Contributions of Material Properties and Structure to Increased Bone Fragility for a Given Bone Mass in the UCD-T2DM Rat Model of Type 2 Diabetes

被引:67
作者
Acevedo, Claire [1 ,2 ,3 ]
Sylvia, Meghan [1 ]
Schaible, Eric [4 ]
Graham, James L. [5 ,6 ]
Stanhope, Kimber L. [5 ,6 ]
Metz, Lionel N. [1 ]
Gludovatz, Bernd [7 ]
Schwartz, Ann V. [8 ]
Ritchie, Robert O. [2 ,9 ]
Alliston, Tamara N. [1 ]
Havel, Peter J. [5 ,6 ]
Fields, Aaron J. [1 ]
机构
[1] Univ Calif San Francisco, Dept Orthopaed Surg, San Francisco, CA USA
[2] Lawrence Berkeley Natl Lab, Div Mat Sci, Berkeley, CA USA
[3] Univ Utah, Dept Mech Engn, Salt Lake City, UT 84112 USA
[4] Adv Light Source, Expt Syst Grp, Berkeley, CA USA
[5] Univ Calif Davis, Dept Mol Biosci, Davis, CA 95616 USA
[6] Univ Calif Davis, Dept Nutr, Davis, CA 95616 USA
[7] UNSW Sydney, Sch Mech & Mfg Engn, Sydney, NSW, Australia
[8] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA
[9] Univ Calif Berkeley, Dept Mat Sci & Engn, Berkeley, CA 94720 USA
基金
美国国家科学基金会; 瑞士国家科学基金会;
关键词
COLLAGEN; BIOMECHANICS; BONE CT; PRECLINICAL STUDIES; METABOLISM; NONENZYMATIC GLYCATION; POSTMENOPAUSAL WOMEN; CORTICAL BONE; MECHANICAL-PROPERTIES; FRACTURE RISK; MINERAL DENSITY; CROSS-LINKS; MELLITUS; MICROARCHITECTURE; STRENGTH;
D O I
10.1002/jbmr.3393
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Adults with type 2 diabetes (T2D) have a higher fracture risk for a given bone quantity, but the mechanisms remain unclear. Using a rat model of polygenic obese T2D, we demonstrate that diabetes significantly reduces whole-bone strength for a given bone mass (CT-derived BMC), and we quantify the roles of T2D-induced deficits in material properties versus bone structure; ie, geometry and microarchitecture. Lumbar vertebrae and ulnae were harvested from 6-month-old lean Sprague-Dawley rats, obese Sprague-Dawley rats, and diabetic obese UCD-T2DM rats (diabetic for 69 +/- 7 days; blood glucose >200mg/dL). Both obese rats and those with diabetes had reduced whole-bone strength for a given BMC. In obese rats, this was attributable to structural deficits, whereas in UCD-T2DM rats, this was attributable to structural deficits and to deficits in tissue material properties. For the vertebra, deficits in bone structure included thinner and more rod-like trabeculae; for the ulnae, these deficits included inefficient distribution of bone mass to resist bending. Deficits in ulnar material properties in UCD-T2DM rats were associated with increased non-enzymatic crosslinking and impaired collagen fibril deformation. Specifically, small-angle X-ray scattering revealed that diabetes reduced collagen fibril ultimate strain by 40%, and those changes coincided with significant reductions in the elastic, yield, and ultimate tensile properties of the bone tissue. Importantly, the biomechanical effects of these material property deficits were substantial. Prescribing diabetes-specific tissue yield strains in high-resolution finite element models reduced whole-bone strength by a similar amount (and in some cases a 3.4-fold greater amount) as the structural deficits. These findings provide insight into factors that increase bone fragility for a given bone mass in T2D; not only does diabetes associate with less biomechanically efficient bone structure, but diabetes also reduces tissue ductility by limiting collagen fibril deformation, and in doing so, reduces the maximum load capacity of the bone. (c) 2018 American Society for Bone and Mineral Research.
引用
收藏
页码:1066 / 1075
页数:10
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