Literature DB >> 26944240

The Natural History of Nonobstructive Hypertrophic Cardiomyopathy.

Virginia B Hebl1, William R Miranda1, Kevin C Ong1, David O Hodge2, J Martijn Bos3, Federico Gentile4, Kyle W Klarich1, Rick A Nishimura1, Michael J Ackerman5, Bernard J Gersh1, Steve R Ommen1, Jeffrey B Geske6.   

Abstract

OBJECTIVE: To describe the survival of a large nonobstructive hypertrophic cardiomyopathy (NO-HCM) cohort and to identify risk factors for increased mortality in this population. PATIENTS AND METHODS: Patients were identified from the Mayo Clinic HCM database from January 1, 1975, through November 30, 2006, for this retrospective observational study. Patients with resting or provocable left ventricular outflow tract gradients were excluded. Echocardiographic, clinical, and genetic data were compared between subgroups, and survival data were compared with expected population rates.
RESULTS: A total of 706 patients with NO-HCM were identified. During median follow-up of 5 years (mean, 7 years), there were 208 deaths. Overall survival was no different than expected compared with age- and sex-matched white US population mortality rates (P=.77). Independent predictors of death were age at diagnosis, "burned out" HCM, and history of transient ischemic attack or stroke; use of an implantable cardioverter defibrillator (ICD) was inversely related to death. After exclusion of patients with an ICD, there was no difference in survival compared with age- and sex- matched individuals (P=.39); age, previous transient ischemic attack/stroke, and burned out HCM were predictors of death.
CONCLUSION: In this cohort, patients with NO-HCM had similar survival rates as age- and sex-matched white US population mortality rates. Although use of an ICD was inversely related to death, no differences in overall survival were seen after those patients were excluded. Burned out HCM was independently associated with an increased risk of death, identifying a subset of patients who may benefit from more aggressive therapies.
Copyright © 2016 Mayo Foundation for Medical Education and Research. Published by Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 26944240     DOI: 10.1016/j.mayocp.2016.01.002

Source DB:  PubMed          Journal:  Mayo Clin Proc        ISSN: 0025-6196            Impact factor:   7.616


  4 in total

1.  Homozygous missense MYBPC3 Pro873His mutation associated with increased risk for heart failure development in hypertrophic cardiomyopathy.

Authors:  Antheia Kissopoulou; Cecilia Trinks; Anna Green; Jan-Erik Karlsson; Jon Jonasson; Cecilia Gunnarsson
Journal:  ESC Heart Fail       Date:  2018-04-16

2.  Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy.

Authors:  Pertti Jääskeläinen; Jagadish Vangipurapu; Joose Raivo; Teemu Kuulasmaa; Tiina Heliö; Katriina Aalto-Setälä; Maija Kaartinen; Erkki Ilveskoski; Sari Vanninen; Liisa Hämäläinen; John Melin; Jorma Kokkonen; Markku S Nieminen; Markku Laakso; Johanna Kuusisto
Journal:  ESC Heart Fail       Date:  2019-02-18

3.  Implantation of ventricular assist devices in hypertrophic cardiomyopathy with left ventricular systolic dysfunction.

Authors:  Nobuichiro Yagi; Osamu Seguchi; Hiroki Mochizuki; Kensuke Kuroda; Seiko Nakajima; Takuya Watanabe; Masanobu Yanase; Naoki Tadokoro; Satsuki Fukushima; Tomoyuki Fujita; Norihide Fukushima
Journal:  ESC Heart Fail       Date:  2021-10-27

4.  Clinical Outcomes in Patients With Nonobstructive, Labile, and Obstructive Hypertrophic Cardiomyopathy.

Authors:  Dai-Yin Lu; Iraklis Pozios; Bereketeab Haileselassie; Ioannis Ventoulis; Hongyun Liu; Lars L Sorensen; Marco Canepa; Susan Phillip; M Roselle Abraham; Theodore P Abraham
Journal:  J Am Heart Assoc       Date:  2018-02-25       Impact factor: 5.501

  4 in total

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