Ko Yu-Lin, Hsu Lung-An, Wu Semon, Teng Ming-Sheng, Chou Hsin-Hua
Department of Research, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan; The Division of Cardiology, Department of Internal Medicine and Cardiovascular Center, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan; School of Medicine, Tzu Chi University, Hualien 97004, Taiwan.
The First Cardiovascular Division, Department of Internal Medicine, Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Taoyuan 33305, Taiwan.
Mediators Inflamm. 2016;2016:5830361. doi: 10.1155/2016/5830361. Epub 2016 May 25.
To test the statistical association of the CRP and SAA1 locus variants with their corresponding circulating levels and metabolic and inflammatory biomarker levels by using mediation analysis, a sample population of 599 Taiwanese subjects was enrolled and five CRP and four SAA1 variants were genotyped. Correlation analysis revealed that C-reactive protein (CRP) and serum amyloid A (SAA) levels were significantly associated with multiple metabolic phenotypes and inflammatory marker levels. Our data further revealed a significant association of CRP and SAA1 variants with both CRP and SAA levels. Mediation analysis revealed that SAA levels suppressed the association between SAA1 genotypes/haplotypes and CRP levels and that CRP levels suppressed the association between CRP haplotypes and SAA levels. In conclusion, genetic variants at the CRP and SAA1 loci independently affect both CRP and SAA levels, and their respective circulating levels act as suppressors. These results provided further evidence of the role of the suppression effect in biological science and may partially explain the missing heritability in genetic association studies.
为了通过中介分析来检验CRP和SAA1基因座变异与其相应的循环水平以及代谢和炎症生物标志物水平之间的统计关联,我们招募了599名台湾受试者作为样本群体,并对五个CRP和四个SAA1变异进行了基因分型。相关性分析显示,C反应蛋白(CRP)和血清淀粉样蛋白A(SAA)水平与多种代谢表型和炎症标志物水平显著相关。我们的数据进一步揭示了CRP和SAA1变异与CRP和SAA水平均存在显著关联。中介分析表明,SAA水平抑制了SAA1基因型/单倍型与CRP水平之间的关联,而CRP水平抑制了CRP单倍型与SAA水平之间的关联。总之,CRP和SAA1基因座的遗传变异独立影响CRP和SAA水平,且它们各自的循环水平起到抑制作用。这些结果为抑制效应在生物科学中的作用提供了进一步的证据,并可能部分解释了基因关联研究中缺失的遗传力。