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. 2023 May 19;12(2):108–126. doi: 10.1007/s13679-023-00503-6

Table 3.

RCT results on butyrate administration

Condition n Dose Administration Time Results Ref
Inflammatory bowel disease 49 1.8 g/day Oral 2 months Increased the growth of bacteria able to produce SCFAs with potentially anti-inflammatory action [25]
Pediatric obesity 54 20 mg/kg body weight Oral 6 months Greater changes in BMI, waist circumference, insulin level, ghrelin level, HOMA-IR, micro-RNA221 relative expression, and IL-6 level [26]
Behçet’s Syndrome 17 2.4 g/day Oral 3 months Reduced leukocyte ROS production and lipid peroxidation in plasma, increased total antioxidant capacity in plasma, improvement in fibrin susceptibility to plasmin-induced lysis [27]
Pediatric inflammatory bowel disease 72 300 mg/day Oral 12 weeks No difference in remission rate or median disease activity [28]
Type 1 diabetes 30 4 g/day Oral 1 month No changes in innate or adaptive immunity in T1DM [29]
Type 2 diabetes 39 100 mg/day Oral 6 weeks No changes in biochemical parameters [30]
Irritable bowel syndrome 66 300 mg/day Oral 12 weeks Decreased frequency of spontaneous abdominal pain, postprandial abdominal pain, abdominal pain during defecation, stool consistency and constipation [31]
Ulcerative colitis 16 6 mmol/day Rectal 20 days No changes in measured parameters of the colonic mucus layer: MUC2 and TFF3 [32]
Ulcerative colitis 11 100 mmol/day Rectal 8 weeks Reduced number of translocated NF-kB-positive macrophages, reduced number of neutrophils in crypt and surface epithelia and of the lamina propria lymphocytes/plasma cells, decreased Disease Activity Index (DAI) [33]
Shigellosis 80 160 mmol/day Rectal 3 days Early reduction of macrophages, pus cells, IL-8 and IL-1β in the stool, induced LL-37 expression in the rectal epithelia [34]