search
Back to results

Adipose Tissue Dysfunction in Type 2 Diabetes and Its Reversibility by Bariatric Surgery (ADIDYS)

Primary Purpose

Adipose Tissue Dysfunction Type 2 Diabetes Mellitus Bariatric Surgery

Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Gastric byspass
Sponsored by
Odense University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Adipose Tissue Dysfunction Type 2 Diabetes Mellitus Bariatric Surgery

Eligibility Criteria

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

Inclusion Criteria:

  • GAD65 antibody negative patients with T2D
  • Treated with either diet alone or diet in combination with metformin, DPP-4 inhibitors, sulphonylureas, GLP1-analogs or insulin (maximum 40 IE long - or intermediate acting insulin).
  • HbA1c < 70 mmol/l for diabetics and <48 mmol/l for obese.
  • Do not have any known diabetic complication (macroalbuminuria, proliferative retinopathy, neuropathy or cardiovascular disease).
  • The use of up to two antihypertensive drugs and one cholesterol lowering drug is allowed in patients with T2D and obese individuals.
  • Both patients with T2D and obese individuals should be eligible for bariatric surgery, and should be able and willing to discontinue all drugs for 1 week prior to the clamp studies
  • Except for the conditions mentioned above, the patients with T2D and the obese individuals should be healthy.
  • Lean controls should be healthy, lean and drug naive.
  • Obese and lean controls should have no first degree family history of diabetes.
  • All participants should be 30-65 years old.
  • All participants should be able to provide informed written consent.

Exclusion Criteria:

  • Any unknown disease or need for medication that occurs after inclusion.
  • Abnormal ECG, screening blood tests and/or severe hypertension (>160/100 mmHg).
  • Impaired glucose tolerance (IGT) or impaired fasting glucose in lean, healthy participants (2-hour plasma glucose > 7.8 mmol/l or fasting plasma glucose > 5.6 mmol/l).
  • Known pregnancy or positive beta-HCG in blood during screening.

Sites / Locations

  • Kristoffer Jensen KolnesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

No Intervention

Arm Label

Gastric bypass with T2DM

Gastric bypass without T2DM

Control group

Arm Description

Outcomes

Primary Outcome Measures

Markers in adipose tissue dysfunction
Changes in morphology of adipocytes, mRNA expression and protein abundance in adipocytes
Muscular insulin sensitivity
Changes in muscle mRNA expression and protein abundance

Secondary Outcome Measures

Rate of disposal
Changes in rate of disposal
Body composition
Changes in body composition
Metabolomics
Changes in metabolomics

