Paré Guillaume, Chasman Daniel I, Kellogg Mark, Zee Robert Y L, Rifai Nader, Badola Sunita, Miletich Joseph P, Ridker Paul M
Center for Cardiovascular Disease Prevention, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.
PLoS Genet. 2008 Jul 4;4(7):e1000118. doi: 10.1371/journal.pgen.1000118.
While circulating levels of soluble Intercellular Adhesion Molecule 1 (sICAM-1) have been associated with diverse conditions including myocardial infarction, stroke, malaria, and diabetes, comprehensive analysis of the common genetic determinants of sICAM-1 is not available. In a genome-wide association study conducted among 6,578 participants in the Women's Genome Health Study, we find that three SNPs at the ICAM1 (19p13.2) locus (rs1799969, rs5498 and rs281437) are non-redundantly associated with plasma sICAM-1 concentrations at a genome-wide significance level (P<5x10(-8)), thus extending prior results from linkage and candidate gene studies. We also find that a single SNP (rs507666, P = 5.1x10(-29)) at the ABO (9q34.2) locus is highly correlated with sICAM-1 concentrations. The novel association at the ABO locus provides evidence for a previously unknown regulatory role of histo-blood group antigens in inflammatory adhesion processes.
虽然可溶性细胞间黏附分子1(sICAM-1)的循环水平与多种疾病相关,包括心肌梗死、中风、疟疾和糖尿病,但目前尚无对sICAM-1常见遗传决定因素的全面分析。在一项针对女性基因组健康研究中6578名参与者开展的全基因组关联研究中,我们发现ICAM1(19p13.2)基因座上的三个单核苷酸多态性(SNP)(rs1799969、rs5498和rs281437)在全基因组显著水平(P<5×10⁻⁸)下与血浆sICAM-1浓度非冗余相关,从而扩展了之前连锁和候选基因研究的结果。我们还发现ABO(9q34.2)基因座上的一个单核苷酸多态性(rs507666,P = 5.1×10⁻²⁹)与sICAM-1浓度高度相关。ABO基因座上的这种新关联为组织血型抗原在炎症黏附过程中以前未知的调节作用提供了证据。