Literature DB >> 29449366

Use of Serum Transthyretin as a Prognostic Indicator and Predictor of Outcome in Cardiac Amyloid Disease Associated With Wild-Type Transthyretin.

Jacquelyn L S Hanson1, Marios Arvanitis1, Clarissa M Koch1, John L Berk1, Frederick L Ruberg1, Tatiana Prokaeva1, Lawreen H Connors2.   

Abstract

BACKGROUND: Wild-type transthyretin amyloidosis (ATTRwt), an underappreciated cause of heart failure in older adults, is challenging to diagnose and monitor in the absence of validated, disease-specific biomarkers. We examined the prognostic use and survival association of serum TTR (transthyretin) concentration in ATTRwt. METHODS AND
RESULTS: Patients with biopsy-proven ATTRwt were retrospectively identified. Serum TTR, cardiac biomarkers, and echocardiographic parameters were assessed at baseline and follow-up evaluations. Statistical analyses included Kaplan-Meier method, Cox proportional hazard survival models, and receiver-operating characteristic curve analysis. Median serum TTR concentration at presentation was 23 mg/dL (n=116). Multivariate predictors of shorter overall survival were decreased TTR, left ventricular ejection fraction and elevated cTn-I (cardiac troponin I); an inclusive model demonstrated superior accuracy in 4-year survival prediction by receiver-operating characteristic curve analysis (area under the curve, 0.77). TTR values lower than the normal limit, <18 mg/dL, were associated with shorter survival (2.8 versus 4.1 years; P=0.03). Further, TTR values at 1- and 2-year follow-ups were significantly lower (P<0.001) in untreated patients (n=23) compared with those treated with TTR stabilizer, diflunisal (n=12), after baseline evaluation. During 2-year follow-up, unchanged TTR corresponded to increased cTn-I (P=0.006) in untreated patients; conversely, the diflunisal-treated group showed increased TTR (P=0.001) and stabilized cTn-I and left ventricular ejection fraction at 1 year.
CONCLUSIONS: In this series of biopsy-proven ATTRwt, lower baseline serum TTR concentration was associated with shorter survival as an independent predictor of outcome. Longitudinal analysis demonstrated that decreasing TTR corresponded to worsening cardiac function. These data suggest that TTR may be a useful prognostic marker and predictor of outcome in ATTRwt.
© 2018 American Heart Association, Inc.

Entities:  

Keywords:  amyloid; biomarker; heart failure; risk factor; survival

Mesh:

Substances:

Year:  2018        PMID: 29449366      PMCID: PMC5819619          DOI: 10.1161/CIRCHEARTFAILURE.117.004000

Source DB:  PubMed          Journal:  Circ Heart Fail        ISSN: 1941-3289            Impact factor:   8.790


  30 in total

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Authors:  Candida Cristina Quarta; Scott D Solomon; Imran Uraizee; Jenna Kruger; Simone Longhi; Marinella Ferlito; Christian Gagliardi; Agnese Milandri; Claudio Rapezzi; Rodney H Falk
Journal:  Circulation       Date:  2014-02-21       Impact factor: 29.690

Review 2.  Senile systemic amyloidosis: are regional differences real or do they reflect different diagnostic suspicion and use of techniques?

Authors:  Rodney H Falk
Journal:  Amyloid       Date:  2012-06       Impact factor: 7.141

Review 3.  Cardiac amyloidosis: the great pretender.

Authors:  Claudio Rapezzi; Massimiliano Lorenzini; Simone Longhi; Agnese Milandri; Christian Gagliardi; Ilaria Bartolomei; Fabrizio Salvi; Mathew S Maurer
Journal:  Heart Fail Rev       Date:  2015-03       Impact factor: 4.214

4.  Analyses of prealbumin mRNAs in individuals with familial amyloidotic polyneuropathy.

Authors:  S Mita; S Maeda; K Shimada; S Araki
Journal:  J Biochem       Date:  1986-11       Impact factor: 3.387

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Authors:  A Myron Johnson; Giampaolo Merlini; Joanna Sheldon; Kiyoshi Ichihara
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6.  Transthyretin cardiac amyloidoses in older North Americans.

Authors:  Kumar Dharmarajan; Mathew S Maurer
Journal:  J Am Geriatr Soc       Date:  2012-02-13       Impact factor: 5.562

7.  Nephelometric measurement of human serum prealbumin and correlation with acute-phase proteins CRP and SAA: results in familial amyloid polyneuropathy.

Authors:  L H Connors; M A Gertz; M Skinner; A S Cohen
Journal:  J Lab Clin Med       Date:  1984-10

8.  METABOLISM OF IODINE-131--LABELED THYROXINE-BINDING PREALBUMIN IN MAN.

Authors:  J H OPPEHNEIMER; M I SURKS; G BERNSTEIN; J C SMITY
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Authors:  M Skinner; L H Connors; A Rubinow; C Libbey; J D Sipe; A S Cohen
Journal:  Am J Med Sci       Date:  1985-01       Impact factor: 2.378

Review 10.  The systemic amyloidoses: clearer understanding of the molecular mechanisms offers hope for more effective therapies.

