Literature DB >> 31950987

Echocardiographic phenotype and prognosis in transthyretin cardiac amyloidosis.

Liza Chacko1, Raffaele Martone1,2, Francesco Bandera3,4, Thirusha Lane1, Ana Martinez-Naharro1, Michele Boldrini1, Tamer Rezk1, Carol Whelan1, Cristina Quarta1, Dorota Rowczenio1, Janet A Gilbertson1, Tanakal Wongwarawipat1, Helen Lachmann1, Ashutosh Wechalekar1, Sajitha Sachchithanantham1, Shameem Mahmood1, Rossella Marcucci5, Daniel Knight1, David Hutt1, James Moon6,7, Aviva Petrie8, Francesco Cappelli2, Marco Guazzi3,4, Philip N Hawkins1, Julian D Gillmore1, Marianna Fontana1.   

Abstract

AIMS: Transthyretin amyloidosis cardiomyopathy (ATTR-CM) is an increasingly recognized cause of heart failure. We sought to characterize the structural and functional echocardiographic phenotype across the spectrum of wild-type (wtATTR-CM) and hereditary (hATTR-CM) transthyretin cardiomyopathy and the echocardiographic features predicting prognosis. METHODS AND
RESULTS: We studied 1240 patients with ATTR-CM who underwent prospective protocolized evaluations comprising full echocardiographic assessment and survival between 2000 and 2019, comprising 766 with wtATTR-CM and 474 with hATTR-CM, of whom 314 had the V122I variant and 127 the T60A variant. At diagnosis, patients with V122I-hATTR-CM had the most severe degree of systolic and diastolic dysfunction across all echocardiographic parameters and patients with T60AhATTR-CM the least; patients with wtATTR-CM had intermediate features. Stroke volume index, right atrial area index, longitudinal strain, and E/e' were all independently associated with mortality (P < 0.05 for all). Severe aortic stenosis (AS) was also independently associated with prognosis, conferring a significantly shorter survival (median survival 22 vs. 53 months, P = 0.001).
CONCLUSION: The three distinct genotypes present with varying degrees of severity. Echocardiography indicates a complex pathophysiology in which both systolic and diastolic function are independently associated with mortality. The presence of severe AS was independently associated with significantly reduced patient survival. Published on behalf of the European Society of Cardiology. All rights reserved.
© The Author(s) 2020. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  Amyloidosis; Aortic stenosis; Cardiomyopathy; Echocardiography; Prognosis; Transthyretin

Mesh:

Substances:

Year:  2020        PMID: 31950987     DOI: 10.1093/eurheartj/ehz905

Source DB:  PubMed          Journal:  Eur Heart J        ISSN: 0195-668X            Impact factor:   29.983


  21 in total

1.  Position Statement on Diagnosis and Treatment of Cardiac Amyloidosis - 2021.

Authors:  Marcus V Simões; Fabio Fernandes; Fabiana G Marcondes-Braga; Philip Scheinberg; Edileide de Barros Correia; Luis Eduardo P Rohde; Fernando Bacal; Silvia Marinho Martins Alves; Sandrigo Mangini; Andréia Biolo; Luis Beck-da-Silva; Roberta Shcolnik Szor; Wilson Marques Junior; Acary Souza Bulle Oliveira; Márcia Waddington Cruz; Bruno Vaz Kerges Bueno; Ludhmila Abrahão Hajjar; Aurora Felice Castro Issa; Felix José Alvarez Ramires; Otavio Rizzi Coelho Filho; André Schmidt; Ibraim Masciarelli Francisco Pinto; Carlos Eduardo Rochitte; Marcelo Luiz Campos Vieira; Cláudio Tinoco Mesquita; Celso Dario Ramos; José Soares-Junior; Minna Moreira Dias Romano; Wilson Mathias Junior; Marcelo Iório Garcia Junior; Marcelo Westerlund Montera; Marcelo Dantas Tavares de Melo; Sandra Marques E Silva; Pedro Manoel Marques Garibaldi; Aristóteles Comte de Alencar Neto; Renato Delascio Lopes; Diane Xavier de Ávila; Denizar Viana; José Francisco Kerr Saraiva; Manoel Fernandes Canesin; Glaucia Maria Moraes de Oliveira; Evandro Tinoco Mesquita
Journal:  Arq Bras Cardiol       Date:  2021-09       Impact factor: 2.000

