Seremak-Mrozikiewicz Agnieszka, Drews Krzysztof, Bartkowiak-Wieczorek Joanna, Kurzawińska Grazyna, Pieńkowski Wojciech, Spaczyński Marek, Mrozikiewicz Przemysław M
Klinika Perinatologii i Chorób Kobiecych, Katedry Perinatologii i Ginekologii AM w Poznaniu.
Ginekol Pol. 2005 Sep;76(9):679-86.
It was suggested that genetic factors play an important role in the regulation of bone mineral density and in the pathogenesis of bone fracture in osteoporosis. PvuII restriction polymorphism in the intron 1 of the gene coding estrogen receptor alpha (ER-alpha) is indicated to play a significant role in osteopenia and osteoporosis development. The goal of our study was to determine the frequency and the significance of PvuII polymorphism of the ER-alpha gene in the group of postmenopausal women with osteopenia and osteoporosis.
93 postmenopausal women with osteopenia and osteoporosis (t-score lower than (-1), and 141 healthy postmenopausal women have been investigated for PvuII polymorphism of the ER-a gene using polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) assays.
We have observed higher frequency of homozygous genotype PP (25.8 vs. 19.8%) and P allele (50.6 vs. 46.1%) in the group of women with low level of t-score. In the osteopenic women (-2.5 < T-score < -1.0) the significant difference in the distribution of t-score index and genotypes has been found. t-score index correlated with body mass index (BMI), mean body weight, BMD aged matched (AM) and BMD young adults (YA) index. The AM and YA index correlated with the number of pregnancies.
The presence of PP genotype and P allele could be connected with higher bone loss and with the development of osteopenia and osteoporosis in postmenopausal women.
有研究表明,遗传因素在骨密度调节以及骨质疏松症骨折发病机制中发挥重要作用。编码雌激素受体α(ER-α)的基因内含子1中的PvuII限制性多态性被认为在骨质减少和骨质疏松症发展中起重要作用。我们研究的目的是确定绝经后骨质减少和骨质疏松症女性群体中ER-α基因PvuII多态性的频率及意义。
采用聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)分析方法,对93例绝经后骨质减少和骨质疏松症女性(t值低于(-1))以及141例健康绝经后女性进行了ER-α基因PvuII多态性研究。
我们观察到,t值较低的女性群体中,纯合基因型PP(25.8%对19.8%)和P等位基因(50.6%对46.1%)的频率更高。在骨质减少女性(-2.5 < T值 < -1.0)中,发现t值指数和基因型分布存在显著差异。t值指数与体重指数(BMI)、平均体重、年龄匹配骨密度(AM)和青年成人骨密度(YA)指数相关。AM和YA指数与怀孕次数相关。
PP基因型和P等位基因的存在可能与绝经后女性更高的骨质流失以及骨质减少和骨质疏松症的发生有关。