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通过对免疫相关基因座的关联和连锁分析,研究东中撒丁岛奠基人群多发性硬化症的遗传易感性。

Investigating multiple sclerosis genetic susceptibility on the founder population of east-central Sardinia via association and linkage analysis of immune-related loci.

机构信息

Department of Brain and Behavioral Science, University of Pavia, Pavia, Italy.

Department of Brain and Behavioral Science, University of Pavia, Pavia, Italy; Institute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Bolzano, Italy.

出版信息

Mult Scler. 2018 Dec;24(14):1815-1824. doi: 10.1177/1352458517732841. Epub 2017 Sep 21.

Abstract

BACKGROUND

A wealth of single-nucleotide polymorphisms (SNPs) responsible for multiple sclerosis (MS) susceptibility have been identified; however, they explain only a fraction of MS heritability.

OBJECTIVES

We contributed to discovery of new MS susceptibility SNPs by studying a founder population with high MS prevalence.

METHODS

We analyzed ImmunoChip data from 15 multiplex families and 94 unrelated controls from the Nuoro Province, Sardinia, Italy. We tested each SNP for both association and linkage with MS, the linkage being explored in terms of identity-by-descent (IBD) sharing excess and using gene dropping to compute a corresponding empirical -value. By targeting regions that are both associated and in linkage with MS, we increase chances of identifying interesting genomic regions.

RESULTS

We identified 486 MS-associated (< 1 × 10) and 18,426 MS-linked (< 0.05) SNPs. A total of 111 loci were both linked and associated with MS, 18 of them pointing to 14 non-major histocompatibility complex (MHC) genes, and 93 of them located in the MHC region.

CONCLUSION

We discovered new suggestive signals and confirmed some previously identified ones. We believe this to represent a significant step toward an understanding of the genetic basis of MS.

摘要

背景

已经发现了许多与多发性硬化症(MS)易感性相关的单核苷酸多态性(SNPs);然而,它们仅解释了 MS 遗传率的一部分。

目的

我们通过研究一个多发性硬化症患病率较高的创始人群体,为发现新的多发性硬化症易感性 SNPs 做出了贡献。

方法

我们分析了来自意大利撒丁岛努罗省的 15 个多态家族和 94 个无关对照的 ImmunoChip 数据。我们测试了每个 SNP 与 MS 的关联和连锁,连锁通过同源性(IBD)共享过剩来探索,并使用基因丢弃来计算相应的经验值。通过针对与 MS 相关且连锁的区域,我们增加了识别有趣基因组区域的机会。

结果

我们确定了 486 个与 MS 相关(<1×10)和 18426 个与 MS 连锁(<0.05)的 SNPs。共有 111 个位点与 MS 连锁且相关,其中 18 个指向 14 个非主要组织相容性复合体(MHC)基因,93 个位于 MHC 区域。

结论

我们发现了新的提示性信号,并证实了一些先前确定的信号。我们相信这是理解多发性硬化症遗传基础的重要一步。

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