Department of Rheumatology and Clinical Immunology, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.
Scand J Rheumatol. 2009;38(4):256-62. doi: 10.1080/03009740802552469.
The association of systemic lupus erythematosus (SLE) with the human leucocyte antigen (HLA) region is well known. In this study, we analysed the involvement of the HLA region in susceptibility for SLE in a stable founder, Caucasian population of SLE patients.
We performed an extensive screen of the entire HLA region on 103 SLE patients and family-based controls. Both single locus association analysis and haplotype sharing analysis were performed. The Additional Disease Locus Test (ADLT) was applied to examine the nature of the observed associations and to distinguish true causal associations from associations due to linkage disequilibrium (LD).
Significant associations were observed at markers in the HLA class I, class II, and class III regions using both haplotype sharing and single locus methods. The haplotype sharing methods revealed the most significant difference at marker D6S1666 in the HLA class II region (p(HSS) = 0.00037, p(CROSS) = 1.7 x 10(-5)). The most significant result for single locus association was shown at marker D6S265 in the HLA class I region (p = 0.00019). The ADLT demonstrated that these markers represent independent associations.
HLA class I, class II, and class III are associated with SLE, but only class I and class II contribute independently to increased risk of SLE.
红斑狼疮(SLE)与人类白细胞抗原(HLA)区域的关联是众所周知的。在这项研究中,我们分析了 HLA 区域在稳定的欧洲血统的 SLE 患者群体中对 SLE 易感性的影响。
我们对 103 名 SLE 患者和基于家族的对照者进行了整个 HLA 区域的广泛筛查。进行了单基因座关联分析和单倍型共享分析。应用附加疾病基因座检验(ADLT)来检验观察到的关联的性质,并将真正的因果关联与由于连锁不平衡(LD)引起的关联区分开来。
使用单倍型共享和单基因座方法,在 HLA Ⅰ类、Ⅱ类和Ⅲ类区域的标记物中观察到了显著的关联。单倍型共享方法在 HLA Ⅱ类区域的标记物 D6S1666 处显示出最显著的差异(p(HSS) = 0.00037,p(CROSS) = 1.7 x 10(-5))。单基因座关联的最显著结果显示在 HLA Ⅰ类区域的标记物 D6S265 处(p = 0.00019)。ADLT 表明这些标记物代表独立的关联。
HLA Ⅰ类、Ⅱ类和Ⅲ类与 SLE 相关,但只有Ⅰ类和Ⅱ类独立增加 SLE 的风险。