• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[北京年轻女性部分遗传因素与骨密度峰值关系的研究]

[Study on the relationship between some genetic factors and peak bone mineral density in Beijing young women].

作者信息

Yang Xin, Zheng Shu-rong, Chen Rong-jing, Chen Shu-ling, Fan Zheng-hong, Li Hui, Lu Yun-hua

机构信息

Department of Obstetrics and Gynecology, First Hospital, Peking University, Beijing 100034, China.

出版信息

Zhonghua Fu Chan Ke Za Zhi. 2003 May;38(5):273-6.

PMID:12895309
Abstract

OBJECTIVE

To evaluate the relationship between the peak bone mineral density (PBMD) and vitamin D receptor (VDR), estrogen receptor (ER) allelic variants in Beijing young women.

METHODS

From March, 2000 to July, 2001, one hundred and fifty-nine young healthy women (25 - 37 years old) in Beijing were voluntarily enrolled in the study. (1) BMD were measured by dual energy X-ray absorptiometry (DXEA) at lumbar and hip. (2) The polymorphism of VDR and ER genes were detected by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). (3) The relationship between BMD and polymorphism of VDR and ER genes were examined.

RESULTS

(1) Lumber BMD was positively correlated to height, weight and body mass index (BMI), whereas, the femoral neck BMD only to weight, and the other sites of hip BMD to BMI. (2) Although subjects with the VDR bb genotype had higher BMD than those with Bb genotype at lumber, femoral neck, inter and troch, no significant difference was found (P > 0.05). (3) In Ward triangle, subjects with ER PP genotype had significantly lower BMD than those in ER Pp and pp genotypes (P < 0.05). (4) Women with BbPP genotype combination had lower BMD levels at lumber and hip, and with bbPP and Bbpp genotypes combination significantly higher lumber BMD levels than BbPP genotype (P < 0.05). However, the differences of BMD among subjects with different VDR and ER genotypes became not significant after adjusting the confounder of body weight.

CONCLUSIONS

(1) Body weight and BMI play important roles to PBMD of Beijing women. (2) There was no significant difference of BMD levels between VDR genotypes at any site. (3) PvuII polymorphism of ER gene was associated with low Ward triangle BMD. (4) There was significant relationship between the combination of ER and VDR polymorphisms at lumbar and hip BMD. Our data suggest that genetic variation at the ER locus, singly and in relation to the VDR locus, may influence the attainment and maintenance of peak bone mass in young women.

摘要

目的

评估北京年轻女性的峰值骨密度(PBMD)与维生素D受体(VDR)、雌激素受体(ER)基因多态性之间的关系。

方法

2000年3月至2001年7月,159名北京年轻健康女性(25 - 37岁)自愿参加本研究。(1)采用双能X线吸收法(DXEA)测量腰椎和髋部的骨密度(BMD)。(2)通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)检测VDR和ER基因的多态性。(3)研究BMD与VDR和ER基因多态性之间的关系。

结果

(1)腰椎骨密度与身高、体重和体重指数(BMI)呈正相关,而股骨颈骨密度仅与体重相关,髋部其他部位骨密度与BMI相关。(2)虽然VDR基因bb基因型受试者在腰椎、股骨颈、转子间和粗隆的骨密度高于Bb基因型受试者,但差异无统计学意义(P>0.05)。(3)在Ward三角区,ER基因PP基因型受试者的骨密度显著低于ER基因Pp和pp基因型受试者(P<0.05)。(4)BbPP基因型组合的女性在腰椎和髋部的骨密度水平较低,而bbPP和Bbpp基因型组合的女性腰椎骨密度水平显著高于BbPP基因型(P<0.05)。然而,在调整体重混杂因素后,不同VDR和ER基因型受试者之间的骨密度差异变得不显著。

