Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review

FL Ruberg, M Grogan, M Hanna, JW Kelly… - Journal of the American …, 2019 - jacc.org
Transthyretin amyloid cardiomyopathy (ATTR-CM) is an under-recognized cause of heart
failure (HF) in older adults, resulting from myocardial deposition of misfolded transthyretin …

Redefining the epidemiology of cardiac amyloidosis. A systematic review and meta‐analysis of screening studies

A Aimo, M Merlo, A Porcari… - European journal of …, 2022 - Wiley Online Library
Aims An algorithm for non‐invasive diagnosis of amyloid transthyretin cardiac amyloidosis
(ATTR‐CA) and novel disease‐modifying therapies have prompted an active search for CA …

Prevalence and outcomes of concomitant aortic stenosis and cardiac amyloidosis

C Nitsche, PR Scully, KP Patel… - Journal of the American …, 2021 - jacc.org
Background Older patients with severe aortic stenosis (AS) are increasingly identified as
having cardiac amyloidosis (CA). It is unknown whether concomitant AS-CA has worse …

Expert consensus recommendations for the suspicion and diagnosis of transthyretin cardiac amyloidosis

MS Maurer, S Bokhari, T Damy, S Dorbala… - Circulation: Heart …, 2019 - Am Heart Assoc
Cardiomyopathy is a manifestation of transthyretin amyloidosis (ATTR), which is an
underrecognized systemic disease whereby the transthyretin protein misfolds to form fibrils …

ASNC/AHA/ASE/EANM/HFSA/ISA/SCMR/SNMMI expert consensus recommendations for multimodality imaging in cardiac amyloidosis: part 1 of 2—evidence base …

S Dorbala, Y Ando, S Bokhari… - Circulation …, 2021 - Am Heart Assoc
Sharmila Dorbala, MD, MPH, FASNC, Chair*; Yukio Ando, MD, PhD†; Sabahat Bokhari,
MD‡; Angela Dispenzieri, MD § ; Rodney H. Falk, MD*; Victor A. Ferrari, MD∥; Marianna …

Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction

E González-López, M Gallego-Delgado… - European heart …, 2015 - academic.oup.com
Aims Heart failure with preserved ejection fraction (HFpEF) is a heterogeneous clinical
syndrome with multiple underlying causes. Wild-type transthyretin (TTR) amyloidosis …

Genotype and phenotype of transthyretin cardiac amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey)

MS Maurer, M Hanna, M Grogan, A Dispenzieri… - Journal of the American …, 2016 - jacc.org
Background: Transthyretin amyloidosis (ATTR) is a heterogeneous disorder with multiorgan
involvement and a genetic or nongenetic basis. Objectives: The goal of this study was to …

Clinical characteristics of wild-type transthyretin cardiac amyloidosis: disproving myths

E González-López, C Gagliardi… - European heart …, 2017 - academic.oup.com
Aims Wild-type transthyretin amyloidosis (ATTRwt) is mostly considered a disease
predominantly of elderly male, characterized by concentric LV hypertrophy, preserved LVEF …

Хроническая сердечная недостаточность. Клинические рекомендации 2020

СН Терещенко, АС Галявич, ТМ Ускач… - Российский …, 2020 - cyberleninka.ru
КТИ—кардиоторакальный индекс КШ—коронарное шунтирование ЛЖ—левый
желудочек МНО—международное нормализованное отношение МРТ—магнитно …

Diagnosis, prognosis, and therapy of transthyretin amyloidosis

MA Gertz, MD Benson, PJ Dyck, M Grogan… - Journal of the American …, 2015 - jacc.org
Transthyretin amyloidosis is a fatal disorder that is characterized primarily by progressive
neuropathy and cardiomyopathy. It occurs in both a mutant form (with autosomal dominant …