• 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

与体重和身体组成相关的[具体基因名称]和[具体基因名称]基因多态性与饮食摄入之间的相互作用:一项探索性研究。

The Interaction between Genetic Polymorphisms in and Genes and Dietary Intake with Regard to Body Mass and Composition: An Exploratory Study.

作者信息

Nasreddine Lara, Akika Reem, Mailhac Aurelie, Tamim Hani, Zgheib Nathalie Khoueiry

机构信息

Department of Nutrition & Food Sciences, Faculty of Agriculture and Food Sciences, American University of Beirut, Beirut, PO Box 11-0236, Riad El-Solh 1107 2020, Lebanon.

Department of Pharmacology and Toxicology, Faculty of Medicine, American University of Beirut, Beirut, PO Box 11-0236, Riad El-Solh 1107 2020, Lebanon.

出版信息

J Pers Med. 2019 Feb 5;9(1):11. doi: 10.3390/jpm9010011.

DOI:10.3390/jpm9010011
PMID:30764585
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6463113/
Abstract

In contrast to the large number of genetic studies on obesity, there has been significantly less nutrigenetics investigation of the interaction between diet and single nucleotide polymorphisms (SNPs) in obesity, especially within Eastern Mediterranean populations. The aim of this study was to evaluate the potential interactions between three candidate SNPs, namely, and in the ( gene and the variant of the ( gene, and macronutrient intake with regard to obesity, body fat, and muscle composition. Three hundred and eight healthy Lebanese adults were included in this study. Data collection included a questionnaire for demographics and lifestyle in addition to a detailed dietary assessment using a culture-specific 80-item semi-quantitative food frequency questionnaire. This was coupled with anthropometric measurements and peripheral blood withdrawal for DNA and genotyping using Taqman allele discrimination assays. The two candidate SNPs were not associated with risk of obesity in this population sample, yet there was a trend, though not a significant one, towards lower muscle mass among carriers of the risk allele of either SNPs. To our knowledge, these results have not been previously reported. As for the variant, results were congruent with the literature, given that individuals who were homozygous for the risk allele had significantly higher body mass index (BMI) and body fat despite lower intakes of saturated fat. Similar interactions, though not significant, were shown with muscle mass, whereby individuals who were homozygous for the risk allele had lower muscle mass with higher intakes of saturated fat, a result that, to our knowledge, has not been previously reported.

摘要

与大量关于肥胖的基因研究相比,饮食与肥胖中单核苷酸多态性(SNP)之间相互作用的营养遗传学研究要少得多,尤其是在东地中海人群中。本研究的目的是评估三个候选SNP,即[具体基因名称1]基因中的[具体SNP名称1]和[具体基因名称2]基因的[具体SNP名称2]变体与肥胖、体脂和肌肉组成方面的常量营养素摄入之间的潜在相互作用。本研究纳入了308名健康的黎巴嫩成年人。数据收集包括一份关于人口统计学和生活方式的问卷,以及使用一份针对特定文化的80项半定量食物频率问卷进行的详细饮食评估。这与人体测量以及采集外周血用于DNA提取和使用Taqman等位基因鉴别分析进行基因分型相结合。在这个人群样本中,这两个[具体基因名称]候选SNP与肥胖风险无关,但在任一[具体SNP名称]的风险等位基因携带者中,存在肌肉量较低的趋势,尽管不显著。据我们所知,这些结果此前尚未见报道。至于[具体SNP名称3]变体,结果与文献一致,因为风险等位基因纯合的个体尽管饱和脂肪摄入量较低,但体重指数(BMI)和体脂显著更高。在肌肉量方面也显示出类似的相互作用,尽管不显著,即风险等位基因纯合的个体在饱和脂肪摄入量较高时肌肉量较低,据我们所知,这一结果此前尚未见报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98fe/6463113/25dd63a2312a/jpm-09-00011-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98fe/6463113/25dd63a2312a/jpm-09-00011-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98fe/6463113/25dd63a2312a/jpm-09-00011-g001.jpg

