• 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

白细胞介素 37 基因变异赋予冠心病的显著风险。

Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery Disease.

机构信息

Key Laboratory of Molecular Biophysics of the Ministry of Education, College of Life Science and Technology, Center for Human Genome Research, Cardio-X Institute, Huazhong University of Science and Technology, Wuhan, P. R. China.

BGI-Wuhan, Wuhan 430075, China; BGI-Shenzhen, Shenzhen 518083, China.

出版信息

Sci Rep. 2017 Feb 9;7:42175. doi: 10.1038/srep42175.

DOI:10.1038/srep42175
PMID:28181534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5299598/
Abstract

The interleukin 1 family plays an important role in the immune and inflammatory responses. Coronary artery disease (CAD) is a chronic inflammatory disease. However, the genetic association between IL-37, the seventh member of the IL-1 family, and CAD is unknown. Here we show that a single nucleotide polymorphism in the IL-37 gene (rs3811047) confers a significant risk of CAD. We have performed an association analysis between rs3811047 and CAD in two independent populations with 2,501 patients and 3,116 controls from China. Quantitative RT-PCR analysis has been performed to determine if the IL-37 expression level is influenced by rs3811047. We show that the minor allele A of rs3811047 is significantly associated with CAD in two independent populations under a recessive model (P = 5.51 × 10/OR = 1.56 in the GeneID Northernern population and P = 1.23 × 10/OR = 1.45 in the GeneID Central population). The association became more significant in the combined population (P = 9.70 × 10/OR = 1.47). Moreover, the association remains significant in a CAD case control population matched for age and sex. Allele A of rs3811047 shows significant association with a decreased mRNA expression level of IL-37 (n = 168, P = 3.78 × 10). These data suggest that IL37 is a new susceptibility gene for CAD, which provides a potential target for the prevention and treatment of CAD.

摘要

白细胞介素 1 家族在免疫和炎症反应中发挥着重要作用。冠心病 (CAD) 是一种慢性炎症性疾病。然而,白细胞介素 1 家族的第七个成员 IL-37 与 CAD 的遗传关联尚不清楚。在这里,我们表明 IL-37 基因中的一个单核苷酸多态性(rs3811047)赋予 CAD 显著风险。我们在中国的两个独立人群中进行了 rs3811047 与 CAD 的关联分析,共有 2501 例患者和 3116 例对照。进行了定量 RT-PCR 分析,以确定 rs3811047 是否影响 IL-37 的表达水平。我们表明,在两个独立的人群中,rs3811047 的次要等位基因 A 在隐性模型下与 CAD 显著相关(GeneID Northernern 人群中 P=5.51×10/OR=1.56,GeneID Central 人群中 P=1.23×10/OR=1.45)。在合并人群中,相关性更加显著(P=9.70×10/OR=1.47)。此外,在年龄和性别匹配的 CAD 病例对照人群中,相关性仍然显著。rs3811047 的等位基因 A 与 IL-37 的 mRNA 表达水平降低显著相关(n=168,P=3.78×10)。这些数据表明,IL37 是 CAD 的一个新的易感基因,为 CAD 的预防和治疗提供了一个潜在的靶点。

