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HLA-DRB1*1501的标签单核苷酸多态性rs3135388与多发性硬化易感性显著相关:通过实时PCR进行经济高效的高通量检测。

The tag SNP for HLA-DRB1*1501, rs3135388, is significantly associated with multiple sclerosis susceptibility: cost-effective high-throughput detection by real-time PCR.

作者信息

Zivković Maja, Stanković Aleksandra, Dincić Evica, Popović Milan, Popović Smiljana, Raicević Ranko, Alavantić Dragan

机构信息

Vinca Institute of Nuclear Sciences, Laboratory for Radiobiology and Molecular Genetics, Belgrade, Serbia.

出版信息

Clin Chim Acta. 2009 Aug;406(1-2):27-30. doi: 10.1016/j.cca.2009.05.004. Epub 2009 May 9.

Abstract

BACKGROUND

Recently a high-resolution HLA and SNP map was defined and the analysis provided informative tag SNPs that capture much of the common variation in the MHC region. This concept enables detection of smaller number of SNPs, making it "surrogate" markers for haplotype associated with certain disease. The SNP rs3135388 was proposed as a tagging SNP for DRB1*1501/DQB10602 alleles, associated with MS. The aim of the study was to investigate the HLA rs3135388 genotypes in association with MS in patients from Serbia.

METHODS

Two hundred sixty nine consecutive patients from Serbia with relapse-remitting and secondary progressive MS were recruited for the study. Genomic DNA was isolated from peripheral blood cells. We designed the TaqMan assay for high-throughput genotyping of HLA rs3135388 on 7500 Real-Time PCR System.

RESULTS

We found significantly higher frequency of rs3135388 A allele carriers in MS patients compared to controls (p<0.001, chi(2)). In our population the carriers of one A allele had adjusted OR 2.09 (95% CI 1.41-3.09, p<0.001) for MS susceptibility.

CONCLUSION

We assessed significant association of rs3135388 A allele carriership with MS in patients from Serbia. This HLA-DRB1*1501 "surrogate" marker is useful in association studies in MS.

摘要

背景

最近定义了一个高分辨率的HLA和SNP图谱,分析提供了信息丰富的标签SNP,可捕获MHC区域的大部分常见变异。这一概念能够检测数量较少的SNP,使其成为与某些疾病相关单倍型的“替代”标记。SNP rs3135388被提议作为与MS相关的DRB1*1501/DQB10602等位基因的标签SNP。本研究的目的是调查塞尔维亚患者中HLA rs3135388基因型与MS的关联。

方法

招募了269名来自塞尔维亚的复发缓解型和继发进展型MS患者进行研究。从外周血细胞中分离基因组DNA。我们设计了TaqMan分析方法,用于在7500实时PCR系统上对HLA rs3135388进行高通量基因分型。

结果

我们发现MS患者中rs3135388 A等位基因携带者的频率显著高于对照组(p<0.001,卡方检验)。在我们的人群中,携带一个A等位基因的个体患MS的校正OR为2.09(95%CI 1.41 - 3.09,p<0.001)。

结论

我们评估了塞尔维亚患者中rs3135388 A等位基因携带者与MS之间的显著关联。这种HLA - DRB1*1501“替代”标记在MS的关联研究中很有用。

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