首页> 外文期刊>European Spine Journal >Polymorphism in vitamin D receptor is associated with bone mineral density in patients with adolescent idiopathic scoliosis
【24h】

Polymorphism in vitamin D receptor is associated with bone mineral density in patients with adolescent idiopathic scoliosis

机译:维生素D受体的多态性与青少年特发性脊柱侧弯患者的骨矿物质密度相关

获取原文
获取原文并翻译 | 示例
           

摘要

Low bone mass and osteopenia have been reported in the axial and peripheral skeleton of adolescent idiopathic scoliosis (AIS) patients. Furthermore, several recent studies have shown that gene polymorphisms are related to osteoporosis. However, no study has yet linked polymorphisms in the vitamin D receptor (VDR) gene and bone mass in AIS. Accordingly, the authors examined the association between bone mass and VDR gene polymorphisms in 198 girls diagnosed with AIS. The VDR BsmI (rs1544410), FokI (rs2228670) and Cdx2 (rs11568820) polymorphisms and bone mineral density at the lumbar spine (LSBMD) and femoral neck (FNBMD) were analyzed and compared to their levels in healthy controls. Mean LSBMD and FNBMD in AIS patients were lower than in age- and sex-matched healthy controls (P = 0.0022 and P = 0.0013, respectively). A comparison of genotype frequencies in AIS patients and controls revealed a significant difference for the BsmI polymorphism only (P = 0.0054). Furthermore, a significant association was found between the VDR BsmI polymorphism and LSBMD. In particular, LSBMD in AIS patients with the AA genotype was found to be significantly lower than in patients with the GA (P < 0.05) or GG (P < 0.01) genotypes. However, no significant association was found between LSBMD or FNBMD and the VDR FokI or Cdx2 polymorphisms. These results suggest that the VDR BsmI polymorphism is associated with LSBMD in girls with AIS.
机译:据报道,青少年特发性脊柱侧凸(AIS)患者的轴向和周围骨骼中骨量低和骨质减少。此外,最近的一些研究表明基因多态性与骨质疏松症有关。但是,尚无研究将维生素D受体(VDR)基因的多态性与AIS中的骨量联系起来。因此,作者检查了198名被诊断为AIS的女孩的骨量与VDR基因多态性之间的关系。分析了VDR BsmI(rs1544410),FokI(rs2228670)和Cdx2(rs11568820)多态性以及腰椎(LSBMD)和股骨颈(FNBMD)的骨矿物质密度,并将其与健康对照中的水平进行比较。 AIS患者的平均LSBMD和FNBMD低于年龄和性别相匹配的健康对照组(分别为P = 0.0022和P = 0.0013)。比较AIS患者和对照组的基因型频率,发现仅BsmI多态性存在显着差异(P = 0.0054)。此外,发现VDR BsmI多态性与LSBMD之间存在显着关联。特别是,发现具有AA基因型的AIS患者的LSBMD显着低于具有GA(P <0.05)或GG(P <0.01)基因型的患者。但是,在LSBMD或FNBMD与VDR FokI或Cdx2多态性之间未发现显着关联。这些结果表明,VDR BsmI基因多态性与AIS女孩的LSBMD有关。

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