Association of estrogen receptor alpha gene polymorphisms with bone mineral density: a meta-analysis

被引:15
作者
Wang Ke-jie [2 ]
Shi Dong-quan [1 ,3 ]
Sun Li-sheng [1 ,3 ]
Jiang Xu [1 ,3 ]
Lu Yan-yun [3 ]
Dai Jin [1 ,3 ]
Chen Dong-yang [1 ,3 ]
Xu Zhi-hong [1 ,3 ]
Jiang Qing [1 ,3 ]
机构
[1] Nanjing Univ, Ctr Diag & Treatment Joint Dis, Drum Tower Hosp, Sch Med, Nanjing 210008, Jiangsu, Peoples R China
[2] Changzhou 1 Peoples Hosp, Dept Orthopaed, Changzhou 213003, Jiangsu, Peoples R China
[3] Nanjing Univ, Lab Bone & Joint Dis, Model Anim Res Ctr, Nanjing 210061, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
bone mineral density; XbaI; PvuII; polymorphisms; estrogen receptor alpha gene; meta-analysis; VITAMIN-D-RECEPTOR; POSTMENOPAUSAL WOMEN; PVUII POLYMORPHISMS; MASS; GENOTYPES; FRACTURE; RISK; DETERMINANTS; SUSCEPTIBILITY; TURNOVER;
D O I
10.3760/cma.j.issn.0366-6999.2012.14.034
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background A number of studies have examined the association between estrogen receptor alpha (ESR-alpha) gene polymorphisms and bone mineral density (BMD), but previous studies of ESR-alpha gene XbaI (rs9340799) and PvuII (rs2234693) polymorphisms have been hampered by small sample size, regional restrictions and inconclusive results. Thus a meta-analysis is needed to assess their pooled effects. Methods This study reviewed all published articles indexed in Pubmed using the keywords in the title or abstract. All data were extracted independently by two reviewers using a standard form, the studies were meta-analyzed and minor discrepancies were resolved by authors' discussion. Results Twenty seven eligible studies involving 8467 women and 2032 men were identified. The XbaI and PvuII polymorphisms were significantly associated with BMD of the lumbar spine. XX and PP homozygotes had a protective effect in comparison with carriers of the x and p alleles, the effects were more significant in premenopausal women or Western women. At the femoral neck, the results were different.)0( served as a protective factor in postmenopausal women, Western women, Western postmenopausal women, and men, while PP was likely to serve as a risk factor in Eastern women, Eastern postmenopausal women, and men. Conclusions The XbaI polymorphism is correlated to BMD at diverse skeletal sites. PP had a protective role for the lumbar spine but might be a risk factor for the femoral neck.
引用
收藏
页码:2589 / 2597
页数:9
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