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Heritability of Cortisol Production and Metabolism Throughout Adolescence

Authors :
Dorret I. Boomsma
Conor V. Dolan
Ruth Andrew
Brian R. Walker
Martijn J J Finken
Hilleke E. Hulshoff Pol
Joost Rotteveel
Britt J van Keulen
Pediatric surgery
ACS - Diabetes & metabolism
AGEM - Endocrinology, metabolism and nutrition
Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep
Amsterdam Reproduction & Development (AR&D)
Source :
van Keulen, B J, Dolan, C V, Andrew, R, Walker, B R, Hulshoff Pol, H E, Boomsma, D I, Rotteveel, J & Finken, M J J 2020, ' Heritability of Cortisol Production and Metabolism Throughout Adolescence ', The Journal of clinical endocrinology and metabolism, vol. 105, no. 2, dgz016 . https://doi.org/10.1210/clinem/dgz016, The Journal of Clinical Endocrinology and Metabolism, The Journal of clinical endocrinology and metabolism, 105(2):dgz016. The Endocrine Society
Publication Year :
2019
Publisher :
The Endocrine Society, 2019.

Abstract

Context Inter-individual differences in cortisol production and metabolism emerge with age and may be explained by genetic factors. Objective To estimate the relative contributions of genetic and environmental factors to inter-individual differences in cortisol production and metabolism throughout adolescence. Design Prospective follow-up study of twins. Setting Nationwide register. Participants 218 mono- and dizygotic twins (N = 109 pairs) born between 1995 amd 1996, recruited from the Netherlands Twin Register. Cortisol metabolites were determined in 213, 169, and 160 urine samples at the ages of 9, 12, and 17, respectively. Main outcome measures The total contribution of genetic factors (broad-sense heritability) and shared and unshared environmental influences to inter-individual differences in cortisol production and activities of 5α-reductase, 5β-reductase, and 11β-hydroxysteroid dehydrogenases and cytochrome P450 3A4. Results For cortisol production rate at the ages of 9, 12, and 17, broad-sense heritability was estimated as 42%, 30%, and 0%, respectively, and the remainder of the variance was explained by unshared environmental factors. For cortisol metabolism indices, the following heritability was observed: for the A-ring reductases (5α-and 5β-reductases), broad-sense heritability increased with age (to >50%), while for the other indices (renal 11β-HSD2, global 11β-HSD, and CYP3A4), the contribution of genetic factors was highest (68%, 18%, and 67%, respectively) at age 12. Conclusions The contribution of genetic factors to inter-individual differences in cortisol production decreased between 12 and 17y, indicative of a predominant role of individual circumstances. For cortisol metabolism, distinct patterns of genetic and environmental influences were observed, with heritability that either increased with age or peaked at age 12y.

Details

ISSN :
19457197 and 0021972X
Volume :
105
Database :
OpenAIRE
Journal :
The Journal of Clinical Endocrinology & Metabolism
Accession number :
edsair.doi.dedup.....188930e24b80fedaec665cca3aeb4a4e
Full Text :
https://doi.org/10.1210/clinem/dgz016