Improved Cardiac Outcomes by Early Treatment with Angiotensin-Converting Enzyme Inhibitors in Becker Muscular Dystrophy.


Journal

Journal of neuromuscular diseases
ISSN: 2214-3602
Titre abrégé: J Neuromuscul Dis
Pays: Netherlands
ID NLM: 101649948

Informations de publication

Date de publication:
2021
Historique:
pubmed: 6 4 2021
medline: 21 12 2021
entrez: 5 4 2021
Statut: ppublish

Résumé

The latest practice guidelines from the American College of Cardiology/American Heart Association recommend the prescription of an ACE-i for patients presenting with non-ischemic cardiomyopathy when left ventricular ejection fraction (LVEF) falls below 40%. To determine if the initiation of treatment with an angiotensin-converting enzyme inhibitor (ACE-i) earlier than recommended by practice guidelines issued by professional societies improves the long-term cardiac outcomes of patients presenting with Becker muscular dystrophy (MD) cardiomyopathy. From a multicenter registry of Becker MD, we selected retrospectively patients presenting between January 1990 and April 2019 with a LVEF ≥40 and ≤49%. We used a propensity score analysis to compare the risk of a) hospitalization for management of heart failure (HF), and b) a decrease in LVEF to <35% in patients who received an ACE-i when LVEF fell below 40% (conventional treatment), versus below 50% (early treatment). From the 183 patients entered in our registry, we identified 85 whose LVEF was between 40 and 49%, 51 of whom received early and 34 received conventional ACE-i treatment. Among patients with early versus conventional treatments, 2 (3.9%) versus 4 (11.8%) were hospitalized for management of HF [hazard ratio (HR) 0.151; 95% confidence interval (CI) 0.028 to 0.822; p = 0.029], and 9 (17.6%) versus 10 (29.4%) had a decrease in LVEF below 35% (HR 0.290; 95% CI 0.121 to 0.694; p = 0.005). The long-term cardiac outcome of patients presenting with Becker MD was significantly better when treatment with ACE-i was introduced after a decrease in LVEF below 50%, instead of below 40% as recommended in the current practice guidelines issued by professional societies.

Sections du résumé

BACKGROUND BACKGROUND
The latest practice guidelines from the American College of Cardiology/American Heart Association recommend the prescription of an ACE-i for patients presenting with non-ischemic cardiomyopathy when left ventricular ejection fraction (LVEF) falls below 40%.
OBJECTIVE OBJECTIVE
To determine if the initiation of treatment with an angiotensin-converting enzyme inhibitor (ACE-i) earlier than recommended by practice guidelines issued by professional societies improves the long-term cardiac outcomes of patients presenting with Becker muscular dystrophy (MD) cardiomyopathy.
METHODS METHODS
From a multicenter registry of Becker MD, we selected retrospectively patients presenting between January 1990 and April 2019 with a LVEF ≥40 and ≤49%. We used a propensity score analysis to compare the risk of a) hospitalization for management of heart failure (HF), and b) a decrease in LVEF to <35% in patients who received an ACE-i when LVEF fell below 40% (conventional treatment), versus below 50% (early treatment).
RESULTS RESULTS
From the 183 patients entered in our registry, we identified 85 whose LVEF was between 40 and 49%, 51 of whom received early and 34 received conventional ACE-i treatment. Among patients with early versus conventional treatments, 2 (3.9%) versus 4 (11.8%) were hospitalized for management of HF [hazard ratio (HR) 0.151; 95% confidence interval (CI) 0.028 to 0.822; p = 0.029], and 9 (17.6%) versus 10 (29.4%) had a decrease in LVEF below 35% (HR 0.290; 95% CI 0.121 to 0.694; p = 0.005).
CONCLUSIONS CONCLUSIONS
The long-term cardiac outcome of patients presenting with Becker MD was significantly better when treatment with ACE-i was introduced after a decrease in LVEF below 50%, instead of below 40% as recommended in the current practice guidelines issued by professional societies.

Identifiants

pubmed: 33814458
pii: JND200620
doi: 10.3233/JND-200620
pmc: PMC8385526
doi:

Substances chimiques

Angiotensin-Converting Enzyme Inhibitors 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