相似文献

1
The Interaction between Genetic Polymorphisms in and Genes and Dietary Intake with Regard to Body Mass and Composition: An Exploratory Study.与体重和身体组成相关的[具体基因名称]和[具体基因名称]基因多态性与饮食摄入之间的相互作用:一项探索性研究。
J Pers Med. 2019 Feb 5;9(1):11. doi: 10.3390/jpm9010011.
2
Assessment of the FTO gene polymorphisms (rs1421085, rs17817449 and rs9939609) in exercise-trained men and women: the effects of a 4-week hypocaloric diet.评估 FTO 基因多态性(rs1421085、rs17817449 和 rs9939609)在运动训练的男性和女性中的影响:4 周低热量饮食的作用。
J Int Soc Sports Nutr. 2019 Sep 2;16(1):36. doi: 10.1186/s12970-019-0307-6.
3
Genetic variation of FTO and TCF7L2 in premature adrenarche.FTO和TCF7L2基因变异与性早熟。
Metabolism. 2009 Sep;58(9):1263-9. doi: 10.1016/j.metabol.2009.03.025. Epub 2009 Jun 18.
4
A complete linkage disequilibrium in a haplotype of three SNPs in Fat Mass and Obesity associated (FTO) gene was strongly associated with anthropometric indices after controlling for calorie intake and physical activity.在控制热量摄入和身体活动后,脂肪量和肥胖相关(FTO)基因中三个单核苷酸多态性(SNP)的单倍型完全连锁不平衡与人体测量指标密切相关。
BMC Med Genet. 2018 Aug 20;19(1):146. doi: 10.1186/s12881-018-0664-z.
5
Effect of Obesity-Linked rs9939609 Variant on Physical Activity and Dietary Patterns in Physically Active Men and Women.肥胖相关的rs9939609变异对体力活动男性和女性的身体活动及饮食模式的影响
J Obes. 2018 Mar 1;2018:7560707. doi: 10.1155/2018/7560707. eCollection 2018.
6
Interaction between FTO gene variants and lifestyle factors on metabolic traits in an Asian Indian population.亚洲印度人群中FTO基因变异与生活方式因素对代谢性状的相互作用。
Nutr Metab (Lond). 2016 Jun 3;13:39. doi: 10.1186/s12986-016-0098-6. eCollection 2016.
7
Obesity risk and preference for high dietary fat intake are determined by FTO rs9939609 gene polymorphism in selected Indonesian adults.在部分印度尼西亚成年人中,肥胖风险及对高膳食脂肪摄入的偏好由FTO rs9939609基因多态性决定。
Asia Pac J Clin Nutr. 2019;28(1):183-191. doi: 10.6133/apjcn.201903_28(1).0024.
8
Contribution of ENPP1, TCF7L2, and FTO polymorphisms to type 2 diabetes in mixed ancestry ethnic population of South Africa.ENPP1、TCF7L2和FTO基因多态性对南非混合血统种族人群2型糖尿病的影响。
Afr Health Sci. 2015 Dec;15(4):1149-60. doi: 10.4314/ahs.v15i4.14.
9
Macronutrient-specific effect of FTO rs9939609 in response to a 10-week randomized hypo-energetic diet among obese Europeans.肥胖欧洲人群中,FTO rs9939609 对 10 周低能量饮食的反应存在宏量营养素特异性。
Int J Obes (Lond). 2009 Nov;33(11):1227-34. doi: 10.1038/ijo.2009.159. Epub 2009 Aug 18.
10
Association of the fat mass and obesity-associated (FTO) gene variant (rs9939609) with dietary intake in the Finnish Diabetes Prevention Study.芬兰糖尿病预防研究中肥胖相关基因(FTO)变异(rs9939609)与饮食摄入的相关性。
Br J Nutr. 2012 Nov 28;108(10):1859-65. doi: 10.1017/S0007114511007410. Epub 2012 Jan 23.

引用本文的文献

1
Interaction between the gene and dietary intake on metabolic syndrome risk factors among Saudi Arabian adults.沙特阿拉伯成年人中基因与饮食摄入对代谢综合征风险因素的相互作用。
Front Nutr. 2025 Mar 18;12:1513088. doi: 10.3389/fnut.2025.1513088. eCollection 2025.
2
A Systematic Review of the Gene-Lifestyle Interactions on Metabolic Disease-Related Outcomes in Arab Populations.一项关于基因-生活方式相互作用对阿拉伯人群代谢性疾病相关结局影响的系统评价。
Nutrients. 2024 Aug 1;16(15):2519. doi: 10.3390/nu16152519.
3
Pharmacogenomics in Lebanon: current status, challenges and opportunities.

