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韩国FcγRIIIB基因多态性与系统性红斑狼疮的关联

The association between fcgammaRIIIB polymorphisms and systemic lupus erythematosus in Korea.

作者信息

Hong C H, Lee J S, Lee H S, Bae S C, Yoo D H

机构信息

Hospital for Rheumatic Diseases, Hanyang University College of Medicine, Seoul, Korea.

出版信息

Lupus. 2005;14(5):346-50. doi: 10.1191/0961203305lu2086oa.

Abstract

Polymorphisms of FcgammaR have been proposed as genetic factors that influence susceptibility to SLE. FcgammaRIIIB polymorphism in systemic lupus erythematosus (SLE) have been studied in various populations, but the results were inconsistent. The aim of this study was to determine the association of FcgammaRIIIB polymorphism in Korean lupus patients. One-hundred and eighty-three SLE patients (166 female, 17 male) meeting 1982 ACR criteria and 300 Korean disease-free controls were enrolled. Genotyping for the FcgammaRIIIB NA1/NA2 was performed by PCR of genomic DNA using allele-specific primers. There was no significant skewing in the distribution of the three FcgammaRIIIB genotypes, and alleles between SLE and the controls. The frequency of FcgammaRIIIB genotypes in SLE patients and controls was FcgammaRIIIB NA1/NA1 27.9% versus 26%, NA1/NA2 55.2% versus 51.7%, NA2/NA2 16.9% versus 22.3%, respectively. The gene frequencies of NA1 allele were 0.56 in the SLE and 0.52 in controls, respectively. Among clinical manifestations, thrombocytopenia was more common in FcgammaRIIIB NA2/NA2 genotype (P = 0.04, OR 2.4, 95% CI 1.0-5.4), and NA2 allele (P = 0.03, OR 1.7, 95% CI 1.1-2.8). Although FcgammaRIIIB polymorphism was not associated with the development of SLE in Korean, thrombocytopenia was associated with FcgammaRIIIB NA2/NA2 genotype, and NA2 allele.

摘要

FcγR多态性被认为是影响系统性红斑狼疮(SLE)易感性的遗传因素。已在不同人群中研究了系统性红斑狼疮(SLE)中的FcγRIIIB多态性,但结果不一致。本研究的目的是确定韩国狼疮患者中FcγRIIIB多态性的相关性。纳入了183例符合1982年美国风湿病学会(ACR)标准的SLE患者(166例女性,17例男性)和300名无疾病的韩国对照者。使用等位基因特异性引物通过基因组DNA的PCR对FcγRIIIB NA1/NA2进行基因分型。SLE患者和对照者之间的三种FcγRIIIB基因型和等位基因分布没有明显偏差。SLE患者和对照者中FcγRIIIB基因型的频率分别为:FcγRIIIB NA1/NA1为27.9%对26%,NA1/NA2为55.2%对51.7%,NA2/NA2为16.9%对22.3%。NA1等位基因的基因频率在SLE患者中为0.56,在对照者中为0.52。在临床表现中,血小板减少症在FcγRIIIB NA2/NA2基因型中更常见(P = 0.04,比值比[OR] 2.4,95%可信区间[CI] 1.0 - 5.4),在NA2等位基因中也更常见(P = 0.03,OR 1.7,95% CI 1.1 - 2.8)。虽然FcγRIIIB多态性与韩国人SLE的发病无关,但血小板减少症与FcγRIIIB NA2/NA2基因型和NA2等位基因相关。

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