Severity of obstructive airway disease and risk of osteoporotic fracture

被引:103
作者
de Vries, F
van Staa, TP
Bracke, MSGM
Cooper, C
Leufkens, HGM
Lammers, JWJ
机构
[1] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Dept Pharmacoepidemiol & Pharmacotherapy 11, NL-3584 CA Utrecht, Netherlands
[2] Utrecht Med Ctr, Dept Pulm Dis, Utrecht, Netherlands
[3] Univ Southampton, Southampton Gen Hosp, Med Res Council, Southampton, Hants, England
[4] Procter & Gamble Pharmaceut, Egham, Surrey, England
关键词
anti-inflammatory agents; bronchodilator agents; hip fractures; obstructive lung diseases; spinal fractures;
D O I
10.1183/09031936.05.00058204
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The use of inhaled corticosteroids has been associated with a dose-related increased risk of fracture. This may be related to systemic absorption. However, several studies have found that patients with more severe reductions in pulmonary function had reduced bone mineral density, independent of inhaled corticosteroids. The objective of this study was to evaluate the relationship between disease severity and fracture risk. A large case-control study (108,754 cases) was conducted using data from the UK General Practice Research Database. It was found that higher doses of inhaled corticosteroids were associated with greater risks of fracture. The crude odds ratio of fracture among patients exposed to > 1,600 mu g beclomethasone equivalents per day was 1.95 (95% confidence interval (CI) 1.68-2.27). When adjustments were made for disease severity and use of bronchodilators, the initial dose-response relationship between inhaled corticosteroids and fracture risk disappeared (adjusted odds ratio of 1.19 (95% CI 1.01-1.41)). In conclusion, patients with severe obstructive airway disease are at risk of fracture. However, adequate adjustment for disease severity is essential when the association between the use of inhaled corticosteroids and risk of osteoporotic fracture is studied in observational research.
引用
收藏
页码:879 / 884
页数:6
相关论文
共 46 条
[1]  
[Anonymous], 2002, COCHRANE DB SYST REV
[2]  
[Anonymous], 2002, ATC CLASSIFICATION I
[3]   Interleukin-8 stimulation of osteoclastogenesis and bone resorption is a mechanism for the increased osteolysis of metastatic bone disease [J].
Bendre, MS ;
Montague, DC ;
Peery, T ;
Akel, NS ;
Gaddy, D ;
Suva, LJ .
BONE, 2003, 33 (01) :28-37
[4]   Associated loss of fat-free mass and bone mineral density in chronic obstructive pulmonary disease [J].
Bolton, CE ;
Ionescu, AA ;
Shiels, KM ;
Pettit, RJ ;
Edwards, PH ;
Stone, MD ;
Nixon, LS ;
Evans, WD ;
Griffiths, TL ;
Shale, DJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (12) :1286-1293
[5]   Osteoclast differentiation and activation [J].
Boyle, WJ ;
Simonet, WS ;
Lacey, DL .
NATURE, 2003, 423 (6937) :337-342
[6]  
*BRIT MED ASS, 1999, BRIT NAT FORM, V37
[7]  
CHUNG K, 2002, ASTHMA COPD BASIC ME
[8]   Bone loss in patients with untreated chronic obstructive pulmonary disease is mediated by an increase in bone resorption associated with hypercapnia [J].
Dimai, HP ;
Domej, W ;
Leb, G ;
Lau, KHW .
JOURNAL OF BONE AND MINERAL RESEARCH, 2001, 16 (11) :2132-2141
[9]   Leisure-time physical activity patterns among US adults with asthma [J].
Ford, ES ;
Heath, GW ;
Mannino, DM ;
Redd, SC .
CHEST, 2003, 124 (02) :432-437
[10]   TETRACYCLINE-BASED HISTOLOGICAL ANALYSIS OF BONE REMODELING [J].
FROST, HM .
CALCIFIED TISSUE RESEARCH, 1969, 3 (03) :211-&