Effects of Mediterranean Diet, Curcumin, and Resveratrol on Mild-to-Moderate Active Ulcerative Colitis: A Multicenter Randomized Clinical Trial

被引:3
|
作者
Dogan, Ozge Erol [1 ,2 ]
Celik, Kezban Esen Karaca [3 ]
Bas, Murat [3 ]
Alan, Eyup Hakan [4 ]
Cagin, Yasir Furkan [5 ]
机构
[1] Acibadem Mehmet Ali Aydinlar Univ, Inst Hlth Sci, Dept Nutr & Dietet, TR-34752 Istanbul, Turkiye
[2] Ardahan Univ, Vocat Sch Hlth Serv, Dept Hlth Care Serv, TR-75002 Ardahan, Turkiye
[3] Acibadem Mehmet Ali Aydinlar Univ, Dept Nutr & Dietet, Fac Hlth Sci, TR-34752 Istanbul, Turkiye
[4] Malatya Training & Res Hosp, Dept Gastroenterol, TR-44330 Malatya, Turkiye
[5] Inonu Univ, Fac Med, Dept Gastroenterol, TR-44280 Malatya, Turkiye
关键词
ulcerative colitis; Mediterranean diet; curcumin; resveratrol; supplementation; inflammatory bowel diseases; INFLAMMATORY BOWEL DISEASES; QUALITY-OF-LIFE; DOUBLE-BLIND; WEIGHT-LOSS; METAANALYSIS; SUPPLEMENTATION; THERAPY; INDEXES; PATIENT; RISK;
D O I
10.3390/nu16101504
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
This study aimed to investigate the effects of the Mediterranean diet (MD), combined with curcumin and resveratrol supplementation, on disease activity, serum inflammatory markers, and quality of life in patients with mild-to-moderate active ulcerative colitis (UC). This study was designed as a prospective multicenter three-arm randomized controlled trial. Participants were randomized to the MD, MD + curcumin, and MD + resveratrol groups. All participants were placed on the MD for 8 weeks. The MD + curcumin group also received 1600 mg/day of curcumin supplementation, whereas the MD + resveratrol group received 500 mg/day of resveratrol supplementation for 8 weeks. Anthropometric measurements, Truelove-Witts Index, Short Form-36, Inflammatory Bowel Disease Questionnaire, Mediterranean Diet Adherence Scale (MEDAS), and laboratory tests were performed at baseline and postintervention. Within-group comparisons showed that MD, MD + curcumin, and MD + resveratrol interventions were effective in reducing disease activity and inflammation and improving quality of life in individuals with UC (p < 0.05). Between-group comparisons revealed no significant difference in all parameters except for the pain subparameter of SF-36 and the MEDAS score (p < 0.05). The MD is an effective and safe intervention to be used in clinical practice in individuals with UC.
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页数:18
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