相似文献

1
Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery Disease.白细胞介素 37 基因变异赋予冠心病的显著风险。
Sci Rep. 2017 Feb 9;7:42175. doi: 10.1038/srep42175.
2
Association of IL-8-251 A/T rs4073 and IL-10 rs1800872 -592C/A Polymorphisms and Coronary Artery Disease in North Indian Population.IL-8基因-251A/T rs4073和IL-10基因rs1800872 -592C/A多态性与北印度人群冠状动脉疾病的关联
Biochem Genet. 2019 Feb;57(1):129-146. doi: 10.1007/s10528-018-9880-7. Epub 2018 Aug 2.
3
Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction.CAV1基因的基因组变异会增加患冠状动脉疾病和心肌梗死的易感性。
Atherosclerosis. 2016 Mar;246:148-156. doi: 10.1016/j.atherosclerosis.2016.01.008. Epub 2016 Jan 8.
4
Gene polymorphism in IL17A and gene-gene interaction in the IL23R/IL17A axis are associated with susceptibility to coronary artery disease.IL17A基因多态性以及IL23R/IL17A轴中的基因-基因相互作用与冠状动脉疾病易感性相关。
Cytokine. 2023 Apr;164:156142. doi: 10.1016/j.cyto.2023.156142. Epub 2023 Feb 18.
5
Functional rare variant in a binding site in gene increases the risk of coronary artery disease.基因中的一个结合位点的功能性罕见变异增加了患冠状动脉疾病的风险。
Aging (Albany NY). 2021 Dec 12;13(23):25393-25407. doi: 10.18632/aging.203755.
6
Analysis of the genetic association between IL27 variants and coronary artery disease in a Chinese Han population.中国汉族人群中IL27基因变异与冠状动脉疾病的遗传关联分析。
Sci Rep. 2016 May 12;6:25782. doi: 10.1038/srep25782.
7
The association of cholesterol absorption gene Numb polymorphism with Coronary Artery Disease among Han Chinese and Uighur Chinese in Xinjiang, China.中国新疆汉族和维吾尔族人群中胆固醇吸收基因Numb多态性与冠状动脉疾病的关联
Lipids Health Dis. 2015 Sep 29;14:120. doi: 10.1186/s12944-015-0102-6.
8
[Association of C1019T polymorphism in the connexin 37 gene and coronary artery disease in Chinese Han population].[中国汉族人群中连接蛋白37基因C1019T多态性与冠状动脉疾病的关联]
Zhonghua Yi Xue Za Zhi. 2007 Jan 9;87(2):100-4.
9
Polymorphism of IL37 gene as a protective factor for autoimmune thyroid disease.白细胞介素37基因多态性作为自身免疫性甲状腺疾病的保护因素
J Mol Endocrinol. 2015 Dec;55(3):209-18. doi: 10.1530/JME-15-0144. Epub 2015 Sep 15.
10
The IL-33-ST2L pathway is associated with coronary artery disease in a Chinese Han population.IL-33-ST2L 通路与汉族人群的冠状动脉疾病相关。
Am J Hum Genet. 2013 Oct 3;93(4):652-60. doi: 10.1016/j.ajhg.2013.08.009. Epub 2013 Sep 26.

引用本文的文献

1
Role of Interleukin 37 and its polymorphism (rs3811047) in children with type I diabetes.白细胞介素37及其多态性(rs3811047)在1型糖尿病儿童中的作用。
Mol Biol Rep. 2025 Jul 7;52(1):678. doi: 10.1007/s11033-025-10779-7.
2
The Protective Role of Interleukin-37 in Cardiovascular Diseases through Ferroptosis Modulation.白细胞介素-37 通过调控铁死亡在心血管疾病中发挥保护作用。
Int J Mol Sci. 2024 Sep 10;25(18):9758. doi: 10.3390/ijms25189758.
3
Inhibition of Hsp90 K284 Acetylation Aalleviates Cardiac Injury After Ischemia-Reperfusion Injury.

