Skip to main content
Erschienen in: Journal of Cardiovascular Translational Research 3/2015

01.04.2015

Absence of Cardiac Benefit with Early Combination ACE Inhibitor and Beta Blocker Treatment in mdx Mice

verfasst von: Alison Blain, Elizabeth Greally, Steven H. Laval, Andrew M. Blamire, Guy A. MacGowan, Volker W. Straub

Erschienen in: Journal of Cardiovascular Translational Research | Ausgabe 3/2015

Einloggen, um Zugang zu erhalten

Abstract

Most patients with Duchenne muscular dystrophy (DMD) will develop cardiomyopathy; however, the evidence for prophylactic treatment of children with cardiac medications is limited. We have used the mdx mouse model of DMD to assess if early combination treatment with beta blocker (BB) and ACE inhibitor (AI) is superior to single treatment with either one of these drugs. Mice were assessed with cardiac MRI (ventricular structure and function, in vivo calcium influx (manganese-enhanced MRI)), pressure–volume loops, and histopathology. Combination treatment did not show benefits over treatment with AI or BB alone. Indeed, some beneficial aspects of BB and AI were lost when used in combination. None of the treatments impacted RV function. Combination treatment had no significant effect on sarcolemmal damage or histopathology. The study suggests that combined BB and AI may not confer an advantage at an early stage in DMD cardiomyopathy. However, limitations of the mdx model should be considered.
Literatur
1.
Zurück zum Zitat Spurney, C. F. (2011). Cardiomyopathy of Duchenne muscular dystrophy: current understanding and future directions. Muscle & Nerve, 44(1), 8–19.CrossRef Spurney, C. F. (2011). Cardiomyopathy of Duchenne muscular dystrophy: current understanding and future directions. Muscle & Nerve, 44(1), 8–19.CrossRef
2.
Zurück zum Zitat Fayssoil, A., Nardi, O., Orlikowski, D., & Annane, D. (2010). Cardiomyopathy in Duchenne muscular dystrophy: pathogenesis and therapeutics. Heart Failure Reviews, 15(1), 103–107.CrossRefPubMed Fayssoil, A., Nardi, O., Orlikowski, D., & Annane, D. (2010). Cardiomyopathy in Duchenne muscular dystrophy: pathogenesis and therapeutics. Heart Failure Reviews, 15(1), 103–107.CrossRefPubMed
3.
Zurück zum Zitat Viollet, L., Thrush, P. T., Flanigan, K. M., Mendell, J. R., & Allen, H. D. (2012). Effects of angiotensin-converting enzyme inhibitors and/or beta blockers on the cardiomyopathy in Duchenne muscular dystrophy. The American Journal of Cardiology, 110(1), 98–102.CrossRefPubMed Viollet, L., Thrush, P. T., Flanigan, K. M., Mendell, J. R., & Allen, H. D. (2012). Effects of angiotensin-converting enzyme inhibitors and/or beta blockers on the cardiomyopathy in Duchenne muscular dystrophy. The American Journal of Cardiology, 110(1), 98–102.CrossRefPubMed
4.
Zurück zum Zitat Bushby, K., Muntoni, F., & Bourke, J. P. (2003). 107th ENMC international workshop: the management of cardiac involvement in muscular dystrophy and myotonic dystrophy. 7th–9th June 2002, Naarden, the Netherlands. (Vol. 13, pp. 166–172). Presented at the Neuromuscular disorders: NMD. Bushby, K., Muntoni, F., & Bourke, J. P. (2003). 107th ENMC international workshop: the management of cardiac involvement in muscular dystrophy and myotonic dystrophy. 7th–9th June 2002, Naarden, the Netherlands. (Vol. 13, pp. 166–172). Presented at the Neuromuscular disorders: NMD.
5.
Zurück zum Zitat Ogata, H., Ishikawa, Y., Ishikawa, Y., & Minami, R. (2009). Beneficial effects of beta-blockers and angiotensin-converting enzyme inhibitors in Duchenne muscular dystrophy. Journal of Cardiology, 53(1), 72–78.CrossRefPubMed Ogata, H., Ishikawa, Y., Ishikawa, Y., & Minami, R. (2009). Beneficial effects of beta-blockers and angiotensin-converting enzyme inhibitors in Duchenne muscular dystrophy. Journal of Cardiology, 53(1), 72–78.CrossRefPubMed
