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全基因组荟萃分析确定与 Modic 改变相关的染色体 9 上的遗传位置。

Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes.

机构信息

Department of Twin Research and Genetic Epidemiology, School of Life Course Sciences, King's College London, London, UK.

Center for Life Course Health Research, Faculty of Medicine, University of Oulu, Oulu, Finland.

出版信息

J Med Genet. 2019 Jul;56(7):420-426. doi: 10.1136/jmedgenet-2018-105726. Epub 2019 Feb 26.

Abstract

BACKGROUND

Low back pain (LBP) is a common disabling condition. Lumbar disc degeneration (LDD) may be a contributing factor for LBP. Modic change (MC), a distinct phenotype of LDD, is presented as a pathological bone marrow signal change adjacent to vertebral endplate on MRI. It is strongly associated with LBP and has heritability around 30%. Our objective was to identify genetic loci associated with MC using a genome-wide meta-analysis.

METHODS

Presence of MC was evaluated in lumbar MRI in the Northern Finland Birth Cohort 1966 (n=1182) and TwinsUK (n=647). Genome-wide association analyses were carried out using linear regression model. Inverse-variance weighting approach was used in the meta-analysis.

RESULTS

A locus associated with MC (p<5e-8) was found on chromosome 9 with the lead SNP rs1934268 in an intron of the gene. It is located in the binding region of BCL11A, SPI1 and PBX3 transcription factors. The SNP was nominally associated with LBP in TwinsUK (p=0.001) but not associated in the UK Biobank (p=0.914). Suggestive signals (p<1e-5) were identified near , , , , and .

CONCLUSION

is a novel candidate gene for MC that may act via the development of cartilage or nervous system; further work is needed to define the mechanisms underlying the pathways leading to development of MC. This is the first genome-wide meta-analysis of MC, and the results pave the way for further studies on the genetic factors underlying the various features of spine degeneration and LBP.

摘要

背景

下腰痛(LBP)是一种常见的致残性疾病。腰椎间盘退变(LDD)可能是 LBP 的一个致病因素。Modic 改变(MC),LDD 的一个独特表型,表现为 MRI 上椎体终板旁的病理性骨髓信号改变。它与 LBP 强烈相关,遗传率约为 30%。我们的目的是使用全基因组荟萃分析来确定与 MC 相关的遗传位点。

方法

在芬兰北部出生队列 1966 年(n=1182)和英国双胞胎研究(n=647)的腰椎 MRI 中评估 MC 的存在。使用线性回归模型进行全基因组关联分析。荟萃分析采用逆方差加权法。

结果

在染色体 9 上发现了一个与 MC 相关的位点(p<5e-8),其主要 SNP 是基因内含子中的 rs1934268。它位于 BCL11A、SPI1 和 PBX3 转录因子的结合区域。该 SNP 在英国双胞胎研究中与 LBP 呈显著相关(p=0.001),但在英国生物库中不相关(p=0.914)。在附近鉴定出了提示信号(p<1e-5),包括 、 、 、 、 。

结论

是 MC 的一个新候选基因,可能通过软骨或神经系统的发育起作用;需要进一步研究来确定导致 MC 发展的途径的机制。这是 MC 的首次全基因组荟萃分析,结果为进一步研究脊柱退变和 LBP 的各种特征的遗传因素铺平了道路。

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