骨质疏松性椎体骨折级联的风险因素
Risk factors for osteoporotic vertebral fracture cascade
  
DOI:10.3969/j.issn.1006-7108.2023.02.009
中文关键词:  椎体骨折级联  骨密度  胸腰段骨折
英文关键词:vertebral fracture cascade  bone mineral density  thoracolumbar fractures
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樊宇宇 丁立祥 宋红星 侯宇 易蒙 王普石 乔军杰 方秀统* 首都医科大学附属北京世纪坛医院北京 100080 
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中文摘要:
      目的 研究椎体骨折级联(vertebral fractures cascade,VFC)发生的相关风险因素。方法 回顾性分析2015年1月1日至2020年12月31日在首都医科大学附属北京世纪坛医院诊断为骨质疏松性椎体骨折的444例患者的临床资料。统计所有患者的年龄、性别、体质量指数(body mass index,BMI)、骨折的部位、骨密度、是否有糖尿病、是否有慢性阻塞性肺疾病(chronic obstructive pulmonary disease,COPD)、是否有口服激素史。分析VFC发生的相关风险因素。按照是否发生VFC将患者分为两组,采用二元Logistic回归模型分析各风险因素。结果 在单因素分析中,椎体骨折级联的危险因素包括既往有糖尿病史(P=0.084)、既往口服糖皮质激素治疗史(P=0.022)、患有COPD(P=0.048)、骨折发生在胸腰段(P<0.001)、严重骨质疏松(T值≤-3.0)(P =0.087)、BMI≥28 kg/m2(P=0.012)。在多因素风险分析中,椎体骨折级联的风险因素包括有糖尿病史(风险比为1.689,P=0.047)、既往口服糖皮质激素治疗史(风险比为1.839,P=0.010)、患有COPD(风险比为2.103,P=0.026)、骨折发生在胸腰段(风险比为2.686,P<0.001)、BMI≥28 kg/m2(风险比为1.769,P=0.010)。结论 有糖尿病史、既往口服糖皮质激素治疗史、患有COPD、骨折发生在胸腰段、BMI≥28 kg/m2被确定为椎体骨折级联的独立危险因素,其中骨折发生在胸腰段为最重要的风险因素。
英文摘要:
      Objective To study the associated risk factors of the cascade of vertebral fractures (VFCs). Methods The clinical data of 444 patients diagnosed with osteoporotic vertebral fractures from January 1, 2015 to December 31, 2020 in Beijing Shijitan Hospital affiliated to Capital Medical University were retrospectively analyzed. All the patients were counted for age, sex, BMI, location of fracture, bone mineral density, presence of diabetes mellitus, presence of chronic obstructive pulmonary disease (COPD), and history of oral hormones. The risk factors associated with cascade (VFC) of vertebral fractures were analyzed. Patients were divided into two groups according to whether VFC occurred or not. The risk factors were analyzed using a binary logistic retrospective model. Results In the univariate analysis, risk factors for VFCs included previous history of diabetes mellitus (P=0.084), history of previous oral glucocorticoid therapy (P=0.022), COPD (P=0.048), fractures occurring in the thoracolumbar segment (P<0.001), severe osteoporosis (T-Score ≤ -3.0, P =0.087), and BMI ≥2 8 kg/m2 (P=0.012). In the multifactor risk analysis, risk factors for VFCs included history of diabetes mellitus (risk ratio 1.689, P=0.047), history of previous oral glucocorticoid therapy (risk ratio 1.839, P=0.010), COPD (risk ratio 2.103, P=0.026), fracture occurring in the thoracolumbar segment (risk ratio 2.686, P<0.001), and BMI ≥28 kg/m2 (risk ratio 1.769, P=0.010). Conclusion History of diabetes mellitus, previous oral glucocorticoid therapy, COPD, fractures in the thoracolumbar region, and BMI≥28 are identified as independent risk factors for VFCs. Among them, the occurrence of fractures in the thoracolumbar region is the most important risk factor.
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