• 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

评价台湾地区肥胖和代谢表型的肾上腺素能受体β2 表面基因谷氨酰胺 27 谷氨酸多态性。

Evaluation of the glutamine 27 glutamic acid polymorphism in the adrenoceptor β2 surface gene on obesity and metabolic phenotypes in Taiwan.

机构信息

From the *College of Public Health and Nutrition, Taipei Medical University; and †Vita Genomics, Inc, Taipei; and ‡Institute of Clinical Medical Science, China Medical University, Taichung, Taiwan.

出版信息

J Investig Med. 2014 Feb;62(2):310-5. doi: 10.2310/JIM.0000000000000030.

DOI:10.2310/JIM.0000000000000030
PMID:24322328
Abstract

BACKGROUND

The single-nucleotide polymorphism (SNP), rs1042714 or glutamine 27 glutamic acid (Gln27Glu), in the adrenoceptor β2 surface (ADRB2) gene has previously been examined for association with obesity with inconclusive results. The objective of this study was to determine whether the ADRB2 rs1042714 SNP could influence obesity and obesity-related metabolic traits in a Taiwanese population.

METHODS

The ADRB2 rs1042714 SNP and obesity-related metabolic traits including blood pressure, total cholesterol, triglyceride, fasting glucose, waist circumference, and body mass index (BMI) were examined in 967 individuals with general health examinations.

RESULTS

Our data revealed that the ADRB2 rs1042714 SNP exhibited a significant association with obesity among the subjects (P = 0.021). Furthermore, the carriers of the GG genotype had a significantly higher BMI than those with the CC genotype (26.0 ± 5.6 vs 24.3 ± 3.8 kg/m; P = 0.009) and those with the CG genotype (26.0 ± 5.6 vs 23.6 ± 3.3 kg/m; P = 0.001). We also found a nominal association with systolic blood pressure (P = 0.058) and triglyceride (P = 0.055) levels in the ADRB2 rs1042714 SNP.

CONCLUSIONS

Our study indicates that the ADRB2 rs1042714 SNP may contribute to the risk of obesity and predict obesity-related metabolic traits such as BMI, triglyceride, and systolic blood pressure in Taiwanese subjects.

摘要

背景

肾上腺素能受体β2 表面(ADRB2)基因中的单核苷酸多态性(SNP)rs1042714 或谷氨酰胺 27 谷氨酸(Gln27Glu)先前曾被研究与肥胖相关,但结果不一致。本研究的目的是确定 ADRB2 rs1042714 SNP 是否会影响台湾人群的肥胖和肥胖相关代谢特征。

方法

在 967 名接受常规体检的个体中,检查了 ADRB2 rs1042714 SNP 与肥胖相关的代谢特征,包括血压、总胆固醇、甘油三酯、空腹血糖、腰围和体重指数(BMI)。

结果

我们的数据显示,ADRB2 rs1042714 SNP 与受试者的肥胖显著相关(P = 0.021)。此外,GG 基因型携带者的 BMI 明显高于 CC 基因型携带者(26.0 ± 5.6 与 24.3 ± 3.8 kg/m;P = 0.009)和 CG 基因型携带者(26.0 ± 5.6 与 23.6 ± 3.3 kg/m;P = 0.001)。我们还发现 ADRB2 rs1042714 SNP 与收缩压(P = 0.058)和甘油三酯(P = 0.055)水平呈名义相关。

