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A Randomized Controlled Trial on the Coloprotective Effect of Coenzyme Q10 on Immune-Inflammatory Cytokines, Oxidative Status, Antimicrobial Peptides, and Microrna-146A Expression in Patients With Mild-To-Moderate Ulcerative Colitis Publisher Pubmed



Farsi F1 ; Ebrahimidaryani N2 ; Golab F3 ; Akbari A4 ; Janani L5 ; Karimi MY6 ; Irandoost P7 ; Alamdari NM7 ; Agah S4 ; Vafa M1
Authors
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Authors Affiliations
  1. 1. Department of Nutrition, School of Public Health, Iran University of Medical Sciences, Tehran, Iran
  2. 2. Head of Gastroenterology Ward, School of Medicine, Imam Khomeini Hospital, Tehran, Iran
  3. 3. Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran
  4. 4. Colorectal Research Center, Iran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Biostatistics, School of Public Health, Iran University of Medical Sciences, Tehran, Iran
  6. 6. Razi Drug Research Center, Iran University of Medical Sciences, Tehran, Iran
  7. 7. Student Research Committee, Department of Nutrition, School of Public Health, Iran University of Medical Sciences, Tehran, Iran

Source: European Journal of Nutrition Published:2021


Abstract

Purpose: Coenzyme Q10 (CoQ10), having potent antioxidant and anti-inflammatory pharmacological properties, has recently been shown to be a safe and promising agent in maintaining remission of ulcerative colitis (UC). This trial was, therefore, designed to determine CoQ10 efficacy on inflammation and antioxidant status, antimicrobial peptides, and microRNA-146a expression in UC patients. Methods: In this randomized double-blind controlled trial, 88 mild-to-moderate UC patients were randomly allocated to receive CoQ10 (200 mg/day) or placebo (rice flour) for 2 months. At the baseline and at an 8-week follow-up, serum levels of Nrf2, cathelicidin LL-37, β-defensin 2, IL-10, IL-17, NF-κB p65 activity in peripheral blood mononuclear cells (PBMCs), simple clinical colitis activity index questionnaire (SCCAIQ), and quality of life (IBDQ-32 score), as well as an expression rate of microRNA-146a were measured. Results: A significant reduction was detected in the serum IL-17 level, activity of NF-κB p65 in PBMCs, and also SCCAI score in the CoQ10 group compared to the placebo group, whereas IL-10 serum concentrations and IBDQ-32 score of the CoQ10 group considerably increased versus the control group; the changes of these variables were also significantly different within and between groups at the end of the study. Furthermore, CoQ10 remarkably increased serum levels of cathelicidin LL-37. A significant change in serum cathelicidin LL-37 levels was also observed between the two groups. No statistical difference, however, was seen between the two groups in terms of the serum levels of Nrf2 and β-defensin 2 and the relative expression of microRNA-146a. Conclusions: Our results indicate that CoQ10 supplementation, along with drug therapy, appears to be an efficient reducer of inflammation in patients with mild-to-moderate UC at a remission phase. Trial Registration: The research has also been registered at the Iranian Registry of Clinical Trials (IRCT): IRCT20090822002365N17. Graphic abstract: [Figure not available: see fulltext.]. © 2021, Springer-Verlag GmbH, DE part of Springer Nature.
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