6.
Zurück zum Zitat Ishikawa, Y., Bach, J. R., & Minami, R. (1999). Cardioprotection for Duchenne’s muscular dystrophy. American Heart Journal, 137(5), 895–902.CrossRefPubMed Ishikawa, Y., Bach, J. R., & Minami, R. (1999). Cardioprotection for Duchenne’s muscular dystrophy. American Heart Journal, 137(5), 895–902.CrossRefPubMed
7.
Zurück zum Zitat Thrush, P., Viollet, L., Flanigan, K., Mendell, J., & Allen, H. (2012). Natural history of cardiomyopathy in Duchenne muscular dystrophy and the effects of angiotensin-converting enzyme inhibitor with or without beta-blocker. Journal of the American College of Cardiology, 59(13_Suppl_S), 820.CrossRef Thrush, P., Viollet, L., Flanigan, K., Mendell, J., & Allen, H. (2012). Natural history of cardiomyopathy in Duchenne muscular dystrophy and the effects of angiotensin-converting enzyme inhibitor with or without beta-blocker. Journal of the American College of Cardiology, 59(13_Suppl_S), 820.CrossRef
8.
Zurück zum Zitat Politano, L., Nigro, V., Passamano, L., Petretta, V., Comi, L. I., Papparella, S., et al. (2001). Evaluation of cardiac and respiratory involvement in sarcoglycanopathies. Neuromuscular Disorders: NMD, 11(2), 178–185.CrossRefPubMed Politano, L., Nigro, V., Passamano, L., Petretta, V., Comi, L. I., Papparella, S., et al. (2001). Evaluation of cardiac and respiratory involvement in sarcoglycanopathies. Neuromuscular Disorders: NMD, 11(2), 178–185.CrossRefPubMed
9.
Zurück zum Zitat Cesario, D. A., & Fonarow, G. C. (2002). Beta-blocker therapy for heart failure: the standard of care. Reviews in Cardiovascular Medicine, 3(1), 14–21.PubMed Cesario, D. A., & Fonarow, G. C. (2002). Beta-blocker therapy for heart failure: the standard of care. Reviews in Cardiovascular Medicine, 3(1), 14–21.PubMed
10.
Zurück zum Zitat Spencer, F. A., Lessard, D., Yarzebski, J., Gore, J. M., & Goldberg, R. J. (2005). Decade-long changes in the use of combination evidence-based medical therapy at discharge for patients surviving acute myocardial infarction. American Heart Journal, 150(4), 838–844.CrossRefPubMed Spencer, F. A., Lessard, D., Yarzebski, J., Gore, J. M., & Goldberg, R. J. (2005). Decade-long changes in the use of combination evidence-based medical therapy at discharge for patients surviving acute myocardial infarction. American Heart Journal, 150(4), 838–844.CrossRefPubMed
11.
Zurück zum Zitat Talameh, J. A., McLeod, H. L., Adams, K. F., & Patterson, J. H. (2012). Genetic tailoring of pharmacotherapy in heart failure: optimize the old, while we wait for something new. Journal of Cardiac Failure, 18(4), 338–349.CrossRefPubMed Talameh, J. A., McLeod, H. L., Adams, K. F., & Patterson, J. H. (2012). Genetic tailoring of pharmacotherapy in heart failure: optimize the old, while we wait for something new. Journal of Cardiac Failure, 18(4), 338–349.CrossRefPubMed
12.
Zurück zum Zitat Kubesova, H. M., Weber, P., Meluzinova, H., Bielakova, K., & Matejovsky, J. (2013). Benefits and pitfalls of cardiovascular medication in seniors. Wiener Klinische Wochenschrift, 125(15–16), 425–436. doi:10.1007/s00508-013-0395-2.CrossRefPubMed Kubesova, H. M., Weber, P., Meluzinova, H., Bielakova, K., & Matejovsky, J. (2013). Benefits and pitfalls of cardiovascular medication in seniors. Wiener Klinische Wochenschrift, 125(15–16), 425–436. doi:10.​1007/​s00508-013-0395-2.CrossRefPubMed
13.
Zurück zum Zitat Kantor, P. F., Abraham, J. R., Dipchand, A. I., Benson, L. N., & Redington, A. N. (2010). The impact of changing medical therapy on transplantation-free survival in pediatric dilated cardiomyopathy. Journal of the American College of Cardiology, 55(13), 1377–1384.CrossRefPubMed Kantor, P. F., Abraham, J. R., Dipchand, A. I., Benson, L. N., & Redington, A. N. (2010). The impact of changing medical therapy on transplantation-free survival in pediatric dilated cardiomyopathy. Journal of the American College of Cardiology, 55(13), 1377–1384.CrossRefPubMed
