首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >SIRT1/HERC4 SIRT1/HERC4 Locus Associated With Bisphosphonate‐Induced Osteonecrosis of the Jaw: An Exome‐Wide Association Analysis
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SIRT1/HERC4 SIRT1/HERC4 Locus Associated With Bisphosphonate‐Induced Osteonecrosis of the Jaw: An Exome‐Wide Association Analysis

机译:SIRT1 / HERC4 SIRT1 / HERC4基因座与双膦酸盐诱导的颌骨骨折:exome-宽的关联分析

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ABSTRACT Osteonecrosis of the jaw (ONJ) is a rare, but serious drug side effect, mainly associated with the use of intravenous (iv) bisphosphonates (BPs). The purpose of this study was to identify genetic variants associated with ONJ in patients of European ancestry treated with iv BPs using whole‐exome sequencing (WES). The WES phase 1 included 44 multiple myeloma patients (22 ONJ cases and 22 controls) and WES phase 2 included 17 ONJ patients with solid tumors. Multivariable logistic regression analysis was performed to estimate the odds ratios (ORs) and 95% confidence intervals (CI), adjusting for age, sex, and principal components for ancestry. Meta‐analysis of WES phase 1 and 2 was performed to estimate the combined ORs. In silico analyses were then performed to identify expression quantitative loci (eQTL) single‐nucleotide polymorphisms (SNPs) that are in high linkage disequilibrium (LD) with the top SNPs. The associations of the potentially functional SNPs were replicated and validated in an independent case‐control study of 48 patients of European ancestry treated with iv BPs (19 ONJ cases and 29 controls). The top SNPs in the exome‐wide association meta‐analysis were two SNPs on chromosome 10: SIRT1 SNP rs7896005 and HERC4 SNP rs3758392 with identical OR of 0.07 (0.01–0.46; p ?=?3.83?×?10 ?5 ). In the in silico functional analyses, two promoter region SNPs (rs7894483 and rs3758391) were identified to be in high LD with the index SNPs and are eQTLs for SIRT1 gene in whole blood in the GTEx database. The ORs were 0.30 (0.10–0.88), 0.26 (0.12–0.55), and 0.26 (0.12–0.55) for the WES top SNP rs7896005 and two promoter SNPs rs7894483 and rs3758391, respectively, in the replication sample. In summary, we identified the SIRT1/HERC4 locus on chromosome 10 to be associated with iv BP‐induced ONJ and two promoter SNPs that might be the potential genetic markers for this association. ? 2017 The Authors. Journal of Bone and Mineral Research Published by Wiley Periodicals Inc.
机译:摘要颌骨骨折(ON​​J)是一种罕见但严重的药物副作用,主要与使用静脉注射(IV)双膦酸盐(BPS)有关。本研究的目的是鉴定欧洲祖先患者与IV BPS治疗的癌症相关的遗传变异,使用全溢位测序(WES)。 WES阶段1包括44名多发性骨髓瘤患者(22个ONJ病例和22例,22例,WES相2包括17名ONJ患者具有实体瘤的患者。进行多变量逻辑回归分析以估计禽类比(或)和95%的置信区间(CI),调整年龄,性别和主要成分的血统。进行WES期1和2的荟萃分析以估计组合或含量。然后在硅分析中进行,以鉴定具有顶部SNP的高连杆不平衡(LD)的表达定量基因座(EQTL)单核苷酸多态性(SNP)。潜在的功能性SNP的关联在用IV BPS治疗的48名欧洲祖先患者(19 ONJ案件和29个对照)的独立病例对照研究中进行复制和验证。 exome-宽的关联元分析中的顶级SNP是染色体10:SIRT1 SNP RS7896005和HERC4 SNP RS3758392,其相同或0.07(0.01-0.46; P?= 3.83?×10?5)。在Silico功能分析中,鉴定出两个启动子区域SNP(RS7894483和RS3758391)与指数SNP的高LD,并且在GTEX数据库中的全血中的SIRT1基因的EQTLS。对于WES顶部SNP RS7896005和两个启动子SNPS RS7894483和RS3758391的0.30(0.12-0.88),0.26(0.12-0.55),0.26(0.12-0.55)和0.26(0.12-0.55)分别在复制样品中。总之,我们鉴定了染色体10上的SIRT1 / HERC4基因座,以与IV BP诱导的ONJ和两个启动子SNP相关联,这可能是该协会的潜在遗传标记。还2017年作者。 Wiley期刊公司骨矿物研究杂志CHINESE。

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