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The correlation between estrogen receptor gene polymorphism and osteoporosis in Han Chinese women

机译:汉族女性雌激素受体基因多态性与骨质疏松的相关性

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摘要

OBJECTIVE: To uncover the role of estrogen receptor gene polymorphism in the onset of osteoporosis in Han Chinese women. PATIENTS AND METHODS: A total of 122 osteoporosis woman patients who were admitted to this hospital between April 2016 and April 2017 were enrolled in this study as the case group, and during the same period, 106 healthy counterparts who took physical examination as the control group. With the genetic samples collected from subjects in two groups, we detected the polymorphisms of Pvu II and Xba I in the estrogen receptor alpha (ERα) gene and the Rsa-I and Aiu-I polymorphisms in the ERβ gene by Restriction Fragment Length Polymorphism (RFLP), and the related-alleles frequency in subjects carrying the genotype of Pvu-1I and Xba-I polymorphisms in the ERα gene or the genotype of Rsa-I and Alu-I polymorphisms in the ERβ gene in the two groups. RESULTS: Comparison of genotype frequencies pp, Pp, and PP of ERα Pvu-II polymorphisms between the case group and the control group showed the differences were statistically significant (p 0.05), and similar results were also found in comparison of the genotype frequencies of rr, Rr, and RR of Rsa-I polymorphisms (p 0.05). By the comparison of genotype frequencies of ERβ Alu-I and Rsa-I polymorphisms in the case group with those in the control group, and by the comparison of genotype frequencies aa, Aa, and AA of ERβ Alu-I polymorphisms in the case group with those in the control group, all the differences were statistically significant (p 0.05 ). CONCLUSIONS: In Han Chinese women, susceptibility to osteoporosis may be affected by ERα Pvu-II polymorphisms and ERβ Alu-I polymorphisms; those carrying genotypes containing A and P alleles may have a higher risk in osteoporosis.
机译:目的:探讨雌激素受体基因多态性在汉族女性骨质疏松症发病中的作用。患者与方法:2016年4月至2017年4月在该医院收治的122名骨质疏松症女性患者作为病例组入组本研究,同期有106名健康体检者作为对照组。利用两组受试者的遗传样本,我们通过限制性片段长度多态性检测了雌激素受体α(ERα)基因中Pvu II和Xba I的多态性以及ERβ基因中Rsa-I和Aiu-I的多态性( RFLP),以及两组中携带ERα基因Pvu-1I和Xba-I基因多态性或ERβ基因Rsa-1和Alu-1基因多态性的受试者的相关等位基因频率。结果:病例组和对照组ERαPvu-II多态性的基因型频率pp,Pp和PP的比较显示差异具有统计学意义(p <0.05),并且在比较两组的基因型频率时也发现了相似的结果。 Rsa-1多态性的rr,Rr和RR(p> 0.05)。通过比较病例组中ERβAlu-I和Rsa-I基因多态性的基因型频率和病例组中ERβAlu-I基因多态性的基因型频率aa,AA和AA与对照组相比,所有差异均具有统计学意义(p <0.05)。结论:在中国汉族妇女中,骨质疏松症易感性可能受ERαPvu-II多态性和ERβAlu-I多态性的影响。那些携带含有A和P等位基因的基因型的人可能会患骨质疏松症。

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