Prevalence, clinical profile, and significance of left ventricular remodeling in the end-stage phase of hypertrophic cardiomyopathy
- PMID: 16831987
- DOI: 10.1161/CIRCULATIONAHA.105.583500
Prevalence, clinical profile, and significance of left ventricular remodeling in the end-stage phase of hypertrophic cardiomyopathy
Abstract
Background: End stage (ES) is a recognized part of the hypertrophic cardiomyopathy (HCM) disease spectrum. Frequency, clinical profile and course, and treatment strategies in these patients remain incompletely defined.
Methods and results: Three HCM cohorts comprised 1259 patients, including 44 (3.5%) characterized as ES with systolic dysfunction (ejection fraction <50% at rest; range 15% to 49%). ES developed at a wide age range (14 to 74 years), with 45% of patients < or = 40 years old. Although 29 patients (66%) died of progressive heart failure, had sudden death events, or underwent heart transplantation, 15 (34%) survived with medical management over 3+/-3 years. Duration from onset of HCM symptoms to ES identification was considerable (14+/-10 years), but ES onset to death/transplantation was brief (2.7+/-2 years). ES occurred with similar frequency in patients with or without prior myectomy (P=0.84). Appropriate defibrillator interventions were 10% per year in patients awaiting donor hearts. Most ES patients (n=23; 52%) showed substantial left ventricular (LV) remodeling with cavity dilatation. Less complete remodeling occurred in 21 patients (48%), including 5 with persistence of a nondilated and markedly hypertrophied LV. Pathology and magnetic resonance imaging showed extensive (transmural) fibrosis in 9 of 11 ES patients. At initial evaluation, patients who developed ES were younger with more severe symptoms, had a larger LV cavity, and more frequently had a family history of ES than other HCM patients.
Conclusions: ES of nonobstructive HCM has an expanded and more diverse clinical expression than previously appreciated, including occurrence in young patients, heterogeneous patterns of remodeling, frequent association with atrial fibrillation, and impaired LV contractility that precedes cavity dilatation, wall thinning, and heart failure symptoms. ES is an unfavorable complication (mortality rate 11% per year) and a sudden death risk factor; it requires vigilance to permit timely recognition and the necessity for defibrillator implantation and heart transplantation.
Similar articles
-
CMR assessment and clinical outcomes of hypertrophic cardiomyopathy with or without ventricular remodeling in the end-stage phase.Int J Cardiovasc Imaging. 2018 Apr;34(4):597-605. doi: 10.1007/s10554-017-1263-3. Epub 2017 Oct 25. Int J Cardiovasc Imaging. 2018. PMID: 29071521
-
Advanced heart failure with preserved systolic function in nonobstructive hypertrophic cardiomyopathy: under-recognized subset of candidates for heart transplant.Circ Heart Fail. 2014 Nov;7(6):967-75. doi: 10.1161/CIRCHEARTFAILURE.114.001435. Epub 2014 Sep 19. Circ Heart Fail. 2014. PMID: 25239116
-
Hypertrophic cardiomyopathy with mild left ventricular remodeling: echocardiographic assessment using left ventricular wall motion score.J Cardiol. 2008 Apr;51(2):95-105. doi: 10.1016/j.jjcc.2008.01.003. J Cardiol. 2008. PMID: 18522782
-
Hypertrophic cardiomyopathy: present and future, with translation into contemporary cardiovascular medicine.J Am Coll Cardiol. 2014 Jul 8;64(1):83-99. doi: 10.1016/j.jacc.2014.05.003. J Am Coll Cardiol. 2014. PMID: 24998133 Review.
-
Hypertrophic cardiomyopathy: risk factors for life and living benefits insurance.J Insur Med. 2002;34(1):43-60. J Insur Med. 2002. PMID: 15303593 Review.
Cited by
-
Hypertrophic cardiomyopathy in 2012.Circulation. 2012 Mar 20;125(11):1432-8. doi: 10.1161/CIRCULATIONAHA.110.017277. Circulation. 2012. PMID: 22431884 Free PMC article. Review. No abstract available.
-
Phenotypes of hypertrophic cardiomyopathy. An illustrative review of MRI findings.Insights Imaging. 2018 Dec;9(6):1007-1020. doi: 10.1007/s13244-018-0656-8. Epub 2018 Oct 22. Insights Imaging. 2018. PMID: 30350182 Free PMC article. Review.
-
Dual genetic tracing reveals a unique fibroblast subpopulation modulating cardiac fibrosis.Nat Genet. 2023 Apr;55(4):665-678. doi: 10.1038/s41588-023-01337-7. Epub 2023 Mar 23. Nat Genet. 2023. PMID: 36959363
-
Clinical features of the dilated phase of hypertrophic cardiomyopathy in comparison with those of dilated cardiomyopathy.Clin Cardiol. 2010 Jul;33(7):E24-8. doi: 10.1002/clc.20533. Clin Cardiol. 2010. PMID: 20641106 Free PMC article.
-
Nuclear Imaging in Pediatric Cardiology: Principles and Applications.Front Pediatr. 2022 Jul 6;10:909994. doi: 10.3389/fped.2022.909994. eCollection 2022. Front Pediatr. 2022. PMID: 35874576 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources