Screening for Genetic Forms of Diabetes in Convention of Care for Children and Adolescents With Diabetes (GENEPEDIAB) (GENEPEDIAB)

Background/Aims: Diabetes, which affects 420 million people worldwide with a continuously rising incidence, is defined by a state of chronic hyperglycemia; a criterion referring to a heterogeneous group of diseases with various etiologies and distinct therapeutic options. Besides the two main forms of diabetes (i.e., type 1 (T1D) and type 2 (T2D)), there are rare subtypes of the disease called monogenic diabetes (or formerly MODY) that are hardly diagnosed because of their resemblance to T1D or T2D. Since these monogenic diabetes may appear early in life, a consortium of expert pediatric clinical centers was created under a clinical research initiative (the GENEPEDIAB study) to develop tools for accurate diagnosis of rare diabetes and to propose appropriate care to these children and adolescents wrongly assigned to T1D or T2D cohorts. The GENEPEDIAB study was initiated in the context of a broader collaborative project (DiaType) with the objective to develop personalized diabetes medicine and better patient care.

Methods: For discrimination of patients with monogenic diabetes from those with classical forms of diabetes using the MODY probability calculator, patients enrolled in the GENEPEDIAB study are phenotyped and genotyped for T1D risk (anti-islet antibodies and HLA). Patients fulfilling sufficient criteria are then genotyped using the routine MODY panel, before being proposed a thorough gene analysis. More comprehensive genetic tests will be conducted in patients without anomalies found after the MODY gene-sequencing test.

Perspective: the GENEPEDIAB study will enable the investigators to adapt treatment to diabetes etiology and help to provide genetic counseling to patients and their family members. The investigators anticipate that its broad genetic analyses will provide them with important information about the genetic susceptibility of these subgroups of patients with atypical diabetes.

Study Overview

• Status: Completed
• Conditions: Diabetes Mellitus; MODY
• Intervention / Treatment: Genetic: Mody test

Detailed Description

BACKGROUND:

Diabetes currently affects 420 million people worldwide, a number that is expected to increase to 642 million in 2040. This disease is responsible for a high morbidity rate and an overall mortality equivalent to 5 million deaths per year. In Belgium, the prevalence of diabetes is estimated at 8% in adults over 35 years of age, the risk of diabetes being 3 to 5 times higher in populations with high consanguinity, mainly due to the susceptibility to generate recessive genetic variants, which are characteristic of atypical forms of diabetes.

Although diabetes is linearly defined by a state of chronic hyperglycaemia, this criterion refers to a heterogeneous group of diseases of various aetiologies and distinct therapeutic options. Ten to 15% of diabetic patients have insulin-dependent type 1 diabetes (T1D), attributed to autoimmune destruction of insulin-producing beta cells, while 80% of patients have type 2 diabetes (T2DM), treated - inter alia - with oral antidiabetic drugs. Despite the diagnosis of T1D is confirmed by the determination of specific antibodies, DT1 and T2D are clinically characterized by the phenotypic type and evolution of the patient, without recourse to specific etiological and/or pathognomonic criteria. Recently, subtypes of T1D and T2D have been categorized to help the clinician choose the best therapeutic interventions for the patient (i.e., dietary approach, physical activity, oral antidiabetic drugs, insulin, combined therapies).

Monogenic causes of diabetes are less common (up to 5% of all cases) and of recent discovery, their molecular basis having been established in the 1990s, under the name "maturity onset diabetes of the young" (MODY). The diagnosis of a genetic origin of diabetes has multiple consequences, primarily at therapeutic level. Despite the implications of a monogenic diabetes diagnosis, this form remains largely underdiagnosed, and it is accepted that 2 to 3% of active patients within diabetes conventions of care suffer from undetected genetic forms.

AIM:

Screening, using routinely diagnostic tools, of monogenic forms of diabetes in cohorts of paediatric patients with atypical forms of diabetes, who are followed in conventions of care for diabetic patients. After diagnosis of monogenic forms of diabetes, screened patients will be monitored and treated according to international recommendations applied to specifically recognized forms of diabetes.

