» Articles » PMID: 36130103

Dose-Response Effect of Coenzyme Q10 Supplementation on Blood Pressure Among Patients with Cardiometabolic Disorders: A Grading of Recommendations Assessment, Development, and Evaluation (GRADE)-Assessed Systematic Review and Meta-Analysis Of...

Overview
Journal Adv Nutr
Publisher Elsevier
Date 2022 Sep 21
PMID 36130103
Authors
Affiliations
Soon will be listed here.
Abstract

Previous studies have shown beneficial effects of coenzyme Q10 (CoQ10) supplementation on blood pressure (BP). However, the optimal intake of CoQ10 for BP regulation in patients with cardiometabolic disorders is unknown, and its effect on circulating CoQ10 is also unclear. We aimed to assess the dose-response relation between CoQ10 and BP, and quantify the effect of CoQ10 supplementation on the concentration of circulating CoQ10 by synthesizing available evidence from randomized controlled trials (RCTs). A comprehensive literature search was performed in 3 databases (PubMed/MEDLINE, Embase, and Cochrane Library) to 21 March, 2022. A novel 1-stage restricted cubic spline regression model was used to evaluate the nonlinear dose-response relation between CoQ10 and BP. Twenty-six studies comprising 1831 subjects were included in our meta-analysis. CoQ10 supplementation significantly reduced systolic blood pressure (SBP) (-4.77 mmHg, 95% CI: -6.57, -2.97) in patients with cardiometabolic diseases; this reduction was accompanied by a 1.62 (95% CI: 1.26, 1.97) μg/mL elevation of circulating CoQ10 compared with the control group. Subgroup analyses revealed that the effects of reducing SBP were more pronounced in patients with diabetes and dyslipidemia and in studies with longer durations (>12 wk). Importantly, a U-shaped dose-response relation was observed between CoQ10 supplementation and SBP level, with an approximate dose of 100-200 mg/d largely reducing SBP (χ2 = 10.84, Pnonlinearity = 0.004). The quality of evidence was rated as moderate, low, and very low for SBP, diastolic blood pressure (DBP), and circulating CoQ10 according to the Grading of Recommendations, Assessment, Development, and Evaluation approach (GRADE), respectively. The current finding demonstrated that the clinically beneficial effects of CoQ10 supplementation may be attributed to the reduction in SBP, and 100-200 mg/d of CoQ10 supplementation may achieve the greatest benefit on SBP in patients with cardiometabolic diseases. This study was registered on PROSPERO as CRD42021252933.

Citing Articles

Current Approaches and Innovations in Managing Preeclampsia: Highlighting Maternal Health Disparities.

Dickerson A, Joseph C, Kashfi K J Clin Med. 2025; 14(4).

PMID: 40004721 PMC: 11856135. DOI: 10.3390/jcm14041190.


Can Coenzyme Q10 Supplementation Reduce Cardiovascular Disease Risk Factors? A Protocol for a GRADE-Assessed Systematic Review and Dose-Response Meta-Analysis of Randomized Controlled Trials.

Jafari A Health Sci Rep. 2025; 8(2):e70452.

PMID: 39931258 PMC: 11808257. DOI: 10.1002/hsr2.70452.


Renoprotective effects of coenzyme Q10 supplementation in patients with chronic kidney disease: a protocol for a systematic review.

Abe Y, Nishiwaki H, Suzuki T, Noma H, Watanabe Y, Ota E BMJ Open. 2025; 14(12):e084088.

PMID: 39806632 PMC: 11664338. DOI: 10.1136/bmjopen-2024-084088.


Exploring the Renoprotective Potential of Bioactive Nutraceuticals in Chronic Kidney Disease Progression: A Narrative Review.

Ghosh A, Muley A, Bhat S, Ainapure A Cureus. 2024; 16(9):e68730.

PMID: 39371767 PMC: 11454842. DOI: 10.7759/cureus.68730.


The Role of Antioxidants in the Therapy of Cardiovascular Diseases-A Literature Review.

Mlynarska E, Hajdys J, Czarnik W, Fularski P, Leszto K, Majchrowicz G Nutrients. 2024; 16(16).

PMID: 39203723 PMC: 11357572. DOI: 10.3390/nu16162587.


References
1.
DerSimonian R, Laird N . Meta-analysis in clinical trials. Control Clin Trials. 1986; 7(3):177-88. DOI: 10.1016/0197-2456(86)90046-2. View

2.
Rodriguez-Carrizalez A, Castellanos-Gonzalez J, Martinez-Romero E, Miller-Arrevillaga G, Pacheco-Moises F, Roman-Pintos L . The effect of ubiquinone and combined antioxidant therapy on oxidative stress markers in non-proliferative diabetic retinopathy: A phase IIa, randomized, double-blind, and placebo-controlled study. Redox Rep. 2015; 21(4):155-63. PMC: 8900707. DOI: 10.1179/1351000215Y.0000000040. View

3.
Hosoe K, Kitano M, Kishida H, Kubo H, Fujii K, Kitahara M . Study on safety and bioavailability of ubiquinol (Kaneka QH) after single and 4-week multiple oral administration to healthy volunteers. Regul Toxicol Pharmacol. 2006; 47(1):19-28. DOI: 10.1016/j.yrtph.2006.07.001. View

4.
Eriksson J, Forsen T, Mortensen S, Rohde M . The effect of coenzyme Q10 administration on metabolic control in patients with type 2 diabetes mellitus. Biofactors. 1999; 9(2-4):315-8. DOI: 10.1002/biof.5520090229. View

5.
Dai Y, Luk T, Yiu K, Wang M, Yip P, Lee S . Reversal of mitochondrial dysfunction by coenzyme Q10 supplement improves endothelial function in patients with ischaemic left ventricular systolic dysfunction: a randomized controlled trial. Atherosclerosis. 2011; 216(2):395-401. DOI: 10.1016/j.atherosclerosis.2011.02.013. View