Lei S-F, Jiang H, Deng F-Y, Deng H-W
Laboratory of Molecular and Statistical Genetics, College of Life Sciences, Hunan Normal University, Changsha, Hunan, 410081, People's Republic of China.
Osteoporos Int. 2007 Sep;18(9):1157-75. doi: 10.1007/s00198-007-0402-4. Epub 2007 May 30.
Osteoporotic fracture (OF) is a public health problem. It is a common practice in the genetics of osteoporosis that bone mineral density (BMD) was studied as a major surrogate phenotype in gene search for risk of OF (ROF) because of their high phenotypic correlation. However, some studies indicate that the genetic correlation between BMD and ROF is very low. This implies that most genes found important for BMD may not be relevant to ROF. Ideally, employing OF per se as a direct study phenotype can directly find the relevant genes underlying ROF.
Here, we summarized some evidence supporting ROF under moderate genetic control, and the current progress of molecular genetic studies employing OF as the direct study phenotype, then give our consideration on the future prospects in the genetics of ROF.
骨质疏松性骨折(OF)是一个公共卫生问题。在骨质疏松症遗传学中,由于骨矿物质密度(BMD)与骨质疏松性骨折风险(ROF)具有高度表型相关性,因此在寻找ROF基因时,将BMD作为主要替代表型进行研究是一种常见做法。然而,一些研究表明,BMD与ROF之间的遗传相关性非常低。这意味着大多数对BMD重要的基因可能与ROF无关。理想情况下,将OF本身作为直接研究表型可以直接找到ROF潜在的相关基因。
在此,我们总结了一些支持在适度遗传控制下ROF的证据,以及以OF作为直接研究表型的分子遗传学研究的当前进展,然后对ROF遗传学的未来前景给出我们的思考。