Coenzyme Q10 deficiency in mitochondrial DNA depletion syndromes


Por: Montero-Sanchez R, Grazina M, López-Gallardo E, Montoya J, Briones P, Navarro-Sastre A, Land JM, Hargreaves IP, Artuch-Iriberri R and Jimenez-Mallebrera C

Publicada: 1 jul 2013
Resumen:
We evaluated coenzyme Q(10) (CoQ) levels in patients studied under suspicion of mitochondrial DNA depletion syndromes (MDS) (n = 39). CoQ levels were quantified by HPLC, and the percentage of mtDNA depletion by quantitative real-time PCR. A high percentage of MDS patients presented with CoQ deficiency as compared to other mitochondrial patients (Mann-Whitney-U test: p = 0.001). Our findings suggest that MDS are frequently associated with CoQ deficiency, as a possible secondary consequence of disease pathophysiology. Assessment of muscle CoQ status seems advisable in MDS patients since the possibility of CoQ supplementation may then be considered as a candidate therapy. (c) 2013 Elsevier B.V. and Mitochondria Research Society. All rights reserved.
ISSN: 15677249





MITOCHONDRION
Editorial
ELSEVIER SCI LTD, 125 London Wall, London EC2Y 5AS, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 13 Número: 4
Páginas: 337-341
WOS Id: 000320294600010
ID de PubMed: 23583954
imagen Green Submitted

MÉTRICAS