Association of Intestinal Microbiota with Metabolic Markers and Dietary Habits in Patients with Type 2 Diabetes

被引:97
作者
Yamaguchi, Yoshiharu [1 ]
Adachi, Kazunori [1 ]
Sugiyama, Tomoya [1 ]
Shimozato, Akihiro [1 ]
Ebi, Masahide [1 ]
Ogasawara, Naotaka [1 ]
Funaki, Yasushi [1 ]
Goto, Chiho [2 ]
Sasaki, Makoto [1 ]
Kasugai, Kunio [1 ]
机构
[1] Aichi Med Univ, Sch Med, Dept Gastroenterol, 1-1 Yazakokarimata, Nagakute, Aichi 4801195, Japan
[2] Nagoya Bunri Univ, Fac Hlth & Human Life, Dept Hlth & Nutr, Inazawa, Japan
关键词
Type; 2; diabetes; Dietary habits; Gut microbiota; Low-carbohydrate diet; Low-protein diet; CARDIOVASCULAR RISK-FACTORS; GUT-MICROBIOTA; DOUBLE-BLIND; WEIGHT-LOSS; FAT; BACTERIA; WOMEN; TRANSGLUCOSIDASE; METAGENOME; DYSBIOSIS;
D O I
10.1159/000447690
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Evidence suggests that intestinal micro biota, along with factors such as diet and host genetics, contributes to obesity, metabolic dysfunction and diabetes. Therefore, we examined the relationship between gut microbiota, blood metabolic markers, dietary habits and fecal short-chain fatty acids (SCFAs) in patients with type 2 diabetes mellitus (T2DM). Methods: Dietary habits, blood and fecal samples from 59 T2DM patients were recruited, and the association of intestinal microbiota with metabolic markers and dietary habits was analyzed. Results: Total energy intake was 1,692 380 kcal/day. Carbohydrate, fat and protein intakes were 57.5 +/- 5.2, 23.2 +/- 5.3 and 13.2 +/- 2.2%, respectively. Dietary habits high carbohydrate, fat, and protein intake were associated with increased counts of Clostridium clusters IV and XI and decreased counts of Bifidobacterium spp., order Lactobacillales and Clostridium cluster IV. Protein intake was negatively correlated with fecal acetate and total SCFAs. Total SCFAs, propionate and acetate were negatively correlated with blood insulin levels and the homeostasis model of insulin resistance. Conclusion: Diets low in protein and carbohydrates favor a healthy gut microbiome and improve glucose tolerance in T2DM patients, although further elucidation of the role of the gut microbiome could lead to better therapies and prophylaxes. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:66 / 72
页数:7
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