Slow growth and short stature in children with attention deficit hyperactivity disorder (ADHD): a retrospective study of 493 children who underwent growth hormone provocation testing at one tertiary paediatric endocrine centre
Abstract
Objectives
We hypothesised that growth hormone (GH) deficiency (GHD) in children with attention deficit hyperactivity disorder (ADHD) is rare. This study aimed to determine any distinct clinical or biochemical parameters, including GH provocation testing, in children with ADHD on psychostimulants or idiopathic short stature (ISS).
Methods
Retrospective cross-sectional study of children who had GH provocative testing between 1998 and 2013 at one tertiary paediatric endocrine centre. Clinical data included age, sex, anthropometry, pubertal staging, bone age, diagnostic code as per the European Society Paediatric Endocrinology (ESPE), GH provocation test results, thyroid function tests, serum insulin-like growth factor-1 (IGF-1) and insulin-like growth factor-binding protein-3 (IGFBP-3) levels.
Results
Four hundred ninety-three subjects underwent GH provocation testing for investigation of short stature to exclude GHD during the study period. Fifty-one children had a diagnosis of ADHD. In the remaining children, the diagnosis was Idiopathic short stature (n=240), GHD +/− hypopituitarism (n=60), and 142 subjects had other causes of short stature. Children with ADHD were older, had higher height and weight SDS and were GH-sufficient. All 51 children with ADHD had a normal serum IGFBP-3, while 20 out of these 51 subjects had a low serum IGF-1.
Conclusions
GHD in children with ADHD on psychostimulant medication is rare. GH testing in children with ADHD may not be necessary, particularly if serum IGFBP-3 is in the normal range. We suggest IGFBP-3 could be used as a surrogate marker of GH sufficiency in children with ADHD. However, this needs to be confirmed with a larger study group.
Acknowledgments
The authors would like to thank A/Prof Tony Hyunh and Dr Mark Harris for reviewing the manuscript, endocrine nurse Sinead Archibald from Mater Children’s Hospital for caring for patients during GH testing, and the participants and their families who participated in this study.
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Research ethics: Ethics approval was obtained from the Mater Health Services Human Research Ethics Committee.
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Informed consent: Not applicable.
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Author contributions: The authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: The authors declare that there is no conflict of interest associated with this manuscript.
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Research funding: None declared.
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Data availability: The raw data can be obtained on request from the corresponding author.
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Articles in the same Issue
- Frontmatter
- Review
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- Original Articles
- Comparison of the effectiveness of prepubertal growth hormone treatment on height and predicted adult height in children with short stature born small for gestational age vs. with a growth hormone deficiency
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- Endocrine sequelae after pediatric craniopharyngioma treatment: a single-center retrospective cohort study
- Premature ovarian insufficiency in pediatric cancer patients: a 10 year Rady Children’s Hospital experience
- Alterations in optical coherence tomography and optical coherence tomography angiography findings in children with partial biotinidase deficiency
- Slow growth and short stature in children with attention deficit hyperactivity disorder (ADHD): a retrospective study of 493 children who underwent growth hormone provocation testing at one tertiary paediatric endocrine centre
- Short Communication
- Assessment of diabetes-specific knowledge and its determinants among children with type 1 diabetes mellitus and their primary caregivers: Experience from a tertiary care center in North India
- Letters to the Editor
- Comment on “Diagnostic utility of the average peak LH levels measured during GnRH stimulation test”
- Author’s reply “Comment on diagnostic utility of the average peak LH levels measured during GnRH stimulation test”
- Case Reports
- Estrogen-insensitivity syndrome (EIS) in a female adolescent patient – a case report
- The complexities of managing a newborn with 6q24 transient neonatal diabetes mellitus: a case report
- Homozygous mutation of KISS1 receptor (KISS1R) gene identified in a Chinese patient with congenital hypogonadotropic hypogonadism (CHH): case report and literature review
- Selpercatinib prior to radioactive iodine for pediatric papillary thyroid carcinoma
Articles in the same Issue
- Frontmatter
- Review
- Selecting optimal progestational agents either alone or in combination in common pediatric endocrine settings: challenges of unmet needs
- Original Articles
- Comparison of the effectiveness of prepubertal growth hormone treatment on height and predicted adult height in children with short stature born small for gestational age vs. with a growth hormone deficiency
- Expanded phenotypic spectrum in MODY 5 patients with 17q12 deletion syndrome: experience from an Indian tertiary care hospital
- Endocrine sequelae after pediatric craniopharyngioma treatment: a single-center retrospective cohort study
- Premature ovarian insufficiency in pediatric cancer patients: a 10 year Rady Children’s Hospital experience
- Alterations in optical coherence tomography and optical coherence tomography angiography findings in children with partial biotinidase deficiency
- Slow growth and short stature in children with attention deficit hyperactivity disorder (ADHD): a retrospective study of 493 children who underwent growth hormone provocation testing at one tertiary paediatric endocrine centre
- Short Communication
- Assessment of diabetes-specific knowledge and its determinants among children with type 1 diabetes mellitus and their primary caregivers: Experience from a tertiary care center in North India
- Letters to the Editor
- Comment on “Diagnostic utility of the average peak LH levels measured during GnRH stimulation test”
- Author’s reply “Comment on diagnostic utility of the average peak LH levels measured during GnRH stimulation test”
- Case Reports
- Estrogen-insensitivity syndrome (EIS) in a female adolescent patient – a case report
- The complexities of managing a newborn with 6q24 transient neonatal diabetes mellitus: a case report
- Homozygous mutation of KISS1 receptor (KISS1R) gene identified in a Chinese patient with congenital hypogonadotropic hypogonadism (CHH): case report and literature review
- Selpercatinib prior to radioactive iodine for pediatric papillary thyroid carcinoma