Type 1 Diabetes Mellitus Clinical Trial
— METYDIAOfficial title:
Mechanisms of Type 1 Diabetes Endophenotypes, by Cluster Analysis
The goal of this observational study consists of performing cluster analysis to decipher underlying disease mechanisms of type 1 diabetes in children and young adults. To this end, we will combine clinical, laboratory, genetic, transcriptomic, and metabolomic datasets of an extensively phenotyped cohort of children and young adults with type 1 diabetes. We will also assess the risk for cardiovascular diseases in this most vulnerable diabetes cohort.
Status | Recruiting |
Enrollment | 150 |
Est. completion date | February 1, 2026 |
Est. primary completion date | February 1, 2026 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 0 Years to 25 Years |
Eligibility | Inclusion Criteria (Type 1 Diabetic patients): - Informed consent as documented by signature - Patient's age: between 0 and 25 years old. - Children, adolescents, and young adult patients followed in diabetology. Exclusion Criteria (Type 1 Diabetic patients): - No exclusion criteria Inclusion Criteria (Controls): - Informed consent as documented by signature - Patient's age: 25 less than 6 years of age and 25 between 6 and 25 years old. - Healthy patient Exclusion Criteria (Controls): - Patient receiving treatment affecting metabolic control (ex: systemic corticoids, beta blocker, immunotherapy etc.) - Concomitant disease that may affect the analysis of the results (ex: cancer, active autoimmune disease requiring treatment) |
Country | Name | City | State |
---|---|---|---|
Switzerland | University Hospital of Geneva | Geneva |
Lead Sponsor | Collaborator |
---|---|
Pediatric Clinical Research Platform | University Hospital, Geneva, University of Geneva, Switzerland |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cluster analysis to decipher underlying mechanisms of type 1 diabetes | We will combine clinical, laboratory, genetic, transcriptomic, and metabolomic datasets of an extensively phenotyped cohort of type 1 diabetes patients (Children and young adults).
We will create clinical and genetic correlates with the following clinical parameters: Age at diabetes onset (years), disease duration (years), BMI (kg/m2), diabetes autoantibodies, C-peptide level (pmol/l) and decline over time, HbA1c (%), insulin dose (U/kg/d), ketoacidosis at disease onset (y/n), lipid levels (Total cholesterol, triglycerides, HLD, LDL, Lipoprotein(a)), macro- and microvascular complications, ethnicity, family history for diabetes, associated autoimmune diseases (e.g., autoimmune thyroiditis or celiac disease) and mixed meal tolerance test. |
blood sampling and analyses |
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