• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

跨种族样本中心血管代谢特征的功能导向分析。

Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample.

机构信息

Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, TN, USA.

Human Genetics Center, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA.

出版信息

Hum Mol Genet. 2019 Apr 1;28(7):1212-1224. doi: 10.1093/hmg/ddy435.

DOI:10.1093/hmg/ddy435
PMID:30624610
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6423424/
Abstract

Interpretation of genetic association results is difficult because signals often lack biological context. To generate hypotheses of the functional genetic etiology of complex cardiometabolic traits, we estimated the genetically determined component of gene expression from common variants using PrediXcan (1) and determined genes with differential predicted expression by trait. PrediXcan imputes tissue-specific expression levels from genetic variation using variant-level effect on gene expression in transcriptome data. To explore the value of imputed genetically regulated gene expression (GReX) models across different ancestral populations, we evaluated imputed expression levels for predictive accuracy genome-wide in RNA sequence data in samples drawn from European-ancestry and African-ancestry populations and identified substantial predictive power using European-derived models in a non-European target population. We then tested the association of GReX on 15 cardiometabolic traits including blood lipid levels, body mass index, height, blood pressure, fasting glucose and insulin, RR interval, fibrinogen level, factor VII level and white blood cell and platelet counts in 15 755 individuals across three ancestry groups, resulting in 20 novel gene-phenotype associations reaching experiment-wide significance across ancestries. In addition, we identified 18 significant novel gene-phenotype associations in our ancestry-specific analyses. Top associations were assessed for additional support via query of S-PrediXcan (2) results derived from publicly available genome-wide association studies summary data. Collectively, these findings illustrate the utility of transcriptome-based imputation models for discovery of cardiometabolic effect genes in a diverse dataset.

摘要

遗传关联结果的解释具有挑战性,因为信号通常缺乏生物学背景。为了生成复杂心脏代谢特征的功能遗传病因假设,我们使用 PrediXcan(1)从常见变体估计基因表达的遗传决定成分,并确定通过特征具有差异预测表达的基因。PrediXcan 使用基因表达变体水平效应从遗传变异推断组织特异性表达水平在转录组数据中。为了探索跨不同祖先群体推断的遗传调节基因表达(GReX)模型的价值,我们评估了在欧洲血统和非洲血统样本中从 RNA 序列数据推断的表达水平的预测准确性全基因组,并使用欧洲衍生模型在非欧洲目标人群中发现了相当大的预测能力。然后,我们在包括血脂水平、体重指数、身高、血压、空腹血糖和胰岛素、RR 间隔、纤维蛋白原水平、因子 VII 水平以及白细胞和血小板计数在内的 15 个心脏代谢特征上测试了 GReX 的关联,在三个祖裔群体的 15755 个人中,结果在祖裔之间产生了 20 个新的基因表型关联达到实验范围的显著水平。此外,我们在特定于我们祖先的分析中确定了 18 个新的显著基因表型关联。通过查询来自公开可用全基因组关联研究汇总数据的 S-PrediXcan(2)结果,对顶级关联进行了额外支持的评估。总的来说,这些发现说明了基于转录组的推断模型在多样化数据集中发现心脏代谢效应基因的实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b920/6423424/14c49240a42c/ddy435f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b920/6423424/14c49240a42c/ddy435f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b920/6423424/14c49240a42c/ddy435f1.jpg

