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胶原 I α1 基因 Sp1 多态性与墨西哥女性腰椎骨质疏松症有关。

Sp1 polymorphism in collagen I α1 gene is associated with osteoporosis in lumbar spine of Mexican women.

机构信息

Department of Genetics, National Rehabilitation Institute, Calzada Mexico-Xochimilco No. 289, Arenal de Guadalupe, Tlalpan, CP 14389 Mexico City, Mexico.

出版信息

Mol Biol Rep. 2011 Jun;38(5):2987-92. doi: 10.1007/s11033-010-9963-y. Epub 2010 Feb 10.

Abstract

The Sp1 binding site polymorphism in collagen type I alpha 1 gene (COLIA1) has been associated with osteoporosis (OP) and bone mineral density (BMD). The aim of this study was to explore the association of this polymorphism with OP and BMD in the Mexican population by polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) procedure. Allelic and genotypic frequencies from the Sp1 polymorphism were determined in 100 women with OP, 100 women without OP and 500 subjects from general Mexican population (GMP). Distribution of Sp1 polymorphism was in Hardy-Weinberg equilibrium. In spite of population structure due to racial mix in Mexican population, associations with OP were demonstrated. The frequency of "s" allele was significantly higher in women with OP (35%) than in women without OP (11%; P < 0.00001). Interestingly, "ss" genotype, was exclusive of women with OP and was associated with low BMD (0.588 ± 0.077 g/cm(2)) in contrast to "SS" genotype (0.733 ± 0.039 g/cm(2); P = 0.0001). This work confirms the association of Sp1 polymorphism with low BMD and OP in Mexican population and make sure to use Sp1 as a genetic marker for OP in our population.

摘要

胶原类型 I 阿尔法 1 基因(COLIA1)Sp1 结合位点多态性与骨质疏松症(OP)和骨密度(BMD)有关。本研究的目的是通过聚合酶链反应和限制性片段长度多态性(PCR-RFLP)程序,探讨这种多态性与墨西哥人群中 OP 和 BMD 的关系。在 100 名 OP 女性、100 名非 OP 女性和 500 名普通墨西哥人群(GMP)中,确定了 Sp1 多态性的等位基因和基因型频率。Sp1 多态性的分布符合 Hardy-Weinberg 平衡。尽管由于墨西哥人口的种族混合导致人群结构发生变化,但仍证明了与 OP 的相关性。在 OP 女性中,“s”等位基因的频率(35%)明显高于非 OP 女性(11%;P<0.00001)。有趣的是,“ss”基因型仅存在于 OP 女性中,与低 BMD(0.588±0.077g/cm2)相关,而“SS”基因型与高 BMD(0.733±0.039g/cm2)相关(P=0.0001)。这项工作证实了 Sp1 多态性与墨西哥人群中低 BMD 和 OP 的相关性,并确定 Sp1 可作为我们人群中 OP 的遗传标志物。

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