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
- PMID: 33620550
- DOI: 10.1007/s00394-021-02514-2
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
Retraction in
-
Retraction Note to: 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.Eur J Nutr. 2022 Sep;61(6):3313. doi: 10.1007/s00394-022-02949-1. Eur J Nutr. 2022. PMID: 35767081 No abstract available.
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.
Keywords: Clinical trial; Coenzyme Q10; Inflammatory bowel disease; Inflammatory markers; Ulcerative colitis.
© 2021. Springer-Verlag GmbH, DE part of Springer Nature.
Similar articles
-
Effects of coenzyme Q10 on health-related quality of life, clinical disease activity and blood pressure in patients with mild to moderate ulcerative colitis: a randomized clinical trial.Med J Islam Repub Iran. 2021 Jan 6;35:3. doi: 10.47176/mjiri.35.3. eCollection 2021. Med J Islam Repub Iran. 2021. PMID: 33996654 Free PMC article.
-
Implication of Nrf2/HO-1 pathway in the coloprotective effect of coenzyme Q10 against experimentally induced ulcerative colitis.Inflammopharmacology. 2017 Feb;25(1):119-135. doi: 10.1007/s10787-016-0305-0. Epub 2017 Jan 3. Inflammopharmacology. 2017. PMID: 28050757
-
Coenzyme Q10 supplementation ameliorates inflammatory markers in patients with multiple sclerosis: a double blind, placebo, controlled randomized clinical trial.Nutr Neurosci. 2015 May;18(4):169-76. doi: 10.1179/1476830513Y.0000000106. Epub 2014 Jan 10. Nutr Neurosci. 2015. PMID: 24621064 Clinical Trial.
-
Effects of coenzyme Q10 supplementation on inflammation, angiogenesis, and oxidative stress in breast cancer patients: a systematic review and meta-analysis of randomized controlled- trials.Inflammopharmacology. 2021 Jun;29(3):579-593. doi: 10.1007/s10787-021-00817-8. Epub 2021 May 18. Inflammopharmacology. 2021. PMID: 34008150
-
Can coenzyme Q10 supplementation effectively reduce human tumor necrosis factor-α and interleukin-6 levels in chronic inflammatory diseases? A systematic review and meta-analysis of randomized controlled trials.Pharmacol Res. 2019 Oct;148:104290. doi: 10.1016/j.phrs.2019.104290. Epub 2019 Jun 8. Pharmacol Res. 2019. PMID: 31185284
Cited by
-
Advances in research on immunocyte iron metabolism, ferroptosis, and their regulatory roles in autoimmune and autoinflammatory diseases.Cell Death Dis. 2024 Jul 4;15(7):481. doi: 10.1038/s41419-024-06807-2. Cell Death Dis. 2024. PMID: 38965216 Free PMC article. Review.
-
Antimicrobial Peptides: From Design to Clinical Application.Antibiotics (Basel). 2022 Mar 6;11(3):349. doi: 10.3390/antibiotics11030349. Antibiotics (Basel). 2022. PMID: 35326812 Free PMC article. Review.
-
Short-Chain and Total Fatty Acid Profile of Faeces or Plasma as Predictors of Food-Responsive Enteropathy in Dogs: A Preliminary Study.Animals (Basel). 2021 Dec 31;12(1):89. doi: 10.3390/ani12010089. Animals (Basel). 2021. PMID: 35011195 Free PMC article.
-
Nomogram to Predict the Overall Survival of Colorectal Cancer Patients: A Multicenter National Study.Int J Environ Res Public Health. 2021 Jul 21;18(15):7734. doi: 10.3390/ijerph18157734. Int J Environ Res Public Health. 2021. PMID: 34360026 Free PMC article.
-
Antioxidant Therapy in Inflammatory Bowel Disease: A Systematic Review and a Meta-Analysis of Randomized Clinical Trials.Pharmaceuticals (Basel). 2023 Sep 28;16(10):1374. doi: 10.3390/ph16101374. Pharmaceuticals (Basel). 2023. PMID: 37895845 Free PMC article. Review.
References
-
- Bai X, Gou X, Cai P, Xu C, Cao L, Zhao Z, Huang M, Jin J (2019) Sesamin enhances Nrf2-mediated protective defense against oxidative stress and inflammation in colitis via AKT and ERK activation. Oxid Med Cell Longev 2019:2432416. https://doi.org/10.1155/2019/2432416 - DOI - PubMed - PMC
-
- Yang L, Song Y, Jin P, Liu Y, Wang Y, Qiao H, Huang Y (2018) Shen–Ling–Bai–Zhu–San for ulcerative colitis: protocol for a systematic review and meta-analysis. Medicine 97(38):e12337. https://doi.org/10.1097/MD.0000000000012337 - DOI - PubMed - PMC
-
- Okabayashi S, Kobayashi T, Hibi T (2020) Inflammatory bowel disease in Japan-is it similar to or different from Westerns? J Anus Rectum Colon 4(1):1–13. https://doi.org/10.23922/jarc.2019-003 - DOI - PubMed - PMC
-
- Ficagna GB, Dalri JL, Malluta EF, Scolaro BL, Bobato ST (2020) Quality of life of patients from a multidisciplinary clinic of inflammatory bowel disease. Arq Gastroenterol 57(1):8–12. https://doi.org/10.1590/s0004-2803.202000000-03 - DOI - PubMed
-
- Malekzadeh MM, Vahedi H, Gohari K, Mehdipour P, Sepanlou SG, Ebrahimi Daryani N, Zali MR, Mansour-Ghanaei F, Safaripour A, Aghazadeh R (2016) Emerging epidemic of inflammatory bowel disease in a middle income country: a nation-wide study from Iran. Arch Iran Med 19(1):2–15 - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical