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主要组织相容性复合体 II 类多态性变异与巴基斯坦拉合尔旁遮普人群的哮喘易感性相关。

Major histocompatibility complex class II polymorphic variants are associated with asthma predisposition in the Punjabi population of Lahore, Pakistan.

机构信息

Centre of Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.

The Children's Hospital and The Institute of Child Health, Pediatric Pulmonology, Lahore, Pakistan.

出版信息

Clin Respir J. 2021 Apr;15(4):374-381. doi: 10.1111/crj.13309. Epub 2020 Nov 30.

Abstract

INTRODUCTION

Various genome wide association studies have manifested that Major Histocompatibility Complex (MHC) region on chromosome 6p21 houses many potential candidate genes for asthma.

OBJECTIVE

This Case-Control association study was planned to determine the association of 10 Single Nucleotide Polymorphisms (SNPs), residing within and around MHC genes' region on chromosome 6p21, with Asthma in Punjabi population of Lahore, Pakistan.

METHODS

A total of 161 subjects, 61 physician-diagnosed asthma patients and 100 age-matched healthy controls, were recruited from Lahore, a city in Punjab. Ten single nucleotide polymorphisms (SNPs) (rs9378249, rs2070600, rs404860, rs6689, rs1049124, rs1063355, rs1049225, rs1049219, rs7773955 and rs928976) located within or near AGER, NOTCH and HLA genes in MHC region, were genotyped in both patients and controls using single base extension reaction and capillary electrophoresis-based genetic analyser. Statistical models were applied using SHEsis Plus. Results were adjusted for various cofactors (age, gender and environment) and by applying multiple corrections. Haplotype and linkage disequilibrium analyses were performed on Haploview software v4.1.

RESULTS

Three of the studied SNPs rs1049124, rs1049219 and rs7773955 show independent significant association with asthma under allelic and genotypic models. Two of the haplotypes, H7 and H13, "CTAATTT" and "CCACTAT", respectively, for rs2070600, rs404860, rs6689, rs1049124, rs1063355, rs1049219 and rs7773955, are found to be significantly associated with the disease.

CONCLUSION

This study reports association of SNP variants residing on HLA-DQB1 and HLA-DQA2 genes and haplotypes H7 and H13 on genomic region 6p21 with Asthma in the Punjabi population of Lahore, Pakistan.

摘要

介绍

多项全基因组关联研究表明,6 号染色体 p21 上的主要组织相容性复合体(MHC)区域存在许多哮喘的潜在候选基因。

目的

本病例对照关联研究旨在确定位于 6 号染色体 p21 上 MHC 基因区域内和周围的 10 个单核苷酸多态性(SNP)与巴基斯坦拉合尔旁遮普人群哮喘之间的关联。

方法

共招募了 161 名受试者,包括 61 名医生诊断的哮喘患者和 100 名年龄匹配的健康对照者,他们均来自旁遮普的拉合尔市。10 个单核苷酸多态性(SNP)(rs9378249、rs2070600、rs404860、rs6689、rs1049124、rs1063355、rs1049225、rs1049219、rs7773955 和 rs928976)位于 MHC 区域内或附近的AGER、NOTCH 和 HLA 基因中,使用单碱基延伸反应和毛细管电泳遗传分析仪在患者和对照者中进行了基因分型。使用 SHEsis Plus 应用统计模型。结果调整了各种协变量(年龄、性别和环境),并进行了多次校正。在 Haploview 软件 v4.1 上进行了单体型和连锁不平衡分析。

结果

在所研究的 3 个 SNP 中,rs1049124、rs1049219 和 rs7773955 在等位基因和基因型模型下均与哮喘有独立的显著关联。rs2070600、rs404860、rs6689、rs1049124、rs1063355、rs1049219 和 rs7773955 上的两个单体型 H7 和 H13,分别为“CTAATTT”和“CCACTAT”,与该疾病显著相关。

结论

本研究报告了位于 HLA-DQB1 和 HLA-DQA2 基因上的 SNP 变体以及位于 6 号染色体 p21 基因组区域上的单体型 H7 和 H13 与巴基斯坦拉合尔旁遮普人群哮喘之间的关联。

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