PreKeto: Pre-meals of 3-hydroxybutyrate in Type 2 Diabetes

Sponsor
University of Aarhus (Other)
Overall Status
Recruiting
CT.gov ID
NCT05581043
Collaborator
Steno Diabetes Center Aarhus, Aarhus University Hospital, Denmark (Other), Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Denmark (Other)
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Study Details

Study Description

Brief Summary

Hyperglycemia following meals in patients with type 2 diabetes mellitus (T2DM) is a common problem. Recently, our group found that oral consumption of the ketone metabolite, 3-hydroxybutyrate (3-OHB), effectively stimulates insulin secretion and delays gastric emptying.The aim of this study is to investigate the dose/response relationship between 3-OHB servings of 0, 10, 20 and 40 grams 30 minutes before an OGTT and, ii) investigate the role of timing by serving 20 grams of 3-OHB at different timepoints ahead of an OGTT (0, 30 and 60 minutes)

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: 3-hydroxybutyrate (3-OHB)
N/A

Detailed Description

Hyperglycemia following meals in patients with type 2 diabetes mellitus (T2DM) is a common problem, which can cause discomfort and fatigue but may also lead to diabetic complications. Small servings of macronutrients, especially protein-rich products, before a main meal (= pre-meals) has been shown to significantly lower postprandial glucose excursions in both healthy individuals and patients with T2DM. The reductions are primarily attributed the fact that protein stimulates insulin secretion and delays gastric emptying. The timing and dose of a premeal are essential for the glycemic reductions following a meal 4. Unfortunately, it often requires a rather large amount of protein (> 50 g) to facilitate clinically relevant reductions in postprandial glucose levels and a large protein intake may be unwanted for some patients (i.e., chronic kidney disease). Recently, our group found that oral consumption of the ketone metabolite, 3- hydroxybutyrate (3-OHB), effectively stimulates insulin secretion and delays gastricemptying. We have also shown that 3-OHB inhibits gluconeogenesis 6, which may further contribute to glucose-lowering effects. Two other clinical studies have shown that serving 3- OHB before an oral glucose tolerance test (OGTT) lowered glucose excursions in healthy volunteers and persons with impaired glucose tolerance. There are no current data available about the effect of 3-OHB premeals in T2DM patients, but we have preliminary data from an ongoing trial showing that 30 g of 3-OHB served 40 min before a mixed meal test effectively lowers postprandial glucose levels (around 3 mM) in patients with T2DM. The optimal dose and timing of 3-OHB pre-meals is unknown but important before initiating long-term clinical trials. We hypothesize that pre-melas of 3-OHB will affect postprandialglucose excursions in a time-dependent matter and servings 30 minutes before an OGTT is Deleted: 4 optimal in order to lower postprandial glucose excursions. The aim of this study is therefore to i) investigate the dose/response relationship between 3-OHB servings of 0, 10, 20 and 40 grams 30 minutes before an OGTT and, ii) investigate the role of timing by serving 20 grams of 3-OHB at different timepoints ahead of an OGTT (0, 30 and 60 minutes). The primary endpoint is glucose trajectories following the OGTT. This study will give important insight into the optimal dose and timing for potential future clinical long-term studies in patients with metabolic diseases (i.e., T2DM, obesity)

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
We will use a randomized cross-over design to investigate 10 volunteers with T2DM on six different occasions separated with at least one week.We will use a randomized cross-over design to investigate 10 volunteers with T2DM on six different occasions separated with at least one week.
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Pre-meals of 3-hydroxybutyrate for People With Type 2 Diabetes
Actual Study Start Date :
Jan 12, 2023
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: 0 gram 3-OHB 30 minutes before an OGTT

0 gram 3-OHB 30 minutes before an OGTT

Dietary Supplement: 3-hydroxybutyrate (3-OHB)
The aim of this study was therefore to i) investigate the dose/response relationship between 3-OHB servings of 0, 10, 20 and 40 grams 30 minutes before an OGTT and, ii) investigate the role of timing by serving 25 grams of 3-OHB at different timepoints ahead of an OGTT (0, 30 and 60 minutes).

