Evolving Therapeutic Strategies for Dystrophinopathies
2005; Lippincott Williams & Wilkins; Volume: 112; Issue: 18 Linguagem: Inglês
10.1161/circulationaha.105.577619
ISSN1524-4539
Autores Tópico(s)Mitochondrial Function and Pathology
ResumoHomeCirculationVol. 112, No. 18Evolving Therapeutic Strategies for Dystrophinopathies Free AccessEditorialPDF/EPUBAboutView PDFView EPUBSections ToolsAdd to favoritesDownload citationsTrack citationsPermissions ShareShare onFacebookTwitterLinked InMendeleyReddit Jump toFree AccessEditorialPDF/EPUBEvolving Therapeutic Strategies for DystrophinopathiesPotential for Conflict Between Cardiac and Skeletal Needs Steven D. Colan, MD Steven D. ColanSteven D. Colan From the Department of Cardiology, Children's Hospital Boston, Department of Pediatrics, Harvard Medical School, Boston, Mass. Originally published1 Nov 2005https://doi.org/10.1161/CIRCULATIONAHA.105.577619Circulation. 2005;112:2756–2758The importance of cardiomyopathy to the clinical course of the dystrophinopathies varies according to the nature of the dystrophin defect. In Becker muscular dystrophy (BMD), cardiac involvement is often the most important determinant of clinical status and long-term outcome. For the Duchenne muscular dystrophy (DMD) patient, cardiac manifestations are often masked by inactivity and respiratory muscle compromise. However, the increasing use of ventilatory assist devices has allowed cardiac failure to emerge as a more prevalent feature of the disease.1 Furthermore, a wide range of therapeutic interventions to improve skeletal muscle strength are being explored,2 some of which may not have equivalent benefit for cardiac muscle. The article by Jefferies et al3 is therefore timely, reporting the potential cardiac benefits of early treatment of patients with DMD and BMD with afterload-reducing therapy. These authors present a retrospective review of the outcome of their patients with DMD or BMD who were managed according to a clinical treatment protocol that included initiation of ACE inhibitor (ACEI) therapy at the time of first recognition of ventricular dysfunction. β-Blocker (BB) therapy was added for patients who had no evidence of improvement in their ventricular function after 3 months. There are at least 3 important findings in their reported experience. First, there were no significant adverse clinical effects attributable to medical therapy. Although these agents have a remarkable safety profile overall, neuromuscular diseases in general are notorious for unanticipated pharmacological responses, and this result is therefore reassuring. Second, over the average follow-up duration of 3.3 years, there was a significant improvement in ventricular function (ejection fraction) and evidence of improved ventricular geometry (reduced sphericity). Third, the authors report an association between cardiac involvement and specific exon deletion, which is perhaps the least expected of these 3 results.Article p 2799Despite the clear improvement in ventricular function documented in this study, it is fair to inquire whether afterload reduction therapy has the potential to fundamentally alter the course of the cardiomyopathy in DMD or BMD. The underlying pathology in the dystrophinopathies is progressive cell destruction with apparently normal contractility of the surviving myocytes,4 at least before the onset of congestive heart failure. Cell loss and secondary reduction in myocardial mass lead to a rise in wall stress, with the typical adverse consequences of afterload excess, which include reduced systolic function, ventricular dilatation and sphericalization, and increased myocardial oxygen consumption. The potential to interrupt this positive feedback loop is one of the more impressive benefits of afterload reduction therapy and can fully explain the improvement in systolic function, reduction in ventricular volume, and normalization of left ventricular shape observed by Jefferies et al.3 Given the nature of the underlying disorder, the primary predicted short-term benefit of afterload reduction therapy is to make it easier for the surviving cardiocytes to do their job, as was seen in this study. The question remains, however, whether this therapy alters the cardiomyopathy or merely masks the manifestations of a relentlessly progressive process. There is precedent for this question. The ventricular mechanics in anthracycline