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Development and Validation of a New Risk Prediction Score for Life-Threatening Ventricular Tachyarrhythmias in Laminopathies.
Wahbi, Karim; Ben Yaou, Rabah; Gandjbakhch, Estelle; Anselme, Frédéric; Gossios, Thomas; Lakdawala, Neal K; Stalens, Caroline; Sacher, Frédéric; Babuty, Dominique; Trochu, Jean-Noel; Moubarak, Ghassan; Savvatis, Kostantinos; Porcher, Raphaël; Laforêt, Pascal; Fayssoil, Abdallah; Marijon, Eloi; Stojkovic, Tanya; Béhin, Anthony; Leonard-Louis, Sarah; Sole, Guilhem; Labombarda, Fabien; Richard, Pascale; Metay, Corinne; Quijano-Roy, Susana; Dabaj, Ivana; Klug, Didier; Vantyghem, Marie-Christine; Chevalier, Philippe; Ambrosi, Pierre; Salort, Emmanuelle; Sadoul, Nicolas; Waintraub, Xavier; Chikhaoui, Khadija; Mabo, Philippe; Combes, Nicolas; Maury, Philippe; Sellal, Jean-Marc; Tedrow, Usha B; Kalman, Jonathan M; Vohra, Jitendra; Androulakis, Alexander F A; Zeppenfeld, Katja; Thompson, Tina; Barnerias, Christine; Bécane, Henri-Marc; Bieth, Eric; Boccara, Franck; Bonnet, Damien; Bouhour, Françoise; Boulé, Stéphane.
Afiliación
  • Wahbi K; APHP, Cochin Hospital, Cardiology Department, FILNEMUS, Centre de Référence de Pathologie Neuromusculaire Nord/Est/Ile de France, Paris-Descartes, Sorbonne Paris Cité University (K.W., D.D.).
  • Ben Yaou R; INSERM Unit 970, Paris Cardiovascular Research Centre (PARCC), France (K.W., C. Stalens, E.J.).
  • Gandjbakhch E; APHP, Centre de référence de pathologie neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department (R.B.Y., A.F., T.S., A.B., S.L.-L., K.C., H.-M.B., B.E.).
  • Anselme F; Sorbonne Universités, INSERM UMRS 974, CNRS, UMR-7215, Center for Research in Myology, Myology Institute,(R.B.Y., G.B.).
  • Gossios T; APHP, Institute of Cardiology (E.G., X.W., P.C.).
  • Lakdawala NK; Sorbonne Universités, UPMC Univ Paris 06, INSERM 1166, Institute of Cardiometabolism and Nutrition (ICAN), France (E.G., P.C.).
  • Stalens C; Centre de Référence des Maladies Cardiaques Héréditaires, Paris, France† (E.G., P.C.).
  • Sacher F; Cardiology Department, University Hospital of Rouen, France (F.A.).
  • Babuty D; Inherited Cardiovascular Diseases Unit, University College London & St. Bartholomew's Hospital, United Kingdom† (T.G., K.S., P.E.).
  • Trochu JN; Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Boston, MA (N.K.L., U.B.T.).
  • Moubarak G; Aix Marseille University, INSERM, GMGF; Department of Medical Genetics, Childrens' Hospital La Timone, France (A.D.S.-G., N.L.).
  • Savvatis K; INSERM Unit 970, Paris Cardiovascular Research Centre (PARCC), France (K.W., C. Stalens, E.J.).
  • Porcher R; Medical Affairs Department, AFM-Telethon, Evry, France (C. Stalens).
  • Laforêt P; Centre de reference des maladies rythmiques héréditaires, Bordeaux University Hospital (CHU), IHU Liryc, Electrophysiology and Heart Modeling Institute, fondation Bordeaux Université, Univ. Bordeaux, INSERM U1045, France (F.S.).
  • Fayssoil A; Université François Rabelais, Cardiology Department, CHU Tours, France (D. Babuty).
  • Marijon E; INSERM, UMR1087, Université de Nantes, L'Institut du Thorax, CHU de Nantes, CIC, Centre de référence pour la prise en charge des maladies rythmiques héréditaires de Nantes, France† (J.-N.T.).
  • Stojkovic T; Department of Electrophysiology and Pacing, InParys Clinical Research Group, Clinique Ambroise Paré, Neuilly-sur-Seine, France (G.M.).
  • Béhin A; Inherited Cardiovascular Diseases Unit, University College London & St. Bartholomew's Hospital, United Kingdom† (T.G., K.S., P.E.).
  • Leonard-Louis S; William Harvey Research Institute, Queen Mary University London, United Kingdom (K.S.).
  • Sole G; APHP, Hôtel-Dieu Hospital, Centre d'Epidémiologie Clinique, INSERM U1153, Université Paris Descartes - Sorbonne Paris Cité, France (R.P.).
  • Labombarda F; APHP, Hôpital Raymond Poincaré, Centre de Référence des maladies neuromusculaires Nord-Est-Île de France, Garches (P.L., A.F.).
  • Richard P; APHP, Centre de référence de pathologie neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department (R.B.Y., A.F., T.S., A.B., S.L.-L., K.C., H.-M.B., B.E.).