14.
Zurück zum Zitat Menon, S. C., Etheridge, S. P., Liesemer, K. N., Williams, R. V., Bardsley, T., Heywood, M. C., & Puchalski, M. D. (2014). Predictive value of myocardial delayed enhancement in duchenne muscular dystrophy. Pediatric Cardiology, 35(7), 1279–1285.CrossRefPubMed Menon, S. C., Etheridge, S. P., Liesemer, K. N., Williams, R. V., Bardsley, T., Heywood, M. C., & Puchalski, M. D. (2014). Predictive value of myocardial delayed enhancement in duchenne muscular dystrophy. Pediatric Cardiology, 35(7), 1279–1285.CrossRefPubMed
15.
Zurück zum Zitat Blain, A., Greally, E., Laval, S., Blamire, A., Straub, V., & MacGowan, G. A. (2013). Beta-blockers, left and right ventricular function, and in-vivo calcium influx in muscular dystrophy cardiomyopathy. PloS One, 8(2), e57260.CrossRefPubMedCentralPubMed Blain, A., Greally, E., Laval, S., Blamire, A., Straub, V., & MacGowan, G. A. (2013). Beta-blockers, left and right ventricular function, and in-vivo calcium influx in muscular dystrophy cardiomyopathy. PloS One, 8(2), e57260.CrossRefPubMedCentralPubMed
16.
Zurück zum Zitat Pfeffer, M. A., Braunwald, E., Moyé, L. A., Basta, L., Brown, E. J., Cuddy, T. E., et al. (1992). Effect of captopril on mortality and morbidity in patients with left ventricular dysfunction after myocardial infarction. Results of the survival and ventricular enlargement trial. The SAVE Investigators. The New England Journal of Medicine, 327(10), 669–677.CrossRefPubMed Pfeffer, M. A., Braunwald, E., Moyé, L. A., Basta, L., Brown, E. J., Cuddy, T. E., et al. (1992). Effect of captopril on mortality and morbidity in patients with left ventricular dysfunction after myocardial infarction. Results of the survival and ventricular enlargement trial. The SAVE Investigators. The New England Journal of Medicine, 327(10), 669–677.CrossRefPubMed
17.
Zurück zum Zitat Eichhorn, E. J., Heesch, C. M., Barnett, J. H., Alvarez, L. G., Fass, S. M., Grayburn, P. A., et al. (1994). Effect of metoprolol on myocardial function and energetics in patients with nonischemic dilated cardiomyopathy: a randomized, double-blind, placebo-controlled study. Journal of the American College of Cardiology, 24(5), 1310–1320.CrossRefPubMed Eichhorn, E. J., Heesch, C. M., Barnett, J. H., Alvarez, L. G., Fass, S. M., Grayburn, P. A., et al. (1994). Effect of metoprolol on myocardial function and energetics in patients with nonischemic dilated cardiomyopathy: a randomized, double-blind, placebo-controlled study. Journal of the American College of Cardiology, 24(5), 1310–1320.CrossRefPubMed
18.
Zurück zum Zitat Kanda, T., Inoue, M., Suzuki, T., & Murata, K. (1993). Low-dose combination therapy with metoprolol and captopril for congestive-heart-failure in mice. Cardiovascular Drugs and Therapy, 7(5), 795–800.CrossRefPubMed Kanda, T., Inoue, M., Suzuki, T., & Murata, K. (1993). Low-dose combination therapy with metoprolol and captopril for congestive-heart-failure in mice. Cardiovascular Drugs and Therapy, 7(5), 795–800.CrossRefPubMed
19.
Zurück zum Zitat Quinlan, J. G., Hahn, H. S., Wong, B. L., Lorenz, J. N., Wenisch, A. S., & Levin, L. S. (2004). Evolution of the mdx mouse cardiomyopathy: physiological and morphological findings. Neuromuscular Disorders: NMD, 14(8–9), 491–496.CrossRef Quinlan, J. G., Hahn, H. S., Wong, B. L., Lorenz, J. N., Wenisch, A. S., & Levin, L. S. (2004). Evolution of the mdx mouse cardiomyopathy: physiological and morphological findings. Neuromuscular Disorders: NMD, 14(8–9), 491–496.CrossRef
20.