相似文献

1
Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample.跨种族样本中心血管代谢特征的功能导向分析。
Hum Mol Genet. 2019 Apr 1;28(7):1212-1224. doi: 10.1093/hmg/ddy435.
2
TIGAR: An Improved Bayesian Tool for Transcriptomic Data Imputation Enhances Gene Mapping of Complex Traits.TIGAR:一种改进的转录组数据插补贝叶斯工具,可增强复杂性状的基因定位。
Am J Hum Genet. 2019 Aug 1;105(2):258-266. doi: 10.1016/j.ajhg.2019.05.018. Epub 2019 Jun 20.
3
Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits.预测祖源多样化人群中的基因表达可发现生活方式和心血管代谢特征的易感性位点。
Am J Hum Genet. 2022 Apr 7;109(4):669-679. doi: 10.1016/j.ajhg.2022.02.013. Epub 2022 Mar 8.
4
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.全基因组综合表型研究中鉴定的与祖先相关的关联强调了基因组多样性的益处,这些关联与红细胞特征有关。
BMC Genomics. 2020 Mar 14;21(1):228. doi: 10.1186/s12864-020-6626-9.
5
Transferability of Single- and Cross-Tissue Transcriptome Imputation Models Across Ancestry Groups.单组织和跨组织转录组插补模型在不同祖先群体间的可转移性
Genet Epidemiol. 2025 Jan;49(1):e22611. doi: 10.1002/gepi.22611.
6
Genetic architecture of gene expression traits across diverse populations.跨多种人群的基因表达性状的遗传结构。
PLoS Genet. 2018 Aug 10;14(8):e1007586. doi: 10.1371/journal.pgen.1007586. eCollection 2018 Aug.
7
The trans-ancestral genomic architecture of glycemic traits.跨祖先的血糖特征的基因组结构。
Nat Genet. 2021 Jun;53(6):840-860. doi: 10.1038/s41588-021-00852-9. Epub 2021 May 31.
8
Genetically regulated gene expression underlies lipid traits in Hispanic cohorts.遗传调控的基因表达是西班牙裔人群脂质特征的基础。
PLoS One. 2019 Aug 8;14(8):e0220827. doi: 10.1371/journal.pone.0220827. eCollection 2019.
9
Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium.跨种族视角下的血糖特征遗传学研究:利用基因组学和流行病学构建人群结构(PAGE)联盟的精细映射研究结果。
Diabetologia. 2017 Dec;60(12):2384-2398. doi: 10.1007/s00125-017-4405-1. Epub 2017 Sep 13.
10
Genetically Regulated Gene Expression in the Brain Associated With Chronic Pain: Relationships With Clinical Traits and Potential for Drug Repurposing.基因调控与慢性疼痛相关的大脑中的基因表达:与临床特征的关系及药物再利用的潜力。
Biol Psychiatry. 2024 Apr 15;95(8):745-761. doi: 10.1016/j.biopsych.2023.08.023. Epub 2023 Sep 9.

引用本文的文献

1
Large-scale multi-omics analyses in Hispanic/Latino populations identify genes for cardiometabolic traits.对西班牙裔/拉丁裔人群的大规模多组学分析确定了心血管代谢特征的相关基因。
Nat Commun. 2025 Apr 11;16(1):3438. doi: 10.1038/s41467-025-58574-z.
2
A gene-level test for directional selection on gene expression.基因表达的定向选择的基因水平测试。
Genetics. 2023 May 26;224(2). doi: 10.1093/genetics/iyad060.
3
DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood.DNA 甲基化分析用于鉴定与血液中循环纤维蛋白原水平相关的新的遗传位点。

