Literature DB >> 34429516

Duchenne muscular dystrophy patients: troponin leak in asymptomatic and implications for drug toxicity studies.

Larry W Markham1, Jonathan H Soslow2, Aryaz Sheybani3, Kim Crum3, Frank J Raucci4, William B Burnette5.   

Abstract

BACKGROUND: Cardiomyopathy is the leading cause of death in Duchenne muscular dystrophy (DMD), but studies suggest heart failure biomarkers correlate poorly with cardiomyopathy severity. DMD clinical trials have used troponin I (cTnI) as a biomarker of toxicity, but it is unclear if asymptomatic DMD patients have elevated cTnI. We longitudinally evaluated cTnI, brain natriuretic peptide (BNP), and N-terminal pro-BNP (NT-proBNP) in a DMD cohort.
METHODS: DMD patients were prospectively enrolled and followed for 3 years. Serum was drawn at the time of cardiac magnetic resonance (CMR). Normal biomarker values were derived from healthy subjects. Biomarkers were correlated with CMR markers.
RESULTS: All subjects were asymptomatic at the time of enrollment. Several DMD subjects had transiently elevated cTnI. Those with elevated cTnI were more likely to have late gadolinium enhancement on baseline CMR. NT-proBNP correlated with indexed left ventricular end diastolic and maximum left atrial volumes. Otherwise, standard cardiac biomarkers did not correlate with CMR markers of cardiomyopathy.
CONCLUSIONS: CTnI, BNP, and NT-proBNP do not correlate with CMR assessment of cardiomyopathy progression. A subset of DMD patients have asymptomatic cTnI leak of uncertain clinical significance, though of critical importance if cTnI is used to assess for cardiac toxicity in future drug trials. IMPACT: Asymptomatic patients with Duchenne muscular dystrophy (DMD) exhibit transient troponin I leak. NT-proBNP correlated with indexed left ventricular end diastolic volume and indexed maximum left atrial volume. Other cardiac biomarkers did not correlate with cardiac magnetic resonance (CMR) markers of cardiomyopathy.
© 2021. The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc.

Entities:  

Year:  2021        PMID: 34429516      PMCID: PMC8866537          DOI: 10.1038/s41390-021-01682-5

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  46 in total

1.  B-type natriuretic peptide and cardiac dysfunction in Duchenne muscular dystrophy.

Authors:  Tayyab Mohyuddin; Irwin B Jacobs; Robert C Bahler
Journal:  Int J Cardiol       Date:  2006-10-31       Impact factor: 4.164

2.  Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.

Authors:  Paul A Harris; Robert Taylor; Robert Thielke; Jonathon Payne; Nathaniel Gonzalez; Jose G Conde
Journal:  J Biomed Inform       Date:  2008-09-30       Impact factor: 6.317

3.  The Role of Matrix Metalloproteinases and Tissue Inhibitors of Metalloproteinases in Duchenne Muscular Dystrophy Cardiomyopathy.

Authors:  Jonathan H Soslow; Meng Xu; James C Slaughter; Kimberly Crum; Joshua D Chew; W Bryan Burnette; Yan Ru Su; Kelsey Tomasek; David A Parra; Larry W Markham
Journal:  J Card Fail       Date:  2019-02-11       Impact factor: 5.712

4.  The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy.

Authors:  G Nigro; L I Comi; L Politano; R J Bain
Journal:  Int J Cardiol       Date:  1990-03       Impact factor: 4.164

5.  Relationship of cardiac troponin to systolic global longitudinal strain in hypertrophic cardiomyopathy.

Authors:  Anushree Agarwal; Rayan Yousefzai; Kambiz Shetabi; Fatima Samad; Saurabh Aggarwal; Chi Cho; Michelle Bush; M Fuad Jan; Bijoy K Khandheria; Timothy E Paterick; A Jamil Tajik
Journal:  Echocardiography       Date:  2017-08-28       Impact factor: 1.724

Review 6.  How well does B-type natriuretic peptide predict death and cardiac events in patients with heart failure: systematic review.

Authors:  Jenny A Doust; Eva Pietrzak; Annette Dobson; Paul Glasziou
Journal:  BMJ       Date:  2005-03-19

7.  Duchenne muscular dystrophy: a 30-year population-based incidence study.

Authors:  Joseph Dooley; Kevin E Gordon; Linda Dodds; Judith MacSween
Journal:  Clin Pediatr (Phila)       Date:  2010-02       Impact factor: 1.168

8.  Cardiac assessment of patients with late stage Duchenne muscular dystrophy.

Authors:  E A P van Bockel; J S Lind; J G Zijlstra; P J Wijkstra; P M Meijer; M P van den Berg; R H J A Slart; L P H J Aarts; J E Tulleken
Journal:  Neth Heart J       Date:  2009-06       Impact factor: 2.380

Review 9.  Biochemical markers of myocyte injury in heart failure.

Authors:  Y Sato; T Kita; Y Takatsu; T Kimura
Journal:  Heart       Date:  2004-10       Impact factor: 5.994

Review 10.  Cardiac Pathophysiology and the Future of Cardiac Therapies in Duchenne Muscular Dystrophy.

Authors:  Tatyana A Meyers; DeWayne Townsend
Journal:  Int J Mol Sci       Date:  2019-08-22       Impact factor: 5.923

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  2 in total

Review 1.  Cardiac care of children with dystrophinopathy and females carrying DMD-gene variations.

Authors:  John Bourke; Cathy Turner; William Bradlow; Ashish Chikermane; Caroline Coats; Matthew Fenton; Maria Ilina; Alexandra Johnson; Stam Kapetanakis; Lisa Kuhwald; Adrian Morley-Davies; Ros Quinlivan; Konstantinos Savvatis; Marianela Schiava; Zaheer Yousef; Michela Guglieri
Journal:  Open Heart       Date:  2022-10

2.  Myricetin (3,3',4',5,5',7-Hexahydroxyflavone) Prevents 5-Fluorouracil-Induced Cardiotoxicity.

Authors:  Azher Arafah; Muneeb U Rehman; Ajaz Ahmad; Khalid M AlKharfy; Saeed Alqahtani; Basit L Jan; Nada M Almatroudi
Journal:  ACS Omega       Date:  2022-01-25
  2 in total

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