• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

HLA - A和 - DRB1对斯堪的纳维亚多发性硬化症患者发病年龄、病程及严重程度的影响。

The impact of HLA-A and -DRB1 on age at onset, disease course and severity in Scandinavian multiple sclerosis patients.

作者信息

Smestad C, Brynedal B, Jonasdottir G, Lorentzen A R, Masterman T, Akesson E, Spurkland A, Lie B A, Palmgren J, Celius E G, Hillert J, Harbo H F

机构信息

Department of Neurology, Ullevål University Hospital, Oslo, Norway.

出版信息

Eur J Neurol. 2007 Aug;14(8):835-40. doi: 10.1111/j.1468-1331.2007.01825.x.

DOI:10.1111/j.1468-1331.2007.01825.x
PMID:17662002
Abstract

The human leucocyte antigen (HLA) class II haplotype DRB115-DQB106 (DR15-DQ6) is associated with susceptibility to multiple sclerosis (MS), and HLA class I associations in MS have also been reported. However, the influence of HLA class I and II alleles on clinical phenotypes in MS has not yet been completely studied. This study aimed at evaluating the impact of HLA-A and -DRB1 alleles on clinical variables in Scandinavian MS patients. The correlation between HLA-A or -DRB1 alleles and age at onset, disease course and Multiple Sclerosis Severity Score (MSSS) were studied in 1457 Norwegian and Swedish MS patients by regression analyses and Kruskal-Wallis rank sum test. Presence of HLA-DRB115 was correlated with younger age at onset of disease (corrected P = 0.009). No correlation was found between HLA-A and the variables studied. This study analysed the effect of HLA-A on clinical variables in a large Scandinavian sample set, but could not identify any significant contribution from HLA-A on the clinical phenotype in MS. However, associations between HLA-DRB115 and age at onset of MS were reproduced in this extended Scandinavian MS cohort.

摘要

人类白细胞抗原(HLA)II类单倍型DRB115 - DQB106(DR15 - DQ6)与多发性硬化症(MS)易感性相关,并且MS中HLA I类关联也已有报道。然而,HLA I类和II类等位基因对MS临床表型的影响尚未得到充分研究。本研究旨在评估HLA - A和 - DRB1等位基因对斯堪的纳维亚MS患者临床变量的影响。通过回归分析和Kruskal - Wallis秩和检验,对1457名挪威和瑞典MS患者的HLA - A或 - DRB1等位基因与发病年龄、病程和多发性硬化症严重程度评分(MSSS)之间的相关性进行了研究。HLA - DRB115的存在与疾病发病时较年轻的年龄相关(校正P = 0.009)。未发现HLA - A与所研究变量之间存在相关性。本研究分析了HLA - A对大量斯堪的纳维亚样本集中临床变量的影响,但未发现HLA - A对MS临床表型有任何显著贡献。然而,在这个扩大的斯堪的纳维亚MS队列中重现了HLA - DRB115与MS发病年龄之间的关联。

相似文献

1
The impact of HLA-A and -DRB1 on age at onset, disease course and severity in Scandinavian multiple sclerosis patients.HLA - A和 - DRB1对斯堪的纳维亚多发性硬化症患者发病年龄、病程及严重程度的影响。
Eur J Neurol. 2007 Aug;14(8):835-40. doi: 10.1111/j.1468-1331.2007.01825.x.
2
HLA-A confers an HLA-DRB1 independent influence on the risk of multiple sclerosis.HLA-A 赋予多发性硬化症风险 HLA-DRB1 独立影响。
PLoS One. 2007 Jul 25;2(7):e664. doi: 10.1371/journal.pone.0000664.
3
HLA-DRB1*1501, -DQB1*0301, -DQB1*0302, -DQB1*0602, and -DQB1*0603 alleles are associated with more severe disease outcome on MRI in patients with multiple sclerosis.HLA-DRB1*1501、-DQB1*0301、-DQB1*0302、-DQB1*0602和-DQB1*0603等位基因与多发性硬化症患者MRI上更严重的疾病结局相关。
Int Rev Neurobiol. 2007;79:521-35. doi: 10.1016/S0074-7742(07)79023-2.
4
Epistasis between HLA-DRB1 parental alleles in a Spanish cohort with multiple sclerosis.西班牙多发性硬化症队列中 HLA-DRB1 亲代等位基因之间的上位性。
J Neurol Sci. 2010 Nov 15;298(1-2):96-100. doi: 10.1016/j.jns.2010.07.026. Epub 2010 Sep 1.
5
Parent-of-origin of HLA-DRB1*1501 and age of onset of multiple sclerosis.人类白细胞抗原-DRB1*1501的亲本来源与多发性硬化症的发病年龄
J Hum Genet. 2009 Sep;54(9):547-9. doi: 10.1038/jhg.2009.69. Epub 2009 Jul 24.
6
Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis.HLA-DRB1基因座的异质性与多发性硬化症风险
Hum Mol Genet. 2006 Sep 15;15(18):2813-24. doi: 10.1093/hmg/ddl223. Epub 2006 Aug 11.
7
Multiple sclerosis: a modifying influence of HLA class I genes in an HLA class II associated autoimmune disease.多发性硬化症:HLA I类基因在一种与HLA II类相关的自身免疫性疾病中的调节作用。
Tissue Antigens. 2000 Feb;55(2):140-8. doi: 10.1034/j.1399-0039.2000.550205.x.
8
Influence of HLA-DRB1 allele heterogeneity on disease risk and clinical course in a West Australian MS cohort: a high-resolution genotyping study.在澳大利亚西部多发性硬化症队列中,HLA-DRB1 等位基因异质性对疾病风险和临床过程的影响:一项高分辨率基因分型研究。
Mult Scler. 2010 May;16(5):526-32. doi: 10.1177/1352458510362997. Epub 2010 Mar 5.
9
Relationship between HLA-DRB1* 11/15 genotype and susceptibility to multiple sclerosis in Iran.伊朗人群中HLA - DRB1*11/15基因型与多发性硬化易感性的关系。
J Neurol Sci. 2014 Oct 15;345(1-2):92-6. doi: 10.1016/j.jns.2014.07.013. Epub 2014 Jul 16.
10
No evidence for an effect of DNA methylation on multiple sclerosis severity at HLA-DRB1*15 or HLA-DRB5.未发现 DNA 甲基化对 HLA-DRB1*15 或 HLA-DRB5 多发性硬化严重程度的影响。
J Neuroimmunol. 2010 Jun;223(1-2):120-3. doi: 10.1016/j.jneuroim.2010.03.002. Epub 2010 Apr 14.

