Endocrine Dysfunctions After Pediatric Traumatic Brain Injury: Present Insights and Future Directions
Ignazio Cammisa1, Elena Malavolta1, Giorgio Sodero2,3
1Department of Life Sciences and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy.
Insights
Childhood traumatic brain injury (TBI) can cause long-term endocrine problems, affecting growth and puberty. Regular monitoring is crucial for early detection and improved outcomes in pediatric patients.
Area of Science:
- Pediatric endocrinology
- Neurotrauma
- Child health
Background:
- Childhood traumatic brain injury (TBI) is a growing global health issue.
- Post-traumatic endocrine dysfunction is an underrecognized complication of pediatric TBI.
- The hypothalamic-pituitary axis (HPA) is particularly vulnerable to injury.
Purpose of the Study:
- To review the spectrum and prevalence of endocrine dysfunction following pediatric TBI.
- To highlight the long-term consequences of these dysfunctions.
- To emphasize the need for structured endocrine surveillance.
Main Methods:
- Literature review of studies on pediatric TBI and endocrine outcomes.
- Analysis of reported prevalence and types of pituitary dysfunction.
- Discussion of diagnostic challenges and management strategies.
Main Results:
- Prevalence of pituitary dysfunction post-TBI ranges from 5% to 57%.
- Growth hormone deficiency (GHD) is the most common abnormality.
- Other issues include gonadal, adrenal, and posterior pituitary disorders, often with delayed onset.
Conclusions:
- Endocrine sequelae can manifest years after TBI, complicating diagnosis.
- Structured, longitudinal endocrine surveillance is essential for pediatric TBI survivors.
- Early recognition and intervention can improve rehabilitation outcomes.
Abstract:
Traumatic brain injury (TBI) in childhood is a major global health concern and a leading cause of morbidity and mortality in the pediatric population. Its incidence is rising worldwide, with early childhood and adolescence representing the most vulnerable age groups. Beyond acute neurological injury, post-traumatic endocrine dysfunction has emerged as an underrecognized but clinically significant sequela, with potential long-term consequences for growth, puberty, metabolism, and overall quality of life. The hypothalamic-pituitary axis (HPA) is uniquely vulnerable due to its anatomical and vascular characteristics, making pituitary cells-particularly somatotrophs and gonadotrophs-susceptible to ischemic, traumatic, and inflammatory damage. Reported prevalence of post-TBI pituitary dysfunction in children ranges from 5 to 57%, reflecting a deep heterogeneity in injury severity, diagnostic methods, and timing of evaluations. Growth hormone deficiency (GHD) is the most frequently reported abnormality, with presentations varying from transient to persistent forms. Gonadal axis disturbances, including hypogonadotropic hypogonadism and, less commonly, central precocious puberty, highlight the impact of TBI on pubertal development. Adrenal dysfunctions, though less frequent, may be life-threatening if unrecognized, while posterior pituitary disorders, such as diabetes insipidus, usually revealed acutely, are often transient. Importantly, many endocrine sequelae manifest months to years after the initial trauma, complicating a timely diagnosis. Current evidence underscores the need for structured, longitudinal endocrine surveillance after pediatric TBI, with baseline and follow-up assessments at defined intervals. Early recognition and intervention, including hormone replacement when appropriate, may improve neurocognitive recovery and overall rehabilitation outcomes. Future multicenter studies and standardized screening protocols should be considered essential to clarify incidence, natural history, and optimal management strategies for post-traumatic endocrine dysfunction in children.
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