Personalized Medicine in Mitochondrial Health and Disease: Molecular Basis of Therapeutic Approaches Based on Nutritional Supplements and Their ..
Academic Article
Publication Date:
2022
abstract:
Abstract: Mitochondrial diseases (MDs) may result from mutations affecting nuclear or mitochondrial genes, encoding mitochondrial proteins, or non-protein-coding mitochondrial RNA. Despite the
great variability of affected genes, in the most severe cases, a neuromuscular and neurodegenerative
phenotype is observed, and no specific therapy exists for a complete recovery from the disease. The
most used treatments are symptomatic and based on the administration of antioxidant cocktails
combined with antiepileptic/antipsychotic drugs and supportive therapy for multiorgan involvement. Nevertheless, the real utility of antioxidant cocktail treatments for patients affected by MDs
still needs to be scientifically demonstrated. Unfortunately, clinical trials for antioxidant therapies
using ?-tocopherol, ascorbate, glutathione, riboflavin, niacin, acetyl-carnitine and coenzyme Q have
met a limited success. Indeed, it would be expected that the employed antioxidants can only be
effective if they are able to target the specific mechanism, i.e., involving the central and peripheral
nervous system, responsible for the clinical manifestations of the disease. Noteworthily, very often
the phenotypes characterizing MD patients are associated with mutations in proteins whose function
does not depend on specific cofactors. Conversely, the administration of the antioxidant cocktails
might determine the suppression of endogenous oxidants resulting in deleterious effects on cell
viability and/or toxicity for patients. In order to avoid toxicity effects and before administering
the antioxidant therapy, it might be useful to ascertain the blood serum levels of antioxidants and
cofactors to be administered in MD patients. It would be also worthwhile to check the localization
of mutations affecting proteins whose function should depend (less or more directly) on the cofactors to be administered, for estimating the real need and predicting the success of the proposed
cofactor/antioxidant-based therapy
Iris type:
01.01 Articolo in rivista
Keywords:
mitochondrial impairment; mitochondrial dysfunction; mitochondrial diseases; vitamins; cofactors; dietary supplement; aminoacyl tRNA synthetase; phospholipids; peptide-based treatments; CRAT deficiency; SLC25A10 and DIC deficiency; MERRF; MELAS; Leigh syndrome; Leigh-like syndromes; MEGDEL; encephalomyopathies; antioxidant cocktails; mitochondrial carriers; complex I; type I NADH dehydrogenase
List of contributors:
Tragni, Vincenzo; Petrosillo, Giuseppe; Marzulli, Domenico
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