Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Begumpet, Hyderabad, A.P, India.
Clin Chim Acta. 2010 Apr 2;411(7-8):597-600. doi: 10.1016/j.cca.2010.01.026. Epub 2010 Jan 29.
Osteoporosis is a multifactorial disorder with a strong genetic component and ESR1 is suggested as a candidate gene for osteoporosis. Therefore the present study is aimed to investigate the role of ESR1 gene polymorphisms and its influence on estradiol levels and BMD in osteoporotic women of Indian ethnicity.
Four-hundred twenty-seven osteoporotic women and 460 age matched controls were included in the study. ESR1 gene polymorphism was assessed by PCR-RFLP method. Serum estradiol was measured by ELISA.
The frequency of pp and xx genotypes as well as p and x alleles was significantly high in pre- and postmenopausal osteoporotics when compared to controls (p<0.001). They had low BMD and estradiol levels in comparison with PP and XX genotype individuals (p<0.05).
The ESR1 gene is associated with low bone mass and low estradiol levels in all our study subjects. It is likely that the allele exerts its influence on the bone in early adulthood leading to an increased risk of osteoporosis later in life.
骨质疏松症是一种具有强烈遗传成分的多因素疾病,ESR1 被认为是骨质疏松症的候选基因。因此,本研究旨在探讨 ESR1 基因多态性及其对印度裔骨质疏松症女性雌二醇水平和 BMD 的影响。
本研究纳入了 427 名骨质疏松症女性和 460 名年龄匹配的对照组。采用 PCR-RFLP 法检测 ESR1 基因多态性。采用 ELISA 法测定血清雌二醇水平。
与对照组相比,绝经前和绝经后骨质疏松症患者的 pp 和 xx 基因型以及 p 和 x 等位基因的频率明显更高(p<0.001)。与 PP 和 XX 基因型个体相比,她们的 BMD 和雌二醇水平较低(p<0.05)。
在我们所有的研究对象中,ESR1 基因与低骨量和低雌二醇水平相关。该等位基因可能在成年早期对骨骼发挥作用,导致晚年骨质疏松症的风险增加。