Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, 17 Haengdang-Dong, Seongdong-Gu, Seoul 133-792, South Korea.
Rheumatol Int. 2012 Jan;32(1):277-80. doi: 10.1007/s00296-010-1789-3. Epub 2011 Jan 18.
PXK was identified as a novel candidate gene for systemic lupus erythematosus (SLE) from genome-wide association studies (GWAS) in Caucasians. But a recent replication study in Hong Kong Chinese reported that PXK was not associated with SLE. The aim of this study was to determine whether PXK is associated with SLE in Koreans. We genotyped single nucleotide polymorphism (SNP) rs6445975 of PXK using the TaqMan assay in 527 Korean patients with SLE and 517 healthy Korean control subjects. Genotypic associations were assessed using multiple logistic regression models. Additional analyses were also performed by subphenotype stratification. No association was detected between PXK rs6445975 and SLE (odds ratio (OR) = 1.06, P = 0.57). PXK rs6445975 showed positive associations with photosensitivity (P = 0.02) and the production of anti-Sm Ab (P = 0.04) among SLE patients. Thus, the association of PXK rs6445975 with SLE that was previously observed in Caucasians was not replicated in Koreans or in Hong Kong Chinese. It is possible that PXK has different genetic contribution on SLE between Caucasians and Asians and that the gene is associated with disease subphenotypes rather than with overall susceptibility.
PXK 是从高加索人群的全基因组关联研究(GWAS)中鉴定出的系统性红斑狼疮(SLE)的一个新的候选基因。但最近在香港华人中的一项复制研究报告称,PXK 与 SLE 无关。本研究旨在确定 PXK 是否与韩国人群中的 SLE 有关。我们使用 TaqMan 检测法对 527 例韩国 SLE 患者和 517 例健康韩国对照的 PXK 单核苷酸多态性(SNP)rs6445975 进行了基因分型。采用多因素逻辑回归模型评估基因型关联。还通过亚表型分层进行了额外的分析。PXK rs6445975 与 SLE 之间未检测到关联(比值比(OR)=1.06,P=0.57)。PXK rs6445975 与 SLE 患者的光敏感(P=0.02)和抗 Sm Ab 的产生(P=0.04)呈正相关。因此,先前在高加索人群中观察到的 PXK rs6445975 与 SLE 的关联在韩国人和香港华人中没有得到复制。PXK 可能在高加索人群和亚洲人群中对 SLE 的遗传贡献不同,并且该基因与疾病亚表型相关,而不是与总体易感性相关。