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ERAP1 多态性相互作用及其与白塞病易感性的关联:基于模型的多因素降维算法 (MB-MDR) 的应用。

ERAP1 polymorphisms interactions and their association with Behçet's disease susceptibly: Application of Model-Based Multifactor Dimension Reduction Algorithm (MB-MDR).

机构信息

Department of Biostatistics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

Medical Biology Research Center, Health Technology Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

PLoS One. 2020 Feb 5;15(2):e0227997. doi: 10.1371/journal.pone.0227997. eCollection 2020.

Abstract

BACKGROUND

Behçet's disease (BD) is a chronic multi-systemic vasculitis with a considerable prevalence in Asian countries. There are many genes associated with a higher risk of developing BD, one of which is endoplasmic reticulum aminopeptidase-1 (ERAP1). In this study, we aimed to investigate the interactions of ERAP1 single nucleotide polymorphisms (SNPs) using a novel data mining method called Model-based multifactor dimensionality reduction (MB-MDR).

METHODS

We have included 748 BD patients and 776 healthy controls. A peripheral blood sample was collected, and eleven SNPs were assessed. Furthermore, we have applied the MB-MDR method to evaluate the interactions of ERAP1 gene polymorphisms.

RESULTS

The TT genotype of rs1065407 had a synergistic effect on BD susceptibility, considering the significant main effect. In the second order of interactions, CC genotype of rs2287987 and GG genotype of rs1065407 had the most prominent synergistic effect (β = 12.74). The mentioned genotypes also had significant interactions with CC genotype of rs26653 and TT genotype of rs30187 in the third-order (β = 12.74 and β = 12.73, respectively).

CONCLUSION

To the best of our knowledge, this is the first study investigating the interaction of a particular gene's SNPs in BD patients by applying a novel data mining method. However, future studies investigating the interactions of various genes could clarify this issue.

摘要

背景

白塞病(BD)是一种慢性多系统血管炎,在亚洲国家有相当高的发病率。有许多基因与更高的 BD 发病风险相关,其中之一是内质网氨肽酶-1(ERAP1)。在这项研究中,我们旨在使用一种新的数据挖掘方法——基于模型的多因素维度缩减(MB-MDR)来研究 ERAP1 单核苷酸多态性(SNP)的相互作用。

方法

我们纳入了 748 名 BD 患者和 776 名健康对照者。采集外周血样本,评估了 11 个 SNP。此外,我们应用 MB-MDR 方法来评估 ERAP1 基因多态性的相互作用。

结果

rs1065407 的 TT 基因型在考虑到显著的主效应时对 BD 易感性有协同作用。在二阶相互作用中,rs2287987 的 CC 基因型和 rs1065407 的 GG 基因型具有最显著的协同作用(β=12.74)。所述基因型与 rs26653 的 CC 基因型和 rs30187 的 TT 基因型在三阶(β=12.74 和β=12.73)中也具有显著的相互作用。

结论

据我们所知,这是第一项应用新的数据挖掘方法研究特定基因 SNP 在 BD 患者中相互作用的研究。然而,未来研究各种基因的相互作用可以阐明这一问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a89e/7001967/e0af51c701f8/pone.0227997.g001.jpg

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