• 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

GNB3 基因 C825T 多态性与台湾人群肥胖及代谢表型的相关性。

Association of the C825T polymorphism in the GNB3 gene with obesity and metabolic phenotypes in a Taiwanese population.

机构信息

College of Public Health and Nutrition, Taipei Medical University, Taipei, Taiwan.

出版信息

Genes Nutr. 2013 Jan;8(1):137-44. doi: 10.1007/s12263-012-0304-8. Epub 2012 Jul 12.

DOI:10.1007/s12263-012-0304-8
PMID:22791279
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3534990/
Abstract

The relationship between obesity and a single nucleotide polymorphism (SNP), rs5443 (C825T), in the guanine nucleotide binding protein beta polypeptide 3 (GNB3) gene is currently inconsistent. In this study, we aimed to reassess whether the GNB3 rs5443 SNP could influence obesity and obesity-related metabolic traits in a Taiwanese population. A total of 983 Taiwanese subjects with general health examinations were genotyped. Based on the criteria defined by the Department of Health in Taiwan, the terms "overweight" and "obesity" are defined as 24 ≦ BMI < 27 and BMI ≧ 27, respectively. Compared to the carrier of the combined CT + TT genotypes of the GNB3 rs5443 polymorphism, triglyceride was significantly higher for the carrier of CC genotype in the complete sample population (128.2 ± 93.2 vs. 114.3 ± 79.1 mg/dl; P = 0.041). In addition, the carriers of CC variant had a higher total cholesterol than those with the combined CT + TT variants (194.5 ± 36.8 vs. 187.9 ± 33.0 mg/dl; P = 0.019) in the complete sample population. In the normal controls, both triglyceride (P = 0.018) and total cholesterol (P = 0.011) were also significantly higher in the CC homozygotes than in the combined CT + TT genotypes. However, the GNB3 rs5443 SNP did not exhibit any significant association with obesity or overweight among the subjects. Our study indicates that the CC genotype of the GNB3 rs5443 SNP may predict higher obesity-related metabolic traits such as triglyceride and total cholesterol in non-obese Taiwanese subjects (but not in obese subjects).

摘要

肥胖与单个核苷酸多态性(SNP)rs5443(C825T)之间的关系在鸟苷三磷酸结合蛋白β多肽 3(GNB3)基因中目前并不一致。在这项研究中,我们旨在重新评估 GNB3 rs5443 SNP 是否会影响台湾人群的肥胖和肥胖相关代谢特征。共有 983 名接受一般健康检查的台湾人进行了基因分型。根据台湾卫生署规定的标准,“超重”和“肥胖”的定义分别为 24 ≦ BMI < 27 和 BMI ≧ 27。与 GNB3 rs5443 多态性的 CT + TT 基因型携带者相比,完全样本人群中 CC 基因型携带者的甘油三酯明显更高(128.2 ± 93.2 与 114.3 ± 79.1 mg/dl;P = 0.041)。此外,CC 变异体携带者的总胆固醇水平高于 CT + TT 变异体携带者(194.5 ± 36.8 与 187.9 ± 33.0 mg/dl;P = 0.019)。在正常对照组中,CC 纯合子的甘油三酯(P = 0.018)和总胆固醇(P = 0.011)也明显高于 CT + TT 基因型。然而,GNB3 rs5443 SNP 与受试者中的肥胖或超重没有显示出任何显著关联。我们的研究表明,GNB3 rs5443 SNP 的 CC 基因型可能预测非肥胖台湾受试者中更高的肥胖相关代谢特征,如甘油三酯和总胆固醇(但在肥胖受试者中则没有)。

