Bone stiffness and failure load are related with clinical parameters in men with chronic obstructive pulmonary disease

ABSTRACT Osteoporosis is frequently seen in patients with chronic obstructive pulmonary disease (COPD). Because research on bone structure and bone strength in COPD patients is limited, the objectives of this pilot study were as follows: (1) to compare bone structure, stiffness, and failure load, me...

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Veröffentlicht in:Journal of bone and mineral research 2013-10, Vol.28 (10), p.2186-2193
Hauptverfasser: Romme, Elisabeth APM, Rutten, Erica PA, Geusens, Piet, de Jong, Joost JA, van Rietbergen, Bert, Smeenk, Frank WJM, Wouters, Emiel FM, van den Bergh, Joop PW
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Sprache:eng
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Zusammenfassung:ABSTRACT Osteoporosis is frequently seen in patients with chronic obstructive pulmonary disease (COPD). Because research on bone structure and bone strength in COPD patients is limited, the objectives of this pilot study were as follows: (1) to compare bone structure, stiffness, and failure load, measured at the peripheral skeleton, between men with and without COPD after stratification for areal bone mineral density (aBMD); and (2) to relate clinical parameters with bone stiffness and failure load in men with COPD. We included 30 men with COPD (normal aBMD, n = 18; osteoporosis, n = 12) and 17 men without COPD (normal aBMD, n = 9; osteoporosis, n = 8). We assessed pack‐years of smoking, body mass index (BMI), fat free mass index (FFMI), pulmonary function (forced expiratory volume in 1 second [FEV1], FEV1/forced vital capacity [FVC], diffusion capacity for carbon monoxide [DLCO], and transfer coefficient for carbon monoxide [KCO]), and extent of emphysema. Bone structure of the distal radius and tibia was assessed by high‐resolution peripheral quantitative computed tomography (HR‐pQCT), and bone stiffness and failure load of the distal radius and tibia were estimated from micro finite element analysis (µFEA). After stratification for aBMD and COPD, men with osteoporosis showed abnormal bone structure (p 
ISSN:0884-0431
1523-4681
DOI:10.1002/jbmr.1947