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 …

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 …

2023 ACC expert consensus decision pathway on comprehensive multidisciplinary care for the patient with cardiac amyloidosis: a report of the American College of …

Writing Committee, MM Kittleson, FL Ruberg… - Journal of the American …, 2023 - jacc.org
The systemic amyloidoses are a broad spectrum of diseases that result from misfolding of
proteins that aggregate into b-sheet amyloid fibrils. Over 35 amyloidogenic precursor …

Natural history, quality of life, and outcome in cardiac transthyretin amyloidosis

T Lane, M Fontana, A Martinez-Naharro, CC Quarta… - Circulation, 2019 - Am Heart Assoc
Background: Transthyretin amyloidosis cardiomyopathy (ATTR-CM) is an increasingly
recognized cause of heart failure in older individuals. We sought to characterize the natural …

Understanding the complexity of heart failure risk and treatment in black patients

A Nayak, AJ Hicks, AA Morris - Circulation: Heart Failure, 2020 - Am Heart Assoc
Although care of patients with heart failure (HF) has improved in the past decade, important
disparities in HF outcomes persist based on race/ethnicity. Age-adjusted HF-related …

ATTR Amyloidosis: Current and Emerging Management Strategies: JACC: CardioOncology State-of-the-Art Review

JM Griffin, JL Rosenthal, JL Grodin, MS Maurer… - Cardio Oncology, 2021 - jacc.org
Transthyretin cardiac amyloidosis (ATTR-CA) is increasingly diagnosed owing to the
emergence of noninvasive imaging and improved awareness. Clinical penetrance of …

Long-term survival with tafamidis in patients with transthyretin amyloid cardiomyopathy

P Elliott, BM Drachman, SS Gottlieb… - Circulation: Heart …, 2022 - Am Heart Assoc
Background: Tafamidis is approved in many countries for the treatment of transthyretin
amyloid cardiomyopathy. This study reports data on the long-term efficacy of tafamidis from …

Addressing common questions encountered in the diagnosis and management of cardiac amyloidosis

MS Maurer, P Elliott, R Comenzo, M Semigran… - Circulation, 2017 - Am Heart Assoc
Advances in cardiac imaging have resulted in greater recognition of cardiac amyloidosis in
everyday clinical practice, but the diagnosis continues to be made in patients with late-stage …

Tenosynovial and cardiac amyloidosis in patients undergoing carpal tunnel release

BW Sperry, BA Reyes, A Ikram, JP Donnelly… - Journal of the American …, 2018 - jacc.org
Background: Patients with cardiac amyloidosis often have carpal tunnel syndrome that
precedes cardiac manifestations by several years. However, the prevalence of cardiac …

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 …