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HLA - A*2402和一个微卫星(D6S248)是巴斯克患者中强直性脊柱炎的次要独立易感性标志物。

HLA-A*2402 and a microsatellite (D6S248) are secondary independent susceptibility markers to ankylosing spondylitis in Basque patients.

作者信息

de Juan M D, Reta A, Belzunegui J, Figueroa M, Maruri N, Cuadrado E

机构信息

Immunology Department, Laboratorio Unificado, Hospital Donosita, San Sebastián, Basque Country, Spain.

出版信息

Hum Immunol. 2004 Feb;65(2):175-80. doi: 10.1016/j.humimm.2003.11.006.

Abstract

Ankylosing spondylitis (AS) is universally associated with human leukocyte antigen B27 (HLA-B27), although other genes could determine the development and clinical expression of the disease. HLA-A9 (A2402) allele was previously found to be associated in Basque patients. The objective of this study is to perform a more precise analysis of microsatellite polymorphisms in HLA-A2402 and B27 haplotypes to elucidate the significance of this association. A group of 50 unrelated AS patients and 113 controls of Basque origin were studied. Eight microsatellites in the class I major histocompatibility complex region with vicinity to HLA-A and -B were analyzed and the strength of allelic associations to AS and linkage disequilibrium (LD) between alleles were evaluated. Allele 15 at the microsatellite locus D6S248, 1000 Kb telomeric to HLA-A showed a strong positive association with the disease (OR:6; pc=4.7x10(-4)) and it could not be explained by LD to HLA-B27, HLA-A2402 or any other loci. We found that D6S248-15 allele together with HLA-A2402 could be B27-independent markers of additional susceptibility gene/s localised in the region telomeric to HLA-A in Basque AS patients.

摘要

强直性脊柱炎(AS)普遍与人类白细胞抗原B27(HLA - B27)相关,尽管其他基因可能决定该疾病的发生发展及临床表现。此前发现HLA - A9(A2402)等位基因在巴斯克患者中存在关联。本研究的目的是对HLA - A2402和B27单倍型中的微卫星多态性进行更精确分析,以阐明这种关联的意义。研究了一组50名无亲缘关系的AS患者和113名巴斯克血统的对照者。分析了I类主要组织相容性复合体区域中靠近HLA - A和 - B的8个微卫星,并评估了等位基因与AS的关联强度以及等位基因之间的连锁不平衡(LD)。位于HLA - A端粒1000 Kb处的微卫星位点D6S248的等位基因15与该疾病呈强正相关(比值比:6;pc = 4.7x10(-4)),且无法用与HLA - B27、HLA - A2402或任何其他位点的LD来解释。我们发现,在巴斯克AS患者中,D6S248 - 15等位基因与HLA - A2402一起可能是位于HLA - A端粒区域的其他易感基因的B27非依赖性标记。

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