Bone brittleness varies with genetic background in A/J and C57BL/6J inbred mice

被引:91
作者
Jepsen, KJ
Pennington, DE
Lee, YL
Warman, M
Nadeau, J
机构
[1] CUNY Mt Sinai Sch Med, Dept Orthoped, New York, NY 10029 USA
[2] Case Western Reserve Univ, Dept Anat, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Dept Genet & Med, Cleveland, OH 44106 USA
关键词
genetics; bone biomechanics; skeletal fragility; inbred mice; bone density; bone quality;
D O I
10.1359/jbmr.2001.16.10.1854
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The contribution of genetic and environmental factors to variations in bone quality are understood poorly. We tested whether bone brittleness varies with genetic background using the A/J and C57BL/6J inbred Mouse strains. Whole bone four-point bending tests revealed a 70% decrease in postyield deflection of A/J femurs compared with C57BL/6J, indicating that A/J femurs failed in a significantly more brittle manner. Cyclic loading studies indicated that A/J femurs accumulated damage differently than C57BL/6J femurs, consistent with their increased brittleness. Differences in matrix composition also were observed between the two mouse strains. A/J femurs had a 4.5% increase in ash content and an 11.8% decrease in collagen content. Interestingly, a reciprocal relationship was observed between femoral geometry and material stiffness; this relationship may have contributed to the brittle phenotype of A/J femurs. A/J femurs are more slender than those of C57BL/6J femurs; however, their 47% smaller moment of inertia appeared to be compensated by an increased tissue stiffness at the expense of altered tissue damageability. Importantly, these differences in whole bone mechanical properties between A/J and C57BL/6J femurs could not have been predicted from bone mass or density measures alone. The results indicated that bone brittleness is a genetically influenced trait and that it is associated with genetically determined differences in whole bone architecture, bone matrix composition, and mechanisms of cyclical damage accumulation.
引用
收藏
页码:1854 / 1862
页数:9
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