结论

我们的研究表明,ADRB2 rs1042714 SNP 可能导致肥胖风险增加,并可预测台湾人群的 BMI、甘油三酯和收缩压等肥胖相关代谢特征。

相似文献

1
Evaluation of the glutamine 27 glutamic acid polymorphism in the adrenoceptor β2 surface gene on obesity and metabolic phenotypes in Taiwan.评价台湾地区肥胖和代谢表型的肾上腺素能受体β2 表面基因谷氨酰胺 27 谷氨酸多态性。
J Investig Med. 2014 Feb;62(2):310-5. doi: 10.2310/JIM.0000000000000030.
2
Association of the FTO and ADRB2 genes with body composition and fat distribution in obese women.肥胖女性中 FTO 和 ADRB2 基因与身体成分和脂肪分布的关系。
Maturitas. 2013 Oct;76(2):165-71. doi: 10.1016/j.maturitas.2013.07.004. Epub 2013 Aug 1.
3
The glutamine 27 glutamic acid polymorphism of the beta2-adrenoceptor gene is associated with abdominal obesity and greater risk of impaired glucose tolerance in men but not in women: a population-based study in Spain.β2肾上腺素能受体基因谷氨酰胺27谷氨酸多态性与男性腹型肥胖及糖耐量受损风险增加有关,而与女性无关:西班牙一项基于人群的研究
Clin Endocrinol (Oxf). 2003 Oct;59(4):476-81. doi: 10.1046/j.1365-2265.2003.01871.x.
4
Gln27Glu polymorphism in the beta2 adrenergic receptor gene and lipid metabolism during exercise in obese women.肥胖女性运动期间β2肾上腺素能受体基因中的Gln27Glu多态性与脂质代谢
Int J Obes Relat Metab Disord. 2002 Nov;26(11):1434-41. doi: 10.1038/sj.ijo.0802129.
5
Association of the rs6235 variant in the proprotein convertase subtilisin/kexin type 1 (PCSK1) gene with obesity and related traits in a Taiwanese population.PCSK1 基因中 proprotein convertase subtilisin/kexin type 1(PCSK1)基因的 rs6235 变异与台湾人群肥胖及相关特征的关联。
Gene. 2014 Jan 1;533(1):32-7. doi: 10.1016/j.gene.2013.10.016. Epub 2013 Oct 17.
6
Gender-dependent association of a β(2)-adrenergic gene variant with obesity parameters in Malaysian Malays.马来西亚马来人中β(2) - 肾上腺素能基因变异与肥胖参数的性别依赖性关联。
Asia Pac J Public Health. 2015 Mar;27(2):NP154-65. doi: 10.1177/1010539511430250. Epub 2011 Dec 23.
7
Role of beta-2 adrenergic receptor polymorphism (rs1042714) on body weight and glucose metabolism response to a meal-replacement hypocaloric diet.β2 肾上腺素能受体多态性(rs1042714)对代餐低热量饮食引起的体重和葡萄糖代谢反应的作用。
Nutrition. 2023 Dec;116:112170. doi: 10.1016/j.nut.2023.112170. Epub 2023 Jul 23.
8
A maximal effort trial in obese women carrying the beta2-adrenoceptor Gln27Glu polymorphism.一项针对携带β2肾上腺素能受体Gln27Glu多态性的肥胖女性的最大努力试验。
J Physiol Biochem. 2002 Jun;58(2):103-8. doi: 10.1007/BF03179845.
9
Genotypes and haplotypes of beta2-adrenergic receptor and parameters of the metabolic syndrome in Korean adolescents.韩国青少年β2-肾上腺素能受体的基因型和单倍型与代谢综合征参数
Metabolism. 2008 Aug;57(8):1064-70. doi: 10.1016/j.metabol.2008.03.009.
10
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.

引用本文的文献

1
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.
2
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.
3
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.
4
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.
5
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.
6
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.
7
Association and interaction effects of Alzheimer's disease-associated genes and lifestyle on cognitive aging in older adults in a Taiwanese population.台湾人群中阿尔茨海默病相关基因与生活方式对老年人认知衰老的关联及交互作用
Oncotarget. 2017 Apr 11;8(15):24077-24087. doi: 10.18632/oncotarget.15269.
8
Association and interaction of APOA5, BUD13, CETP, LIPA and health-related behavior with metabolic syndrome in a Taiwanese population.在台湾人群中,APOA5、BUD13、CETP、LIPA 与健康相关行为与代谢综合征的关联和相互作用。
Sci Rep. 2016 Nov 9;6:36830. doi: 10.1038/srep36830.
9
Association of a common rs9939609 variant in the fat mass and obesity-associated (FTO) gene with obesity and metabolic phenotypes in a Taiwanese population: a replication study.脂肪量和肥胖相关(FTO)基因常见rs9939609变异与台湾人群肥胖及代谢表型的关联:一项重复研究
J Genet. 2016 Sep;95(3):595-601. doi: 10.1007/s12041-016-0671-9.
10
Study of seven single-nucleotide polymorphisms identified in East Asians for association with obesity in a Taiwanese population.对东亚人群中鉴定出的七个单核苷酸多态性与台湾人群肥胖相关性的研究。
BMJ Open. 2016 Aug 10;6(8):e011713. doi: 10.1136/bmjopen-2016-011713.