Association between prophylactic angiotensin-converting enzyme inhibitors and overall survival in Duchenne muscular dystrophy—analysis of registry data

Author:

Porcher Raphaël1ORCID,Desguerre Isabelle2,Amthor Helge3,Chabrol Brigitte4,Audic Frédérique5,Rivier François67,Isapof Arnaud8,Tiffreau Vincent9,Campana-Salort Emmanuelle10ORCID,Leturcq France11,Tuffery-Giraud Sylvie12ORCID,Ben Yaou Rabah1314,Annane Djillali15ORCID,Amédro Pascal716,Barnerias Christine2,Bécane Henri Marc14,Béhin Anthony14,Bonnet Damien17ORCID,Bassez Guillaume14,Cossée Mireille12,de La Villéon Grégoire16,Delcourte Claire18,Fayssoil Abdallah1419ORCID,Fontaine Bertand20ORCID,Godart François21,Guillaumont Sophie16,Jaillette Emmanuelle22,Laforêt Pascal19,Leonard-Louis Sarah14,Lofaso Frederic23,Mayer Michele8,Morales Raul Juntas20,Meune Christophe24ORCID,Orlikowski David25ORCID,Ovaert Caroline26ORCID,Prigent Hélène27,Saadi Malika28,Sochala Maximilien28,Tard Celine29ORCID,Vaksmann Guy29ORCID,Walther-Louvier Ulrike6,Eymard Bruno13,Stojkovic Tanya13ORCID,Ravaud Philippe1,Duboc Denis28,Wahbi Karim2830

Affiliation:

1. Université de Paris, CRESS UMR1153, INSERM, INRA, F-75004, Paris, France; Centre d'Epidémiologie Clinique, AP-HP, Hôtel-Dieu, F-75004 Paris, France

2. AP-HP, Centre de Référence des Maladies Neuromusculaires Nord/Est/Ile de France, Service de Neurologie Pédiatrique, Hôpital Necker, GH Necker-Enfants Malades, Paris, France

3. Versailles Saint-Quentin-en-Yvelines University, INSERM U1179, LIA BAHN CSM, Montigny-le-Bretonneux, 78180, Neuromuscular Reference Centre, Paediatric Department, University Hospital Raymond Poincaré, Garches, 92380, France

4. Hôpital Timone Enfants, Marseille, France

5. Centre de Référence des Maladies Neuromusculaires Nord/Est/Ile de France, Service de Neuropédiatrie, Hôpital Roger Salengro, CHRU Lille, Lille, France

6. Department of Paediatric Neurology & Reference Centre for Neuromuscular Diseases AOC, CHU Montpellier, France

7. PhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France

8. Centre de Référence des Maladies Neuromusculaires Nord/Est/Ile de France, Service de Neuropédiatrie, Hôpital Trousseau, Paris, France

9. Physical and Rehabilitation Medicine Unit, University Hospital, Lille, France, URePSSS (Pluridisciplinary Research Unit: Sports, Health, Society) EA, 7369, Lille University

10. APHM, Department of Neurology, Neuromuscular and ALS Reference Centre, La Timone University Hospital, Marseille, FranceAix Marseille Université, INSERM, GMGF, Marseille, France

11. Laboratoire de Biochimie et Génétique Moléculaire, Hôpital Cochin et Institut de Myologie, Groupe Hospitalier La Pitié Salpétrière, APHP, France

12. Laboratory of Genetics of Rare Diseases (LGMR), University of Montpellier, Montpellier, France

13. Sorbonne Universités, INSERM UMRS 974, CNRS, UMR-7215, Centre for Research in Myology, Institut de Myologie, Pitié-Salpêtrière University Hospital, Paris, France

14. APHP, Centre de Référence de Pathologie Neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department, Pitié-Salpêtrière Hospital, Paris, France

15. General Intensive Care Unit, Raymond Poincaré Hospital (AP-HP), Lab Inflammation & Infection, U1173 University Paris Saclay-UVSQ/INSERM, Garches, France

