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一项针对同卵双胞胎对的全基因组关联研究表明,存在一个与血清高密度脂蛋白胆固醇变异性相关的基因座。

A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.

作者信息

Surakka Ida, Whitfield John B, Perola Markus, Visscher Peter M, Montgomery Grant W, Falchi Mario, Willemsen Gonneke, de Geus Eco J C, Magnusson Patrik K E, Christensen Kaare, Sørensen Thorkild I A, Pietiläinen Kirsi H, Rantanen Taina, Silander Kaisa, Widén Elisabeth, Muilu Juha, Rahman Iffat, Liljedahl Ulrika, Syvänen Ann-Christine, Palotie Aarno, Kaprio Jaakko, Kyvik Kirsten O, Pedersen Nancy L, Boomsma Dorret I, Spector Tim, Martin Nicholas G, Ripatti Samuli, Peltonen Leena

机构信息

Institute for Molecular Medicine, University of Helsinki, Finland.

出版信息

Twin Res Hum Genet. 2012 Dec;15(6):691-9. doi: 10.1017/thg.2012.63. Epub 2012 Oct 3.

Abstract

Genome-wide association analysis on monozygotic twin-pairs offers a route to discovery of gene environment interactions through testing for variability loci associated with sensitivity to individual environment/lifestyle. We present a genome-wide scan of loci associated with intra-pair differences in serum lipid and apolipoprotein levels. We report data for 1,720 monozygotic female twin-pairs from GenomEUtwin project with 2.5 million SNPs, imputed or genotyped, and measured serum lipid fractions for both twins. We found one locus associated with intra-pair differences in high-density lipoprotein cholesterol, rs2483058 in an intron of SRGAP2, where twins carrying the C allele are more sensitive to environmental factors(P=3.98 x 10-8). We followed up the association in further genotyped monozygotic twins (N= 1,261),which showed a moderate association for the variant (P= 0.200, same direction of an effect). In addition,we report a new association on the level of apolipoprotein A-ll (P= 4.03 x 1 o-8).

摘要

对同卵双胞胎进行全基因组关联分析,通过检测与个体环境/生活方式敏感性相关的可变位点,为发现基因-环境相互作用提供了一条途径。我们对与血清脂质和载脂蛋白水平的双胞胎内差异相关的位点进行了全基因组扫描。我们报告了来自GenomEUtwin项目的1720对同卵女性双胞胎的数据,这些双胞胎有250万个单核苷酸多态性(SNP),通过估算或基因分型获得,并对双胞胎双方的血清脂质成分进行了测量。我们发现一个与高密度脂蛋白胆固醇的双胞胎内差异相关的位点,位于SRGAP2基因内含子中的rs2483058,携带C等位基因的双胞胎对环境因素更敏感(P = 3.98×10⁻⁸)。我们在另外基因分型的同卵双胞胎(N = 1261)中对该关联进行了随访,结果显示该变异存在中度关联(P = 0.200,效应方向相同)。此外,我们报告了载脂蛋白A-II水平的一个新关联(P = 4.03×10⁻⁸)。

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