Effects of Inulin and Resistant Starch on Postprandial SCFA, Glucose, Insulin, and Gut Hormone Responses in Lean and Overweight Subjects
This study aims to investigate how Inulin and Resistant Starch affect post-meal responses of certain gut hormones, glucose, insulin, and a specific fatty acid called acetate in both lean and overweight individuals.
Glucose
+ Inulin
+ Resistant Starch
Body Weight+5
+ Nutrition Disorders
+ Nutritional and Metabolic Diseases
Basic Science Study
Summary
Study start date: February 1, 2012
Actual date on which the first participant was enrolled.This study explores how two types of fermentable fibers, inulin and resistant starch, affect certain body responses in lean and overweight or obese individuals. The body naturally breaks down these fibers into short-chain fatty acids (SCFA), which have been linked to both obesity promotion and diabetes prevention. By comparing the effects of these fibers, the study aims to understand their role in health and disease better. This research is particularly important as it could help improve our understanding of how dietary fiber impacts metabolism and potentially lead to new strategies for managing obesity and diabetes. During this study, participants from both lean and overweight/obese groups consume a drink containing either glucose alone or glucose combined with either inulin or resistant starch. This happens on three separate occasions, following a randomized, single-blind design. The study measures the body's responses, specifically focusing on short-chain fatty acids, glucose, insulin, free fatty acids, and gut hormones. Participants also receive a standard lunch four hours after consuming the test drink. The primary outcome of interest is the incremental area under the serum acetate response curve, which is a measure of how much acetate, a type of short-chain fatty acid, is produced over time.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.25 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Basic Science Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Group II
Study Objectives
Primary Objectives
Secondary Objectives