Vegan meal kit delivery offers consumer convenience and has shown benefit in cardiometabolic parameters such as low-density lipoprotein cholesterol (LDL-c) and weight. The purpose of this study is to evaluate the impact of meal kit facilitated vegan diet on LDL-c and trimethylamine N-oxide (TMAO) when compared to an omnivorous diet control.
This study will compare the impact of a vegan diet to a non-vegan diet, when provided with meal kits in participants who are overweight. A vegan diet includes foods that come from plants and excludes foods that come from animals like meat, dairy, and eggs. Dietary modifications such as adopting a vegan diet are associated with significant improvements in cardiometabolic parameters, making it one of the preferred treatment options for obesity and preventing associated health conditions. Meal kits are packages that include: a quick (\~30-45 minutes) and simple recipe, all the recipe's required ingredients, and are conveniently delivered to patient homes. In this study, a facilitated vegan diet is defined as a change from an omnivorous diet to a vegan diet with the aid of boxed vegan meal kit delivery. A facilitated vegan diet has shown LDL-c and weight improvements over continuing an omnivorous diet in a preliminary study. TMAO, changes in gut microbiome, and compliance to dietary modification impact cardiovascular and overall health. TMAO is a diet dependent biomarker for CVD, as elevated TMAO levels are associated with a 62% increased risk of heart attack, stroke, or death. TMAO increases platelet hyperactivity, inflammation, and foam cell generation, all of which contribute to atherosclerosis and may explain the increased risk of CVD. Additionally, TMAO predicts risk of major adverse cardiovascular events independently of other cardiovascular risk factors. Consumption of animal products elevate TMAO levels due to its abundance of TMAO precursors: choline and carnitine. Chronic dietary red meat was associated with increased TMAO levels over white meat and non-meat protein. One study found that consuming plant-based alternative meat products improved TMAO levels over a mostly red meat diet. Both study interventions replaced protein sources but did not remove animal products such as eggs and dairy, which have conflicting evidence relative to TMAO. This study intervention will have participants adopt a full vegan diet, eliminating animal products. The gut microbiome plays a crucial role in converting dietary precursors into TMAO. TMAO levels post l-carnitine ingestion were significantly higher in patients on a long-term omnivorous diet vs patients on a long-term vegan or vegetarian diet. This suggests that the gut microbiome in a plant-based diet lowers the formation of TMAO via the diet. This study will explore changes in gut microbiome from a dietary intervention in relation to TMAO and explore if these changes are sustained after discontinuing a 4-week facilitated vegan diet. Additionally, changes in gut microbiome will be explored in relation to microbiota changes seen in other disease states such as anxiety, irritable bowel disease, and other inflammatory diseases. The impact of dietary modifications on controlling obesity and associated health conditions has room for improvement. Dietary modifications have long been one of the preferred treatments in obesity and CVD prevention, yet the obesity rates continue to rise. One potential area of improvement is compliance to dietary modification. This study will explore changes in food group restricted free diet patterns after a 4-week vegan meal kit intervention.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
70
Vegan boxed meal kits
Non-vegan boxed meal kits
David Grant U.S. Air Force Medical Center
Travis Air Force Base, California, United States
Change between intervention arms in baseline adjusted LDL-c at 4 weeks
Change in LDL-c
Time frame: 4 weeks
Change between intervention arms in baseline adjusted TMAO at 4 weeks
Change in TMAO
Time frame: 4 weeks
Change between intervention arms in baseline adjusted LDL-c at 8 weeks
Change in LDL-c
Time frame: 8 weeks
Change between intervention arms in baseline adjusted LDL-c at 12 weeks
Change in LDL-c
Time frame: 12 weeks
Change between intervention arms in baseline adjusted TMAO at 8 weeks
Change in TMAO
Time frame: 8 weeks
Change between intervention arms in baseline adjusted TMAO at 12 weeks
Change in TMAO
Time frame: 12 weeks
Change between intervention arms in baseline adjusted lipid panel parameters at 4 weeks
Change in lipid panel
Time frame: 4 weeks
Change between intervention arms in baseline adjusted lipid panel parameters at 8 weeks
Change in lipid panel
Time frame: 8 weeks
Change between intervention arms in baseline adjusted lipid panel parameters at 12 weeks
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Change in lipid panel
Time frame: 12 weeks
Change between intervention arms in baseline adjusted BMI at 4 weeks
Weight and height will be combined to report BMI in kg/m\^2
Time frame: 4 weeks
Change between intervention arms in baseline adjusted BMI at 8 weeks
Weight and height will be combined to report BMI in kg/m\^2
Time frame: 8 weeks
Change between intervention arms in baseline adjusted BMI at 12 weeks
Weight and height will be combined to report BMI in kg/m\^2
Time frame: 12 weeks
Change between intervention arms in baseline adjusted blood pressure at 4 weeks
Measured with Sphygmocor device, both systolic and diastolic blood pressures
Time frame: 4 weeks
Change between intervention arms in baseline adjusted blood pressure at 8 weeks
Measured with Sphygmocor device, both systolic and diastolic blood pressures
Time frame: 8 weeks
Change between intervention arms in baseline adjusted blood pressure at 12 weeks
Measured with Sphygmocor device, both systolic and diastolic blood pressures
Time frame: 12 weeks
Change between intervention arms in baseline adjusted hemoglobin A1c at 4 weeks
Change in hemoglobin A1c
Time frame: 4 weeks
Change between intervention arms in baseline adjusted hemoglobin A1c at 8 weeks
Change in hemoglobin A1c
Time frame: 8 weeks
Change between intervention arms in baseline adjusted hemoglobin A1c at 12 weeks
Change in hemoglobin A1c
Time frame: 12 weeks