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HLA-DRB1 等位基因异质性影响多发性硬化症的严重程度以及在西澳大利亚的发病风险。

HLA-DRB1 allele heterogeneity influences multiple sclerosis severity as well as risk in Western Australia.

机构信息

Centre for Neuromuscular and Neurological Disorders, University of Western Australia.

出版信息

J Neuroimmunol. 2010 Feb 26;219(1-2):109-13. doi: 10.1016/j.jneuroim.2009.11.015. Epub 2009 Dec 16.

Abstract

Susceptibility to multiple sclerosis (MS) has been consistently associated with the Human Leukocyte Antigen (HLA)-DRB11501 genotype, however effects on disease severity and clinical outcome have varied in different populations. We present the results of a high-resolution HLA-DRB1 genotyping and genotype-phenotype correlation study in a large West Australian MS cohort. Our findings indicate that in this population, which is of largely Anglo-Celtic and Northern European origin, HLA-DRB11501 is not only a strong determinant of disease risk but may also be associated with disease severity as measured by the Multiple Sclerosis Severity Score (MSSS), with the MSSS increasing by an estimated 0.51 per DRB11501 allele. We also found evidence that the HLA-DRB11201 allele is associated with less severe disease.

摘要

多发性硬化症(MS)的易感性与人类白细胞抗原(HLA)-DRB11501 基因型一直相关,然而在不同人群中,其对疾病严重程度和临床结果的影响有所不同。我们报告了在一个大型西澳大利亚 MS 队列中进行的 HLA-DRB1 高分辨率基因分型和基因型-表型相关性研究的结果。我们的研究结果表明,在这个主要由盎格鲁-撒克逊人和北欧血统的人群中,HLA-DRB11501 不仅是疾病风险的强决定因素,而且可能与多发性硬化严重程度评分(MSSS)有关,估计每增加一个 DRB11501 等位基因,MSSS 就会增加 0.51。我们还发现证据表明 HLA-DRB11201 等位基因与疾病的严重程度较低有关。

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