Blood Pressure, Body Composition, Immune Function
Conditions
Brief summary
Accordingly, the purpose of this study is to evaluate the efficacy of 1) supplementation with Synbiotic (Plexus® Triplex), 2) commercially-available Probiotic, or 3) placebo control over 30 days on the gut microbiome, cardiometabolic health, body weight and body composition in healthy individuals.
Detailed description
Specific Aim 1. Explore the changes in the gut microbiome using 16s rRNA sequencing to determine total bacterial counts, microbial diversity (alpha- and beta-diversity), short chain fatty acid (SCFA) concentration, circulating inflammatory biomarkers and mucosal immunity as a result of synbiotic vs. probiotic vs. placebo control. Specific Aim 2. Document the functional changes in cardiometabolic health-related parameters; specifically, heart rate, heart rate variability (HRV), blood pressure (central and peripheral), vascular stiffness (augmentation index, AIx, and pulse wave velocity, PWV), body weight and composition, blood glucose and lipids as a result of synbiotic vs. probiotic vs. placebo control. Specific Aim 3. Characterize the impact of synbiotic vs. probiotic vs. placebo control on perceptions of fullness/hunger, self-reported gastrointestinal health (questionnaire), and mood states. Hypothesis: We hypothesize that the synbiotic will result in greater changes in total gut bacterial count, microbial diversity, SCFA, while reducing circulating markers of inflammation and increasing determinants of mucosal immunity. Second, the synbiotic will result in greater enhancement of cardiometabolic health over the probiotic or placebo control. Third, the synbiotic will maintain or improve perceptual indicators of fullness/hunger, gastrointestinal health, and mood states over probiotic alone or placebo control.
Interventions
DIETARY_SUPPLEMENTSynbiotic, Probiotic, Placebo
Use of dietary supplements to improve gut microbiome and cardiometabolic health
Sponsors
Skidmore College
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)
Masking description
Actives and placebos made by 3rd party in discreet containers inconspicuously labeled.
Intervention model description
Randomized placebo-controlled double-blind parallel study
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
* To be included participants must be healthy, weight stable (± 4.4 lb for \> 6 months prior), and 18 to 60 years of age. Participants will be expected to be relatively healthy without uncontrolled chronic disease (e.g. cardiovascular, metabolic, or pulmonary) and 1 or fewer positive risk factors for cardiovascular disease (e.g. high blood pressure, high cholesterol, etc.) as described by the American College of Sports Medicine/American Heart Association Criteria and presented in the table 1 below. Per College policy, participants who are visitors are required to be fully vaccinated against COVID-19, including a booster, and participants who are faculty, staff or students are required to be fully vaccinated against COVID-19 and receive a booster by January 24, 2022 or within 30 days of becoming eligible, unless a medical or religious exemption has been granted. Participants will be screened for eligibility by health history form in person baseline measurements are made (Figure 1). To ensure greater inclusion, ecological validity and representation, women will be included in this study; however, we will not control for menstrual cycle phase, but will document for possible statistical consideration.
Exclusion criteria
* Given the focus of the study those who are currently, or have recently used (\<3 months), oral antibiotics or have diagnosed irritable bowel syndrome or gut/bowel maladies (short bowel syndrome, etc.) will be excluded. Subjects who present with 2 or more CVD risk factors (table above) or have uncontrolled/overt cardiovascular, pulmonary, or metabolic disease (Diabetes Mellitus), or recent blood donation (\<8 weeks) will be excluded. Those who have cancer or are being treated for cancer will also be excluded. Women who are currently pregnant, breastfeeding, attempting to conceive, or amenorrheic (not associated with menopause or use of contraceptive medications) will also be excluded from the study. Anyone who is being treated for hypothyroid with levothyroxine will be excluded as one of the supplement ingredients, chromium polynicotinate, may interfere with this medication . Anyone with severe illness or compromised or suppressed immune system (e.g. taking immune suppressants, chronic viral infection or treatment) will be excluded. Anyone recently diagnosed (\<1yr) with an eating disorder or food allergies will also be excluded.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Gut microbial diversity | Baseline, 15 days, 30 days | alpha- and beta-diversity |
| Gut microbial count | Baseline, 15 days, 30 days | Gut microbial species identification and quantification |
| Short Chain fatty acids | Baseline, 15 days, 30 days | Short Chain Fatty Acid concentration |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Heart Rate Variability | Baseline, 15 days, 30 days | Time and frequency domain HRV parameters |
| Dietary Analysis | Baseline, 15 days, 30 days | Dietary analysis using the ASA24 system |
| Blood pressure | Baseline, 15 days, 30 days | Brachial and estimated central blood pressure |
| Blood Lipids | Baseline, 15 days, 30 days | Blood lipid profile using Cholestech system |
| Salivary inflammation profile | Baseline, 15 days, 30 days | Salimetrics ELISA for key inflammatory and immunity parameters (SIgA, IgG, alpha amylase, cortisol, c-reactive protein) |
| Body Composition | Baseline, 15 days, 30 days | Body mass, % body fat using Tanita RD 545 |
| Vascular Stiffness | Baseline, 15 days, 30 days | Aortic vascular stiffness |
| Vascular reactivity | Baseline, 15 days, 30 days | Using the near-infrared vascular occlusion test |
Countries
United States
Contacts
Primary ContactSteve Ives, PhD
Outcome results
None listed