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 …
neuropathy and cardiomyopathy. It occurs in both a mutant form (with autosomal dominant …
Management of arrhythmias in cardiac amyloidosis
S Giancaterino, MA Urey, D Darden, JC Hsu - Clinical Electrophysiology, 2020 - jacc.org
Cardiac amyloidosis is characterized by extracellular protein fibril deposition in the
myocardium leading to restrictive heart failure. Both atrial and ventricular arrhythmias, along …
myocardium leading to restrictive heart failure. Both atrial and ventricular arrhythmias, along …
[HTML][HTML] Inflammatory and molecular pathways in heart failure—ischemia, HFpEF and transthyretin cardiac amyloidosis
D Michels da Silva, H Langer, T Graf - International journal of molecular …, 2019 - mdpi.com
Elevated pro-inflammatory biomarkers and cytokines are associated with morbidity and
mortality in heart failure (HF). Preclinical and clinical studies have shown multiple …
mortality in heart failure (HF). Preclinical and clinical studies have shown multiple …
Atrial fibrillation in amyloidotic cardiomyopathy: prevalence, incidence, risk factors and prognostic role
S Longhi, CC Quarta, A Milandri, M Lorenzini… - Amyloid, 2015 - Taylor & Francis
Background: Although atrial fibrillation (AF) is a known complication of amyloidotic
cardiomyopathy (AC), a precise pathophysiological and prognostic characterization is not …
cardiomyopathy (AC), a precise pathophysiological and prognostic characterization is not …
[HTML][HTML] Multidisciplinary approaches for transthyretin amyloidosis
H Koike, T Okumura, T Murohara, M Katsuno - Cardiology and Therapy, 2021 - Springer
Amyloidosis caused by systemic deposition of transthyretin (TTR) is called ATTR
amyloidosis and mainly includes hereditary ATTR (ATTRv) amyloidosis and wild-type ATTR …
amyloidosis and mainly includes hereditary ATTR (ATTRv) amyloidosis and wild-type ATTR …
Role of imaging in the diagnosis and management of patients with cardiac amyloidosis: state of the art review and focus on emerging nuclear techniques
Amyloidosis is an infiltrative disease characterized by deposition of amyloid fibrils within the
extracellular tissue of one or multiple organs. Involvement of the heart, cardiac amyloidosis …
extracellular tissue of one or multiple organs. Involvement of the heart, cardiac amyloidosis …
Heart failure with preserved ejection fraction, atrial fibrillation, and the role of senile amyloidosis
MP van den Berg, BA Mulder… - European Heart …, 2019 - academic.oup.com
Heart failure with preserved ejection fraction (HFpEF) and atrial fibrillation (AF) are very
common conditions, particularly in the elderly. However, the mechanisms underlying the two …
common conditions, particularly in the elderly. However, the mechanisms underlying the two …
[HTML][HTML] Restrictive cardiomyopathies: the importance of noninvasive cardiac imaging modalities in diagnosis and treatment—a systematic review
A Rammos, V Meladinis, G Vovas… - Radiology research and …, 2017 - hindawi.com
Restrictive cardiomyopathy (RCM) is the least common among cardiomyopathies. It can be
idiopathic, familial, or secondary to systematic disorders. Marked increase in left and/or right …
idiopathic, familial, or secondary to systematic disorders. Marked increase in left and/or right …
Inotropic myocardial reserve deficiency is the predominant feature of exercise haemodynamics in cardiac amyloidosis
TS Clemmensen, H Mølgaard… - European Journal of …, 2017 - Wiley Online Library
Aims This study aimed to characterize invasive haemodynamics during exercise in subjects
with cardiac amyloidosis (CA). Methods and results The study population numbered 44 …
with cardiac amyloidosis (CA). Methods and results The study population numbered 44 …
[HTML][HTML] Imaging findings of right cardiac amyloidosis: impact on prognosis and clinical course
Cardiac involvement from amyloidosis is of growing interest in the overall literature. Despite
cardiac amyloidosis (CA) has been considered for a long time a rare disease, the diagnostic …
cardiac amyloidosis (CA) has been considered for a long time a rare disease, the diagnostic …