Cargando…

Diagnostic utility of cardiac troponin T level in patients with cardiac amyloidosis

AIM: The aim of this study was to evaluate the diagnostic utility of high‐sensitivity cardiac troponin T (hs‐cTnT) levels in discriminating cardiac amyloidosis from patients with cardiac hypertrophy caused by aetiologies other than cardiac amyloidosis. METHODS AND RESULTS: Serum hs‐cTnT levels were...

Descripción completa

Detalles Bibliográficos
Autores principales:	Takashio, Seiji, Yamamuro, Megumi, Izumiya, Yasuhiro, Hirakawa, Kyoko, Marume, Kyohei, Yamamoto, Masahiro, Ueda, Mitsuharu, Yamashita, Taro, Ishibashi‐Ueda, Hatsue, Yasuda, Satoshi, Ogawa, Hisao, Ando, Yukio, Anzai, Toshihisa, Tsujita, Kenichi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2017
Materias:	Original Research Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793964/ https://www.ncbi.nlm.nih.gov/pubmed/28869340 http://dx.doi.org/10.1002/ehf2.12203

Ejemplares similares

Non‐Val30Met mutation, septal hypertrophy, and cardiac denervation in patients with mutant transthyretin amyloidosis
por: Hirakawa, Kyoko, et al.
Publicado: (2018)

Can myocardial susceptibility quantification be an imaging biomarker for cardiac amyloidosis?
por: Hayashi, Hidetaka, et al.
Publicado: (2021)

Persistent increase in cardiac troponin T at hospital discharge predicts repeat hospitalization in patients with acute decompensated heart failure
por: Takashio, Seiji, et al.
Publicado: (2017)

Trends in the Clinical and Pathological Characteristics of Cardiac Rupture in Patients With Acute Myocardial Infarction Over 35 Years
por: Honda, Satoshi, et al.
Publicado: (2014)

Late gadolinium enhancement on cardiac magnetic resonance predicts coronary vasomotor abnormality and myocardial lactate production in patients with chronic heart failure
por: Uemura, Tomoaki, et al.
Publicado: (2016)

Lymph Vessel Proliferation on Cardiac Biopsy May Help in the Diagnosis of Cardiac Sarcoidosis
por: Oe, Yukiko, et al.
Publicado: (2019)

Decreased Myocardial Dendritic Cells is Associated With Impaired Reparative Fibrosis and Development of Cardiac Rupture After Myocardial Infarction in Humans
por: Nagai, Toshiyuki, et al.
Publicado: (2014)

Plasma growth differentiation factor 15: a novel tool to detect early changes of hereditary transthyretin amyloidosis
por: Okada, Masamitsu, et al.
Publicado: (2020)

Correlation Between Cardiac Images, Biomarkers, and Amyloid Load in Wild‐Type Transthyretin Amyloid Cardiomyopathy
por: Morioka, Mami, et al.
Publicado: (2022)

Presence of increased inflammatory infiltrates accompanied by activated dendritic cells in the left atrium in rheumatic heart disease
por: Shiba, Mikio, et al.
Publicado: (2018)

Recent advances in transthyretin amyloidosis therapy
por: Ueda, Mitsuharu, et al.
Publicado: (2014)

Prognostic value of right ventricular global longitudinal strain in patients with immunoglobulin light-chain cardiac amyloidosis
por: Usuku, Hiroki, et al.
Publicado: (2023)

Differential Expression of Cardiac Troponin T and I in a Patient with Isolated Skeletal Muscular Sarcoidosis
por: Mannoji, Hiroshi, et al.
Publicado: (2016)

P-wave characteristics and atrium voltage mapping in cardiac amyloidosis with paroxysmal atrial fibrillation
por: Ohe, Masatsugu, et al.
Publicado: (2023)

Usefulness of automatic assessment for longitudinal strain to diagnose wild-type transthyretin amyloid cardiomyopathy
por: Usuku, Hiroki, et al.
Publicado: (2023)

Prognostic impact of blood pressure response plus gadolinium enhancement in dilated cardiomyopathy
por: Tateishi, Emi, et al.
Publicado: (2015)

Pathological Investigation of Congenital Bicuspid Aortic Valve Stenosis, Compared with Atherosclerotic Tricuspid Aortic Valve Stenosis and Congenital Bicuspid Aortic Valve Regurgitation
por: Hamatani, Yasuhiro, et al.
Publicado: (2016)