16. Paediatric Cardiology, CHU Montpellier, France

17. AP-HP, Unité Médico-Chirurgicale de Cardiologie Congénitale et Pédiatrique, Centre de Référence des Malformations Cardiaques Congénitales Complexes-M3C, Hôpital Necker Enfants Malades, Université Paris Descartes, Sorbonne Paris-Cité, Paris, France

18. Critical Care Centre, University Hospital of Lille, Lille Cedex, France

19. APHP, Hôpital Raymond Poincaré, Centre de Référence des Maladies Neuromusculaires Nord-Est-Île de France, Garches, France

20. Department of Neurology & Reference Centre for Neuromuscular Diseases AOC, CHU Montpellier, France

21. Pediatric Cardiology Department, Lille University Hospital, University Nord de France, Lille, France

22. Intensive Care Unit, CHU de Lille, Lille, France

23. Service d'Explorations Fonctionnelles, Hôpital Raymond Poincaré, Garches, FranceINSERM Université de Versailles Saint Quentin en Yvelines, France

24. APHP, Department of Cardiology, Bobigny Hospital, Paris, XIII University, INSERM UMR S-942, Paris, France

25. Réanimation Adultes, APHP, Hôpitaux Universitaires Paris Ile de France Ouest, site R. Poincaré, Garches, France; CIC1429 INSERM AP-HP, Hôpitaux Universitaires Paris Ile de France Ouest, site R. Poincaré, Garches, France

26. Pediatric and Congenital Cardiology, M3C Regional Reference CHD Centre, University Hospital, Marseille Medical Genetics, INSERM UMR 1251, Aix Marseille University, Marseille, France

27. Réanimation adultes, APHP, Hôpitaux Universitaires Paris Ile de France Ouest, site R. Poincaré, Garches, France

28. APHP, Cochin Hospital, Cardiology Department, FILNEMUS, Paris-Descartes, Sorbonne Paris Cité University, Paris, France

29. Unité de Cardiologie Congénitale, Hôpital Privé de La Louvière, Lille, France

30. INSERM Unit 970, Paris Cardiovascular Research Centre (PARCC), Paris, France

Abstract

Abstract Aims To estimate the effect of prophylactic angiotensin-converting enzyme inhibitors (ACEi) on survival in Duchenne muscular dystrophy (DMD). Methods and results We analysed the data from the French multicentre DMD Heart Registry (ClinicalTrials.gov: NCT03443115). We estimated the association between the prophylactic prescription of ACEi and event-free survival in 668 patients aged 8 to 13 years, with normal left ventricular function, using (i) a Cox model with intervention as a time-dependent covariate, (ii) a propensity-based analysis comparing ACEi treatment vs. no treatment, and (iii) a set of sensitivity analyses. The study outcomes were overall survival and hospitalizations for heart failure (HF) or acute respiratory failure. Among the 668 patients included in the DMD Heart Registry, 576 (mean age 6.1 ± 2.8 years) were eligible for this study, of whom 390 were treated with ACEi prophylactically. Death occurred in 53 patients (13.5%) who were and 60 patients (32.3%) who were not treated prophylactically with ACEi, respectively. In a Cox model with intervention as a time-dependent variable, the hazard ratio (HR) associated with ACEi treatment was 0.49 [95% confidence interval (CI) 0.34–0.72] and 0.47 (95% CI 0.31–0.17) for overall mortality after adjustment for baseline variables. In the propensity-based analysis, 278 patients were included in the treatment group and 834 in the control group, with 18.5% and 30.4% 12-year estimated probability of death, respectively. ACEi were associated with a lower risk of death (HR 0.39; 95% CI 0.17–0.92) and hospitalization for HF (HR 0.16; 95% CI 0.04–0.62). All other sensitivity analyses yielded similar results. Conclusion Prophylactic ACEi treatment in DMD was associated with a significantly higher overall survival and lower rates of hospitalization for HF.

Funder

Association Monégasque contre les Myopathies

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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