The Association of Accelerated Early Growth, Timing of Puberty, and Metabolic Consequences in Children

Youn Hee Jee1,2,3, Sanjay Jumani1, Veronica Mericq4

  • 1Section on Growth, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.

Insights

Children born small for gestational age (SGA) or with premature adrenarche (PA) face increased metabolic syndrome risks due to accelerated growth and early puberty. This review explores the links between early development and metabolic health consequences.

Area of Science:

  • Pediatric Endocrinology
  • Metabolic Health
  • Developmental Biology

Background:

  • Children born small for gestational age (SGA) exhibit higher risks for metabolic syndrome, type 2 diabetes, insulin resistance, and cardiovascular diseases, particularly with accelerated early growth.
  • Premature adrenarche (PA) is also linked to metabolic disturbances and earlier pubertal timing.
  • Early pubertal timing in both SGA and PA populations is associated with increased metabolic risks, necessitating further investigation.

Approach:

  • This review synthesizes recent research on the relationship between early infantile growth patterns and pubertal timing.
  • It examines the association between these developmental factors and the subsequent risk of metabolic syndrome.
  • The review aims to elucidate the underlying pathophysiology connecting early growth, puberty, and metabolic health.

Key Points:

  • Accelerated early growth and early puberty are identified risk factors for metabolic syndrome.
  • SGA children, especially those with catch-up growth, are at higher long-term metabolic risk.
  • Early pubertal timing in SGA and PA children correlates with various metabolic risks.

Conclusions:

  • Understanding the interplay between early growth, pubertal timing, and metabolic health is crucial for identifying at-risk children.
  • Further research into the pathophysiology can inform preventative strategies for metabolic syndrome in vulnerable pediatric populations.
  • This review highlights the need for continued investigation into the long-term metabolic consequences of early developmental trajectories.

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