引用本文的文献

1
A two-years real-word study with fingolimod: early predictors of efficacy and an association between EBNA-1 IgG titers and multiple sclerosis progression.一项为期两年的芬戈莫德真实世界研究:疗效的早期预测指标以及 EBNA-1 IgG 滴度与多发性硬化进展之间的关联。
Front Immunol. 2024 Jun 7;15:1384411. doi: 10.3389/fimmu.2024.1384411. eCollection 2024.
2
The gut microbiome molecular mimicry piece in the multiple sclerosis puzzle.肠道微生物组分子模拟在多发性硬化症谜题中的作用。
Front Immunol. 2022 Aug 15;13:972160. doi: 10.3389/fimmu.2022.972160. eCollection 2022.
3
The influence of HLA-DRB1*15 on the relationship between microglia and neurons in multiple sclerosis normal appearing cortical grey matter.
HLA-DRB1*15 对多发性硬化症正常外观皮质灰质中小胶质细胞和神经元之间关系的影响。
Brain Pathol. 2022 Jul;32(4):e13041. doi: 10.1111/bpa.13041. Epub 2021 Dec 13.
4
The global prevalence of familial multiple sclerosis: an updated systematic review and meta-analysis.家族性多发性硬化症的全球患病率:一项更新的系统评价和荟萃分析。
BMC Neurol. 2021 Jun 28;21(1):246. doi: 10.1186/s12883-021-02267-9.
5
Anti-Myelin Oligodendrocyte Glycoprotein and Human Leukocyte Antigens as Markers in Pediatric and Adolescent Multiple Sclerosis: on Diagnosis, Clinical Phenotypes, and Therapeutic Responses.抗髓鞘少突胶质细胞糖蛋白和人类白细胞抗原作为儿童及青少年多发性硬化症的标志物:关于诊断、临床表型及治疗反应
Mult Scler Int. 2018 Nov 22;2018:8487471. doi: 10.1155/2018/8487471. eCollection 2018.
6
Onset Symptoms, Tobacco Smoking, and Progressive-Onset Phenotype Are Associated With a Delayed Onset of Multiple Sclerosis, and Marijuana Use With an Earlier Onset.起病症状、吸烟与渐进性起病表型与多发性硬化症的延迟发病相关,而使用大麻则与较早发病相关。
Front Neurol. 2018 Jun 8;9:418. doi: 10.3389/fneur.2018.00418. eCollection 2018.
7
Deconstruction of HLA-DRB1*04:01:01 and HLA-DRB1*15:01:01 class II haplotypes using next-generation sequencing in European-Americans with multiple sclerosis.采用新一代测序技术对多发性硬化症欧洲裔美国人 HLA-DRB1*04:01:01 和 HLA-DRB1*15:01:01 Ⅱ类单体型进行解构。
Mult Scler. 2019 May;25(6):772-782. doi: 10.1177/1352458518770019. Epub 2018 Apr 23.
8
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies.多发性硬化症风险基因座与 10 项研究的 7125 名个体疾病严重程度的关联
Neurol Genet. 2016 Aug 4;2(4):e87. doi: 10.1212/NXG.0000000000000087. eCollection 2016 Aug.
9
Association of HLA Genetic Risk Burden With Disease Phenotypes in Multiple Sclerosis.HLA 遗传风险负担与多发性硬化症疾病表型的关联。
JAMA Neurol. 2016 Jul 1;73(7):795-802. doi: 10.1001/jamaneurol.2016.0980.
10
Genetic determinants of risk and progression in multiple sclerosis.多发性硬化症风险及病情进展的遗传决定因素。
Clin Chim Acta. 2015 Sep 20;449:16-22. doi: 10.1016/j.cca.2015.01.034. Epub 2015 Feb 4.