Bone marrow fat composition as a novel imaging biomarker in postmenopausal women with prevalent fragility fractures

被引:285
作者
Patsch, Janina M. [1 ]
Li, Xiaojuan [1 ]
Baum, Thomas [1 ]
Yap, Samuel P. [1 ]
Karampinos, Dimitrios C. [1 ]
Schwartz, Ann V. [2 ]
Link, Thomas M. [1 ]
机构
[1] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, Musculoskeletal Quantitat Imaging Res Grp, San Francisco, CA 94107 USA
[2] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94107 USA
基金
奥地利科学基金会;
关键词
FRAGILITY FRACTURES; MR SPECTROSCOPY; BONE MARROW FAT; UNSATURATION LEVEL; TYPE 2 DIABETES MELLITUS; PROTON MR SPECTROSCOPY; MINERAL DENSITY; ADIPOSE-TISSUE; OLDER-ADULTS; DOCOSAHEXAENOIC ACID; IN-VIVO; OSTEOPOROSIS; RISK; INSIGHTS; RATIO;
D O I
10.1002/jbmr.1950
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The goal of this magnetic resonance (MR) imaging study was to quantify vertebral bone marrow fat content and composition in diabetic and nondiabetic postmenopausal women with fragility fractures and to compare them with nonfracture controls with and without type 2 diabetes mellitus. Sixty-nine postmenopausal women (mean age 63 +/- 5 years) were recruited. Thirty-six patients (47.8%) had spinal and/or peripheral fragility fractures. Seventeen fracture patients were diabetic. Thirty-three women (52.2%) were nonfracture controls. Sixteen women were diabetic nonfracture controls. To quantify vertebral bone marrow fat content and composition, patients underwent MR spectroscopy (MRS) of the lumbar spine at 3 Tesla. Bone mineral density (BMD) was determined by dual-energy X-ray absorptiometry (DXA) of the hip and lumbar spine (LS) and quantitative computed tomography (QCT) of the LS. To evaluate associations of vertebral marrow fat content and composition with spinal and/or peripheral fragility fractures and diabetes, we used linear regression models adjusted for age, race, and spine volumetric bone mineral density (vBMD) by QCT. At the LS, nondiabetic and diabetic fracture patients had lower vBMD than controls and diabetics without fractures (p = 0.018; p = 0.005). However, areal bone mineral density (aBMD) by DXA did not differ between fracture and nonfracture patients. After adjustment for age, race, and spinal vBMD, the prevalence of fragility fractures was associated with -1.7% lower unsaturation levels (confidence interval [CI] -2.8% to -0.5%, p = 0.005) and +2.9% higher saturation levels (CI 0.5% to 5.3%, p = 0.017). Diabetes was associated with -1.3% (CI -2.3% to -0.2%, p = 0.018) lower unsaturation and +3.3% (CI 1.1% to 5.4%, p = 0.004) higher saturation levels. Diabetics with fractures had the lowest marrow unsaturation and highest saturation. There were no associations of marrow fat content with diabetes or fracture. Our results suggest that altered bone marrow fat composition is linked with fragility fractures and diabetes. MRS of spinal bone marrow fat may therefore serve as a novel tool for BMD-independent fracture risk assessment. (C) 2013 American Society for Bone and Mineral Research.
引用
收藏
页码:1721 / 1728
页数:8
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