相似文献

1
Association of the C825T polymorphism in the GNB3 gene with obesity and metabolic phenotypes in a Taiwanese population.GNB3 基因 C825T 多态性与台湾人群肥胖及代谢表型的相关性。
Genes Nutr. 2013 Jan;8(1):137-44. doi: 10.1007/s12263-012-0304-8. Epub 2012 Jul 12.
2
The Pro12Ala polymorphism in the peroxisome proliferator-activated receptor gamma (PPARG) gene in relation to obesity and metabolic phenotypes in a Taiwanese population.台湾人群中过氧化物酶体增殖物激活受体γ(PPARG)基因Pro12Ala多态性与肥胖及代谢表型的关系
Endocrine. 2015 Apr;48(3):786-93. doi: 10.1007/s12020-014-0407-7. Epub 2014 Sep 3.
3
Weight loss and body fat reduction under sibutramine therapy in obesity with the C825T polymorphism in the GNB3 gene.在伴有GNB3基因C825T多态性的肥胖症患者中,西布曲明治疗下的体重减轻和体脂减少。
Pharmacogenet Genomics. 2009 Sep;19(9):730-3. doi: 10.1097/FPC.0b013e3283307cf1.
4
Analysis of SNPs of MC4R, GNB3 and FTO gene polymorphism in obese Saudi subjects.沙特肥胖受试者中MC4R、GNB3和FTO基因多态性的单核苷酸多态性分析
Afr Health Sci. 2017 Dec;17(4):1059-1069. doi: 10.4314/ahs.v17i4.14.
5
The associations among GNB3 C825T polymorphism, erectile dysfunction, and related risk factors.GNB3基因C825T多态性、勃起功能障碍及相关危险因素之间的关联。
J Sex Med. 2008 Sep;5(9):2061-8. doi: 10.1111/j.1743-6109.2008.00938.x.
6
Influence of G-protein β-Polypeptide 3 C825T Polymorphism on Antihypertensive Response to Telmisartan and Amlodipine in Chinese Patients.G蛋白β多肽3 C825T基因多态性对中国患者替米沙坦和氨氯地平降压反应的影响
Chin Med J (Engl). 2016 Jan 5;129(1):8-14. doi: 10.4103/0366-6999.172548.
7
The c.825CT (rs5443) polymorphism and protection against fatal outcome of corona virus disease 2019 (COVID-19).c.825C>T(rs5443)多态性与2019冠状病毒病(COVID-19)致命结局的防护
Front Genet. 2022 Aug 9;13:960731. doi: 10.3389/fgene.2022.960731. eCollection 2022.
8
GNB3 gene 825 TT variant predicts hard coronary events in the population-based Heinz Nixdorf Recall study.在基于人群的海因茨·尼克斯多夫召回研究中,GNB3基因825位点TT变异可预测严重冠状动脉事件。
Atherosclerosis. 2014 Dec;237(2):437-42. doi: 10.1016/j.atherosclerosis.2014.08.025. Epub 2014 Aug 28.
9
The guanine nucleotide binding protein beta polypeptide 3 gene C825T polymorphism is associated with elite endurance athletes.鸟嘌呤核苷酸结合蛋白β多肽3基因C825T多态性与优秀耐力运动员相关。
Exp Physiol. 2009 Mar;94(3):344-9. doi: 10.1113/expphysiol.2008.045138. Epub 2009 Jan 12.
10
Association study on GNB3 gene polymorphism with essential hypertension in Xinjiang Uygur group.新疆维吾尔族人群中GNB3基因多态性与原发性高血压的关联性研究
Front Med China. 2007 May;1(2):230-3. doi: 10.1007/s11684-007-0045-z.

引用本文的文献

1
Influence of genetic polymorphism on sports talent performance versus non-athletes: a systematic review and meta-analysis.基因多态性对运动员与非运动员运动天赋表现的影响:一项系统评价与荟萃分析。
BMC Sports Sci Med Rehabil. 2024 Oct 31;16(1):223. doi: 10.1186/s13102-024-01001-5.
2
G Protein Subunit Beta 3 (GNB3) Variant Is Associated with Biochemical Changes in Brazilian Patients with Hypertension.G 蛋白亚基β 3(GNB3)变体与巴西高血压患者生化变化相关。
Arq Bras Cardiol. 2023 Dec;120(12):e20230396. doi: 10.36660/abc.20230396.
3
Pathophysiological Role of Genetic Factors Associated With Gestational Diabetes Mellitus.与妊娠期糖尿病相关的遗传因素的病理生理作用
Front Physiol. 2022 Apr 4;13:769924. doi: 10.3389/fphys.2022.769924. eCollection 2022.
4
The Relationships between Leptin, Genotype, and Chinese Medicine Body Constitution for Obesity.瘦素、基因型与肥胖的中医体质之间的关系
Evid Based Complement Alternat Med. 2021 May 7;2021:5510552. doi: 10.1155/2021/5510552. eCollection 2021.
5
Detection of susceptibility loci on and associated with metabolic syndrome using a genome-wide association study in a Taiwanese population.利用全基因组关联研究在台湾人群中检测与代谢综合征相关的位于[具体染色体]和[具体染色体]上的易感基因座。
Oncotarget. 2017 Sep 16;8(55):93349-93359. doi: 10.18632/oncotarget.20967. eCollection 2017 Nov 7.
6
INSIG2 rs7566605 single nucleotide variant and global DNA methylation index levels are associated with weight loss in a personalized weight reduction program.INSIG2 rs7566605 单核苷酸变异和全球 DNA 甲基化指数水平与个性化减肥计划中的体重减轻有关。
Mol Med Rep. 2018 Jan;17(1):1699-1709. doi: 10.3892/mmr.2017.8039. Epub 2017 Nov 14.
7
Transforming growth factor-β signaling pathway-associated genes SMAD2 and TGFBR2 are implicated in metabolic syndrome in a Taiwanese population.转化生长因子-β信号通路相关基因 SMAD2 和 TGFBR2 参与台湾人群的代谢综合征。
Sci Rep. 2017 Oct 19;7(1):13589. doi: 10.1038/s41598-017-14025-4.
8
Effects of circadian clock genes and environmental factors on cognitive aging in old adults in a Taiwanese population.昼夜节律时钟基因和环境因素对台湾老年人群认知衰老的影响。
Oncotarget. 2017 Apr 11;8(15):24088-24098. doi: 10.18632/oncotarget.15493.
9
Effects of circadian clock genes and health-related behavior on metabolic syndrome in a Taiwanese population: Evidence from association and interaction analysis.昼夜节律时钟基因和健康相关行为对台湾人群代谢综合征的影响:来自关联和交互分析的证据。
PLoS One. 2017 Mar 15;12(3):e0173861. doi: 10.1371/journal.pone.0173861. eCollection 2017.
10
The ADAMTS9 gene is associated with cognitive aging in the elderly in a Taiwanese population.ADAMTS9基因与台湾老年人群的认知衰老有关。
PLoS One. 2017 Feb 22;12(2):e0172440. doi: 10.1371/journal.pone.0172440. eCollection 2017.

