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NFKB1-94ATTG 插入/缺失多态性(rs28362491)与寻常型天疱疮的关联。

Association of NFKB1 -94ATTG ins/del polymorphism (rs28362491) with pemphigus vulgaris.

机构信息

Laboratory of Medical Biology-Genetics, Medical School, Aristotle University, Thessaloniki, Greece.

2nd Department of Dermatology, Papageorgiou General Hospital, Medical School, Aristotle University, Thessaloniki, Greece.

出版信息

Exp Dermatol. 2019 Aug;28(8):972-975. doi: 10.1111/exd.13957. Epub 2019 Jun 6.

Abstract

Pemphigus vulgaris is a rare chronic blistering skin disease resulting from IgG autoantibodies directed against transmembrane desmosomal glycoprotein desmoglein 3 and is the most common form of pemphigus. Since interleukin-1 receptor-associated kinase (IRAK-1)/nuclear factor-kappa B (NF-kappa B) pathway plays an essential role in the pathogenesis of autoimmune diseases, the aim of the present study was to explore the role of polymorphisms in three genes, named IRAK1 (rs3027898), NFKBIA (rs696) and NFKB1 (-94ATTG insertion/deletion variant, - rs28362491), in PV susceptibility. Forty-four unrelated patients with PV (23 males) were enrolled in the study. Additionally, 77 ethnic matching healthy volunteers (45 males) with no personal or family history of chronic autoimmune or infectious diseases were studied. Strong statistical significant difference was observed between PV patients and controls for polymorphism -94 insertion/deletion ATTG in the promoter region of NFKB1 gene (P = 0.00005). Additional dedicated studies in larger groups of patients of various ethnicities are needed to replicate and confirm the preliminary findings.

摘要

寻常型天疱疮是一种罕见的慢性水疱性皮肤病,由针对跨膜桥粒糖蛋白桥粒芯糖蛋白 3 的 IgG 自身抗体引起,是天疱疮中最常见的类型。由于白介素-1 受体相关激酶 (IRAK-1)/核因子-κB (NF-κB) 途径在自身免疫性疾病的发病机制中起着至关重要的作用,本研究旨在探讨三个基因(IRAK1(rs3027898)、NFKBIA(rs696)和 NFKB1(-94ATTG 插入/缺失变体,-rs28362491))中的多态性在 PV 易感性中的作用。研究纳入了 44 名无关的 PV 患者(23 名男性)。此外,还研究了 77 名无慢性自身免疫或感染性疾病个人或家族史的、与患者种族匹配的健康志愿者(45 名男性)。在 NFKB1 基因启动子区域的 NFKB1 基因多态性 -94 插入/缺失 ATTG 中,PV 患者与对照组之间存在显著统计学差异(P=0.00005)。需要在更大的不同种族患者群体中进行专门的研究,以复制和确认初步发现。

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