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突尼斯患者中HLA - DR/DQ多态性与慢性炎性脱髓鞘性多发性神经根神经病(CIDP)的关联。

Association of HLA-DR/DQ polymorphism with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) in Tunisian patients.

作者信息

Mrad Meriem, Fekih-Mrissa Najiba, Mansour Malek, Seyah Aicha, Riahi Anis, Gritli Nasreddine, Mrissa Ridha

机构信息

Université Tunis el Manar, Faculté des Science de Tunis, El Manar, Tunisia; Hôpital Militaire Principal d'Instruction de Tunis, Service d'Hématologie, Laboratoire de Biologie Moléculaire, 1008 Montfleury, Tunisia.

出版信息

Transfus Apher Sci. 2013 Dec;49(3):623-6. doi: 10.1016/j.transci.2013.07.024. Epub 2013 Aug 3.

Abstract

BACKGROUND AND OBJECTIVE

Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an immune-mediated disorder of the peripheral nervous system (PNS). The aim of this study was to investigate associations between HLA-DR/DQ alleles and CIDP in Tunisian patients.

PATIENTS AND METHODS

HLA DR/DQ genotyping was performed using polymerase chain reaction sequence-specific primers (PCR-SSP) with 36 CIDP patients and 100 healthy individuals serving as the control group.

RESULTS

CIDP in Tunisian patients was found to be associated with the HLA-DRB113 allele (pc=0.03) (where pc denotes the Bonferroni corrected probability value). Moreover, the two haplotypes, DRB113/DQB106 (22.22% of patients vs. 8.5% of controls, pc=0.017) and DRB107/DQB1*03 (13.88% of patients vs. 3% of controls, pc=0.005), were found to confer a susceptibility to CIDP.

CONCLUSION

To our knowledge, this is the first study performed to analyze the association of HLA-DRB1/DQB1 alleles on CIDP susceptibility in a Tunisian population.

摘要

背景与目的

慢性炎症性脱髓鞘性多发性神经根神经病(CIDP)是一种免疫介导的周围神经系统(PNS)疾病。本研究旨在调查突尼斯患者中HLA - DR/DQ等位基因与CIDP之间的关联。

患者与方法

采用聚合酶链反应序列特异性引物(PCR - SSP)对36例CIDP患者和100名健康个体作为对照组进行HLA DR/DQ基因分型。

结果

发现突尼斯患者中的CIDP与HLA - DRB113等位基因相关(pc = 0.03)(其中pc表示经Bonferroni校正的概率值)。此外,还发现两种单倍型,DRB113/DQB106(患者中占22.22%,对照组中占8.5%,pc = 0.017)和DRB107/DQB1*03(患者中占13.88%,对照组中占3%,pc = 0.005),会使患者易患CIDP。

结论

据我们所知,这是第一项分析突尼斯人群中HLA - DRB1/DQB1等位基因与CIDP易感性之间关联的研究。

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