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Determinants of Glycaemic Control in Children With Type 1 Diabetes

Recruiting
Conditions
Diabetes Mellitus, Type 1
Interventions
Other: Determinants of T1D glycaemic control
Registration Number
NCT06325111
Lead Sponsor
IRCCS Burlo Garofolo
Brief Summary

Type 1 diabetes (T1D) is a common chronic disease of childhood associated with a significantly increased risk of micro- and macro-vascular complications, including neuropathy, nephropathy and cardiovascular diseases. The risk of development T1D comorbidities is associated with glycaemic control, a complex mechanism involving biological, physiological environmental factors.

While more than 60 genetic variants were already associated with Glycated hemoglobin (HbA1c) in healthy subjects, very few genes have been identified in T1D individuals. Also, hyperglycaemia could be the cause of epigenetic changes at specific target genes, such as DNA methylation, histone modifications and microRNAs, correlated to accelerated development of diabetes-related complications. Most recently, increasing evidence also suggested that human microbiome may play a crucial role in the onset and progression of T1D and dysbiosis of the gut and oral microbiota was reported as a typical feature of hyperglycaemia.

However, potential differences among poorly and good managed T1D subjects have not been still studied. Also, the exact mechanism by long-term hyperglycaemia's acts in T1D remains poorly understood. Therefore, this project will explore an emerging area of research by the study of possible genetic, epigenetic and environmental biomarkers among T1D subjects with different glycaemic control.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
800
Inclusion Criteria
  • Type 1 diabetes subjects
  • Age from 6 to 20 years old
  • At least 5 years of duration of disease
Exclusion Criteria
  • Type 1 diabetes subjects incapable of giving valid informed consent or whose parents are incapable of giving valid informed consent.
  • Type 1 diabetes subjects for whom it is not possible to collect information on the clinical history, starting from the onset of diabetes
  • Subjects with other types of diabetes (i.e. type 2, monogenic diabetes, cystic fibrosis related diabetes)

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Patients with T1D and poor glycaemic controlDeterminants of T1D glycaemic controlPoor glycemic control will be defined as HbA1c value ≥7%
Patients with T1D and optimal glycaemic controlDeterminants of T1D glycaemic controlOptimal glycaemic control will be defined as HbA1c values \<7%
Primary Outcome Measures
NameTimeMethod
Identification of genes involved in T1D glycaemic controlThrough study completion, an average of 18 months

DNA will be isolated from saliva by Genefix Saliva DNA/RNA collection kit (Isohelix, UK) and whole genome genotyping will be performed using Illumina chip arrays (CA, USA).

Identification of microRNAs involved in T1D glycaemic controlThrough study completion, an average of 18 months

Peripheral blood will be collected from each participant into Ethylenediaminetetraacetic acid (EDTA)-containing tubes for microRNAs sequencing. Illumina TruSeq Small RNA Sample Preparation kit will be used for library preparation, and sequencing will be conducted by Illumina platform (CA, USA).

Identification of DNA methylation patterns involved in T1D glycaemic controlThrough study completion, an average of 18 months

Peripheral blood will be collected from each participant into EDTA-containing tubes and Genome-wide DNA methylation will be performed using the Illumina Infinium Human Methylation EPIC BeadChip array

Identification of oral microbiome characteristics associated to T1D glycaemic controlThrough study completion, an average of 18 months

Bacterial DNA will be extracted from saliva and a 500 base pair region of the V1-V3 portion of the 16S ribosomal RNA gene as well as the 200 base pair region of the V3 portion will be amplified. The V3 amplicon will be used for template preparation and will be sequenced using the Ion PGM Hi-Q View sequencing kit (Life Technologies, New York, NY, USA) with the IonPGM™System technology

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Institute for Maternal and Child Health - IRCCS "Burlo Garofolo"

🇮🇹

Trieste, Italy

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