结论

(1)体重和BMI对北京女性的PBMD起重要作用。(2)任何部位VDR基因型之间的骨密度水平无显著差异。(3)ER基因的PvuII多态性与Ward三角区低骨密度有关。(4)ER和VDR基因多态性组合与腰椎和髋部骨密度之间存在显著关系。我们的数据表明,ER基因位点的遗传变异,单独或与VDR基因位点相关,可能影响年轻女性峰值骨量的获得和维持。

相似文献

1
[Study on the relationship between some genetic factors and peak bone mineral density in Beijing young women].[北京年轻女性部分遗传因素与骨密度峰值关系的研究]
Zhonghua Fu Chan Ke Za Zhi. 2003 May;38(5):273-6.
2
[Association of bone mineral density with gene polymorphisms and environmental factors in Chinese postmenopausal women].中国绝经后女性骨密度与基因多态性及环境因素的关联
Wei Sheng Yan Jiu. 2006 Mar;35(2):196-200.
3
[Relationship between estrogen receptor genotypes and female bone mineral density].雌激素受体基因分型与女性骨密度的关系
Zhonghua Fu Chan Ke Za Zhi. 2001 Jun;36(6):344-7.
4
[The influence of hormonal replacement therapy on bone density in postmenopausal women depending on polymorphism of vitamin D receptor (VDR) and estrogen receptor (ER) genes].[激素替代疗法对绝经后女性骨密度的影响:取决于维生素D受体(VDR)和雌激素受体(ER)基因的多态性]
Ann Acad Med Stetin. 2003;49:111-30.
5
Prediction of bone mineral density from vitamin D receptor polymorphisms is uncertain in representative samples of Japanese Women. The Japanese Population-based Osteoporosis (JPOS) Study.在日本女性的代表性样本中,从维生素D受体多态性预测骨矿物质密度尚不确定。基于日本人群的骨质疏松症(JPOS)研究。
Int J Epidemiol. 2004 Oct;33(5):979-88. doi: 10.1093/ije/dyh245. Epub 2004 Sep 9.
6
Vitamin D receptor gene start codon polymorphisms (FokI) and bone mineral density: interaction with age, dietary calcium, and 3'-end region polymorphisms.维生素D受体基因起始密码子多态性(FokI)与骨密度:与年龄、膳食钙及3'-末端区域多态性的相互作用
J Bone Miner Res. 1998 Jun;13(6):925-30. doi: 10.1359/jbmr.1998.13.6.925.
7
Vitamin D receptor gene polymorphisms are not related to bone turnover, rate of bone loss, and bone mass in postmenopausal women: the OFELY Study.维生素D受体基因多态性与绝经后女性的骨转换、骨质流失率及骨量无关:OFELY研究
J Bone Miner Res. 1996 Jun;11(6):827-34. doi: 10.1002/jbmr.5650110614.
8
The BsmI vitamin D receptor restriction fragment length polymorphism (bb) influences the effect of calcium intake on bone mineral density.BsmI维生素D受体限制性片段长度多态性(bb)影响钙摄入对骨矿物质密度的作用。
J Bone Miner Res. 1997 Jul;12(7):1049-57. doi: 10.1359/jbmr.1997.12.7.1049.
9
Determinants of peak bone mass: clinical and genetic analyses in a young female Canadian cohort.峰值骨量的决定因素:加拿大年轻女性队列的临床与遗传分析
J Bone Miner Res. 1999 Apr;14(4):633-43. doi: 10.1359/jbmr.1999.14.4.633.
10
Vitamin D receptor start codon polymorphism ( FokI) is related to bone mineral density in healthy adolescent boys.维生素D受体起始密码子多态性(FokI)与健康青春期男孩的骨矿物质密度有关。
J Bone Miner Metab. 2003;21(2):109-13. doi: 10.1007/s007740300018.

引用本文的文献

1
Association of estrogen receptor alpha gene polymorphisms with bone mineral density in Chinese women: a meta-analysis.雌激素受体α基因多态性与中国女性骨密度的关联:一项荟萃分析。
Osteoporos Int. 2007 Mar;18(3):295-305. doi: 10.1007/s00198-006-0239-2. Epub 2006 Nov 7.