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Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms.
Gonzalez-Lopez, Esther; Escobar-Lopez, Luis; Obici, Laura; Saturi, Giulia; Bezard, Mélanie; Saith, Sunil E; AbouEzzeddine, Omar F; Mussinelli, Roberta; Gagliardi, Christian; Kharoubi, Mounira; Griffin, Jan M; Dispenzieri, Angela; Vilches, Silvia; Perlini, Stefano; Longhi, Simone; Oghina, Silvia; Rivas, Adrian; Grogan, Martha; Maurer, Mathew S; Damy, Thibaud; Palladini, Giovanni; Rapezzi, Claudio; Garcia-Pavia, Pablo.
Affiliation
  • Gonzalez-Lopez E; Heart Failure and Inherited Cardiac Diseases Unit, Department of Cardiology, Hospital Universitario Puerta de Hierro, IDIPHISA, CIBERCV, Madrid, Spain.
  • Escobar-Lopez L; Heart Failure and Inherited Cardiac Diseases Unit, Department of Cardiology, Hospital Universitario Puerta de Hierro, IDIPHISA, CIBERCV, Madrid, Spain.
  • Obici L; Amyloidosis Research and Treatment Center, Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.
  • Saturi G; Cardiology, Department of Diagnostic, Experimental and Specialty Medicine, University of Bologna and S. Orsola-Malpighi Hospital, Bologna, Italy.
  • Bezard M; Referral Center for Cardiac Amyloidosis, GRC Amyloid Research Institute, Department of Cardiology, Center Hospitalier Universitaire Henri Mondor, DHU-ATVB Créteil, France.
  • Saith SE; Inserm U955, Université Paris-Est Créteil, Créteil, France.
  • AbouEzzeddine OF; Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center, New York New York, USA.
  • Mussinelli R; Department of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota, USA.
  • Gagliardi C; Amyloidosis Research and Treatment Center, Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.
  • Kharoubi M; Cardiology, Department of Diagnostic, Experimental and Specialty Medicine, University of Bologna and S. Orsola-Malpighi Hospital, Bologna, Italy.
  • Griffin JM; Referral Center for Cardiac Amyloidosis, GRC Amyloid Research Institute, Department of Cardiology, Center Hospitalier Universitaire Henri Mondor, DHU-ATVB Créteil, France.
  • Dispenzieri A; Inserm U955, Université Paris-Est Créteil, Créteil, France.
  • Vilches S; Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center, New York New York, USA.
  • Perlini S; Department of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota, USA.
  • Longhi S; Heart Failure and Inherited Cardiac Diseases Unit, Department of Cardiology, Hospital Universitario Puerta de Hierro, IDIPHISA, CIBERCV, Madrid, Spain.
  • Oghina S; Amyloidosis Research and Treatment Center, Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.
  • Rivas A; Emergency Department, Fondazione IRCCS Policlinico S. Matteo, Internal Medicine Department, University of Pavia, Pavia, Italy.
  • Grogan M; Cardiology, Department of Diagnostic, Experimental and Specialty Medicine, University of Bologna and S. Orsola-Malpighi Hospital, Bologna, Italy.
  • Maurer MS; Referral Center for Cardiac Amyloidosis, GRC Amyloid Research Institute, Department of Cardiology, Center Hospitalier Universitaire Henri Mondor, DHU-ATVB Créteil, France.
  • Damy T; Inserm U955, Université Paris-Est Créteil, Créteil, France.
  • Palladini G; Heart Failure and Inherited Cardiac Diseases Unit, Department of Cardiology, Hospital Universitario Puerta de Hierro, IDIPHISA, CIBERCV, Madrid, Spain.
  • Rapezzi C; Department of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota, USA.
  • Garcia-Pavia P; Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center, New York New York, USA.
JACC CardioOncol ; 4(4): 442-454, 2022 Nov.
Article in En | MEDLINE | ID: mdl-36444226
Background: Transthyretin amyloid cardiomyopathy (ATTR-CM) is increasingly recognized as a treatable cause of heart failure (HF). Advances in diagnosis and therapy have increased the number of patients diagnosed at early stages, but prognostic data on patients without HF symptoms are lacking. Moreover, it is unknown whether asymptomatic patients benefit from early initiation of transthyretin (TTR) stabilizers. Objectives: The aim of this study was to describe the natural history and prognosis of ATTR-CM in patients without HF symptoms. Methods: Clinical characteristics and outcomes of patients with ATTR-CM without HF symptoms were retrospectively collected at 6 international amyloidosis centers. Results: A total of 118 patients (78.8% men, median age 66 years [IQR: 53.8-75 years], 68 [57.6%] with variant transthyretin amyloidosis, mean left ventricular ejection fraction 60.5% ± 9.9%, mean left ventricular wall thickness 15.4 ± 3.1 mm, and 53 [45%] treated with TTR stabilizers at baseline or during follow-up) were included. During a median follow-up period of 3.7 years (IQR: 1-6 years), 38 patients developed HF symptoms (23 New York Heart Association functional class II and 14 functional class III or IV), 32 died, and 2 required cardiac transplantation. Additionally, 20 patients received pacemakers, 13 developed AF, and 1 had a stroke. Overall survival was 96.5% (95% CI: 91%-99%), 90.4% (95% CI: 82%-95%), and 82% (95% CI: 71%-89%) at 1, 3, and 5 years, respectively. Treatment with TTR stabilizers was associated with improved survival (HR: 0.31; 95% CI: 0.12-0.82; P = 0.019) and remained significant after adjusting for sex, age, ATTR-CM type, and estimated glomerular filtration rate (HR: 0.18; 95% CI: 0.06-0.55; P = 0.002). Conclusions: After a median follow-up period of 3.7 years, 1 in 3 patients with asymptomatic ATTR-CM developed HF symptoms, and nearly as many died or required cardiac transplantation. Treatment with TTR stabilizers was associated with improved prognosis.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: JACC CardioOncol Year: 2022 Document type: Article Affiliation country: Spain Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Prognostic_studies Language: En Journal: JACC CardioOncol Year: 2022 Document type: Article Affiliation country: Spain Country of publication: United States