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Recruiting NCT06384313

NCT06384313 Butyrate-enriched Triglyceride and Diabetes Prevention

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Clinical Trial Summary
NCT ID NCT06384313
Status Recruiting
Phase
Sponsor Maastricht University Medical Center
Condition Type 2 Diabetes
Study Type INTERVENTIONAL
Enrollment 48 participants
Start Date 2024-09-19
Primary Completion 2027-09-01

Trial Parameters

Condition Type 2 Diabetes
Sponsor Maastricht University Medical Center
Study Type INTERVENTIONAL
Phase N/A
Enrollment 48
Sex ALL
Min Age 20 Years
Max Age 70 Years
Start Date 2024-09-19
Completion 2027-09-01
Interventions
butyrate/hexanoate-enriched triglycerides

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Brief Summary

A body of animal studies as well as observational studies in humans demonstrated that butyrate is one SCFA that has pronounced positive effects on body weight control, inflammation, and insulin resistance. Even though the SCFA hexanoate is less researched, it has been shown to be involved in anti-inflammatory processes. Of note, acute human studies showed that fibre-induced metabolic improvements are linked to higher SCFA levels in the systemic circulation. It has been shown that a butyrate/hexanoate-enriched triglyceride oil enhanced systemic butyrate and hexanoate concentrations for a prolonged time. Yet, it remains to be determined whether a chronic increase in circulating butyrate and hexanoate concentrations translate into long-term benefits. In this study it is hypothesized that a chronic increase of butyrate/hexanoate in the circulation may improve host metabolism and metabolic health by improving adipose tissue function, reducing systemic lipid overflow and inflammation thereby increasing peripheral insulin sensitivity in individual with overweight/obesity and prediabetes.

Eligibility Criteria

Inclusion Criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: * Age 20-70 years * BMI ≥ 28 and \< 40 kg/m2 * Weight stable for at least 3 months * Normal blood pressure (systolic blood pressure 100-140 mmHg, diastolic blood pressure 60-90 mmHg) * One or more of the following criteria to determine disturbed glucose/insulin homeostasis * Fasting glucose 5.6-6.9 mmol/L * Two-hour glucose of 7.8-11.1 mmol/L * HOMA-IR ≥ 2.2 * HbA1c (5.7-6.4%) Exclusion Criteria: * Diabetes mellitus (type 1 or 2) * Cardiovascular disease: including no history or myocardial infarction, heart failure, arrhythmias * Pulmonary disease: no history of chronic obstructive pulmonary disease, emphysema, bronchitis, asthma * Kidney (e.g. kidney failure) or liver (e.g. cirrhosis, non-alcoholic fatty acid) malfunction * Gastrointestinal disease (no inflammatory bowel disease, irritable bowel syndrome or digestive disorders) or a history of abdominal surgery

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