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本文引用的文献

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Replication and extension of genome-wide association study results for obesity in 4923 adults from northern Sweden.瑞典北部4923名成年人肥胖症全基因组关联研究结果的重复验证与扩展
Hum Mol Genet. 2009 Apr 15;18(8):1489-96. doi: 10.1093/hmg/ddp041. Epub 2009 Jan 22.
2
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.
3
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.
4
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.全基因组关联研究在七个与肥胖指标相关的基因座上发现了新的序列变异。
Nat Genet. 2009 Jan;41(1):18-24. doi: 10.1038/ng.274. Epub 2008 Dec 14.
5
Obesity and the metabolic syndrome in developing countries.发展中国家的肥胖与代谢综合征
J Clin Endocrinol Metab. 2008 Nov;93(11 Suppl 1):S9-30. doi: 10.1210/jc.2008-1595.
6
Epidemiology of obesity in the Western Hemisphere.西半球肥胖症流行病学
J Clin Endocrinol Metab. 2008 Nov;93(11 Suppl 1):S1-8. doi: 10.1210/jc.2008-1356.
7
Common nonsynonymous variants in PCSK1 confer risk of obesity.前蛋白转化酶枯草溶菌素1(PCSK1)中常见的非同义变异会增加肥胖风险。
Nat Genet. 2008 Aug;40(8):943-5. doi: 10.1038/ng.177. Epub 2008 Jul 6.
8
Obesity prevalence from a European perspective: a systematic review.从欧洲视角看肥胖症患病率:一项系统综述
BMC Public Health. 2008 Jun 5;8:200. doi: 10.1186/1471-2458-8-200.
9
Occupational social class, risk factors and cardiovascular disease incidence in men and women: a prospective study in the European Prospective Investigation of Cancer and Nutrition in Norfolk (EPIC-Norfolk) cohort.职业社会阶层、危险因素与男性和女性心血管疾病发病率:诺福克欧洲癌症与营养前瞻性调查(EPIC-Norfolk)队列中的一项前瞻性研究。
Eur J Epidemiol. 2008;23(7):449-58. doi: 10.1007/s10654-008-9262-2. Epub 2008 May 29.
10
Common variants near MC4R are associated with fat mass, weight and risk of obesity.MC4R基因附近的常见变异与脂肪量、体重及肥胖风险相关。
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在欧洲癌症与营养前瞻性调查(EPIC-Norfolk)研究中,前蛋白转化酶枯草溶菌素1(PCSK1)基因变异与肥胖的关联。

Association of variants in the PCSK1 gene with obesity in the EPIC-Norfolk study.

作者信息

Kilpeläinen Tuomas O, Bingham Sheila A, Khaw Kay-Tee, Wareham Nicholas J, Loos Ruth J F

机构信息

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

出版信息

Hum Mol Genet. 2009 Sep 15;18(18):3496-501. doi: 10.1093/hmg/ddp280. Epub 2009 Jun 15.

DOI:10.1093/hmg/ddp280
PMID:19528091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2729665/
Abstract

Recently, the rs6232 (N221D) and rs6235 (S690T) SNPs in the PCSK1 gene were associated with obesity in a meta-analysis comprising more than 13 000 individuals of European ancestry. Each additional minor allele of rs6232 or rs6235 was associated with a 1.34- or 1.22-fold increase in the risk of obesity, respectively. So far, only one relatively small study has aimed to replicate these findings, but could not confirm the association of the rs6235 SNP and did not study the rs6232 variant. In the present study, we examined the associations of the rs6232 and rs6235 SNPs with obesity in a population-based cohort consisting of 20 249 individuals of European descent from Norfolk, UK. Logistic regression and generalized linear models were used to test the associations of the risk alleles with obesity and related quantitative traits, respectively. Neither of the SNPs was significantly associated with obesity, BMI or waist circumference under the additive genetic model (P > 0.05). However, we observed an interaction between rs6232 and age on the level of BMI (P = 0.010) and risk of obesity (P = 0.020). The rs6232 SNP was associated with BMI (P = 0.021) and obesity (P = 0.022) in the younger individuals [less than median age (59 years)], but not among the older age group (P = 0.81 and P = 0.68 for BMI and obesity, respectively). In conclusion, our data suggest that the PCSK1 rs6232 and rs6235 SNPs are not major contributors to common obesity in the general population. However, the effect of rs6232 may be age-dependent.

摘要

最近,在一项纳入了超过13000名欧洲血统个体的荟萃分析中,前蛋白转化酶枯草溶菌素1(PCSK1)基因中的rs6232(N221D)和rs6235(S690T)单核苷酸多态性(SNP)与肥胖相关。rs6232或rs6235的每一个额外的次要等位基因分别与肥胖风险增加1.34倍或1.22倍相关。到目前为止,仅有一项相对较小的研究旨在重复这些发现,但未能证实rs6235 SNP的相关性,且未研究rs6232变异。在本研究中,我们在一个基于人群的队列中检测了rs6232和rs6235 SNP与肥胖的相关性,该队列由来自英国诺福克的20249名欧洲血统个体组成。分别使用逻辑回归和广义线性模型来检验风险等位基因与肥胖及相关定量性状的相关性。在加性遗传模型下,这两个SNP均与肥胖、体重指数(BMI)或腰围无显著相关性(P>0.05)。然而,我们观察到rs6232与年龄在BMI水平(P = 0.010)和肥胖风险(P = 0.020)上存在相互作用。rs6232 SNP在较年轻个体[年龄小于中位数(59岁)]中与BMI(P = 0.021)和肥胖(P = 0.022)相关,但在较年长组中无相关性(BMI和肥胖的P值分别为0.81和0.68)。总之,我们的数据表明,PCSK1基因的rs6232和rs6235 SNP不是普通人群中常见肥胖的主要影响因素。然而,rs6232的作用可能与年龄有关。