Improved Cardiac Outcomes by Early Treatment with Angiotensin-Converting Enzyme Inhibitors in Becker Muscular Dystrophy.
Adult
Angiotensin-Converting Enzyme Inhibitors
/ therapeutic use
Cardiomyopathies
/ drug therapy
Female
Heart Failure
/ drug therapy
Hospitalization
Humans
Male
Middle Aged
Muscular Dystrophy, Duchenne
/ complications
Registries
Retrospective Studies
Treatment Outcome
Ventricular Function, Left
/ drug effects
Young Adult
Becker muscular dystrophy
angiotensin-converting enzyme inhibitor
heart failure
inherited myopathy
non-ischemic cardiomyopathy
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
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
495-502Références
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