Resistant Starch Wheat for Improved Metabolic Health
Study Details
Study Description
Brief Summary
The objective of this study is to determine the effect of wheat enriched in resistant starch (RS) on the generation of fermentation products by the lower gut microbes, the fecal microbiota profile, intestinal metabolites, and the glycemic response to a test meal compared to regular wheat.
Condition or Disease | Intervention/Treatment | Phase |
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N/A |
Detailed Description
Resistant starch (RS) is a type of dietary fiber that provides fermentable carbohydrate (FC) in the lower bowel yielding positive effects on postprandial glycemia and weight management as well as digestive tract health. RS is defined as the portion of starch resistant to digestion by amylases, allowing it to reach the distal intestine where it can be fermented by the resident intestinal microbiota. A limited number of human studies using RS from high amylose corn have demonstrated that RS increases synthesis of gut peptides that improve glucose homeostasis and insulin secretion. Based on these studies, the FDA has recently approved the following health claims for resistant starch derived from corn (RS2): lowering of blood glucose, blood cholesterol, and blood pressure; increased mineral absorption; improved laxation; and reduced energy intake. The purpose in the proposed "proof of concept" study here is to show that RS provided in the form of wheat flour products has similar beneficial effects. The investigators aim to further explore the effect of RS on the gut microbiota. The intestinal microbiome is comprised of over one trillion bacterial cells comprised of approximately one thousand species that perform diverse functions ranging from energy harvest, angiogenesis, immunomodulation, and regulation of mood and behavior. Some of the major products of bacterial metabolism include acetate, propionate, and butyrate, the major short chain fatty acids (SCFA). These bioactive fermentation products have been associated with improved glucose homeostasis, attributed, in part, by their interactions with receptors on intestinal cells to augment secretion of glucagon-like peptide-1 (GLP-1), an incretin hormone known to stimulate insulin secretion.
This study is a randomized, cross-over design consisting of two 1-week dietary intervention periods as well as a 2-week washout period in between. Subjects will be randomly assigned to receive either RS wheat first or regular wheat first, then will be crossed over to the opposite treatment following a 2-week washout period. Wheat products made from RS wheat and regular wheat will be provided and the volunteers will be instructed to incorporate the products into their usual diet for 7 days. This study will probe the associations between the gut microbiota profiles, fermentation of RS wheat, microbial-mediated alterations in bile acids, and glycemia. The investigators will measure these effects in healthy, middle-aged humans using an interdisciplinary approach that integrates nutrition, microbiology, intestinal physiology, and analytical chemistry.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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Experimental: Group 1 Order of treatments: A. Resistant Starch Wheat B. Regular Wheat |
Dietary Supplement: Resistant Starch Wheat
The investigators will be testing high amylose wheat varieties developed by Arcadia Biosciences that have high levels of RS in the endosperm, the source of refined flour. Compared to regular wheat varieties with RS levels of less than 1%, Arcadia's wheat varieties contain between 16% and 34% RS.
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Experimental: Group 2 Order of treatments: A. Regular Wheat B. Resistant Starch Wheat |
Dietary Supplement: Resistant Starch Wheat
The investigators will be testing high amylose wheat varieties developed by Arcadia Biosciences that have high levels of RS in the endosperm, the source of refined flour. Compared to regular wheat varieties with RS levels of less than 1%, Arcadia's wheat varieties contain between 16% and 34% RS.
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Outcome Measures
Primary Outcome Measures
- Changes in Gut Microbiota Composition [Days 1, 7, 22, and 29]
Gut microbiota community composition will be determined by 16S ribosomal ribonucleic acid (rRNA) gene sequencing from stool samples
Secondary Outcome Measures
- Changes in Glucose Metabolism [0, 1, 2, and 3 hours postprandial]
Fasting and postprandial measures of blood glucose, insulin, GLP-1
- Changes in Gut Microbiota Metabolism [0, 0.5, 1, 1.5, 2, 2.5, 3 hours postprandial]
Fasting and postprandial measures of hydrogen and methane in breath
- Changes in Gut Microbiota Metabolism [0, 1, 2, and 3 hours postprandial]
Fasting and postprandial measures of SCFA and bile acids in plasma
- Evaluation of Consumer Acceptance [Days 8 and 30]
Participant-reported liking and taste
- Dietary Intake [Days 3, 5, 8, 25, 27, and 30]
24-hour dietary recalls
Eligibility Criteria
Criteria
Inclusion Criteria:
- Healthy adults. Healthy means that the candidate reports that s/he feels well and can perform normal activities.
Exclusion Criteria:
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BMI <18.5 and >39.9 kg/m2
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Presence of of untreated or uncontrolled metabolic diseases
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Presence of gastrointestinal disorders that could interfere with the study outcome (i.e. Crohn's disease, Irritable bowel syndrome, Colitis)
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Use of oral antibiotics within the past 3 months
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Presence of cancer or other serious chronic disease by self report
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Current use of prescribed or over the counter weight loss medications
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Pregnant
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Lactating
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Current use of tobacco
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Dietary restrictions that would interfere with consuming the intervention foods
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | Western Human Nutrition Research Center | Davis | California | United States | 95616 |
Sponsors and Collaborators
- USDA, Western Human Nutrition Research Center
- University of California, Davis
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 984621-1