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Updated: May 13, 2026

Isolating Central Nervous System Tissues and Associated Meninges for the Downstream Analysis of Immune cells
Published on: May 19, 2020
Pituitary function in children following infectious diseases of the central nervous system
Yael Levy-Shraga1, Inbal Gazit, Dalit Modan-Moses
1Pediatric Endocrine and Diabetes Unit, Safra Children's Hospital, Sheba Medical Center, 52621, Tel Hashomer, Israel, yael.levy.shraga@gmail.com.
Insights
Infectious meningitis rarely causes pituitary deficiencies in children. Most children recover fully, with routine growth and puberty monitoring by primary care physicians being sufficient for follow-up. Invasive testing is only needed for specific concerns.
Area of Science:
- Pediatric Endocrinology
- Infectious Diseases
- Neurology
Background:
- Studies indicate a notable incidence of pituitary deficiencies post-infectious meningitis in adults.
- The long-term effects of meningitis on pituitary function in children require further investigation.
Purpose of the Study:
- To assess the pituitary function in children following recovery from infectious meningitis.
- To determine the frequency of pituitary deficiencies in pediatric meningitis survivors.
Main Methods:
- Evaluated 14 children with a history of meningitis through medical history, physical exams, auxological measurements, and basal hormone levels (TSH, fT4, cortisol, IGF1).
- Followed children with abnormal results for one year, including dynamic testing when indicated.
- Collected data on age at meningitis, age at evaluation, and time interval between events.
Main Results:
- All children exhibited normal thyroid function tests and basal cortisol levels.
- Three children had low IGF1 levels; two normalized over follow-up, suggesting growth hormone deficiency was unlikely.
- One child with low height SDS showed a normal response to growth hormone stimulation testing.
Conclusions:
- Pituitary dysfunction with overt clinical symptoms is uncommon in children after acute meningitis.
- Routine monitoring of growth and puberty by primary care physicians is likely adequate for most pediatric meningitis survivors.
- Invasive pituitary assessments should be reserved for children with slow growth or clinical suspicion of hypopituitarism.
Abstract:
Recent studies in adults suggest that pituitary deficiencies develop in a considerable proportion of patients who recover from infectious meningitis. The aim of this study was to evaluate pituitary function of children with a history of meningitis. Seventy-nine children were admitted to the Safra Children's Hospital due to meningitis between 2007 and 2010. Twenty-four families were lost for follow-up, 55 were interviewed by phone and 14 (9 males) participated in the study. Evaluation included medical history, physical examination, auxological measurements and basal levels of TSH, fT4, cortisol and IGF1. Children with abnormal results were followed for a year and dynamic testing was performed when indicated. Mean age at time of infectious meningitis was 3.8 ± 5.4 years (range 0.03-15.8), and at clinical evaluation 6.4 ± 6.4 (range 1.2-20). The interval between the acute event and evaluation was 2.7 ± 1.2 years. Thyroid function tests and basal cortisol levels were normal for all children. Three children had low IGF1 levels; however over a year of follow-up two of them had normal height and growth velocity, making growth hormone deficiency unlikely. One child had low height SDS, but exhibited a normal response to a growth hormone stimulation test. Pituitary dysfunction with overt clinical symptoms is not a frequent consequence of acute meningitis in children. Follow-up of growth and puberty of children post-meningitis by the primary care physician is probably sufficient. Invasive assessments should be reserved for selected cases where there is slow growth or other clinical suspicion of hypopituitarism.
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