Bandrés E, Pombo I, González-Huarriz M, Rebollo A, López G, García-Foncillas J
Laboratory of Biotechnology and Pharmacogenomics, Clinica Universitaria de Navarra, University of Navarra, Pamplona, Spain.
J Endocrinol Invest. 2005 Apr;28(4):312-21. doi: 10.1007/BF03347196.
Bone mineral density (BMD), the major determinant of osteoporotic fracture risk, has a strong genetic component, and several candidate gene polymorphisms have been implicated in the regulation of this process. In view of the reported associations between the BMD and polymorphisms in the collagen type I alpha 1 gene (COL1A1), vitamin D receptor (VDR), estrogen receptor (ER)alpha and calcitonin receptor (CTR) genes, an association study was performed between VDR, COL1A1, CTR and ER genotypes and lumbar spine, femoral neck and Ward's triangle BMD in postmenopausal Spanish women. We statistically controlled for many confounding factors, such as height, weight, age, years since menopause, use of hormone replacement therapy (HRT), tobacco consumption, use of oral contraceptives, calcium dietary intake or exercise practice. No association between COL1A1 or ER genotypes and BMD was detected. However, we described a statistically significant association between a personal history of fractures and COL1A1 genotype. The ss genotype was found to be over-represented between those women who had a personal history of fractures. The analyses of the VDR polymorphisms showed that FF subjects reached the highest values of BMD at the three measured sites, whereas Ff individuals had an intermediate BMD and ff women had the lowest values. However, the VDR-BsmI gene polymorphism was not found to be associated with adjusted BMD. For the CTR polymorphisms, our study showed that women with the aa genotype had a lower adjusted BMD at the femoral neck. In conclusion, in our postmenopausal Spanish women cohort we found a statistically significant association beteween the VDR and CTR gene polymorphisms and the BMD. However, we did not find any association between the ER and COL1A1 gene and the BMD. The COL1A1 gene was found to be associated with the prevalence of osteoporotic fractures. Of all the studied gene polymorphisms, the FokI VDR gene polymorphism seems to be the strongest BMD genetic determinant of postmenopausal Spanish women.
骨矿物质密度(BMD)是骨质疏松性骨折风险的主要决定因素,具有很强的遗传成分,几种候选基因多态性与该过程的调节有关。鉴于已报道的BMD与I型胶原蛋白α1基因(COL1A1)、维生素D受体(VDR)、雌激素受体(ER)α和降钙素受体(CTR)基因多态性之间的关联,我们对绝经后西班牙女性的VDR、COL1A1、CTR和ER基因型与腰椎、股骨颈和沃德三角区的BMD进行了关联研究。我们对许多混杂因素进行了统计学控制,如身高、体重、年龄、绝经年限、激素替代疗法(HRT)的使用、吸烟、口服避孕药的使用、饮食钙摄入量或运动习惯。未检测到COL1A1或ER基因型与BMD之间存在关联。然而,我们描述了骨折个人史与COL1A1基因型之间存在统计学显著关联。发现ss基因型在有骨折个人史的女性中占比过高。对VDR多态性的分析表明,FF受试者在三个测量部位的BMD值最高,而Ff个体的BMD处于中间水平,ff女性的BMD值最低。然而,未发现VDR - BsmI基因多态性与校正后的BMD相关。对于CTR多态性,我们的研究表明,aa基因型的女性股骨颈校正后的BMD较低。总之,在我们的绝经后西班牙女性队列中,我们发现VDR和CTR基因多态性与BMD之间存在统计学显著关联。然而,我们未发现ER和COL1A1基因与BMD之间存在任何关联。发现COL1A1基因与骨质疏松性骨折的患病率相关。在所有研究的基因多态性中,FokI VDR基因多态性似乎是绝经后西班牙女性BMD最强的遗传决定因素。