Hypopituitarism in pediatric survivors of inflicted traumatic brain injury

Bethany A Auble1, Sureka Bollepalli, Kathi Makoroff

  • 11 Division of Pediatric Endocrinology, Cincinnati Children's Hospital Medical Center and University of Cincinnati School of Medicine , Cincinnati, Ohio.

Journal of Neurotrauma
|September 14, 2013
PubMed

Insights

Inflicted traumatic brain injury (iTBI) in children frequently causes endocrine dysfunction, with 86% experiencing abnormalities. Elevated prolactin and growth issues are common, highlighting the need for careful monitoring after iTBI.

Area of Science:

  • Pediatric Endocrinology
  • Pediatric Neurology
  • Child Abuse Research

Background:

  • Endocrine dysfunction is a known complication of accidental traumatic brain injury (TBI).
  • The prevalence and spectrum of endocrine dysfunction following inflicted traumatic brain injury (iTBI) in children remain largely uncharacterized.
  • iTBI represents a significant cause of pediatric brain injury, necessitating investigation into its long-term sequelae.

Purpose of the Study:

  • To investigate the prevalence and types of endocrine dysfunction in children who have sustained moderate-to-severe iTBI.
  • To characterize hormonal abnormalities, including growth hormone, thyroid, adrenal, and prolactin axes, in this vulnerable population.
  • To establish the clinical significance of endocrine sequelae following iTBI.

Main Methods:

  • Retrospective evaluation of 14 children with a history of iTBI.
  • Comprehensive assessment including anthropometric measurements and detailed hormonal evaluations (GH, IGF-1, IGFBP-3, TSH, free T4, cortisol, PRL, osmolality).
  • Statistical analysis using Fisher's exact test and Wilcoxon's rank-sum test to compare findings with general population data.

Main Results:

  • A high prevalence of endocrine dysfunction was observed, with 86% of subjects exhibiting at least one abnormality and 50% showing two or more.
  • Common endocrine abnormalities included elevated prolactin (64%), abnormal thyroid function (33%), short stature (29%), and low growth hormone (GH) peak (17%).
  • Elevated prolactin levels were frequently associated with other endocrine dysfunctions. Two children required thyroid hormone treatment, and two may need GH therapy.

Conclusions:

  • Children with a history of iTBI are at a significantly elevated risk for developing endocrine dysfunction, including hyperprolactinemia and growth abnormalities.
  • The findings underscore a critical, under-recognized complication of iTBI in pediatric populations.
  • Close monitoring of growth velocity and pubertal development, coupled with endocrine evaluation for children with iTBI, is strongly recommended.

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