ESPE Abstracts (2024) 98 P1-54

ESPE2024 Poster Category 1 GH and IGFs 1 (11 abstracts)

Should MRI Be Performed on the Pituitary Gland in Short Stature Children with Peak Growth Hormone Levels Between 5 and 7 Micrograms/Liter Following Provocation Tests?"

Noor Hamed , Ashraf Soliman , Fawzia Alyafei , Nada Alaaraj , Shayma Ahmed , Mohamed Qusad & Sohair Elsiddig


Hamad General Hospital, Doha, Qatar


Background: The precise growth hormone (GH) cut-off value for diagnosing growth hormone deficiency (GHD) in children is a subject of ongoing debate. With GH provocative tests typically using cut-offs between 4.7 and 6.5 µg/L, the traditional threshold of <10 µg/L is being reconsidered in favor of <7 µg/L due to advancements in GH assay standardization. Magnetic resonance imaging (MRI) of the pituitary gland is a crucial diagnostic tool, although the prevalence of MRI abnormalities in GHD patients varies widely across studies.

Methods: We conducted a retrospective review of the radiological, clinical, and laboratory records of 43 short stature children (aged 5–11 years, mean 7.2 ± 2.3 years) with confirmed GHD (Peak GH response to clonidine and glucagon provocation <7 µg/L), who underwent brain MRI. Patients were categorized into two groups based on their peak GH response to provocation: Group 1 (<5 µg/L, n = 34) and Group 2 (>5 and <7 µg/L, n = 9).

Results: MRI evaluations revealed pituitary gland abnormalities in 10 out of 34 children in Group 1 and 2 out of 9 children in Group 2. The findings indicate that MRI evaluation of the hypothalamic-pituitary axis is warranted in short children with peak GH responses >5 and <7 µg/L, as it effectively reveals pituitary morphological characteristics and aids in the diagnosis of GHD. • MRI abnormalities included: • 6 Small/ hypoplastic pituitary gland for patient's age, 1 Partial empty sella with the pituitary gland small and flattened, 1 Caudally located sella tissue, 1 Non-enhancing asymmetrical thickening of the left pre-chiasmatic optic nerve, 1 small anterior pituitary gland, with delayed myelination and Chairi type 1 malformation, 1 Persistent type II craniopharyngeal canal, as described, with inferior descent and partial herniation of the anterior lobe of the pituitary gland and 1 Ectopic posterior pituitary with reduced caliber of the pituitary infundibulum.

Table The percentage of MRI abnormalities in GHD children with different peak GH levels,
Group Number of Children Peak GH µg/L Abnormal Pituitary Findings Percentage of Abnormalities
Group 1 34 <5 10 29.41%
Group 2 9 >5 and <7 2 22.22%

Conclusion: Our study supports the use of MRI for the pituitary gland in the diagnostic evaluation of short-stature children with peak GH levels between 5 and 7 µg/L. MRI findings can contribute valuable diagnostic information in patients with lower peak GH levels, suggesting a broader application for MRI in the assessment of GHD.

Volume 98

62nd Annual ESPE (ESPE 2024)

Liverpool, UK
16 Nov 2024 - 18 Nov 2024

European Society for Paediatric Endocrinology 

Browse other volumes

Article tools

My recent searches

No recent searches.