Longitudinal Study of the GLUcagon REsponse to Hypoglycemia in Children and Adolescents With New-onset Type 1 DIAbetes

A regiszterben nem jelölt feltételek

• WP1 :
• Inclusion criteria:
  • De novo type 1 diabetic patient, as per ISPAD criteria;
  • Symptoms of hyperglycemia: polyuria-polydipsia-amaigrin +/- Acido ketosis.
  • Fasting blood glucose ≥126 mg/dL AND/OR blood glucose ≥200 mg/dL at 120 minutes of an OGTT AND/OR HbA1c ≥6.5% AND/OR a patient with symptoms of hyperglycemia/hyperglycemic crisis (see 8. a. 2.) with random blood glucose ≥200 mg/dL.
  • Presence in serum of one or more anti-islet autoantibodies (anti-insulin, anti-IA2, anti-GAD65, anti-ZnT8)
• Patients aged between 2 and 30 years
• Minimum weight: 17 kg (for blood samples)
• Male - female patients
• Free, written and oral consent.
  • Exclusion criteria:
• Child under 2 years of age.
• Taking treatments interfering with insulin secretion and sensitivity (e.g. sulfonylureas, diazoxide, somatostatin, methylxanthine derivatives, corticosteroids, biguanide, incretins).
• Presence of newly diagnosed (within 1 month) celiac disease (diagnosed on pathological duodenal biopsy) at inclusion.
• Autoimmune/autoinflammatory disease (other than type 1 diabetes) or active malignancy present at inclusion.
• Obesity defined as a BMI with a z-score >+3 SD.
• Hepatic, renal or adrenal insufficiency.
• History of bone marrow transplantation.
• History of diabetes after hemolytic-uremic syndrome.
• Epileptic patient
• Absence of anti-islet autoantibodies.
• Dysmorphia with suspicion of underlying genetic syndrome.
• Participation in another study in the previous 3 months, with administration of blood derivatives or potentially immunomodulating treatments.
  • WP2 :
• Inclusion Criteria:
  • De novo type 1 diabetic patient, as per ISPAD criteria;
  • Symptoms of hyperglycemia: polyuria-polydipsia-amaigrin +/- Acido ketosis.
  • Fasting blood glucose ≥126 mg/dL AND/OR blood glucose ≥200 mg/dL at 120 minutes of an OGTT AND/OR HbA1c ≥6.5% AND/OR a patient with symptoms of hyperglycemia/hyperglycemic crisis (see 8. a. 2.) with random blood glucose ≥200 mg/dL.
  • Presence in serum of one or more anti-islet autoantibodies (anti-insulin, anti-IA2, anti-GAD65, anti-ZnT8)
  • Patients aged between 2 years and 18 years (<18 years).
  • Male - female patients
  • Free, written and oral consent.
• Exclusion criteria:
  • Child under 2 years of age.
  • Taking treatments that interfere with insulin secretion and sensitivity (e.g. sulfonylureas, diazoxide, somatostatin, methylxanthine derivatives, corticosteroids, biguanide, incretins).
  • Presence of newly diagnosed (within 1 month) celiac disease (diagnosed on pathological duodenal biopsy) at inclusion.
  • Autoimmune/autoinflammatory disease (other than type 1 diabetes) or active malignancy present at inclusion.
  • Obesity defined as a BMI with a z-score >+3 SD.
  • Hepatic, renal or adrenal insufficiency.
  • History of bone marrow transplantation.
  • History of diabetes after hemolytic-uremic syndrome.
  • Absence of anti-islet autoantibodies.
  • Dysmorphia with suspected underlying genetic syndrome.
  • Participation in another study within the previous 3 months with administration of blood derivatives or potentially immunomodulatory treatments.
  • WP3 :
• Inclusion Criteria:
  • Adult older than 18 years.
  • Absence of blood marker of diabetes (Absence of antibodies, HbA1C <6.5%, C-peptide > 0.18 nmol/L, Fasting blood glucose < 100 mg/dL, blood glucose at any time < 200 mg/dL).
  • Be a first-degree relative with a patient being followed for diabetes (meeting ISPAD criteria).
  • Male - Female
  • Free written and oral consent
• Exclusion criteria:
  • Taking treatments that interfere with insulin secretion and sensitivity (e.g. sulfonylureas, diazoxide, somatostatin, methylxanthine derivatives, corticosteroids, biguanide, incretins).
  • Presence of newly diagnosed (within 1 month) celiac disease (diagnosed on pathological duodenal biopsy) at inclusion.
  • Autoimmune/autoinflammatory disease (other than type 1 diabetes) or active malignancy present at inclusion.
  • Obesity defined as a BMI with a z-score >+3 SD.
  • Hepatic, renal or adrenal insufficiency.
  • History of bone marrow transplantation.
  • History of diabetes after hemolytic-uremic syndrome.
  • Ischemic cardiomyopathy
  • Pregnant participant
  • Epileptic patient
  • WP4 :
• Inclusion Criteria:
  • Cohort of patients followed for cystic fibrosis:
• Pediatric patient between 2 and 18 years of age.
• Diagnosed with cystic fibrosis with impaired pancreatic endocrine function.
• Presents glucose homeostasis disorders (regular hypo/hyper-glycemia).
• Male - female patient
• Free, written and oral consent
  • Cohort of patients with (sub)total pancreatectomy:
• Pediatric patients between 2 and 18 years of age.
