Abstract
Objectives
Copeptin is secreted in isomolar amounts along with AVP. Its stability makes it a perfect biomarker of AVP deficiency. In children, dynamic GH tests were shown to stimulate copeptin. Here, we retrospectively studied the effect of clonidine on copeptin release.
Methods
This is a monocentric retrospective analysis of donated residual serum samples from 42 children with suspected growth hormone deficiency (GHD) who underwent clonidine stimulation between 2020 and 2023. Copeptin was measured in baseline, 30-, 60-, 90- and 120-min samples by BRAHMS Copeptin proAVP Kryptor immunofluorescence assay.
Results
There were 20 patients with GHD and 22 without; no patient had polyuria-polydipsia syndrome. Median age was 6.7 years (quartiles; 5.6–7.8), and the median height was −2.92 SDS (−3.42 to −2.34). The median baseline level of copeptin was 5.6 pmol/L (3.4–9.6). Median copeptin mildly decreased to 4.5 pmol/L (3.0–10.0) after 30 min; this change was not significant (p=0.45). Thereafter, median values remained low at 4.6, 4.6, and 4.6 pmol/L (60, 90, and 120 min). There was no correlation between baseline copeptin levels and the diagnosis of GHD.
Conclusions
The clonidine stimulation test does not stimulate copeptin release and is not suitable for the assessment of AVP deficiency in children.
Acknowledgments
We are grateful to families and patients for providing residual blood samples.
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Research ethics: This study and the use of biobank samples were approved by the Ethics Committee of the Medical Faculty of Tübingen (768/2023BO2).
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Informed consent: All care givers gave their written informed consent for the unrestricted scientific use of the biobank samples.
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Author contributions: GB: Conceptualization, methodology, writing the original draft, and editing; KW: Methodology, formal analysis, editing, and review; AP: Methodology, formal analysis, editing, and review; RS: Methodology, formal analysis, editing, and review. All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Use of Large Language Models, AI and Machine Learning Tools: None declared.
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Conflict of interest: The authors state no conflict of interest.
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Research funding: None declared.
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Data availability: The data that support the findings of this study are available from the corresponding author G.B. upon reasonable request.
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© 2024 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Original Articles
- Effects of orlistat on body mass index and serum lipids in overweight and obese adolescents: a meta-analysis
- Psychological and behavioral assessments in girls with idiopathic central precocious puberty
- The effect of phlebotomy and placement of an intravenous catheter on plasma catecholamine and serum copeptin concentrations
- Laparoscopic adrenalectomy in children with diverse adrenal pathologies: the impact of pre-operative imaging in decision making process
- Short- to medium-term follow-up of normoponderal children and adolescents with subclinical hypothyroidism: a retrospective study of the last 15 years
- Newborn screening follow-up in Bavaria: height and weight in paediatric patients with congenital adrenal hyperplasia
- Patterns and determinants of serum amylase, lipase concentrations in Indian adolescents and youth with type 1 diabetes
- Pediatric Graves’ disease in Argentina: analyzing treatment strategies and outcomes
- Nephrogenic diabetes insipidus results from a novel in-frame deletion of AVPR2 gene in monozygotic-twin boys and their mother and grandmother
- Short Communication
- Does clonidine stimulate copeptin in children?
- Case Report and Review of the Literature
- Sialidosis type 1 in a Turkish family: a case report and review of literatures
- Case Reports
- Central precocious puberty in a toddler with hypothalamic hamartoma
- Autosomally dominantly inherited isolated gonadotropin deficiency via maternal assisted reproduction due to SOX10 mutation
- Unclear symptoms, early diagnosis and perfect outcome: a case diagnosed as sepiapterin reductase deficiency hidden behind vitamin B12 deficiency
Articles in the same Issue
- Frontmatter
- Original Articles
- Effects of orlistat on body mass index and serum lipids in overweight and obese adolescents: a meta-analysis
- Psychological and behavioral assessments in girls with idiopathic central precocious puberty
- The effect of phlebotomy and placement of an intravenous catheter on plasma catecholamine and serum copeptin concentrations
- Laparoscopic adrenalectomy in children with diverse adrenal pathologies: the impact of pre-operative imaging in decision making process
- Short- to medium-term follow-up of normoponderal children and adolescents with subclinical hypothyroidism: a retrospective study of the last 15 years
- Newborn screening follow-up in Bavaria: height and weight in paediatric patients with congenital adrenal hyperplasia
- Patterns and determinants of serum amylase, lipase concentrations in Indian adolescents and youth with type 1 diabetes
- Pediatric Graves’ disease in Argentina: analyzing treatment strategies and outcomes
- Nephrogenic diabetes insipidus results from a novel in-frame deletion of AVPR2 gene in monozygotic-twin boys and their mother and grandmother
- Short Communication
- Does clonidine stimulate copeptin in children?
- Case Report and Review of the Literature
- Sialidosis type 1 in a Turkish family: a case report and review of literatures
- Case Reports
- Central precocious puberty in a toddler with hypothalamic hamartoma
- Autosomally dominantly inherited isolated gonadotropin deficiency via maternal assisted reproduction due to SOX10 mutation
- Unclear symptoms, early diagnosis and perfect outcome: a case diagnosed as sepiapterin reductase deficiency hidden behind vitamin B12 deficiency