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      Sex specific associations between common glucocorticoid receptor gene variants and hypothalamus-pituitary-adrenal axis responses to psychosocial stress.

      Biological Psychiatry
      Adaptation, Physiological, genetics, Adaptation, Psychological, Adrenocorticotropic Hormone, blood, drug effects, Adult, Analysis of Variance, Contraceptives, Oral, pharmacology, Ethinyl Estradiol, Female, Genetic Variation, Haplotypes, Humans, Hydrocortisone, metabolism, Hypothalamo-Hypophyseal System, physiology, Linkage Disequilibrium, Male, Pituitary-Adrenal System, Polymorphism, Genetic, Receptors, Glucocorticoid, Reference Values, Saliva, Sex Factors, Stress, Psychological

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          Abstract

          Alterations in glucocorticoid (GC) signaling have been associated with a number of psychiatric disorders. Genetic variation of the glucocorticoid receptor (GR) might be one of the factors underlying susceptibility to stress related disease. We investigated 206 healthy subjects and assessed associations between four common GR gene (NR3C1) polymorphisms (ER22/23EK, N363S, BclI, 9beta) and hypothalamic-pituitary-adrenal (HPA) axis responses to psychosocial stress (Trier Social Stress Test, TSST) and glucocorticoid sensitivity measured by a dexamethasone suppression test (DST). Male 9beta AG carriers displayed the highest adrenocorticotropic hormone (ACTH) and total cortisol TSST responses (for ACTH: main effect genotype p = .02) whereas male BclI GG carriers showed diminished responses. Remarkably, the BclI GG genotype in women (all using oral contraceptives) was associated with the highest total cortisol TSST responses, resulting in a significant sex by genotype interaction (p = .03). Following the DST, male 9beta AG carriers had elevated ACTH levels (sex by genotype interaction p = .03). We observed significant sex specific associations between GR gene polymorphisms and HPA axis responses to psychosocial stress as well as GC sensitivity. These findings support the relevance of GR gene polymorphisms in HPA axis regulation. Genetic variations of the GR might constitute a risk factor in development of HPA axis related disorders.

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