• 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

印度人群中C反应蛋白的全基因组关联研究重复了常见变异的已知关联。

Genomewide association study for C-reactive protein in Indians replicates known associations of common variants.

作者信息

Prasad Gauri, Giri Anil K, Basu Analabha, Tandon Nikhil, Bharadwaj Dwaipayan

机构信息

Genomics and Molecular Medicine Unit, CSIR-Institute of Genomics and Integrative Biology, New Delhi 110 020, India.

出版信息

J Genet. 2019 Mar;98.

PMID:30945673
Abstract

Elevated C-reactive protein (CRP) serves as an independent biomarker for acute and chronic inflammation, and is also associated with metabolic diseases. Genomewide loci regulating CRP level in Indian population, a high-risk group for metabolic illness, is unexplored. Therefore, we aimed to discover common polymorphisms associated with plasma CRP level in 4493 Indians of Indo-European origin using genomewide association study. Genomewide strong associations of two known intronic variants in hepatocyte nuclear factor-1 α gene () were identified among Indian subjects. We also detected prior associations of several variants in/near metabolic and inflammatory process genes: , , , , and with modest associations. This study confirms that Indians from Indo-European origin display similar core universal genetic factors for CRP levels.

摘要

C反应蛋白(CRP)水平升高是急性和慢性炎症的独立生物标志物,还与代谢性疾病相关。在代谢疾病高危人群印度人群中,尚未探索调控CRP水平的全基因组位点。因此,我们旨在通过全基因组关联研究,在4493名印欧血统的印度人中发现与血浆CRP水平相关的常见多态性。在印度受试者中,鉴定出肝细胞核因子-1α基因()中两个已知内含子变异的全基因组强关联。我们还检测到代谢和炎症过程基因中/附近的几个变异的先前关联:、、、、和具有适度关联。本研究证实,印欧血统的印度人在CRP水平上表现出相似的核心普遍遗传因素。

相似文献

1
Genomewide association study for C-reactive protein in Indians replicates known associations of common variants.印度人群中C反应蛋白的全基因组关联研究重复了常见变异的已知关联。
J Genet. 2019 Mar;98.
2
Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans.关于C反应蛋白水平的大型多民族候选基因研究:在非裔美国人中鉴定出CD36基因的一种新关联。
Hum Genet. 2014 Aug;133(8):985-95. doi: 10.1007/s00439-014-1439-z. Epub 2014 Mar 19.
3
Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore?在新加坡的亚洲人群中,C 反应蛋白相关遗传变异与血清水平和微血管病变的视网膜标志物有关吗?
PLoS One. 2013 Jul 2;8(7):e67650. doi: 10.1371/journal.pone.0067650. Print 2013.
4
Genome-wide association with C-reactive protein levels in CLHNS: evidence for the CRP and HNF1A loci and their interaction with exposure to a pathogenic environment.全基因组关联研究显示 CLHNS 与 C 反应蛋白水平相关:CRP 和 HNF1A 基因座及其与致病环境暴露相互作用的证据。
Inflammation. 2012 Apr;35(2):574-83. doi: 10.1007/s10753-011-9348-y.
5
Association of exome sequences with plasma C-reactive protein levels in >9000 participants.9000多名参与者外显子组序列与血浆C反应蛋白水平的关联
Hum Mol Genet. 2015 Jan 15;24(2):559-71. doi: 10.1093/hmg/ddu450. Epub 2014 Sep 3.
6
Plasma C-reactive protein, genetic risk score, and risk of common cancers in the Atherosclerosis Risk in Communities study.血浆 C 反应蛋白、遗传风险评分与社区动脉粥样硬化风险研究中常见癌症的风险。
Cancer Causes Control. 2013 Dec;24(12):2077-87. doi: 10.1007/s10552-013-0285-y. Epub 2013 Sep 14.
7
Pleiotropy among common genetic loci identified for cardiometabolic disorders and C-reactive protein.在为心脏代谢紊乱和C反应蛋白所确定的常见基因座之间的多效性。
PLoS One. 2015 Mar 13;10(3):e0118859. doi: 10.1371/journal.pone.0118859. eCollection 2015.
8
Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study.在利用基因与流行病学人群结构研究(PAGE)研究中的代谢芯片,在多民族人群中发现、精细定位与 C 反应蛋白相关的遗传变异,并进行条件分析。
Hum Mol Genet. 2018 Aug 15;27(16):2940-2953. doi: 10.1093/hmg/ddy211.
9
Common variants in CRP and LEPR influence high sensitivity C-reactive protein levels in North Indians.常见的 CRP 和 LEPR 变异体影响北印度人的高敏 C 反应蛋白水平。
PLoS One. 2011;6(9):e24645. doi: 10.1371/journal.pone.0024645. Epub 2011 Sep 8.
10
Single-nucleotide polymorphisms at five loci are associated with C-reactive protein levels in a cohort of Filipino young adults.在菲律宾青年成年人队列中,五个基因位点的单核苷酸多态性与 C 反应蛋白水平相关。
J Hum Genet. 2011 Dec;56(12):823-7. doi: 10.1038/jhg.2011.106. Epub 2011 Sep 22.