Zurück zum Zitat Bauer, R., Straub, V., Blain, A., Bushby, K., & MacGowan, G. A. (2009). Contrasting effects of steroids and angiotensin-converting-enzyme inhibitors in a mouse model of dystrophin-deficient cardiomyopathy. European Journal of Heart Failure, 11(5), 463–471.CrossRefPubMed Bauer, R., Straub, V., Blain, A., Bushby, K., & MacGowan, G. A. (2009). Contrasting effects of steroids and angiotensin-converting-enzyme inhibitors in a mouse model of dystrophin-deficient cardiomyopathy. European Journal of Heart Failure, 11(5), 463–471.CrossRefPubMed
21.
Zurück zum Zitat Bauer, R., Blain, A., Greally, E., Bushby, K., Lochmüller, H., Laval, S., et al. (2010). Intolerance to β-blockade in a mouse model of δ-sarcoglycan-deficient muscular dystrophy cardiomyopathy. European Journal of Heart Failure, 12(11), 1163–1170.CrossRefPubMed Bauer, R., Blain, A., Greally, E., Bushby, K., Lochmüller, H., Laval, S., et al. (2010). Intolerance to β-blockade in a mouse model of δ-sarcoglycan-deficient muscular dystrophy cardiomyopathy. European Journal of Heart Failure, 12(11), 1163–1170.CrossRefPubMed
22.
Zurück zum Zitat Steendijk, P., Staal, E., Jukema, J. W., & Baan, J. (2001). Hypertonic saline method accurately determines parallel conductance for dual-field conductance catheter. American Journal of Physiology - Heart and Circulatory Physiology, 281(2), H755–H763.PubMed Steendijk, P., Staal, E., Jukema, J. W., & Baan, J. (2001). Hypertonic saline method accurately determines parallel conductance for dual-field conductance catheter. American Journal of Physiology - Heart and Circulatory Physiology, 281(2), H755–H763.PubMed
23.
Zurück zum Zitat Raff, G. L., & Glantz, S. A. (1981). Volume loading slows left ventricular isovolumic relaxation rate. Evidence of load-dependent relaxation in the intact dog heart. Circulation Research, 48(6 Pt 1), 813–824.CrossRefPubMed Raff, G. L., & Glantz, S. A. (1981). Volume loading slows left ventricular isovolumic relaxation rate. Evidence of load-dependent relaxation in the intact dog heart. Circulation Research, 48(6 Pt 1), 813–824.CrossRefPubMed
24.
Zurück zum Zitat Bauer, R., Macgowan, G. A., Blain, A., Bushby, K., & Straub, V. (2008). Steroid treatment causes deterioration of myocardial function in the {delta}-sarcoglycan-deficient mouse model for dilated cardiomyopathy. Cardiovascular Research, 79(4), 652–661.CrossRefPubMed Bauer, R., Macgowan, G. A., Blain, A., Bushby, K., & Straub, V. (2008). Steroid treatment causes deterioration of myocardial function in the {delta}-sarcoglycan-deficient mouse model for dilated cardiomyopathy. Cardiovascular Research, 79(4), 652–661.CrossRefPubMed
25.
Zurück zum Zitat Greally, E., Davison, B. J., Blain, A., Laval, S., Blamire, A., Straub, V., & MacGowan, G. A. (2013). Heterogeneous abnormalities of in-vivo left ventricular calcium influx and function in mouse models of muscular dystrophy cardiomyopathy. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance, 15, 4.CrossRef Greally, E., Davison, B. J., Blain, A., Laval, S., Blamire, A., Straub, V., & MacGowan, G. A. (2013). Heterogeneous abnormalities of in-vivo left ventricular calcium influx and function in mouse models of muscular dystrophy cardiomyopathy. Journal of Cardiovascular Magnetic Resonance: Official Journal of the Society for Cardiovascular Magnetic Resonance, 15, 4.CrossRef
26.
Zurück zum Zitat Massie, B. M. (2002). Neurohormonal blockade in chronic heart failure. How much is enough? Can there be too much? Journal of the American College of Cardiology, 39(1), 79–82.CrossRefPubMed Massie, B. M. (2002). Neurohormonal blockade in chronic heart failure. How much is enough? Can there be too much? Journal of the American College of Cardiology, 39(1), 79–82.CrossRefPubMed
27.
Zurück zum Zitat Anand, I. S. (2004). Is too much neurohormonal blockade harmful? Current Cardiology Reports, 6(3), 169–175.CrossRefPubMed Anand, I. S. (2004). Is too much neurohormonal blockade harmful? Current Cardiology Reports, 6(3), 169–175.CrossRefPubMed
