Major histocompatibility complex class II polymorphic variants are associated with asthma predisposition in the Punjabi population of Lahore, Pakistan. (30th November 2020)

• Record Type: Journal Article
• Authors: Aslam, Raheela; Shahid, Mariam; Bano, Iqbal; Ayoub, Muhammad; Sabar, Muhammad Farooq; Altaf, Saba; Kousar, Samra; Ghani, Muhammad Usman; Husnain, Tayyab; Shahid, Ahmad Ali
• Is Part Of: Clinical respiratory journal. Volume 15:Number 4(2021)
• Page Start: 374
• Page End: 381
• Publication Date: 2020-11-30
• Subjects: asthma -- biomarker -- genetics -- MHC class II -- single nucleotide polymorphism; Respiratory organs -- Diseases -- Periodicals; Respiratory organs -- Periodicals; 616.24
• DOI: 10.1111/crj.13309
• Languages: English
• ISSNs: 1752-6981

Abstract

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.