Jian Gao, Xiaoyu Guo, Wei Wei, Ran Li, Ke Hu, Xin Liu, Wenbo Jiang, Siyao Liu, Weiqi Wang, Hu Sun, Huanyu Wu, Yuntao Zhang, Wenbo Gu, Ying Li, Changhao Sun, Tianshu Han
Journal: Diabetes care 2021;44(9):1970-1979
PMID: 34253560
OBJECTIVE
This randomized controlled-feeding trial aimed to determine the impact of fried meat intake on the gut microbiota and fecal cometabolites and whether such impacts influenced host glucose homoeostasis, intestinal endotoxin levels, and systemic inflammation.
RESEARCH DESIGN AND METHODS
A total of 117 overweight adults were randomized into two groups. Fifty-nine participants were provided fried meat four times per week, and 58 participants were restricted from fried meat intake, while holding food group and nutrient compositions constant, for 4 weeks. The gut microbiota was analyzed by 16S rRNA sequencing. Glucose and insulin concentrations at 0, 30, 60, and 120 min of an oral glucose tolerance test, fecal microbiota-host cometabolite levels, and intestinal endotoxin and inflammation serum biomarker levels were measured. The area under the curve (AUC) for insulin, insulinogenic index (IGI), and muscle insulin resistance index (MIRI) were calculated.
RESULTS
The participants who consumed fried meat had lower IGI values than the control subjects, but they had higher MIRI and AUC values of insulin and lipopolysaccharide (LPS), TNF-α, IL-10, and IL-1β levels ( < 0.05). Fried meat intake lowered microbial community richness and decreased and abundances while increasing , , and abundances ( FDR <0.05), provoking a significant shift in the fecal cometabolite profile, with lower 3-indolepropionic acid, valeric acid, and butyric acid concentrations and higher carnitine and methylglutaric acid concentrations ( FDR <0.05). Changes in these cometabolite levels were significantly associated with changes in IGI and MIRI values and LPS, FGF21, TNF-α, IL-1β, and IL-10 levels ( < 0.05).
CONCLUSIONS
Fried meat intake impaired glucose homoeostasis and increased intestinal endotoxin and systemic inflammation levels by influencing the gut microbiota and microbial-host cometabolites.
© 2021 by the American Diabetes Association.
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