Authors:  G Merlini; P Westermark
Journal:  J Intern Med       Date:  2004-02       Impact factor: 8.989

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  18 in total

1.  Stabilization of Cardiac Function With Diflunisal in Transthyretin (ATTR) Cardiac Amyloidosis.

Authors:  Graham Lohrmann; Alexandra Pipilas; Roberta Mussinelli; Deepa M Gopal; John L Berk; Lawreen H Connors; Nirupama Vellanki; Jennifer Hellawell; Omar K Siddiqi; Jonathan Fox; Mathew S Maurer; Frederick L Ruberg
Journal:  J Card Fail       Date:  2019-12-02       Impact factor: 5.712

2.  Predictive model of response to tafamidis in hereditary ATTR polyneuropathy.

Authors:  Cecília Monteiro; Jaleh S Mesgazardeh; João Anselmo; Joana Fernandes; Marta Novais; Carla Rodrigues; Gabriel J Brighty; David L Powers; Evan T Powers; Teresa Coelho; Jeffery W Kelly
Journal:  JCI Insight       Date:  2019-06-20

3.  A circulating, disease-specific, mechanism-linked biomarker for ATTR polyneuropathy diagnosis and response to therapy prediction.

Authors:  Xin Jiang; Richard Labaudinière; Joel N Buxbaum; Cecília Monteiro; Marta Novais; Teresa Coelho; Jeffery W Kelly
Journal:  Proc Natl Acad Sci U S A       Date:  2021-03-02       Impact factor: 11.205

4.  Position Statement on Diagnosis and Treatment of Cardiac Amyloidosis - 2021.

Authors:  Marcus V Simões; Fabio Fernandes; Fabiana G Marcondes-Braga; Philip Scheinberg; Edileide de Barros Correia; Luis Eduardo P Rohde; Fernando Bacal; Silvia Marinho Martins Alves; Sandrigo Mangini; Andréia Biolo; Luis Beck-da-Silva; Roberta Shcolnik Szor; Wilson Marques Junior; Acary Souza Bulle Oliveira; Márcia Waddington Cruz; Bruno Vaz Kerges Bueno; Ludhmila Abrahão Hajjar; Aurora Felice Castro Issa; Felix José Alvarez Ramires; Otavio Rizzi Coelho Filho; André Schmidt; Ibraim Masciarelli Francisco Pinto; Carlos Eduardo Rochitte; Marcelo Luiz Campos Vieira; Cláudio Tinoco Mesquita; Celso Dario Ramos; José Soares-Junior; Minna Moreira Dias Romano; Wilson Mathias Junior; Marcelo Iório Garcia Junior; Marcelo Westerlund Montera; Marcelo Dantas Tavares de Melo; Sandra Marques E Silva; Pedro Manoel Marques Garibaldi; Aristóteles Comte de Alencar Neto; Renato Delascio Lopes; Diane Xavier de Ávila; Denizar Viana; José Francisco Kerr Saraiva; Manoel Fernandes Canesin; Glaucia Maria Moraes de Oliveira; Evandro Tinoco Mesquita
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Review 5.  Update on Disease-Specific Biomarkers in Transthyretin Cardiac Amyloidosis.

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6.  Diflunisal treatment is associated with improved survival for patients with early stage wild-type transthyretin (ATTR) amyloid cardiomyopathy: the Boston University Amyloidosis Center experience.

Authors:  Omar K Siddiqi; Yuliya Y Mints; John L Berk; Lawreen Connors; Gheorghe Doros; Deepa M Gopal; Shivangi Kataria; Graham Lohrmann; Alexandra R Pipilas; Frederick L Ruberg
Journal:  Amyloid       Date:  2022-01-27       Impact factor: 6.571

Review 7.  Estimating the Gender Distribution of Patients with Wild-Type Transthyretin Amyloid Cardiomyopathy: A Systematic Review and Meta-Analysis.

Authors:  Florint Kroi; Nils Fischer; Ana Gezin; Mahmoud Hashim; Mark Hermannes Rozenbaum
Journal:  Cardiol Ther       Date:  2020-12-14

8.  Hepatocyte Growth Factor and Cardiac Amyloidosis.

Authors:  Frederick L Ruberg; Omar K Siddiqi
Journal:  JACC CardioOncol       Date:  2020-03-17

Review 9.  Cardiac Transthyretin-derived Amyloidosis: An Emerging Target in Heart Failure with Preserved Ejection Fraction?

Authors:  Sebastiaan Hc Klaassen; Dirk J van Veldhuisen; Hans LA Nienhuis; Maarten P van den Berg; Bouke Pc Hazenberg; Peter van der Meer
Journal:  Card Fail Rev       Date:  2020-08-07

Review 10.  Storage diseases with hypertrophic cardiomyopathy phenotype.

Authors:  Luis Ruiz-Guerrero; Roberto Barriales-Villa
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