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Published on: November 16, 2011
Exaggerated adrenarche and altered cortisol metabolism in Type 1 diabetic children
Thomas Remer1, Christiane Maser-Gluth, Kai R Boye
1Department of Nutrition and Health, Research Institute of Child Nutrition, Dortmund, Germany. remer@fke-do.de
Insights
Type 1 diabetes mellitus in children shows an exaggerated adrenarche, indicated by elevated urinary steroid markers. Cortisol inactivation is reduced, suggesting potential links to hyperandrogenic symptoms in female patients.
Area of Science:
- Endocrinology
- Pediatric Endocrinology
- Metabolic Disorders
Background:
- Steroid metabolism is reportedly dysregulated in Type 1 diabetes mellitus (T1DM).
- Adrenarche, the maturation of the adrenal gland, may be affected by T1DM and its treatment.
Purpose of the Study:
- To non-invasively examine cortisol metabolism in children with T1DM.
- To test if adrenarche is affected in children with T1DM under intensive insulin therapy.
Main Methods:
- Gas chromatography-mass spectrometry profiling of urinary steroids in 109 children with T1DM (aged 4-18 years).
- Quantification of urinary free cortisol (UFF) and cortisone (UFE) using RIA.
- Assessment of enzyme activities (5alpha-reductase, 11beta-HSD2) via metabolite ratios, compared to 400 healthy controls.
Main Results:
- Elevated urinary markers of adrenarche (dehydroepiandrosterone metabolites) and 6beta-hydroxycortisol, UFE, and 11beta-HSD2 activity in T1DM patients.
- Normal overall cortisol secretion but reduced 5alpha-reductase activity.
- Evidence of exaggerated adrenarche and reduced cortisol inactivation in T1DM children.
Conclusions:
- T1DM in children is associated with exaggerated adrenarche, potentially explaining hyperandrogenic symptoms in females.
- Reduced cortisol inactivation via 5alpha-reductase is not compensated by decreased cortisol secretion.
- Elevated urinary 6beta-hydroxycortisol and cortisone warrant further investigation as potential non-invasive clinical stress markers.
Abstract:
Reported literature data strongly suggest that steroid metabolism is dysregulated in Type 1 diabetes mellitus. The aim of this study was to non-invasively examine the cortisol metabolism in children with Type 1 diabetes mellitus (T1DM) in detail and to test the hypothesis that adrenarche is affected under conventional intensive insulin therapy. In 24-h urine samples of 109 patients aged 4-18 years with T1DM of more than 1 year, steroids were profiled using gas chromatography-mass spectrometry. Additionally, urinary free cortisol (UFF) and cortisone (UFE) were quantified by RIA after extraction and chromatographic purification. Data on urinary steroids from 400 healthy controls served as reference values. Enzyme activities were assessed by established steroid metabolite ratios, e.g. 5alpha-reductase and 11beta-hydroxysteroid dehydrogenase Type 2 (11beta-HSD2) by 5alpha-tetrahydrocortisol/tetrahydrocortisol and UFE/UFF, respectively. Urinary markers of adrenarche, especially dehydroepiandrosterone and its direct metabolites were elevated in patients, as were urinary 6beta-hydroxycortisol, UFE, and 11beta-HSD2 activity. However, overall cortisol secretion, as reflected by the sum of major urinary cortisol metabolites, was mostly normal and activity of 5alpha-reductase clearly reduced. Our study provides evidence for an exaggerated adrenarche in T1DM children, which may help to understand reported sequelae in female patients like hyperandrogenic symptoms. The findings also suggest a reduced cortisol inactivation via 5alpha-reductase that is not compensated by a fall in cortisol secretion. Whether the elevated urinary 6beta-hydroxycortisol and cortisone excretion, observed in the patients, are also present in other forms of hypercortisolism and may thus serve as non-invasive clinical stress markers deserves further study.
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