Association of PECAM1/CD31 polymorphisms with cerebral malaria.

International journal of molecular epidemiology and genetics Pub Date : 2016-06-01 eCollection Date: 2016-01-01
Jun Ohashi, Izumi Naka, Hathairad Hananantachai, Jintana Patarapotikul
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Abstract

Platelet/endothelial cell adhesion molecule-1 (PECAM1/CD31), a receptor recognized by P. falciparum-infected red blood cells (iRBCs), on the vascular endothelium has been implicated in mediating cytoadherence in patients with P. falciparum malaria. To examine associations of PECAM1 polymorphisms with cerebral malaria, 11 tag single nucleotide polymorphisms (SNPs) of PECAM1 were analysed for 312 Thai patients with P. falciparum malaria (109 with cerebral malaria and 203 with mild malaria). The rs1122800-C allele was significantly associated with protection from cerebral malaria (P = 0.017), and the rs9912957-A significantly increased the risk for cerebral malaria (P = 0.0065) in malaria patients. Fine-scale mapping using genotyped and imputed SNPs and linkage disequilibrium (LD) analysis revealed that rs1122800 and rs9912957 were located in two distinct LD blocks and were independently associated with cerebral malaria. The rs1122800-C allele was significantly associated with lower expression level of PECAM1 in EBV-transformed lymphoblastoid cell lines (P = 0.045). The present results suggest that PECAM1-mediated cytoadherence of iRBCs to brain endothelium plays a crucial role in the pathogenesis of cerebral malaria.

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PECAM1/CD31多态性与脑型疟疾的关系
血小板/内皮细胞粘附分子-1 (PECAM1/CD31)是恶性疟原虫感染的红细胞(irbc)在血管内皮上识别的受体,与介导恶性疟原虫疟疾患者的细胞粘附有关。为了研究PECAM1多态性与脑型疟疾的相关性,对312例泰国恶性疟原虫疟疾患者(109例脑型疟疾和203例轻度疟疾)的11个标签单核苷酸多态性(snp)进行了分析。rs1122800-C等位基因与预防脑疟疾显著相关(P = 0.017), rs9912957-A等位基因显著增加疟疾患者患脑疟疾的风险(P = 0.0065)。利用基因分型和估算SNPs以及连锁不平衡(LD)分析进行精细定位发现,rs1122800和rs9912957位于两个不同的LD区,并与脑型疟疾独立相关。rs1122800-C等位基因与PECAM1在ebv转化的淋巴母细胞样细胞系中的低表达水平显著相关(P = 0.045)。目前的研究结果表明,pecam1介导的irbc对脑内皮的细胞粘附在脑疟疾的发病机制中起着至关重要的作用。
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