• Follow-up for total pancreatectomy or caudal pancreatectomy
• Presents disorders of carbohydrate homeostasis (regular hypo-/hyper-glycemia)
• Male - female patient
• Free, written and oral consent
  • Exclusion criteria:
• Child under 2 years of age.
• Body weight less than 17 kg.
• Taking treatments that interfere with insulin secretion and sensitivity (e.g. sulfonylureas, diazoxide, somatostatin, methylxanthine derivatives, corticosteroids, biguanide, incretins).
• Presence of newly diagnosed (within 1 month) celiac disease (diagnosed on pathological duodenal biopsy) at inclusion.
• Autoimmune/autoinflammatory disease (other than type 1 diabetes) or active malignancy present at inclusion.
• Obesity defined as a BMI with a z-score >+3 SD.
• Hepatic, renal or adrenal insufficiency.
• History of bone marrow transplantation.
• History of diabetes after hemolytic-uremic syndrome.
• Dysmorphia with suspected underlying genetic syndrome.
• Participation in another study within the last 3 months, with administration of blood derivatives or potentially immunomodulatory treatments.
  • WP5 :
• Inclusion Criteria:
  • Patient who has undergone insulin testing due to suspected growth hormone deficiency or adrenal insufficiency or hypopituitarism.
  • Patients between the ages of 2 years and 18 years (<18 years).
  • Male - female patient.
  • Free written and oral consent.
• Exclusion criteria:
  • Child under 2 years of age.
  • Body weight less than 17 kg.
  • Taking treatments that interfere with insulin secretion and sensitivity (e.g. sulfonylureas, diazoxide, somatostatin, methylxanthine derivatives, corticosteroids, biguanide, incretins).
  • Presence of newly diagnosed (within 1 month) celiac disease (diagnosed on pathological duodenal biopsy) at inclusion.
  • Autoimmune/autoinflammatory disease (other than type 1 diabetes) or active malignancy present at inclusion.
  • Obesity defined as a BMI with a z-score >+3 SD..
  • History of bone marrow transplantation.
  • History of diabetes after hemolytic-uremic syndrome.
  • Participation in another study within the last 3 months, with administration of blood derivatives or potentially immunomodulatory treatments.
  • WP6 :
• Inclusion Criteria:
  • Type 1 diabetic patient, as per ISPAD criteria;
  • Symptoms of hyperglycemia: polyuria-polydipsia-amaigrin +/- Acido ketosis.
  • Fasting blood glucose ≥126 mg/dL AND/OR blood glucose ≥200 mg/dL at 120 minutes of an OGTT AND/OR HbA1c ≥6.5% AND/OR a patient with symptoms of hyperglycemia/hyperglycemic crisis (see 8. a. 2.) with random blood glucose ≥200 mg/dL.
  • Presence in serum of one or more anti-islet autoantibodies (anti-insulin, anti-IA2, anti-GAD65, anti-ZnT8)
  • Patients aged between 2 and 18 years (<18 years).
  • Male - female patients
  • Free, written and oral consent.
• Exclusion criteria:
  • Child under 2 years of age.
  • Taking treatments interfering with insulin secretion and sensitivity (e.g. sulfonylureas, diazoxide, somatostatin, methylxanthine derivatives, corticosteroids, biguanide, incretins).
  • Autoimmune/autoinflammatory disease (other than type 1 diabetes) or active malignancy present at inclusion.
  • Obesity defined as a BMI with a z-score >+3 SD.
  • Hepatic, renal or adrenal insufficiency.
  • History of bone marrow transplantation.
  • History of diabetes after hemolytic-uremic syndrome.
  • Epileptic patient
  • Dysmorphia with suspicion of underlying genetic syndrome.
  • Participation in another study in the previous 3 months, with administration of blood derivatives or potentially immunomodulating treatments.
  • WP7 :
• Inclusion Criteria:
  • De novo type 1 diabetic patient, as per ISPAD criteria;
  • Symptoms of hyperglycemia: polyuria-polydipsia-amaigrin +/- Acido ketosis.
  • Fasting blood glucose ≥126 mg/dL AND/OR blood glucose ≥200 mg/dL at 120 minutes of an OGTT AND/OR HbA1c ≥6.5% AND/OR a patient with symptoms of hyperglycemia/hyperglycemic crisis (see 8. a. 2.) with random blood glucose ≥200 mg/dL.
  • Presence in serum of one or more anti-islet autoantibodies (anti-insulin, anti-IA2, anti-GAD65, anti-ZnT8)
  • Patients aged between 2 and 18 years
  • Minimum weight: 17 kg (for blood samples)
  • Male - female patients
  • Free, written and oral consent.
• Exclusion criteria:
  • Child under 2 years of age.
  • Taking treatments interfering with insulin secretion and sensitivity (e.g. sulfonylureas, diazoxide, somatostatin, methylxanthine derivatives, corticosteroids, biguanide, incretins).
  • Presence of newly diagnosed (within 1 month) celiac disease (diagnosed on pathological duodenal biopsy) at inclusion.
  • Autoimmune/autoinflammatory disease (other than type 1 diabetes) or active malignancy present at inclusion.
  • Obesity defined as a BMI with a z-score >+3 SD.
  • Hepatic, renal or adrenal insufficiency.
  • History of bone marrow transplantation.
  • History of diabetes after hemolytic-uremic syndrome.
  • Epileptic patient
  • Absence of anti-islet autoantibodies.
  • Dysmorphia with suspicion of underlying genetic syndrome.
  • Participation in another study in the previous 3 months, with administration of blood derivatives or potentially immunomodulating treatments.