First Nationwide Survey of 199 Patients with Amyloid A Amyloidosis in Japan
por: Okuda, Yasuaki, et al.
Publicado: (2018)

Mitral Regurgitation and Heart Failure as the First Presentation in a Patient with Features of Two Connective Tissue Disorders: A Rare Combination of Mucopolysaccharidosis and Osteogenesis Imperfecta?
por: Hamatani, Yasuhiro, et al.
Publicado: (2017)

Step‐by‐step typing for the accurate diagnosis of concurrent light chain and transthyretin cardiac amyloidosis
por: Moriyama, Hidenori, et al.
Publicado: (2022)

Prognostic value of high-sensitivity cardiac troponin T in patients with endomyocardial-biopsy proven cardiac amyloidosis
por: Qian, Geng, et al.
Publicado: (2014)

Direct Oral Anticoagulants Form Thrombus Different From Warfarin in a Microchip Flow Chamber System
por: Ishii, Masanobu, et al.
Publicado: (2017)

Usefulness of quantitative (99m)Tc-pyrophosphate SPECT/CT for predicting the prognosis of patients with wild-type transthyretin cardiac amyloidosis
por: Ogasawara, Kouji, et al.
Publicado: (2022)

Anti-Kv1.4 Antibody Without Myasthenia Gravis: A Rare Cause of Autoimmune Myocarditis and Myositis
por: Kuyama, Naoto, et al.
Publicado: (2023)

Myocardial Immunocompetent Cells and Macrophage Phenotypes as Histopathological Surrogates for Diagnosis of Cardiac Sarcoidosis in Japanese
por: Honda, Yasuyuki, et al.
Publicado: (2016)

Significance of myocardial tenascin‐C expression in left ventricular remodelling and long‐term outcome in patients with dilated cardiomyopathy
por: Yokokawa, Tetsuro, et al.
Publicado: (2016)

How to Identify Transthyretin Cardiac Amyloidosis at an Early Stage
por: Izumiya, Yasuhiro, et al.
Publicado: (2020)

Prognostic Impact of the Increase in Cardiac Troponin Levels during Tafamidis Therapy in Patients with Transthyretin Cardiac Amyloidosis
por: Nakamura, Makiko, et al.
Publicado: (2023)

Rapid decline in ejection fraction and persistent elevation of troponin associated with cardiac amyloidosis
por: Abe, Temidayo, et al.
Publicado: (2020)

Clinical characteristics, outcome, and therapeutic effect of tafamidis in wild‐type transthyretin amyloid cardiomyopathy
por: Takashio, Seiji, et al.
Publicado: (2023)

Left atrial intramural haematoma: a fatal complication of cardiac amyloidosis—a case report
por: Terashima, Rika, et al.
Publicado: (2023)

Urinary Transthyretin as a Biomarker in ATTRv Val50Met Amyloidosis
por: Matsushita, Hiroaki, et al.
Publicado: (2022)

Successful surgical treatment for recurrent cardiac fibroma 21 years after resection
por: Kusajima, Kunio, et al.
Publicado: (2015)

Pathology after a combination of sequential and simultaneous unipolar radiofrequency ablation of ventricular tachycardia in a postmortem heart with cardiac sarcoidosis
por: Miyamoto, Koji, et al.
Publicado: (2018)

Earlier Right Ventricular Pacing in Cardiac Resynchronization Therapy for a Patient with Right Axis Deviation
por: Hattori, Yusuke, et al.
Publicado: (2017)

Early Progression of Aortic Stenosis Associated With Iatrogenic Variant Transthyretin Amyloidosis After Domino Liver Transplantation
por: Hosoda, Yasuhito, et al.
Publicado: (2020)

Multimodality assessment of left ventricular dysfunction in Takayasu arteritis and familial hypercholesterolaemia
por: Okada, Atsushi, et al.
Publicado: (2017)

Utility of left atrial and ventricular strain for diagnosis of transthyretin amyloid cardiomyopathy in aortic stenosis
por: Oike, Fumi, et al.
Publicado: (2022)

Decrease in exhaled hydrogen as marker of congestive heart failure
por: Shibata, Atsushi, et al.
Publicado: (2018)

Base-to-apex gradient pattern of cardiac impairment identified on myocardial T1 mapping in cardiac amyloidosis
por: Oda, Seitaro, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_p3rb1ura28cindmj74j0hu6sm6