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五聚素3基因中的rs1840680单核苷酸多态性:重症社区获得性肺炎的潜在保护性生物标志物

rs1840680 single nucleotide polymorphism in Pentraxin 3: a potential protective biomarker of severe community-acquired pneumonia.

作者信息

Zeng Qiaojun, Tang Tiantian, Huang Biru, Bu Shiyi, Xiao Yingqi, Dai Yumeng, Wei Zixin, Huang Linjie, Jiang Shanping

机构信息

Department of Pulmonary and Critical Care Medicine, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.

Institute of Pulmonary Diseases, Sun Yat-sen University, Guangzhou, Guangdong, China.

出版信息

J Int Med Res. 2021 Apr;49(4):3000605211010621. doi: 10.1177/03000605211010621.

Abstract

OBJECTIVE

Single nucleotide polymorphisms (SNPs) of () are associated with various outcomes of lung infections. This study aimed to analyze the relationship between polymorphisms and the severity of community-acquired pneumonia (CAP).

METHODS

This is a retrospective case-control study comprising 43 patients with severe CAP (SCAP) and 97 patients with non-severe CAP. Three SNPs in the gene (rs2305619, rs3816527, and rs1840680) from peripheral blood samples were genotyped by real-time polymerase chain reaction. The association between each SNP and the CAP severity was analyzed by logistic regression analysis.

RESULTS

We found that the rs1840680 polymorphism was significantly associated with CAP clinical severity. However, no such association was observed for the genotypes and allele frequencies of rs2305619 or rs3816527. The rs1840680 AG genotype was an independent factor for a lower risk of SCAP after multivariate logistic regression analysis. Male sex and coronary heart disease were associated with an increased risk of SCAP.

CONCLUSIONS

The rs1840680 AG genotype was found to be associated with a lower risk of SCAP, and may serve as a potential protective biomarker to help clinical judgment and management.

摘要

目的

()的单核苷酸多态性(SNPs)与肺部感染的多种结局相关。本研究旨在分析()多态性与社区获得性肺炎(CAP)严重程度之间的关系。

方法

这是一项回顾性病例对照研究,包括43例重症CAP(SCAP)患者和97例非重症CAP患者。通过实时聚合酶链反应对外周血样本中()基因的三个SNP(rs2305619、rs3816527和rs1840680)进行基因分型。通过逻辑回归分析每个SNP与CAP严重程度之间的关联。

结果

我们发现rs1840680多态性与CAP临床严重程度显著相关。然而,未观察到rs2305619或rs3816527的基因型和等位基因频率与CAP严重程度之间存在此类关联。多因素逻辑回归分析后,rs1840680 AG基因型是SCAP风险较低的独立因素。男性和冠心病与SCAP风险增加相关。

结论

发现rs1840680 AG基因型与SCAP风险较低相关,可能作为一种潜在的保护性生物标志物,有助于临床判断和管理。

相似文献

本文引用的文献

2
Genetics in community-acquired pneumonia.社区获得性肺炎的遗传学研究。
Curr Opin Pulm Med. 2019 May;25(3):323-329. doi: 10.1097/MCP.0000000000000580.

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