Saito Mitsuru, Marumo Keishi
Department of Orthopaedic Surgery, Jikei University School of Medicine, Tokyo, Japan.
Clin Calcium. 2016 Jan;26(1):29-41.
Bone mineral density(BMD)and bone microstructure are regulated mainly by bone remodeling. In contrast, bone collagen enzymatic immature and mature cross-links and advanced glycation end products such as pentosidine and carboxyl methyl lysine are affected by various factors. Aging bone tissue is repaired in the process of bone remodeling. However, deterioration of bone material properties markedly advances due to increases in oxidative stress, glycation stress, reactive oxygen species, carbonyl stress associated with aging and reduced sex hormone levels, and glucocorticoid use. To improve bone material properties in osteoporosis, we should use different drug (Saito M, Calcif Tissue Int, REVIEW, 97;242-261, 2015). In this review, we summarized determinants of bone quality and strength independent of bone remodeling.
骨矿物质密度(BMD)和骨微结构主要由骨重塑调节。相比之下,骨胶原的酶促未成熟和成熟交联以及晚期糖基化终产物(如戊糖苷和羧甲基赖氨酸)受多种因素影响。老化的骨组织在骨重塑过程中得到修复。然而,由于与衰老相关的氧化应激、糖基化应激、活性氧、羰基应激增加以及性激素水平降低和糖皮质激素的使用,骨材料特性的恶化明显加剧。为改善骨质疏松症中的骨材料特性,我们应使用不同药物(斋藤M,《钙化组织国际》,综述,97;242 - 261,2015)。在本综述中,我们总结了独立于骨重塑的骨质量和强度的决定因素。