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| Name | Class |
|---|---|
| Montana State Agricultural Experiment Station | UNKNOWN |
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Polyphenol-rich Haskap berries (Haskap) have untapped therapeutic potential to improve human health, and agricultural producers in northern U.S. states are poised to increase production if consumer demand increases. A critical knowledge gap is that little is known about the interactions between gut microbes and Haskap polyphenols to produce bioactive metabolites linked to downstream health impacts. Additionally, little is known about which Haskap varieties and harvest timing yield the greatest bioactive potential. This study aims to address these gaps by investigating the interaction of bioactive components in Haskap with gut microbiota and the resultant gut and serum metabolites, inflammation, and metabolic health, and then couple this with analysis of berries from different Haskap varieties and harvest times.
The long-term goal of this project is to form a partnership linking the health impacts of Haskap varieties and management practices that maximize health-promoting compounds to benefit both consumers and producers. Specific objectives of this study are to determine 1) the impact of Haskap on the gut microbiome and metabolome, 2) how gut microbiome composition and production of bioactive metabolites from Haskap impacts health and inflammation biomarkers, and 3) which Haskap varieties and growing practices increase production of health-promoting compounds.
To accomplish this, a four-armed, randomized, triple-blind, placebo controlled clinical trial of Haskap versus placebo for two separate groups with distinctly low and high metabolic syndrome status will be completed. Participants will be assessed for health biometrics, fat oxidation, gut microbiome composition, inflammation, and both the gut and serum metabolome before and after 8 weeks of intervention. Haskap fruit from twenty varieties will primarily come from the randomized block design field trial and fruit will be harvested at four stages of fruit maturity, then analyzed for polyphenol content. This part of the study will be replicated over three growing seasons.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo, Metabolically Healthy | Placebo Comparator | The placebo supplement will have no polyphenol content and will be carbohydrate-matched to the experimental group. A twice daily dose (10-12 hours apart) will be consumed for 8 weeks. |
|
| Haskap, Metabolically Healthy | Experimental | The haskap supplement will consist of a haskap berry smoothie. A twice daily dose (10-12) hours apart will be consumed for 8 weeks. |
|
| Placebo, Metabolically Unhealthy | Placebo Comparator | The placebo supplement will have no polyphenol content and will be carbohydrate-matched to the experimental group. A twice daily dose (10-12 hours apart) will be consumed for 8 weeks. |
|
| Haskap, Metabolically Unhealthy | Experimental | The haskap supplement will consist of a haskap berry smoothie. A twice daily dose (10-12) hours apart will be consumed for 8 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Haskap berry smoothie | Dietary Supplement | A smoothie blend of berries and water |
|
| Measure | Description | Time Frame |
|---|---|---|
| 16 subunit ribosomal ribonucleic acid (16S rRNA) gut microbial composition | fecal microbial composition | 8 weeks |
| Inflammation (pg/mL) | Serum interleukin (IL) IL-1B, IL-6, IL-10, IL-17, IL-23, tumor necrosis factor alpha (TNF-alpha), granulocyte-macrophage colony-stimulating factor (GM-CSF), interferon gamma (IFN-gamma) | 8 weeks |
| Lipid Panel (mg/dL) | Serum triglycerides (TG), low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, total cholesterol (CHOL), glucose (GLU) | 8 weeks |
| F2 isoprostanes | urine | 8 weeks |
| Untargeted metabolomic analysis | Serum metabolome | 8 weeks |
| Untargeted metabolomic analysis | Fecal metabolome | 8 weeks |
| Exercise Induced Fat Oxidation | Measurement in g/min of fat being utilized during exercise at 40-60% of the participants estimated VO2max | 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Acute Diet | 24-hour dietary recall using the Automated Self-Administered 24-hour Dietary. Assessment Tool (ASA24). Outcome is macronutrient and micronutrient composition of food entry. | 8 weeks |
| Habitual Diet |
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Inclusion Criteria for Metabolically Healthy Group:
All of the following:
Inclusion Criteria for Metabolically Unhealthy Group:
Required:
- Waist circumference: men ≥ 40, women ≥ 35 inches
AND ≥ 1 of the following:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Mary P Miles, PhD | Contact | 406-994-6678 | mmiles@montana.edu | |
| Zachary T Miller, PhD | Contact | (406) 961-3025 | zachariah.miller@montana.edu |
| Name | Affiliation | Role |
|---|---|---|
| Mary P Miles, PhD | Montana State University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Montana State University | Recruiting | Bozeman | Montana | 59717 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 42087172 | Derived | Chamberlin ML, Spears ML, Cooper G, Miller ZJ, Bothner B, Walk ST, Yeoman CJ, Miles MP. Impact of the gut microbiome on health impacts of Haskap berries: study protocol for a randomized control trial. Trials. 2026 May 5;27(1):451. doi: 10.1186/s13063-026-09759-4. |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Nov 5, 2024 | Nov 6, 2024 | Prot_000.pdf |
| SAP | No | Yes | No | Statistical Analysis Plan | Nov 5, 2024 | Nov 6, 2024 | SAP_001.pdf |
| ICF | No | No | Yes | Informed Consent Form | Nov 5, 2024 | Nov 6, 2024 | ICF_002.pdf |
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| ID | Term |
|---|---|
| D008659 | Metabolic Diseases |
| D007249 | Inflammation |
| D003141 | Communicable Diseases |
| ID | Term |
|---|---|
| D009750 | Nutritional and Metabolic Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D007239 | Infections |
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Placebo and haskap interventions were designed to be comparable in taste and appearance.
| Placebo comparator | Dietary Supplement | A smoothie with no polyphenolic content and matched in carbohydrate composition to the experimental haskap smoothie |
|
Habitual diet recall using Dietary History Questionnaire (DHQ) III (1 year recall). Outcome measures are healthy eating index (HEI) scores which include nine components based on adequacy (total fruit, whole fruit, total vegetables, greens and beans, whole grains, dairy, total protein foods, seafood and plant proteins, fatty acids) and four components based on moderation (refined grains, so-dium, added sugars, saturated fats). Each component is ranked 1-10 in order of increasing health. Total HEI score is reported as the sum of all components (100 possible points) with more points indicating increased health of diet.
| Baseline |
| Anthropometric Assessments | waist circumference (cm) | 8 weeks |
| Anthropometric Assessments | visceral adipose (L) | 8 weeks |
| Anthropometric Assessments | BMI (kg/m2) | 8 weeks |
| Anthropometric Assessments | fat free mass (%) | 8 weeks |
| Blood pressure | SBP/DBP (mmHG) | 8 weeks |
| Estimated VO2 max | Estimation of participants VO2 max (ml/k/min) from a Fatmax test | 0 weeks |
| D020969 | Disease Attributes |