Hyperthyroid-associated osteoporosis is exacerbated by the loss of TSH signaling

被引:95
作者
Baliram, Ramkumarie [3 ]
Sun, Li [1 ,2 ]
Cao, Jay [4 ]
Li, Jianhua [1 ,2 ]
Latif, Rauf [3 ]
Huber, Amanda K. [3 ]
Yuen, Tony [1 ,2 ]
Blair, Harry C. [5 ,6 ]
Zaidi, Mone [1 ,2 ]
Davies, Terry F. [3 ]
机构
[1] Mt Sinai Sch Med, Mt Sinai Bone Program, Dept Med, New York, NY 10029 USA
[2] James J Peters VA Med Ctr, New York, NY USA
[3] Mt Sinai Sch Med, Thyroid Res Unit, New York, NY 10029 USA
[4] ARS, USDA, Human Nutr Res Ctr, Grand Forks, ND USA
[5] Univ Pittsburgh, Dept Pathol & Cell Biol, Pittsburgh, PA USA
[6] Pittsburgh VA Med Ctr, Pittsburgh, PA USA
关键词
THYROID-STIMULATING HORMONE; BONE-MINERAL DENSITY; SERUM TSH; POSTMENOPAUSAL WOMEN; RECOMBINANT TSH; OSTEOPROTEGERIN; POLYMORPHISM; FRACTURES; REGULATOR; TURNOVER;
D O I
10.1172/JCI63948
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The osteoporosis associated with human hyperthyroidism has traditionally been attributed to elevated thyroid hormone levels. There is evidence, however, that thyroid-stimulating hormone (TSH), which is low in most hyperthyroid states, directly affects the skeleton. Importantly, Tshr-knockout mice are osteopenic. In order to determine whether low TSH levels contribute to bone loss in hyperthyroidism, we compared the skeletal phenotypes of wild-type and Tshr-knockout mice that were rendered hyperthyroid. We found that hyperthyroid mice lacking TSHR had greater bone loss and resorption than hyperthyroid wild-type mice, thereby demonstrating that the absence of TSH signaling contributes to bone loss. Further, we identified a TSH-like factor that may confer osteoprotection. These studies suggest that therapeutic suppression of TSH to very low levels may contribute to bone loss in people.
引用
收藏
页码:3737 / 3741
页数:5
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