cardiomyopathy are quite similar to what is found in the dystrophinopathies, with reduced cell mass leading to sustained excess afterload. We were disappointed to find that administration of an ACEI in patients with ventricular dysfunction secondary to anthracycline therapy resulted in transient improvement but no long-term impact on the trajectory of deterioration.5 Is there any reason to anticipate a greater benefit in DMD and BMD?The mdx mouse, a naturally occurring animal model of the dystrophin defect, has a high susceptibility to contraction-induced skeletal muscle injury. Interestingly, this is observed primarily during eccentric contractions, that is, contraction that occurs during muscle lengthening. This mode of contraction is common in skeletal muscles but not in cardiac muscle. Evidence that cardiac muscle in the mdx mouse has increased susceptibility to contraction-induced injury derives from the observation that cardiac dysfunction, which is otherwise subclinical, can be induced in the mdx mouse by prolonged exercise or by administration of β-adrenergic agents.6,7 Dystrophin, in conjunction with the dystrophin glycoprotein complex, is believed to play a structural role in force transmission by providing a mechanical link between the intracellular cytoskeleton and the extracellular matrix.8 The pathogenesis of the muscle dysfunction in the dystrophinopathies is thought to include progressive cell death secondary to a mechanically induced increase in sarcolemmal permeability due to membrane injury6 or to stretch-induced increase of traffic across ion channels.9 Similar to the mdx mouse, predisposition to exercise-induced cardiac damage is noted in acute myocarditis, a disorder associated with loss of sarcolemmal integrity due to cleavage of dystrophin by enteroviral protease 2A.10 Observations such as these have led to the conclusion that in both skeletal and cardiac muscle, abnormal or deficient dystrophin predisposes to contraction-induced cell disruption and loss, and furthermore, the magnitude of force generation is an important determinant of cellular damage.It is therefore reasonable to speculate that attenuation of the mechanical forces on the sarcolemma by means of pharmacological afterload reduction would reduce the rate of cell loss. The article by Jefferies et al3 does not permit any conclusions in this regard, but a recent study by Duboc et al11 provides some support to this hypothesis. These authors reported the results of a placebo-controlled trial of the ACEI perindopril in DMD patients older than 9.5 years who had normal ventricular function at the time of study entry. After 3 years of randomized therapy, all patients were changed to treatment with open-label drug. No difference in outcome was seen at the completion of the first 3 years, but after 2 years of open-label drug, the group of patients who had initially received placebo experienced a higher incidence of moderate to severe ventricular dysfunction. This observation supports the hypothesis that afterload reduction therapy during the initial time period led to better preservation of the myocardium, because therapy in the second phase was the same in both groups.The ultimate cure for DMD and BMD depends on the ability to introduce a functional dystrophin gene into myocytes, and the recent phase I study of plasmid-based gene transfer is a promising step in that direction.12 Nonetheless, it is unpredictable when such therapies will be available. In the mean time, interventions that protect muscle mass could improve the length and quality of life for these patients. However, therapeutic strategies that target skeletal muscle may well be at odds with the best interests of cardiac muscle. The 2 stressors that have been used to elicit clinically apparent cardiomyopathy in the mdx mouse model are exercise and infusion of β-adrenergic agents. It is therefore possible that the markedly reduced exercise capacity of the DMD phenotype serves to limit cardiac injury. This relationship has been suggested to explain the severe cardiomyopathy of the BMD phenotype, in which the less severe skeletal muscle compromise permits exposure of the heart to the stress of exercise.13 If this hypothesis is correct, then pharmacological therapies that selectively improve skeletal muscle function, such as pharmacological stimulation or disinhibition of regenerative satellite cells with insulin-like