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在一组年轻白种成年人中,LRP5基因中的rs3736228多态性与跟骨超声参数相关,但与身体成分无关。

The rs3736228 polymorphism in the LRP5 gene is associated with calcaneal ultrasound parameter but not with body composition in a cohort of young Caucasian adults.

作者信息

Correa-Rodríguez María, Schmidt-RioValle Jacqueline, Rueda-Medina Blanca

机构信息

Faculty of Health Sciences, University of Granada, Av. Ilustración S/N, 18007, Granada, Spain.

出版信息

J Bone Miner Metab. 2017 Nov;35(6):694-700. doi: 10.1007/s00774-016-0808-1. Epub 2016 Dec 27.

Abstract

The aim of the present study was to investigate the possible influence of low-density lipoprotein receptor-related protein 5 (LRP5) and sclerostin (SOST) genes as genetic factors contributing to calcaneal quantitative ultrasound (QUS) and body composition variables in a population of young Caucasian adults. The study population comprised a total of 575 individuals (mean age 20.41years; SD 2.36) whose bone mass was assessed through QUS to determine broadband ultrasound attenuation (BUA, dB/MHz). Body composition measurements were performed using a body composition analyser. Seven single-nucleotide polymorphisms (SNPs) of LRP5 (rs2306862, rs599083, rs556442 and rs3736228) and SOST (rs4792909, rs851054 and rs2023794) were selected as genetic markers and genotyped using TaqMan OpenArray technology. Linear regression analysis was used to test the possible association of the tested SNPs with QUS and body composition parameters. Linear regression analysis revealed that the rs3736228 SNP of LPR5 was significantly associated with BUA after adjustment for age, sex, weight, height, physical activity and calcium intake (P = 0.028, β (95% CI) = 0.089 (0.099-1.691). For the remaining SNPs, no significant association with the QUS measurement was observed. Regarding body composition, no significant association was found between LRP5 and SOST polymorphisms and body mass index, total fat mass and total lean mass after adjustment for age and sex as covariates. We concluded that the rs3736228 LRP5 genetic polymorphism influences calcaneal QUS parameter in a population of young Caucasian adults. This finding suggests that LRP5 might be an important genetic marker contributing to bone mass accrual early in life.

摘要

本研究旨在调查低密度脂蛋白受体相关蛋白5(LRP5)和硬化蛋白(SOST)基因作为遗传因素,对年轻白种人成年人群跟骨定量超声(QUS)和身体成分变量可能产生的影响。研究人群共有575人(平均年龄20.41岁;标准差2.36),通过QUS评估其骨量,以确定宽带超声衰减(BUA,dB/MHz)。使用身体成分分析仪进行身体成分测量。选择LRP5的7个单核苷酸多态性(SNP,rs2306862、rs599083、rs556442和rs3736228)和SOST的7个单核苷酸多态性(SNP,rs4792909、rs851054和rs2023794)作为遗传标记,并使用TaqMan OpenArray技术进行基因分型。采用线性回归分析来检验所测SNP与QUS和身体成分参数之间可能存在的关联。线性回归分析显示,在对年龄、性别、体重、身高、身体活动和钙摄入量进行校正后,LPR5的rs3736228 SNP与BUA显著相关(P = 0.028,β(95%可信区间)= 0.089(0.099 - 1.691)。对于其余的SNP,未观察到与QUS测量值有显著关联。关于身体成分,在校正年龄和性别作为协变量后,未发现LRP5和SOST多态性与体重指数、总脂肪量和总瘦体重之间存在显著关联。我们得出结论,rs3736228 LRP5基因多态性影响年轻白种人成年人群的跟骨QUS参数。这一发现表明,LRP5可能是在生命早期对骨量积累有重要作用的遗传标记。

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