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Sci Rep ; 9(1): 13909, 2019 09 26.
Artigo em Inglês | MEDLINE | ID: mdl-31558765

RESUMO

Primary carnitine deficiency (PCD) not treated with L-Carnitine can lead to sudden cardiac death. To our knowledge, it is unknown if asymptomatic patients treated with L-Carnitine suffer from myocardial scarring and thus be at greater risk of potentially serious arrhythmia. Cardiac evaluation of function and myocardial scarring is non-invasively best supported by cardiac magnetic resonance imaging (CMR) with late gadolinium enhancement (LGE). The study included 36 PCD patients, 17 carriers and 17 healthy subjects. A CMR cine stack in the short-axis plane were acquired to evaluate left ventricle (LV) systolic and diastolic function and a similar LGE stack to evaluate myocardial scarring and replacement fibrosis. LV volumes and ejection fraction were not different between PCD patients, carriers and healthy subjects. However, LV mass was higher in PCD patients with the severe homozygous mutation, c.95 A > G (p = 0.037; n = 17). Among homozygous PCD patients there were two cases of unexplained myocardial scarring and this is in contrast to no myocardial scarring in any of the other study participants (p = 0.10). LV mass was increased in PCD patients. L-carnitine supplementation is essential in order to prevent potentially lethal cardiac arrhythmia and serious adverse cardiac remodeling.


Assuntos
Carnitina/deficiência , Cicatriz/epidemiologia , Coração/diagnóstico por imagem , Imageamento por Ressonância Magnética , Doenças Musculares/diagnóstico por imagem , Miocárdio/patologia , Adulto , Carnitina/genética , Cicatriz/diagnóstico por imagem , Meios de Contraste , Feminino , Gadolínio , Heterozigoto , Homozigoto , Humanos , Masculino , Pessoa de Meia-Idade , Doenças Musculares/genética , Doenças Musculares/patologia , Mutação , Função Ventricular
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