Relationship between serum fibroblast growth factor 19 and vascular endothelial growth factor and soluble klotho

Yanjun Zhang1,2, Guimei Li3,4, Feifei Xiao2

  • 1Department of Pediatric Endocrinology, Shandong Provincial Hospital, Shandong University, 9677 Jingshi Road, Lixia Area, 250021, Jinan, Shandong, China.

BMC Pediatrics
|March 17, 2023
PubMed

Insights

This study found lower serum levels of Fibroblast Growth Factor 19 (FGF19) and soluble klotho protein (sklotho) in children with type 1 diabetes (T1D), alongside higher vascular endothelial growth factor (VEGF). These factors correlate with HbA1c levels and may influence T1D complications.

Area of Science:

  • Endocrinology
  • Pediatrics
  • Metabolic Disorders

Background:

  • Fibroblast Growth Factor 19 (FGF19) plays a role in glycolipid metabolism and may be implicated in type 1 diabetes (T1D) complications.
  • Understanding the interplay of FGF19 with other biomarkers is crucial for pediatric T1D management.

Purpose of the Study:

  • To evaluate the relationship between serum FGF19, vascular endothelial growth factor (VEGF), and soluble klotho protein (sklotho) in children with T1D.
  • To explore potential correlations with diabetes duration and glycemic control (HbA1c).

Main Methods:

  • A cross-sectional study involving 66 children with T1D and 30 healthy controls.
  • Serum concentrations of FGF19, VEGF, and sklotho were measured using ELISA.
  • Participants were analyzed based on T1D duration and HbA1c levels.

Main Results:

  • Children with T1D exhibited lower serum FGF19 and sklotho levels, and higher VEGF levels compared to controls.
  • FGF19, VEGF, and sklotho levels correlated significantly with HbA1c, but not with diabetes duration.
  • Positive correlation found between FGF19 and sklotho; negative correlation between FGF19 and VEGF.

Conclusions:

  • Serum FGF19 levels are closely related to VEGF and sklotho levels in pediatric T1D patients.
  • FGF19 may contribute to T1D complications in children through interactions with VEGF and sklotho.
Abstract