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  • Title: 1,25-dihydroxyvitamin D deficiency accelerates alveolar bone loss independent of aging and extracellular calcium and phosphorus.
    Author: Gong A, Chen J, Wu J, Li J, Wang L, Goltzman D, Miao D.
    Journal: J Periodontol; 2018 Aug; 89(8):983-994. PubMed ID: 29637561.
    Abstract:
    BACKGROUND: Vitamin D is critical for bone homeostasis and immunomodulation. We therefore assessed whether 1,25-dihydroxyvitamin D (1,25(OH)2 D) deficiency in mice with targeted deletion of the gene encoding 25-hydroxyvitamin D-1α-hydroxylase (1α(OH)ase [1αOH)ase-/- mice]) results in alveolar bone loss and periodontal inflammation in vivo. METHODS: Ten-week-old and 12-month-old 1α(OH)ase-/- mice and wild-type littermates were fed a normal diet or a rescue diet, and the phenotype of the periodontium was then analyzed using microcomputed tomography, histology, immunohistochemistry, and real-time Reverse transcription-polymerase chain reaction (RT-PCR). RESULTS: Alveolar bone loss was increased and maxillary bone mineral density (BMD), osteoblast numbers, and the number of osterix-positive cells were decreased significantly in 1α(OH)ase-/- mice compared with wild-type mice. Although aging from 10 weeks to 12 months accentuated these changes, and a rescue diet reduced them, the alterations in the 1α(OH)ase-/- mice exceeded the effects of aging and diet change. Nuclear factor kappa light-chain-enhancer of activated B cells (NF-кB) p65 and CD3 positive cells, and the gene expression levels of interleukin (IL)-1β, tumor necrosis factor (TNF)-α, matrix metalloproteinase (MMP)-3 and -8 were all increased significantly in periodontal tissues of 1α(OH)ase-/- mice compared with wild-type mice. Aging from 10 weeks to 12 months also accentuated these changes, and a rescue diet reduced them, however, the alterations in the 1α(OH)ase-/- mice exceeded the effects of aging and diet change. CONCLUSION: 1,25(OH)2 D deficiency in the 1α(OH)ase-/- mice accelerated alveolar bone loss by inhibiting osteoblastic bone formation and enhancing periodontal tissue degeneration in a calcium- and phosphorus- as well as an age-independent manner.
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