Thyroid-stimulating hormone decreases the risk of osteoporosis by regulating osteoblast proliferation and differentiation
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Abstract
Background: As the incidence of secretory osteoporosis has increased, bone loss, osteoporosis and their relationships with thyroid-stimulating hormone (TSH) have received increased attention. In this study, the role of TSH in bone metabolism and its possible underlying mechanisms were investigated. Methods: We analyzed the serum levels of free triiodothyronine (FT3), free thyroxine (FT4), and TSH and the bone mineral density (BMD) levels of 114 men with normal thyroid function. In addition, osteoblasts from rat calvarial samples were treated with different doses of TSH for different lengths of time. The related gene and protein expression levels were investigated. Results: A comparison of the BMD between the high-level and low-level serum TSH groups showed that the TSH serum concentration was positively correlated with BMD. TSH at concentrations of 10 mU/mL and 100 mU/mL significantly increased the mRNA levels of ALP, COI1 and Runx2 compared with those of the control ( P < 0.05, P < 0.01). Bone morphogenetic protein (BMP)2 activity was enhanced with both increased TSH concentration and increased time. The protein levels of Runx2 and osterix were increased in a dose-dependent manner. Conclusions: The circulating concentrations of TSH and BMD were positively correlated with normal thyroid function in males. TSH promoted osteoblast proliferation and differentiation in rat primary osteoblasts.
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TSH can promote the proliferation and differentiation of osteoblasts in rat primary osteoblasts.
“Additionally, it has been found that TSH can promote the proliferation and differentiation of osteoblasts in rat primary osteoblasts [6].”
From Effects of levothyroxine therapy on bone and mineral metabolism in hypothyroidism: a systematic review and meta-analysis (2025) · cites this paper as [6]
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Sorted by citations
Li, X., Zhang, T., Zhang, H., Liu, S., & Tian, L. (2025) · BMC Endocrine Disorders · doi:10.1186/s12902-024-01819-7 · Cited by 10 · see citing works
- Authors
- Deng, T., Zhang, W., Zhang, Y., Zhang, M., Huan, Z., Yu, C., Zhang, X., Wang, Y., & Xu, J.
- Affiliations
- Shandong University (CN)
- Corresponding author
- Xu, Jin
- Venue
- BMC Endocrine Disorders
- Published
- 2021-03-16
- Volume
- 21
- Issue
- 1
- Pages
- 49-49
- ISSN
- 1472-6823 (ISSN-L)
- PMC
- PMC7968288
- OpenAlex
- W3137335283
- Cited by
- 32
- References
- 5
- Citations by year
- 2026: 4 · 2025: 10 · 2024: 8 · 2023: 3 · 2022: 6 · 2021: 1
- FWCI
- 1.41
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- BMC Endocrine Disorders (publishedVersion, cc-by)
- Research Square (acceptedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Key Technology Research and Development Program of Shandong (2017G006006, 2016GGH3118)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Thyroid Disorders and Treatments
- Keywords
- thyroid-stimulating hormone, osteoporosis, bone mineral density, osteoblast proliferation, osteogenic differentiation, bone metabolism, Runx2, Osterix, BMP-2, calvarial osteoblasts, thyroid function
- MeSH terms
- Adult, Animals, Animals, Newborn, Cell Differentiation, Cells, Cultured, China, Cross-Sectional Studies, Humans, Male, Middle Aged, Osteoblasts, Osteoporosis, Risk Factors, Thyrotropin, Thyroxine, Triiodothyronine, Bone Density, Cell Proliferation, Rats
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