INSERM U606 and Univ Paris Diderot, Sorbonne Paris Cité, Bone and Joint Laboratory, 75010 Paris, France.
Bone. 2013 Jan;52(1):48-55. doi: 10.1016/j.bone.2012.09.020. Epub 2012 Sep 23.
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.
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.
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 ± 9 yrs, p=0.01). BMD Z-score at the total-hip was significantly lower in IMO F+ (-1.3 ± 0.5 vs. -0.9 ± 0.8 g/cm(2), 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 ± 60 mg/cm(3), p=0.03), while cortical thickness was not different.
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.
确定与特发性男性骨质疏松症(IMO)患者脆性骨折相关的生化、影像学和微观结构骨因素。IMO 是一种罕见疾病,其特征为低面积骨矿物质密度(aBMD)(Z 评分<-2),发生在排除低 BMD 继发原因后的 40 岁以上男性。
我们对 31 例年龄在 40 岁以上发生脆性骨折(IMO F+)的 IMO 患者和 37 例无骨折 IMO 患者(IMO F-)进行了病例对照研究。我们首先将 IMO 组与 40 名年龄匹配的无疾病男性进行比较。我们使用 HR-pQCT 扫描(XtremeCT)测量桡骨和胫骨远端的 aBMD 和骨微观结构指数,采用标准和扩展皮质分析。采集尿液和血液样本以确定骨转换标志物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素,比较各组。
与对照组相比,IMO 患者的胫骨和桡骨微观结构参数明显紊乱,影响了骨小梁和皮质参数。IMO F+ 患者明显比 IMO F-患者年龄大(58 ± 8 岁比 53 ± 9 岁,p=0.01)。IMO F+ 的全髋 BMD Z 评分明显低于 IMO F-(-1.3 ± 0.5 比-0.9 ± 0.8 g/cm(2),p=0.01)。调整后,两组间骨小梁微观结构参数、生化标志物和激素参数无差异。在胫骨远端,IMO F+ 患者的皮质 v-BMD 明显较低(799 ± 73 比 858 ± 60 mg/cm(3),p=0.03),而皮质厚度无差异。
我们的结果表明,IMO 患者的骨小梁和皮质骨微观结构明显紊乱,年龄和低皮质密度是骨折发生的决定因素。