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Cardiac Outcomes in Adults With Mitochondrial Diseases

Authors :
Konstantinos Savvatis
Christoffer Rasmus Vissing
Lori Klouvi
Anca Florian
Mehjabin Rahman
Anthony Béhin
Abdallah Fayssoil
Marion Masingue
Tanya Stojkovic
Henri Marc Bécane
Nawal Berber
Fanny Mochel
Denis Duboc
Bertrand Fontaine
Bjørg Krett
Caroline Stalens
Julie Lejeune
Robert D.S. Pitceathly
Luis Lopes
Malika Saadi
Thomas Gossios
Vincent Procaccio
Marco Spinazzi
Céline Tard
Pascal De Groote
Claire-Marie Dhaenens
Claire Douillard
Andoni Echaniz-Laguna
Ros Quinlivan
Michael G. Hanna
Ali Yilmaz
John Vissing
Pascal Laforêt
Perry Elliott
Karim Wahbi
Queen Mary University of London (QMUL)
IT University of Copenhagen (ITU)
Association française contre les myopathies (AFM-Téléthon)
University Hospital Münster - Universitaetsklinikum Muenster [Germany] (UKM)
University College of London [London] (UCL)
CHU Pitié-Salpêtrière [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
Hôpital Raymond Poincaré [Garches]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Université de Versailles Saint-Quentin-en-Yvelines - UFR Sciences de la santé Simone Veil (UVSQ Santé)
Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)
Université Paris Cité (UPCité)
Sorbonne Université (SU)
Hôpital Cochin [AP-HP]
Aristotle University of Thessaloniki
MitoVasc - Physiopathologie Cardiovasculaire et Mitochondriale (MITOVASC)
Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Département de Biochimie et Génétique [Angers]
Université d'Angers (UA)-Centre Hospitalier Universitaire d'Angers (CHU Angers)
PRES Université Nantes Angers Le Mans (UNAM)-PRES Université Nantes Angers Le Mans (UNAM)
Lille Neurosciences & Cognition - U 1172 (LilNCog)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)
Institut Pasteur de Lille
Réseau International des Instituts Pasteur (RIIP)
Hôpital Claude Huriez [Lille]
CHU Lille
AP-HP Hôpital Bicêtre (Le Kremlin-Bicêtre)
Handicap neuromusculaire : Physiopathologie, Biothérapie et Pharmacologies appliquées (END-ICAP)
Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut National de la Santé et de la Recherche Médicale (INSERM)
MR/S005021/1
Association Française contre les Myopathies, AFM
Medical Research Council, MRC: MR/S002065/1
Department of Health and Social Care, DH
University College London Hospitals NHS Foundation Trust, UCLH
NIHR Cambridge Biomedical Research Centre
This study was funded by grants from the Association Française contre les Myopathies (French Alliance against Myopathies), which was not involved in the design and conduct of the study
the collection, management, analysis, and interpretation of the data
the preparation, review or approval of the manuscript
nor in the decision to submit the manuscript for publication. Dr Pitceathly is supported by a Medical Research Council (United Kingdom) Clinician Scientist Fellowship (MR/S002065/1). Drs Pitceathly and Hanna receive funding from a Medical Research Council (United Kingdom) strategic award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases (ICGNMD) (MR/S005021/1). Dr Lopes is supported by a Medical Research Council (United Kingdom) clinical academic partnership (CARP) award. Dr Quinlivan was funded by National Institute for Health and Care Research Biomedical Research Centre, University College Hospitals Foundation Trust. The University College London Hospitals/University College London Queen Square Institute of Neurology sequencing facility receives a proportion of funding from the Department of Health's National Institute for Health and Care Research Biomedical Research Centre’s funding scheme. The clinical and diagnostic 'Rare Mitochondrial Disorders' Service in London is funded by the U.K. NHS Highly Specialised Commissioners. Dr Elliott has received consultancy fees from Pfizer, Sanofi, Sarepta, DinaQor, Freeline, Novo Nordisk, and Bristol Myers Squibb. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
Source :
Journal of the American College of Cardiology, Journal of the American College of Cardiology, 2022, 80 (15), pp.1421-1430. ⟨10.1016/j.jacc.2022.08.716⟩
Publication Year :
2022
Publisher :
HAL CCSD, 2022.

Abstract

International audience; Background: Patients with mitochondrial diseases are at risk of heart failure (HF) and arrhythmic major adverse cardiac events (MACE). Objectives: We developed prediction models to estimate the risk of HF and arrhythmic MACE in this population. Methods: We determined the incidence and searched for predictors of HF and arrhythmic MACE using Cox regression in 600 adult patients from a multicenter registry with genetically confirmed mitochondrial diseases. Results: Over a median follow-up time of 6.67 years, 29 patients (4.9%) reached the HF endpoint, including 19 hospitalizations for nonterminal HF, 2 cardiac transplantations, and 8 deaths from HF. Thirty others (5.1%) reached the arrhythmic MACE, including 21 with third-degree or type II second-degree atrioventricular blocks, 4 with sinus node dysfunction, and 5 sudden cardiac deaths. Predictors of HF were the m.3243A>G variant (HR: 4.3; 95% CI: 1.8-10.1), conduction defects (HR: 3.0; 95% CI: 1.3-6.9), left ventricular (LV) hypertrophy (HR: 2.6; 95% CI: 1.1-5.8), LV ejection fraction

Details

Language :
English
ISSN :
07351097 and 15583597
Database :
OpenAIRE
Journal :
Journal of the American College of Cardiology, Journal of the American College of Cardiology, 2022, 80 (15), pp.1421-1430. ⟨10.1016/j.jacc.2022.08.716⟩
Accession number :
edsair.doi.dedup.....d02e3babcfab5edc418372f23ceac8a2