Sulfur Amino Acids, Energy Metabolism and Obesity
- Conditions
- Overweight and Obesity
- Interventions
- Other: High SAA dietOther: Low SAA diet
- Registration Number
- NCT04701346
- Lead Sponsor
- University of Oslo
- Brief Summary
The primary objective of the trial is to establish the effects of dietary sulfur amino acid (SAA) restriction on body weight, body composition and energy expenditure in humans.
- Detailed Description
Dietary SAA restriction is an established model for increasing lifespan and improving metabolic health in animal studies. Data from human studies are limited.
In this study the investigators will perform an 8-week dietary intervention with SAA restriction to characterise the effects on several parameters related to metabolic health including body weight, body composition, energy expenditure, lipid profile and gene expression profiles in adipose tissue. The aim is to translate findings from previous animal experiments to humans
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 61
- Healthy participants with overweight and obesity (BMI 27-35 kg/m2)
- Waist circumference > 80 cm for women and > 94 cm for men
- Smoking
- Presence of chronic disease
- Established co-morbidities
- Already on a vegan diet or have been the last month
- Pregnancy
- Breastfeeding the last 3 months
- Unstable body weight the last 3 months
- High intensity training > 3 times weekly
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description High SAA diet High SAA diet Dietary intervention Low SAA diet Low SAA diet Dietary intervention
- Primary Outcome Measures
Name Time Method Changes in body weight At baseline, 4 and 8 weeks Kilograms
- Secondary Outcome Measures
Name Time Method Changes in resting energy expenditure At baseline, 4 and 8 weeks Kilocalories
Changes in plasma concentrations of SAA and related intermediates and compounds At baseline, 4 and 8 weeks Sulfite, thiosulfate, rhodanide, sulfate, total aminothiols (homocysteine, cysteine, glutathione gamma-glutamylcysteine, cysteinylglycine, cysteamine), and fractions of total cysteine, total glutathione and total homocysteine, cystathionine, lanthionine, homolanthionine, taurine hypotaurine, sarcosine, hydrogen sulfide, S-adenosylmethionine and S-adenosylhomocysteine
Changes in concentrations of plasma lipid profile At baseline, 4 and 8 weeks Fatty acids, total cholesterol, LDL-cholesterol, HDL-cholesterol, triglycerides, ApoA1, ApoB
Changes in plasma concentrations of adipokines and appetite hormones At baseline, 4 and 8 weeks Leptin, adiponectin, gastrin, ghrelin, cholecystokinin (CCK), glucagon-like peptide (GLP-1), oxyntomodulin, gastric inhibitory peptide (GIP), peptide YY (PYY), and pancreatic peptide (PP).
Changes in fibroblast growth factor 21 (FGF21) At baseline, 4 and 8 weeks Serum concentrations
Changes in gut microbiota At baseline, 4 and 8 weeks Sequencing of fecal samples
Changes in body composition At baseline, 4 and 8 weeks Fat mass (kilograms) and lean mass (kilograms)
Changes in substrate oxidation At baseline, 4 and 8 weeks Respiratory quotient
Changes in urine concentrations of SAA and related intermediates and compounds At baseline, 4 and 8 weeks Including sulfite, thiosulfate, rhodanide, sulfate, total aminothiols (homocysteine, cysteine, glutathione gamma-glutamylcysteine, cysteinylglycine, cysteamine)
Changes in plasma makers of insulin sensitivity At baseline, 4 and 8 weeks Concentrations of glucose and insulin
Changes in biomarkers related to obesity and energy metabolism At baseline, 4 and 8 weeks Untargeted analyses of plasma, serum and tissue concentrations
Changes in gene expression At baseline, 4 and 8 weeks mRNA of proteins involved in SAA metabolism, lipid and energy metabolism in leucocytes and subcutaneous white adipose tissue samples
Vitamin status At baseline, 4 and 8 weeks Plasma concentrations of folate, B12 and methylmalonic acid (MMA)
Changes in short chain fatty acids At baseline, 4 and 8 weeks Fecal concentrations
Nitrogen balance At baseline, 4 and 8 weeks 24 h-urine urea nitrogen
Trial Locations
- Locations (1)
Centre for Clinical Nutrition, University of Oslo/Oslo University Hospital
🇳🇴Oslo, Norway