Human leukocyte antigen-DRB1 alleles in patients with sarcoidosis from Northeast Iran

Z. Mirfeizi, M. Sahebari, S. Nabavi, Masoumeh Salari, Masoud Saghafi, Z. Rezaieyazdi, N. Valizadeh, Houshang Raaftpanah
{"title":"Human leukocyte antigen-DRB1 alleles in patients with sarcoidosis from Northeast Iran","authors":"Z. Mirfeizi, M. Sahebari, S. Nabavi, Masoumeh Salari, Masoud Saghafi, Z. Rezaieyazdi, N. Valizadeh, Houshang Raaftpanah","doi":"10.22631/RR.2018.69997.1052","DOIUrl":null,"url":null,"abstract":"Sarcoidosis a systemic granulomatous disorder of unknown etiology with varying clinical pictures. HLA genes, especially HLA-DRB1, have been shown to be candidates for the etiology of sarcoidosis. This study examined the association between the polymorphism of HLA-DRB1 alleles and sarcoidosis in Iranian subjects. The study population included 58 patients with sarcoidosis and 68 healthy controls. Genomic DNA was extracted, and the polymorphisms of the HLA-DRB1 alleles were determined using a polymerase chain reaction with sequence-specific primer (PCR-SSP). The frequency of HLA-DRB1*07 was higher in sarcoidosis patients (25.8%) than in controls (15.3%); however no significant difference was observed between the two groups (P>0.05). The frequency of HLA-DRB1*11 was higher in the control group (31.9%) than in cases (22.4%), but no significant difference was detected between the groups (P>0.05). The results of the present study showed that there is no association between HLA-DRB1 alleles and susceptibility to sarcoidosis in Mashhad, Northeast Iran. Further studies with large sample sizes are required in order to clarify this issue.","PeriodicalId":87314,"journal":{"name":"Journal of rheumatology research","volume":"12 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of rheumatology research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22631/RR.2018.69997.1052","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Sarcoidosis a systemic granulomatous disorder of unknown etiology with varying clinical pictures. HLA genes, especially HLA-DRB1, have been shown to be candidates for the etiology of sarcoidosis. This study examined the association between the polymorphism of HLA-DRB1 alleles and sarcoidosis in Iranian subjects. The study population included 58 patients with sarcoidosis and 68 healthy controls. Genomic DNA was extracted, and the polymorphisms of the HLA-DRB1 alleles were determined using a polymerase chain reaction with sequence-specific primer (PCR-SSP). The frequency of HLA-DRB1*07 was higher in sarcoidosis patients (25.8%) than in controls (15.3%); however no significant difference was observed between the two groups (P>0.05). The frequency of HLA-DRB1*11 was higher in the control group (31.9%) than in cases (22.4%), but no significant difference was detected between the groups (P>0.05). The results of the present study showed that there is no association between HLA-DRB1 alleles and susceptibility to sarcoidosis in Mashhad, Northeast Iran. Further studies with large sample sizes are required in order to clarify this issue.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
伊朗东北部结节病患者白细胞抗原- drb1等位基因分析
结节病是一种病因不明、临床表现各异的系统性肉芽肿性疾病。HLA基因,特别是HLA- drb1,已被证明是结节病病因的候选基因。本研究探讨了伊朗人HLA-DRB1等位基因多态性与结节病之间的关系。研究人群包括58例结节病患者和68例健康对照。提取基因组DNA,采用序列特异性引物聚合酶链反应(PCR-SSP)测定HLA-DRB1等位基因多态性。结节病患者HLA-DRB1*07的表达频率(25.8%)高于对照组(15.3%);两组间差异无统计学意义(P>0.05)。HLA-DRB1*11阳性率对照组(31.9%)高于对照组(22.4%),组间差异无统计学意义(P>0.05)。本研究结果表明,在伊朗东北部马什哈德,HLA-DRB1等位基因与结节病易感性之间没有关联。为了澄清这个问题,需要进一步的大样本研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
The prevalence of Covid-19 in patients with Rheumatoid Arthritis receiving classic Disease-Modifying Anti Rheumatic Drugs The association of main blood groups and development of Systemic Lupus Erythematosus and its organ involvements Syndrome of Inappropriate Secretion of Antidiuretic Hormone and Severe Thrombocytopenia in an Immunosuppressive Systemic Lupus Erythematosus Patient: A Case Report Pituitary involvement in a case of granulomatosis with polyangiitis: case report and literature review Musculoskeletal Manifestations of COVID-19: A Systematic Search and Review
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1