本文引用的文献

1
Prevalence of systemic autoimmune rheumatic diseases and clinical significance of ANA profile: data from a tertiary hospital in Shanghai, China.中国上海某三级医院系统性自身免疫性风湿病的患病率及抗核抗体谱的临床意义
APMIS. 2016 Sep;124(9):805-11. doi: 10.1111/apm.12564. Epub 2016 Jun 22.
2
Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation.基因-基因相互作用的分子基础:基因表达的循环交叉调控与心房颤动相关的全基因组关联研究后基因-基因相互作用
PLoS Genet. 2015 Aug 12;11(8):e1005393. doi: 10.1371/journal.pgen.1005393. eCollection 2015 Aug.
3
抑制热休克蛋白90(Hsp90)K284位点乙酰化可减轻缺血再灌注损伤后的心脏损伤。
J Cardiovasc Transl Res. 2024 Dec;17(6):1427-1441. doi: 10.1007/s12265-024-10548-0. Epub 2024 Jul 24.
4
Polymorphism Analysis of Interleukin-18 and Interleukin-37 Genes in Hepatitis B Infections with Different Outcomes: A Preliminary Report from an Iranian Population.白细胞介素-18 和白细胞介素-37 基因多态性分析在不同结局乙型肝炎感染中的作用:伊朗人群的初步报告。
Asian Pac J Cancer Prev. 2023 Feb 1;24(2):411-416. doi: 10.31557/APJCP.2023.24.2.411.
5
A Critical Appraisal of the Diagnostic and Prognostic Utility of the Anti-Inflammatory Marker IL-37 in a Clinical Setting: A Case Study of Patients with Diabetes Type 2.在临床环境下评估抗炎标志物 IL-37 的诊断和预后效用的批判性研究:以 2 型糖尿病患者为例。
Int J Environ Res Public Health. 2023 Feb 19;20(4):3695. doi: 10.3390/ijerph20043695.
6
Serum levels of IL-37 and correlation with inflammatory cytokines and clinical outcomes in patients with coronary artery disease.血清 IL-37 水平与冠心病患者炎症细胞因子的相关性及其与临床结局的关系。
J Investig Med. 2022 Dec;70(8):1720-1727. doi: 10.1136/jim-2021-002134. Epub 2022 May 30.
7
Functional rare variant in a binding site in gene increases the risk of coronary artery disease.基因中的一个结合位点的功能性罕见变异增加了患冠状动脉疾病的风险。
Aging (Albany NY). 2021 Dec 12;13(23):25393-25407. doi: 10.18632/aging.203755.
8
Association of the Polymorphisms with Transaminases and Alkaline Phosphatase Levels in Premature Coronary Artery Disease Patients and Healthy Controls. Results of the Genetics of Atherosclerotic (GEA) Mexican Study.多态性与早发冠心病患者及健康对照者转氨酶和碱性磷酸酶水平的关联。动脉粥样硬化遗传学(GEA)墨西哥研究结果
Diagnostics (Basel). 2021 Jun 2;11(6):1018. doi: 10.3390/diagnostics11061018.
9
IL-37-a putative therapeutic agent in cardiovascular diseases.IL-37——心血管疾病的一种潜在治疗药物。
QJM. 2022 Nov 14;115(11):719-725. doi: 10.1093/qjmed/hcab011.
10
IL-37 Gene and Cholesterol Metabolism: Association of Polymorphisms with the Presence of Hypercholesterolemia and Cardiovascular Risk Factors. The GEA Mexican Study.IL-37 基因与胆固醇代谢:多态性与高胆固醇血症和心血管危险因素存在的关联。墨西哥 GEA 研究。
Biomolecules. 2020 Oct 5;10(10):1409. doi: 10.3390/biom10101409.
Identification of rare variants in TNNI3 with atrial fibrillation in a Chinese GeneID population.
在中国基因识别(GeneID)人群中对与心房颤动相关的肌钙蛋白I3(TNNI3)罕见变异的识别。
Mol Genet Genomics. 2016 Feb;291(1):79-92. doi: 10.1007/s00438-015-1090-y. Epub 2015 Jul 14.
4
Association of SNP Rs9943582 in APLNR with Left Ventricle Systolic Dysfunction in Patients with Coronary Artery Disease in a Chinese Han GeneID Population.中国汉族人群中APLNR基因的SNP Rs9943582与冠心病患者左心室收缩功能障碍的关联
PLoS One. 2015 May 19;10(5):e0125926. doi: 10.1371/journal.pone.0125926. eCollection 2015.
5
Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population.中国汉族人群中7p31上的CAV1基因变体rs3807989与心房颤动之间的显著关联。
J Am Heart Assoc. 2015 May 7;4(5):e001980. doi: 10.1161/JAHA.115.001980.
6
Candidate pathway-based genome-wide association studies identify novel associations of genomic variants in the complement system associated with coronary artery disease.基于候选通路的全基因组关联研究确定了补体系统中与冠状动脉疾病相关的基因组变异的新关联。
Circ Cardiovasc Genet. 2014 Dec;7(6):887-94. doi: 10.1161/CIRCGENETICS.114.000738. Epub 2014 Sep 23.
7
IL-37 ameliorates the inflammatory process in psoriasis by suppressing proinflammatory cytokine production.IL-37 通过抑制促炎细胞因子的产生来改善银屑病的炎症过程。
J Immunol. 2014 Feb 15;192(4):1815-23. doi: 10.4049/jimmunol.1300047. Epub 2014 Jan 22.
8
Regulation of CARD8 expression by ANRIL and association of CARD8 single nucleotide polymorphism rs2043211 (p.C10X) with ischemic stroke.由 ANRIL 调控的 CARD8 表达及其单核苷酸多态性 rs2043211(p.C10X)与缺血性脑卒中的关联。
Stroke. 2014 Feb;45(2):383-8. doi: 10.1161/STROKEAHA.113.003393. Epub 2014 Jan 2.
9
BRG1 variant rs1122608 on chromosome 19p13.2 confers protection against stroke and regulates expression of pre-mRNA-splicing factor SFRS3.BRG1 变体 rs1122608 位于 19p13.2 染色体上,可预防中风,并调节前体 mRNA 剪接因子 SFRS3 的表达。
Hum Genet. 2014 May;133(5):499-508. doi: 10.1007/s00439-013-1389-x. Epub 2013 Nov 5.
10
Association of interleukin-33 gene single nucleotide polymorphisms with ischemic stroke in north Chinese population.白细胞介素-33 基因单核苷酸多态性与中国北方人群缺血性脑卒中的相关性研究。
BMC Med Genet. 2013 Oct 9;14:109. doi: 10.1186/1471-2350-14-109.