本文引用的文献

1
The GNB3 C825T polymorphism as a pharmacogenetic marker in the treatment of hypertension, obesity, and depression.GNB3 C825T 多态性作为治疗高血压、肥胖和抑郁症的药物遗传学标志物。
Pharmacogenet Genomics. 2011 Sep;21(9):594-606. doi: 10.1097/FPC.0b013e3283491153.
2
Chipping away the 'missing heritability': GIANT steps forward in the molecular elucidation of obesity - but still lots to go.破解“遗传缺失之谜”:肥胖分子解析领域的重大进展——但仍有许多工作要做。
Obes Facts. 2010 Oct;3(5):294-303. doi: 10.1159/000321537. Epub 2010 Oct 15.
3
Recent progress in the genetics of common obesity.常见肥胖症遗传学的最新进展。
Br J Clin Pharmacol. 2009 Dec;68(6):811-29. doi: 10.1111/j.1365-2125.2009.03523.x.
4
A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.基于基因数据预测慢性疲劳综合征的分类方法比较。
J Transl Med. 2009 Sep 22;7:81. doi: 10.1186/1479-5876-7-81.
5
Weight loss and body fat reduction under sibutramine therapy in obesity with the C825T polymorphism in the GNB3 gene.在伴有GNB3基因C825T多态性的肥胖症患者中,西布曲明治疗下的体重减轻和体脂减少。
Pharmacogenet Genomics. 2009 Sep;19(9):730-3. doi: 10.1097/FPC.0b013e3283307cf1.
6
Gene-gene interactions among genetic variants from obesity candidate genes for nonobese and obese populations in type 2 diabetes.2型糖尿病非肥胖和肥胖人群中肥胖候选基因的遗传变异之间的基因-基因相互作用。
Genet Test Mol Biomarkers. 2009 Aug;13(4):485-93. doi: 10.1089/gtmb.2008.0145.
7
Interaction of serotonin-related genes affects short-term antidepressant response in major depressive disorder.血清素相关基因的相互作用影响重度抑郁症的短期抗抑郁反应。
Prog Neuropsychopharmacol Biol Psychiatry. 2009 Oct 1;33(7):1167-72. doi: 10.1016/j.pnpbp.2009.06.015. Epub 2009 Jun 26.
8
Association and interaction analyses of genetic variants in ADIPOQ, ENPP1, GHSR, PPARgamma and TCF7L2 genes for diabetic nephropathy in a Taiwanese population with type 2 diabetes.在一个台湾的 2 型糖尿病人群中,对 ADIPOQ、ENPP1、GHSR、PPARγ 和 TCF7L2 基因中的遗传变异与糖尿病肾病的关联和相互作用进行分析。
Nephrol Dial Transplant. 2009 Nov;24(11):3360-6. doi: 10.1093/ndt/gfp271. Epub 2009 Jun 8.
9
A controlled pharmacogenetic trial of sibutramine on weight loss and body composition in obese or overweight adults.西布曲明对肥胖或超重成年人减肥及身体成分影响的对照药物遗传学试验。
Gastroenterology. 2008 Oct;135(4):1142-54. doi: 10.1053/j.gastro.2008.07.009. Epub 2008 Jul 16.
10
Global burden of obesity in 2005 and projections to 2030.2005年全球肥胖负担及到2030年的预测。
Int J Obes (Lond). 2008 Sep;32(9):1431-7. doi: 10.1038/ijo.2008.102. Epub 2008 Jul 8.