Back to Search
Start Over
Heritability of Cortisol Production and Metabolism Throughout Adolescence
- 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.
- Subjects :
- Male
0301 basic medicine
Hypothalamo-Hypophyseal System
medicine.medical_specialty
Adolescent
Hydrocortisone
Endocrinology, Diabetes and Metabolism
Clinical Biochemistry
Physiology
Context (language use)
Quantitative trait locus
Biology
Biochemistry
Dizygotic twins
03 medical and health sciences
Quantitative Trait, Heritable
0302 clinical medicine
Endocrinology
3-Oxo-5-alpha-Steroid 4-Dehydrogenase
Internal medicine
Twins, Dizygotic
medicine
Cytochrome P-450 CYP3A
Humans
Prospective Studies
Registries
Child
Prospective cohort study
Clinical Research Articles
Netherlands
Biochemistry (medical)
Metabolism
Heritability
Twin study
Biosynthetic Pathways
030104 developmental biology
11-beta-Hydroxysteroid Dehydrogenases
Female
Oxidoreductases
030217 neurology & neurosurgery
Follow-Up Studies
Production rate
Subjects
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