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利用英国生物库数据进行全基因组分析为骨关节炎的遗传结构提供了新的见解。

Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis.

机构信息

Department of Oncology and Metabolism, University of Sheffield, Sheffield, UK.

5th Psychiatric Department, Dromokaiteio Psychiatric Hospital, Athens, Greece.

出版信息

Nat Genet. 2018 Apr;50(4):549-558. doi: 10.1038/s41588-018-0079-y. Epub 2018 Mar 20.

Abstract

Osteoarthritis is a common complex disease imposing a large public-health burden. Here, we performed a genome-wide association study for osteoarthritis, using data across 16.5 million variants from the UK Biobank resource. After performing replication and meta-analysis in up to 30,727 cases and 297,191 controls, we identified nine new osteoarthritis loci, in all of which the most likely causal variant was noncoding. For three loci, we detected association with biologically relevant radiographic endophenotypes, and in five signals we identified genes that were differentially expressed in degraded compared with intact articular cartilage from patients with osteoarthritis. We established causal effects on osteoarthritis for higher body mass index but not for triglyceride levels or genetic predisposition to type 2 diabetes.

摘要

骨关节炎是一种常见的复杂疾病,给公共健康带来了巨大负担。在这里,我们利用英国生物库资源中超过 1650 万个变体的数据,对骨关节炎进行了全基因组关联研究。在对多达 30727 例病例和 297191 例对照进行复制和荟萃分析后,我们确定了 9 个新的骨关节炎位点,在所有这些位点中,最可能的因果变异是非编码的。对于三个位点,我们检测到与生物学上相关的放射影像学表型的关联,在五个信号中,我们鉴定出在与骨关节炎患者的关节软骨相比,降解的软骨中表达差异的基因。我们确定了较高的体重指数对骨关节炎有因果影响,但对甘油三酯水平或 2 型糖尿病的遗传易感性没有影响。

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