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有父母骨折病史患者发生脆性骨折和低骨密度的预测因素。

Predictors of fragility fracture and low bone mineral density in patients with a history of parental fracture.

作者信息

Dey Mrinalini, Bukhari Marwan

机构信息

University Hospitals of Morecambe Bay NHS Foundation Trust, Royal Lancaster Infirmary, Rheumatology, Ashton Road, Lancaster, Lancashire, UK.

出版信息

Osteoporos Sarcopenia. 2019 Mar;5(1):6-10. doi: 10.1016/j.afos.2019.03.001. Epub 2019 Mar 15.

Abstract

OBJECTIVES

Bone mineral density (BMD) and fragility fracture (FF) have high heritability, but few data exist on impact of other factors on families with fracture history. We aimed to evaluate predictors of FF and low BMD, in patients with family history of FF.

METHODS

This was a retrospective study on patients undergoing dual energy X-ray absorptiometry at a district general hospital (DGH), 2004-2016. Parameters recorded (in addition to standard dual energy X-ray absorptiometry parameters): age, smoking, alcohol, corticosteroids, aromatase inhibitors, Depo-Provera, hormone replacement therapy, rheumatoid arthritis, polymyalgia rheumatica, breast or prostate cancer, coeliac disease, and fracture site. Logistic regression was used to model fracture risk and site, and linear regression for impact of factors on L1-4 and femoral BMD. Factor analyses with polychoric correlation matrices and calculation of Eigenvalues were applied to determine association between fracture sites and associated risk factors.

RESULTS

A total of 6053 patients were included, 91.1% female. 2094 had sustained at least one FF. Smoking, alcoholism, increased age, height, and fat mass increased FF risk. Sites analysed: femur, tibia/fibula, humerus, forearm, ribs, and vertebrae. Alcoholism, and increasing tissue thickness and fat mass significantly increased FF risk. Decreased right femoral and vertebral BMD increased overall FF risk.

CONCLUSIONS

Our study confirms the effect of certain factors on vertebral BMD, but suggests a differential effect on the upper and lower spine, as well as in the dominant and nondominant hip. Different sites of fracture are associated with different risk factors, the most common sites of fracture being the peripheral long bones and vertebrae.

摘要

目的

骨密度(BMD)和脆性骨折(FF)具有较高的遗传度,但关于其他因素对有骨折病史家庭的影响的数据较少。我们旨在评估有脆性骨折家族史患者中脆性骨折和低骨密度的预测因素。

方法

这是一项对2004年至2016年在一家地区综合医院(DGH)接受双能X线吸收测定的患者进行的回顾性研究。记录的参数(除标准双能X线吸收测定参数外):年龄、吸烟、饮酒、皮质类固醇、芳香化酶抑制剂、醋酸甲羟孕酮、激素替代疗法、类风湿性关节炎、风湿性多肌痛、乳腺癌或前列腺癌、乳糜泻以及骨折部位。采用逻辑回归对骨折风险和部位进行建模,采用线性回归分析各因素对L1 - 4和股骨骨密度的影响。应用具有多序相关矩阵的因子分析和特征值计算来确定骨折部位与相关危险因素之间的关联。

结果

共纳入6053例患者,其中91.1%为女性。2094例患者至少发生过一次脆性骨折。吸烟、酗酒、年龄增加、身高增加和脂肪量增加会增加脆性骨折风险。分析的骨折部位包括:股骨、胫腓骨、肱骨、前臂、肋骨和椎骨。酗酒、组织厚度增加和脂肪量增加显著增加脆性骨折风险。右侧股骨和椎骨骨密度降低会增加总体脆性骨折风险。

结论

我们的研究证实了某些因素对椎骨骨密度的影响,但提示对上下脊柱以及优势髋和非优势髋有不同影响。不同的骨折部位与不同的危险因素相关,最常见的骨折部位是外周长骨和椎骨。

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