Choi Han Seok, Park So Young, Kim Yoo Mee, Kim Se Hwa, Kim Kyoung Min, Chung Yoon-Sok
Division of Endocrinology and Metabolism, Department of Internal Medicine, Dongguk University Ilsan Hospital, Koyang, Gyeonggi-do, South Korea.
Division of Endocrinology and Metabolism, Department of Internal Medicine, Cheil General Hospital and Women's Healthcare Center, Dankook University College of Medicine, Seoul, South Korea.
Osteoporos Sarcopenia. 2016 Mar;2(1):13-19. doi: 10.1016/j.afos.2016.02.003. Epub 2016 Mar 16.
Osteoporosis is a metabolic bone disease characterized by decreased bone strength, leading to an increased risk of fracture. The World Health Organization (WHO) defines osteoporosis as a bone mineral density (BMD) of 2.5 standard deviations below that of a young adults (T-score of -2.5 or lower). Severe osteoporosis is differentiated from osteoporosis by the presence of one or more fragility fractures in addition to this T-score. However, the current WHO definition may be insufficient to reflect the diverse spectrum of osteoporosis or severe osteoporosis, which can encompass various number and severity of prevalent fractures. To overcome these shortcomings of the WHO definition of osteoporosis, we propose a concept of 'advanced severe osteoporosis', which is defined by the presence of proximal femur fragility fracture or two or more fragility fractures in addition to BMD T-score of -2.5 or less. Based on the previous clinical trials and analyses, we recommend selective estrogen receptor modulators, bisphosphonates, receptor activator of nuclear factor kappa-B ligand (RANKL) monoclonal antibody, and parathyroid hormone for the medical treatment of severe osteoporosis. In cases of advanced severe osteoporosis or osteoporosis that does not respond to previous anti-osteoporotic treatments, we also recommend parathyroid hormone, bisphosphonates, and RANKL monoclonal antibody. In conclusion, we need more precise assessment of osteoporosis and further stratification of the disease by number of prevalent fractures in addition to BMD. More aggressive managements should be provided for those with advanced severe osteoporosis.
骨质疏松症是一种代谢性骨病,其特征是骨强度降低,导致骨折风险增加。世界卫生组织(WHO)将骨质疏松症定义为骨矿物质密度(BMD)比年轻成年人低2.5个标准差(T值为-2.5或更低)。严重骨质疏松症与骨质疏松症的区别在于,除了这个T值外,还存在一处或多处脆性骨折。然而,目前WHO的定义可能不足以反映骨质疏松症或严重骨质疏松症的多种情况,这些情况可能包括各种数量和严重程度的既往骨折。为了克服WHO骨质疏松症定义的这些缺点,我们提出了“晚期严重骨质疏松症”的概念,其定义为除了BMD T值为-2.5或更低外,还存在股骨近端脆性骨折或两处或更多处脆性骨折。根据先前的临床试验和分析,我们推荐选择性雌激素受体调节剂、双膦酸盐、核因子κB受体活化因子配体(RANKL)单克隆抗体和甲状旁腺激素用于严重骨质疏松症的药物治疗。对于晚期严重骨质疏松症或对先前抗骨质疏松治疗无反应的骨质疏松症患者,我们还推荐甲状旁腺激素、双膦酸盐和RANKL单克隆抗体。总之,除了BMD外,我们还需要更精确地评估骨质疏松症,并根据既往骨折的数量对该疾病进行进一步分层。对于晚期严重骨质疏松症患者,应提供更积极的管理。