Laboratory of Ecobiomonitoring and Quality Control, Yaroslavl State University, 150003 Yaroslavl, Russia.
Center of Bioelementology and Human Ecology, Institute of Biodesign and Modeling of Complex Systems, Department of Therapy of the Institute of Postgraduate Education, IM Sechenov First Moscow State Medical University (Sechenov University), 119435 Moscow, Russia.
Biomolecules. 2023 Jun 17;13(6):1006. doi: 10.3390/biom13061006.
The objective of the present study was to review recent epidemiological and clinical data on the association between selected minerals and trace elements and osteoporosis, as well as to discuss the molecular mechanisms underlying these associations. We have performed a search in the PubMed-Medline and Google Scholar databases using the MeSH terms "osteoporosis", "osteogenesis", "osteoblast", "osteoclast", and "osteocyte" in association with the names of particular trace elements and minerals through 21 March 2023. The data demonstrate that physiological and nutritional levels of trace elements and minerals promote osteogenic differentiation through the up-regulation of BMP-2 and Wnt/β-catenin signaling, as well as other pathways. miRNA and epigenetic effects were also involved in the regulation of the osteogenic effects of trace minerals. The antiresorptive effect of trace elements and minerals was associated with the inhibition of osteoclastogenesis. At the same time, the effect of trace elements and minerals on bone health appeared to be dose-dependent with low doses promoting an osteogenic effect, whereas high doses exerted opposite effects which promoted bone resorption and impaired bone formation. Concomitant with the results of the laboratory studies, several clinical trials and epidemiological studies demonstrated that supplementation with Zn, Mg, F, and Sr may improve bone quality, thus inducing antiosteoporotic effects.
本研究旨在回顾近年来有关特定矿物质和微量元素与骨质疏松症之间关联的流行病学和临床数据,并讨论这些关联的分子机制。我们使用 MeSH 术语“骨质疏松症”、“成骨”、“成骨细胞”、“破骨细胞”和“骨细胞”,并结合特定微量元素和矿物质的名称,在 PubMed-Medline 和 Google Scholar 数据库中进行了搜索,截至 2023 年 3 月 21 日。数据表明,微量元素和矿物质的生理和营养水平通过上调 BMP-2 和 Wnt/β-catenin 信号通路以及其他途径促进成骨分化。miRNA 和表观遗传效应也参与了微量元素对成骨作用的调节。微量元素和矿物质的抗吸收作用与抑制破骨细胞生成有关。同时,微量元素和矿物质对骨骼健康的影响似乎呈剂量依赖性,低剂量促进成骨作用,而高剂量则产生相反的作用,促进骨吸收并损害骨形成。与实验室研究结果一致,几项临床试验和流行病学研究表明,补充 Zn、Mg、F 和 Sr 可能改善骨质量,从而产生抗骨质疏松作用。