Suppr超能文献

常见肥胖症遗传学的最新进展。

Recent progress in the genetics of common obesity.

机构信息

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

出版信息

Br J Clin Pharmacol. 2009 Dec;68(6):811-29. doi: 10.1111/j.1365-2125.2009.03523.x.

Abstract

The genetic contribution to interindividual variation in common obesity has been estimated at 40-70%. Yet, despite a relatively high heritability, the search for obesity susceptibility genes has been an arduous task. This paper reviews recent progress made in the obesity genetics field with an emphasis on established obesity susceptibility loci identified through candidate gene as well as genome-wide studies. For the last 15 years, candidate gene and genome-wide linkage studies have been the two main genetic epidemiological approaches to identify genetic loci for common traits, yet progress has been slow and success limited. Only recently have candidate gene studies started to succeed; by means of large-scale studies and meta-analyses at least five variants in four candidate genes have been found to be robustly associated with obesity-related traits. Genome-wide linkage studies, however, have so far not been able to pinpoint genetic loci for common obesity. The genome-wide association approach, which has become available in recent years, has dramatically changed the pace of gene discoveries for common disease, including obesity. Three waves of large-scale high-density genome-wide association studies have already discovered at least 15 previously unanticipated genetic loci incontrovertibly associated with body mass index and extreme obesity risk. Although the combined contribution of these loci to the variation in obesity risk at the population level is small and their predictive value is typically low, these recently discovered loci are set to improve fundamentally our insights into the pathophysiology of obesity.

摘要

个体间常见肥胖的遗传差异可归因于 40-70%。尽管遗传率相对较高,但寻找肥胖易感基因一直是一项艰巨的任务。本文重点介绍了通过候选基因和全基因组研究确定的已建立的肥胖易感基因座,回顾了肥胖遗传学领域的最新进展。在过去的 15 年中,候选基因和全基因组连锁研究一直是识别常见性状遗传基因座的两种主要遗传流行病学方法,但进展缓慢,成功有限。直到最近,候选基因研究才开始取得成功;通过大规模研究和荟萃分析,至少在四个候选基因中的五个变体与肥胖相关特征具有稳健的相关性。然而,全基因组连锁研究迄今为止还无法确定常见肥胖的遗传基因座。近年来出现的全基因组关联研究方法极大地改变了包括肥胖症在内的常见疾病的基因发现速度。三波大规模高密度全基因组关联研究已经发现了至少 15 个以前未预料到的与体重指数和极端肥胖风险明显相关的遗传基因座。尽管这些基因座在人群水平上对肥胖风险变异的综合贡献很小,并且其预测价值通常较低,但这些新发现的基因座将从根本上改善我们对肥胖症病理生理学的认识。

相似文献

1
Recent progress in the genetics of common obesity.
Br J Clin Pharmacol. 2009 Dec;68(6):811-29. doi: 10.1111/j.1365-2125.2009.03523.x.
2
Progress in the genetics of common obesity and type 2 diabetes.
Expert Rev Mol Med. 2010 Feb 26;12:e7. doi: 10.1017/S1462399410001389.
3
Developments in obesity genetics in the era of genome-wide association studies.
J Nutrigenet Nutrigenomics. 2011;4(4):222-38. doi: 10.1159/000332158. Epub 2011 Nov 2.
4
Advancement in genetic variants conferring obesity susceptibility from genome-wide association studies.
Front Med. 2015 Jun;9(2):146-61. doi: 10.1007/s11684-014-0373-8. Epub 2014 Dec 29.
7
Candidate genes for obesity-susceptibility show enriched association within a large genome-wide association study for BMI.
Hum Mol Genet. 2012 Oct 15;21(20):4537-42. doi: 10.1093/hmg/dds283. Epub 2012 Jul 12.
10
A genome-wide search for gene-by-obesity interaction loci of dyslipidemia in Koreans shows diverse genetic risk alleles.
J Lipid Res. 2019 Dec;60(12):2090-2101. doi: 10.1194/jlr.P119000226. Epub 2019 Oct 29.

