骨强度的遗传调控:动物模型研究综述。

BoneKEy reports Pub Date : 2015-07-08 eCollection Date: 2015-01-01 DOI:10.1038/bonekey.2015.83
Douglas J Adams, Cheryl L Ackert-Bicknell
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引用次数: 14

摘要

基于人口和家庭的研究已经确定,脆性骨折风险是遗传的;然而,迄今为止发表的全基因组关联研究仅占股骨或腰椎骨折风险已知变异的一小部分。为了寻找与骨骼强度相关的基因位点,人们在动物模型上做了很多工作。使用动物模型的研究克服了与使用患者数据相关的一些问题,但在解释结果时需要谨慎。在这篇综述中,我们研究了在动物模型中用于鉴定调节骨强度的位点和/或基因的正向遗传作图的测试类型,并讨论了这些测试方法的局限性。此外,我们还对小鼠、大鼠和鸡骨强度的数量性状位点进行了综述。这些基因座中的大多数与骨大小和/或几何形状的基因座共图,因此可能通过调节骨大小来决定强度。在比较近交系小鼠时,已经证明了骨基质组成的差异,这些基质差异可能与骨强度的差异有关。然而,需要进一步的工作来确定在材料水平上对骨强度起作用的位点。
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Genetic regulation of bone strength: a review of animal model studies.

Population- and family-based studies have established that fragility fracture risk is heritable; yet, the genome-wide association studies published to date have only accounted for a small fraction of the known variation for fracture risk of either the femur or the lumbar spine. Much work has been carried out using animal models toward finding genetic loci that are associated with bone strength. Studies using animal models overcome some of the issues associated with using patient data, but caution is needed when interpreting the results. In this review, we examine the types of tests that have been used for forward genetics mapping in animal models to identify loci and/or genes that regulate bone strength and discuss the limitations of these test methods. In addition, we present a summary of the quantitative trait loci that have been mapped for bone strength in mice, rats and chickens. The majority of these loci co-map with loci for bone size and/or geometry and thus likely dictate strength via modulating bone size. Differences in bone matrix composition have been demonstrated when comparing inbred strains of mice, and these matrix differences may be associated with differences in bone strength. However, additional work is needed to identify loci that act on bone strength at the materials level.

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