4.7 Article

Volumetric Cortical Bone Porosity Assessment with MR Imaging: Validation and Clinical Feasibility

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RADIOLOGY
卷 276, 期 2, 页码 526-535

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RADIOLOGICAL SOC NORTH AMERICA
DOI: 10.1148/radiol.15141850

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  1. National Institutes of Health [K25 AR 060283, R01 AR 50068, R03 AR 064577]

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Purpose: To develop a method to assess volumetric cortical bone porosity in clinically practical acquisition times by measuring the signal decay at only two echo times (TEs) as part of a single three-dimensional ultrashort TE (UTE) magnetic resonance (MR) examination. Materials and Methods: The study was approved by the institutional review board and complied with HIPAA guidelines. Written informed consent was obtained from all subjects. A marker of cortical bone porosity called porosity index was defined as the ratio of UTE image intensities at a long and short TE, and the results were compared with biexponential analysis. Porosity index of midtibia cortical bone samples obtained from 16 donors was compared with ground-truth porosity by using micro-computed tomographic (CT) imaging and bone mineral density by peripheral quantitative CT scanner. Reproducibility of porosity index were tested in volunteers, and clinical feasibility was evaluated in postmenopausal women. Interparameter associations were assessed by using Pearson or Spearman correlation coefficient. Results: Bone specimen porosity index was correlated with micro-CT imaging porosity (R-2 = 0.79) and pore size (R-2 = 0.81); age (R-2 = 0.64); peripheral quantitative CT scanner density (R-2 = 0.49, negatively); and pore water fraction (R-2 = 0.62) and T2* (R-2 = 0.64) by biexponential analysis. The reproducibility study yielded a coefficient of variation of 2.2% and intraclass correlation coefficient of 0.97. The study that involved postmenopausal women showed a wide range of porosity index (15%-38%). Conclusion: A two-point MR imaging method to assess cortical bone porosity in humans was conceived and validated. This approach has the potential for clinical use to assess changes in cortical bone porosity that result from disease or in response to therapy. (C)RSNA, 2015

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