Evaluation of epicardial adipose tissue in children with type 1 diabetes

Gül Trabzon1, Şükrü Güngör2, Şeyma Demiray Güllü3

  • 1Hatay Mustafa Kemal University Medical Faculty Department of Pediatric Endocrinology, Hatay, Turkey. gldirekk@gmail.com.

Pediatric Research
|June 15, 2024
PubMed

Insights

Children with type 1 diabetes exhibit increased epicardial adipose tissue (EAT), a visceral fat surrounding the heart. This finding suggests EAT may indicate cardiac risk and poor glycemic control in pediatric type 1 diabetes patients.

Area of Science:

  • Cardiology
  • Endocrinology
  • Pediatrics

Background:

  • Epicardial adipose tissue (EAT) is visceral fat surrounding the heart.
  • Type 1 diabetes (T1D) is increasingly recognized to have associations with cardiovascular health.
  • The relationship between EAT and T1D in children requires further investigation.

Purpose of the Study:

  • To investigate the association between epicardial adipose tissue (EAT) and type 1 diabetes (T1D) in a pediatric cohort.
  • To determine if EAT thickness differs between children with T1D and healthy controls.
  • To explore the potential of EAT as a biomarker for cardiac risk in pediatric T1D.

Main Methods:

  • Retrospective study comparing children with T1D and healthy children.
  • Measurement of epicardial fat thickness.
  • Documentation of HbA1c levels and time to diabetes diagnosis.

Main Results:

  • Children with T1D (n=51) had significantly higher EAT values compared to healthy controls (n=69).
  • Mean HbA1c in the T1D group was 9.4 ± 0.2, with a mean insulin dose of 0.94 units/kg/day.
  • Epicardial fat thickness demonstrated potential as a specific and sensitive indicator in type 1 diabetics.

Conclusions:

  • Increased EAT is observed in children with T1D, suggesting a link between EAT and the condition.
  • EAT thickness may be associated with glycemic control and serve as a potential indicator of cardiac risks in pediatric T1D.
  • Further research is essential to fully understand the complex mechanisms underlying the EAT-T1D relationship and its clinical implications.
Abstract

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