The Journal of Clinical Endocrinology & Metabolism · 1999 · 74 citations · 19 references
Life SciencesEndocrinologyPhysiologyHormone BiochemistryMetabolic RegulationSteroid BiochemistryAdrenal Steroid HormonesAdrenal SteroidogenesisSteroid Hormone BiochemistrySteroid Metabolism11 Beta-hydroxylase11 Beta-hydroxysteroid DehydrogenaseAldosterone MetabolismDizygotic TwinsMonozygotic TwinsPlasma Steroid ProfilesPlasma Steroid ProfilingSteroid Metabolite Profiling
Corticosteroids are important in the regulation of normal physiology and are key factors in regulating cardiovascular physiology and disease, the development of which is known to have a genetic component. However, there is little information on the extent to which plasma and urine steroid levels are determined by familial and genetic factors. We have examined basal and ACTH-stimulated plasma steroid levels and 24-h corticosteroid metabolite excretion rates in 146 pairs of adult twins [75 monozygotic (MZ); 71 dizygotic (DZ)]. Intraclass correlation coefficients were measured for all variables; several plasma steroid measurements were strongly related in both (MZ) and (DZ) twins, consistent with a familial pattern. These included basal levels of 11-deoxycortisol and aldosterone. ACTH-stimulated plasma aldosterone levels were also significantly correlated, to a significant degree, in both MZ and DZ twins. The index of 11beta-hydroxysteroid dehydrogenase activity (tetrahydrocortisol + allotetrahydrocortisol/tetrahydrocortisone) and of the more specific index of activity of the type 2 isoform of this enzyme (urine free cortisol/cortisone) also correlated, to a similar degree, in DZ and MZ twins. In contrast, for the basal and ACTH-stimulated plasma concentrations and 24-h urine excretion rates of several corticosteroids, there was evidence of significant heritability (H2), in that correlation in MZ twins was greater than in DZ. For example, basal plasma corticosterone concentrations (B) (H2 = 0.44), basal and stimulated 11-deoxycorticosterone concentrations (DOC) (H2 = 0.44 and 0.41, respectively), stimulated 11-deoxycortisol concentrations (H2 = 0.53), and the index of 11beta-hydroxylase activity DOC/B (H2 = 0.49) were all significantly heritable. For the urinary variables, 24-h tetrahydrodeoxycortisol (H2 = 0.59) and free aldosterone (H2 = 0.56) were significantly heritable. Our data provide the first evidence that plasma and urine levels of important glucocorticoids and mineralocorticoids show a strong familial pattern, and in some instances, there is evidence of a genetic component to this. This suggests that corticosteroids have a plausible role in essential hypertension that has a similar heritable component.
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Roland Rosmond, Mary F. Dallman, Per Björntorp · The Journal of Clinical Endocrinology & Metabolism · 1998 · 876 citations · Full text
Cortisol Effects on Body Mass, Blood Pressure, and Cholesterol in the General Population
Robert Fraser, M Ingram, Niall Anderson et al. · Hypertension · 1999 · 371 citations · Full text
Graham Watt, Stephen Harrap, Christopher Foy et al. · Journal of Hypertension · 1992 · 304 citations
Life Sciences, Genetics, Physiology +13
Nannette A. T. M. Huizenga, Jan W. Koper, Pieter de Lange et al. · The Journal of Clinical Endocrinology & Metabolism · 1998 · 249 citations · Full text