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A case-control study of fractures in men with idiopathic osteoporosis: Fractures are associated with older age and low cortical bone density

机译:特发性骨质疏松症男性骨折的病例对照研究:骨折与年龄较大和皮质骨密度低有关

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Objectives: To determine biochemical, radiological and micro-architectural bone factors related to fragility fractures in idiopathic male osteoporosis (IMO) patients. IMO is a rare disorder characterized by low areal bone mineral density (aBMD) (Z-score - 2) occurring in men after excluding secondary causes of low BMD. Methods: We conducted a case-control study in 31 patients with fragility fracture (IMO F. +) that had occurred after the age of 40. years and 37 without fracture (IMO F-). We first compared IMO group to 40 age-matched disease-free men. We measured aBMD and bone micro-architectural indices at distal radius and tibia sites with a HR-pQCT scan (XtremeCT) using standard and extended cortical analysis. Urine and blood samples were collected in order to determine the levels of bone-turnover markers and the potential determinant of bone fragility. Models of analysis of covariance, including age, height and weight as adjustment factors, were used to compare the groups. Results: Compared to their controls, IMO patients showed marked disturbance of their micro-architectural parameters at tibia and radius affecting both trabecular and cortical parameters. IMO F+ subjects were significantly older than IMO F- subjects (58±8 vs. 53±9yrs, p=0.01). BMD Z-score at the total-hip was significantly lower in IMO F+ (-1.3±0.5 vs. -0.9±0.8g/cm2, p=0.01). After adjustment, trabecular micro-architectural parameters, biochemical markers and hormonal parameters were not different in the 2 groups. At distal tibia, cortical v-BMD was significantly lower in IMO F+ patients (799±73 vs. 858±60mg/cm3, p=0.03), while cortical thickness was not different. Conclusion: Our results show that patients with IMO display a marked disturbance of trabecular and cortical bone micro-architecture, and that age and low cortical density are determinants of the fracture occurrence.
机译:目的:确定与特发性男性骨质疏松症(IMO)患者脆性骨折有关的生化,放射学和微体系结构骨因素。 IMO是一种罕见疾病,其特征是排除了低BMD的继发原因后,男性发生了较低的面骨矿物质密度(aBMD)(Z评分<-2)。方法:我们对40岁以后发生的31例易碎性骨折(IMO F. +)和37例未发生骨折(IMO F-)的患者进行了病例对照研究。我们首先将IMO组与40名年龄匹配的无病男性进行了比较。我们使用标准和扩展皮层分析通过HR-pQCT扫描(XtremeCT)测量了radius骨远端和胫骨部位的aBMD和骨骼微结构指数。收集尿液和血液样本,以确定骨转换指标的水平和骨脆性的潜在决定因素。使用协方差分析模型(包括年龄,身高和体重作为调整因子)来比较各组。结果:与对照组相比,IMO患者的胫骨和radius骨微结构参数明显受到干扰,从而影响了小梁和皮质参数。 IMO F +受试者的年龄明显大于IMO F-受试者(58±8岁vs. 53±9岁,p = 0.01)。在IMO F +中,全髋关节的BMD Z评分显着降低(-1.3±0.5对-0.9±0.8g / cm2,p = 0.01)。调整后,两组的骨小梁微结构参数,生化指标和激素参数无差异。在胫骨远端,IMO F +患者的皮质v-BMD显着降低(799±73 vs. 858±60mg / cm3,p = 0.03),而皮质厚度没有差异。结论:我们的结果表明,IMO患者显示出明显的小梁和皮质骨微结构紊乱,年龄和低皮质密度是骨折发生的决定因素。

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