Department of Physiology, Istanbul University, Istanbul Faculty of Medicine, Capa 34093, Istanbul, Turkey.
Arthritis Res Ther. 2012 Feb 6;14(1):R27. doi: 10.1186/ar3730.
HLA-B51 and HLA-B52 are two close human leukocyte antigen (HLA) allele groups with minor amino acid differences. However, they are associated with two different vasculitides (HLA-B51 in Behçet's disease and HLA-B52 in Takayasu's arteritis (TAK)) and with major clinical and immunological differences. In this study, we aimed to screen a large cohort of TAK patients from Turkey for the presence of HLA-B51 and HLA-B52 as susceptibility and severity factors.
TAK patients (n = 330) followed at a total of 15 centers were included in the study. The mean age of the patients was 37.8 years, and 86% were women. DNA samples from the patients and healthy controls (HC; n = 210) were isolated, and the presence of HLA-B51 or HLA-B52 was screened for by using PCR with sequence-specific primers.
We found a significant association of HLA-B52 with TAK (20.9% vs HC = 6.7%, P = 0.000, OR = 3.7, 95% CI = 2.02 to 6.77). The distribution of HLA-B51 did not differ between TAK patients and HCs (22.7% vs 24.8%, OR = 0.9, 95% CI = 0.60 to 1.34). The presence of HLA-B52 decreased in late-onset patients (> 40 years of age; 12.0%, P = 0.024, OR = 0.43, 95% CI = 0.20 to 0.91). Patients with angiographic type I disease with limited aortic involvement also had a lower presence of HLA-B52 compared to those with all other disease subtypes (13.1% vs 26%, P = 0.005, OR = 0.43, 95% CI = 0.23 to 0.78).
In this study, the previously reported association of TAK with HLA-B52 in other populations was confirmed in patients from Turkey. The functional relevance of HLA-B52 in TAK pathogenesis needs to be explored further.
HLA-B51 和 HLA-B52 是两个密切相关的人类白细胞抗原(HLA)等位基因群体,仅存在微小的氨基酸差异。然而,它们与两种不同的血管炎(HLA-B51 与 Behçet 病相关,HLA-B52 与 Takayasu 动脉炎(TAK)相关)以及主要的临床和免疫学差异相关。在这项研究中,我们旨在筛选来自土耳其的大量 TAK 患者,以确定 HLA-B51 和 HLA-B52 是否为易感性和严重程度的因素。
本研究纳入了在 15 家中心就诊的 330 例 TAK 患者。患者的平均年龄为 37.8 岁,86%为女性。从患者和健康对照者(HC;n=210)中分离出 DNA 样本,使用聚合酶链反应(PCR)和序列特异性引物来筛选 HLA-B51 或 HLA-B52 的存在。
我们发现 HLA-B52 与 TAK 显著相关(20.9% vs HC=6.7%,P=0.000,OR=3.7,95%CI=2.02 至 6.77)。TAK 患者和 HC 之间 HLA-B51 的分布无差异(22.7% vs 24.8%,OR=0.9,95%CI=0.60 至 1.34)。HLA-B52 在发病年龄晚于 40 岁的患者中减少(12.0%,P=0.024,OR=0.43,95%CI=0.20 至 0.91)。与其他疾病亚型相比,HLA-B52 在仅有局限性主动脉受累的血管造影 I 型疾病患者中的存在率较低(13.1% vs 26%,P=0.005,OR=0.43,95%CI=0.23 至 0.78)。
在本研究中,我们在来自土耳其的患者中证实了先前报道的 HLA-B52 与 TAK 之间的关联。需要进一步探讨 HLA-B52 在 TAK 发病机制中的功能相关性。