Correa-Rodríguez M, Schmidt Rio-Valle J, Rueda-Medina B
Department of Nursing, Faculty of Health Sciences, University of Granada (Spain), Av. Ilustración S/N, 18007, Granada, Spain.
Osteoporos Int. 2016 Mar;27(3):1057-1061. doi: 10.1007/s00198-015-3379-4. Epub 2015 Oct 28.
Bone mineral content is influenced by genetic factors. We investigated the role of WNT16 in bone properties determined using quantitative ultrasound (QUS) on young adults. Three WNT16 genetic markers (rs2908007, rs2908004, and rs2707466) were found to have a significant association with the broadband ultrasound attenuation (BUA) measurement, suggesting that WNT16 influences bone mass in young adults.
The aim of this study was to investigate whether genetic markers on the WNT16 gene are associated with bone mass, as assessed using QUS in a population of healthy young Spanish adults.
A cross-sectional study was conducted on 575 individuals (mean age 20.41 ± 2.69). Bone quality was assessed using BUA measurements (dB/MHz) on the right calcaneus. Six single nucleotide polymorphisms (SNPs) (rs2908007, rs2908004, rs3801387, rs3801385, rs2707466, and rs2536184) covering the WNT16 gene were selected as genetic markers and genotyped to test their association with BUA variations.
The rs2908007, rs2908004, and rs2707466 SNPs were found to have a significant association with BUA (p = 0.004, p = 0.001, and p = 0.004, respectively).
We demonstrate for the first time that WNT16 genetic polymorphisms influence QUS traits in a population of young adults. This finding suggests that WNT16 might be an important genetic factor in determining peak bone mass acquisition.
骨矿物质含量受遗传因素影响。我们研究了WNT16在年轻成年人通过定量超声(QUS)测定的骨特性中的作用。发现三个WNT16基因标记(rs2908007、rs2908004和rs2707466)与宽带超声衰减(BUA)测量值存在显著关联,表明WNT16影响年轻成年人的骨量。
本研究的目的是调查WNT16基因上的遗传标记是否与骨量相关,该骨量通过QUS在一群健康的西班牙年轻成年人中进行评估。
对575名个体(平均年龄20.41±2.69)进行了横断面研究。使用右跟骨的BUA测量值(dB/MHz)评估骨质量。选择覆盖WNT16基因的六个单核苷酸多态性(SNP)(rs2908007、rs2908004、rs3801387、rs3801385、rs2707466和rs2536184)作为遗传标记并进行基因分型,以测试它们与BUA变化的关联。
发现rs2908007、rs2908004和rs2707466这三个SNP与BUA存在显著关联(p分别为0.004、0.001和0.004)。
我们首次证明WNT16基因多态性影响年轻成年人群体的QUS特征。这一发现表明WNT16可能是决定峰值骨量获取的一个重要遗传因素。