This study is focused on assessing potential health benefits of daily consumption of potatoes, specifically its resistant starch content (i.e. nondigestible carbohydrate), on blood vessel and gut health function in adults with metabolic syndrome. It is expected that the daily consumption of potatoes for two weeks, within a diet that follows the Dietary Guidelines for Americans, will improve blood vessel function in association with decreasing gut permeability ("leaky gut") that results in the absorption of bacterial toxins that reside in the intestine. Outcomes will therefore support dietary recommendations for potatoes to support vascular and gastrointestinal health.
Cardiovascular disease is a major public health concern in the United States, where it accounts for 1 in 4 deaths every year. Vascular endothelial dysfunction is an early event leading to cardiovascular disease and can be caused by postprandial hyperglycemia. Cardiovascular disease is also characterized by metabolic endotoxemia. Metabolic endotoxemia describes increased circulating levels of gut-derived endotoxin (lipopolysaccharide; a bacterial product derived from Gram-negative bacteria in the intestines) that results from gut barrier dysfunction, a phenomenon that is common in metabolic syndrome. Studies in animals and humans have shown that consumption of resistant starch (a type of carbohydrate found in potatoes among other foods) can help to improve vascular and gut health. This clinical trial will therefore investigate the extent to which potatoes can improve microbiota composition, alleviate metabolic endotoxemia, and improve vascular function. It is hypothesized that 2-week daily ingestion of potatoes within a diet that meets the Dietary Guidelines for Americans will limit metabolic endotoxemia by decreasing gut barrier permeability and alleviating gut dysbiosis while separately improving vascular function by limiting postprandial hyperglycemia. This study will address the following objectives: 1) define changes in gut barrier function in association with improved gut microbiota composition, increased fecal short chain fatty acid (SCFA) production, and decreased serum endotoxin, 2) define changes in postprandial glycemic responses and endotoxemia, and 3) define changes in gut hormones that promote glycemic control and changes in markers of oxidative stress in relation to improvements in endothelial vascular function, all following 2-week potato consumption. To test the hypothesis, all participants will complete a randomized cross-over trial where they will receive a potato or bagel along with a diet that meets the Dietary Guidelines for Americans for 2 weeks. They will then undergo a 2-h postprandial study to define the influence of potato consumption on vascular function, glycemic control, and endotoxin translocation. Upon completing the intervention, participants will undergo a gut permeability test, fecal samples will be collected for microbiota composition analysis, and blood samples will be collected to assess endotoxin and inflammatory markers. Upon successfully completing this study, it is anticipated that chronic consumption of potatoes will be demonstrated to be an effective dietary strategy to reduce metabolic endotoxemia, improve gut health, and improve vascular function.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Enrollment
32
Ohio State University
Columbus, Ohio, United States
Endotoxin
Fasting serum endotoxin concentration
Time frame: Day 14
Vascular Endothelial Function
Area under curve (change from baseline) for brachial artery flow-mediated dilation (FMD). The unit for FMD is %, which is calculated as: \[vessel diameter in millimeters (post-occlusion) - vessel diameter in millimeters (pre-occlusion)\] / vessel diameter in millimeters (pre-occlusion) x 100. FMD(%) is then used to caluclate area under the curve based on independent measures of FMD at 0-120 minutes)
Time frame: Day 14 Postprandial (0, 30, 60, 90, 120 minutes)
Fasting Glucose Day 0
Fasting plasma glucose
Time frame: Fasting glucose on Day 0
Fasting Glucose Day 14
Fasting plasma glucose Day 14
Time frame: Fasting glucose on Day 14
Fasting Insulin Day 0
Fasting plasma insulin
Time frame: Fasting insulin on Day 0
Fasting Insulin Day 14
Fasting plasma insulin Day 14
Time frame: Fasting insulin on Day 14
Postprandial Insulin
Plasma insulin concentration area under curve change from baseline
Time frame: Day 14 postprandial (0, 30, 60, 90, 120 minutes)
Postprandial Glucose
Postprandial plasma glucose concentration area under curve change from baseline
Time frame: Day 14 postprandial (0, 30, 60, 90, 120 minutes)
Fasting Endotoxin
Fasting serum endotoxin concentration
Time frame: Day 0
Postprandial Endotoxin
Postprandial serum endotoxin concentration area under curve change from baseline
Time frame: Day 14 postprandial (0, 30, 60, 90, 120 minutes)
Lactulose/Mannitol Ratio
Urinary concentration of the non-digestible sugars lactulose/mannitol (mg/mg)
Time frame: Day 14, 0-5 hours post-consumption of sugar probes
Sucralose/Erythritol Ratio
Urinary concentration of the non-digestible sugars sucralose/erythritol
Time frame: Day 14, 6-24 hours post-consumption of sugar probes
Fecal Butyrate
Fecal concentration of butyrate
Time frame: Day 14
Fecal Acetate
Fecal concentration of acetate
Time frame: Day 14
Fecal Propionate
Fecal concentration of propionate
Time frame: Day 14
Postprandial Cholecystokinin
Plasma CCK area under curve change from baseline
Time frame: Day 14 postprandial (0, 30, 60, 90, 120 minutes)
Fasting Cholecystokinin
Fasting plasma concentration of CCK
Time frame: Day 14
Postprandial NOx
Plasma total nitrite/nitrate area under curve change from baseline
Time frame: Day 14 postprandial (0, 30, 60, 90, 120 minutes)
Fasting NOx
Fasting plasma concentration of nitrite/nitrate
Time frame: Day 14
Postprandial Malondialdehyde (MDA)
Plasma MDA concentration, biomarker of oxidative stress area under curve change from baseline
Time frame: Day 14 postprandial (0, 30, 60, 90, 120 minutes)
Fasting Malondialdehyde (MDA)
Fasting plasma MDA concentration, biomarker of oxidative stress
Time frame: Day 14
Fasting Vascular Endothelial Function
Fasting flow-mediated dilation of the brachial artery. Measure is calculated as: \[post-occlusion vessel diameter (mm) - pre-occlusion vessel diameter (mm) / pre-occlusion vessel diameter (mm)\] x 100
Time frame: Day 14
Vitamin C
Fasting vitamin C concentration, biomarker of oxidative stress
Time frame: Day 14
cIMT
Carotid intima-media thickness. Mean thickness of left and right carotid artery intima media.
Time frame: Day 14
Day 14 BMI
Body mass index calculated as kg weight per meters squared
Time frame: Day 14
Day 0 Waist Circumference
Waist circumference in centimeters
Time frame: Day 0
Day 14 Waist Circumference
Waist circumference in centimeters
Time frame: Day 14
Day 0 Diastolic Blood Pressure
Diastolic blood pressure on Day 0
Time frame: Day 0
Day 14 Diastolic Blood Pressure
Diastolic blood pressure on Day 14
Time frame: Day 14
Day 0 Systolic Blood Pressure
Systolic blood pressure on Day 0
Time frame: Day 0
Day 14 Systolic Blood Pressure
Systolic blood pressure on Day 14
Time frame: Day 14
Day 0 BMI
Body mass index calculated as kg weight per meters squared
Time frame: Day 0
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