• 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

相似文献

1
Candidate genes for obesity-susceptibility show enriched association within a large genome-wide association study for BMI.肥胖易感性候选基因在 BMI 的全基因组关联研究中存在丰富的关联。
Hum Mol Genet. 2012 Oct 15;21(20):4537-42. doi: 10.1093/hmg/dds283. Epub 2012 Jul 12.
2
Analyses of shared genetic factors between asthma and obesity in children.儿童哮喘和肥胖症之间共享遗传因素的分析。
J Allergy Clin Immunol. 2010 Sep;126(3):631-7.e1-8. doi: 10.1016/j.jaci.2010.06.030.
3
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.
4
Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis.全基因组遗传分析突出了丝裂原活化蛋白激酶(MAPK)信号通路在子宫内膜异位症发病机制中的作用。
Hum Reprod. 2017 Apr 1;32(4):780-793. doi: 10.1093/humrep/dex024.
5
Dissecting shared genetic architecture between depression and body mass index.解析抑郁症和体重指数之间的共享遗传结构。
BMC Med. 2024 Oct 11;22(1):455. doi: 10.1186/s12916-024-03681-9.
6
A Candidate-Gene Approach Identifies Novel Associations Between Common Variants in/Near Syndromic Obesity Genes and BMI in Pediatric and Adult European Populations.候选基因方法鉴定了综合征性肥胖基因内/附近常见变异与儿科和成人欧洲人群 BMI 之间的新关联。
Diabetes. 2019 Apr;68(4):724-732. doi: 10.2337/db18-0986. Epub 2019 Jan 28.
7
Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways.子宫内膜异位症和哮喘的遗传重叠分析确定了与性激素和甲状腺信号通路相关的共同位点。
Hum Reprod. 2022 Jan 28;37(2):366-383. doi: 10.1093/humrep/deab254.
8
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.
9
The role of eating behavior traits in mediating genetic susceptibility to obesity.饮食行为特征在介导肥胖遗传易感性中的作用。
Am J Clin Nutr. 2018 Sep 1;108(3):445-452. doi: 10.1093/ajcn/nqy130.
10
GWA-based pleiotropic analysis identified potential SNPs and genes related to type 2 diabetes and obesity.基于 GWA 的多效性分析确定了与 2 型糖尿病和肥胖相关的潜在 SNPs 和基因。
J Hum Genet. 2021 Mar;66(3):297-306. doi: 10.1038/s10038-020-00843-4. Epub 2020 Sep 18.

引用本文的文献

1
A Systematic Review of the Effect of Gene-Lifestyle Interactions on Metabolic-Disease-Related Traits in South Asian Populations.南亚人群中基因-生活方式相互作用对代谢疾病相关性状影响的系统评价
Nutr Rev. 2025 Jun 1;83(6):1061-1082. doi: 10.1093/nutrit/nuae115.
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
Risky Early Family Environment and Genetic Associations with Adult Metabolic Dysregulation.危险的早期家庭环境与成年代谢失调的遗传关联。
Int J Environ Res Public Health. 2022 Oct 28;19(21):14032. doi: 10.3390/ijerph192114032.
4
Genetic polymorphisms in neuroendocrine disorder-related candidate genes associated with pre-pregnancy obesity in gestational diabetes mellitus patients by using a stratification approach.采用分层方法研究妊娠期糖尿病患者孕前肥胖相关神经内分泌紊乱候选基因中的遗传多态性。
Ann Transl Med. 2020 Sep;8(17):1060. doi: 10.21037/atm-20-1579.
5
A Nutrigenetic Approach to Investigate the Relationship between Metabolic Traits and Vitamin D Status in an Asian Indian Population.一种营养遗传学方法,用于研究亚洲人群中代谢特征与维生素 D 状况之间的关系。
Nutrients. 2020 May 9;12(5):1357. doi: 10.3390/nu12051357.
6
Characterizing the Relation Between Expression QTLs and Complex Traits: Exploring the Role of Tissue Specificity.表征表达数量性状基因座与复杂性状之间的关系:探索组织特异性的作用。
Behav Genet. 2018 Sep;48(5):374-385. doi: 10.1007/s10519-018-9914-2. Epub 2018 Jul 20.
7
Identification of genetic elements in metabolism by high-throughput mouse phenotyping.通过高通量小鼠表型分析鉴定代谢中的遗传元件。
Nat Commun. 2018 Jan 18;9(1):288. doi: 10.1038/s41467-017-01995-2.
8
Interaction between TCF7L2 polymorphism and dietary fat intake on high density lipoprotein cholesterol.TCF7L2基因多态性与膳食脂肪摄入对高密度脂蛋白胆固醇的相互作用。
PLoS One. 2017 Nov 28;12(11):e0188382. doi: 10.1371/journal.pone.0188382. eCollection 2017.
9
A molecular census of arcuate hypothalamus and median eminence cell types.弓状下丘脑和正中隆起细胞类型的分子普查。
Nat Neurosci. 2017 Mar;20(3):484-496. doi: 10.1038/nn.4495. Epub 2017 Feb 6.
10
A GWA study reveals genetic loci for body conformation traits in Chinese Laiwu pigs and its implications for human BMI.一项全基因组关联研究揭示了中国莱芜猪体型性状的基因座及其对人类体重指数的影响。
Mamm Genome. 2016 Dec;27(11-12):610-621. doi: 10.1007/s00335-016-9657-4. Epub 2016 Jul 29.

