Glucose metabolism and diet-based prevention of liver dysfunction in MPV17 mutant patients.

TitleGlucose metabolism and diet-based prevention of liver dysfunction in MPV17 mutant patients.
Publication TypeJournal Article
Year of Publication2009
AuthorsParini, R, Furlan, F, Notarangelo, L, Spinazzola, A, Uziel, G, Strisciuglio, P, Concolino, D, Corbetta, C, Nebbia, G, Menni, F, Rossi, G, Maggioni, M, Zeviani, M
JournalJ Hepatol
Volume50
Issue1
Pagination215-21
Date Published2009 Jan
ISSN0168-8278
KeywordsAdolescent, Alanine Transaminase, Aspartate Aminotransferases, Biopsy, Child, Preschool, Disease Progression, Female, Glucose, Humans, Infant, Liver, Liver Diseases, Male, Membrane Proteins, Mitochondrial Diseases, Mitochondrial Proteins, Mutation, Pedigree
Abstract

BACKGROUND/AIMS: To describe in detail the specific clinical and biological characteristics of three patients with MPV17 gene mutations, a rare hepatocerebral mitochondrial DNA depletion syndrome (MDS) and the positive effects of a novel dietetic treatment based on avoidance of fasting.METHODS: We describe the case histories of three members of the same family with MPV17 mutations.RESULTS: Two patients had a very severe and progressive liver disease: 1 died in the first year of life and the other underwent liver transplantation. The third patient, now 13 years of age, had a milder form of liver disease and developed progressive ataxia. Psychomotor involvement at onset of disease was mild or absent. No patient had severe hyperlactataemia. In vivo functional studies on two patients showed no hyperlactataemia even after intravenous and oral glucose loading, regular fasting hypoglycemia 3-4h after meals and no response to glucagon. Liver function tests improved when patients received continuous iv glucose infusion or were regularly fed every 3h.CONCLUSIONS: These clinical and biochemical features allow us to differentiate patients with MPV17 mutations from other liver MDS and suggest that regular glucose intake at short intervals may be beneficial in slowing the progression of the disease.

DOI10.1016/j.jhep.2008.08.019
Alternate JournalJ. Hepatol.
Citation Key10.1016/j.jhep.2008.08.019
PubMed ID19012992