Acute and Long-term Health Effects of Various Carbohydrates on Blood Glucose Management in Humans
- Conditions
- Nutrition, Healthy
- Interventions
- Other: ControlOther: Treatment
- Registration Number
- NCT06554002
- Lead Sponsor
- Clinical Nutrition Research Centre, Singapore
- Brief Summary
Dietary fibre, especially soluble fibre, has several health benefits such as lowering the risks for cardiovascular disease, stroke, diabetes, obesity, and gastrointestinal diseases. Resistant dextrin is a non-viscous soluble fibre, can be introduced quite easily in foods or as drinks, and it is well tolerated. This study aims to investigate if daily supplementation of habitual diets with resistant dextrin over 8 weeks affect glycaemic control via insulin sensitivity, intestinal fermentation, energy expenditure and fat oxidation in adults with increased risk for type 2 diabetes. The primary outcome is the effect on glycaemic control (fasting glucose, insulin, insulin sensitivity and 24 hour glycaemic response from CGMS). The secondary outcomes are the effects on fasting lipids, energy expenditure and fuel utilization in a whole room calorimeter and appetite regulation.
- Detailed Description
Dietary fibre has several health benefits such as lowering the risks for cardiovascular disease, stroke, diabetes, obesity, and gastrointestinal diseases. Dietary fibre intake has regularly been reported to be below the daily recommended levels. Based on the 2010 National Nutrition Survey, 21% of Singaporeans did not meet the recommended daily intake of dietary fibre. While increasing fruit and vegetables intake remains the primary strategy to promote fibre intake, an alternative is to supplement a daily diet with dietary fibre, especially soluble fibre, to improve health.
Resistant dextrin is a non-viscous soluble fibre that exhibits prebiotic properties and it has been shown to alter gastrointestinal ecology. Emerging evidence suggests that resistant dextrin reduced insulin resistance in both healthy individuals and adults with type 2 diabetes, resulting in better blood glucose control. In term of its cardio-protective effects, resistant dextrin has also been shown to lower blood cholesterol levels and reduced inflammation biomarkers. Resistant dextrin has also been shown to suppress hunger and increase satiety, leading to reduced daily energy intake and greater body weight loss.
To date, evidence from clinical trials, notably among Asians is still insufficient to make dietary recommendations. In addition, the possibility of short-chain fatty acid production in stimulating diet-induced thermogenesis and fat oxidation has not been explored. These are the novel aspects that our proposed study aims to investigate.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 98
- 21 to 60 years old
- Group A: 21 - 25 kg/m2, with first degree family history of type 2 diabetes, or Group B: 23 - 30 kg/m2, with waist circumference >85 cm for males and >82 cm for females
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• Consume fibre supplements or any other supplements that is likely to interfere with study outcomes
- Have any major organ dysfunction (e.g. cardiovascular, respiratory, hepatic, renal, gastrointestinal) that may influence taste, olfaction, appetite, digestion, metabolism, absorption or elimination of test foods, nutraceutical or drug
- Smoking
- Have any metabolic diseases (e.g. diabetes, hypertension)
- Have medical conditions and/or taking medications known to affect glycaemia (e.g. glucocorticoids, thyroid hormones, thiazide diuretics)
- Have glucose-6-phosphate dehydrogenase (G6PD) deficiency
- Have any severe food allergy (e.g. anaphylaxis to peanuts), or any other known food allergy/intolerance
- Have active Tuberculosis (TB) or currently receiving treatment for TB
- Have any known Chronic infection or known to suffer from or have previously suffered from or is a carrier of Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), Human Immunodeficiency Virus (HIV)
- A team member of the study or their immediate family members (i.e. spouse, parent, child, or sibling, whether biological or legally adopted)
- Enrolled in a concurrent research study judged not to be scientifically or medically compatible with the study of the CNRC.
- Intentionally restricting food intake
- Have poor veins impeding venous access
- Have any history of severe vasovagal syncope (blackouts or near faints) following blood draws
- Have claustrophobia
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Control Control Flavoured beverage powder with 3g glucose, twice a day Treatment Treatment Flavoured beverage powder with 20g resistant dextrin, twice a day
- Primary Outcome Measures
Name Time Method Glucose will be measured from fasting blood samples that will be collected at baseline (0 week), follow up visit (at 4 weeks) and at the end of the intervention (at 8 weeks). Mid intervention visit on Week 4 Fasting blood biochemistry from 14mL of venous blood sample collected via venipuncture.
Insulin will be measured from fasting blood samples that will be collected at baseline (0 week), follow up visit (at 4 weeks) and at the end of the intervention (at 8 weeks). Mid intervention visit on Week 4 Fasting blood biochemistry from 14mL of venous blood sample collected via venipuncture.
Insulin sensitivity will be measured from fasting blood samples that will be collected at baseline and final visit. Mid intervention visit on Week 4 Fasting blood biochemistry from 14mL of venous blood sample collected via venipuncture.
24 hour glycaemic response will measured in all participants during the baseline and at the end of the intervention (at 8 weeks). Inserted on the Baseline visit (0 week) (Days 1-3) and Final visit (8 week) (Days 1-3) On Day 1 of the baseline and final test visits, participants will come to the laboratory in the evening (1600h) for continuous glucose monitoring system, CGMS (IPro®2, Medtronic, USA) insertion.
- Secondary Outcome Measures
Name Time Method In a subset of 10 participants per study arm, energy expenditure will be measured in a whole room calorimeter on the baseline visit (0 week) and final visit (8 week), On Day 2 of baseline visit (0 week) for 9 hours Energy expenditure measured in a whole room calorimeter (WRC).
Subjective appetite sensations collected before breakfast and lunch, and 4 hours postprandially at every half an hour, using validated 100mm visual analog scale questionnaires. Before breakfast and lunch, and 4 hours postprandial breakfast and lunch, obtained every half an hour. VAS conducted on Day 2 of baseline (0 week) and final visit (8 week). Subjective appetite sensations collected using validated 100mm visual analog scale questionnaires. Four questions on hunger, fullness, desire to eat, prospective consumption. Questions anchored at 0 mm being the "least" and at 100 mm being "most". For example, for prospective consumption " How much food do you think you can eat now?", at 0mm (nothing at all) to 100 mm (a large amount). Results captured electronically using the software AVAS (available at: http://www.nrlc-group.net/software/AdaptiveVisual.php).
Lipids will be measured measured from fasting blood samples that will be collected at baseline (0 week), follow up visit (at 4 weeks) and at the end of the intervention (at 8 weeks). Mid intervention visit on Week 4 Fasting blood biochemistry from 14mL of venous blood sample collected via venipuncture.
Trial Locations
- Locations (1)
Clinical Nutrition Research Centre (CNRC)
🇸🇬Singapore, Singapore