Cardiovascular Benefits of Moderate Exercise Training in Marfan Syndrome: Insights From an Animal Model

Background Marfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary cardiomyopathy. Overall, regular physical exercise is recommended for a healthy lifestyle, but dynamic sports are strongly discouraged in MF pat...

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Published inJournal of the American Heart Association Vol. 6; no. 9
Main Authors Mas‐Stachurska, Aleksandra, Siegert, Anna‐Maria, Batlle, Monsterrat, Gorbenko del Blanco, Darya, Meirelles, Thayna, Rubies, Cira, Bonorino, Fabio, Serra‐Peinado, Carla, Bijnens, Bart, Baudin, Julio, Sitges, Marta, Mont, Lluís, Guasch, Eduard, Egea, Gustavo
Format Journal Article
LanguageEnglish
Published England John Wiley and Sons Inc 01.09.2017
Wiley
Subjects
Online AccessGet full text
ISSN2047-9980
2047-9980
DOI10.1161/JAHA.117.006438

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Abstract Background Marfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary cardiomyopathy. Overall, regular physical exercise is recommended for a healthy lifestyle, but dynamic sports are strongly discouraged in MF patients. Nonetheless, evidence supporting this recommendation is lacking. Therefore, we studied the role of long‐term dynamic exercise of moderate intensity on the MF cardiovascular phenotype. Methods and Results In a transgenic mouse model of MF (Fbn1C1039G/+), 4‐month‐old wild‐type and MF mice were subjected to training on a treadmill for 5 months; sedentary littermates served as controls for each group. Aortic and cardiac remodeling was assessed by echocardiography and histology. The 4‐month‐old MF mice showed aortic root dilatation, elastic lamina rupture, and tunica media fibrosis, as well as cardiac hypertrophy, left ventricular fibrosis, and intramyocardial vessel remodeling. Over the 5‐month experimental period, aortic root dilation rate was significantly greater in the sedentary MF group, compared with the wild‐type group (∆mm, 0.27±0.07 versus 0.13±0.02, respectively). Exercise significantly blunted the aortic root dilation rate in MF mice compared with sedentary MF littermates (∆mm, 0.10±0.04 versus 0.27±0.07, respectively). However, these 2 groups were indistinguishable by aortic root stiffness, tunica media fibrosis, and elastic lamina ruptures. In MF mice, exercise also produced cardiac hypertrophy regression without changes in left ventricular fibrosis. Conclusions Our results in a transgenic mouse model of MF indicate that moderate dynamic exercise mitigates the progression of the MF cardiovascular phenotype.
AbstractList BackgroundMarfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary cardiomyopathy. Overall, regular physical exercise is recommended for a healthy lifestyle, but dynamic sports are strongly discouraged in MF patients. Nonetheless, evidence supporting this recommendation is lacking. Therefore, we studied the role of long‐term dynamic exercise of moderate intensity on the MF cardiovascular phenotype. Methods and ResultsIn a transgenic mouse model of MF (Fbn1C1039G/+), 4‐month‐old wild‐type and MF mice were subjected to training on a treadmill for 5 months; sedentary littermates served as controls for each group. Aortic and cardiac remodeling was assessed by echocardiography and histology. The 4‐month‐old MF mice showed aortic root dilatation, elastic lamina rupture, and tunica media fibrosis, as well as cardiac hypertrophy, left ventricular fibrosis, and intramyocardial vessel remodeling. Over the 5‐month experimental period, aortic root dilation rate was significantly greater in the sedentary MF group, compared with the wild‐type group (∆mm, 0.27±0.07 versus 0.13±0.02, respectively). Exercise significantly blunted the aortic root dilation rate in MF mice compared with sedentary MF littermates (∆mm, 0.10±0.04 versus 0.27±0.07, respectively). However, these 2 groups were indistinguishable by aortic root stiffness, tunica media fibrosis, and elastic lamina ruptures. In MF mice, exercise also produced cardiac hypertrophy regression without changes in left ventricular fibrosis. ConclusionsOur results in a transgenic mouse model of MF indicate that moderate dynamic exercise mitigates the progression of the MF cardiovascular phenotype.
Marfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary cardiomyopathy. Overall, regular physical exercise is recommended for a healthy lifestyle, but dynamic sports are strongly discouraged in MF patients. Nonetheless, evidence supporting this recommendation is lacking. Therefore, we studied the role of long-term dynamic exercise of moderate intensity on the MF cardiovascular phenotype. In a transgenic mouse model of MF ( ), 4-month-old wild-type and MF mice were subjected to training on a treadmill for 5 months; sedentary littermates served as controls for each group. Aortic and cardiac remodeling was assessed by echocardiography and histology. The 4-month-old MF mice showed aortic root dilatation, elastic lamina rupture, and tunica media fibrosis, as well as cardiac hypertrophy, left ventricular fibrosis, and intramyocardial vessel remodeling. Over the 5-month experimental period, aortic root dilation rate was significantly greater in the sedentary MF group, compared with the wild-type group (∆mm, 0.27±0.07 versus 0.13±0.02, respectively). Exercise significantly blunted the aortic root dilation rate in MF mice compared with sedentary MF littermates (∆mm, 0.10±0.04 versus 0.27±0.07, respectively). However, these 2 groups were indistinguishable by aortic root stiffness, tunica media fibrosis, and elastic lamina ruptures. In MF mice, exercise also produced cardiac hypertrophy regression without changes in left ventricular fibrosis. Our results in a transgenic mouse model of MF indicate that moderate dynamic exercise mitigates the progression of the MF cardiovascular phenotype.
BACKGROUND: Marfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary cardiomyopathy. Overall, regular physical exercise is recommended for a healthy lifestyle, but dynamic sports are strongly discouraged in MF patients. Nonetheless, evidence supporting this recommendation is lacking. Therefore, we studied the role of long-term dynamic exercise of moderate intensity on the MF cardiovascular phenotype. METHODS AND RESULTS: In a transgenic mouse model of MF (Fbn1C1039G/+), 4-month-old wild-type and MF mice were subjected to training on a treadmill for 5 months; sedentary littermates served as controls for each group. Aortic and cardiac remodeling was assessed by echocardiography and histology. The 4-month-old MF mice showed aortic root dilatation, elastic lamina rupture, and tunica media fibrosis, as well as cardiac hypertrophy, left ventricular fibrosis, and intramyocardial vessel remodeling. Over the 5-month experimental period, aortic root dilation rate was significantly greater in the sedentary MF group, compared with the wild-type group (∆mm, 0.27±0.07 versus 0.13±0.02, respectively). Exercise significantly blunted the aortic root dilation rate in MF mice compared with sedentary MF littermates (∆mm, 0.10±0.04 versus 0.27±0.07, respectively). However, these 2 groups were indistinguishable by aortic root stiffness, tunica media fibrosis, and elastic lamina ruptures. In MF mice, exercise also produced cardiac hypertrophy regression without changes in left ventricular fibrosis. CONCLUSIONS: Our results in a transgenic mouse model of MF indicate that moderate dynamic exercise mitigates the progression of the MF cardiovascular phenotype.
Background Marfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary cardiomyopathy. Overall, regular physical exercise is recommended for a healthy lifestyle, but dynamic sports are strongly discouraged in MF patients. Nonetheless, evidence supporting this recommendation is lacking. Therefore, we studied the role of long‐term dynamic exercise of moderate intensity on the MF cardiovascular phenotype. Methods and Results In a transgenic mouse model of MF (Fbn1C1039G/+), 4‐month‐old wild‐type and MF mice were subjected to training on a treadmill for 5 months; sedentary littermates served as controls for each group. Aortic and cardiac remodeling was assessed by echocardiography and histology. The 4‐month‐old MF mice showed aortic root dilatation, elastic lamina rupture, and tunica media fibrosis, as well as cardiac hypertrophy, left ventricular fibrosis, and intramyocardial vessel remodeling. Over the 5‐month experimental period, aortic root dilation rate was significantly greater in the sedentary MF group, compared with the wild‐type group (∆mm, 0.27±0.07 versus 0.13±0.02, respectively). Exercise significantly blunted the aortic root dilation rate in MF mice compared with sedentary MF littermates (∆mm, 0.10±0.04 versus 0.27±0.07, respectively). However, these 2 groups were indistinguishable by aortic root stiffness, tunica media fibrosis, and elastic lamina ruptures. In MF mice, exercise also produced cardiac hypertrophy regression without changes in left ventricular fibrosis. Conclusions Our results in a transgenic mouse model of MF indicate that moderate dynamic exercise mitigates the progression of the MF cardiovascular phenotype.
Marfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary cardiomyopathy. Overall, regular physical exercise is recommended for a healthy lifestyle, but dynamic sports are strongly discouraged in MF patients. Nonetheless, evidence supporting this recommendation is lacking. Therefore, we studied the role of long-term dynamic exercise of moderate intensity on the MF cardiovascular phenotype.BACKGROUNDMarfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary cardiomyopathy. Overall, regular physical exercise is recommended for a healthy lifestyle, but dynamic sports are strongly discouraged in MF patients. Nonetheless, evidence supporting this recommendation is lacking. Therefore, we studied the role of long-term dynamic exercise of moderate intensity on the MF cardiovascular phenotype.In a transgenic mouse model of MF (Fbn1C1039G/+), 4-month-old wild-type and MF mice were subjected to training on a treadmill for 5 months; sedentary littermates served as controls for each group. Aortic and cardiac remodeling was assessed by echocardiography and histology. The 4-month-old MF mice showed aortic root dilatation, elastic lamina rupture, and tunica media fibrosis, as well as cardiac hypertrophy, left ventricular fibrosis, and intramyocardial vessel remodeling. Over the 5-month experimental period, aortic root dilation rate was significantly greater in the sedentary MF group, compared with the wild-type group (∆mm, 0.27±0.07 versus 0.13±0.02, respectively). Exercise significantly blunted the aortic root dilation rate in MF mice compared with sedentary MF littermates (∆mm, 0.10±0.04 versus 0.27±0.07, respectively). However, these 2 groups were indistinguishable by aortic root stiffness, tunica media fibrosis, and elastic lamina ruptures. In MF mice, exercise also produced cardiac hypertrophy regression without changes in left ventricular fibrosis.METHODS AND RESULTSIn a transgenic mouse model of MF (Fbn1C1039G/+), 4-month-old wild-type and MF mice were subjected to training on a treadmill for 5 months; sedentary littermates served as controls for each group. Aortic and cardiac remodeling was assessed by echocardiography and histology. The 4-month-old MF mice showed aortic root dilatation, elastic lamina rupture, and tunica media fibrosis, as well as cardiac hypertrophy, left ventricular fibrosis, and intramyocardial vessel remodeling. Over the 5-month experimental period, aortic root dilation rate was significantly greater in the sedentary MF group, compared with the wild-type group (∆mm, 0.27±0.07 versus 0.13±0.02, respectively). Exercise significantly blunted the aortic root dilation rate in MF mice compared with sedentary MF littermates (∆mm, 0.10±0.04 versus 0.27±0.07, respectively). However, these 2 groups were indistinguishable by aortic root stiffness, tunica media fibrosis, and elastic lamina ruptures. In MF mice, exercise also produced cardiac hypertrophy regression without changes in left ventricular fibrosis.Our results in a transgenic mouse model of MF indicate that moderate dynamic exercise mitigates the progression of the MF cardiovascular phenotype.CONCLUSIONSOur results in a transgenic mouse model of MF indicate that moderate dynamic exercise mitigates the progression of the MF cardiovascular phenotype.
