Genetic aspects of the oxidative phosphorylation dysfunction in dilated cardiomyopathy

Bayona-Bafaluy, M.P. (Universidad de Zaragoza) ; Iglesias, E. (Universidad de Zaragoza) ; López-Gallardo, E. (Universidad de Zaragoza) ; Emperador, S. (Universidad de Zaragoza) ; Pacheu-Grau, D. (Universidad de Zaragoza) ; Labarta, L. ; Montoya, J. (Universidad de Zaragoza) ; Ruiz-Pesini, E. (Universidad de Zaragoza)

Resumen: Dilated cardiomyopathy is a frequent and extremely heterogeneous medical condition. Deficits in the oxidative phosphorylation system have been described in patients suffering from dilated cardiomyopathy. Hence, mutations in proteins related to this biochemical pathway could be etiological factors for some of these patients. Here, we review the clinical phenotypes of patients harboring pathological mutations in genes related to the oxidative phosphorylation system, either encoded in the mitochondrial or in the nuclear genome, presenting with dilated cardiomyopathy. In addition to the clinical heterogeneity of these patients, the large genetic heterogeneity has contributed to an improper allocation of pathogenicity for many candidate mutations. We suggest criteria to avoid incorrect assignment of pathogenicity to newly found mutations and discuss possible therapies targeting the oxidative phosphorylation function.

Idioma: Inglés

DOI: 10.1016/j.mrrev.2020.108334

Año: 2020

Publicado en: MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH 786, 108334 (2020), [13 pp]
ISSN: 1383-5742

Factor impacto JCR: 5.657 (2020)

Categ. JCR: BIOTECHNOLOGY & APPLIED MICROBIOLOGY rank: 26 / 158 = 0.165 (2020) - Q1 - T1
Categ. JCR: TOXICOLOGY rank: 11 / 93 = 0.118 (2020) - Q1 - T1
Categ. JCR: GENETICS & HEREDITY rank: 31 / 175 = 0.177 (2020) - Q1 - T1

Factor impacto SCIMAGO: 2.036 - Health, Toxicology and Mutagenesis (Q1) - Genetics (Q1)

Tipo y forma: Revisión (Versión definitiva)

Área (Departamento): Area Histología (Dpto. Anatom.Histolog.Humanas)
Área (Departamento): Área Bioquímica y Biolog.Mole. (Dpto. Bioq.Biolog.Mol. Celular)