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- W2147323739 endingPage "221" @default.
- W2147323739 startingPage "209" @default.
- W2147323739 abstract "Euthyroid status is essential for normal skeletal development and the maintenance of adult bone structure and strength. Established thyrotoxicosis has long been recognised as a cause of high bone turnover osteoporosis and fracture but more recent studies have suggested that subclinical hyperthyroidism and long-term suppressive doses of thyroxine (T 4 ) may also result in decreased bone mineral density (BMD) and an increased risk of fragility fracture, particularly in postmenopausal women. Furthermore, large population studies of euthyroid individuals have demonstrated that a hypothalamic–pituitary–thyroid axis set point at the upper end of the normal reference range is associated with reduced BMD and increased fracture susceptibility. Despite these findings, the cellular and molecular mechanisms of thyroid hormone action in bone remain controversial and incompletely understood. In this review, we discuss the role of thyroid hormones in bone and the skeletal consequences of hyperthyroidism." @default.
- W2147323739 created "2016-06-24" @default.
- W2147323739 creator A5031268979 @default.
- W2147323739 creator A5058291070 @default.
- W2147323739 creator A5068860861 @default.
- W2147323739 creator A5076653057 @default.
- W2147323739 date "2012-03-27" @default.
- W2147323739 modified "2023-10-14" @default.
- W2147323739 title "The skeletal consequences of thyrotoxicosis" @default.
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