Genome-wide analysis in northern Chinese twins identifies twelve new susceptibility loci for pulmonary function.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2024-12-30 DOI:10.1186/s12864-024-11165-6
Tong Wang, Weijing Wang, Chunsheng Xu, Xiaocao Tian, Dongfeng Zhang
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Abstract

Background: Previous genome-wide association studies (GWAS) have established association between genetic variants and pulmonary function across various ethnics, whereas such associations are scarcely reported in Chinese adults. Therefore, we conducted an GWAS to explore relationships between genetic variants and pulmonary function among middle-aged Chinese dizygotic twins and further validated the top variants using data from the UK Biobank (UKB).

Methods: In the discovery phase, 139 dizygotic twin pairs were drawn from the Qingdao Twin Registry. Pulmonary function was assessed using three parameters: forced expiratory volume the first second (FEV1), forced vital capacity (FVC), and FEV1/FVC ratio. GWAS was performed using GEMMA, Gene-based analysis was conducted by VEGAS2. And pathway enrichment analysis was performed using PASCAL. In the validation phase, Single-nucleotide polymorphisms (SNPs) with suggestive significance were examined through linear regression analysis of the additive effect model among 1573 Chinese ethnic participants from UKB.

Results: The median age of twin pairs in the study was 49 years. 3 SNPs (rs80345886, rs117883876, and 75139439) related to FEV1 achieved genome-wide significance. Moreover, 222, 150, and 73 SNPs surpassed suggestive evidence level (p < 1 × 10- 5) for FEV1, FVC, and FEV1/FVC, respectively. Among them, 16 SNPs located in TBC1D16 for FEV1, 25 SNPs located in GPR126 for FVC, and 2 SNPs located in CCDC110 for FEV1/FVC, the three genes were also revealed by gene-based analysis. Moreover, 12 novel SNPs related to pulmonary function were validated to reach the nominal significance level (p < 0.05) in the UKB, with some located in the TBC1D16, TAFA5, and MTHFD1L genes.

Conclusion: Our GWAS results on Chinese dizygotic twins provide new references for the genetic regulation on pulmonary function. Twelve novel susceptibility loci are considered as possible crucial to pulmonary function.

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中国北方双胞胎的全基因组分析发现了12个新的肺功能易感位点。
背景:以前的全基因组关联研究(GWAS)已经在不同种族中建立了遗传变异与肺功能之间的关联,然而这种关联在中国成年人中几乎没有报道。因此,我们对中国中年双卵双胞胎进行了GWAS研究,以探索遗传变异与肺功能之间的关系,并利用英国生物银行(UKB)的数据进一步验证了顶级变异。方法:在发现阶段,从青岛双胞胎登记处抽取139对异卵双胞胎。使用三个参数评估肺功能:第一秒用力呼气量(FEV1)、用力肺活量(FVC)和FEV1/FVC比值。GWAS采用GEMMA,基因分析采用VEGAS2。利用PASCAL进行途径富集分析。在验证阶段,通过加性效应模型的线性回归分析,对1573名来自UKB的中国少数民族参与者进行了具有提示意义的单核苷酸多态性(snp)检验。结果:研究中双胞胎的中位年龄为49岁。与FEV1相关的3个snp (rs80345886、rs117883876和75139439)具有全基因组意义。此外,在FEV1、FVC和FEV1/FVC中,分别有222、150和73个snp超过了暗示证据水平(p - 5)。其中FEV1的snp位于TBC1D16中16个,FVC的snp位于GPR126中25个,FEV1/FVC的snp位于CCDC110中2个,通过基因分析也发现了这3个基因。此外,12个与肺功能相关的新snp被验证达到名义显著性水平(p)。结论:我们对中国异卵双胞胎的GWAS结果为肺功能的遗传调控提供了新的参考。12个新的易感位点被认为可能对肺功能至关重要。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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