495-502

Références

Am J Hum Genet. 1989 Oct;45(4):498-506
pubmed: 2491009
Orphanet J Rare Dis. 2017 Feb 20;12(1):39
pubmed: 28219442
J Am Coll Cardiol. 2005 Mar 15;45(6):855-7
pubmed: 15766818
JAMA Cardiol. 2017 Feb 1;2(2):190-199
pubmed: 27926769
Lancet Neurol. 2015 Feb;14(2):153-61
pubmed: 25554404
J Neurol. 1993 Feb;240(2):105-12
pubmed: 8437017
Pediatr Cardiol. 2014 Oct;35(7):1279-85
pubmed: 24830760
PLoS Curr. 2013 Dec 12;5:
pubmed: 24459612
BMC Med Res Methodol. 2012 May 30;12:70
pubmed: 22646911
Am J Cardiol. 2012 Jul 1;110(1):98-102
pubmed: 22463839
Eur Heart J Cardiovasc Imaging. 2019 Aug 1;20(8):906-915
pubmed: 30590561
JAMA. 2007 Jan 17;297(3):314-6
pubmed: 17227985
J Am Coll Cardiol. 2015 Jul 28;66(4):403-69
pubmed: 25553722
Eur J Heart Fail. 2005 Jun;7(4):684-8
pubmed: 15921812
Am Heart J. 2007 Sep;154(3):596-602
pubmed: 17719312
Am Heart J. 1996 Sep;132(3):642-7
pubmed: 8800037
J Am Heart Assoc. 2019 Oct;8(19):e013501
pubmed: 31549577
J Am Coll Cardiol. 2017 Aug 8;70(6):776-803
pubmed: 28461007
Nucleic Acids Res. 1988 Dec 9;16(23):11141-56
pubmed: 3205741
J Cardiovasc Magn Reson. 2014 Sep 25;16:81
pubmed: 25315351
Cochrane Database Syst Rev. 2018 Oct 16;10:CD009068
pubmed: 30326162
J Am Coll Cardiol. 2011 Apr 19;57(16):1641-9
pubmed: 21492761
Trends Cardiovasc Med. 2018 Jul;28(5):330-337
pubmed: 29292032
J Neurol. 1997 Oct;244(10):657-63
pubmed: 9402544
J Am Coll Cardiol. 1993 Dec;22(7):1927-34
pubmed: 8245351
Orphanet J Rare Dis. 2019 May 10;14(1):105
pubmed: 31077250
Brain. 1994 Feb;117 ( Pt 1):1-14
pubmed: 8149204
Stat Sci. 2010 Feb 1;25(1):1-21
pubmed: 20871802

Auteurs

Caroline Stalens (C)

Medical Affairs Department, AFM-Téléthon, Evry, France.
INSERM Unit 970, Paris Cardiovascular Research Centre (PARCC), Paris, France.

Leslie Motté (L)

AP-HP, Cochin Hospital, Cardiology Department, Paris, France.

Anthony Béhin (A)

AP-HP, Pitié-Salpêtrière Hospital, Reference Center for Muscle Diseases Paris-Est, Myology Institute, Paris, France.

Rabah Ben Yaou (R)

AP-HP, Pitié-Salpêtrière Hospital, Reference Center for Muscle Diseases Paris-Est, Myology Institute, Paris, France.

France Leturcq (F)

AP-HP, Cochin Hospital, Department of Genetics and Molecular Biology, Paris, France.

Guillaume Bassez (G)

AP-HP, Pitié-Salpêtrière Hospital, Reference Center for Muscle Diseases Paris-Est, Myology Institute, Paris, France.

Pascal Laforêt (P)

Neurology Department, CHU Paris IdF Ouest-Hôpital Raymond Poincaré, Garches, France.

Bertrand Fontaine (B)

AP-HP, Pitié-Salpêtrière Hospital, Reference Center for Muscle Diseases Paris-Est, Myology Institute, Paris, France.

Stéphane Ederhy (S)

AP-HP, Saint Antoine Hospital, Cardiology Department, Paris, France.

Marion Masingue (M)

AP-HP, Pitié-Salpêtrière Hospital, Reference Center for Muscle Diseases Paris-Est, Myology Institute, Paris, France.

Malika Saadi (M)

AP-HP, Cochin Hospital, Cardiology Department, Paris, France.

Sarah Leonard Louis (SL)

AP-HP, Pitié-Salpêtrière Hospital, Reference Center for Muscle Diseases Paris-Est, Myology Institute, Paris, France.

Nawal Berber (N)

AP-HP, Pitié-Salpêtrière Hospital, Reference Center for Muscle Diseases Paris-Est, Myology Institute, Paris, France.

Tanya Stojkovic (T)

AP-HP, Pitié-Salpêtrière Hospital, Reference Center for Muscle Diseases Paris-Est, Myology Institute, Paris, France.

Denis Duboc (D)

AP-HP, Cochin Hospital, Cardiology Department, Paris, France.
Université Paris Descartes-Sorbonne Paris Cité, Paris, France.

Karim Wahbi (K)

AP-HP, Cochin Hospital, Cardiology Department, Paris, France.
Université Paris Descartes-Sorbonne Paris Cité, Paris, France.
Inserm, UMRS, Paris, France.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH