Early Treatment with ACE Inhibitors in Becker Muscular Dystrophy Patients Improves Cardiac Health
Starting cardioprotective treatments as soon as cardiac function drops below the lower limit of the normal range is associated with better cardiac outcomes in patients with Becker muscular dystrophy, report investigators in JND
The prevention of endstage heart failure, one of the most common causes of death in patients with BMD, is central in their management. BMD is a form of muscular dystrophy related to Duchenne muscular dystrophy (DMD) in that both result from a mutation in the dystrophin gene, but with a milder course in the case of BMD. The latest practice guidelines from the American College of Cardiology/American Heart Association recommend prescribing an angiotensin-converting enzyme inhibitor (ACE-i) for patients with non-ischemic cardiomyopathy when left ventricular ejection fraction (LVEF) falls below 40%. There is, however, no consensus on when to start treatment in patients with BMD.
“While there is extensive literature showing a beneficial effect of cardioprotective treatments such as ACE inhibitors in DMD, thus far there was only limited evidence of a similar effect in BMD,” explained lead investigator Karim Wahbi, MD, PhD, AP-HP, Myology Institute; Cochin Hospital; Université de Paris; and Inserm, UMRS, Paris, France. “As a result, there is no consensus to date among experts in the field of neuromuscular cardiomyopathies. And there remains a great variability regarding the use of ACE inhibitors in BMD from one country to another and from one center to another. Should this treatment be initiated when cardiac function is normal like in DMD? Or when overt cardiac failure is present (left ventricular ejection below 40%) as recommended in the general population? Or somewhere in between? We wanted to fill that gap.”
The investigators sought to determine if starting treatment with an ACE inhibitor earlier than recommended by practice guidelines issued by professional societies improves the long-term cardiac outcomes of patients with BMD. They analyzed data retrospectively from 183 patients entered in a French multicenter registry of BMD between January 1990 and April 2019 using a complex statistical analysis called propensity score analysis. They found that the long-term cardiac outcome of patients with BMD was significantly better when treatment with an ACE inhibitor was introduced earlier than recommended in the current practice guidelines.
Among patients with early treatment (when LVEF was below 50%) versus conventional treatment (when LVEF was below 40%), fewer than 4% were hospitalized for management of heart failure compared to 11.8% who were treated conventionally, and 17.6% versus 29.4% had a decrease in LVEF below 35%.
The magnitude of benefit conferred by ACE inhibitors in this study of patients with BMD is similar to that observed in an earlier randomized study of patients with DMD, adding support to their high efficacy in the prevention of myocardial dysfunction, especially when introduced early in the course of the disease.
“This is the first study to show that treatment with an ACE inhibitor can be beneficial for long-term cardiac health in patients with BMD, reducing the risk of developing severe cardiomyopathy and heart failure. Furthermore, it provides important information on the best moment to start ACE inhibitors, as soon as cardiac function drops below the lower limit of the normal range,” noted Dr. Wahbi. “We hope these results will result in a larger and earlier use of ACE inhibitors for patients with BMD worldwide.”
NOTES FOR EDITORS
Full open access study: “Improved Cardiac Outcomes by Early Treatment with Angiotensin-Converting Enzyme Inhibitors in Becker Muscular Dystrophy” by Caroline Stalens, Leslie Motté, Anthony Béhin, Rabah Ben Yaou, France Leturcq, Guillaume Bassez, Pascal Laforêt , Bertrand Fontaine, Stéphane Ederhy, Marion Masingue, Malika Saadi, Sarah Leonard Louis, Nawal Berber, Tanya Stojkovic, Denis Duboc, and Karim Wahbi (DOI: 10.3233/JND-200620), Journal of Neuromuscular Diseases, Volume 8, issue 4. The article is freely available at: content.iospress.com/articles/journal-of-neuromuscular-diseases/jnd200620.
This study was funded by the AFM-Téléthon.
For additional information contact Diana Murray, IOS Press (+1 718-640-5678 or email@example.com). Journalists who wish to interview the authors should contact the press office of AFM-Téléthon, the French Muscular Dystrophy Association (+33 1 69 47 12 78 or firstname.lastname@example.org).
About the Journal of Neuromuscular Diseases
The Journal of Neuromuscular Diseases facilitates progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis, and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias, and myositis). The journal publishes research reports, reviews, and short communications. Guided by Editors-in-Chief Carsten G. Bönnemann (National Institute of Neurological Disorders and Stroke, NIH) and Hanns Lochmüller (Children’s Hospital of Eastern Ontario Research Institute, Ottawa, Canada), the journal is dedicated to providing an open forum for original research in basic science, translational, and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases. iospress.com/journal-of-neuromuscular-diseases
About IOS Press
IOS Press is headquartered in Amsterdam with satellite offices in the USA, Germany, India, and China and serves the information needs of scientific and medical communities worldwide. IOS Press now publishes more about 90 international peer-reviewed journals and about 70 book titles each year on subjects ranging from computer science, artificial intelligence, and engineering to medicine, neuroscience, and cancer research. iospress.com