引用本文的文献

1
Genetic insights into CRP levels in Indian adolescents: confirming adult genetic associations.印度青少年CRP水平的遗传学见解:证实与成人的遗传关联
Mol Genet Genomics. 2025 Jan 23;300(1):17. doi: 10.1007/s00438-024-02213-7.
2
Engineering CRISPR/Cas9 therapeutics for cancer precision medicine.为癌症精准医疗设计CRISPR/Cas9疗法。
Front Genet. 2024 Apr 25;15:1309175. doi: 10.3389/fgene.2024.1309175. eCollection 2024.
3
Genetic analysis of over half a million people characterises C-reactive protein loci.对超过 50 万人的基因分析确定了 C 反应蛋白基因座。

本文引用的文献

1
Reverse phenotyping comes of age.反向表型分析已走向成熟。
Mol Genet Metab. 2016 Aug;118(4):230-1. doi: 10.1016/j.ymgme.2016.05.010. Epub 2016 May 14.
2
625 kb microduplication at Xp22.12 including RPS6KA3 in a child with mild intellectual disability.一名轻度智力残疾儿童Xp22.12处625 kb的微重复,包含RPS6KA3基因。
J Hum Genet. 2015 Dec;60(12):777-80. doi: 10.1038/jhg.2015.106. Epub 2015 Sep 10.
3
CNVs conferring risk of autism or schizophrenia affect cognition in controls.CNVs 导致自闭症或精神分裂症的风险会影响对照组的认知能力。
Nat Commun. 2022 Apr 22;13(1):2198. doi: 10.1038/s41467-022-29650-5.
4
Pro-inflammatory cytokine polymorphisms and interactions with dietary alcohol and estrogen, risk factors for invasive breast cancer using a post genome-wide analysis for gene-gene and gene-lifestyle interaction.促炎细胞因子多态性与饮食酒精和雌激素的相互作用,以及使用全基因组后分析进行基因-基因和基因-生活方式相互作用的侵袭性乳腺癌的危险因素。
Sci Rep. 2021 Jan 13;11(1):1058. doi: 10.1038/s41598-020-80197-1.
5
Pro-inflammatory cytokine polymorphisms in ONECUT2 and HNF4A and primary colorectal carcinoma: a post genome-wide gene-lifestyle interaction study.ONECUT2和HNF4A基因中的促炎细胞因子多态性与原发性结直肠癌:一项全基因组后基因-生活方式相互作用研究。
Am J Cancer Res. 2020 Sep 1;10(9):2955-2976. eCollection 2020.
6
Genome-wide Association Analysis of Proinflammatory Cytokines and Gene-lifestyle Interaction for Invasive Breast Cancer Risk: The WHI dbGaP Study.全基因组关联分析促炎细胞因子与基因-生活方式相互作用对浸润性乳腺癌风险的影响:WHI dbGaP 研究。
Cancer Prev Res (Phila). 2021 Jan;14(1):41-54. doi: 10.1158/1940-6207.CAPR-20-0256. Epub 2020 Sep 14.
7
Genome-Wide Association Study of Metabolic Syndrome Reveals Primary Genetic Variants at Locus in Indians.代谢综合征的全基因组关联研究揭示了印度人群中位于 Locus 的主要遗传变异。
Biomolecules. 2019 Jul 30;9(8):321. doi: 10.3390/biom9080321.
8
Genome-wide association study of blood lipids in Indians confirms universality of established variants.全基因组关联研究证实了已确定的变异在印度人群中的普遍性。
J Hum Genet. 2019 Jun;64(6):573-587. doi: 10.1038/s10038-019-0591-7. Epub 2019 Mar 25.
Nature. 2014 Jan 16;505(7483):361-6. doi: 10.1038/nature12818. Epub 2013 Dec 18.
4
An Xp22.12 microduplication including RPS6KA3 identified in a family with variably affected intellectual and behavioral disabilities.一个家族中存在 Xp22.12 微重复,该重复包含 RPS6KA3,受影响的个体表现出不同程度的智力和行为障碍。
J Hum Genet. 2013 Nov;58(11):755-7. doi: 10.1038/jhg.2013.88. Epub 2013 Aug 29.
5
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.染色质修饰基因 KANSL1 突变导致 17q21.31 微缺失综合征。
Nat Genet. 2012 Apr 29;44(6):639-41. doi: 10.1038/ng.2262.
6
A child with mild X-linked intellectual disability and a microduplication at Xp22.12 including RPS6KA3.一名患有轻度 X 连锁智力障碍的儿童,其 Xp22.12 区域存在微重复,包括 RPS6KA3。
Pediatrics. 2011 Oct;128(4):e1029-33. doi: 10.1542/peds.2010-0388. Epub 2011 Sep 19.
7
Coffin-Lowry syndrome.考芬-洛里综合征。
Eur J Hum Genet. 2010 Jun;18(6):627-33. doi: 10.1038/ejhg.2009.189. Epub 2009 Nov 4.
8
The genetic landscape of intellectual disability arising from chromosome X.由X染色体引发的智力残疾的遗传图谱。
Trends Genet. 2009 Jul;25(7):308-16. doi: 10.1016/j.tig.2009.05.002. Epub 2009 Jun 24.
9
Characterization of interstitial Xp duplications in two families by tiling path array CGH.通过平铺路径阵列比较基因组杂交技术对两个家族中的间质性Xp重复进行特征分析。
Am J Med Genet A. 2008 Jan 15;146A(2):197-203. doi: 10.1002/ajmg.a.32070.
10
X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation.采用X染色体平铺路径阵列检测X连锁智力障碍患者的拷贝数变异
BMC Genomics. 2007 Nov 29;8:443. doi: 10.1186/1471-2164-8-443.