Current experience in testing mitochondrial nutrients in disorders featuring oxidative stress and mitochondrial dysfunction: rational design of chemoprevention trials.

Giovanni Pagano, Annarita Aiello Talamanca, Giuseppe Castello, Mario D Cordero, Marco d'Ischia, Maria Nicola Gadaleta, Federico V Pallardó, Sandra Petrović, Luca Tiano, Adriana Zatterale

Journal: International journal of molecular sciences 2015;15(11):20169-208

PMID: 25380523

Plain Language Summary

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Many conditions are associated with mitochondrial dysfunction (MDF) and oxidative stress (OS). For example; some genetic diseases, aging and age-associated disorders, neurologic and psychiatric diseases, malignancies and autoimmune diseases. This review looks at the clinical trials focused on the use of mitochondrial cofactors (mitochondrial nutrients - MN) such as alpha-lipoic acid (ALA), Coenzyme Q 10 (CoQ10) and L-carnitine (CARN) which are essential in the functioning of mitochondria. Of the trials that were used in the review, 81 tested ALA, 107 tested CoQ10, 74 reports tested CARN, 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. Further studies are therefore needed.

Abstract

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.

Address: Istituto Nazionale Tumori Fondazione G. Pascale-Cancer Research Center at Mercogliano (CROM)-IRCCS, Naples I-80131, Italy. [email protected].; Istituto Nazionale Tumori Fondazione G. Pascale-Cancer Research Center at Mercogliano (CROM)-IRCCS, Naples I-80131, Italy. [email protected].; Istituto Nazionale Tumori Fondazione G. Pascale-Cancer Research Center at Mercogliano (CROM)-IRCCS, Naples I-80131, Italy. [email protected].; Research Laboratory, Dental School, Universidad de Sevilla, Sevilla 41009, Spain. [email protected].; Department of Chemical Sciences, University of Naples "Federico II", Naples I-80126, Italy. [email protected].; National Research Council, Institute of Biomembranes and Bioenergetics, Bari I-70126, Italy. [email protected].; CIBERER (Centro de Investigación Biomédica en Red de Enfermedades Raras), University of Valencia-INCLIVA, Valencia 46010, Spain. [email protected].; Vinca" Institute of Nuclear Sciences, University of Belgrade, Belgrade 11001, Serbia. [email protected].; Biochemistry Unit, Department of Clinical and Dental Sciences, Polytechnical University of Marche, Ancona I-60131, Italy. [email protected].; Genetics Unit, Azienda Sanitaria Locale (ASL) Napoli 1 Centro, Naples I-80136, Italy. [email protected].
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