Literature DB >> 31333131

The Association Between Knee Osteoarthritis and HLA-DRB1*0101 in the East of Iran.

Omid Kooshkaki1,2, Elham Atabati3, Majid Shayesteh4, Fatemeh Salmani5, Gholamreza A Sarab6.   

Abstract

BACKGROUND: Osteoarthritis (OA) is a painful social problem, which breaks down the articular cartilage, causes the failure of synovial joints and subchondral bone sclerosis. OA etiology is not completely understood, but joint trauma, infection, obesity, and diseases are the most important risk factors for OA developing. Recent studies suggested inflammatory factors and genetic components can be involved in the pathogenesis of OA. Experimental evidences suggest a linkage between Human Leukocyte Antigen (HLA) genetic diversity and OA. But a few studies have been conducted in this subject.
OBJECTIVE: To investigate the association between HLA-DRB1*0101 and OA in Iranian patients.
METHODS: Thirty patients with knee osteoarthritis and 30 healthy people as the control group were included in the study. Sex, weight, age, Body mass index (BMI) and height of all participants were recorded. HLA-DRB1*0101 was typed by PCR using the sequence-specific primer.
RESULTS: Our results showed 80% of knee osteoarthritis patients were positively HLA-DRB1*0101 (n=24), while only 26.7% of controls were positive (n=8) (P= 0.015).
CONCLUSION: These findings proposed that there is a significant association between HLADRB1* 0101 and susceptibility to knee osteoarthritis. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

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Keywords:  HLA; HLA-DR alleles; HLA-DRB1 haplotypes; Osteoarthritis; iranian population; tissue Antigens.

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Year:  2020        PMID: 31333131     DOI: 10.2174/1573397115666190716114738

Source DB:  PubMed          Journal:  Curr Rheumatol Rev        ISSN: 1573-3971


  1 in total

1.  An integrative analysis of DNA methylation and transcriptome showed the dysfunction of MAPK pathway was involved in the damage of human chondrocyte induced by T-2 toxin.

Authors:  Xuena Yang; Xue Xiao; Lu Zhang; Bo Wang; Ping Li; Bolun Cheng; Chujun Liang; Mei Ma; Xiong Guo; Feng Zhang; Yan Wen
Journal:  BMC Mol Cell Biol       Date:  2022-01-17
  1 in total

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