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髓样分化因子88样衔接蛋白基因多态性rs8177374在调节巴基斯坦人群疟疾严重程度中的作用。

Role of MyD88-adaptor-like gene polymorphism rs8177374 in modulation of malaria severity in the Pakistani population.

作者信息

Rani Asima, Nawaz Syed Kashif, Irfan Shazia, Arshad Muhammad, Bashir Razia, Shaheen Najma

机构信息

University of Sargodha, Department of Zoology, Sargodha, Pakistan.

University of Sargodha, Department of Zoology, Sargodha, Pakistan.

出版信息

Braz J Infect Dis. 2017 Jul-Aug;21(4):418-423. doi: 10.1016/j.bjid.2017.04.002. Epub 2017 May 6.

Abstract

INTRODUCTION

The present study was designed to investigate the association between rs8177374 polymorphism and malaria symptoms due to exposure of Plasmodium vivax and Plasmodium falciparum.

MATERIALS AND METHODS

A total of 454 samples were included in the study (228 malaria patients and 226 healthy individuals). Malaria patients, divided into P. vivax and P. falciparum groups on the basis of the causative species of Plasmodium, were categorized into mild and severe on the basis of clinical outcomes according to WHO criteria. Healthy individuals were used as controls. Allele specific PCR based strategy was used for the identification of rs8177374 SNP.

RESULTS

MyD88-adaptor-like gene polymorphism was associated with susceptibility to malaria (p<0.001). C allele frequency (0.74) was higher in the population compared to T allele frequency (0.26). CT genotype increased the susceptibility of malaria (OR: 2.661; 95% CI: 1.722-4.113) and was positively associated with mild malaria (OR: 5.609; 95% CI: 3.479-9.044, p=0.00). On the other hand, CC genotype was associated with severe malaria (OR: 3.116; 95% CI: 1.560-6.224, p=0.00). P. vivax infection rate was higher in CT genotype carriers compared to other genotypes (OR: 3.616; 95% CI: 2.219-5.894, p<0.001).

CONCLUSION

MyD88-adaptor-like/TIR domain containing adaptor protein polymorphism for single nucleotide polymorphism rs8177374 is related with the susceptibility of malaria.

摘要

引言

本研究旨在调查rs8177374多态性与间日疟原虫和恶性疟原虫感染所致疟疾症状之间的关联。

材料与方法

本研究共纳入454个样本(228例疟疾患者和226例健康个体)。疟疾患者根据疟原虫致病种类分为间日疟原虫组和恶性疟原虫组,并根据世界卫生组织标准依据临床结果分为轻症和重症。健康个体作为对照。采用基于等位基因特异性PCR的策略鉴定rs8177374单核苷酸多态性。

结果

MyD88衔接蛋白样基因多态性与疟疾易感性相关(p<0.001)。人群中C等位基因频率(0.74)高于T等位基因频率(0.26)。CT基因型增加了疟疾易感性(比值比:2.661;95%置信区间:1.722 - 4.113),并与轻症疟疾呈正相关(比值比:5.609;95%置信区间:3.479 - 9.044,p = 0.00)。另一方面,CC基因型与重症疟疾相关(比值比:3.116;95%置信区间:1.560 - 6.224,p = 0.00)。CT基因型携带者的间日疟原虫感染率高于其他基因型(比值比:3.616;95%置信区间:2.219 - 5.894,p<0.001)。

结论

含MyD88衔接蛋白样/TIR结构域衔接蛋白的单核苷酸多态性rs8177374与疟疾易感性相关。

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