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β-防御素1单核苷酸多态性与特应性皮炎的关联

Association of beta-defensin 1 single nucleotide polymorphism with atopic dermatitis.

作者信息

Mohamed Hala Ghareeb, Abbas Amal, El-Kabarity Rania Hamdy, Diab Heba Mahmoud El-sayed

机构信息

Department of Clinical Pathology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

出版信息

Egypt J Immunol. 2009;16(2):125-38.

Abstract

Atopic dermatitis (AD) is a chronic relapsing, pruritic, inflammatory skin disease, which results from a complex interplay between genetic and environmental factors. Defensins are broadly dispersed family of antimicrobial peptides which are classified into 2 distinct families: the alpha-defensins and the beta-defensins. The primary function of defensins is to protect the skin from invasion by foreign pathogens. Previous studies suggested that single nucleotide polymorphisms (SNPs) of the beta-defensin 1 gene (DEFB1) could be involved in the development of AD. The Aim of the study is to examine DEFB1 gene to gain a better understanding of their role in the pathophysiology of AD patients and their involvement in AD susceptibility and severity. 35 atopic patients and 10 healthy volunteers as controls were investigated. They were subjected to analysis of absolute eosinophil count, total and specific IgE and detection of Beta-defensin-1 gene polymorphism at position 692 and 1654 using PCR amplification and restriction analysis. We observed significant difference in the distribution of the DEFB1 AIG polymorphism at 692 (P<0.01) in AD patients compared to controls, but not at 1654. A statistical significant association between DEFB1 692 GG genotype and elevated total serum IgE level (P<0.01), and between DEFB1 692 GG and AG genotypes & 1654 AA genotype and high absolute eosinophil count (P<0.05) were found. Concerning Specific IgE there was significant association between DEFB1 692 GG genotype and positive specific IgE to dermatophytes and HDM (House Dust Mite) (P1<0.01) while DEFB1 1654AA genotype shows significant association with positive specific IgE to cockroaches (P<0.05). Regarding SCORAD severity index, there was significant statistical association between DEFB1 692 GG and AG & DEFB1 1654 AA and AG genotype with severe AD disease (P<0.05). The correlation between atopic markers and SCORAD severity index shows that there was a significant statistical relationship between serum levels of total IgE (P<0.01), absolute eosinophil count (P<0.01), specific IgE to cat (P<0.05), HDM (P<0.01) and cockroaches (P<0.01) and SCORAD. Our findings support previously studies suggesting that DEFB1 gene is one of the candidate genes for atopy. G allele at site 692& AA genotype at site 1654 may be useful as markers for AD susceptibility and severity

摘要

特应性皮炎(AD)是一种慢性复发性、瘙痒性炎症性皮肤病,由遗传和环境因素之间的复杂相互作用引起。防御素是广泛分布的一类抗菌肽,分为两个不同的家族:α-防御素和β-防御素。防御素的主要功能是保护皮肤免受外来病原体的侵袭。先前的研究表明,β-防御素1基因(DEFB1)的单核苷酸多态性(SNP)可能与AD的发生有关。本研究的目的是检测DEFB1基因,以更好地了解其在AD患者病理生理学中的作用及其与AD易感性和严重程度的关系。对35例特应性患者和10名健康志愿者作为对照进行了研究。他们接受了绝对嗜酸性粒细胞计数、总IgE和特异性IgE分析,并使用PCR扩增和限制性分析检测了692和1654位点的β-防御素-1基因多态性。我们观察到,与对照组相比,AD患者中692位点的DEFB1 AIG多态性分布存在显著差异(P<0.01),但1654位点没有。发现DEFB1 692 GG基因型与血清总IgE水平升高之间存在统计学显著关联(P<0.01),以及DEFB1 692 GG和AG基因型与1654 AA基因型与高绝对嗜酸性粒细胞计数之间存在统计学显著关联(P<0.05)。关于特异性IgE,DEFB1 692 GG基因型与对皮肤癣菌和屋尘螨(HDM)的特异性IgE阳性之间存在显著关联(P1<0.01),而DEFB1 1654AA基因型与对蟑螂的特异性IgE阳性之间存在显著关联(P<0.05)。关于SCORAD严重程度指数,DEFB1 692 GG和AG与DEFB1 1654 AA和AG基因型与重度AD疾病之间存在显著统计学关联(P<0.05)。特应性标志物与SCORAD严重程度指数之间的相关性表明,血清总IgE水平(P<0.01)、绝对嗜酸性粒细胞计数(P<0.01)、对猫的特异性IgE(P<0.05)、HDM(P<0.01)和蟑螂的特异性IgE(P<0.01)与SCORAD之间存在显著统计学关系。我们的研究结果支持先前的研究,表明DEFB1基因是特应性的候选基因之一。692位点的G等位基因和1654位点的AA基因型可能作为AD易感性和严重程度的标志物。

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