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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 >Identification of Novel Loci Associated With Hip Shape: A Meta-Analysis of Genomewide Association Studies
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Identification of Novel Loci Associated With Hip Shape: A Meta-Analysis of Genomewide Association Studies

机译:与髋关节形状相关的新型基因座的鉴定:基因组结合研究的荟萃分析

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摘要

We aimed to report the first genomewide association study (GWAS) meta-analysis of dual-energy X-ray absorptiometry (DXA)-derived hip shape, which is thought to be related to the risk of both hip osteoarthritis and hip fracture. Ten hip shape modes (HSMs) were derived by statistical shape modeling using SHAPE software, from hip DXA scans in the Avon Longitudinal Study of Parents and Children (ALSPAC; adult females), TwinsUK (mixed sex), Framingham Osteoporosis Study (FOS; mixed), Osteoporotic Fractures in Men study (MrOS), and Study of Osteoporotic Fractures (SOF; females) (total N = 15,934). Associations were adjusted for age, sex, and ancestry. Five genomewide significant (p 5 x 10(-9), adjusted for 10 independent outcomes) single-nucleotide polymorphisms (SNPs) were associated with HSM1, and three SNPs with HSM2. One SNP, in high linkage disequilibrium with rs2158915 associated with HSM1, was associated with HSM5 at genomewide significance. In a look-up of previous GWASs, three of the identified SNPs were associated with hip osteoarthritis, one with hip fracture, and five with height. Seven SNPs were within 200 kb of genes involved in endochondral bone formation, namely SOX9, PTHrP, RUNX1, NKX3-2, FGFR4, DICER1, and HHIP. The SNP adjacent to DICER1 also showed osteoblast cis-regulatory activity of GSC, in which mutations have previously been reported to cause hip dysplasia. For three of the lead SNPs, SNPs in high LD (r(2) 0.5) were identified, which intersected with open chromatin sites as detected by ATAC-seq performed on embryonic mouse proximal femora. In conclusion, we identified eight SNPs independently associated with hip shape, most of which were associated with height and/or mapped close to endochondral bone formation genes, consistent with a contribution of processes involved in limb growth to hip shape and pathological sequelae. These findings raise the possibility that genetic studies of hip shape might help in understanding potential pathways involved in hip osteoarthritis and hip fracture. (c) 2018 The Authors. Journal of Bone and Mineral Research Published by Wiley Periodicals, Inc.
机译:我们旨在报告第一种基因组缔合作研究(GWAS)荟萃分析的双能X射线吸收测定法(DXA)的髋关节形状,被认为与Hip骨关节炎和髋部骨折的风险有关。通过使用形状软件的统计形状建模来源于统计形状模型,从父母和儿童(Alspac;成人女性),骨笼(混合性),FOS骨质疏松研究(FOS;混合),男性研究(MRO)的骨质疏松骨折,以及骨质疏松骨折的研究(SOF;女性)(总N = 15,934)。协会调整为年龄,性别和血统。五个基因面积显着(P <5×10(-9),调整为10个独立结果)单核苷酸多态性(SNPs)与HSM1和HSM2的三个SNP相关。在与HSM1相关的RS2158915的高键合不平衡中的一种SNP与HSM5在基因面内意义上有关。在先前的Gwass的查询中,三种已识别的SNP与髋关节骨关节炎,一个具有髋部骨折,五个具有高度。七个SNP在200KB内涉及子宫内骨形成,即SOX9,PTHRP,RUNX1,NKX3-2,FGFR4,DICER1和HHIP。与Dicer1相邻的SNP还显示出GSC的骨赘CIS调节活性,其中先前据报道突变引起髋关节发育性。对于三个铅SnP,鉴定了高LD(R(2)& 0.5)中的SNP,其与ATAC-SEQ检测到的开口染色质位点相交,如ATAC-SEQ对胚胎小鼠近端股骨。总之,我们鉴定了八个与髋部形状相关的SNP,其中大部分与高度和/或贴上靠近内骨骨形成基因的映射,这与肢体生长的过程的贡献一致,其含量与髋部形状和病理后遗症相关。这些发现引发了髋关节形状的遗传研究可能有助于了解患有髋关节骨关节炎和髋关节骨折的潜在途径。 (c)2018作者。 Wiley期刊上发表的骨质研究杂志CHINESE。

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