The Association of HLA-A, B and DRB1 with Buerger's Disease

Publish Year: 1398
نوع سند: مقاله ژورنالی
زبان: English
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JR_RBMB-8-2_008

تاریخ نمایه سازی: 22 دی 1399

Abstract:

Background: Thromboangiitis obliterans (TAO), also known as Burger’s disease, is a devastating disease affecting the arteries and veins of the upper and lower distal limbs most commonly afflicting young male smokers of low socioeconomic status. The expression of human leukocyte antigen (HLA)-A, B and –DRB1 genes have been implicated in the pathogenesis of TAO. Our study aimed to examine the association of different HLA-A, B and –DRB1 genes in TAO patients in the Iranian population. Methods: A case-control study examining 55 Iranian patients with TAO and 500 healthy subjects was performed in Imam Reza hospital, Mashhad, Iran. The prevalence of major histocompatibility complex (MHC) class I (-A, -B) and class II (-DRB) alleles were determined for each participant. Results: Our results revealed the HLA-A*03 (odds ratio [OR]=5.394), HLA-A*24 (OR=5.143), HLA-A*31 (OR=4.251), HLA-A*11 (OR=3.034), HLA-B*27 (OR=6.680), HLA-B*15 (OR=3.959), HLA-B*07 (OR=3.698), HLA-B*51 (OR=3.370), HLA-B*44 (OR=3.326), HLA-DRB1*16 (OR=20.583), HLA-DRB1*04 (OR=8.960), HLA-DRB1*14 (OR=3.746), HLA-DRB1*03 (OR=2.303), and HLA-DRB1*15 (OR=2.111) alleles to occur at a significantly higher frequency in TAO patients compared to controls (p<0.05). The HLA-A*25, HLA-A*66, HLA-DRB1*08, HLA-DRB1*10, and HLA-DRB1*12 alleles resulted in infinite OR, and was associated with an increased risk of TAO. However, the alleles HLA-A*30, HLA-B*08, HLA-B*45, HLA-B*46, and HLA-B*53 were associated with a protective role against TAO with an OR = 0. Conclusions: This is the first study examining the HLA pattern in patients with Burger’s disease in the Iranian population. Our findings have revealed an association between HLA class I and II alleles with TAO.

Authors

Abbas Shapouri-Moghaddam

Immunology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Mojgan Mohammadi

Immunology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. & Allergy Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Hamid Reza Rahimi

Neurogenic Inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. & Department of Modern Sciences and Technologies, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Habibolah Esmaeili

Social Determination of Health Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Mahmoud Mahmoudi

Immunology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Mohammad-Hadi Saeed Modaghegh

Vascular and Endovascular Surgery Research Center, Imam Reza Hospital, Mashhad University of Medical Sciences, Iran.

Jalil Tavakol Afshari

Immunology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.