Page last updated: 2024-10-19

niacinamide and Mitochondrial Diseases

niacinamide has been researched along with Mitochondrial Diseases in 4 studies

nicotinamide : A pyridinecarboxamide that is pyridine in which the hydrogen at position 3 is replaced by a carboxamide group.

Mitochondrial Diseases: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.

Research Excerpts

ExcerptRelevanceReference
"Mitochondrial disorders are highly heterogeneous conditions characterized by defects of the mitochondrial respiratory chain."1.40NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial disease. ( Auwerx, J; Cerutti, R; Dantzer, F; Lamperti, C; Leoni, V; Li, W; Marchet, S; Pirinen, E; Sauve, AA; Schon, EA; Viscomi, C; Zeviani, M, 2014)

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (50.00)24.3611
2020's2 (50.00)2.80

Authors

AuthorsStudies
Orlandi, I1
Vai, M1
Zhao, N1
Xia, J1
Xu, B1
Cerutti, R1
Pirinen, E1
Lamperti, C1
Marchet, S1
Sauve, AA1
Li, W1
Leoni, V1
Schon, EA1
Dantzer, F1
Auwerx, J1
Viscomi, C1
Zeviani, M1
Hathorn, T1
Snyder-Keller, A1
Messer, A1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
The Effect of Niacin Supplementation on Systemic Nicotinamide Adenine Dinucleotide (NAD+) Metabolism, Physiology and Muscle Performance in Healthy Controls and Mitochondrial Myopathy Patients[NCT03973203]15 participants (Actual)Interventional2014-06-01Completed
NiaMIT (NiaMIT_0001) Continuation for Early-stage Mitochondrial Myopathy Patients to Investigate the Effect of Niacin Supplementation on Systemic Nicotinamide Adenine Dinucleotide (NAD+) Metabolism, Physiology and Muscle Performance[NCT04538521]3 participants (Actual)Interventional2019-02-11Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Other Studies

4 other studies available for niacinamide and Mitochondrial Diseases

ArticleYear
Assays for Monitoring the Effects of Nicotinamide Supplementation on Mitochondrial Activity in Saccharomyces cerevisiae.
    Methods in molecular biology (Clifton, N.J.), 2020, Volume: 2138

    Topics: Aging; Cell Respiration; Dietary Supplements; Membrane Potential, Mitochondrial; Mitochondria; Mitoc

2020
Physical exercise may exert its therapeutic influence on Alzheimer's disease through the reversal of mitochondrial dysfunction via SIRT1-FOXO1/3-PINK1-Parkin-mediated mitophagy.
    Journal of sport and health science, 2021, Volume: 10, Issue:1

    Topics: Adenosine Triphosphate; Alzheimer Disease; Amyloid beta-Peptides; Brain-Derived Neurotrophic Factor;

2021
NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial disease.
    Cell metabolism, 2014, Jun-03, Volume: 19, Issue:6

    Topics: Animals; Dietary Supplements; Disease Models, Animal; Electron Transport Complex IV; Energy Metaboli

2014
NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial disease.
    Cell metabolism, 2014, Jun-03, Volume: 19, Issue:6

    Topics: Animals; Dietary Supplements; Disease Models, Animal; Electron Transport Complex IV; Energy Metaboli

2014
NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial disease.
    Cell metabolism, 2014, Jun-03, Volume: 19, Issue:6

    Topics: Animals; Dietary Supplements; Disease Models, Animal; Electron Transport Complex IV; Energy Metaboli

2014
NAD(+)-dependent activation of Sirt1 corrects the phenotype in a mouse model of mitochondrial disease.
    Cell metabolism, 2014, Jun-03, Volume: 19, Issue:6

    Topics: Animals; Dietary Supplements; Disease Models, Animal; Electron Transport Complex IV; Energy Metaboli

2014
Nicotinamide improves motor deficits and upregulates PGC-1α and BDNF gene expression in a mouse model of Huntington's disease.
    Neurobiology of disease, 2011, Volume: 41, Issue:1

    Topics: Animals; Brain-Derived Neurotrophic Factor; Disease Models, Animal; Female; Humans; Huntington Disea

2011