• 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

相似文献

1
TRIB1 rs17321515 and rs2954029 gene polymorphisms increase the risk of non-alcoholic fatty liver disease in Chinese Han population.TRIB1 rs17321515 和 rs2954029 基因多态性增加中国汉族人群非酒精性脂肪性肝病的风险。
Lipids Health Dis. 2019 Mar 9;18(1):61. doi: 10.1186/s12944-019-1001-z.
2
TRIB1 rs17321515 gene polymorphism increases the risk of coronary heart disease in general population and non-alcoholic fatty liver disease patients in Chinese Han population.TRIB1 rs17321515 基因多态性增加汉族人群冠心病和非酒精性脂肪性肝病患者的发病风险。
Lipids Health Dis. 2019 Aug 31;18(1):165. doi: 10.1186/s12944-019-1108-2.
3
rs662, rs854560 and rs17321515, rs2954029 Gene Polymorphisms Are Associated with Lipid Parameters in Patients with Unstable Angina.rs662、rs854560 和 rs17321515、rs2954029 基因多态性与不稳定型心绞痛患者的血脂参数有关。
Genes (Basel). 2024 Jul 2;15(7):871. doi: 10.3390/genes15070871.
4
Association of the TRIB1 tribbles homolog 1 gene rs17321515 A>G polymorphism and serum lipid levels in the Mulao and Han populations.TRIB1 同源物 1 基因 rs17321515 A>G 多态性与中国毛南族和汉族人群血清脂质水平的关联。
Lipids Health Dis. 2011 Dec 6;10:230. doi: 10.1186/1476-511X-10-230.
5
The A>T polymorphism of the tribbles homolog 1 gene is associated with serum triglyceride concentrations in Japanese community-dwelling women.TRIB1基因的A>T多态性与日本社区居住女性的血清甘油三酯浓度相关。
Tohoku J Exp Med. 2014 Jun;233(2):149-53. doi: 10.1620/tjem.233.149.
6
TRIB1 constitutes a molecular link between regulation of sleep and lipid metabolism in humans.TRIB1 在人类睡眠调节和脂代谢中构成了一个分子联系。
Transl Psychiatry. 2012 Mar 20;2(3):e97. doi: 10.1038/tp.2012.20.
7
Associations for , , and Polymorphism and Lifestyle Factors with Ischemic Stroke: A Nested Case-Control Study.与缺血性中风相关的 、 、 多态性和生活方式因素的巢式病例对照研究。
Yonsei Med J. 2019 Jul;60(7):659-666. doi: 10.3349/ymj.2019.60.7.659.
8
TRIB1 and TRPS1 variants, G × G and G × E interactions on serum lipid levels, the risk of coronary heart disease and ischemic stroke.TRIB1 和 TRPS1 变体、G×G 和 G×E 相互作用对血清脂质水平、冠心病和缺血性脑卒中风险的影响。
Sci Rep. 2019 Feb 20;9(1):2376. doi: 10.1038/s41598-019-38765-7.
9
Polymorphisms of TRIB1 genes for coronary artery disease and stroke risk: A systematic review and meta-analysis.TRIB1 基因多态性与冠心病和卒中风险:系统评价和荟萃分析。
Gene. 2023 Sep 5;880:147613. doi: 10.1016/j.gene.2023.147613. Epub 2023 Jul 4.
10
Association study of genetic variants at newly identified lipid gene TRIB1 with coronary heart disease in Chinese Han population.中国汉族人群中新发现的脂质基因TRIB1的基因变异与冠心病的关联研究。
Lipids Health Dis. 2015 May 19;14:46. doi: 10.1186/s12944-015-0043-0.