Author Gorbenko del Blanco, Darya
Guasch, Eduard
Batlle, Monsterrat
Sitges, Marta
Serra‐Peinado, Carla
Mas‐Stachurska, Aleksandra
Meirelles, Thayna
Egea, Gustavo
Rubies, Cira
Bonorino, Fabio
Baudin, Julio
Siegert, Anna‐Maria
Bijnens, Bart
Mont, Lluís
AuthorAffiliation 5 CIBERCV Barcelona Spain
1 Institut Cardiovascular Hospital Clínic de Barcelona Universitat de Barcelona Spain
4 Institut d'Investigacions Biomédiques August Pi i Sunyer (IDIBAPS) Barcelona Spain
3 Institut de Nanociències i Nanotecnologia (IN2UB) Universitat de Barcelona Spain
6 ICREA Barcelona Spain
2 Departament de Biomedicina Facultat de Medicina Universitat de Barcelona Spain
7 Universitat Pompeu Fabra Barcelona Spain
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Keywords fibrosis
endurance exercise
myocardiopathy
Marfan syndrome
aortic disease
Language English
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2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.
This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
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Dr Mas‐Stachurska and Dr Siegert contributed equally to this work and are joint first authors.
Dr Guasch and Dr Egea contributed equally to this work and are joint last authors.
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  year: 2017
  text: September 2017
PublicationDecade 2010
PublicationPlace England
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– name: Hoboken
PublicationTitle Journal of the American Heart Association
PublicationTitleAlternate J Am Heart Assoc
PublicationYear 2017
Publisher John Wiley and Sons Inc
Wiley
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References 1991; 352
2015; 78
1991; 18
2007; 101
2012; 586
2009; 64
2009; 20
2006; 98
2001; 280
2013; 127
2013; 62
2015; 101
2015; 32
2017; 23
2010; 121
2016; 121
1995; 333
2001; 88
2016; 18
2007; 33
2007; 13
2009; 158
2006; 112
2012; 98
2016; 13
2017; 74
2016; 7
2004; 114
2017; 14
2013; 34
2015; 114
1997; 241
2015; 66
2016; 310
1999; 99
2016; 111
2016; 80
2011; 28
2001; 219
2014; 147
2014; 124
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28947564 - J Am Heart Assoc. 2017 Sep 25;6(9)
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– reference: 28947564 - J Am Heart Assoc. 2017 Sep 25;6(9):
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Snippet Background Marfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary...
Marfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary...
BACKGROUND: Marfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary...
BackgroundMarfan syndrome (MF) leads to aortic root dilatation and a predisposition to aortic dissection, mitral valve prolapse, and primary and secondary...
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SubjectTerms Aneurismes aòrtics
Aneurysm, Dissecting - genetics
Aneurysm, Dissecting - pathology
Aneurysm, Dissecting - physiopathology
Aneurysm, Dissecting - prevention & control
Animal models in research
Animals
Aorta - pathology
Aorta - physiopathology
Aortic Aneurysm - genetics
Aortic Aneurysm - pathology
Aortic Aneurysm - physiopathology
Aortic Aneurysm - prevention & control
Aortic aneurysms
aortic disease
Cardiomyopathies - genetics
Cardiomyopathies - pathology
Cardiomyopathies - physiopathology
Cardiomyopathies - prevention & control
Dilatation, Pathologic
Disease Models, Animal
Disease Progression
endurance exercise
Exercici
Exercise
Exercise Therapy
Female
Fibrillin-1 - genetics
Fibrosis
Genetic diseases
Genetic Predisposition to Disease
Malalties hereditàries
Male
Marfan syndrome
Marfan Syndrome - genetics
Marfan Syndrome - pathology
Marfan Syndrome - physiopathology
Marfan Syndrome - therapy
Mice, Inbred C57BL
Mice, Transgenic
Models animals en la investigació
myocardiopathy
Original Research
Phenotype
Physical Conditioning, Animal - methods
Sex Factors
Time Factors
Vascular Remodeling
Ventricular Function, Left
Ventricular Remodeling
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Title Cardiovascular Benefits of Moderate Exercise Training in Marfan Syndrome: Insights From an Animal Model
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https://www.ncbi.nlm.nih.gov/pubmed/28947563
https://www.proquest.com/docview/1943287747
https://recercat.cat/handle/2072/293071
https://pubmed.ncbi.nlm.nih.gov/PMC5634291
https://doaj.org/article/8f8f08a782a14322b78942e702882ae2
Volume 6
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