28.
Zurück zum Zitat Cohn, J. N., Pfeffer, M. A., Rouleau, J., Sharpe, N., Swedberg, K., Straub, M., et al. (2003). Adverse mortality effect of central sympathetic inhibition with sustained-release moxonidine in patients with heart failure (MOXCON). European Journal of Heart Failure, 5(5), 659–667.CrossRefPubMed Cohn, J. N., Pfeffer, M. A., Rouleau, J., Sharpe, N., Swedberg, K., Straub, M., et al. (2003). Adverse mortality effect of central sympathetic inhibition with sustained-release moxonidine in patients with heart failure (MOXCON). European Journal of Heart Failure, 5(5), 659–667.CrossRefPubMed
29.
Zurück zum Zitat Stuckey, D. J., Carr, C. A., Camelliti, P., Tyler, D. J., Davies, K. E., & Clarke, K. (2012). In vivo MRI characterization of progressive cardiac dysfunction in the mdx mouse model of muscular dystrophy. PloS One, 7(1), e28569.CrossRefPubMedCentralPubMed Stuckey, D. J., Carr, C. A., Camelliti, P., Tyler, D. J., Davies, K. E., & Clarke, K. (2012). In vivo MRI characterization of progressive cardiac dysfunction in the mdx mouse model of muscular dystrophy. PloS One, 7(1), e28569.CrossRefPubMedCentralPubMed
30.
Zurück zum Zitat Banerjee, D., Haddad, F., Zamanian, R. T., & Nagendran, J. (2010). Right ventricular failure: a novel era of targeted therapy. Current Heart Failure Reports, 7(4), 202–211.CrossRefPubMed Banerjee, D., Haddad, F., Zamanian, R. T., & Nagendran, J. (2010). Right ventricular failure: a novel era of targeted therapy. Current Heart Failure Reports, 7(4), 202–211.CrossRefPubMed
31.
Zurück zum Zitat Silversides, C. K., Webb, G. D., Harris, V. A., & Biggar, D. W. (2003). Effects of deflazacort on left ventricular function in patients with Duchenne muscular dystrophy. The American Journal of Cardiology, 91(6), 769–772.CrossRefPubMed Silversides, C. K., Webb, G. D., Harris, V. A., & Biggar, D. W. (2003). Effects of deflazacort on left ventricular function in patients with Duchenne muscular dystrophy. The American Journal of Cardiology, 91(6), 769–772.CrossRefPubMed
32.
Zurück zum Zitat Markham, L. W., Spicer, R. L., Khoury, P. R., Wong, B. L., Mathews, K. D., & Cripe, L. H. (2005). Steroid therapy and cardiac function in Duchenne muscular dystrophy. Pediatric Cardiology, 26(6), 768–771.CrossRefPubMed Markham, L. W., Spicer, R. L., Khoury, P. R., Wong, B. L., Mathews, K. D., & Cripe, L. H. (2005). Steroid therapy and cardiac function in Duchenne muscular dystrophy. Pediatric Cardiology, 26(6), 768–771.CrossRefPubMed
33.
Zurück zum Zitat Morales, M. G., Cabrera, D., Céspedes, C., Vio, C. P., Vazquez, Y., Brandan, E., & Cabello-Verrugio, C. (2013). Inhibition of the angiotensin-converting enzyme decreases skeletal muscle fibrosis in dystrophic mice by a diminution in the expression and activity of connective tissue growth factor (CTGF/CCN-2). Cell and Tissue Research, 353(1), 173–187.CrossRefPubMed Morales, M. G., Cabrera, D., Céspedes, C., Vio, C. P., Vazquez, Y., Brandan, E., & Cabello-Verrugio, C. (2013). Inhibition of the angiotensin-converting enzyme decreases skeletal muscle fibrosis in dystrophic mice by a diminution in the expression and activity of connective tissue growth factor (CTGF/CCN-2). Cell and Tissue Research, 353(1), 173–187.CrossRefPubMed
Metadaten
Titel
Absence of Cardiac Benefit with Early Combination ACE Inhibitor and Beta Blocker Treatment in mdx Mice
verfasst von
Alison Blain
Elizabeth Greally
Steven H. Laval
Andrew M. Blamire
Guy A. MacGowan
Volker W. Straub
Publikationsdatum
01.04.2015
Verlag
Springer US
Erschienen in
Journal of Cardiovascular Translational Research / Ausgabe 3/2015
Print ISSN: 1937-5387
Elektronische ISSN: 1937-5395
DOI
https://doi.org/10.1007/s12265-015-9623-7

