Pubertal development in children born small for gestational age

Margreet A Veening1, Mirjam M van Weissenbruch, John J Roord

  • 1Department of Pediatrics, Research Institute for Endocrinology, Reproduction and Metabolism, VU University Medical Center, Amsterdam, The Netherlands.

Insights

Children born small for gestational age (SGA) experience accelerated puberty, particularly girls. This study found elevated dehydroepiandrosterone sulfate (DHEAS) in SGA children, indicating early signs of adrenarche.

Area of Science:

  • Pediatric endocrinology
  • Reproductive health
  • Growth and development

Background:

  • Reduced fetal growth is linked to early puberty and potential fertility issues.
  • Children born small for gestational age (SGA) may face long-term health consequences.
  • Precocious adrenarche and polycystic ovary syndrome are associated with reduced fetal growth.

Purpose of the Study:

  • To investigate pubertal development in children born small for gestational age (SGA) compared to those born appropriate for gestational age (AGA).
  • To assess dehydroepiandrosterone sulfate (DHEAS) levels in SGA and AGA children during development.
  • To determine if low birth weight impacts pubertal timing and androgenization.

Main Methods:

  • Physical examinations and pubertal staging were conducted twice on SGA and AGA children.
  • Pubic hair development was assessed as an indicator of androgenization.
  • Hormone levels, including estradiol, testosterone, and dehydroepiandrosterone sulfate (DHEAS), were measured.

Main Results:

  • Prepubertal SGA children exhibited higher DHEAS levels than AGA children.
  • SGA girls showed a more rapid pubertal progression compared to AGA girls.
  • DHEAS levels tended to remain higher in SGA children throughout puberty.

Conclusions:

  • Low birth weight may have lasting effects on pubertal development, with accelerated progression observed in SGA girls.
  • Exaggerated adrenarche in prepubertal SGA children appears to persist into puberty.
  • Findings suggest a link between reduced fetal growth and altered pubertal timing and androgenization.
Abstract

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