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Heritability of Cortisol Production and Metabolism Throughout Adolescence.
van Keulen, Britt J; Dolan, Conor V; Andrew, Ruth; Walker, Brian R; Hulshoff Pol, Hilleke E; Boomsma, Dorret I; Rotteveel, Joost; Finken, Martijn J J.
Afiliação
  • van Keulen BJ; Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Pediatric Endocrinology, Amsterdam, The Netherlands.
  • Dolan CV; Department of Biological Psychology, Vrije Universiteit Amsterdam, The Netherlands.
  • Andrew R; Centre for Cardiovascular Science, University of Edinburgh, Queen's Medical Research Institute, Edinburgh, UK.
  • Walker BR; Centre for Cardiovascular Science, University of Edinburgh, Queen's Medical Research Institute, Edinburgh, UK.
  • Hulshoff Pol HE; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
  • Boomsma DI; Department of Psychiatry, Brian Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Rotteveel J; Department of Biological Psychology, Vrije Universiteit Amsterdam, The Netherlands.
  • Finken MJJ; Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Pediatric Endocrinology, Amsterdam, The Netherlands.
J Clin Endocrinol Metab ; 105(2)2020 02 01.
Article em En | MEDLINE | ID: mdl-31608377
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, 5ß-reductase, and 11ß-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 5ß-reductases), broad-sense heritability increased with age (to >50%), while for the other indices (renal 11ß-HSD2, global 11ß-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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Gêmeos Dizigóticos / Hidrocortisona / Vias Biossintéticas Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adolescent / Child / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: J Clin Endocrinol Metab Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Gêmeos Dizigóticos / Hidrocortisona / Vias Biossintéticas Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adolescent / Child / Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: J Clin Endocrinol Metab Ano de publicação: 2020 Tipo de documento: Article