Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.

Genetic analysis of hypertrophic cardiomyopathy (HCM), a mendelian form of cardiac hypertrophy, indicates that the primary defect is in sarcomeric function. However, the initial proposal that depressed myocardial contraction leads to a 'compensatory' hypertrophy has proven inconsistent wit...

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Автори: Ashrafian, H, Redwood, C, Blair, E, Watkins, H
Формат: Journal article
Мова:English
Опубліковано: 2003
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author Ashrafian, H
Redwood, C
Blair, E
Watkins, H
author_facet Ashrafian, H
Redwood, C
Blair, E
Watkins, H
author_sort Ashrafian, H
collection OXFORD
description Genetic analysis of hypertrophic cardiomyopathy (HCM), a mendelian form of cardiac hypertrophy, indicates that the primary defect is in sarcomeric function. However, the initial proposal that depressed myocardial contraction leads to a 'compensatory' hypertrophy has proven inconsistent with laboratory and clinical evidence. Drawing on observations of mutant contractile protein function, together with mouse models and clinical studies, we propose that sarcomeric HCM mutations lead to inefficient ATP utilization. The suggestion that energy depletion underlies HCM is supported by the HCM-like phenotype found with mutations in a variety of metabolic genes. A central role for compromised energetics would also help explain the unresolved clinical observations of delayed onset and asymmetrical hypertrophy in HCM, and would have implications for therapy in HCM and, potentially, in more-common forms of cardiac hypertrophy and failure.
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spelling oxford-uuid:06f4558c-825d-4da8-9eeb-82a0c50f68792022-03-26T09:05:07ZHypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:06f4558c-825d-4da8-9eeb-82a0c50f6879EnglishSymplectic Elements at Oxford2003Ashrafian, HRedwood, CBlair, EWatkins, HGenetic analysis of hypertrophic cardiomyopathy (HCM), a mendelian form of cardiac hypertrophy, indicates that the primary defect is in sarcomeric function. However, the initial proposal that depressed myocardial contraction leads to a 'compensatory' hypertrophy has proven inconsistent with laboratory and clinical evidence. Drawing on observations of mutant contractile protein function, together with mouse models and clinical studies, we propose that sarcomeric HCM mutations lead to inefficient ATP utilization. The suggestion that energy depletion underlies HCM is supported by the HCM-like phenotype found with mutations in a variety of metabolic genes. A central role for compromised energetics would also help explain the unresolved clinical observations of delayed onset and asymmetrical hypertrophy in HCM, and would have implications for therapy in HCM and, potentially, in more-common forms of cardiac hypertrophy and failure.
spellingShingle Ashrafian, H
Redwood, C
Blair, E
Watkins, H
Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.
title Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.
title_full Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.
title_fullStr Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.
title_full_unstemmed Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.
title_short Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.
title_sort hypertrophic cardiomyopathy a paradigm for myocardial energy depletion
work_keys_str_mv AT ashrafianh hypertrophiccardiomyopathyaparadigmformyocardialenergydepletion
AT redwoodc hypertrophiccardiomyopathyaparadigmformyocardialenergydepletion
AT blaire hypertrophiccardiomyopathyaparadigmformyocardialenergydepletion
AT watkinsh hypertrophiccardiomyopathyaparadigmformyocardialenergydepletion