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韩国哮喘患者的全基因组关联研究:与英国哮喘患者的比较。

Genome-Wide Association Study of Korean Asthmatics: A Comparison With UK Asthmatics.

作者信息

An Jin, Do Ah Ra, Kang Hae Yeon, Kim Woo Jin, Lee Sanghun, Lee Ji Hyang, Song Woo Jung, Kwon Hyouk Soo, Cho You Sook, Moon Hee Bom, Hu Sile, Adcock Ian M, Chung Kian Fan, Won Sungho, Kim Tae Bum

机构信息

Department of Allergy and Clinical Immunology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Department of Pulmonary, Allergy and Critical Care Medicine, Kyung Hee University Hospital at Gangdong, College of Medicine, Kyung Hee University, Seoul, Korea.

出版信息

Allergy Asthma Immunol Res. 2021 Jul;13(4):609-622. doi: 10.4168/aair.2021.13.4.609.

Abstract

PURPOSE

Although genome-wide association studies (GWASs) represent the most powerful approach for identifying genes that influence asthma, to date, no studies have established genetic susceptibility to asthma in the Korean population. This study aimed to identify genetic variants associated with adult Korean asthmatics and compare them with the significant single nucleotide polymorphisms (SNPs) of UK asthmatics from the UK Biobank.

METHODS

Patients were defined as having asthma if they were diagnosed by a doctor or taking medications for asthma. Controls were defined as individuals without asthma or chronic obstructive pulmonary disease. We performed quality control, genotype imputation, GWAS, and PrediXcan analyses. In the GWAS, a value of < 5 × 10 was considered significant. We compared significant SNPs between Korean and UK patients with asthma.

RESULTS

A total of 1,386 asthmatic patients and 5,205 controls were analyzed. The SNP rs1770, located near the human leukocyte antigen (HLA)-DQB1, was the most significant SNP ( = 4.5 × 10). In comparison with 24 SNPs in a GWAS of UK asthmatics, six SNPs were significant with the same odds ratio (OR) direction, including signals related to type 2 inflammation (, IL1RL1, TSLP, and GATA3) and mucus plugging (, MUC5AC). HLA-DQA1 showed an opposite OR direction. The HLA-DQB1 gene demonstrated significantly imputed mRNA expression in the lung tissue and whole blood.

CONCLUSIONS

The SNP rs1770 of HLA-DQB1 was the most significant in Korean asthmatics. Similarities and discrepancies were found in the genetic variants between Korean and UK asthmatics. GWAS of Korean asthmatics should be replicated and compared with those of GWAS of other ethnicities.

摘要

目的

尽管全基因组关联研究(GWAS)是识别影响哮喘的基因的最有效方法,但迄今为止,尚无研究确定韩国人群对哮喘的遗传易感性。本研究旨在识别与成年韩国哮喘患者相关的基因变异,并将其与来自英国生物银行的英国哮喘患者的显著单核苷酸多态性(SNP)进行比较。

方法

如果患者被医生诊断为哮喘或正在服用哮喘药物,则定义为患有哮喘。对照组定义为无哮喘或慢性阻塞性肺疾病的个体。我们进行了质量控制、基因型推算、GWAS和PrediXcan分析。在GWAS中,p值<5×10⁻⁸被认为具有显著性。我们比较了韩国和英国哮喘患者之间的显著SNP。

结果

共分析了1386例哮喘患者和5205例对照。位于人类白细胞抗原(HLA)-DQB1附近的SNP rs1770是最显著的SNP(p = 4.5×10⁻¹²)。与英国哮喘患者GWAS中的24个SNP相比,6个SNP在相同的优势比(OR)方向上具有显著性,包括与2型炎症(IL1RL1、TSLP和GATA3)和黏液阻塞(MUC5AC)相关的信号。HLA-DQA1显示出相反的OR方向。HLA-DQB1基因在肺组织和全血中显示出显著的推算mRNA表达。

结论

HLA-DQB1的SNP rs1770在韩国哮喘患者中最为显著。在韩国和英国哮喘患者的基因变异中发现了相似性和差异。韩国哮喘患者的GWAS应进行重复,并与其他种族的GWAS进行比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f493/8255356/c7052c5a707e/aair-13-609-g001.jpg

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