» Articles » PMID: 32583356

Coenzyme Q10 Supplementation and Oxidative Stress Parameters: a Systematic Review and Meta-analysis of Clinical Trials

Overview
Specialty Pharmacology
Date 2020 Jun 26
PMID 32583356
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: Oxidative stress (OS) is associated with several chronic complications and diseases. The use of coenzyme Q10 (CoQ10) as an adjuvant treatment with routine clinical therapy against metabolic diseases has shown to be beneficial. However, the impact of CoQ10 as a preventive agent against OS has not been systematically investigated.

Methods: A systematic literature search was performed using the PubMed, SCOPUS, EMBASE, and Cochrane Library databases to identify randomized clinical trials evaluating the efficacy of CoQ10 supplementation on OS parameters. Standard mean differences and 95% confidence intervals were calculated for net changes in OS parameters using a random-effects model.

Results: Seventeen randomized clinical trials met the eligibility criteria to be included in the meta-analysis. Overall, CoQ10 supplementation was associated with a statistically significant decrease in malondialdehyde (MDA) (SMD - 0.94; 95% CI - 1.46, - 0.41; I = 87.7%) and a significant increase in total antioxidant capacity (TAC) (SMD 0.67; 95% CI 0.28, 1.07; I = 74.9%) and superoxide dismutase (SOD) activity (SMD 0.40; 95% CI 1.12, 0.67; I = 9.6%). The meta-analysis found no statistically significant impact of CoQ10 supplementation on nitric oxide (NO) (SMD - 1.40; 95% CI - 0.12, 1.93; I = 92.6%), glutathione (GSH) levels (SMD 0.41; 95% CI - 0.09, 0.91; I = 70.0%), catalase (CAT) activity (SMD 0.36; 95% CI - 0.46, 1.18; I = 90.0%), or glutathione peroxidase (GPx) activities (SMD - 1.40; 95% CI: - 0.12, 1.93; I = 92.6%).

Conclusion: CoQ10 supplementation, in the tested range of doses, was shown to reduce MDA concentrations, and increase TAC and antioxidant defense system enzymes. However, there were no significant effects of CoQ10 on NO, GSH concentrations, or CAT activity.

Citing Articles

Association between dietary coenzyme Q10 intake and hyperuricemia in Chinese adults: a nationwide cross-sectional study.

Kuang H, Zhao D, Tian Z, Liu Z, Dai S, Zheng Y BMC Public Health. 2025; 25(1):806.

PMID: 40016661 PMC: 11869573. DOI: 10.1186/s12889-024-21041-3.


Mitigation of Neuroinflammation and Oxidative Stress in Rotenone-Induced Parkinson Mouse Model through Liposomal Coenzyme-Q10 Intervention: A Comprehensive In-vivo Study.

Umer H, Sharif A, Majeed Khan H, Anjum S, Akhtar B, Ali S Inflammation. 2025; .

PMID: 39836283 DOI: 10.1007/s10753-025-02237-0.


Inflammation, Oxidative Stress, and Endothelial Dysfunction in the Pathogenesis of Vascular Damage: Unraveling Novel Cardiovascular Risk Factors in Fabry Disease.

Faro D, Di Pino F, Monte I Int J Mol Sci. 2024; 25(15).

PMID: 39125842 PMC: 11312754. DOI: 10.3390/ijms25158273.


The Interplay between Endogenous and Foodborne Pro-Oxidants and Antioxidants in Shaping Redox Homeostasis.

Jakubek P, Parchem K, Wieckowski M, Bartoszek A Int J Mol Sci. 2024; 25(14).

PMID: 39063068 PMC: 11276820. DOI: 10.3390/ijms25147827.


Inflammation in Fabry disease: stages, molecular pathways, and therapeutic implications.

Kurdi H, Lavalle L, Moon J, Hughes D Front Cardiovasc Med. 2024; 11:1420067.

PMID: 38932991 PMC: 11199868. DOI: 10.3389/fcvm.2024.1420067.