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The Effect of Selenium Supplementation on Disease Activity and Immune-Inflammatory Biomarkers in Patients With Mild-To-Moderate Ulcerative Colitis: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial Publisher Pubmed



Khazdouz M1, 2 ; Daryani NE3 ; Cheraghpour M4 ; Alborzi F3 ; Hasani M5 ; Ghavami SB4 ; Shidfar F1, 6
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. Growth and Development Research Center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Gastroenterology and Hepatology, Imam Khomeini Hospital, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  5. 5. Department of Nutrition, School of Public Health, Golestan University of Medical Sciences, Gorgan, Iran
  6. 6. Colorectal Research Center, Iran University of Medical Sciences, Tehran, Iran

Source: European Journal of Nutrition Published:2023


Abstract

Purpose: Selenium (Se) supplementation may help reduce inflammation and disease activity in ulcerative colitis (UC) patients. We investigated the therapeutic effects of Se administration in cases with mild-to-moderate active UC. Methods: A multicenter, double-blind, randomized clinical trial (RCT) was conducted on 100 cases with active mild-to-moderate UC. The patients were randomly allocated to be given an oral selenomethionine capsule (200 mcg/day, n = 50) or a placebo capsule (n = 50) for 10 weeks. The primary outcome was defined as disease activity via the Simple Clinical Colitis Activity Index (SCCAI), and secondary outcomes were measured at the end of the study. Results: After 10 weeks, the SCCAI score's mean was reduced in the Se group (P < 0.001). At the end of the intervention, clinical improvement (decline of 3 ≥ score from baseline score) was observed in 19 patients (38%) of the Se group and 3 patients (6%) of the placebo group. The patients with clinical remission (defined as SCCAI ≤ 2) were assigned in the Se group (P = 0.014). The Se group’s quality of life and Se serum levels were enhanced at the end of the study (P < 0/001). In the Se group, the mean concentration of interleukin-17 decreased (P < 0/001). However, the levels of interleukin-10 showed no considerable change between the two groups in the 10th week (P = 0.23). Conclusion: Se supplementation as add-on therapy with medical management induced remission and improved the quality of life in patients with active mild-to-moderate UC. Trial registration number and date of registration: IRCT20091114002709N51; 2020-04-13. © 2023, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.
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