引用本文的文献

1
The miR-668 binding site variant rs1046322 on is associated with obesity in Southeast Asians.
Front Endocrinol (Lausanne). 2023 Oct 4;14:1185956. doi: 10.3389/fendo.2023.1185956. eCollection 2023.
3
In the context of the triple burden of malnutrition: A systematic review of gene-diet interactions and nutritional status.
Crit Rev Food Sci Nutr. 2024;64(11):3235-3263. doi: 10.1080/10408398.2022.2131727. Epub 2022 Oct 12.
4
Specific Functions of Melanocortin 3 Receptor (MC3R).
J Clin Res Pediatr Endocrinol. 2023 Feb 27;15(1):1-6. doi: 10.4274/jcrpe.galenos.2022.2022-5-21. Epub 2022 Sep 2.
5
Obesity: The Fat Tissue Disease Version of Cancer.
Cells. 2022 Jun 9;11(12):1872. doi: 10.3390/cells11121872.
6
Peri-Operative Glycemic Dynamics in a Chinese Patient With Type 2 Diabetes Undergoing Laparoscopic Sleeve Gastrectomy.
Cureus. 2021 Oct 25;13(10):e19029. doi: 10.7759/cureus.19029. eCollection 2021 Oct.
7
Identifying actionable lifestyle risk factors for obesity research and intervention: Challenges and opportunities for Pacific Island health researchers.
Lancet Reg Health West Pac. 2020 Oct 16;4:100040. doi: 10.1016/j.lanwpc.2020.100040. eCollection 2020 Nov.
8
Integrative Analysis Revealing Human Adipose-Specific Genes and Consolidating Obesity Loci.
Sci Rep. 2019 Feb 28;9(1):3087. doi: 10.1038/s41598-019-39582-8.
9
Are gene polymorphisms associated with body mass regulation? A cross-sectional study.
BMJ Open. 2017 Nov 15;7(11):e017875. doi: 10.1136/bmjopen-2017-017875.
10
An autonomous metabolic role for Spen.
PLoS Genet. 2017 Jun 22;13(6):e1006859. doi: 10.1371/journal.pgen.1006859. eCollection 2017 Jun.

本文引用的文献

1
Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry.
Obesity (Silver Spring). 2009 Jul;17(7):1461-5. doi: 10.1038/oby.2009.53. Epub 2009 Mar 5.
2
FTO gene variation and measures of body mass in an African population.
BMC Med Genet. 2009 Mar 5;10:21. doi: 10.1186/1471-2350-10-21.
3
Combined effects of MC4R and FTO common genetic variants on obesity in European general populations.
J Mol Med (Berl). 2009 May;87(5):537-46. doi: 10.1007/s00109-009-0451-6. Epub 2009 Mar 3.
5
Inactivation of the Fto gene protects from obesity.
Nature. 2009 Apr 16;458(7240):894-8. doi: 10.1038/nature07848. Epub 2009 Feb 22.
8
Association of codon 16 and codon 27 beta 2-adrenergic receptor gene polymorphisms with obesity: a meta-analysis.
Obesity (Silver Spring). 2008 Sep;16(9):2096-106. doi: 10.1038/oby.2008.327.
9
The common variant in the FTO gene did not modify the effect of lifestyle changes on body weight: the Finnish Diabetes Prevention Study.
Obesity (Silver Spring). 2009 Apr;17(4):832-6. doi: 10.1038/oby.2008.618. Epub 2009 Jan 29.
10
FTO genotype is associated with body mass index after the age of seven years but not with energy intake or leisure-time physical activity.
J Clin Endocrinol Metab. 2009 Apr;94(4):1281-7. doi: 10.1210/jc.2008-1199. Epub 2009 Jan 21.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验