本文引用的文献

1
Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system.30 个与运动和恢复时心率反应相关的基因座,提示涉及自主神经系统。
Nat Commun. 2018 May 16;9(1):1947. doi: 10.1038/s41467-018-04148-1.
2
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics.从 GWAS 汇总统计数据推断组织特异性基因表达变异的表型后果。
Nat Commun. 2018 May 8;9(1):1825. doi: 10.1038/s41467-018-03621-1.
3
Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey.
J Thromb Haemost. 2023 May;21(5):1135-1147. doi: 10.1016/j.jtha.2023.01.015. Epub 2023 Jan 28.
4
Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits.预测祖源多样化人群中的基因表达可发现生活方式和心血管代谢特征的易感性位点。
Am J Hum Genet. 2022 Apr 7;109(4):669-679. doi: 10.1016/j.ajhg.2022.02.013. Epub 2022 Mar 8.
5
Genetically regulated expression in late-onset Alzheimer's disease implicates risk genes within known and novel loci.迟发性阿尔茨海默病中基因调控的表达提示了已知和新发病位中的风险基因。
Transl Psychiatry. 2021 Dec 6;11(1):618. doi: 10.1038/s41398-021-01677-0.
6
Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues.颈动脉内膜中层厚度与全血基因表达及 48 种组织中基因表达的遗传预测的关联。
Hum Mol Genet. 2022 Mar 31;31(7):1171-1182. doi: 10.1093/hmg/ddab236.
7
Tracing the Evolution of Human Gene Regulation and Its Association with Shifts in Environment.追溯人类基因调控的演变及其与环境变化的关联。
Genome Biol Evol. 2021 Nov 5;13(11). doi: 10.1093/gbe/evab237.
8
Short Time-Series Expression Transcriptome Data Reveal the Gene Expression Patterns of Dairy Cow Mammary Gland as Milk Yield Decreased Process.短时间序列表达转录组数据揭示了奶牛乳腺产奶量下降过程中的基因表达模式。
Genes (Basel). 2021 Jun 20;12(6):942. doi: 10.3390/genes12060942.
9
Mining GWAS and eQTL data for CF lung disease modifiers by gene expression imputation.通过基因表达推断挖掘 GWAS 和 eQTL 数据以寻找 CF 肺病修饰因子。
PLoS One. 2020 Nov 30;15(11):e0239189. doi: 10.1371/journal.pone.0239189. eCollection 2020.
10
Genetically regulated gene expression underlies lipid traits in Hispanic cohorts.遗传调控的基因表达是西班牙裔人群脂质特征的基础。
PLoS One. 2019 Aug 8;14(8):e0220827. doi: 10.1371/journal.pone.0220827. eCollection 2019.
在中国健康与营养调查中鉴定和功能分析血糖特征部位。
PLoS Genet. 2018 Apr 5;14(4):e1007275. doi: 10.1371/journal.pgen.1007275. eCollection 2018 Apr.
4
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.与体重指数相关的蛋白变异体提示了控制能量摄入和消耗的途径在肥胖中的作用。
Nat Genet. 2018 Jan;50(1):26-41. doi: 10.1038/s41588-017-0011-x. Epub 2017 Dec 22.
5
Genetic effects on gene expression across human tissues.基因对人体各组织基因表达的影响。
Nature. 2017 Oct 11;550(7675):204-213. doi: 10.1038/nature24277.
6
Analysis of genome-wide association data highlights candidates for drug repositioning in psychiatry.全基因组关联数据分析突显了精神医学药物再定位的候选者。
Nat Neurosci. 2017 Oct;20(10):1342-1349. doi: 10.1038/nn.4618. Epub 2017 Aug 14.
7
Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition.全基因组认知同理心的荟萃分析:遗传率,以及与性别、神经精神状况和认知的相关性。
Mol Psychiatry. 2018 Jun;23(6):1402-1409. doi: 10.1038/mp.2017.122. Epub 2017 Jun 6.
8
Rare and low-frequency coding variants alter human adult height.罕见和低频编码变异会改变人类成年身高。
Nature. 2017 Feb 9;542(7640):186-190. doi: 10.1038/nature21039. Epub 2017 Feb 1.
9
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog).新的NHGRI-EBI已发表全基因组关联研究目录(GWAS目录)。
Nucleic Acids Res. 2017 Jan 4;45(D1):D896-D901. doi: 10.1093/nar/gkw1133. Epub 2016 Nov 29.
10
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.人类血细胞性状变异的等位基因图谱及其与常见复杂疾病的关联。
Cell. 2016 Nov 17;167(5):1415-1429.e19. doi: 10.1016/j.cell.2016.10.042.