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Adipose Tissue Heterogeneity and Its Link to Type 2 Diabetes (DiaSpax)

Primary Purpose

Type 2 Diabetes

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Pioglitazone 45 mg
Empagliflozin 25 MG
Semaglutide 7 MG
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes

Eligibility Criteria

30 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Signed informed consent
  • BMI 27-35 kg/m2
  • HbA1c 48 mmol/mol or higher
  • For fertile women, effective contraception

Exclusion Criteria:

  • HbA1c 65 mmol/mol or higher
  • Established cardiovascular disease and/or heart failure
  • Severe psychiatric condition
  • Active alcoholism
  • Insulin treatment
  • Anticoagulant therapy (vitamin K antagonists or equivalent)
  • Pregnancy, lactation
  • Positive GAD or IA2 antibodies
  • Low C-peptide/glucose ratio (less than 2 measured as pmol/mg per dL)
  • NT-proBNP above the upper normal reference value
  • Kidney disease
  • Liver disease or hepatic values over twice the upper reference value
  • Severe concomitant disease including ongoing cancer

Sites / Locations

  • Karolinska University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

Pioglitazone

Empagliflozin

Semaglutide

Arm Description

Pioglitazone is known to affect fat cells and is used as an active comparator. It reduces HbA1c but increase fat mass slightly. We hypothesize that pioglitazone may have particular benefits in individuals with a specific adipose cellularity.

Empagliflozin reduces HbA1c and increase lipolysis possibly due to increased glucagon secretion. It also reduces fat mass weight to a minor degree.

Semaglutide reduces body weight, including fat mass, to a more significant degree than empagliflozin but has no known direct effects on adipose tissue.

Outcomes

Primary Outcome Measures

Changes in fat cell lipolysis after 6 months of treatment
Change in isoprenaline-induced (over basal) lipolysis in isolated fat cells

Secondary Outcome Measures

Changes in fat cell heterogeneity after 6 months of treatment
Changes in the adiponectin/leptin mRNA expression ratio in adipose tissue measured by quantitative PCR

Full Information

First Posted
August 10, 2022
Last Updated
October 2, 2023
Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05501483
Brief Title
Adipose Tissue Heterogeneity and Its Link to Type 2 Diabetes
Acronym
DiaSpax
Official Title
Adipose Tissue Heterogeneity and Its Link to Type 2 Diabetes: A Randomized Open Intervention Study That Compares Empagliflozin, Pioglitazone and Semaglutide
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 8, 2023 (Actual)
Primary Completion Date
September 1, 2024 (Anticipated)
Study Completion Date
December 31, 2032 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
People with newly diagnosed type 2 diabetes treated with metformin that have not reached their HbA1c target (49-64 mmol/mol) will be recruited to the study. If they fulfill the inclusion and none of the exclusion criteria, they will be, after signing informed consent, randomized to a six-month intervention with either pioglitazone, empagliflozin or semaglutide. Fat biopsies are obtained from the subcutaneous abdominal area before and after a hyperinsulinemic-euglycemic clamp at baseline and after six months. Participants are regularly followed during this the intervention. The overall goal is to determine how antidiabetic-drugs affect white adipose tissue cellularity and whether adipose heterogeneity impacts on drug response. The primary outcome measure is the change in fat tissue lipolysis (glycerol release in isolated fat cells after hormone stimulation) before and after treatment.
Detailed Description
A detailed description of the protocol has been approved by the Swedish Medical Products Agency and the study is registered as EudraCT: 2021-002367-21.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants are recruited to either of three groups where they receive (in addition to metformin) any of the three study drugs.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pioglitazone
Arm Type
Active Comparator
Arm Description
Pioglitazone is known to affect fat cells and is used as an active comparator. It reduces HbA1c but increase fat mass slightly. We hypothesize that pioglitazone may have particular benefits in individuals with a specific adipose cellularity.
Arm Title
Empagliflozin
Arm Type
Experimental
Arm Description
Empagliflozin reduces HbA1c and increase lipolysis possibly due to increased glucagon secretion. It also reduces fat mass weight to a minor degree.
Arm Title
Semaglutide
Arm Type
Experimental
Arm Description
Semaglutide reduces body weight, including fat mass, to a more significant degree than empagliflozin but has no known direct effects on adipose tissue.
Intervention Type
Drug
Intervention Name(s)
Pioglitazone 45 mg
Intervention Description
Starts with 45 mg
Intervention Type
Drug
Intervention Name(s)
Empagliflozin 25 MG
Intervention Description
Starts with 25 mg
Intervention Type
Drug
Intervention Name(s)
Semaglutide 7 MG
Intervention Description
Starts with 3 mg daily for the first 2 weeks
Primary Outcome Measure Information:
Title
Changes in fat cell lipolysis after 6 months of treatment
Description
Change in isoprenaline-induced (over basal) lipolysis in isolated fat cells
Time Frame
Baseline and after six months intervention
Secondary Outcome Measure Information:
Title
Changes in fat cell heterogeneity after 6 months of treatment
Description
Changes in the adiponectin/leptin mRNA expression ratio in adipose tissue measured by quantitative PCR
Time Frame
Baseline and after six months intervention
Other Pre-specified Outcome Measures:
Title
Changes in tissue cellularity after 6 months of treatment (explorative outcome)
Description
Changes in adipose tissue cellularity measured by single-cell transcriptomic analyses of fat tissue biopsies
Time Frame
Baseline and after six months intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Signed informed consent BMI 27-35 kg/m2 HbA1c 48 mmol/mol or higher For fertile women, effective contraception Exclusion Criteria: HbA1c 65 mmol/mol or higher Established cardiovascular disease and/or heart failure Severe psychiatric condition Active alcoholism Insulin treatment Anticoagulant therapy (vitamin K antagonists or equivalent) Pregnancy, lactation Positive GAD or IA2 antibodies Low C-peptide/glucose ratio (less than 2 measured as pmol/mg per dL) NT-proBNP above the upper normal reference value Kidney disease Liver disease or hepatic values over twice the upper reference value Severe concomitant disease including ongoing cancer
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mikael Ryden, MD, PhD
Phone
+46736995215
Email
mikael.ryden@ki.se
First Name & Middle Initial & Last Name or Official Title & Degree
Jesper Bäckdahl, MD, PhD
Phone
+46702297237
Email
jesper.backdahl@ki.se
Facility Information:
Facility Name
Karolinska University Hospital
City
Stockholm
ZIP/Postal Code
14186
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mikael Rydén, MD, PhD
Phone
0736995215
Email
mikael.ryden@ki.se
First Name & Middle Initial & Last Name & Degree
Jesper Bäckdahl, MD, PhD
Phone
+46702297237
Email
jesper.backdahl@ki.se
First Name & Middle Initial & Last Name & Degree
Niklas Mejhert, PhD
First Name & Middle Initial & Last Name & Degree
Daniel P Andersson, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
According to the ethical approval, we are not allowed to share participant data that can allow identification of the individual participants. We will present data at a group level and anonymized data in the publications that are planned to result from this study.

Learn more about this trial

Adipose Tissue Heterogeneity and Its Link to Type 2 Diabetes

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