Residual β-cell mass influences growth of prepubertal children with type 1 diabetes

Carla Bizzarri1, Danila Benevento, Ippolita Patrizia Patera

  • 1Unit of Endocrinology and Diabetes, Bambino Gesù Children's Hospital, Rome, Italy.

Insights

Type 1 diabetes (T1D) impacts child growth even with intensive insulin therapy. Preserving residual beta-cell function positively influences growth, independent of glycemic control quality.

Area of Science:

  • Pediatric Endocrinology
  • Metabolic Disorders
  • Diabetes Research

Background:

  • Childhood growth deceleration is linked to type 1 diabetes (T1D) and poor glycemic control.
  • The persistence of growth impairment despite optimized T1D therapy remains unclear.
  • This study investigates the impact of intensive insulin treatment on prepubertal growth in children with T1D.

Purpose of the Study:

  • To evaluate the long-term effects of intensive insulin therapy on the growth of prepubertal children with type 1 diabetes.
  • To determine the relationship between residual beta-cell function, glycemic control, and growth outcomes in T1D.
  • To assess if growth impairment persists in T1D children even with optimized treatment.

Main Methods:

  • Longitudinal evaluation of 104 children with T1D from diagnosis to puberty onset.
  • Regular monitoring of height, weight, insulin requirements, and glycated hemoglobin (HbA1c).
  • Estimation of residual beta-cell mass using fasting C-peptide levels at T1D onset.

Main Results:

  • Height SDS showed a slight but significant decrease from 0.52 at onset to 0.36 at follow-up (p=0.04).
  • BMI SDS significantly increased from -0.04 to 0.32 (p=0.01).
  • Height velocity was positively associated with C-peptide and insulin requirement, and inversely with HbA1c. BMI gain was negatively influenced by HbA1c.

Conclusions:

  • Intensive insulin therapy does not fully prevent the negative impact of type 1 diabetes on prepubertal growth.
  • Residual beta-cell mass plays a crucial role in promoting growth in T1D children.
  • The positive effect of residual beta-cell function on growth is independent of glycemic control levels (HbA1c).
Abstract

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