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 in | Journal of the American Heart Association Vol. 6; no. 9 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley and Sons Inc
01.09.2017
Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 2047-9980 2047-9980 |
DOI | 10.1161/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. |
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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 |
AuthorAffiliation_xml | – name: 2 Departament de Biomedicina Facultat de Medicina Universitat de Barcelona Spain – name: 6 ICREA Barcelona Spain – name: 4 Institut d'Investigacions Biomédiques August Pi i Sunyer (IDIBAPS) Barcelona Spain – name: 7 Universitat Pompeu Fabra Barcelona Spain – name: 1 Institut Cardiovascular Hospital Clínic de Barcelona Universitat de Barcelona Spain – name: 5 CIBERCV Barcelona Spain – name: 3 Institut de Nanociències i Nanotecnologia (IN2UB) Universitat de Barcelona Spain |
Author_xml | – sequence: 1 givenname: Aleksandra surname: Mas‐Stachurska fullname: Mas‐Stachurska, Aleksandra organization: Universitat de Barcelona – sequence: 2 givenname: Anna‐Maria surname: Siegert fullname: Siegert, Anna‐Maria organization: Universitat de Barcelona – sequence: 3 givenname: Monsterrat surname: Batlle fullname: Batlle, Monsterrat organization: CIBERCV – sequence: 4 givenname: Darya surname: Gorbenko del Blanco fullname: Gorbenko del Blanco, Darya organization: Universitat de Barcelona – sequence: 5 givenname: Thayna surname: Meirelles fullname: Meirelles, Thayna organization: Universitat de Barcelona – sequence: 6 givenname: Cira surname: Rubies fullname: Rubies, Cira organization: Institut d'Investigacions Biomédiques August Pi i Sunyer (IDIBAPS) – sequence: 7 givenname: Fabio surname: Bonorino fullname: Bonorino, Fabio organization: Universitat de Barcelona – sequence: 8 givenname: Carla surname: Serra‐Peinado fullname: Serra‐Peinado, Carla organization: Universitat de Barcelona – sequence: 9 givenname: Bart surname: Bijnens fullname: Bijnens, Bart organization: Universitat Pompeu Fabra – sequence: 10 givenname: Julio surname: Baudin fullname: Baudin, Julio organization: Institut d'Investigacions Biomédiques August Pi i Sunyer (IDIBAPS) – sequence: 11 givenname: Marta surname: Sitges fullname: Sitges, Marta organization: CIBERCV – sequence: 12 givenname: Lluís surname: Mont fullname: Mont, Lluís organization: CIBERCV – sequence: 13 givenname: Eduard surname: Guasch fullname: Guasch, Eduard email: eguasch@clinic.cat organization: CIBERCV – sequence: 14 givenname: Gustavo surname: Egea fullname: Egea, Gustavo email: gegea@ub.edu organization: Institut d'Investigacions Biomédiques August Pi i Sunyer (IDIBAPS) |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28947563$$D View this record in MEDLINE/PubMed |
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Keywords | fibrosis endurance exercise myocardiopathy Marfan syndrome aortic disease |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 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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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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