• 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

遗传风险评分与临床试验中拉丁裔女性的体重指数无关。

Genetic risk score does not correlate with body mass index of Latina women in a clinical trial.

机构信息

Department of Medicine, Division of Gastroenterology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

出版信息

Clin Transl Sci. 2011 Oct;4(5):323-7. doi: 10.1111/j.1752-8062.2011.00314.x.

DOI:10.1111/j.1752-8062.2011.00314.x
PMID:22029802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3205467/
Abstract

Obesity disproportionately affects Latina women. Common genetic variants are convincingly associated with body mass index (BMI) and may be used to create genetic risk scores (GRS) for obesity that could define genetically influenced forms of obesity and alter response to clinical trial interventions. The objective of this study was (1) to identify the frequency and effect size of common obesity genetic variants in Latina women; (2) to determine the clinical utility of a GRS for obesity with Latina women participating in a community-based clinical trial. DNA from 85 Latina women was genotyped for eight genetic variants previously associated with BMI in Caucasians, but not yet assessed in Latina populations. The main outcome measure was the correlation of GRS (sum of eight risk alleles) with BMI, waist circumference, and percent body fat. A majority (83%) of participants had a BMI ≥25. Frequency of loci near FTO, MC4R, and GNPDA2 were lower in Latinas than Caucasians. Association of each locus with BMI was lower in Latinas compared to Caucasians with no significant correlations with BMI. We conclude that an eight locus GRS has no clinical utility for explaining obesity or predicting response to intervention in Latina women participating in a clinical trial.

摘要

肥胖症在拉丁裔女性中不成比例地高发。常见的遗传变异与体重指数(BMI)有明显关联,这些变异可用于构建肥胖遗传风险评分(GRS),以确定受遗传影响的肥胖类型,并改变对临床试验干预的反应。本研究的目的是:(1)确定拉丁裔女性常见肥胖遗传变异的频率和效应大小;(2)确定在参与社区临床研究的拉丁裔女性中,肥胖 GRS 的临床实用性。对 85 名拉丁裔女性的 DNA 进行了 8 种先前与白种人 BMI 相关但尚未在拉丁裔人群中评估的遗传变异的基因分型。主要观察指标是 GRS(8 个风险等位基因的总和)与 BMI、腰围和体脂百分比的相关性。大多数(83%)参与者的 BMI≥25。与白种人相比,FTO、MC4R 和 GNPDA2 附近的位点频率在拉丁裔中较低。与白种人相比,每个位点与 BMI 的关联较低,与 BMI 无显著相关性。我们得出结论,一个包含 8 个基因座的 GRS 对于解释肥胖症或预测参与临床试验的拉丁裔女性对干预的反应没有临床实用性。

相似文献

1
Genetic risk score does not correlate with body mass index of Latina women in a clinical trial.遗传风险评分与临床试验中拉丁裔女性的体重指数无关。
Clin Transl Sci. 2011 Oct;4(5):323-7. doi: 10.1111/j.1752-8062.2011.00314.x.
2
Associations between body mass index-related genetic variants and adult body composition: The Fenland cohort study.体重指数相关基因变异与成人体成分之间的关联:芬兰德队列研究。
Int J Obes (Lond). 2017 Apr;41(4):613-619. doi: 10.1038/ijo.2017.11. Epub 2017 Jan 18.
3
Analysis of FTO gene variants with obesity and glucose homeostasis measures in the multiethnic Insulin Resistance Atherosclerosis Study cohort.多民族胰岛素抵抗动脉粥样硬化研究队列中 FTO 基因变异与肥胖和葡萄糖稳态指标的分析。
Int J Obes (Lond). 2011 Sep;35(9):1173-82. doi: 10.1038/ijo.2010.244. Epub 2010 Nov 23.
4
Association of a Genetic Risk Score With Body Mass Index Across Different Birth Cohorts.遗传风险评分与不同出生队列体重指数的关联。
JAMA. 2016 Jul 5;316(1):63-9. doi: 10.1001/jama.2016.8729.
5
Fat mass- and obesity-associated genotype, dietary intakes and anthropometric measures in European adults: the Food4Me study.欧洲成年人中与脂肪量和肥胖相关的基因型、饮食摄入量及人体测量指标:Food4Me研究
Br J Nutr. 2016 Feb 14;115(3):440-8. doi: 10.1017/S0007114515004675. Epub 2015 Dec 1.
6
Cumulative effects and predictive value of common obesity-susceptibility variants identified by genome-wide association studies.全基因组关联研究鉴定的常见肥胖易感性变异的累积效应和预测价值。
Am J Clin Nutr. 2010 Jan;91(1):184-90. doi: 10.3945/ajcn.2009.28403. Epub 2009 Oct 7.
7
Sexual Dimorphism of a Genetic Risk Score for Obesity and Related Traits among Chinese Patients with Type 2 Diabetes.中国 2 型糖尿病患者肥胖及相关特征的遗传风险评分的性别二态性。
Obes Facts. 2019;12(3):328-343. doi: 10.1159/000500490. Epub 2019 Jun 5.
8
Adult obesity susceptibility variants are associated with greater childhood weight gain and a faster tempo of growth: the 1946 British Birth Cohort Study.成人肥胖易感性变异与儿童期体重增加较多和生长速度较快有关:1946 年英国出生队列研究。
Am J Clin Nutr. 2012 May;95(5):1150-6. doi: 10.3945/ajcn.111.027870. Epub 2012 Mar 28.
9
FTO genetic variants and risk of obesity and type 2 diabetes: a meta-analysis of 28,394 Indians.FTO 基因变异与肥胖和 2 型糖尿病风险:28394 名印度人的荟萃分析。
Obesity (Silver Spring). 2014 Mar;22(3):964-70. doi: 10.1002/oby.20606. Epub 2013 Sep 20.
10
Associations of variants in FTO and near MC4R with obesity traits in South Asian Indians.FTO 和 MC4R 附近的变异与南亚印度人肥胖特征的关联。
Obesity (Silver Spring). 2012 Nov;20(11):2268-77. doi: 10.1038/oby.2012.64. Epub 2012 Mar 16.

本文引用的文献

1
Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.两个新的体重调节基因座在法国和德国研究组的早发性极端肥胖全基因组关联研究的联合分析中被发现。
PLoS Genet. 2010 Apr 22;6(4):e1000916. doi: 10.1371/journal.pgen.1000916.
2
Cumulative effects and predictive value of common obesity-susceptibility variants identified by genome-wide association studies.全基因组关联研究鉴定的常见肥胖易感性变异的累积效应和预测价值。
Am J Clin Nutr. 2010 Jan;91(1):184-90. doi: 10.3945/ajcn.2009.28403. Epub 2009 Oct 7.
3
A power primer.强力底漆。
Psychol Bull. 1992 Jul;112(1):155-9. doi: 10.1037//0033-2909.112.1.155.
4
The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI.全基因组关联研究中鉴定的肥胖相关基因座在儿童 BMI 测定中的作用。
Obesity (Silver Spring). 2009 Dec;17(12):2254-7. doi: 10.1038/oby.2009.159. Epub 2009 May 28.
5
Narrowing down the role of common variants in the genetic predisposition to obesity.缩小常见变异在肥胖遗传易感性中的作用。
Genome Med. 2009 Mar 11;1(3):31. doi: 10.1186/gm31.
6
The role of genes in the current obesity epidemic.基因在当前肥胖流行中的作用。
Ann Acad Med Singap. 2009 Jan;38(1):45-3.
7
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.早发性心肌梗死与单核苷酸多态性和拷贝数变异的全基因组关联研究
Nat Genet. 2009 Mar;41(3):334-41. doi: 10.1038/ng.327. Epub 2009 Feb 8.
8
Missing heritability and GWAS utility.缺失的遗传力与全基因组关联研究的效用。
Obesity (Silver Spring). 2009 Feb;17(2):209-10. doi: 10.1038/oby.2008.613.
9
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.针对早发性和病态成人肥胖的全基因组关联研究在欧洲人群中发现了三个新的风险基因座。
Nat Genet. 2009 Feb;41(2):157-9. doi: 10.1038/ng.301. Epub 2009 Jan 18.
10
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.六个与体重指数相关的新基因座凸显了神经元对体重调节的影响。
Nat Genet. 2009 Jan;41(1):25-34. doi: 10.1038/ng.287. Epub 2008 Dec 14.