2.  Prevalence and Outcomes of p.Val142Ile TTR Amyloidosis Cardiomyopathy: A Systematic Review.

Authors:  Pranav Chandrashekar; Laith Alhuneafat; Meghan Mannello; Lana Al-Rashdan; Morris M Kim; Jason Dungu; Kevin Alexander; Ahmad Masri
Journal:  Circ Genom Precis Med       Date:  2021-08-31

3.  Yield of bone scintigraphy screening for transthyretin-related cardiac amyloidosis in different conditions: Methodological issues and clinical implications.

Authors:  Giacomo Tini; Eugenio Sessarego; Stefano Benenati; Pier Filippo Vianello; Beatrice Musumeci; Camillo Autore; Marco Canepa
Journal:  Eur J Clin Invest       Date:  2021-08-22       Impact factor: 5.722

4.  Correlation Between Cardiac Images, Biomarkers, and Amyloid Load in Wild-Type Transthyretin Amyloid Cardiomyopathy.

Authors:  Mami Morioka; Seiji Takashio; Naoya Nakashima; Masato Nishi; Akira Fujiyama; Kyoko Hirakawa; Shinsuke Hanatani; Hiroki Usuku; Eiichiro Yamamoto; Masafumi Kidoh; Seitaro Oda; Kenichi Matsushita; Mitsuharu Ueda; Kenichi Tsujita
Journal:  J Am Heart Assoc       Date:  2022-06-14       Impact factor: 6.106

5.  Poor right ventricular function is associated with impaired exercise capacity and ventilatory efficiency in transthyretin cardiac amyloid patients.

Authors:  Simone Bartolini; Samuele Baldasseroni; Francesco Fattirolli; Maria Vittoria Silverii; Lucrezia Piccioli; Federico Perfetto; Niccolò Marchionni; Carlo Di Mario; Raffaele Martone; Giulia Taborchi; Sofia Morini; Elisa Vignini; Francesco Cappelli
Journal:  Intern Emerg Med       Date:  2020-09-12       Impact factor: 3.397

6.  Clinical comparison of V122I genotypic variant of transthyretin amyloid cardiomyopathy with wild-type and other hereditary variants: a systematic review.

Authors:  Amandeep Goyal; Shubham Lahan; Tarun Dalia; Sagar Ranka; Venugopal Brijmohan Bhattad; Ronak R Patel; Zubair Shah
Journal:  Heart Fail Rev       Date:  2021-03-25       Impact factor: 4.214

Review 7.  Estimating the Gender Distribution of Patients with Wild-Type Transthyretin Amyloid Cardiomyopathy: A Systematic Review and Meta-Analysis.

Authors:  Florint Kroi; Nils Fischer; Ana Gezin; Mahmoud Hashim; Mark Hermannes Rozenbaum
Journal:  Cardiol Ther       Date:  2020-12-14

Review 8.  Imaging-Guided Treatment for Cardiac Amyloidosis.

Authors:  Adam Ioannou; Rishi Patel; Julian D Gillmore; Marianna Fontana
Journal:  Curr Cardiol Rep       Date:  2022-05-07       Impact factor: 3.955

Review 9.  Cardiac Amyloidosis: Multimodal Imaging of Disease Activity and Response to Treatment.

Authors:  Rishi K Patel; Marianna Fontana; Frederick L Ruberg
Journal:  Circ Cardiovasc Imaging       Date:  2021-06-15       Impact factor: 8.589

Review 10.  The Role of Multi-modality Imaging in the Diagnosis of Cardiac Amyloidosis: A Focused Update.

Authors:  Shaun Khanna; Ivy Wen; Aditya Bhat; Henry H L Chen; Gary C H Gan; Faraz Pathan; Timothy C Tan
Journal:  Front Cardiovasc Med       Date:  2020-10-30
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