growth factor I or myostatin inhibitors,2 may increase the rate of cardiac muscle deterioration. Similarly, oral administration of the β-adrenergic agent albuterol to DMD and BMD patients has been reported to improve skeletal muscle function,14 but based on the experience in the mdx mouse, it would be predicted to exacerbate cardiac damage. In general, it cannot be assumed that interventions that improve skeletal muscle function will have a similarly beneficial effect on cardiac muscle.Perhaps the most intriguing finding in the report by Jefferies et al3 is the relationship between the exon-specific location of the deletion and the risk of cardiomyopathy. It is somewhat surprising that DMD patients, in whom dystrophin is usually absent from the sarcolemma, should manifest such genotype-phenotype correlations. Deletions in specific locations previously have been noted to predispose to cardiomyopathy in DMD.15 In some patients with DMD, expression of dystrophin fragments may be important. For example, expression and localization at the cell membrane of dystrophin lacking the C-terminus and the β-dystroglycan binding domain have been described in DMD patients.16–18 There are other observations that support the concept that the loss of dystrophin per se is not sufficient to explain the differences in severity of muscular dystrophy. For example, there is marked disparity in pathology between species and muscle types in the dystrophinopathies. Differences in the severity of muscle dysfunction between heart and skeletal muscle are of particular interest. Point mutations in the dystrophin gene have been described in X-linked dilated cardiomyopathy, despite the absence of skeletal muscle involvement, which suggests that the function of dystrophin is not the same in the 2 locations.19 Observed differences in the pattern of cellular location between cardiac and skeletal muscle lend support to this hypothesis.8 Overall, these observations argue strongly in favor of the importance of epigenetic factors in disease severity and progression. They also provide further evidence of the potential for dissociation between cardiac and skeletal response to therapeutic strategies.The opinions expressed in this editorial are not necessarily those of the editors or of the American Heart Association.FootnotesCorrespondence to Steven D. Colan, MD, Department of Cardiology, Children's Hospital Boston, Department of Pediatrics, Harvard Medical School, 300 Longwood Ave, Boston, MA 02115. References 1 Eagle M, Baudouin SV, Chandler C, Giddings DR, Bullock R, Bushby K. Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation. Neuromuscul Disord. 2002; 12: 926–929.CrossrefMedlineGoogle Scholar2 Bogdanovich S, Perkins KJ, Krag TO, Khurana TS. Therapeutics for Duchenne muscular dystrophy: current approaches and future directions. J Mol Med. 2004; 82: 102–115.CrossrefMedlineGoogle Scholar3 Jefferies JL, Eidem BW, Belmont JW, Craigen WJ, Ware SM, Fernbach SD, Neish SR, Smith EO, Towbin JA. Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy. Circulation. 2005; 112: 2799–2804.LinkGoogle Scholar4 Shapiro F, Sethna N, Colan S, Wohl ME, Specht L. Spinal fusion in Duchenne muscular dystrophy: a multidisciplinary approach. Muscle Nerve. 1992; 15: 604–614.CrossrefMedlineGoogle Scholar5 Lipshultz SE, Lipsitz SR, Sallan SE, Simbre VC II, Shaikh SL, Mone SM, Gelber RD, Colan SD. Long-term enalapril therapy for left ventricular dysfunction in doxorubicin-treated survivors of childhood cancer. J Clin Oncol. 2002; 20: 4517–4522.CrossrefMedlineGoogle Scholar6 Yasuda S, Townsend D, Michele DE, Favre EG, Day SM, Metzger JM. Dystrophic heart failure blocked by membrane sealant poloxamer. Nature. 2005; 436: 1025–1029.CrossrefMedlineGoogle Scholar7 Janssen PM, Hiranandani N, Mays TA, Rafael-Fortney JA. Utrophin deficiency worsens cardiac contractile dysfunction present in dystrophin-deficient mdx mice. Am J Physiol Heart Circ Physiol. 2005; July 15[Epub ahead of print].Google Scholar8 Lapidos KA, Kakkar R, McNally EM. The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma. Circ Res. 2004; 94: 1023–1031.LinkGoogle Scholar9 Yeung EW, Whitehead NP, Suchyna TM, Gottlieb PA, Sachs F, Allen DG. Effects of stretch-activated channel blockers on [Ca2+]i and muscle damage in the mdx mouse. J Physiol. 