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吸烟与骨折风险:一项荟萃分析。

Smoking and fracture risk: a meta-analysis.

作者信息

Kanis J A, Johnell O, Oden A, Johansson H, De Laet C, Eisman J A, Fujiwara S, Kroger H, McCloskey E V, Mellstrom D, Melton L J, Pols H, Reeve J, Silman A, Tenenhouse A

机构信息

WHO Collaborating Centre for Metabolic Bone Diseases, University of Sheffield Medical School, Beech Hill Road, Sheffield, S10 2RX, UK.

出版信息

Osteoporos Int. 2005 Feb;16(2):155-62. doi: 10.1007/s00198-004-1640-3. Epub 2004 Jun 3.

Abstract

Smoking is widely considered a risk factor for future fracture. The aim of this study was to quantify this risk on an international basis and to explore the relationship of this risk with age, sex and bone mineral density (BMD). We studied 59,232 men and women (74% female) from ten prospective cohorts comprising EVOS/EPOS, DOES, CaMos, Rochester, Sheffield, Rotterdam, Kuopio, Hiroshima and two cohorts from Gothenburg. Cohorts were followed for a total of 250,000 person-years. The effect of current or past smoking, on the risk of any fracture, any osteoporotic fracture and hip fracture alone was examined using a Poisson model for each sex from each cohort. Covariates examined were age, sex and BMD. The results of the different studies were merged using the weighted beta-coefficients. Current smoking was associated with a significantly increased risk of any fracture compared to non-smokers (RR=1.25; 95% Confidence Interval (CI)=1.15-1.36). Risk ratio (RR) was adjusted marginally downward when account was taken of BMD, but it remained significantly increased (RR=1.13). For an osteoporotic fracture, the risk was marginally higher (RR=1.29; 95% CI=1.13-1.28). The highest risk was observed for hip fracture (RR=1.84; 95% CI=1.52-2.22), but this was also somewhat lower after adjustment for BMD (RR=1.60; 95% CI=1.27-2.02). Risk ratios were significantly higher in men than in women for all fractures and for osteoporotic fractures, but not for hip fracture. Low BMD accounted for only 23% of the smoking-related risk of hip fracture. Adjustment for body mass index had a small downward effect on risk for all fracture outcomes. For osteoporotic fracture, the risk ratio increased with age, but decreased with age for hip fracture. A smoking history was associated with a significantly increased risk of fracture compared with individuals with no smoking history, but the risk ratios were lower than for current smoking. We conclude that a history of smoking results in fracture risk that is substantially greater than that explained by measurement of BMD. Its validation on an international basis permits the use of this risk factor in case finding strategies.

摘要

吸烟被广泛认为是未来骨折的一个风险因素。本研究的目的是在国际范围内量化这一风险,并探讨该风险与年龄、性别和骨密度(BMD)之间的关系。我们研究了来自EVOS/EPOS、DOES、CaMos、罗切斯特、谢菲尔德、鹿特丹、库奥皮奥、广岛以及哥德堡的两个队列的59232名男性和女性(74%为女性)。这些队列总共随访了250000人年。使用泊松模型对每个队列中的每种性别,研究当前或过去吸烟对任何骨折、任何骨质疏松性骨折和仅髋部骨折风险的影响。所检查的协变量包括年龄、性别和骨密度。不同研究的结果使用加权β系数进行合并。与不吸烟者相比,当前吸烟与任何骨折风险显著增加相关(风险比(RR)=1.25;95%置信区间(CI)=1.15 - 1.36)。考虑骨密度后,风险比(RR)略有下调,但仍显著增加(RR = 1.13)。对于骨质疏松性骨折,风险略高(RR = 1.29;95% CI = 1.13 - 1.28)。髋部骨折的风险最高(RR = 1.84;95% CI = 1.52 - 2.22),但在调整骨密度后也有所降低(RR = 1.60;95% CI = 1.27 - 2.02)。所有骨折和骨质疏松性骨折的风险比在男性中显著高于女性,但髋部骨折并非如此。低骨密度仅占吸烟相关髋部骨折风险的23%。调整体重指数对所有骨折结局的风险有小幅下调作用。对于骨质疏松性骨折,风险比随年龄增加,但髋部骨折的风险比随年龄降低。与无吸烟史的个体相比,吸烟史与骨折风险显著增加相关,但风险比低于当前吸烟。我们得出结论,吸烟史导致的骨折风险远大于通过骨密度测量所解释的风险。其在国际范围内的验证使得该风险因素可用于病例发现策略。

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