首页> 外文期刊>Orthopedics >Genetic traits of avascular necrosis of the femoral head analyzed by array comparative genomic hybridization and real-time polymerase chain reaction.
【24h】

Genetic traits of avascular necrosis of the femoral head analyzed by array comparative genomic hybridization and real-time polymerase chain reaction.

机译:通过阵列比较基因组杂交和实时聚合酶链反应分析了股骨头缺血性坏死的遗传特征。

获取原文
获取原文并翻译 | 示例
           

摘要

In an attempt to observe the genetic traits of avascular necrosis of the femoral head, we analyzed the genomic alterations in blood samples of 18 patients with avascular necrosis of the femoral head (9 idiopathic and 9 alcoholic cases) using the array comparative genomic hybridization method and real-time polymerase chain reaction. Several candidate genes were identified that may induce avascular necrosis of the femoral head, and we investigated their role in the pathomechanism of osteonecrosis of bone. The frequency of each candidate gene over all the categories of avascular necrosis of the femoral head was also calculated by real-time polymerase chain reaction. The highest frequency specific genes in each category were FLJ40296, CYP27C1, and CTDP1. FLJ40296 and CYP27C1 had the highest frequency (55.6%) in the idiopathic category. FLJ40296 had a high frequency (44.4%) in the alcoholic category, but CYP27C1 had a relatively low frequency (33.3%) in the alcoholic category. However, CTDP1 showed a significantly high frequency (55.6%) in the alcoholic category and a low frequency (22.2%) in the idiopathic category. Although we statistically analyzed the frequency of each gene with Fisher's exact test, we could not prove statistical significance due to the small number of samples. Further studies are needed with larger sample numbers. If the causal genes of avascular necrosis of the femoral head are found, they may be used for early detection, prognosis prediction, and genomic treatment of avascular necrosis of the femoral head in the future.
机译:为了观察股骨头缺血性坏死的遗传学特征,我们采用阵列比较基因组杂交方法,分析了18例股骨头缺血性坏死患者(9例特发性和9例酒精中毒)的血液样本中的基因组变化。实时聚合酶链反应。确定了几种可能导致股骨头缺血性坏死的候选基因,我们研究了它们在骨坏死的发病机理中的作用。还通过实时聚合酶链反应计算了在整个股骨头坏死类别中每个候选基因的频率。每个类别中频率最高的特异性基因是FLJ40296,CYP27C1和CTDP1。在特发性类别中,FLJ40296和CYP27C1的频率最高(55.6%)。在酒精中,FLJ40296的频率较高(44.4%),而在酒精中,CYP27C1的频率相对较低(33.3%)。但是,CTDP1在酒精性类别中显示出明显较高的频率(55.6%),在特发性类别中显示出较低的频率(22.2%)。尽管我们使用Fisher精确检验对每个基因的频率进行了统计分析,但由于样本数量少,我们无法证明其统计学意义。需要更大的样本数量进行进一步的研究。如果发现了股骨头缺血性坏死的病因基因,将来它们可用于股骨头缺血性坏死的早期发现,预后预测和基因组治疗。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号