Tsukamoto Manabu, Mori Toshiharu, Nakamura Eiichiro, Okada Yasuaki, Fukuda Hokuto, Yamanaka Yoshiaki, Sabanai Ken, Wang Ke-Yong, Hanagiri Takeshi, Kuboi Satoshi, Yatera Kazuhiro, Sakai Akinori
Department of Orthopedic Surgery, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Department of Orthopedic Surgery, Shin-Kokura Hospital, Federation of National Public Service, Kitakyushu, Japan.
Osteoporos Sarcopenia. 2020 Dec;6(4):179-184. doi: 10.1016/j.afos.2020.11.003. Epub 2020 Nov 24.
Chronic obstructive pulmonary disease (COPD) is a risk factor for osteoporosis. Nevertheless, much remains unclear regarding the bone metabolism dynamics associated with COPD. The present study focuses on the associations between the COPD severity and serum bone metabolism biomarkers.
We enrolled 40 patients who visited the orthopedics departments at our institutions and underwent dual-energy X-ray absorptiometry between September 2015 and December 2017. Only male osteoporosis patients over 45 years of age were included, and 5 patients were excluded due to disease or use of internal medicines affecting bone metabolism. All subjects underwent lung function testing, spine radiography, and blood tests. We measured percent forced expiratory volume in 1 second (%FEV), which reflects COPD severity, and we examined the relationships between %FEV and serum levels of bone metabolism biomarkers.
All subjects were diagnosed with osteoporosis based on T-scores. %FEV correlated with body weight, body mass index (BMI), and Z-score/T-scores. %FEV moderately correlated with serum levels of alkaline phosphatase (ALP), procollagen type 1 N-terminal propeptide (P1NP), and tartrate-resistant acid phosphatase 5b in the partial correlation analysis adjusted for BMI or T-score in the lumbar vertebrae. We performed a hierarchical multiple regression analysis to identify that serum ALP and P1NP were the independent explanatory variables to %FEV independent of other factors.
The data suggest that the COPD severity in middle-aged and older men with osteoporosis associates with decreased bone formation. COPD patients may exhibit bone metabolism dynamics characterized by low bone turnover with osteogenesis dysfunction as COPD becomes severe.
慢性阻塞性肺疾病(COPD)是骨质疏松症的一个危险因素。然而,与COPD相关的骨代谢动态仍有许多不清楚的地方。本研究聚焦于COPD严重程度与血清骨代谢生物标志物之间的关联。
我们纳入了2015年9月至2017年12月期间到我院骨科就诊并接受双能X线吸收测定的40例患者。仅纳入45岁以上的男性骨质疏松症患者,5例因疾病或使用影响骨代谢的内服药而被排除。所有受试者均接受了肺功能测试、脊柱X线摄影和血液检查。我们测量了反映COPD严重程度的1秒用力呼气量百分比(%FEV),并研究了%FEV与血清骨代谢生物标志物水平之间的关系。
所有受试者均根据T值诊断为骨质疏松症。%FEV与体重、体重指数(BMI)和Z值/T值相关。在根据腰椎BMI或T值进行校正的偏相关分析中,%FEV与血清碱性磷酸酶(ALP)、1型前胶原N端前肽(P1NP)和抗酒石酸酸性磷酸酶5b水平中度相关。我们进行了分层多元回归分析,以确定血清ALP和P1NP是独立于其他因素的%FEV的独立解释变量。
数据表明,患有骨质疏松症的中老年男性的COPD严重程度与骨形成减少有关。随着COPD病情加重,COPD患者可能表现出以骨转换低和成骨功能障碍为特征的骨代谢动态变化。