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一种多性状方法鉴定出了7个与背痛相关的新基因。

A multi-trait approach identified 7 novel genes for back pain.

作者信息

Belonogova Nadezhda M, Elgaeva Elizaveta E, Zorkoltseva Irina V, Kirichenko Anatoliy V, Svishcheva Gulnara R, Freidin Maxim B, Williams Frances M K, Suri Pradeep, Axenovich Tatiana I, Tsepilov Yakov A

机构信息

Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia.

Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russia.

出版信息

Pain Rep. 2024 Dec 24;10(1):e1218. doi: 10.1097/PR9.0000000000001218. eCollection 2025 Feb.

Abstract

INTRODUCTION

Back pain (BP) is a complex heritable trait with an estimated heritability of 40% to 60%. Less than half of this can be explained by known genetic variants identified in genome-wide association studies.

OBJECTIVES

We applied a powerful multi-trait and gene-based approach to association analysis of BP to identify novel genes associated with BP.

METHODS

Using phenotypes and imputed genotypes from the UK Biobank 500k dataset, we generated a multi-trait phenotype by combining 3 BP-related phenotypes: chronic BP, dorsalgia, and intervertebral disk disorders. We performed gene-based association analysis for 3 BP-related phenotypes and multi-trait phenotype. Conditional analysis was applied to account for the effects of genetic variants outside the gene. Finally, we replicated significantly associated genes using the FinnGen database.

RESULTS

We identified 32 genes associated with BP and replicated 16 of them. Thirteen genes were detected using the multi-trait phenotype. Seven of the detected genes, , , , , , , and , were not previously reported. Several new genes are known to be associated with traits genetically correlated with BP or to be involved in pathways associated with BP.

CONCLUSION

Using new powerful methods of association analysis, we identified 7 novel genes associated with BP. Our results provide new insights into the genetics of back pain.

摘要

引言

背痛(BP)是一种复杂的可遗传性状,估计遗传率为40%至60%。其中不到一半可由全基因组关联研究中确定的已知基因变异来解释。

目的

我们应用一种强大的多性状和基于基因的方法对背痛进行关联分析,以确定与背痛相关的新基因。

方法

利用英国生物银行50万数据集的表型和推算基因型,我们通过合并3种与背痛相关的表型(慢性背痛、背痛和椎间盘疾病)生成了一种多性状表型。我们对3种与背痛相关的表型和多性状表型进行了基于基因的关联分析。应用条件分析来考虑基因外遗传变异的影响。最后,我们使用芬兰基因数据库对显著相关基因进行了验证。

结果

我们鉴定出32个与背痛相关的基因,并验证了其中16个。使用多性状表型检测到13个基因。检测到的7个基因,即 、 、 、 、 、 和 ,此前未被报道。已知几个新基因与与背痛遗传相关的性状有关,或参与与背痛相关的途径。

结论

通过使用新的强大关联分析方法,我们鉴定出7个与背痛相关的新基因。我们的结果为背痛的遗传学提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/461e/11671072/bf197a0a5af6/painreports-10-e1218-g001.jpg

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