Full Information

First Posted
March 14, 2022
Last Updated
March 14, 2022
Sponsor
Odense University Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT05291013
Brief Title
Adipose Tissue Dysfunction in Type 2 Diabetes and Its Reversibility by Bariatric Surgery
Acronym
ADIDYS
Official Title
Adipose Tissue Dysfunction in Type 2 Diabetes and Its Reversibility by Bariatric Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2022 (Anticipated)
Primary Completion Date
April 30, 2023 (Anticipated)
Study Completion Date
April 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Odense University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
ABSTRACT Background: Insulin resistance (IR) plays a major role in the pathogenesis of type 2 diabetes (T2D). Adipose tissue (AT) dysfunction leading to systemic low-grade inflammation and ectopic lipid deposition plays an important role in obesity-induced IR, but its role in T2D pathogenesis and to what extent insulin-sensitizing interventions can reverse AT dysfunction remain to be clarified. Hypothesis/aims: To test the hypotheses 1) that T2D is associated with exaggerated AT dysfunction compared with obesity alone, 2) that increased insulin sensitivity and remission of T2D after bariatric surgery is in part explained by improved AT function Research plan: Novel markers of exaggerated AT dysfunction will be identified and studied together with known markers of AT dysfunction in patients with T2D compared with non-diabetic obese and lean individuals. Then the effects of bariatric surgery on all these markers of AT dysfunction in obesity and T2D will be studied. Adipose tissue and skeletal muscle biopsies and blood samples will be used for 1) next generation RNA sequencing, 2) targeted analysis of mRNA and protein content/activities, 3) metabolomics, 4) morphological analysis and 5) analysis of adipokines/myokines. Abnormalities in T2D and changes in response to bariatric surgery will be related to substrate metabolism, insulin sensitivity and secretion and insulin signalling in muscle. Perspectives: This project provides novel insight into the role of AT dysfunction in T2D pathogenesis in humans and the potential of bariatric surgery to reverse AT dysfunction and improve insulin sensitivity. We ultimately expect that this will help us to identify novel pharmaceutical targets for the treatment of IR.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adipose Tissue Dysfunction Type 2 Diabetes Mellitus Bariatric Surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Gastric bypass with T2DM
Arm Type
Experimental
Arm Title
Gastric bypass without T2DM
Arm Type
Experimental
Arm Title
Control group
Arm Type
No Intervention
Intervention Type
Procedure
Intervention Name(s)
Gastric byspass
Intervention Description
Test will be before and 9-12 month after gastric bypass
Primary Outcome Measure Information:
Title
Markers in adipose tissue dysfunction
Description
Changes in morphology of adipocytes, mRNA expression and protein abundance in adipocytes
Time Frame
3 year
Title
Muscular insulin sensitivity
Description
Changes in muscle mRNA expression and protein abundance
Time Frame
3 year
Secondary Outcome Measure Information:
Title
Rate of disposal
Description
Changes in rate of disposal
Time Frame
3 year
Title
Body composition
Description
Changes in body composition
Time Frame
3 year
Title
Metabolomics
Description
Changes in metabolomics
Time Frame
3 year

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: GAD65 antibody negative patients with T2D Treated with either diet alone or diet in combination with metformin, DPP-4 inhibitors, sulphonylureas, GLP1-analogs or insulin (maximum 40 IE long - or intermediate acting insulin). HbA1c < 70 mmol/l for diabetics and <48 mmol/l for obese. Do not have any known diabetic complication (macroalbuminuria, proliferative retinopathy, neuropathy or cardiovascular disease). The use of up to two antihypertensive drugs and one cholesterol lowering drug is allowed in patients with T2D and obese individuals. Both patients with T2D and obese individuals should be eligible for bariatric surgery, and should be able and willing to discontinue all drugs for 1 week prior to the clamp studies Except for the conditions mentioned above, the patients with T2D and the obese individuals should be healthy. Lean controls should be healthy, lean and drug naive. Obese and lean controls should have no first degree family history of diabetes. All participants should be 30-65 years old. All participants should be able to provide informed written consent. Exclusion Criteria: Any unknown disease or need for medication that occurs after inclusion. Abnormal ECG, screening blood tests and/or severe hypertension (>160/100 mmHg). Impaired glucose tolerance (IGT) or impaired fasting glucose in lean, healthy participants (2-hour plasma glucose > 7.8 mmol/l or fasting plasma glucose > 5.6 mmol/l). Known pregnancy or positive beta-HCG in blood during screening.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kristoffer Jensen Kolnes, MD, PhD-student
Phone
+4593988934
Email
kristoffer.jensen.kolnes@rsyd.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Kurt Højlund, Professor, consultant doctor
Email
Kurt.Hoejlund@rsyd.dk
Facility Information:
Facility Name
Kristoffer Jensen Kolnes
City
Odense
ZIP/Postal Code
5000
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kristoffer J Kolnes, Doctor
Phone
93988934
Email
kristoffer.jensen.kolnes@rsyd.dk
First Name & Middle Initial & Last Name & Degree
Tine Hylle, secretary
Phone
+4523741691
Email
tine.hylle@rsyd.dk

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Adipose Tissue Dysfunction in Type 2 Diabetes and Its Reversibility by Bariatric Surgery

We'll reach out to this number within 24 hrs