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Current Experience in Testing Mitochondrial Nutrients in Disorders Featuring Oxidative Stress and Mitochondrial Dysfunction: Rational Design of Chemoprevention Trials

An extensive number of pathologies are associated with mitochondrial dysfunction (MDF) and oxidative stress (OS). Thus, mitochondrial cofactors termed “mitochondrial nutrients” (MN), such as α-lipoic acid (ALA), Coenzyme Q10 (CoQ10), and l-carnitine (CARN) (or its derivatives) have been tested in a...

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Autores principales: Pagano, Giovanni, Aiello Talamanca, Annarita, Castello, Giuseppe, Cordero, Mario D., d’Ischia, Marco, Gadaleta, Maria Nicola, Pallardó, Federico V., Petrović, Sandra, Tiano, Luca, Zatterale, Adriana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264162/
https://www.ncbi.nlm.nih.gov/pubmed/25380523
http://dx.doi.org/10.3390/ijms151120169
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author Pagano, Giovanni
Aiello Talamanca, Annarita
Castello, Giuseppe
Cordero, Mario D.
d’Ischia, Marco
Gadaleta, Maria Nicola
Pallardó, Federico V.
Petrović, Sandra
Tiano, Luca
Zatterale, Adriana
author_facet Pagano, Giovanni
Aiello Talamanca, Annarita
Castello, Giuseppe
Cordero, Mario D.
d’Ischia, Marco
Gadaleta, Maria Nicola
Pallardó, Federico V.
Petrović, Sandra
Tiano, Luca
Zatterale, Adriana
author_sort Pagano, Giovanni
collection PubMed
description An extensive number of pathologies are associated with mitochondrial dysfunction (MDF) and oxidative stress (OS). Thus, mitochondrial cofactors termed “mitochondrial nutrients” (MN), such as α-lipoic acid (ALA), Coenzyme Q10 (CoQ10), and l-carnitine (CARN) (or its derivatives) have been tested in a number of clinical trials, and this review is focused on the use of MN-based clinical trials. The papers reporting on MN-based clinical trials were retrieved in MedLine up to July 2014, and evaluated for the following endpoints: (a) treated diseases; (b) dosages, number of enrolled patients and duration of treatment; (c) trial success for each MN or MN combinations as reported by authors. The reports satisfying the above endpoints included total numbers of trials and frequencies of randomized, controlled studies, i.e., 81 trials testing ALA, 107 reports testing CoQ10, and 74 reports testing CARN, while only 7 reports were retrieved testing double MN associations, while no report was found testing a triple MN combination. A total of 28 reports tested MN associations with “classical” antioxidants, such as antioxidant nutrients or drugs. Combinations of MN showed better outcomes than individual MN, suggesting forthcoming clinical studies. The criteria in study design and monitoring MN-based clinical trials are discussed.
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spelling pubmed-42641622014-12-12 Current Experience in Testing Mitochondrial Nutrients in Disorders Featuring Oxidative Stress and Mitochondrial Dysfunction: Rational Design of Chemoprevention Trials Pagano, Giovanni Aiello Talamanca, Annarita Castello, Giuseppe Cordero, Mario D. d’Ischia, Marco Gadaleta, Maria Nicola Pallardó, Federico V. Petrović, Sandra Tiano, Luca Zatterale, Adriana Int J Mol Sci Review An extensive number of pathologies are associated with mitochondrial dysfunction (MDF) and oxidative stress (OS). Thus, mitochondrial cofactors termed “mitochondrial nutrients” (MN), such as α-lipoic acid (ALA), Coenzyme Q10 (CoQ10), and l-carnitine (CARN) (or its derivatives) have been tested in a number of clinical trials, and this review is focused on the use of MN-based clinical trials. The papers reporting on MN-based clinical trials were retrieved in MedLine up to July 2014, and evaluated for the following endpoints: (a) treated diseases; (b) dosages, number of enrolled patients and duration of treatment; (c) trial success for each MN or MN combinations as reported by authors. The reports satisfying the above endpoints included total numbers of trials and frequencies of randomized, controlled studies, i.e., 81 trials testing ALA, 107 reports testing CoQ10, and 74 reports testing CARN, while only 7 reports were retrieved testing double MN associations, while no report was found testing a triple MN combination. A total of 28 reports tested MN associations with “classical” antioxidants, such as antioxidant nutrients or drugs. Combinations of MN showed better outcomes than individual MN, suggesting forthcoming clinical studies. The criteria in study design and monitoring MN-based clinical trials are discussed. MDPI 2014-11-05 /pmc/articles/PMC4264162/ /pubmed/25380523 http://dx.doi.org/10.3390/ijms151120169 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Pagano, Giovanni
Aiello Talamanca, Annarita
Castello, Giuseppe
Cordero, Mario D.
d’Ischia, Marco
Gadaleta, Maria Nicola
Pallardó, Federico V.
Petrović, Sandra
Tiano, Luca
Zatterale, Adriana
Current Experience in Testing Mitochondrial Nutrients in Disorders Featuring Oxidative Stress and Mitochondrial Dysfunction: Rational Design of Chemoprevention Trials
title Current Experience in Testing Mitochondrial Nutrients in Disorders Featuring Oxidative Stress and Mitochondrial Dysfunction: Rational Design of Chemoprevention Trials
title_full Current Experience in Testing Mitochondrial Nutrients in Disorders Featuring Oxidative Stress and Mitochondrial Dysfunction: Rational Design of Chemoprevention Trials
title_fullStr Current Experience in Testing Mitochondrial Nutrients in Disorders Featuring Oxidative Stress and Mitochondrial Dysfunction: Rational Design of Chemoprevention Trials
title_full_unstemmed Current Experience in Testing Mitochondrial Nutrients in Disorders Featuring Oxidative Stress and Mitochondrial Dysfunction: Rational Design of Chemoprevention Trials
title_short Current Experience in Testing Mitochondrial Nutrients in Disorders Featuring Oxidative Stress and Mitochondrial Dysfunction: Rational Design of Chemoprevention Trials
title_sort current experience in testing mitochondrial nutrients in disorders featuring oxidative stress and mitochondrial dysfunction: rational design of chemoprevention trials
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4264162/
https://www.ncbi.nlm.nih.gov/pubmed/25380523
http://dx.doi.org/10.3390/ijms151120169
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