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Association between prophylactic angiotensin-converting enzyme inhibitors and overall survival in Duchenne muscular dystrophy-analysis of registry data.
Porcher, Raphaël; Desguerre, Isabelle; Amthor, Helge; Chabrol, Brigitte; Audic, Frédérique; Rivier, François; Isapof, Arnaud; Tiffreau, Vincent; Campana-Salort, Emmanuelle; Leturcq, France; Tuffery-Giraud, Sylvie; Ben Yaou, Rabah; Annane, Djillali; Amédro, Pascal; Barnerias, Christine; Bécane, Henri Marc; Béhin, Anthony; Bonnet, Damien; Bassez, Guillaume; Cossée, Mireille; de La Villéon, Grégoire; Delcourte, Claire; Fayssoil, Abdallah; Fontaine, Bertand; Godart, François; Guillaumont, Sophie; Jaillette, Emmanuelle; Laforêt, Pascal; Leonard-Louis, Sarah; Lofaso, Frederic; Mayer, Michele; Morales, Raul Juntas; Meune, Christophe; Orlikowski, David; Ovaert, Caroline; Prigent, Hélène; Saadi, Malika; Sochala, Maximilien; Tard, Celine; Vaksmann, Guy; Walther-Louvier, Ulrike; Eymard, Bruno; Stojkovic, Tanya; Ravaud, Philippe; Duboc, Denis; Wahbi, Karim.
Afiliação
  • Porcher R; Université de Paris, CRESS UMR1153, INSERM, INRA, F-75004, Paris, France; Centre d'Epidémiologie Clinique, AP-HP, Hôtel-Dieu, F-75004 Paris, France.
  • Desguerre I; 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.
  • Amthor H; 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.
  • Chabrol B; Hôpital Timone Enfants, Marseille, France.
  • Audic F; Centre de Référence des Maladies Neuromusculaires Nord/Est/Ile de France, Service de Neuropédiatrie, Hôpital Roger Salengro, CHRU Lille, Lille, France.
  • Rivier F; Department of Paediatric Neurology & Reference Centre for Neuromuscular Diseases AOC, CHU Montpellier, France.
  • Isapof A; PhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
  • Tiffreau V; Centre de Référence des Maladies Neuromusculaires Nord/Est/Ile de France, Service de Neuropédiatrie, Hôpital Trousseau, Paris, France.
  • Campana-Salort E; Physical and Rehabilitation Medicine Unit, University Hospital, Lille, France, URePSSS (Pluridisciplinary Research Unit: Sports, Health, Society) EA, 7369, Lille University.
  • Leturcq F; APHM, Department of Neurology, Neuromuscular and ALS Reference Centre, La Timone University Hospital, Marseille, FranceAix Marseille Université, INSERM, GMGF, Marseille, France.
  • Tuffery-Giraud S; Laboratoire de Biochimie et Génétique Moléculaire, Hôpital Cochin et Institut de Myologie, Groupe Hospitalier La Pitié Salpétrière, APHP, France.
  • Ben Yaou R; Laboratory of Genetics of Rare Diseases (LGMR), University of Montpellier, Montpellier, France.
  • Annane D; Sorbonne Universités, INSERM UMRS 974, CNRS, UMR-7215, Centre for Research in Myology, Institut de Myologie, Pitié-Salpêtrière University Hospital, Paris, France.
  • Amédro P; APHP, Centre de Référence de Pathologie Neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department, Pitié-Salpêtrière Hospital, Paris, France.
  • Barnerias C; General Intensive Care Unit, Raymond Poincaré Hospital (AP-HP), Lab Inflammation & Infection, U1173 University Paris Saclay-UVSQ/INSERM, Garches, France.
  • Bécane HM; PhyMedExp, University of Montpellier, INSERM, CNRS, Montpellier, France.
  • Béhin A; Paediatric Cardiology, CHU Montpellier, France.
  • Bonnet D; 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.
  • Bassez G; APHP, Centre de Référence de Pathologie Neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department, Pitié-Salpêtrière Hospital, Paris, France.
