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Influence of Polymorphisms in the RANKL/RANK/OPG Signaling Pathway on Volumetric Bone Mineral Density and Bone Geometry at the Forearm in Men

机译:RANKL / RANK / OPG信号通路中的多态性对男性前臂体积骨矿物质密度和骨几何形状的影响

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摘要

We sought to determine the influence of single-nucleotide polymorphisms (SNPs) in RANKL, RANK, and OPG on volumetric bone mineral density (vBMD) and bone geometry at the radius in men. Pairwise tag SNPs (r (2) ≥ 0.8) for RANKL (n = 8), RANK (n = 44), and OPG (n = 22) and five SNPs near RANKL and OPG strongly associated with areal BMD in genomewide association studies were previously genotyped in men aged 40-79 years in the European Male Ageing Study (EMAS). Here, these SNPs were analyzed in a subsample of men (n = 589) who had peripheral quantitative computed tomography (pQCT) performed at the distal (4%) and mid-shaft (50%) radius. Estimated parameters were total and trabecular vBMD (mg/mm(3)) and cross-sectional area (mm(2)) at the 4% site and cortical vBMD (mg/mm(3)); total, cortical, and medullary area (mm(2)); cortical thickness (mm); and stress strain index (SSI) (mm(3)) at the 50% site. We identified 12 OPG SNPs associated with vBMD and/or geometric parameters, including rs10505348 associated with total vBMD (β [95% CI] = 9.35 [2.12-16.58], P = 0.011), cortical vBMD (β [95% CI] = 5.62 [2.10-9.14], P = 0.002), cortical thickness (β [95% CI] = 0.08 [0.03-0.13], P = 0.002), and medullary area (β [95% CI] = -2.90 [-4.94 to -0.86], P = 0.005) and rs2073618 associated with cortical vBMD (β [95% CI] = -4.30 [-7.78 to -0.82], P = 0.015) and cortical thickness (β [95% CI] = -0.08 [-0.13 to -0.03], P = 0.001). Three RANK SNPs were associated with vBMD, including rs12956925 associated with trabecular vBMD (β [95% CI] = -7.58 [-14.01 to -1.15], P = 0.021). There were five RANK SNPs associated with geometric parameters, including rs8083511 associated with distal radius cross-sectional area (β [95% CI] = 8.90 [0.92-16.88], P = 0.029). No significant association was observed between RANKL SNPs and pQCT parameters. Our findings suggest that genetic variation in OPG and RANK influences radius vBMD and geometry in men.
机译:我们试图确定RANKL,RANK和OPG中的单核苷酸多态性(SNP)对男性volume骨体积骨矿物质密度(vBMD)和骨骼几何形状的影响。在全基因组关联研究中,RANKL(n = 8),RANK(n = 44)和OPG(n = 22)的成对标签SNP(r(2)≥0.8)和与区域BMD密切相关的RANKL和OPG附近的五个SNPs之前在欧洲男性衰老研究(EMAS)中对40-79岁的男性进行了基因分型。在这里,这些SNP在男性(n = 589)的子样本中进行了分析,他们在远端(4%)和中轴(50%)半径进行了外周定量计算机体层摄影(pQCT)。估计参数为总和小梁vBMD(mg / mm(3))和4%部位和皮质vBMD的横截面积(mm(2))(mg / mm(3));总,皮质和髓样区域(mm(2));皮层厚度(mm);和应力应变指数(SSI)(mm(3))在50%的位置。我们确定了12个与vBMD和/或几何参数相关的OPG SNP,包括与总vBMD(β[95%CI] = 9.35 [2.12-16.58],P = 0.011),皮质vBMD(β[95%CI] = 5.62 [2.10-9.14],P = 0.002),皮质厚度(β[95%CI] = 0.08 [0.03-0.13],P = 0.002),髓质区域(β[95%CI] =-2.90 [-4.94]至-0.86],P = 0.005)和rs2073618与皮质vBMD(β[95%CI] =-4.30 [-7.78至-0.82],P = 0.015)和皮质厚度(β[95%CI] =-0.08)相关[-0.13至-0.03],P = 0.001)。三个RANK SNP与vBMD相关,包括与小梁vBMD相关的rs12956925(β[95%CI] =-7.58 [-14.01至-1.15],P = 0.021)。有五个与几何参数相关联的RANK SNP,包括与远端radius骨横截面积相关联的rs8083511(β[95%CI] = 8.90 [0.92-16.88],P = 0.029)。没有观察到RANKL SNP和pQCT参数之间的显着关联。我们的发现表明,OPG和RANK的遗传变异会影响男性的vBMD半径和几何形状。

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