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Pituitary dysfunction in traumatic brain injury: Is evaluation in the acute phase worthwhile?
Pradip P Dalwadi1, Nikhil M Bhagwat1, Parimal S Tayde1
1Department of Endocrinology, Topiwala National Medical College, Bai Yamunabai Laxman Nair Charitable Hospital, Mumbai, Maharashtra, India.
Indian Journal of Endocrinology and Metabolism
|February 21, 2017
Summary
Traumatic brain injury (TBI) frequently causes pituitary hormone deficiencies, particularly affecting growth hormone and gonadotropin axes. Low triiodothyronine (T3) levels in acute TBI predict mortality, highlighting the need for prompt pituitary function assessment.
Area of Science:
- Endocrinology
- Neuroscience
- Trauma Care
Background:
- Traumatic brain injury (TBI) is an under-recognized cause of hypopituitarism.
- Recent data suggest TBI-induced hypopituitarism may be more prevalent than previously thought.
- There is a notable scarcity of data regarding TBI and hypopituitarism in the Indian population.
Purpose of the Study:
- To determine the prevalence of pituitary hormone deficiencies in the acute phase following TBI.
- To correlate trauma severity with basal pituitary hormone levels.
- To investigate whether initial hormone deficiencies predict mortality in TBI patients.
Main Methods:
- A cohort of 49 TBI patients (41 men, 8 women) was enrolled.
- Pituitary function was assessed within 24 hours of hospital admission.
- Hormone levels were correlated with TBI severity and mortality outcomes.
Main Results:
- Gonadotropin deficiency occurred in 65.3% of patients; 46.9% had low insulin-like growth factor-1.
- Cortisol levels <7 mcg/dl were observed in 12.24% of patients.
- Low free triiodothyronine (fT3) levels were significantly associated with increased mortality risk.
Conclusions:
- Pituitary dysfunction is common post-TBI, with growth hormone and gonadotropin axes most frequently affected.
- Low fT3 levels demonstrate the strongest correlation with mortality after TBI.
- Assessing cortisol levels during the acute phase of TBI is crucial due to the life-threatening risk of undetected deficiency.

