Department of Pharmacy Practice and Science, University of Arizona College of Pharmacy, Tucson, AZ.
Department of Hemostasis, Regional University Hospital Centre Tours, Tours, France.
Blood Adv. 2022 Jul 26;6(14):4137-4146. doi: 10.1182/bloodadvances.2022007673.
Heparin, a widely used anticoagulant, carries the risk of an antibody-mediated adverse drug reaction, heparin-induced thrombocytopenia (HIT). A subset of heparin-treated patients produces detectable levels of antibodies against complexes of heparin bound to circulating platelet factor 4 (PF4). Using a genome-wide association study (GWAS) approach, we aimed to identify genetic variants associated with anti-PF4/heparin antibodies that account for the variable antibody response seen in HIT. We performed a GWAS on anti-PF4/heparin antibody levels determined via polyclonal enzyme-linked immunosorbent assays. Our discovery cohort (n = 4237) and replication cohort (n = 807) constituted patients with European ancestry and clinical suspicion of HIT, with cases confirmed via functional assay. Genome-wide significance was considered at α = 5 × 10-8. No variants were significantly associated with anti-PF4/heparin antibody levels in the discovery cohort at a genome-wide significant level. Secondary GWAS analyses included the identification of variants with suggestive associations in the discovery cohort (α = 1 × 10-4). The top variant in both cohorts was rs1555175145 (discovery β = -0.112 [0.018], P = 2.50 × 10-5; replication β = -0.104 [0.051], P = .041). In gene set enrichment analysis, 3 gene sets reached false discovery rate-adjusted significance (q < 0.05) in both discovery and replication cohorts: "Leukocyte Transendothelial Migration," "Innate Immune Response," and "Lyase Activity." Our results indicate that genomic variation is not significantly associated with anti-PF4/heparin antibody levels. Given our power to identify variants with moderate frequencies and effect sizes, this evidence suggests genetic variation is not a primary driver of variable antibody response in heparin-treated patients with European ancestry.
肝素是一种广泛使用的抗凝剂,存在抗体介导的药物不良反应风险,即肝素诱导的血小板减少症(HIT)。在接受肝素治疗的患者中,有一部分会产生可检测水平的针对与循环血小板因子 4(PF4)结合的肝素复合物的抗体。本研究采用全基因组关联研究(GWAS)方法,旨在鉴定与抗 PF4/肝素抗体相关的遗传变异,这些变异可解释 HIT 中所见的可变抗体反应。我们通过多克隆酶联免疫吸附试验测定抗 PF4/肝素抗体水平进行 GWAS。我们的发现队列(n = 4237)和复制队列(n = 807)由具有 HIT 临床疑似表现的欧洲血统患者组成,通过功能测定确认病例。在全基因组显著性水平上,认为 α = 5 × 10-8 时有显著意义。在发现队列中,没有变异在全基因组显著水平上与抗 PF4/肝素抗体水平显著相关。二次 GWAS 分析包括在发现队列中鉴定具有提示关联的变异(α = 1 × 10-4)。两个队列中的最高变异是 rs1555175145(发现 β = -0.112 [0.018],P = 2.50 × 10-5;复制 β = -0.104 [0.051],P =.041)。在基因集富集分析中,在发现和复制队列中,有 3 个基因集达到了错误发现率校正显著性(q < 0.05):“白细胞跨内皮迁移”、“先天免疫反应”和“裂解酶活性”。我们的研究结果表明,基因组变异与抗 PF4/肝素抗体水平无显著相关性。考虑到我们识别具有中等频率和效应大小的变异的能力,这一证据表明,在欧洲血统的肝素治疗患者中,遗传变异不是可变抗体反应的主要驱动因素。