The aim of GENEPEDIAB study is to improve the diagnosis of atypical forms of diabetes in children and adolescents, and not to evaluate the effects of treatment modification following genetic screening.

INTERVENTION:

1. Retrospective analysis of data from active and historical diabetic patients within diabetes care conventions of paediatric endocrinology services; screening of patients with atypical diabetes; use of clinical routine tests to allow genetic diagnosis of the condition.
2. Prospective analysis of the evolution of new diabetic patients followed in paediatric diabetes care conventions; screening of patients with atypical diabetes; use of clinical routine tests to allow genetic diagnosis of the condition.

3. Screening of patients with atypical diabetes:

   • The monogenic diabetes probability will initially be assessed using the MODY probability calculator (old terminology for monogenic diabetes), which identifies at risk patients based on clinical history (age, sex, body mass index, HbA1C, type of therapy, presence of diabetes in the family). This calculator is available on Internet at www.diabetesgenes.org.
   • In addition, other clinical criteria will be used to improve the sensitivity and specificity of screening for monogenic diabetes.

4. Genetic diagnosis of the condition:

   • The diagnosis of T1D will first be completed based on factors currently recognized by the International Society for Paediatric and Adolescent Diabetes (ISPAD): anti islet antibodies and at risk HLA genotype. Residual insulin secretion will be also evaluated.
   • Subjects that are detected using criteria described above will be screened using the routine MODY gene sequencing test, which includes GCK, HNF1A, HNF4A, HNF1B, KCNJ11, ABCC8, and INS gene sequencing.
   • More comprehensive genetic tests will be conducted in patients without anomalies found after the MODY gene-sequencing test.

PARTICIPATING SITES:

GENEPEDIAB is a multicentre study that include various diabetes care conventions of paediatric endocrinology services in Belgium.

• Main site: Cliniques universitaires Saint-Luc (UCLouvain), Brussel (Belgium)

  • Principal investigator : Dr. Philippe Lysy, Paediatric Endocrinology Unit
  • Co-investigators : PhD student Sophie Welsch, PhD Caroline Daems, Paediatric Endocrinology Unit
  • Clinical Research Coordinator : Paola Gallo, Paediatric Endocrinology Unit

• Other sites:

  • CHU ND-des Bruyeres (ULg), Liege (Belgium) - Prof. Marie-Christine Lebrethon;
  • CHU UCL Namur site Mont-Godinne & CHU UCL Namur site Sainte-Elisabeth (UCLouvain), Namur (Belgium) - Dr. Dominique Beckers & Dr. Thierry Mouraux;
  • CHC, Liege (Belgium) - Dr. Nicole Seret;
  • Grand Hopital de Charleroi site Notre Dame (GHdC), Charleroi (Belgium) - Dr. Jacques Louis.

• Study Type: Interventional
• Enrollment (Actual): 446
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Belgium
  • Brussel, Belgium, 1200
    • Cliniques universitaires Saint-Luc - UCLouvain

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: No older than 46 years (Child, Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Age between 0 and 18 years at the age of diabetes diagnosis.
• Patients followed and/or diagnosed within diabetes care agreements of the pediatric endocrinology departments participating in the study.

Exclusion Criteria:

• none

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Diagnostic
• Allocation: Non-Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: T1D Group; Retrospective analysis of data from active and historical diabetic patients within diabetes care conventions of pediatric endocrinology services; screening of patients with atypical diabetes; use of tests used in clinical routine to allow referral to the genetic diagnosis of the condition.; Prospective analysis of the evolution of new diabetic patients followed in pediatric endocrinology services of diabetes care conventions; screening of patients with atypical diabetes; use of tests used in clinical routine to allow the genetic diagnosis of the condition.; Screening of patients with atypical diabetes: first evaluated according to the "MODY" probability calculator. In addition, other clinical criteria will be used to improve the sensitivity and specificity of pediatric monogenic diabetes screening.	Genetic: Mody test; Subjects will be screened using a MODY gene-sequencing test, which includes GCK, HNF1A, HNF4A, HNF1B, KCNJ11, ABCC8, and INS gene sequencing. More comprehensive genetic tests will be conducted in patients without anomalies found after the MODY gene-sequencing test.
Experimental: MODY Group; Retrospective analysis of data from active and historical diabetic patients within diabetes care conventions of pediatric endocrinology services; screening of patients with atypical diabetes; use of tests used in clinical routine to allow referral to the genetic diagnosis of the condition.; Prospective analysis of the evolution of new diabetic patients followed in pediatric endocrinology services of diabetes care conventions; screening of patients with atypical diabetes; use of tests used in clinical routine to allow the genetic diagnosis of the condition.; Screening of patients with atypical diabetes: first evaluated according to the "MODY" probability calculator. In addition, other clinical criteria will be used to improve the sensitivity and specificity of pediatric monogenic diabetes screening.	Genetic: Mody test; Subjects will be screened using a MODY gene-sequencing test, which includes GCK, HNF1A, HNF4A, HNF1B, KCNJ11, ABCC8, and INS gene sequencing. More comprehensive genetic tests will be conducted in patients without anomalies found after the MODY gene-sequencing test.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Diagnostic of atypical diabetes using follow-up of clinical parameters: Weight	Weight in kilograms (Kg)	At diabetes diagnosis
Diagnostic of atypical diabetes using follow-up of clinical parameters: Height	Height in meters (m)	At diabetes diagnosis
Diagnostic of atypical diabetes using follow-up of clinical parameters: BMI	Body Mass Index (Kg/m²)	At diabetes diagnosis
Diagnostic of atypical diabetes using follow-up of laboratory results: HbA1c (%)	Glicated hemoglobin (%)	from diabetes diagnosis to study inclusion. (The study inclusion will be from 18 months after diagnosis to several years)
Diagnostic of atypical diabetes using follow-up of laboratory results: HbA1c (mmol/mol)	Glicated hemoglobin (mmol/mol)	from diabetes diagnosis to study inclusion. (The study inclusion will be from 18 months after diagnosis to several years)
Diagnostic of atypical diabetes using follow-up of laboratory results: Glycaemia	Glycaemia (mg/dL)	from diabetes diagnosis to study inclusion
Diagnostic of atypical diabetes using follow-up of laboratory results: C-peptide	C-peptide (pmol/mL)	from diabetes diagnosis to study inclusion. (The study inclusion will be from 18 months after diagnosis to several years)
Genetic diagnosis of diabetes: Anti-islets antibodies	Presence of measurable Anti-islets antibodies	from diabetes diagnosis to study inclusion. (The study inclusion will be from 18 months after diagnosis to several years)
Genetic diagnosis of diabetes: HLA genotype	Presence of at risk HLA genotype	from diabetes diagnosis to study inclusion. (The study inclusion will be from 18 months after diagnosis to several years)
Genetic diagnosis of atypical diabetes: MODY gene-sequencing test	MODY gene-sequencing test (GCK, HNF1A, HNF4A, HNF1B, KCNJ11, ABCC8, and INS gene sequencing)	at inclusion in the study
Genetic diagnosis of atypical diabetes: More comprehensive genetic tests	More comprehensive genetic tests will be conducted in patients without anomalies found after the MODY gene-sequencing test.	After MODY gene-sequencing test, from 3 months to 1.5 year after study inclusion

Collaborators and Investigators

• Sponsor: Université Catholique de Louvain
• Investigators: Principal Investigator: Philippe Lysy, Cliniques universitaires Saint-Luc - UCLouvain

Study record dates

Study Major Dates

• Study Start (Actual): October 22, 2018
• Primary Completion (Actual): October 22, 2021
• Study Completion (Actual): June 22, 2022

Study Registration Dates

• First Submitted: July 2, 2019
• First Submitted That Met QC Criteria: July 15, 2019
• First Posted (Actual): July 16, 2019

Study Record Updates

• Last Update Posted (Actual): July 15, 2022
• Last Update Submitted That Met QC Criteria: July 14, 2022
• Last Verified: July 1, 2022

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Glucose Metabolism Disorders; Metabolic Diseases; Endocrine System Diseases; Diabetes Mellitus
• Other Study ID Numbers: GENEPEDIAB

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No