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首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Association of Multiple Nucleotide Variations in the Pituitary Glutaminyl Cyclase Gene (QPCT) With Low Radial BMD in Adult Women.
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Association of Multiple Nucleotide Variations in the Pituitary Glutaminyl Cyclase Gene (QPCT) With Low Radial BMD in Adult Women.

机译:垂体谷氨酰胺基环化酶基因(QPCT)中的多个核苷酸变异与成年女性低径向骨密度的关联。

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摘要

Correlation between 13 genetic variations of the glutaminyl-peptide cyclotransferase gene and adjusted aBMD was tested among 384 adult women. Among 13 variations with strong linkage disequilibrium, R54W showed a prominent association (p = 0.0003), which was more striking when examined among 309 elder subjects (>/=50 years; p = 0.0001). Contribution for postmenopausal bone loss was suggested. INTRODUCTION: Alterations in homeostatic regulation of estrogen through the hypothalamus-pituitary-gonadal axis (HPG axis) importantly affect the pathogenesis of osteoporosis. Osteoporosis-susceptibility genes have been proposed in this hormonal axis, such as estrogen receptor genes and the gonadotropin-releasing hormone gene (GnRH). Here we report another example of genes: glutaminyl-peptide cyclotransferase gene (QPCT), an essential modifier of pituitary peptide hormones, including GnRH. MATERIALS AND METHODS: Analyses of association of 13 single nucleotide polymorphisms (SNPs) at the QPCT locus with adjusted areal BMD (adj-aBMD) were carried out among 384 adult women. Linkage disequilibrium (LD) was analyzed by haplotype estimation and calculation of D' and r(2). Multiple regression analysis was applied for evaluating the combined effects of the variations. RESULTS AND CONCLUSIONS: LD analysis indicated strong linkage disequilibrium within the entire 30-kb region of the QPCT gene. Significant correlations were observed between the genotypes of the six SNPs and the radial adj-aBMD, among which R54W (nt + 160C>T) presented the most prominent association (p = 0.0003). Striking association was observed for these SNPs among the 309 subjects >50 years of age (R54W, p = 0.0001; -1095T>C, p = 0.0002; -1844C>T, p = 0.0002). Multiple regression analyses indicated that multiple SNPs in the gene might act in combination to determine the radial adj-aBMD. These results indicate that genetic variations in QPCT are the important factors affecting the BMD of adult women that contribute to susceptibility for osteoporosis. The datashould provide new insight into the etiology of the disease and may suggest a new target to be considered during treatment.
机译:在384名成年妇女中测试了谷氨酰胺肽环转移酶基因的13种遗传变异与调整后的aBMD之间的相关性。在13个具有强烈连锁不平衡的变异中,R54W表现出显着的关联性(p = 0.0003),在309位年龄较大的受试者(> / = 50岁; p = 0.0001)中进行检查时更为显着。建议对绝经后骨丢失做出贡献。简介:下丘脑-垂体-性腺轴(HPG轴)对雌激素的体内稳态调节的改变对骨质疏松症的发病机制有重要影响。已经在这个激素轴上提出了骨质疏松症易感基因,例如雌激素受体基因和促性腺激素释放激素基因(GnRH)。在这里我们报告基因的另一个示例:谷氨酰胺肽环转移酶基因(QPCT),是包括GnRH在内的垂体肽激素的重要修饰剂。材料与方法:在384名成年女性中,对QPCT位点的13个单核苷酸多态性(SNP)与调整后的面积BMD(adj-aBMD)的关联进行了分析。通过单倍型估计和D'和r(2)的计算分析了连锁不平衡(LD)。应用多元回归分析来评估变化的综合影响。结果与结论:LD分析表明在QPCT基因的整个30kb区域内存在强烈的连锁不平衡。六个SNP的基因型与放射状adj-aBMD之间存在显着相关性,其中R54W(nt + 160C> T)表现出最显着的相关性(p = 0.0003)。在年龄大于50岁的309名受试者中观察到了这些SNP的惊人关联(R54W,p = 0.0001; -1095T> C,p = 0.0002; -1844C> T,p = 0.0002)。多元回归分析表明,该基因中的多个SNP可能共同起作用,以确定径向adj-aBMD。这些结果表明,QPCT的遗传变异是影响成年女性BMD的重要因素,而BMD易患骨质疏松症。数据应提供对疾病病因的新见解,并可能建议在治疗期间考虑新的靶标。

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