Tall stature: a clinical, endocrinological and radiological study
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Updated: Nov 3, 2026

Assessment of Child Anthropometry in a Large Epidemiologic Study
Published on: February 2, 2017
Insights
This study investigated growth hormone (GH) secretion in tall children, finding that pubertal changes can cause
Area of Science:
- Pediatric Endocrinology
- Growth Hormone Physiology
- Adolescent Medicine
Background:
- Tall stature in children necessitates investigation into growth hormone (GH) secretory dynamics.
- Puberty is a period of significant physiological changes affecting endocrine function.
Purpose of the Study:
- To analyze GH secretory patterns in children with tall stature.
- To correlate endocrine and radiological findings in this cohort.
Main Methods:
- Studied 38 children (25 F, 13 M) with tall stature (Height SD score > 1.8).
- Assessed GH levels via basal measurements, TRH stimulation, oral glucose tolerance tests, insulin-induced hypoglycemia, and 24-hour GH profiling.
- Performed pituitary radiology.
Main Results:
- Some children showed elevated basal GH, abnormal GH responses to TRH, or paradoxical GH responses to oral glucose.
- No concordance between peak GH after insulin-induced hypoglycemia and stage IV sleep GH.
- Increased GH pulse amplitude and area during puberty; morning GH secretion observed.
- Pituitary microadenomata suggested in 17 patients, potentially linked to sex hormones in late puberty.
Conclusions:
- 'Abnormal' endocrine and radiological findings in tall pubertal children require cautious interpretation.
- Physiological pubertal increases in GH secretion may explain some observed paradoxical responses.
- Distinguishing somatotroph pathology from hormonal effects of puberty is crucial.
Abstract:
We have studied GH secretory dynamics in 38 (25 F, 13 M) children referred for investigation and treatment of tall stature (Height SD score (SDS) greater than 1.8). Five children had elevated basal GH levels (mean 20.4 mU/l) and a further four had abnormal GH responses to exogenous TRH. Two other children had paradoxical GH responses to oral glucose loading. Although one of these was receiving high dose testosterone to limit final height. All these children were pubertal and did not show concordance between peak GH concentration observed after insulin-induced hypoglycaemia and during stage IV sleep. Twenty-four hour GH profiles revealed increased GH pulse amplitude and area under the pulse during puberty. Morning GH secretion was also regularly observed and it is possible that the paradoxical responses seen by us and reported by others reflect this increased physiological secretion. Pituitary radiology revealed morphological abnormalities suggestive of microadenomata in 17 patients but these were all in late puberty and these changes may be related more to the effects of sex hormones than to somatotroph pathology. 'Abnormal' endocrinology and radiology are seen in tall children in puberty and must be interpreted with caution.
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