Literature DB >> 35083944

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

Omar K Siddiqi1,2, Yuliya Y Mints2, John L Berk1,3, Lawreen Connors1,4, Gheorghe Doros5, Deepa M Gopal1,2, Shivangi Kataria5, Graham Lohrmann3, Alexandra R Pipilas2, Frederick L Ruberg1,2,6.   

Abstract

BACKGROUND: Diflunisal is a non-steroidal anti-inflammatory drug that stabilises transthyretin (TTR) and reduces neurologic deterioration in patients with polyneuropathy caused by hereditary transthyretin amyloidosis (ATTRv).
METHODS: We conducted a retrospective cohort study of patients with wild-type transthyretin cardiac amyloidosis (ATTRwt-CM) treated with diflunisal for at least one year between 2009 and 2016 at the Boston University Amyloidosis Centre. Baseline and one year follow up characteristics were measured, including plasma chemistries and echocardiography. Cox proportional hazards analysis assessed the primary outcome of all-cause mortality.
RESULTS: A total of 104 ATTRwt-CM patients were evaluated with 35 patients receiving diflunisal. Patients in the diflunisal group were younger (73.8 vs 76.8 years, p = 0.034), with lower B-type natriuretic peptide (BNP, 335 +/- 67 vs. 520 +/- 296 pg/mL, p = 0.006), similar troponin I (0.1 +/- 0.1 vs 0.2 +/- 0.3 ng/mL, p = 0.09), and better renal function (eGFR 67 +/- 17 vs 53 +/- 18 mL/min/1.73m2, p = 0.0002) at baseline. Over a median follow-up of 3.2 years, 52 deaths occurred. Diflunisal administration was associated with improved survival in unadjusted analysis (HR 0.13, 95% CI 0.05 - 0.36, p < 0.001) that persisted after adjustment for age, baseline BNP, eGFR, troponin I, interventricular septal thickness, and left ventricular ejection fraction (HR 0.18, 95% CI 0.06 - 0.51, p = 0.0006). Over the observation period, no significant changes in BNP, troponin I, interventricular septal thickness or left ventricular ejection fraction were observed with diflunisal treatment. A total of 14 patients (40%) discontinued diflunisal in this study, but only 3 within the first year. Mean eGFR in treated patients was 59 ml/min/1.73m2 at 1 year (change from baseline p = 0.03).
CONCLUSION: Diflunisal administration in ATTRwt-CM was associated with improved survival and overall stability in clinical and echocardiographic markers of disease with decrement renal function.

Entities:  

Keywords:  Cardiac amyloidosis; diflunisal; echocardiography; heart failure; transthyretin

Mesh:

Substances:

Year:  2022        PMID: 35083944      PMCID: PMC9258521          DOI: 10.1080/13506129.2021.2000388

Source DB:  PubMed          Journal:  Amyloid        ISSN: 1350-6129            Impact factor:   6.571


  22 in total

Review 1.  Transthyretin Amyloid Cardiomyopathy: JACC State-of-the-Art Review.

Authors:  Frederick L Ruberg; Martha Grogan; Mazen Hanna; Jeffery W Kelly; Mathew S Maurer
Journal:  J Am Coll Cardiol       Date:  2019-06-11       Impact factor: 24.094

2.  Pilot study for left ventricular imaging phenotype of patients over 65 years old with heart failure and preserved ejection fraction: the high prevalence of amyloid cardiomyopathy.

Authors:  Youssef Bennani Smires; Gérard Victor; David Ribes; Matthieu Berry; Thomas Cognet; Simon Méjean; Antoine Huart; Murielle Roussel; Antoine Petermann; Jérôme Roncalli; Didier Carrié; Hervé Rousseau; Isabelle Berry; Dominique Chauveau; Michel Galinier; Olivier Lairez
Journal:  Int J Cardiovasc Imaging       Date:  2016-05-30       Impact factor: 2.357

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

Authors:  Jacquelyn L S Hanson; Marios Arvanitis; Clarissa M Koch; John L Berk; Frederick L Ruberg; Tatiana Prokaeva; Lawreen H Connors
Journal:  Circ Heart Fail       Date:  2018-02       Impact factor: 8.790

4.  Transthyretin Cardiac Amyloidosis as Diagnosed by 99mTc-PYP Scanning in Patients with Acute Heart Failure and Preserved Ejection Fraction.

Authors:  Saberio Lo Presti; Sofia A Horvath; Christos G Mihos; Chetan Rajadhyaksha; Veronica McCloskey; Orlando Santana
Journal:  Crit Pathw Cardiol       Date:  2019-12

5.  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

6.  Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction.

Authors:  Esther González-López; Maria Gallego-Delgado; Gonzalo Guzzo-Merello; F Javier de Haro-Del Moral; Marta Cobo-Marcos; Carolina Robles; Belén Bornstein; Clara Salas; Enrique Lara-Pezzi; Luis Alonso-Pulpon; Pablo Garcia-Pavia
Journal:  Eur Heart J       Date:  2015-07-28       Impact factor: 29.983

7.  Left ventricular amyloid deposition in patients with heart failure and preserved ejection fraction.

Authors:  Selma F Mohammed; Sultan A Mirzoyev; William D Edwards; Ahmet Dogan; Donna R Grogan; Shannon M Dunlay; Veronique L Roger; Morie A Gertz; Angela Dispenzieri; Steven R Zeldenrust; Margaret M Redfield
Journal:  JACC Heart Fail       Date:  2014-04       Impact factor: 12.035

8.  TTR (Transthyretin) Stabilizers Are Associated With Improved Survival in Patients With TTR Cardiac Amyloidosis.

Authors:  Hannah Rosenblum; Adam Castano; Julissa Alvarez; Jeff Goldsmith; Stephen Helmke; Mathew S Maurer
Journal:  Circ Heart Fail       Date:  2018-04       Impact factor: 8.790

9.  Synthesis and characterization of potent bivalent amyloidosis inhibitors that bind prior to transthyretin tetramerization.

Authors:  Nora S Green; Satheesh K Palaninathan; James C Sacchettini; Jeffery W Kelly
Journal:  J Am Chem Soc       Date:  2003-11-05       Impact factor: 15.419

10.  Clinical characteristics of wild-type transthyretin cardiac amyloidosis: disproving myths.

Authors:  Esther González-López; Christian Gagliardi; Fernando Dominguez; Cristina Candida Quarta; F Javier de Haro-Del Moral; Agnese Milandri; Clara Salas; Mario Cinelli; Marta Cobo-Marcos; Massimiliano Lorenzini; Enrique Lara-Pezzi; Serena Foffi; Luis Alonso-Pulpon; Claudio Rapezzi; Pablo Garcia-Pavia
Journal:  Eur Heart J       Date:  2017-06-21       Impact factor: 29.983

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  1 in total

Review 1.  Treatment of Transthyretin Amyloid Cardiomyopathy: The Current Options, the Future, and the Challenges.

Authors:  Carsten Tschöpe; Ahmed Elsanhoury
Journal:  J Clin Med       Date:  2022-04-12       Impact factor: 4.964

  1 in total

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