• 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

BRAP 基因中的单核苷酸多态性降低了中国青年人群代谢综合征的风险。

The single nucleotide polymorphisms in BRAP decrease the risk of metabolic syndrome in a Chinese young adult population.

机构信息

Department of Epidemiology, Capital Institute of Pediatrics, Beijing, People's Republic of China.

出版信息

Diab Vasc Dis Res. 2013 May;10(3):202-7. doi: 10.1177/1479164112455535. Epub 2012 Sep 10.

DOI:10.1177/1479164112455535
PMID:22965072
Abstract

The single nucleotide polymorphisms (SNPs) in the gene of breast cancer suppressor protein (BRCA1)-associated protein (BRAP) are significantly associated with coronary artery disease, but the molecular mechanisms are not understood. We examined the associations of the SNPs (rs11066001 and rs3782886) in BRAP with metabolic syndrome (MetS), which is a strong predictor of cardiovascular disease, and potential associations between these SNPs and factors related to inflammation. There were significant associations of both the SNPs with MetS [rs11066001, odds ratio (OR) 0.70, 95% confidence interval (CI) 0.51-0.96, p = 0.028; rs3782886, OR 0.69, 95% CI 0.50-0.94, p = 0.020] under a dominant model after age and gender adjustment. Both SNPs were significantly associated with waist circumference, plasma glucose, glycated haemoglobin, triglycerides and nonesterified fatty acid. Our data provide evidence that the SNPs (rs11066001 and rs3782886) in BRAP decrease the risk of MetS, and associations of the SNPs with various components of MetS are different. Moreover, there are significant associations of both the SNPs with nonesterified fatty acid that could be involved in the inflammatory activity of electronegative low-density lipoprotein.

摘要

乳腺癌抑制蛋白相关蛋白 (BRAP) 基因中的单核苷酸多态性 (SNPs) 与冠状动脉疾病显著相关,但分子机制尚不清楚。我们研究了 BRAP 中 SNP(rs11066001 和 rs3782886) 与代谢综合征 (MetS) 的关联,MetS 是心血管疾病的强烈预测因子,以及这些 SNP 与与炎症相关的因素之间的潜在关联。这两个 SNP 与 MetS 都存在显著关联[rs11066001,比值比 (OR) 0.70,95%置信区间 (CI) 0.51-0.96,p = 0.028;rs3782886,OR 0.69,95%CI 0.50-0.94,p = 0.020],在年龄和性别调整后的显性模型下。这两个 SNP 与腰围、血浆葡萄糖、糖化血红蛋白、甘油三酯和非酯化脂肪酸均有显著关联。我们的数据提供了证据表明,BRAP 中的 SNPs(rs11066001 和 rs3782886) 降低了 MetS 的风险,并且 SNP 与 MetS 的各种成分之间的关联是不同的。此外,这两个 SNP 与非酯化脂肪酸都有显著的关联,这可能与电负性低密度脂蛋白的炎症活性有关。

相似文献

1
The single nucleotide polymorphisms in BRAP decrease the risk of metabolic syndrome in a Chinese young adult population.BRAP 基因中的单核苷酸多态性降低了中国青年人群代谢综合征的风险。
Diab Vasc Dis Res. 2013 May;10(3):202-7. doi: 10.1177/1479164112455535. Epub 2012 Sep 10.
2
Effect of dietary energy and polymorphisms in BRAP and GHRL on obesity and metabolic traits.饮食能量和 BRAP 和 GHRL 多态性对肥胖和代谢特征的影响。
Obes Res Clin Pract. 2018 Jan-Feb;12(Suppl 2):39-48. doi: 10.1016/j.orcp.2016.05.004. Epub 2016 May 27.
3
Single nucleotide polymorphisms (SNPs) involved in insulin resistance, weight regulation, lipid metabolism and inflammation in relation to metabolic syndrome: an epidemiological study.与代谢综合征相关的胰岛素抵抗、体重调节、脂质代谢和炎症中单核苷酸多态性(SNPs):一项流行病学研究。
Cardiovasc Diabetol. 2012 Oct 29;11:133. doi: 10.1186/1475-2840-11-133.
4
An obesity genetic risk score is associated with metabolic syndrome in Chinese children.肥胖遗传风险评分与中国儿童代谢综合征相关。
Gene. 2014 Feb 10;535(2):299-302. doi: 10.1016/j.gene.2013.11.006. Epub 2013 Nov 19.
5
Associations of the PTEN -9C>G polymorphism with insulin sensitivity and central obesity in Chinese.PTEN-9C>G 多态性与中国人的胰岛素敏感性和中心性肥胖的关联。
Gene. 2013 Sep 25;527(2):545-52. doi: 10.1016/j.gene.2013.06.026. Epub 2013 Jun 21.
6
Validation of eight genetic risk factors in East Asian populations replicated the association of BRAP with coronary artery disease.在东亚人群中验证了 8 个遗传风险因素,这些因素与 BRAP 与冠状动脉疾病的关联得到了复制。
J Hum Genet. 2009 Nov;54(11):642-6. doi: 10.1038/jhg.2009.87. Epub 2009 Aug 28.
7
The Association of Type 2 Diabetes Loci Identified in Genome-Wide Association Studies with Metabolic Syndrome and Its Components in a Chinese Population with Type 2 Diabetes.2型糖尿病全基因组关联研究中鉴定出的位点与中国2型糖尿病患者代谢综合征及其组分的关联
PLoS One. 2015 Nov 24;10(11):e0143607. doi: 10.1371/journal.pone.0143607. eCollection 2015.
8
MFGE8 polymorphisms are significantly associated with metabolism-related indicators rather than metabolic syndrome in Chinese people: A nested case-control study.MFGE8 多态性与中国人的代谢相关指标显著相关,而与代谢综合征无关:一项巢式病例对照研究。
Gene. 2018 Nov 30;677:176-181. doi: 10.1016/j.gene.2018.07.060. Epub 2018 Jul 24.
9
A two-stage association study suggests BRAP as a susceptibility gene for schizophrenia.一项两阶段关联研究提示 BRAP 是精神分裂症的易感基因。
PLoS One. 2014 Jan 15;9(1):e86037. doi: 10.1371/journal.pone.0086037. eCollection 2014.
10
A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains.基于表型组学的策略确定了与代谢综合征表型领域相关的 APOC1、BRAP 和 PLCG1 基因座。
PLoS Genet. 2011 Oct;7(10):e1002322. doi: 10.1371/journal.pgen.1002322. Epub 2011 Oct 13.

