4.7 Article

Sex-specific metabolic profiles of androgens and its main binding protein SHBG in a middle aged population without diabetes

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SCIENTIFIC REPORTS
卷 7, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41598-017-02367-y

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  1. German Federal Ministry of Education and Research (BMBF) [01ZZ0403, 01ZZ0103, 01GI0883, AtheroSysMed 03IS2061B]
  2. Ministry for Education, Research and Cultural Affairs
  3. Ministry of Social Affairs of the Federal State of Mecklenburg-West Pomerania
  4. Federal Ministry of Education and Research
  5. Ministry of Cultural Affairs of the Federal State of Mecklenburg-West Pomerania [03IS2061A]
  6. German Center Diabetes Research (DZD e.V.) grant

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The role of androgens in metabolism with respect to sex-specific disease associations is poorly understood. Therefore, we aimed to provide molecular signatures in plasma and urine of androgen action in a sex-specific manner using state-of-the-art metabolomics techniques. Our study population consisted of 430 men and 343 women, aged 20-80 years, who were recruited for the cross-sectional population-based Study of Health in Pomerania (SHIP-TREND), Germany. We used linear regression models to identify associations between testosterone, androstenedione and dehydroepiandrosterone-sulfate (DHEAS) as well as sex hormone-binding globulin and plasma or urine metabolites measured by mass spectrometry. The analyses revealed major sex-specific differences in androgen-associated metabolites, particularly for levels of urate, lipids and metabolic surrogates of lifestyle factors, like cotinine or piperine. In women, in particular in the postmenopausal state, androgens showed a greater impact on the metabolome than in men (especially DHEAS and lipids were highly related in women). We observed a novel association of androstenedione on the metabolism of biogenic amines and only a small sex-overlap of associations within steroid metabolism. The present study yields new insights in the interaction between androgens and metabolism, especially about their implication in female metabolism.

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