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功能性多态性的花生四烯酸途径与风险和临床结果的过敏性疾病。

Functional Polymorphisms of the Arachidonic Acid Pathway Associate with Risks and Clinical Outcomes of Allergic Diseases.

机构信息

Department of Biological Sciences, National University of Singapore, Singapore, Singapore,

Department of Biological Sciences, National University of Singapore, Singapore, Singapore.

出版信息

Int Arch Allergy Immunol. 2023;184(6):609-623. doi: 10.1159/000530393. Epub 2023 May 10.

Abstract

INTRODUCTION

The arachidonic acid (AA) pathway plays a crucial role in allergic inflammatory diseases; however, the functional roles of allergy-associated single nucleotide polymorphisms (SNPs) in this pathway remain incompletely illustrated.

METHODS

This study belongs to a part of an ongoing Singapore/Malaysia cross-sectional genetics and epidemiological study (SMCSGES). We performed population genotyping on n = 2,880 individuals from the SMCSGES cohort to assess the associations of SNPs in the AA pathway genes with asthma and allergic rhinitis (AR). Spirometry assessments were performed to identify associations between SNPs and lung function among n = 74 pediatric asthmatic patients from the same cohort. Allergy-associated SNPs were functionally characterized using in vitro promoter luciferase assay, along with DNA methylome and transcriptome data of n = 237 peripheral blood mononuclear cell (PBMC) samples collected from a subset of the SMCSGES cohort.

RESULTS

Genetic association analysis showed 5 tag-SNPs from 4 AA pathway genes were significantly associated with asthma (rs689466 at COX2, rs35744894 at hematopoietic PGD2 synthase (HPGDS), rs11097414 at HPGDS, rs7167 at CRTH2, and rs5758 at TBXA2R, p < 0.05), whereas 3 tag-SNPs from HPGDS (rs35744894, rs11097414, and rs11097411) and 2 tag-SNPs from PTGDR (rs8019916 and rs41312470) were significantly associated with AR (p < 0.05). The asthma-associated rs689466 regulates COX2 promoter activity and associates with COX2 mRNA expression in PBMC. The allergy-associated rs1344612 was significantly associated with poorer lung function, increased risks of asthma and AR, and increased HPGDS promoter activity. The allergy-associated rs8019916 regulates PTGDR promoter activity and DNA methylation levels of cg23022053 and cg18369034 in PBMC. The asthma-associated rs7167 affects CRTH2 expression by regulating the methylation level of cg19192256 in PBMC.

CONCLUSIONS

The present study identified multiple allergy-associated SNPs that modulate the transcript expressions of key genes in the AA pathway. The development of a "personalized medicine" approach with consideration of genetic influences on the AA pathway may hopefully result in efficacious strategies to manage and treat allergic diseases.

摘要

简介

花生四烯酸(AA)途径在过敏性炎症性疾病中起着至关重要的作用;然而,该途径中与过敏相关的单核苷酸多态性(SNP)的功能作用仍不完全清楚。

方法

本研究属于正在进行的新加坡/马来西亚横断面遗传学和流行病学研究(SMCSGES)的一部分。我们对 SMCSGES 队列中的 2880 名个体进行了群体基因分型,以评估 AA 途径基因中的 SNP 与哮喘和过敏性鼻炎(AR)之间的关联。对来自同一队列的 74 名儿科哮喘患者进行肺功能测定,以确定 SNP 与肺功能之间的关系。对来自 SMCSGES 队列一部分的 237 个外周血单核细胞(PBMC)样本的 DNA 甲基组和转录组数据进行功能表征,以鉴定与过敏相关的 SNP。

结果

遗传关联分析显示,4 个 AA 途径基因中的 5 个标签 SNP 与哮喘显著相关(COX2 中的 rs689466、HPGDS 中的 rs35744894、HPGDS 中的 rs11097414、CRTH2 中的 rs7167 和 TBXA2R 中的 rs5758,p < 0.05),而 HPGDS 中的 3 个标签 SNP(rs35744894、rs11097414 和 rs11097411)和 PTGDR 中的 2 个标签 SNP(rs8019916 和 rs41312470)与 AR 显著相关(p < 0.05)。与哮喘相关的 rs689466 调节 COX2 启动子活性,并与 PBMC 中的 COX2 mRNA 表达相关。与过敏相关的 rs1344612 与较差的肺功能、哮喘和 AR 的风险增加以及 HPGDS 启动子活性的增加显著相关。与过敏相关的 rs8019916 调节 PTGDR 启动子活性和 PBMC 中 cg23022053 和 cg18369034 的 DNA 甲基化水平。与哮喘相关的 rs7167 通过调节 PBMC 中 cg19192256 的甲基化水平来影响 CRTH2 的表达。

结论

本研究鉴定了多个与过敏相关的 SNP,这些 SNP 调节 AA 途径中关键基因的转录表达。考虑到 AA 途径的遗传影响,采用“个体化医疗”方法可能有望制定出有效的策略来管理和治疗过敏性疾病。

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