatenin..., Ovid Technologies (Wolters Kluwer Health)
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2018
High Risk of Fatal and Nonfatal Venous Thromboembolism in Myotonic Dystrophy, Ovid Technologies (Wolters Kluwer Health)
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2016
Incidence and predictors of sudden death, major conduction defects and sustai..., Oxford University Press (OUP)
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2015
Long-term cardiac prognosis and risk stratification in 260 adults presenting ..., Oxford University Press (OUP)
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2012
Electrophysiological Study With Prophylactic Pacing and Survival in Adults Wi..., American Medical Association (AMA)