Cargando…
Myocardial late gadolinium enhancement is associated with clinical presentation in Duchenne muscular dystrophy carriers
BACKGROUND: Duchenne muscular dystrophy (DMD) is an X-linked recessive disease that occurs in males leading to immobility and death in early adulthood. Female carriers of DMD are generally asymptomatic, yet frequently develop dilated cardiomyopathy. This study aims to detect early cardiac manifestat...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034448/ https://www.ncbi.nlm.nih.gov/pubmed/27660108 http://dx.doi.org/10.1186/s12968-016-0281-y |
_version_ | 1782455270689996800 |
---|---|
author | Wexberg, Paul Avanzini, Marion Mascherbauer, Julia Pfaffenberger, Stefan Freudenthaler, Birgit Bittner, Reginald Bernert, Günther Weidinger, Franz |
author_facet | Wexberg, Paul Avanzini, Marion Mascherbauer, Julia Pfaffenberger, Stefan Freudenthaler, Birgit Bittner, Reginald Bernert, Günther Weidinger, Franz |
author_sort | Wexberg, Paul |
collection | PubMed |
description | BACKGROUND: Duchenne muscular dystrophy (DMD) is an X-linked recessive disease that occurs in males leading to immobility and death in early adulthood. Female carriers of DMD are generally asymptomatic, yet frequently develop dilated cardiomyopathy. This study aims to detect early cardiac manifestation in DMD using cardiovascular magnetic resonance (CMR) and to evaluate its association with clinical symptoms. METHODS: Clinical assessment of DMD carriers included six minutes walk tests (6MWT), blood analysis, electrocardiography, echocardiography, and CMR using FLASH sequences to detect late gadolinium enhancement (LGE). T1-mapping using the Modified Look-Locker Inversion recovery (MOLLI) sequence was performed quantify extracellular volume (ECV). RESULTS: Of 20 carriers (age 39.47 ± 12.96 years) 17 (89.5 %) were clinically asymptomatic. ECV was mildly elevated (29.79 ± 2.92 %) and LGE was detected in nine cases (45 %). LGE positive carriers had lower left ventricular ejection fraction in CMR (64.36 ± 5.78 vs. 56.67 ± 6.89 %, p = 0.014), higher bothCK (629.89 ± 317.48 vs. 256.18 ± 109.10 U/l, p = 0.002) and CK-MB (22.13 ± 5.25 vs. 12.11 ± 2.21 U/l, p = 0.001), as well as shorter walking distances during the 6MWT (432.44 ± 96.72 vs. 514.91 ± 66.80 m, p = 0.037). 90.9 % of subjects without LGE had normal pro-BNP, whereas in 66.7 % of those presenting LGE pro-BNP was elevated (p = 0.027). All individuals without LGE were in the NYHA class I, whereas all those in NYHA classes II and III showed positive for LGE (p = 0.066). CONCLUSIONS: Myocardial involvement shown as LGE in CMR occurs in a substantial number of DMD carriers; it is associated with clinical and morphometric signs of incipient heart failure. LGE is thus a sensitive parameter for the early diagnosis of cardiomyopathy in DMD carriers. TRIAL REGISTRATION: Clinicaltrials.gov, NCT01712152 Trial registration: October 19, 2012. First patient enrolled: September 27, 2012 (retrospectively registered). |
format | Online Article Text |
id | pubmed-5034448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50344482016-09-29 Myocardial late gadolinium enhancement is associated with clinical presentation in Duchenne muscular dystrophy carriers Wexberg, Paul Avanzini, Marion Mascherbauer, Julia Pfaffenberger, Stefan Freudenthaler, Birgit Bittner, Reginald Bernert, Günther Weidinger, Franz J Cardiovasc Magn Reson Research BACKGROUND: Duchenne muscular dystrophy (DMD) is an X-linked recessive disease that occurs in males leading to immobility and death in early adulthood. Female carriers of DMD are generally asymptomatic, yet frequently develop dilated cardiomyopathy. This study aims to detect early cardiac manifestation in DMD using cardiovascular magnetic resonance (CMR) and to evaluate its association with clinical symptoms. METHODS: Clinical assessment of DMD carriers included six minutes walk tests (6MWT), blood