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Chinese Journal of Lung Diseases(Electronic Edition) ›› 2025, Vol. 18 ›› Issue (04): 546-551. doi: 10.3877/cma.j.issn.1674-6902.2025.04.009

• Original Article • Previous Articles    

Relationship between serum osteoprotegerin and diagnosis of chronic obstructive pulmonary bone loss and osteoporosis

Hui Yu1, Shuanglan Wang2, Qingneng Wu1, Changqi Yang1, Fengyang Peng1, Dengliang Guo1, Yi Zhang3, Li Cui4, Jiajia Wu5,()   

  1. 1Department of Orthopedics, Macheng People′s Hospital(Hubei University of Science and Technology Affiliated Hospital), Macheng 438300, China
    2Department of Respiratory Medicine, Macheng People′s Hospital(Hubei University of Science and Technology Affiliated Hospital), Macheng 438300, China
    3Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Hubei University of Science and Technology, Xianning 437100, China
    4Epartment of Respiratory Medicine, The First Affiliated Hospital of Changjiang University, Jingzhou 434000, China
    5Department of Respiratory and Critical Care Medicine, The First People′s Hospital of Wuxue City, Wuxue 435400, China
  • Received:2025-05-12 Online:2025-08-25 Published:2025-09-08
  • Contact: Jiajia Wu

Abstract:

Objective

To explore the relationship between serum osteoprotegerin (OPG) and the diagnosis of bone loss and osteoporosis in patients with chronic obstructive pulmonary disease (COPD).

Methods

From January 2021 to March 2024, ninety-five COPD patients with stable disease were recruited from Our hospital, and were divided into the normal bone mineral density (BMD) group (n=35), the reduced BMD group (n=37), and the osteoporosis group (n=23) according to the dual-energy X-ray absorptiometry (DEXA), and enzyme-linked immunosorbent assay (ELISA) was used to determine the serum OPG levels.

Results

Body mass index (BMI) and forceful lung capacity (FVC) were higher in the BMD normal group than in the BMD reduced and osteoporotic patients (P<0.05). Glycosylated hemoglobin (HbA1c) was lower in osteoporotic patients than in the BMD normal and reduced BMD groups, in addition to lower force expiratory volume in 1 second (FEV1) than in the BMD normal group (P<0.05). As BMD decreased, lumbar spine BMD and T scores as well as hip BMD and T scores gradually decreased (P<0.001); while serum OPG levels gradually increased (F=23.257, P<0.001). Serum OPG levels were significantly lower in patients with Global Initiative for Chronic Obstructive Lung Disease (GOLD) classification 1-2 than in patients with GOLD classification 3-4 (t=-3.332, P=0.001). Spearman′s correlation showed a weak negative correlation between serum OPG levels and FEV1(Rho=-0.205, P=0.046), FEV1/FVC (Rho=-0.236, P=0.022), and FEV25_75 (Rho=-0.226, P=0.028). The above BMI, HbA1c, FVC, FEV1, and OPG were included as independent variables in the multiple linear regression equation, and the results showed that BMI, HbA1c, and serum OPG were independently correlated with lumbar spine T-scores (P<0.05); whereas, BMI and serum OPG were also independently correlated with hip T-scores (P<0.05). The BMD normal group was used as a control, and serum OPG diagnosed decreased BMD with an AUC was 0.737(95%CI: 0.617~0.857), and the cutoff value was 187.01 pg/ml; with the patients with normal BMD and reduced BMD as the control, the AUC of serum OPG for diagnosing osteoporosis was 0.825 (95%CI: 0.741~0.909), and the cutoff value was 206.39 pg/ml; with the reduced BMD group as a control, the AUC of serum OPG for diagnosis of BMD reduction was 0.683 (95%CI: 0.550~0.815), and the cutoff value was 187.01 pg/ml; all P<0.05.

Conclusion

High serum OPG levels are associated with the risk of osteoporosis in COPD patients, therefore OPG may be a biomarker for this COPD related comorbidity.

Key words: Chronic obstructive pulmonary disease, Osteoprotegerin, Osteoporosis, Biomarker, Diagnosis

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