Kim Daniel S, Burt Amber A, Ranchalis Jane E, Richter Rebecca J, Marshall Julieann K, Eintracht Jason F, Rosenthal Elisabeth A, Furlong Clement E, Jarvik Gail P
Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA.
J Lipids. 2012;2012:476316. doi: 10.1155/2012/476316. Epub 2012 May 22.
Background. Paraoxonase 1 (PON1) enzymatic activity has been consistently predictive of cardiovascular disease, while the genotypes at the four functional polymorphisms at PON1 have not. The goal of this study was to identify additional variation at the PON gene cluster that improved prediction of PON1 activity and determine if these variants predict carotid artery disease (CAAD). Methods. We considered 1,328 males in a CAAD cohort. 51 tagging single-nucleotide polymorphisms (tag SNPs) across the PON cluster were evaluated to determine their effects on PON1 activity and CAAD status. Results. Six SNPs (four in PON1 and one each in PON2/3) predicted PON1 arylesterase (AREase) activity, in addition to the four previously known functional SNPs. In total, the 10 SNPs explained 30.1% of AREase activity, 5% of which was attributable to the six identified predictive SNPs. We replicate rs854567 prediction of 2.3% of AREase variance, the effects of rs3917510, and a PON3 haplotype that includes rs2375005. While AREase activity strongly predicted CAAD, none of the 10 SNPs predicting AREase predicted CAAD. Conclusions. This study identifies new genetic variants that predict additional PON1 AREase activity. Identification of SNPs associated with PON1 activity is required when evaluating the many phenotypes associated with genetic variation near PON1.
背景。对氧磷酶1(PON1)的酶活性一直是心血管疾病的预测指标,而PON1四个功能多态性位点的基因型并非如此。本研究的目的是在PON基因簇中识别出能改善PON1活性预测的其他变异,并确定这些变异是否能预测颈动脉疾病(CAAD)。方法。我们纳入了一个CAAD队列中的1328名男性。对PON基因簇中的51个标签单核苷酸多态性(tag SNPs)进行评估,以确定它们对PON1活性和CAAD状态的影响。结果。除了四个先前已知的功能SNP外,六个SNP(四个在PON1中,一个在PON2/3中各一个)可预测PON1芳基酯酶(AREase)活性。总的来说,这10个SNP解释了AREase活性的30.1%,其中5%可归因于六个已识别的预测性SNP。我们重复了rs854567对AREase变异的2.3%的预测、rs3917510的效应以及包含rs2375005的PON3单倍型。虽然AREase活性强烈预测CAAD,但预测AREase的10个SNP均未预测CAAD。结论。本研究识别出了可预测额外PON1 AREase活性的新遗传变异。在评估与PON1附近遗传变异相关的众多表型时,需要识别与PON1活性相关的SNP。