  • Metay C; APHP, Hôpital Raymond Poincaré, Centre de Référence des maladies neuromusculaires Nord-Est-Île de France, Garches (P.L., A.F.).
  • Quijano-Roy S; Hôpital Européen Georges Pompidou, Département de Cardiologie, Unité de Rythmologie, Paris, France (E.M.).
  • Dabaj I; APHP, Centre de référence de pathologie neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department (R.B.Y., A.F., T.S., A.B., S.L.-L., K.C., H.-M.B., B.E.).
  • Klug D; APHP, Centre de référence de pathologie neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department (R.B.Y., A.F., T.S., A.B., S.L.-L., K.C., H.-M.B., B.E.).
  • Vantyghem MC; APHP, Centre de référence de pathologie neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department (R.B.Y., A.F., T.S., A.B., S.L.-L., K.C., H.-M.B., B.E.).
  • Chevalier P; Centre de référence des maladies neuromusculaires AOC, Hôpital Pellegrin, CHU Bordeaux, France (G.S., X.F.).
  • Ambrosi P; Cardiology Department, University Hospital of Caen, France (F.L.).
  • Salort E; APHP, UF Cardiogénétique et Myogénétique, Centre de Génétique, GH Pitié Salpêtrière, Paris, France (P.R., C.M.).
  • Sadoul N; APHP, UF Cardiogénétique et Myogénétique, Centre de Génétique, GH Pitié Salpêtrière, Paris, France (P.R., C.M.).
  • Waintraub X; APHP, Centre de référence des maladies neuromusculaires Nord/Est/Ile de France, Service de Neurologie, Réanimation et Réeducation Pediatriques, Hôpital Raymond Poincaré, Garches, France; UMR 1179 INSERM, Université Versailles Saint-Quentin-en-Yvelines, Montigny-le-Bretonneux (S.Q.-R., I. Dabaj).
  • Chikhaoui K; APHP, Centre de référence des maladies neuromusculaires Nord/Est/Ile de France, Service de Neurologie, Réanimation et Réeducation Pediatriques, Hôpital Raymond Poincaré, Garches, France; UMR 1179 INSERM, Université Versailles Saint-Quentin-en-Yvelines, Montigny-le-Bretonneux (S.Q.-R., I. Dabaj).
  • Mabo P; Cardiologie A, University Hospital, Lille, France (D.K.).
  • Combes N; CHU Lille, Endocrinology, Diabetology and Metabolism, Univ Lille, Inserm, UMR 1190 -Translational research in diabetes; EGID European Genomic Institute for Diabetes, France (M.-C.V.).
  • Maury P; Sorbonne Universités, UPMC Univ Paris 06, INSERM 1166, Institute of Cardiometabolism and Nutrition (ICAN), France (E.G., P.C.).
  • Sellal JM; Centre de Référence des Maladies Cardiaques Héréditaires, Paris, France† (E.G., P.C.).
  • Tedrow UB; Service de Cardiologie, Hôpital Est, Lyon, France† (P.C.).
  • Kalman JM; Department of Cardiology, La Timone Hospital, Aix-Marseille Université, France (P.A.).
  • Vohra J; APHM, Centre de référence des maladies neuromusculaires PACA-Réunion-Rhône Alpes, Hôpital Timone; Aix Marseille Université, Inserm UMR_S 910, GMGF, France (E.S.).
  • Androulakis AFA; Department of Cardiology, Institut Lorrain du Coeur et des Vaisseaux, CHU Nancy-Brabois, Vandoeuvre les Nancy Cedex, France (N.S.).
  • Zeppenfeld K; APHP, Institute of Cardiology (E.G., X.W., P.C.).
  • Thompson T; APHP, Centre de référence de pathologie neuromusculaire Paris-Est, FILNEMUS, Myology Institute, Neurology Department (R.B.Y., A.F., T.S., A.B., S.L.-L., K.C., H.-M.B., B.E.).
  • Barnerias C; Univ Rennes, CHU Rennes, Inserm, LTSI - UMR 1099, France (P. Mabo, R.M.).
  • Bécane HM; Département de Rythmologie, Clinique Pasteur, Toulouse, France (N.C.).
  • Bieth E; University Hospital Rangueil, Cardiology department; Unité Inserm U1048, Toulouse, France (P. Maury).
  • Boccara F; Département de Cardiologie, Centre Hospitalier Universitaire de Nancy; INSERM-IADI U1254, Vandœuvre lès-Nancy, France (J.-M.S.).
  • Bonnet D; Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Boston, MA (N.K.L., U.B.T.).
  • Bouhour F; Department of Cardiology, Division of Medicine (J.M.K., J.V.), The Royal Melbourne Hospital and University of Melbourne, Victoria, Australia.
  • Boulé S; Department of Cardiology, Division of Medicine (J.M.K., J.V.), The Royal Melbourne Hospital and University of Melbourne, Victoria, Australia.
Circulation ; 140(4): 293-302, 2019 07 23.
Article en En | MEDLINE | ID: mdl-31155932
ABSTRACT