Experimental: 10 gram 3-OHB 30 minutes before an OGTT

10 gram 3-OHB 30 minutes before an OGTT

Dietary Supplement: 3-hydroxybutyrate (3-OHB)
The aim of this study was therefore to i) investigate the dose/response relationship between 3-OHB servings of 0, 10, 20 and 40 grams 30 minutes before an OGTT and, ii) investigate the role of timing by serving 25 grams of 3-OHB at different timepoints ahead of an OGTT (0, 30 and 60 minutes).

Experimental: 20 gram 3-OHB 30 minutes before an OGTT

20 gram 3-OHB 30 minutes before an OGTT

Dietary Supplement: 3-hydroxybutyrate (3-OHB)
The aim of this study was therefore to i) investigate the dose/response relationship between 3-OHB servings of 0, 10, 20 and 40 grams 30 minutes before an OGTT and, ii) investigate the role of timing by serving 25 grams of 3-OHB at different timepoints ahead of an OGTT (0, 30 and 60 minutes).

Experimental: 40 gram 3-OHB 30 minutes before an OGTT

40 gram 3-OHB 30 minutes before an OGTT

Dietary Supplement: 3-hydroxybutyrate (3-OHB)
The aim of this study was therefore to i) investigate the dose/response relationship between 3-OHB servings of 0, 10, 20 and 40 grams 30 minutes before an OGTT and, ii) investigate the role of timing by serving 25 grams of 3-OHB at different timepoints ahead of an OGTT (0, 30 and 60 minutes).

Experimental: 20 gram 3-OHB 0 minutes before an OGTT

20 gram 3-OHB 0 minutes before an OGTT

Dietary Supplement: 3-hydroxybutyrate (3-OHB)
The aim of this study was therefore to i) investigate the dose/response relationship between 3-OHB servings of 0, 10, 20 and 40 grams 30 minutes before an OGTT and, ii) investigate the role of timing by serving 25 grams of 3-OHB at different timepoints ahead of an OGTT (0, 30 and 60 minutes).

Experimental: 20 gram 3-OHB 60 minutes before an OGTT

20 gram 3-OHB 60 minutes before an OGTT

Dietary Supplement: 3-hydroxybutyrate (3-OHB)
The aim of this study was therefore to i) investigate the dose/response relationship between 3-OHB servings of 0, 10, 20 and 40 grams 30 minutes before an OGTT and, ii) investigate the role of timing by serving 25 grams of 3-OHB at different timepoints ahead of an OGTT (0, 30 and 60 minutes).

Outcome Measures

Primary Outcome Measures

  1. Blood glucose following the OGTT [Blood samples will be obtained -60, -30, -15, 0, 15, 30, 45, 60, 90, 120, 150, 180 minutes from the OGTT]

    Change in blood glucose following the OGTT and compared between the different visits. Measured with laboratory kits.

Secondary Outcome Measures

  1. Plasma concentrations of 3-OHB, insulin, C-peptide, glucagon like peptide-1 (GLP-1), cholecystokinin (CCK), acetaminophen, free fatty acids along others. [Blood samples will be obtained -60, -30, -15, 0, 15, 30, 45, 60, 90, 120, 150, 180 minutes from the OGTT]

    Change in plasma concentrations of 3-OHB, insulin, C-peptide, glucagon like peptide-1 (GLP-1) following the OGGT and compared between the different visits. Measured with laboratory kits.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Older than 18 years of age

  • Type 2 diabetes diagnosis

  • No antiglycemic treatment or monotherapy with metformin

Exclusion Criteria:
  • Hba1c > 70

  • Severe liver disease (Child-Pugh score >10) or kidney disease (eGFR< 40 ml/min)

  • Anemia (Hgb < 6.5 mM)

  • History with pancreatitis

  • Practicing ketogenic diets (i.e., low-carb diet, fasting regime)

  • Inability to understand Danish or English

  • Ongoing cancer or other acute/chronic serious diseases (PI will determine)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Endocrinology and Internal Medicine Aarhus Denmark 8200

Sponsors and Collaborators

  • University of Aarhus
  • Steno Diabetes Center Aarhus, Aarhus University Hospital, Denmark
  • Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Denmark

Investigators

  • Study Director: Niels Møller, Professor, Professor

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Aarhus
ClinicalTrials.gov Identifier:
NCT05581043
Other Study ID Numbers:
  • V4_03052022
First Posted:
Oct 14, 2022
Last Update Posted:
Jan 19, 2023
Last Verified:
Oct 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 19, 2023