Weitere Artikel der Ausgabe 3/2015

Journal of Cardiovascular Translational Research 3/2015 Zur Ausgabe

Screening-Mammografie offenbart erhöhtes Herz-Kreislauf-Risiko

26.04.2024 Mammografie Nachrichten

Routinemäßige Mammografien helfen, Brustkrebs frühzeitig zu erkennen. Anhand der Röntgenuntersuchung lassen sich aber auch kardiovaskuläre Risikopatientinnen identifizieren. Als zuverlässiger Anhaltspunkt gilt die Verkalkung der Brustarterien.

Niedriger diastolischer Blutdruck erhöht Risiko für schwere kardiovaskuläre Komplikationen

25.04.2024 Hypotonie Nachrichten

Wenn unter einer medikamentösen Hochdrucktherapie der diastolische Blutdruck in den Keller geht, steigt das Risiko für schwere kardiovaskuläre Ereignisse: Darauf deutet eine Sekundäranalyse der SPRINT-Studie hin.

Therapiestart mit Blutdrucksenkern erhöht Frakturrisiko

25.04.2024 Hypertonie Nachrichten

Beginnen ältere Männer im Pflegeheim eine Antihypertensiva-Therapie, dann ist die Frakturrate in den folgenden 30 Tagen mehr als verdoppelt. Besonders häufig stürzen Demenzkranke und Männer, die erstmals Blutdrucksenker nehmen. Dafür spricht eine Analyse unter US-Veteranen.

Adipositas-Medikament auch gegen Schlafapnoe wirksam

24.04.2024 Adipositas Nachrichten

Der als Antidiabetikum sowie zum Gewichtsmanagement zugelassene Wirkstoff Tirzepatid hat in Studien bei adipösen Patienten auch schlafbezogene Atmungsstörungen deutlich reduziert, informiert der Hersteller in einer Vorab-Meldung zum Studienausgang.

Update Kardiologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.