Animal and Plant Proteins and Glucose Metabolism
- Conditions
- Glucose Metabolism DisordersMetabolic SyndromeMetabolic Syndrome, Protection Against
- Interventions
- Other: High plant protein isolateOther: High animal protein isolateOther: High plant protein whole foodOther: High animal protein whole food
- Registration Number
- NCT03994367
- Lead Sponsor
- University of Missouri-Columbia
- Brief Summary
The goal of this proposal is to determine the effect of a high protein diet in which the increase in protein intake is derived from different sources (animal vs plant and protein-rich whole foods vs protein isolates) on: i) liver and muscle insulin sensitivity; ii) the metabolic response to a meal, and iii) 24-h plasma concentration profiles of glucose, glucoregulatory hormones, and protein-derived metabolites purported to cause metabolic dysfunction.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 100
- age: ≥21 and ≤70 years;
- BMI: >24.5 and <32.5 kg/m2;
- habitual protein intake <0.9 g/kg/day (assessed on 2 weekdays and 2 weekend days by using the HealthWatch 360 app); and
- weight stable (i.e., ≤3% change) and untrained (≤150 min of structured exercise/week) for at least 2 months before entering the study.
- prediabetes or type 2 diabetes;
- evidence of chronic kidney disease by medical history or laboratory tests (glomerular filtration rate <60 ml/min/1.73 m2 or an albumin to creatinine ratio in urine ≥30 mg/g);
- vegetarians or vegans;
- intolerance or allergies to ingredients in the metabolic meal or intervention diet;
- take dietary supplements (e.g., pre- and probiotics, fiber, fish oil) or medications known to affect our study outcomes;
- received antibiotic or antifungal treatment (which affect the microbiome and therefore microbial metabolite production) 2 months before entering the study;
- consume tobacco products or excessive alcohol (women: >14 drinks/week; men: >21 drinks/week);
- evidence of significant organ system dysfunction or diseases (e.g., cirrhosis), and
- unwilling or unable to provide informed consent.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description High plant protein isolate High plant protein isolate - High animal protein isolate High animal protein isolate - High plant protein whole food High plant protein whole food - High animal protein whole food High animal protein whole food -
- Primary Outcome Measures
Name Time Method 24-hour plasma glucose concentration up to 12 weeks after the intervention Insulin sensitivity assessed as insulin-mediated glucose disposal during a hyperinsulinemic-euglycemic clamp procedure up to 12 weeks after the intervention
- Secondary Outcome Measures
Name Time Method Postprandial plasma glucose concentration up to 12 weeks after the intervention mTOR signaling (phospho-S6 content) in circulating monocytes up to 12 weeks after the intervention Endothelial function, assessed as reactive hyperemia index up to 12 weeks after the intervention Postprandial plasma insulin concentration up to 12 weeks after the intervention Postprandial plasma amino acid concentration up to 12 weeks after the intervention
Trial Locations
- Locations (1)
University of Missouri School of Medicine
🇺🇸Columbia, Missouri, United States