维生素D受体等位基因多态性与骨密度相关性分析  被引量:6

An analysis of the correlation between vitamin D receptor gene polymorphisms and bone mineral density

在线阅读下载全文

作  者:黄啸原[1] 褚为靖[1] 刘玉涛 安晓霞[1] 陈训华[2] 

机构地区:[1]北京积水潭医院北京市创伤骨科研究所,100035 [2]中医研究院骨伤科研究所

出  处:《中华骨科杂志》2000年第6期372-374,共3页Chinese Journal of Orthopaedics

摘  要:目的调查维生素D受体(vitamin D receptor, VDR)基因多态性在我国人群中的分布,分析 VDR基因型与骨密度的关系。方法采用聚合酶链反应(polymerase chain reaction, PCR)和限制性酶切技术,检测北京地区100例围绝经期与48例绝经期妇女维生素D受体基因多态性,同时用双能X线骨密度仪检测腰椎骨密度。结果发现VDR基因型分布频率为BB,2.7%;Bb,8.1%;bb,89. 2%。围绝经期妇女中腰椎骨密度值: BB基因型为(1. 123 ± 0. 105) g/cm~2, Bb基因型为( 1. 290 ±0. 141) g/cm~2,bb基因型为(1.185 ±0. 130) g/cm~2。绝经期妇女腰椎骨密度(0. 822 ±0. 118) g/cm~2,明显低于围绝经期妇女(1. 193±0. 134) g/cm~2(P<0.01)。绝经期妇女中骨质疏松发生率为 34%。结论中国北京地区这部分绝经期和围绝经期妇女VDR基因型分布频率与某些西方国家人群分布不同,她们VDR基因型与骨密度无明显相关性。To investigate the frequency distribution of vitamin D receptor(VDR) genotype in Chinese population and evaluate the correlation between VDR gene polymorphisms and bone mineral density(BMD). Methods Polymerase chain reaction (PCR) and restriction analysis were used to determine VDR genotypes in 148 Chinese women. Their L_2-4 lumbar spine BMD was measured by dual - energy X - ray absorptiometry (DEXA). Results The frequency distribution of the VDR genotype was: BB, 2. 7%; Bb, 8. 1%; bb, 89. 2%. The BMD in perimenopasal women of different genotypes were (1. 123 ± 0. 105 ) g/cm^2 (BB), (1. 290 ±0. 141 ) g/cm^2 (Bb) and (1. 185 ±0. 130) g/cm^2 (bb) respectively. The BMD was significantly lower in postmenopausal women than perimenopausal women (P < 0. 01). The incidence of osteoporosis in postmenopausal women was 34%. Conclusion The frequency distribution of the VDR genotype in Chinese peri - and postmenopausal women were apparently different from that in Western countries. The correlation between the VDR genotype and BMD was not found.

关 键 词:骨密度 维生素D受体 基因多态性 骨质疏松 

分 类 号:R392[医药卫生—免疫学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象