Coenzyme Q10 Supplementation Improves Adipokine Levels and Alleviates Inflammation and Lipid Peroxidation in Conditions of Metabolic Syndrome: A Meta-Analysis of Randomized Controlled Trials.
Phiwayinkosi Vusi DludlaPatrick OrlandoSonia SilvestriFabio MarcheggianiIlenia CirilliTawanda Maurice NyambuyaVuyolwethu MxinwaKabelo MokgalaboniBongani B NkambuleRabia JohnsonSithandiwe E Mazibuko-MbejeChristo John Frederick MullerJohan LouwLuca TianoPublished in: International journal of molecular sciences (2020)
Evidence from randomized controlled trials (RCTs) suggests that coenzyme Q10 (CoQ10) can regulate adipokine levels to impact inflammation and oxidative stress in conditions of metabolic syndrome. Here, prominent electronic databases such as MEDLINE, Cochrane Library, and EMBASE were searched for eligible RCTs reporting on any correlation between adipokine levels and modulation of inflammation and oxidative stress in individuals with metabolic syndrome taking CoQ10. The risk of bias was assessed using the modified Black and Downs checklist, while the Grading of Recommendations Assessment, Development and Evaluation (GRADE) tool was used to evaluate the quality of evidence. Results from the current meta-analysis, involving 318 participants, showed that CoQ10 supplementation in individuals with metabolic syndrome increased adiponectin levels when compared to those on placebo (SMD: 1.44 [95% CI: -0.13, 3.00]; I2 = 96%, p < 0.00001). Moreover, CoQ10 supplementation significantly lowered inflammation markers in individuals with metabolic syndrome in comparison to those on placebo (SMD: -0.31 [95% CI: -0.54, -0.08]; I2 = 51%, p = 0.07). Such benefits with CoQ10 supplementation were related to its ameliorative effects on lipid peroxidation by reducing malondialdehyde levels, concomitant to improving glucose control and liver function. The overall findings suggest that optimal regulation of adipokine function is crucial for the beneficial effects of CoQ10 in improving metabolic health.
Keyphrases
- metabolic syndrome
- oxidative stress
- systematic review
- insulin resistance
- uric acid
- healthcare
- dna damage
- randomized controlled trial
- ischemia reperfusion injury
- cardiovascular risk factors
- cardiovascular disease
- induced apoptosis
- type diabetes
- clinical trial
- adipose tissue
- machine learning
- risk assessment
- emergency department
- double blind
- health information
- signaling pathway
- skeletal muscle
- study protocol
- open label
- adverse drug
- weight loss
- drug induced