Impact of glycemic control on serum lipoprotein (a) in Arab children with type 1 diabetes

M Alsaeid1, M Qabazard, A Shaltout

  • 1Department of Pediatrics, Faculty of Medicine, Kuwait University, Kuwait. mayra@hsc.kuniv.edu.kw

Insights

Poor glycemic control in Arab children with type 1 diabetes is linked to elevated Lipoprotein (a) levels, increasing cardiovascular risk. This highlights the importance of metabolic control in managing diabetes complications.

Area of Science:

  • Pediatrics
  • Endocrinology
  • Cardiovascular Medicine

Background:

  • Lipoprotein (a) (Lp (a)) is an independent risk factor for coronary artery disease (CAD).
  • Type 1 diabetes and CAD are significant health concerns, particularly in Kuwait.
  • Limited data exist on Lp (a) levels in diabetic children, especially Arab populations.

Purpose of the Study:

  • To analyze serum Lp (a) levels in type 1 diabetic children compared to non-diabetic children.
  • To investigate the impact of glycemic control on Lp (a) levels in diabetic children.

Main Methods:

  • Serum Lp (a) levels were measured in 60 non-diabetic and 58 type 1 diabetic prepubertal children.
  • Diabetic children were categorized into good-to-fair control (GHb <11%) and poor control (GHb ≥11%) groups.
  • Lp (a) concentrations were compared across these groups.

Main Results:

  • Mean serum Lp (a) was higher in diabetic children (187.62 mg/L) than controls (162.88 mg/L).
  • Children with poor glycemic control exhibited significantly higher median Lp (a) levels (147.50 mg/L) compared to those with good control (95 mg/L) and controls (125 mg/L).
  • Poorly controlled diabetic children showed a higher prevalence of elevated Lp (a) levels (≥250 mg/L) than other groups.

Conclusions:

  • Elevated Lp (a) levels in Arab children are strongly associated with poor metabolic control in type 1 diabetes.
  • The prevalence of cardiovascular risk-associated Lp (a) levels is higher in poorly controlled diabetic children.
  • Increased Lp (a) may contribute to the heightened risk of CAD in diabetic patients.
Abstract

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