  • Cossée M; APHP, Centre de Référence de Pathologie Neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department, Pitié-Salpêtrière Hospital, Paris, France.
  • de La Villéon G; 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.
  • Delcourte C; APHP, Centre de Référence de Pathologie Neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department, Pitié-Salpêtrière Hospital, Paris, France.
  • Fayssoil A; Laboratory of Genetics of Rare Diseases (LGMR), University of Montpellier, Montpellier, France.
  • Fontaine B; Paediatric Cardiology, CHU Montpellier, France.
  • Godart F; Critical Care Centre, University Hospital of Lille, Lille Cedex, France.
  • Guillaumont S; APHP, Centre de Référence de Pathologie Neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department, Pitié-Salpêtrière Hospital, Paris, France.
  • Jaillette E; APHP, Hôpital Raymond Poincaré, Centre de Référence des Maladies Neuromusculaires Nord-Est-Île de France, Garches, France.
  • Laforêt P; Department of Neurology & Reference Centre for Neuromuscular Diseases AOC, CHU Montpellier, France.
  • Leonard-Louis S; Pediatric Cardiology Department, Lille University Hospital, University Nord de France, Lille, France.
  • Lofaso F; Paediatric Cardiology, CHU Montpellier, France.
  • Mayer M; Intensive Care Unit, CHU de Lille, Lille, France.
  • Morales RJ; APHP, Hôpital Raymond Poincaré, Centre de Référence des Maladies Neuromusculaires Nord-Est-Île de France, Garches, France.
  • Meune C; APHP, Centre de Référence de Pathologie Neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department, Pitié-Salpêtrière Hospital, Paris, France.
  • Orlikowski D; Service d'Explorations Fonctionnelles, Hôpital Raymond Poincaré, Garches, FranceINSERM Université de Versailles Saint Quentin en Yvelines, France.
  • Ovaert C; Centre de Référence des Maladies Neuromusculaires Nord/Est/Ile de France, Service de Neuropédiatrie, Hôpital Trousseau, Paris, France.
  • Prigent H; Department of Neurology & Reference Centre for Neuromuscular Diseases AOC, CHU Montpellier, France.
  • Saadi M; APHP, Department of Cardiology, Bobigny Hospital, Paris, XIII University, INSERM UMR S-942, Paris, France.
  • Sochala M; 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.
  • Tard C; Pediatric and Congenital Cardiology, M3C Regional Reference CHD Centre, University Hospital, Marseille Medical Genetics, INSERM UMR 1251, Aix Marseille University, Marseille, France.
  • Vaksmann G; Réanimation adultes, APHP, Hôpitaux Universitaires Paris Ile de France Ouest, site R. Poincaré, Garches, France.
  • Walther-Louvier U; APHP, Cochin Hospital, Cardiology Department, FILNEMUS, Paris-Descartes, Sorbonne Paris Cité University, Paris, France.
  • Eymard B; APHP, Cochin Hospital, Cardiology Department, FILNEMUS, Paris-Descartes, Sorbonne Paris Cité University, Paris, France.
  • Stojkovic T; Unité de Cardiologie Congénitale, Hôpital Privé de La Louvière, Lille, France.
  • Ravaud P; Unité de Cardiologie Congénitale, Hôpital Privé de La Louvière, Lille, France.
  • Duboc D; Department of Paediatric Neurology & Reference Centre for Neuromuscular Diseases AOC, CHU Montpellier, France.
  • Wahbi K; Sorbonne Universités, INSERM UMRS 974, CNRS, UMR-7215, Centre for Research in Myology, Institut de Myologie, Pitié-Salpêtrière University Hospital, Paris, France.
Eur Heart J ; 42(20): 1976-1984, 2021 05 21.
Article em En | MEDLINE | ID: mdl-33748842
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofia Muscular de Duchenne / Insuficiência Cardíaca Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Humans Idioma: En Revista: Eur Heart J Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Distrofia Muscular de Duchenne / Insuficiência Cardíaca Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Humans Idioma: En Revista: Eur Heart J Ano de publicação: 2021 Tipo de documento: Article País de afiliação: França