本文引用的文献

1
genotype, dietary protein intake, and body weight in a multiethnic population of young adults: a cross-sectional study.年轻成年人多民族群体中的基因型、膳食蛋白质摄入量和体重:一项横断面研究。
Genes Nutr. 2018 Feb 20;13:4. doi: 10.1186/s12263-018-0593-7. eCollection 2018.
2
Short Telomere Length is Associated with Aging, Central Obesity, Poor Sleep and Hypertension in Lebanese Individuals.端粒长度缩短与黎巴嫩人群的衰老、中心性肥胖、睡眠不佳及高血压相关。
Aging Dis. 2018 Feb 1;9(1):77-89. doi: 10.14336/AD.2017.0310. eCollection 2018 Feb.
3
FTO genotype and weight loss: systematic review and meta-analysis of 9563 individual participant data from eight randomised controlled trials.
黎巴嫩的药物基因组学:现状、挑战与机遇
Pharmacogenomics J. 2024 May 22;24(3):16. doi: 10.1038/s41397-024-00336-z.
4
In the context of the triple burden of malnutrition: A systematic review of gene-diet interactions and nutritional status.在营养不良的三重负担背景下:基因-饮食相互作用与营养状况的系统评价。
Crit Rev Food Sci Nutr. 2024;64(11):3235-3263. doi: 10.1080/10408398.2022.2131727. Epub 2022 Oct 12.
5
Meta-Analysis and Systematic Review of Micro- and Macro-Nutrient Intakes and Trajectories of Macro-Nutrient Supply in the Eastern Mediterranean Region.东地中海地区微量和常量营养素摄入量及常量营养素供应轨迹的Meta分析与系统评价
Nutrients. 2021 Apr 30;13(5):1515. doi: 10.3390/nu13051515.
6
TCF7L2 rs7903146 polymorphism modulates the association between adherence to a Mediterranean diet and the risk of gestational diabetes mellitus.TCF7L2基因rs7903146多态性调节地中海饮食依从性与妊娠期糖尿病风险之间的关联。
Metabol Open. 2020 Nov 26;8:100069. doi: 10.1016/j.metop.2020.100069. eCollection 2020 Dec.
7
Science and Healthy Meals in the World: Nutritional Epigenomics and Nutrigenetics of the Mediterranean Diet.世界的科学与健康饮食:地中海饮食的营养表观基因组学和营养遗传学。
Nutrients. 2020 Jun 11;12(6):1748. doi: 10.3390/nu12061748.
FTO基因分型与体重减轻:对来自八项随机对照试验的9563名个体参与者数据的系统评价和荟萃分析。
BMJ. 2016 Sep 20;354:i4707. doi: 10.1136/bmj.i4707.
4
FTO genotype and weight loss in diet and lifestyle interventions: a systematic review and meta-analysis.FTO基因分型与饮食及生活方式干预中的体重减轻:一项系统评价与荟萃分析。
Am J Clin Nutr. 2016 Apr;103(4):1162-70. doi: 10.3945/ajcn.115.123448. Epub 2016 Feb 17.
5
Gene-based meta-analysis of genome-wide association studies implicates new loci involved in obesity.基于基因的全基因组关联研究荟萃分析揭示了与肥胖相关的新基因座。
Hum Mol Genet. 2015 Dec 1;24(23):6849-60. doi: 10.1093/hmg/ddv379. Epub 2015 Sep 16.
6
Gene-environment interactions and obesity: recent developments and future directions.基因-环境相互作用与肥胖:最新进展与未来方向。
BMC Med Genomics. 2015;8 Suppl 1(Suppl 1):S2. doi: 10.1186/1755-8794-8-S1-S2. Epub 2015 Jan 15.
7
Diet, physical activity and socio-economic disparities of obesity in Lebanese adults: findings from a national study.黎巴嫩成年人肥胖的饮食、身体活动及社会经济差异:一项全国性研究的结果
BMC Public Health. 2015 Mar 21;15:279. doi: 10.1186/s12889-015-1605-9.
8
Obesity: interactions of genome and nutrients intake.肥胖:基因组与营养摄入的相互作用。
Prev Nutr Food Sci. 2015 Mar;20(1):1-7. doi: 10.3746/pnf.2015.20.1.1. Epub 2015 Mar 31.
9
The association of MC4R rs17782313 polymorphism with dietary intake in Iranian adults.伊朗成年人中黑素皮质素4受体基因(MC4R)rs17782313多态性与饮食摄入的关联。
Gene. 2015 Jun 1;563(2):125-9. doi: 10.1016/j.gene.2015.03.013. Epub 2015 Mar 11.
10
Dietary patterns interact with APOA1/APOC3 polymorphisms to alter the risk of the metabolic syndrome: the Tehran Lipid and Glucose Study.饮食模式与载脂蛋白A1/载脂蛋白C3基因多态性相互作用,改变代谢综合征风险:德黑兰脂质与血糖研究
Br J Nutr. 2015 Feb 28;113(4):644-53. doi: 10.1017/S0007114514003687. Epub 2015 Feb 5.