引用本文的文献

1
SNP-based and haplotype-based genome-wide association on drug dependence in Han Chinese.基于 SNP 和基于单体型的全基因组关联分析在中国汉族人群中的药物依赖。
BMC Genomics. 2024 Mar 6;25(1):255. doi: 10.1186/s12864-024-10117-4.
2
Converging vulnerability factors for compulsive food and drug use.强迫性食物和药物使用的趋同脆弱性因素。
Neuropharmacology. 2021 Sep 15;196:108556. doi: 10.1016/j.neuropharm.2021.108556. Epub 2021 Apr 20.
3
Possible mechanisms underlying the association between human T-cell leukemia virus type 1 (HTLV-1) and hypertension in elderly Japanese population.
人类 T 细胞白血病病毒 1 型(HTLV-1)与老年日本人群高血压相关的潜在机制。
Environ Health Prev Med. 2021 Jan 29;26(1):17. doi: 10.1186/s12199-021-00938-0.
4
BRCA1-associated protein inhibits glioma cell proliferation and migration and glioma stem cell self-renewal via the TGF-β/PI3K/AKT/mTOR signalling pathway.BRCA1 相关蛋白通过 TGF-β/PI3K/AKT/mTOR 信号通路抑制神经胶质瘤细胞增殖、迁移和神经胶质瘤干细胞自我更新。
Cell Oncol (Dordr). 2020 Apr;43(2):223-235. doi: 10.1007/s13402-019-00482-8. Epub 2019 Nov 27.
5
Central catalytic domain of BRAP (RNF52) recognizes the types of ubiquitin chains and utilizes oligo-ubiquitin for ubiquitylation.BRAP(RNF52)的中央催化结构域可识别泛素链的类型,并利用寡聚泛素来进行泛素化。
Biochem J. 2017 Sep 7;474(18):3207-3226. doi: 10.1042/BCJ20161104.
6
Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels.代谢综合征相关基因的三种错义变体与α-1抗胰蛋白酶水平相关。
Nat Commun. 2015 Jul 15;6:7754. doi: 10.1038/ncomms8754.
7
Interactome of the negative regulator of nuclear import BRCA1-binding protein 2.核输入负调控因子BRCA1结合蛋白2的相互作用组
Sci Rep. 2015 Mar 30;5:9459. doi: 10.1038/srep09459.
8
A two-stage association study suggests BRAP as a susceptibility gene for schizophrenia.一项两阶段关联研究提示 BRAP 是精神分裂症的易感基因。
PLoS One. 2014 Jan 15;9(1):e86037. doi: 10.1371/journal.pone.0086037. eCollection 2014.
9
Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure.从泰国人群基因结构洞察东南亚大陆的人口构成。
PLoS One. 2013 Nov 4;8(11):e79522. doi: 10.1371/journal.pone.0079522. eCollection 2013.
10
Lack of association between a functional variant of the BRCA-1 related associated protein (BRAP) gene and ischemic stroke.BRCA-1 相关关联蛋白(BRAP)基因的功能性变异与缺血性卒中之间缺乏关联。
BMC Med Genet. 2013 Jan 28;14:17. doi: 10.1186/1471-2350-14-17.