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Growth Hormone Treatment Improves Cognitive Function in Short Children with Growth Hormone Deficiency
Insights
Growth hormone (GH) treatment significantly improved IQ, particularly fluid intelligence, in short children with GH deficiency. Pre-treatment GH/IGF-I levels predicted cognitive gains in these children.
Area of Science:
- Pediatric Endocrinology
- Neurodevelopmental Pediatrics
- Growth Hormone Therapy
Background:
- Short stature in prepubertal children can be associated with varying degrees of GH secretion.
- Understanding the impact of GH status and treatment on cognitive function is crucial for these children.
Purpose of the Study:
- To investigate the association between cognitive function and growth hormone (GH) status.
- To evaluate the effects of GH treatment on cognition in short prepubertal children with GH deficiency (GHD) and idiopathic short stature (ISS).
Main Methods:
- A randomized study involving 99 short prepubertal children (3-11 years) with GHD (n=41) or ISS (n=58).
- Children received either a fixed GH dose or an individualized dose for 24 months.
- Cognitive changes, including full-scale IQ (FSIQ) and secondary indices, were assessed using Cohen's d effect sizes.
Main Results:
- GH-deficient children showed significant medium effect size increases in FSIQ (d=0.63), performance IQ (d=0.65), and processing speed (d=0.71).
- Perceptual organization improved only in the ISS group (d=0.53).
- Baseline GHmax and IGF-ISDS explained 40% of the variance in processing speed changes.
Conclusions:
- IQ, specifically fluid intelligence, significantly increased in children with GH deficiency following treatment.
- Pre-treatment GH/IGF-I axis status was a significant predictor of cognitive improvements.
Background/Aims:
We investigated the association between cognition and growth hormone (GH) status and GH treatment in short prepubertal children with broadly ranging GH secretion.
Methods:
A total of 99 children (age 3-11 years), 41 with GH deficiency (GHD) and 58 with idiopathic short stature (ISS), were randomized to a fixed dose (43 µg/kg/day) or a prediction model-guided individualized dose (17-100 µg/kg/day) and followed up for 24 months. In a longitudinal and mixed within- and between-subjects study, we examined clinical effect size changes, measured by Cohen's d, in full-scale IQ (FSIQ) and secondary IQ indices.
Results:
Significant increases giving medium effect size in FSIQ (p = 0.001, Cohen's d = 0.63), performance IQ (p = 0.001, Cohen's d = 0.65) and processing speed (p = 0.005, Cohen's d = 0.71) were found in the GH-deficient group. In contrast, perceptual organization only increased in the ISS group (p = 0.001, Cohen's d = 0.53). Baseline IQ was normally distributed with small but significant differences between the groups: GH-deficient children had lower FSIQ (p = 0.042) and lower performance IQ (p = 0.021). Using multiple regression analysis, 40% of the variance in delta processing speed scores (0-24 months) was explained by GHmax and IGF-ISDS at baseline.
Conclusion:
IQ, specifically fluid intelligence, increased in the GH-deficient children. The pretreatment status of the GH/IGF-I axis was significantly predictive for these changes.
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