引用本文的文献

1
"Oh, Dear We Are in Tribble": An Overview of the Oncogenic Functions of Tribbles 1.“哦,天哪,我们遇到麻烦了”:TRIB1致癌功能概述
Cancers (Basel). 2024 May 16;16(10):1889. doi: 10.3390/cancers16101889.
2
Advances in genetic variation in metabolism-related fatty liver disease.代谢相关脂肪性肝病中基因变异的进展
Front Genet. 2023 Sep 11;14:1213916. doi: 10.3389/fgene.2023.1213916. eCollection 2023.
3
Association of single nucleotide polymorphisms with dyslipidemia and risk of metabolic disorders in the State of Qatar.单核苷酸多态性与血脂异常及卡塔尔代谢紊乱风险的关联。
Mol Genet Genomic Med. 2023 Aug;11(8):e2178. doi: 10.1002/mgg3.2178. Epub 2023 May 5.
4
The genetic interactions between non-alcoholic fatty liver disease and cardiovascular diseases.非酒精性脂肪性肝病与心血管疾病之间的遗传相互作用。
Front Genet. 2022 Aug 10;13:971484. doi: 10.3389/fgene.2022.971484. eCollection 2022.
5
Association between the LRP5 rs556442 gene polymorphism and the risks of NAFLD and CHD in a Chinese Han population.LRP5 rs556442 基因多态性与中国汉族人群非酒精性脂肪肝和冠心病风险的相关性。
BMC Gastroenterol. 2022 Jun 22;22(1):305. doi: 10.1186/s12876-022-02385-9.
6
TRIB1 regulates LDL metabolism through CEBPα-mediated effects on the LDL receptor in hepatocytes.TRIB1 通过 CEBPα 介导的对肝细胞 LDL 受体的影响来调节 LDL 代谢。
J Clin Invest. 2021 Nov 15;131(22). doi: 10.1172/JCI146775.
7
Mitochondrial Mutations and Genetic Factors Determining NAFLD Risk.线粒体突变与决定非酒精性脂肪性肝病风险的遗传因素
Int J Mol Sci. 2021 Apr 24;22(9):4459. doi: 10.3390/ijms22094459.
8
PIN1, a perspective on genetic biomarker for nonalcoholic fatty liver disease (NAFLD).PIN1,非酒精性脂肪性肝病(NAFLD)遗传生物标志物的研究视角。
Metabol Open. 2019 Aug 6;3:100014. doi: 10.1016/j.metop.2019.100014. eCollection 2019 Sep.
9
Peroxisome Proliferator-Activated Receptors and Their Novel Ligands as Candidates for the Treatment of Non-Alcoholic Fatty Liver Disease.过氧化物酶体增殖物激活受体及其新型配体作为非酒精性脂肪性肝病治疗的候选药物。
Cells. 2020 Jul 8;9(7):1638. doi: 10.3390/cells9071638.
10
Interaction between Coffee Drinking and TRIB1 rs17321515 Single Nucleotide Polymorphism on Coronary Heart Disease in a Taiwanese Population.咖啡饮用与 TRIB1 rs17321515 单核苷酸多态性在台湾人群冠心病中的交互作用。
Nutrients. 2020 May 2;12(5):1301. doi: 10.3390/nu12051301.

本文引用的文献

1
Lipid mediators of liver injury in nonalcoholic fatty liver disease.非酒精性脂肪性肝病中肝损伤的脂质介质。
Am J Physiol Gastrointest Liver Physiol. 2019 Jan 1;316(1):G75-G81. doi: 10.1152/ajpgi.00170.2018. Epub 2018 Nov 1.
2
Non-alcoholic fatty liver disease: a narrative review of genetics.非酒精性脂肪性肝病:遗传学的叙述性综述
J Biomed Res. 2018 Nov 20;32(5):389-400. doi: 10.7555/JBR.32.20180045.
3
Intake of stigmasterol and β-sitosterol alters lipid metabolism and alleviates NAFLD in mice fed a high-fat western-style diet.摄入豆甾醇和β-谷甾醇可改变高脂西式饮食喂养小鼠的脂代谢,减轻非酒精性脂肪性肝病。
Biochim Biophys Acta Mol Cell Biol Lipids. 2018 Oct;1863(10):1274-1284. doi: 10.1016/j.bbalip.2018.08.004. Epub 2018 Aug 7.
4
Patient-Reported Outcomes and the Economic Effects of Nonalcoholic Fatty Liver Disease and Nonalcoholic Steatohepatitis: The Value Proposition.患者报告结局与非酒精性脂肪性肝病和非酒精性脂肪性肝炎的经济影响:价值主张。
Hepatology. 2018 Dec;68(6):2405-2412. doi: 10.1002/hep.30125.
5
Future trends in the treatment of non-alcoholic steatohepatitis.非酒精性脂肪性肝炎治疗的未来趋势
Pharmacol Res. 2018 Aug;134:289-298. doi: 10.1016/j.phrs.2018.07.014. Epub 2018 Jul 17.
6
Mechanisms of NAFLD development and therapeutic strategies.非酒精性脂肪性肝病发病机制及治疗策略。
Nat Med. 2018 Jul;24(7):908-922. doi: 10.1038/s41591-018-0104-9. Epub 2018 Jul 2.
7
Should we undertake surveillance for HCC in patients with NAFLD?我们是否应该对非酒精性脂肪性肝病患者进行 HCC 监测?
J Hepatol. 2018 Feb;68(2):326-334. doi: 10.1016/j.jhep.2017.10.006. Epub 2017 Nov 6.
8
Genetics and epigenetics of NAFLD and NASH: Clinical impact.非酒精性脂肪性肝病和非酒精性脂肪性肝炎的遗传学和表观遗传学:临床影响。
J Hepatol. 2018 Feb;68(2):268-279. doi: 10.1016/j.jhep.2017.09.003. Epub 2017 Nov 6.
9
New trends on obesity and NAFLD in Asia.亚洲肥胖和非酒精性脂肪性肝病的新趋势。
J Hepatol. 2017 Oct;67(4):862-873. doi: 10.1016/j.jhep.2017.06.003. Epub 2017 Jun 19.
10
Non-Alcoholic Fatty Liver Disease.非酒精性脂肪性肝病
Adv Exp Med Biol. 2017;960:443-467. doi: 10.1007/978-3-319-48382-5_19.

