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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05291013
Acronym
ADIDYS
Enrollment
45
Registered
2022-03-22
Start date
2022-07-01
Completion date
2023-04-30
Last updated
2022-03-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adipose Tissue Dysfunction Type 2 Diabetes Mellitus Bariatric Surgery

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.

Interventions

PROCEDUREGastric byspass

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

Sponsors

Odense University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 65 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Markers in adipose tissue dysfunction3 yearChanges in morphology of adipocytes, mRNA expression and protein abundance in adipocytes
Muscular insulin sensitivity3 yearChanges in muscle mRNA expression and protein abundance

Secondary

MeasureTime frameDescription
Rate of disposal3 yearChanges in rate of disposal
Body composition3 yearChanges in body composition
Metabolomics3 yearChanges in metabolomics

Countries

Denmark

Contacts

Primary ContactKristoffer Jensen Kolnes, MD, PhD-student
kristoffer.jensen.kolnes@rsyd.dk+4593988934
Backup ContactKurt Højlund, Professor, consultant doctor
Kurt.Hoejlund@rsyd.dk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026