Genotype and Phenotype of Transthyretin Cardiac Amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey).

doi:10.1016/j.jacc.2016.03.596

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Article

Genotype and Phenotype of Transthyretin Cardiac Amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey).

Journal of the American College of Cardiology - 12 Jul 2016

Maurer Mathew S, Hanna Mazen, Grogan Martha, Dispenzieri Angela, Witteles Ronald, Drachman Brian, Judge Daniel P, Lenihan Daniel J, Gottlieb Stephen S, Shah Sanjiv J, Steidley D Eric, Ventura Hector, Murali Srinivas, Silver Marc A, Jacoby Daniel, Fedson Savitri, Hummel Scott L, Kristen Arnt V, Damy Thibaud, Planté-Bordeneuve Violaine, Coelho Teresa, Mundayat Rajiv, Suhr Ole B, Waddington Cruz Márcia, Rapezzi Claudio

Abstract excerpt

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 describe ATTR in the United States by using data from the THAOS (Transthyretin Amyloidosis Outcomes Survey) registry. METHODS: Demographic, clinical, and genetic features of patients enrolled in the THAOS registry in the United States...

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PMID: 27386769
DOI: 10.1016/j.jacc.2016.03.596
PMCID: PMC4940135

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