Exercise was associated with changes in gut microbial composition, an increase in butyrate producing bacteria and an increase in fecal butyrate concentrations independent of diet in rodents and humans. The overall quality of evidence in the studies in humans was low and the risk of bias was unclear. Future studies with standardized reporting and rigorous dietary control in larger samples are needed to further determine the influence of exercise on gut microbial composition.
Prediabetes is associated with low-grade chronic inflammation that
increases the risk for developing type 2 diabetes (T2D) and cardiovascular
disease (CVD). An elevated lipopolysaccharide concentration, associated with
dysbiosis of the intestinal microbiota, has been implicated in the development
of both T2D and CVD. Selective modulation of the intestinal microbiota with
prebiotics reduces intestinal permeability and endotoxin concentrations,
inflammation, and metabolic dysfunction in rodents. The effect of prebiotic
supplementation on cardio-metabolic function in those at risk for T2D is not
known. The primary aim of this trial is to determine the influence of prebiotic
supplementation with inulin on insulin sensitivity and skeletal muscle metabolic
flexibility in adults at risk for T2D. We hypothesize that prebiotic
supplementation with inulin will improve insulin sensitivity and skeletal muscle
metabolic flexibility. We will randomize 48 adults (40–75 yrs) with
prediabetes or a score ≥5 on the American Diabetes Association (ADA)
risk screener to 6 weeks of prebiotic supplementation with inulin (10 g/day) or
placebo. Subjects will be provided with all food for the duration of the study,
to avoid potential confounding through differences in dietary intake between
individuals. Intestinal permeability, serum endotoxin concentrations, insulin
sensitivity, skeletal muscle metabolic flexibility, endothelial function,
arterial stiffness, and fecal bacterial composition will be measured at baseline
and following treatment. The identification of prebiotic supplementation with
inulin as an efficacious strategy for reducing cardio-metabolic risk in
individuals at risk of T2M could impact clinical practice by informing dietary
recommendations and increasing acceptance of prebiotics by the scientific and
medical community.
Trimethylamine N-oxide (TMAO) is associated with type 2 diabetes (T2DM) and increased risk of adverse cardiovascular events. Prebiotic supplementation has been purported to reduce TMAO production, but whether prebiotics reduce fasting or postprandial TMAO levels is unclear. Sedentary, overweight/obese adults at risk for T2DM (n = 18) were randomized to consume a standardized diet (55% carbohydrate, 30% fat) with 10 g/day of either an inulin supplement or maltodextrin placebo for 6 weeks. Blood samples were obtained in the fasting state and hourly during a 4-h high-fat challenge meal (820 kcal; 25% carbohydrate, 63% fat; 317.4 mg choline, 62.5 mg betaine, 8.1 mg l-carnitine) before and after the diet. Plasma TMAO and trimethylamine (TMA) moieties (choline, l-carnitine, betaine, and γ-butyrobetaine) were measured using isocratic ultraperformance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). There were no differences in fasting or postprandial TMAO or TMA moieties between the inulin and placebo groups at baseline (all p > 0.05). There were no significant changes in fasting or postprandial plasma TMAO or TMA moiety concentrations following inulin or placebo. These findings suggest that inulin supplementation for 6 weeks did not reduce fasting or postprandial TMAO in individuals at risk for T2DM. Future studies are needed to identify efficacious interventions that reduce plasma TMAO concentrations.
OBJECTIVES: This study evaluated the association between quality of life and non-insulin-dependent diabetes mellitus (NIDDM) status, and whether this association differs between Hispanics and non-Hispanic Whites. METHODS: Between 1986 and 1989, cross-sectional data on perceived quality of life (PQOL) were collected from 223 persons with NIDDM and 753 non-diabetic subjects. RESULTS: After adjustment, persons with NIDDM rated their PQOL significantly lower than did control subjects. The relationship of diabetes and PQOL did not differ by ethnicity. The number of complications of diabetes was not associated with lower PQOL scores. CONCLUSIONS: Control and treatment strategies should reflect an understanding of the impact that diabetes has on social functioning, leisure activities, and physical and mental health.
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