TRIB1 rs17321515 和 rs2954029 基因多态性增加中国汉族人群非酒精性脂肪性肝病的风险。

TRIB1 rs17321515 and rs2954029 gene polymorphisms increase the risk of non-alcoholic fatty liver disease in Chinese Han population.

机构信息

Medical College of Qingdao University, Qingdao, 266071, China.

Department of Gastroenterology, Qingdao Municipal Hospital, 1 Jiaozhou Road, Qingdao, 266011, Shandong Province, China.

出版信息

Lipids Health Dis. 2019 Mar 9;18(1):61. doi: 10.1186/s12944-019-1001-z.

DOI:10.1186/s12944-019-1001-z
PMID:30851741
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6408849/
Abstract

BACKGROUND

Dysregulation of the lipid homeostasis is an independent risk factor for non-alcoholic fatty liver disease (NAFLD). Some studies had demonstrated that TRIB1 gene polymorphisms affect the plasma lipids metabolism, but no related data was available for TRIB1 gene polymorphisms in the lipids metabolism in Chinses Han population. The present study was conducted to investigate the association between TRIB1 gene polymorphisms (rs17321515 and rs2954029) and the risk of NAFLD in Chinese Han population and their effects on serum lipid profiles.

PATIENTS AND METHODS

TRIB1 rs17321515 and rs2954029 gene polymorphisms were genotyped using the polymerase chain reaction (PCR) in B-type ultrasonography-proven NAFLD patients (n = 146) and healthy controls (n = 175). Serum lipid profiles were determined using biochemical methods. Statistical analyses were performed using SPSS 22.0 statistical software.

RESULTS

The allele distributions of TRIB1 rs17321515 A and rs2954029 A were significant different between the NAFLD patients and healthy controls (P = 0.026, P = 0.045, respectively). The genotype distribution of TRIB1 rs17321515 was significant different between NAFLD patients and healthy controls (P = 0.038). The TRIB1 rs17321515 GA + AA genotype and TRIB1 rs2954029 TA + AA genotype markedly increase the NAFLD risk (OR = 1.885; 95%CI: 1.157-3.070; OR = 1.627; 95%CI: 1.011-2.619, respectively), after adjusted for age, gender, and body mass index, the NAFLD risk still significant (OR = 2.240; 95%CI: 1.196-4.197; OR = 2.050; 95%CI: 1.110-3.786, respectively). In addition, TRIB1 rs17321515 A and rs2954029 A carriers possess the higher lipid profiles in the included subjects.

CONCLUSIONS

TRIB1 rs17321515 and rs2954029 were significant associated with the risk of NAFLD in Chinese Han population. The rs17321515 A and rs2954029 A allele increases the serum lipid profiles in Chinese Han population.

摘要

背景

脂质稳态失调是非酒精性脂肪性肝病(NAFLD)的独立危险因素。一些研究表明 TRIB1 基因多态性影响血浆脂质代谢,但中国汉族人群中TRIB1 基因多态性与脂质代谢的相关数据尚不清楚。本研究旨在探讨 TRIB1 基因多态性(rs17321515 和 rs2954029)与中国汉族人群 NAFLD 风险的关系及其对血清脂质谱的影响。

患者和方法

采用聚合酶链反应(PCR)法对 B 型超声证实的 NAFLD 患者(n=146)和健康对照者(n=175)的 TRIB1 rs17321515 和 rs2954029 基因多态性进行基因分型。采用生化方法测定血清脂质谱。采用 SPSS 22.0 统计软件进行统计学分析。

结果

TRIB1 rs17321515 的 A 等位基因和 rs2954029 的 A 等位基因在 NAFLD 患者和健康对照组之间的分布差异有统计学意义(P=0.026,P=0.045)。TRIB1 rs17321515 的基因型分布在 NAFLD 患者和健康对照组之间有显著差异(P=0.038)。TRIB1 rs17321515 GA+AA 基因型和 rs2954029 TA+AA 基因型显著增加 NAFLD 发病风险(OR=1.885;95%CI:1.157-3.070;OR=1.627;95%CI:1.011-2.619),经年龄、性别和体重指数校正后,NAFLD 发病风险仍显著升高(OR=2.240;95%CI:1.196-4.197;OR=2.050;95%CI:1.110-3.786)。此外,TRIB1 rs17321515 A 和 rs2954029 A 携带者在纳入的研究对象中具有更高的血脂谱。

结论

TRIB1 rs17321515 和 rs2954029 与中国汉族人群的 NAFLD 发病风险显著相关。TRIB1 rs17321515 的 A 等位基因和 rs2954029 的 A 等位基因增加了中国汉族人群的血清脂质谱。