Genotype-Phenotype Correlation in Hypertrophic Cardiomyopathy: New Variant p.Arg652Lys in MYH7

Hypertrophic cardiomyopathy (HCM) is a genetic disease characterised by increased left ventricle (LV) wall thickness caused by mutations in sarcomeric genes. Finding a causal mutation can help to better assess the proband's risk, as it allows the presence of the mutation to be evaluated in rela...

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Detalles Bibliográficos
Autores: Antoniutti, Guido, Caimi-Martinez, Fiama, Álvarez-Rubio, Jorge, Morlanes-Gracia, Paula, Pons Llinares, Jaume, Rodríguez-Picón, Blanca, Fortuny Frau, Elena, Torres-Juan, Laura, Heine-Suñer, Damián, Ripoll-Vera, Tomás
Tipo de recurso: artículo
Fecha de publicación:2022
País:España
Institución:Instituto de Salud Carlos III (ISCIII)
Repositorio:Repisalud
Idioma:inglés
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/23441
Acceso en línea:https://hdl.handle.net/20.500.12105/23441
Access Level:acceso abierto
Palabra clave:NGS for diagnostics of CVDs
cardiomyopathies
cardiomyopathy
genetic
genetic testing
hypertrophic cardiomyopathy
next-generation sequencing
variant classification
variant interpretation
Sarcómeros
Cadenas Pesadas de Miosina
Cardiomiopatía Hipertrófica
Muerte Súbita
Humanos
Miosinas Cardíacas
Estudios de Asociación Genética
Fenotipo
Cardiac Myosins
Phenotype
Death, Sudden
Sarcomeres
Humans
Cardiomyopathy, Hypertrophic
Genetic Association Studies
Myosin Heavy Chains
Descripción
Sumario:Hypertrophic cardiomyopathy (HCM) is a genetic disease characterised by increased left ventricle (LV) wall thickness caused by mutations in sarcomeric genes. Finding a causal mutation can help to better assess the proband's risk, as it allows the presence of the mutation to be evaluated in relatives and the follow-up to be focused on carriers. We performed an observational study of patients with HCM due to the novel p.Arg652Lys variant in the MYH7 gene. Eight families and 59 patients are described in the follow-up for a median of 63 months, among whom 39 (66%) carry the variant. Twenty-five (64%) of carriers developed HCM. A median maximum LV wall thickness of 16.5 mm was described. The LV hypertrophy was asymmetric septal in 75% of cases, with LV outflow tract obstruction in 28%. The incidence of a composite of serious adverse cardiovascular events (sudden death, aborted sudden death, appropriate implantable cardiac defibrillator discharge, an embolic event, or admission for heart failure) was observed in five (20%) patients. Given the finding of the p.Arg652Lys variant in patients with HCM, but not in controls, with evident segregation in patients with HCM from eight families and the location in an active site of the protein, we can define this variant as likely pathogenic and associated with the development of HCM.