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

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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 ( Fbn1 C1039G/+), 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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          Most cited references34

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          2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM guidelines for the diagnosis and management of patients with Thoracic Aortic Disease: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Thoracic Surgery, American College of Radiology, American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons, and Society for Vascular Medicine.

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            Angiotensin II type 1 receptor blockade attenuates TGF-beta-induced failure of muscle regeneration in multiple myopathic states.

            Skeletal muscle has the ability to achieve rapid repair in response to injury or disease. Many individuals with Marfan syndrome (MFS), caused by a deficiency of extracellular fibrillin-1, exhibit myopathy and often are unable to increase muscle mass despite physical exercise. Evidence suggests that selected manifestations of MFS reflect excessive signaling by transforming growth factor (TGF)-beta (refs. 2,3). TGF-beta is a known inhibitor of terminal differentiation of cultured myoblasts; however, the functional contribution of TGF-beta signaling to disease pathogenesis in various inherited myopathic states in vivo remains unknown. Here we show that increased TGF-beta activity leads to failed muscle regeneration in fibrillin-1-deficient mice. Systemic antagonism of TGF-beta through administration of TGF-beta-neutralizing antibody or the angiotensin II type 1 receptor blocker losartan normalizes muscle architecture, repair and function in vivo. Moreover, we show TGF-beta-induced failure of muscle regeneration and a similar therapeutic response in a dystrophin-deficient mouse model of Duchenne muscular dystrophy.
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              Role of exercise in the prevention of cardiovascular disease: results, mechanisms, and new perspectives.

              On an empirical basis, exercise has been regarded as a fundamental pre-requisite for human well-being and physical integrity since classical times. Only in the last decades, however, scientific evidence has accumulated proving its role in the prevention and treatment of multiple chronic diseases beyond any reasonable doubt. Few treatment strategies in medicine have been tested so rigorously in large cohorts of patients as regular physical exercise. With the advent of molecular biology, the underlying mechanisms, such as NO bioavailability and mobilization of progenitor cells, could be identified. This enhances our understanding of this therapeutic tool. Unfortunately, the low compliance rate of the patients is the major drawback of the intervention exercise training (ET). The objective of this manuscript is to summarize the current knowledge with respect to ET on cardiovascular disease (CVD) and the molecular changes elicited by ET. Finally, we will critically assess reasons why ET as therapeutic option is not as effective at the population level in preventing CVD and what we may change in the future to make ET the most effective intervention to fight the development of CVD.
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                Author and article information

                Contributors
                eguasch@clinic.cat
                gegea@ub.edu
                Journal
                J Am Heart Assoc
                J Am Heart Assoc
                10.1002/(ISSN)2047-9980
                JAH3
                ahaoa
                Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
                John Wiley and Sons Inc. (Hoboken )
                2047-9980
                22 September 2017
                September 2017
                : 6
                : 9 ( doiID: 10.1002/jah3.2017.6.issue-9 )
                : e006438
                Affiliations
                [ 1 ] Institut Cardiovascular Hospital Clínic de Barcelona Universitat de Barcelona Spain
                [ 2 ] Departament de Biomedicina Facultat de Medicina Universitat de Barcelona Spain
                [ 3 ] Institut de Nanociències i Nanotecnologia (IN2UB) Universitat de Barcelona Spain
                [ 4 ] Institut d'Investigacions Biomédiques August Pi i Sunyer (IDIBAPS) Barcelona Spain
                [ 5 ] CIBERCV Barcelona Spain
                [ 6 ] ICREA Barcelona Spain
                [ 7 ] Universitat Pompeu Fabra Barcelona Spain
                Author notes
                [*] [* ] Correspondence to: Eduard Guasch, MD, PhD, Cardiovascular Institute, Hospital Clínic, C/Villarroel 170, 08036 Barcelona, Spain. E‐mail: eguasch@ 123456clinic.cat and Gustavo Egea, PhD, Department of Biomedical Sciences, University of Barcelona School of Medicine, C/Casanova 136, 08036 Barcelona, Spain. E‐mail: gegea@ 123456ub.edu
                [†]

                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.

                Article
                JAH32581
                10.1161/JAHA.117.006438
                5634291
                28947563
                44373b0a-69b8-4441-b9a2-eb8974ecf1a7
                © 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.

                History
                : 24 April 2017
                : 10 August 2017
                Page count
                Figures: 6, Tables: 2, Pages: 13, Words: 8412
                Funding
                Funded by: Instituto de Salud Carlos III
                Award ID: PI13/01580
                Award ID: PI16/00703
                Funded by: Sociedad Española de Cardiología
                Funded by: National Marfan Foundation
                Funded by: Ministerio de Economia y Competitividad
                Award ID: SAF2015‐64136R
                Award ID: TIN2014‐52923‐R
                Funded by: Fondo Europeo de Desarrollo Regional
                Funded by: Agència de Gestió d'Ajuts Universitaris i de Recerca
                Award ID: 2014SGR334
                Funded by: CERCA Programme/Generalitat de Catalunya and Centro de Investigación Biomédica en RED
                Award ID: 16/11/00354
                Categories
                Original Research
                Original Research
                Vascular Medicine
                Custom metadata
                2.0
                jah32581
                September 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.2.0 mode:remove_FC converted:26.09.2017

                Cardiovascular Medicine
                aortic disease,endurance exercise,fibrosis,marfan syndrome,myocardiopathy,animal models of human disease,exercise,aneurysm

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