Phetfong Jitrada, Sanvoranart Tanwarat, Nartprayut Kuneerat, Nimsanor Natakarn, Seenprachawong Kanokwan, Prachayasittikul Virapong, Supokawej Aungkura
Department of Clinical Microscopy, Faculty of Medical Technology, Mahidol University, Phuttamonthon, Salaya, Nakhon Pathom 73170 Thailand.
Department of Clinical Microbiology and Applied Technology, Faculty of Medical Technology, Mahidol University, Phuttamonthon, Salaya, Nakhon Pathom 73170 Thailand.
Cell Mol Biol Lett. 2016 Aug 12;21:12. doi: 10.1186/s11658-016-0013-1. eCollection 2016.
Osteoporosis, or bone loss, is a progressive, systemic skeletal disease that affects millions of people worldwide. Osteoporosis is generally age related, and it is underdiagnosed because it remains asymptomatic for several years until the development of fractures that confine daily life activities, particularly in elderly people. Most patients with osteoporotic fractures become bedridden and are in a life-threatening state. The consequences of fracture can be devastating, leading to substantial morbidity and mortality of the patients. The normal physiologic process of bone remodeling involves a balance between bone resorption and bone formation during early adulthood. In osteoporosis, this process becomes imbalanced, resulting in gradual losses of bone mass and density due to enhanced bone resorption and/or inadequate bone formation. Several growth factors underlying age-related osteoporosis and their signaling pathways have been identified, such as osteoprotegerin (OPG)/receptor activator of nuclear factor B (RANK)/RANK ligand (RANKL), bone morphogenetic protein (BMP), wingless-type MMTV integration site family (Wnt) proteins and signaling through parathyroid hormone receptors. In addition, the pathogenesis of osteoporosis has been connected to genetics. The current treatment of osteoporosis predominantly consists of antiresorptive and anabolic agents; however, the serious adverse effects of using these drugs are of concern. Cell-based replacement therapy via the use of mesenchymal stem cells (MSCs) may become one of the strategies for osteoporosis treatment in the future.
骨质疏松症,即骨质流失,是一种渐进性的全身性骨骼疾病,影响着全球数百万人。骨质疏松症通常与年龄相关,而且由于在骨折发生之前的数年里一直没有症状,所以该疾病常常未被诊断出来,而骨折的发生会限制日常生活活动,在老年人中尤为如此。大多数骨质疏松性骨折患者会卧床不起,生命垂危。骨折的后果可能是毁灭性的,会导致患者出现严重的发病情况和死亡。在成年早期,骨骼重塑的正常生理过程涉及骨吸收和骨形成之间的平衡。在骨质疏松症中,这个过程会失衡,由于骨吸收增强和/或骨形成不足,导致骨量和骨密度逐渐流失。已经确定了一些与年龄相关的骨质疏松症相关的生长因子及其信号通路,如骨保护素(OPG)/核因子κB受体激活剂(RANK)/RANK配体(RANKL)、骨形态发生蛋白(BMP)、无翅型MMTV整合位点家族(Wnt)蛋白以及通过甲状旁腺激素受体的信号传导。此外,骨质疏松症的发病机制还与遗传学有关。目前骨质疏松症的治疗主要包括抗吸收和促合成药物;然而,使用这些药物的严重不良反应令人担忧。通过使用间充质干细胞(MSCs)进行基于细胞的替代疗法可能会成为未来骨质疏松症治疗的策略之一。