本文引用的文献

1
Genomics and the multifactorial nature of human autoimmune disease.基因组学与人类自身免疫性疾病的多因素性质
N Engl J Med. 2011 Oct 27;365(17):1612-23. doi: 10.1056/NEJMra1100030.
2
Using functional annotation for the empirical determination of Bayes Factors for genome-wide association study analysis.使用功能注释来经验确定全基因组关联研究分析的贝叶斯因子。
PLoS One. 2011 Apr 27;6(4):e14808. doi: 10.1371/journal.pone.0014808.
3
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.对 249796 人的关联分析揭示了 18 个与体重指数相关的新位点。
Nat Genet. 2010 Nov;42(11):937-48. doi: 10.1038/ng.686. Epub 2010 Oct 10.
4
Hundreds of variants clustered in genomic loci and biological pathways affect human height.数以百计的变异体聚集在基因组位置和生物途径中,影响人类身高。
Nature. 2010 Oct 14;467(7317):832-8. doi: 10.1038/nature09410. Epub 2010 Sep 29.
5
Self-contained gene-set analysis of expression data: an evaluation of existing and novel methods.基于表达数据的独立基因集分析:现有和新型方法的评估。
PLoS One. 2010 Sep 17;5(9):e12693. doi: 10.1371/journal.pone.0012693.
6
Biological, clinical and population relevance of 95 loci for blood lipids.95 个与血脂相关的生物学、临床和人群相关性位点。
Nature. 2010 Aug 5;466(7307):707-13. doi: 10.1038/nature09270.
7
Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS.与性状相关的 SNPs 更有可能是 eQTLs:注释可增强 GWAS 中的发现。
PLoS Genet. 2010 Apr 1;6(4):e1000888. doi: 10.1371/journal.pgen.1000888.
8
Were genome-wide linkage studies a waste of time? Exploiting candidate regions within genome-wide association studies.全基因组连锁研究是否浪费时间?在全基因组关联研究中利用候选区域。
Genet Epidemiol. 2010 Feb;34(2):107-18. doi: 10.1002/gepi.20438.
9
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.全基因组关联位点对人类疾病和性状的潜在病因学及功能影响。
Proc Natl Acad Sci U S A. 2009 Jun 9;106(23):9362-7. doi: 10.1073/pnas.0903103106. Epub 2009 May 27.
10
Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk.全基因组关联数据集的基因层面分析:精神分裂症和双相情感障碍存在多个常见风险等位基因及遗传风险重叠的证据。
Mol Psychiatry. 2009 Mar;14(3):252-60. doi: 10.1038/mp.2008.133. Epub 2008 Dec 9.

肥胖易感性候选基因在 BMI 的全基因组关联研究中存在丰富的关联。

Candidate genes for obesity-susceptibility show enriched association within a large genome-wide association study for BMI.

机构信息

MRC Epidemiology Unit, Institute of Metabolic Science, Addenbrooke’s Hospital, Cambridge, UK.

出版信息

Hum Mol Genet. 2012 Oct 15;21(20):4537-42. doi: 10.1093/hmg/dds283. Epub 2012 Jul 12.

DOI:10.1093/hmg/dds283
PMID:22791748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3607467/
Abstract

Before the advent of genome-wide association studies (GWASs), hundreds of candidate genes for obesity-susceptibility had been identified through a variety of approaches. We examined whether those obesity candidate genes are enriched for associations with body mass index (BMI) compared with non-candidate genes by using data from a large-scale GWAS. A thorough literature search identified 547 candidate genes for obesity-susceptibility based on evidence from animal studies, Mendelian syndromes, linkage studies, genetic association studies and expression studies. Genomic regions were defined to include the genes ±10 kb of flanking sequence around candidate and non-candidate genes. We used summary statistics publicly available from the discovery stage of the genome-wide meta-analysis for BMI performed by the genetic investigation of anthropometric traits consortium in 123 564 individuals. Hypergeometric, rank tail-strength and gene-set enrichment analysis tests were used to test for the enrichment of association in candidate compared with non-candidate genes. The hypergeometric test of enrichment was not significant at the 5% P-value quantile (P = 0.35), but was nominally significant at the 25% quantile (P = 0.015). The rank tail-strength and gene-set enrichment tests were nominally significant for the full set of genes and borderline significant for the subset without SNPs at P < 10(-7). Taken together, the observed evidence for enrichment suggests that the candidate gene approach retains some value. However, the degree of enrichment is small despite the extensive number of candidate genes and the large sample size. Studies that focus on candidate genes have only slightly increased chances of detecting associations, and are likely to miss many true effects in non-candidate genes, at least for obesity-related traits.

摘要

在全基因组关联研究(GWAS)出现之前,通过多种方法已经确定了数百个肥胖易感性候选基因。我们通过使用大规模 GWAS 的数据,研究了这些肥胖候选基因是否与体重指数(BMI)相关联的可能性比非候选基因更为丰富。通过对动物研究、孟德尔综合征、连锁研究、遗传关联研究和表达研究的证据进行全面的文献检索,确定了 547 个肥胖易感性候选基因。候选基因和非候选基因的基因组区域定义为包含候选基因和非候选基因周围±10kb 的侧翼序列的基因。我们使用遗传分析人体测量特征联盟在 123564 个人中进行的 BMI 全基因组荟萃分析发现阶段公开的汇总统计数据。使用超几何检验、秩尾强度检验和基因集富集分析检验候选基因与非候选基因之间关联的富集情况。在 5% P 值分位数(P=0.35)时,富集的超几何检验没有显著意义,但在 25%分位数(P=0.015)时具有名义上的显著意义。秩尾强度和基因集富集检验对于完整的基因集和 P<10(-7)的没有 SNP 的子集都是名义上显著的,边缘显著。总的来说,观察到的富集证据表明候选基因方法仍然具有一定的价值。然而,尽管候选基因数量众多且样本量庞大,但富集程度很小。关注候选基因的研究仅略微增加了检测关联的机会,并且很可能会错过非候选基因中的许多真实效应,至少对于肥胖相关特征是如此。