BACKGROUND:

An accurate estimation of the risk of life-threatening (LT) ventricular tachyarrhythmia (VTA) in patients with LMNA mutations is crucial to select candidates for implantable cardioverter-defibrillator implantation.

METHODS:

We included 839 adult patients with LMNA mutations, including 660 from a French nationwide registry in the development sample, and 179 from other countries, referred to 5 tertiary centers for cardiomyopathies, in the validation sample. LTVTA was defined as (1) sudden cardiac death or (2) implantable cardioverter defibrillator-treated or hemodynamically unstable VTA. The prognostic model was derived using the Fine-Gray regression model. The net reclassification was compared with current clinical practice guidelines. The results are presented as means (SD) or medians [interquartile range].

RESULTS:

We included 444 patients, 40.6 (14.1) years of age, in the derivation sample and 145 patients, 38.2 (15.0) years, in the validation sample, of whom 86 (19.3%) and 34 (23.4%) experienced LTVTA over 3.6 [1.0-7.2] and 5.1 [2.0-9.3] years of follow-up, respectively. Predictors of LTVTA in the derivation sample were male sex, nonmissense LMNA mutation, first degree and higher atrioventricular block, nonsustained ventricular tachycardia, and left ventricular ejection fraction (https//lmna-risk-vta.fr). In the derivation sample, C-index (95% CI) of the model was 0.776 (0.711-0.842), and the calibration slope 0.827. In the external validation sample, the C-index was 0.800 (0.642-0.959), and the calibration slope was 1.082 (95% CI, 0.643-1.522). A 5-year estimated risk threshold ≥7% predicted 96.2% of LTVTA and net reclassified 28.8% of patients with LTVTA in comparison with the guidelines-based approach.

CONCLUSIONS:

In comparison with the current standard of care, this risk prediction model for LTVTA in laminopathies significantly facilitated the choice of candidates for implantable cardioverter defibrillators. CLINICAL TRIAL REGISTRATION URL https//www.clinicaltrials.gov. Unique identifier NCT03058185.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Taquicardia Ventricular / Desfibriladores Implantables / Cardiomiopatías Tipo de estudio: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Circulation Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Taquicardia Ventricular / Desfibriladores Implantables / Cardiomiopatías Tipo de estudio: Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Circulation Año: 2019 Tipo del documento: Article