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Auer, Matthias K.; Paizoni, Luisa; Hofbauer, Lorenz C.; Rauner, Martina; Chen, Yiqing; Schmidt, Heinrich; Huebner, Angela; Bidlingmaier, Martin und Reisch, Nicole (2020): Effects of androgen excess and glucocorticoid exposure on bone health in adult patients with 21-hydroxylase deficiency. In: Journal of Steroid Biochemistry and Molecular Biology, Bd. 204, 105734

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Abstract

Context: This study aimed to determine the role of modifiable predictors on bone health in congenital adrenal hyperplasia (CAH). Design: Cross-sectional, single center study, including 97 patients (N = 42 men) with classic CAH due to 21hydroxylase deficiency (N = 65 salt wasting, N = 32 simple virilizing). Main Outcome Measures: Treatment-related predictors of bone health. Results: Average T scores (-0.9 1.4 vs. -0.4 +/- 1.4;p = 0.036) as well as Z scores (-1.0 +/- 1.3 vs. -0.1 +/- 1.4;p = 0.012) at the spine in patients with CAH were significantly lower in men than women. While osteoporosis was rare in women, it was documented in 9.1% of men with CAH. There was a significant positive correlation of Z scores at the spine with advancing age in women with CAH (R-2 = 0.178;p = 0.003). In multivariate analysis, the intake of conventional hydrocortisone (HC) instead of synthetic glucocorticoids was independently associated with a higher bone mineral density (BMD) at the hip region in both sexes. In women, there was a positive association with vitamin D concentrations. Interestingly, higher sodium levels were associated with a lower BMD independent of renin levels and fludrocortisone dosage. Neither in men nor in women, markers of androgen control were predictive for BMD at any site. Markers of bone turnover indicated low bone turnover. No pathological fractures were documented. Conclusions: Men with CAH are particularly prone to low bone density, while women seem to be relatively protected by androgen excess compared to the general female population. The use of HC instead of synthetic GCs for hormone replacement may translate into better bone health.

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