Volkman Suzanne K, Galecki Andrzej T, Burke David T, Paczas Michael R, Moalli Maria R, Miller Richard A, Goldstein Steven A
Orthopaedic Research Laboratories, Department of Orthopaedic Surgery, University of Michigan, Ann Arbor, Michigan 48109, USA.
J Bone Miner Res. 2003 Aug;18(8):1497-505. doi: 10.1359/jbmr.2003.18.8.1497.
The aim of this study was to examine the genetic effects on cortical bone geometry. Genotypes from 487 mice were compared with geometric traits obtained from microCT. We found 14 genetic markers that associate with geometric traits, showing the complexity of genetic control over bone geometry.
Previous studies have shown that genetic background affects bone characteristics, particularly bone mineral density, in both mouse and human populations. Much less is known, however, about the effects of polymorphic genes on bone size, shape, and mechanical integrity. In this study, we investigated the genetic determinants of geometric properties of cortical bone in mice.
This study used a genetically heterogeneous mouse population, which is denoted UM-HET3 stock and is derived as the progeny of (BALB/cJ X C57BL/6J) F1 females and (C3H/HeJ X DBA/2J) F1 males. The experimental group consisted of 487 female UM-HET3 mice. Genotypic data from 99 polymorphic genetic loci was obtained from the mice at 4 weeks of age. At 18 months of age, the mice were humanely killed, and the right femurs were scanned with microcomputed tomography to assess geometric properties of cortical bone. A permutation-based test was used to detect significant associations between genetic markers and geometric traits. This test generates experiment-wise p values, which account for the effect of testing multiple hypotheses. An experiment-wise p < or = 0.05 was considered statistically significant.
Fourteen genetic markers were found to significantly associate with one or more geometric traits. Two markers (D3Mit62 and D4Mit155) were associated with traits describing bone size; 2 (D12Mit167 and D14Mit170) were linked with traits describing bone shape; and 10 (D1Nds2, D5Mit95, D6Mit216, D7Mit91, D8Mit51, D9Mit110, D11Mit83, D15Mit100, D15Mit171, and D17Mit46) were associated with both size and shape.
Our results indicate that the genetic control of cortical bone geometry is complex and that femoral size and shape may be influenced by different, although overlapping, groups of polymorphic loci.
本研究的目的是研究基因对皮质骨几何形状的影响。将487只小鼠的基因型与通过微型计算机断层扫描获得的几何特征进行比较。我们发现了14个与几何特征相关的基因标记,这表明基因对骨几何形状的控制具有复杂性。
先前的研究表明,基因背景会影响小鼠和人类群体的骨特征,尤其是骨矿物质密度。然而,关于多态性基因对骨大小、形状和力学完整性的影响,我们知之甚少。在本研究中,我们调查了小鼠皮质骨几何特性的基因决定因素。
本研究使用了一个基因异质性小鼠群体,即UM-HET3品系,它是(BALB/cJ×C57BL/6J)F1雌性与(C3H/HeJ×DBA/2J)F1雄性的后代。实验组由487只雌性UM-HET3小鼠组成。在小鼠4周龄时获得了来自99个多态性基因位点的基因型数据。在18月龄时,对小鼠实施安乐死,并用微型计算机断层扫描对右侧股骨进行扫描,以评估皮质骨的几何特性。采用基于排列的检验来检测基因标记与几何特征之间的显著关联。该检验生成实验水平的p值,该值考虑了检验多个假设的影响。实验水平的p≤0.05被认为具有统计学意义。
发现14个基因标记与一种或多种几何特征显著相关。两个标记(D3Mit62和D4Mit155)与描述骨大小的特征相关;2个(D12Mit167和D14Mit170)与描述骨形状的特征相关;10个(D1Nds2、D5Mit95、D6Mit216、D7Mit91、D8Mit51、D9Mit110、D11Mit83、D15Mit100、D15Mit171和D17Mit46)与大小和形状都相关。
我们的结果表明,皮质骨几何形状的基因控制是复杂的,股骨的大小和形状可能受到不同但有重叠的多态性基因座组的影响。