analysis, electrocardiography, echocardiography, and CMR using FLASH sequences to detect late gadolinium enhancement (LGE). T1-mapping using the Modified Look-Locker Inversion recovery (MOLLI) sequence was performed quantify extracellular volume (ECV). RESULTS: Of 20 carriers (age 39.47 ± 12.96 years) 17 (89.5 %) were clinically asymptomatic. ECV was mildly elevated (29.79 ± 2.92 %) and LGE was detected in nine cases (45 %). LGE positive carriers had lower left ventricular ejection fraction in CMR (64.36 ± 5.78 vs. 56.67 ± 6.89 %, p = 0.014), higher bothCK (629.89 ± 317.48 vs. 256.18 ± 109.10 U/l, p = 0.002) and CK-MB (22.13 ± 5.25 vs. 12.11 ± 2.21 U/l, p = 0.001), as well as shorter walking distances during the 6MWT (432.44 ± 96.72 vs. 514.91 ± 66.80 m, p = 0.037). 90.9 % of subjects without LGE had normal pro-BNP, whereas in 66.7 % of those presenting LGE pro-BNP was elevated (p = 0.027). All individuals without LGE were in the NYHA class I, whereas all those in NYHA classes II and III showed positive for LGE (p = 0.066). CONCLUSIONS: Myocardial involvement shown as LGE in CMR occurs in a substantial number of DMD carriers; it is associated with clinical and morphometric signs of incipient heart failure. LGE is thus a sensitive parameter for the early diagnosis of cardiomyopathy in DMD carriers. TRIAL REGISTRATION: Clinicaltrials.gov, NCT01712152 Trial registration: October 19, 2012. First patient enrolled: September 27, 2012 (retrospectively registered). BioMed Central 2016-09-22 /pmc/articles/PMC5034448/ /pubmed/27660108 http://dx.doi.org/10.1186/s12968-016-0281-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Wexberg, Paul Avanzini, Marion Mascherbauer, Julia Pfaffenberger, Stefan Freudenthaler, Birgit Bittner, Reginald Bernert, Günther Weidinger, Franz Myocardial late gadolinium enhancement is associated with clinical presentation in Duchenne muscular dystrophy carriers |
title | Myocardial late gadolinium enhancement is associated with clinical presentation in Duchenne muscular dystrophy carriers |
title_full | Myocardial late gadolinium enhancement is associated with clinical presentation in Duchenne muscular dystrophy carriers |
title_fullStr | Myocardial late gadolinium enhancement is associated with clinical presentation in Duchenne muscular dystrophy carriers |
title_full_unstemmed | Myocardial late gadolinium enhancement is associated with clinical presentation in Duchenne muscular dystrophy carriers |
title_short | Myocardial late gadolinium enhancement is associated with clinical presentation in Duchenne muscular dystrophy carriers |
title_sort | myocardial late gadolinium enhancement is associated with clinical presentation in duchenne muscular dystrophy carriers |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5034448/ https://www.ncbi.nlm.nih.gov/pubmed/27660108 http://dx.doi.org/10.1186/s12968-016-0281-y |
work_keys_str_mv | AT wexbergpaul myocardiallategadoliniumenhancementisassociatedwithclinicalpresentationinduchennemusculardystrophycarriers AT avanzinimarion myocardiallategadoliniumenhancementisassociatedwithclinicalpresentationinduchennemusculardystrophycarriers AT mascherbauerjulia myocardiallategadoliniumenhancementisassociatedwithclinicalpresentationinduchennemusculardystrophycarriers AT pfaffenbergerstefan myocardiallategadoliniumenhancementisassociatedwithclinicalpresentationinduchennemusculardystrophycarriers AT freudenthalerbirgit myocardiallategadoliniumenhancementisassociatedwithclinicalpresentationinduchennemusculardystrophycarriers AT bittnerreginald myocardiallategadoliniumenhancementisassociatedwithclinicalpresentationinduchennemusculardystrophycarriers AT bernertgunther myocardiallategadoliniumenhancementisassociatedwithclinicalpresentationinduchennemusculardystrophycarriers AT weidingerfranz myocardiallategadoliniumenhancementisassociatedwithclinicalpresentationinduchennemusculardystrophycarriers |