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Estrogens and bone disease in chronic kidney disease: role of FGF23
Jorge B Cannata-Andía1, Natalia Carrillo-López, Manuel Naves-Díaz
1Bone and Mineral Research Unit, Hospital Universitario Central de Asturias, Instituto Reina Sofía de Investigación, REDinREN del ISCIII, Universidad de Oviedo, Oviedo, Asturias, Spain. metoseo@hca.es
Purpose Of Review:
To describe the direct and indirect effects of estrogen on bone with special emphasis on the analysis of the recent findings related to the putative role of FGF23 in the estrogen-dependent parathyroid hormone (PTH) suppression.
Recent Findings:
Estrogens act directly on bone cells, downregulating osteoclast precursors and differentiation, increasing osteoclast apoptosis and stimulating osteoblast proliferation and differentiation. However, estrogens can also act indirectly on bone, modulating the calcium-phosphorus-vitamin D-PTH axis. It has been recently demonstrated that estrogens suppress PTH synthesis and secretion in a dose-dependent manner and reduce serum calcitriol and phosphorus levels by an indirect mechanism. In-vivo and in-vitro experiments demonstrated that FGF23 positively correlated, also in a dose-dependent manner, with the dose of estrogens and with the observed changes in calcitriol and phosphorus.
Summary:
These new findings support the importance of the indirect effects of estrogens on bone, suggesting a role for FGF23 in the regulation of PTH by estrogens.
Insights
Estrogen impacts bone directly by affecting bone cells and indirectly by influencing the calcium-phosphorus-vitamin D-parathyroid hormone (PTH) axis. Recent findings suggest Fibroblast Growth Factor 23 (FGF23) plays a role in estrogen-mediated PTH suppression.
Area of Science:
- Endocrinology
- Bone Biology
- Mineral Metabolism
Background:
- Estrogen exerts significant influence on bone health through both direct and indirect mechanisms.
- Understanding the interplay between estrogen, bone cells, and mineral metabolism is crucial for bone health management.
Purpose of the Study:
- To elucidate the direct and indirect effects of estrogen on bone.
- To analyze recent findings on the role of Fibroblast Growth Factor 23 (FGF23) in estrogen-dependent parathyroid hormone (PTH) suppression.
Main Methods:
- Review of existing literature on estrogen's effects on bone cells (osteoblasts and osteoclasts).
- Analysis of in-vivo and in-vitro studies investigating the calcium-phosphorus-vitamin D-PTH axis.
- Examination of the correlation between estrogen dosage, FGF23 levels, and changes in calcitriol and phosphorus.
Main Results:
- Estrogens directly modulate bone cells, inhibiting osteoclast precursors and promoting osteoblast activity.
- Estrogens indirectly influence bone by regulating the calcium-phosphorus-vitamin D-PTH axis.
- Estrogen administration suppressed PTH secretion and reduced serum calcitriol and phosphorus levels, with FGF23 showing a dose-dependent positive correlation.
Conclusions:
- Recent findings highlight the significance of indirect estrogen effects on bone.
- FGF23 emerges as a potential mediator in the regulation of PTH by estrogens, impacting bone metabolism.
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