Structural determinants of vertebral fracture risk

Structural determinants of vertebral fracture risk
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DOI:
10.1359/jbmr.070728
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发表时间:
2007-12-01
影响因子:
6.2
通讯作者:
Khosla, Sundeep
Khosla, Sundeep
中科院分区:
医学1区
文献类型:
--
作者:
Melton, L. Joseph, III;Riggs, B. Lawrence;Khosla, Sundeep

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椎体骨折与特定骨密度、结构和强度参数的相关性比与区域BMD的相关性更强,但所有这些变量都是相关的。引言:目前尚不清楚区域BMD(aBMD)与椎体骨折风险的相关性是否取决于骨密度本身、骨宏观或微观结构、总体骨强度或脊柱负荷/骨强度比。我们从明尼苏达州罗切斯特的女性年龄分层样本中,确定了40名临床诊断为中度创伤引起的椎骨骨折(经血清定量证实)(例;平均年龄,78.6 ± 9.0岁),并将其与40名无骨质疏松性骨折的对照组进行比较(平均年龄,70.9 ± 6.8岁)。腰椎体积BMD(vBMD)和几何形状通过中央QCT进行评估,而微观结构通过高分辨率pQCT在超远端桡骨进行评估。从基于体素的有限元模型估计椎骨失效载荷(类似于强度),并且将风险因子(())确定为施加的脊柱载荷与失效载荷的比率。90 °前屈,2639与2706 N;年龄调整后p = 0.173)。然而,骨折病例的大多数骨密度和结构变量值较低。骨强度指标也降低了,在脊椎骨折的女性中,风险因素增加了35-37%。通过年龄调整的逻辑回归分析,五个主要变量类别中最强的骨折预测因子的相对风险是骨密度(总腰椎vBMD:OR/SD变化,2.2; 95% CI,1.1-4.3),骨几何结构(椎体表观皮质厚度:OR,2.1; 95% CI,1.1-4.1),骨显微结构(无显著性);骨强度(“皮质”[外部2 mm]抗压强度:OR,2.5; 95% CI,1.3-4.8)和风险因素((90 °前屈/整体椎体压缩强度:OR,3.2; 95% CI,1.4-7.5)。这些变量与脊柱aBMD(部分r,-0.32至0.75),但每一个都是一个更强的预测骨折的logistic回归analysis.Conclusions:aBMD与椎骨骨折风险的关联解释其相关性与更具体的骨密度,结构和强度参数。这些可以使更深入的了解骨折的发病机制。
Vertebral fractures are more strongly associated with specific bone density, structure, and strength parameters than with areal BMD, but all of these variables are correlated.Introduction: It is unclear whether the association of areal BMD (aBMD) with vertebral fracture risk depends on bone density per se, bone macro- or microstructure, overall bone strength, or spine load/bone strength ratios.Materials and Methods: From an age-stratified sample of Rochester, MN, women, we identified 40 with a clinically diagnosed vertebral fracture (confirmed serniquantitatively) caused by moderate trauma (cases; mean age, 78.6 +/- 9.0 yr) and compared them with 40 controls with no osteoporotic fracture (mean age, 70.9 +/- 6.8 yr). Lumbar spine volumetric BMD (vBMD) and geometry were assessed by central QCT, whereas microstructure was evaluated by high-resolution pQCT at the ultradistal radius. Vertebral failure load (similar to strength) was estimated from voxel-based finite element models, and the factor-of-risk (() was determined as the ratio of applied spine loads to failure load.Results: Spine loading (axial compressive force on L-3) was similar in vertebral fracture cases and controls (e.g., for 90 degrees forward flexion, 2639 versus 2706 N; age-adjusted p = 0.173). However, fracture cases had inferior values for most bone density and structure variables. Bone strength measures were also reduced, and the factor-of-risk was 35-37% greater (worse) among women with a vertebral fracture. By age-adjusted logistic regression, relative risks for the strongest fracture predictor in each of the five main variable categories were bone density (total lumbar spine vBMD: OR per SD change, 2.2; 95% CI, 1.1-4.3), bone geometry (vertebral apparent cortical thickness: OR, 2.1; 95% CI, 1.1-4.1), bone microstructure (none significant); bone strength ("cortical" [outer 2 mm] compressive strength: OR, 2.5; 95% CI, 1.3-4.8), and factor-of-risk (( for 90 degrees forward flexion/overall vertebral compressive strength: OR, 3.2; 95% CI, 1.4-7.5). These variables were correlated with spine aBMD (partial r, -0.32 to 0.75), but each was a stronger predictor of fracture in the logistic regression analyses.Conclusions: The association of aBMD with vertebral fracture risk is explained by its correlation with more specific bone density, structure, and strength parameters. These may allow deeper insights into fracture pathogenesis.