2005; 562: 367–380.CrossrefMedlineGoogle Scholar10 Badorff C, Knowlton KU. Dystrophin disruption in enterovirus-induced myocarditis and dilated cardiomyopathy: from bench to bedside. Med Microbiol Immunol (Berl). 2004; 193: 121–126.CrossrefMedlineGoogle Scholar11 Duboc D, Meune C, Lerebours G, Devaux JY, Vaksmann G, Becane HM. Effect of perindopril on the onset and progression of left ventricular dysfunction in Duchenne muscular dystrophy. J Am Coll Cardiol. 2005; 45: 855–857.CrossrefMedlineGoogle Scholar12 Romero NB, Braun S, Benveniste O, Leturcq F, Hogrel JY, Morris GE, Barois A, Eymard B, Payan C, Ortega V, Boch AL, Lejean L, Thioudellet C, Mourot B, Escot C, Choquel A, Recan D, Kaplan JC, Dickson G, Klatzmann D, Molinier-Frenckel V, Guillet JG, Squiban P, Herson S, Fardeau M. Phase I study of dystrophin plasmid-based gene therapy in Duchenne/Becker muscular dystrophy. Hum Gene Ther. 2004; 15: 1065–1076.CrossrefMedlineGoogle Scholar13 Cox GF, Kunkel LM. Dystrophies and heart disease. Curr Opin Cardiol. 1997; 12: 329–343.CrossrefMedlineGoogle Scholar14 Fowler EG, Graves MC, Wetzel GT, Spencer MJ. Pilot trial of albuterol in Duchenne and Becker muscular dystrophy. Neurology. 2004; 62: 1006–1008.CrossrefMedlineGoogle Scholar15 Nigro G, Politano L, Nigro V, Petretta VR, Comi LI. Mutation of dystrophin gene and cardiomyopathy. Neuromuscul Disord. 1994; 4: 371–379.CrossrefMedlineGoogle Scholar16 Hoffman EP, Garcia CA, Chamberlain JS, Angelini C, Lupski JR, Fenwick R. Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophy. Ann Neurol. 1991; 30: 605–610.CrossrefMedlineGoogle Scholar17 Helliwell TR, Ellis JM, Mountford RC, Appleton RE, Morris GE. A truncated dystrophin lacking the C-terminal domains is localized at the muscle membrane. Am J Hum Genet. 1992; 50: 508–514.MedlineGoogle Scholar18 Bies RD, Caskey CT, Fenwick R. An intact cysteine-rich domain is required for dystrophin function. J Clin Invest. 1992; 90: 666–672.CrossrefMedlineGoogle Scholar19 Ortiz-Lopez R, Li H, Su J, Goytia V, Towbin JA. Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy. Circulation. 1997; 95: 2434–2440.CrossrefMedlineGoogle Scholar Previous Back to top Next FiguresReferencesRelatedDetailsCited By Kennedy T, Swiderski K, Murphy K, Gehrig S, Curl C, Chandramouli C, Febbraio M, Delbridge L, Koopman R and Lynch G (2016) BGP-15 Improves Aspects of the Dystrophic Pathology in mdx and dko Mice with Differing Efficacies in Heart and Skeletal Muscle, The American Journal of Pathology, 10.1016/j.ajpath.2016.08.008, 186:12, (3246-3260), Online publication date: 1-Dec-2016. Vianello S, Bouyon S, Benoit E, Sebrié C, Boerio D, Herbin M, Roulot M, Fromes Y and de la Porte S (2014) Arginine butyrate per os protects mdx mice against cardiomyopathy, kyphosis and changes in axonal excitability, Neurobiology of Disease, 10.1016/j.nbd.2014.08.023, 71, (325-333), Online publication date: 1-Nov-2014. Finsterer J and Cripe L (2014) Treatment of dystrophin cardiomyopathies, Nature Reviews Cardiology, 10.1038/nrcardio.2013.213, 11:3, (168-179), Online publication date: 1-Mar-2014. Schram G, Fournier A, Leduc H, Dahdah N, Therien J, Vanasse M and Khairy P (2013) All-Cause Mortality and Cardiovascular Outcomes With Prophylactic Steroid Therapy in Duchenne Muscular Dystrophy, Journal of the American College of Cardiology, 10.1016/j.jacc.2012.12.008, 61:9, (948-954), Online publication date: 1-Mar-2013. Viollet L, Thrush P, Flanigan K, Mendell J and Allen H (2012) Effects of Angiotensin-Converting Enzyme Inhibitors and/or Beta Blockers on the Cardiomyopathy in Duchenne Muscular Dystrophy, The American Journal of Cardiology, 10.1016/j.amjcard.2012.02.064, 110:1, (98-102), Online publication date: 1-Jul-2012. Fayssoil A, Nardi O, Orlikowski D and Annane D (2009) Cardiomyopathy in Duchenne muscular dystrophy: pathogenesis and therapeutics, Heart Failure Reviews, 10.1007/s10741-009-9156-8, 15:1, (103-107), Online publication date: 1-Jan-2010. Echigoya Y, Lim K, Nakamura A and Yokota T (2018) Multiple Exon Skipping in the Duchenne Muscular Dystrophy Hot Spots: Prospects and Challenges, Journal of Personalized Medicine, 10.3390/jpm8040041, 8:4, (41) November 1, 2005Vol 112, Issue 18 Advertisement Article InformationMetrics https://doi.org/10.1161/CIRCULATIONAHA.105.577619PMID: 16267247 Originally publishedNovember 1, 2005 Keywordsmuscular dystrophycardiomyopathyEditorialsmyocardiumPDF download Advertisement SubjectsCardiomyopathyPharmacology
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