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

NCT05291013 | Unknown

• 1 other identifier: S-20190162
• Study Type: interventional
• Target: 45
• Locations: 1 country
• Sites: 1

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.

Conditions

Adipose Tissue Dysfunction Type 2 Diabetes Mellitus Bariatric Surgery

Outcome Measures

Primary Outcomes (2)

• Markers in adipose tissue dysfunction

  Changes in morphology of adipocytes, mRNA expression and protein abundance in adipocytes

  3 year

• Muscular insulin sensitivity

  Changes in muscle mRNA expression and protein abundance

  3 year

Secondary Outcomes (3)

• Rate of disposal

  3 year

• Body composition

  3 year

• Metabolomics

  3 year

Study Arms (3)

Gastric bypass with T2DM

EXPERIMENTAL

Procedure: Gastric byspass

Gastric bypass without T2DM

EXPERIMENTAL

Procedure: Gastric byspass

Control group

NO INTERVENTION

Interventions

Gastric byspass PROCEDURE

Test will be before and 9-12 month after gastric bypass

Gastric bypass with T2DM; Gastric bypass without T2DM

Eligibility Criteria

• Age: 30 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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.

You may not qualify if:

• 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.

Sponsors & Collaborators

• Odense University Hospital: lead

Study Sites (1)

Kristoffer Jensen Kolnes

Odense, 5000, Denmark

RECRUITING

Central Study Contacts

Kristoffer Jensen Kolnes, MD, PhD-student

CONTACT

+4593988934; kristoffer.jensen.kolnes@rsyd.dk

Kurt Højlund, Professor, consultant doctor

CONTACT

Kurt.Hoejlund@rsyd.dk

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: MD, PhD-student

Study Record Dates

• First Submitted: March 14, 2022
• First Posted: March 22, 2022
• Study Start: July 1, 2022
• Primary Completion: April 30, 2023
• Study Completion: April 30, 2023
• Last Updated: March 22, 2022

Record last verified: 2022-03

Locations

DK (1)