Department of Family Medicine, Poznań University of Medical Sciences, Przybyszewskiego Street 49, 60-355 Poznań, Poland.
Mol Biol Rep. 2013 Jan;40(1):383-90. doi: 10.1007/s11033-012-2072-3. Epub 2012 Oct 17.
The goal of the study was to investigate the possibility of an association between polymorphisms and single alleles of BsmI, ApaI, TaqI of the vitamin D receptor (VDR) gene with bone mineral density (BMD) and prevalence of vertebral/non-vertebral fractures in a group of postmenopausal Polish women with osteoporosis. The study group comprised of 501 postmenopausal females with osteoporosis (mean age 66.4 ± 8.9), who were diagnosed on the basis of either the WHO criteria or self-reported history of low-energy fractures. The three polymorphisms were determined by PCR (polymerase chain reaction) and RFLP (restriction fragment length polymorphism). BMD at the lumbar spine and femoral neck was assessed by dual energy X-ray absorptiometry (DXA). 285 fractures were reported in the whole group (168 vertebral and 117 non-vertebral). Incidence of non-vertebral fractures was significantly higher in the carriers of single alleles a of ApaI, b of BsmI and T of TaqI VDR gene polymorphisms (p = 0.021, 0.032, 0.020, respectively). No significant associations between allelic variants of the studied polymorphisms and BMD or fracture incidence were found. (1).The presence of single alleles a,b and T of ApaI, BsmI, TaqI VDR gene polymorphisms respectively, might serve as an indicator of non-vertebral fractures. (2). Lack of association between the VDR gene polymorphisms and BMD suggests that VDR contributes to low-energy fractures also through other ways.
本研究旨在探讨维生素 D 受体(VDR)基因 BsmI、ApaI、TaqI 多态性和单等位基因与波兰骨质疏松绝经后妇女骨密度(BMD)和椎体/非椎体骨折发生率之间的相关性。研究组包括 501 例骨质疏松绝经后女性(平均年龄 66.4±8.9 岁),根据世界卫生组织(WHO)标准或低能量骨折的自述病史诊断为骨质疏松症。通过聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)确定三种多态性。采用双能 X 线吸收法(DXA)测定腰椎和股骨颈的 BMD。全组报告 285 例骨折(168 例椎体骨折和 117 例非椎体骨折)。ApaI、BsmI 和 TaqI VDR 基因多态性单等位基因 a、b 和 T 的携带者中,非椎体骨折的发生率明显较高(分别为 p=0.021、0.032、0.020)。未发现研究多态性的等位基因变异与 BMD 或骨折发生率之间存在显著相关性。(1)ApaI、BsmI、TaqI VDR 基因多态性的单等位基因 a、b 和 T 的存在可能是非椎体骨折的指标。(2)VDR 基因多态性与 BMD 之间缺乏关联表明,VDR 也通过其他途径导致低能量骨折。