Department of Neurology, University Medical Center of the Johannes Gutenberg-University Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.
Neurogenetics. 2012 Feb;13(1):83-6. doi: 10.1007/s10048-011-0305-6. Epub 2011 Nov 18.
Recent genome-wide association studies have implicated the "signal transducer and activator of transcription 3" gene (STAT3) as a putative new multiple sclerosis (MS) susceptibility locus. However, independent validation studies are sparse. Therefore, we performed a genetic association study of two STAT3 polymorphisms (rs744166 and rs2293152) in a large and independent German case-control sample of 5,904 subjects. We observed a nominally significant, albeit weak association between rs744166 and MS susceptibility (odds ratio = 1.09, P = 0.012) in our sample. This study supports the association between STAT3 and an increase in MS risk. Taking into account the functional role of STAT3, our results favour an involvement of T(h)17 lymphocytes in MS.
最近的全基因组关联研究表明,“信号转导和转录激活因子 3”基因(STAT3)可能是多发性硬化症(MS)的新易感基因位点。然而,独立的验证研究很少。因此,我们在一个包含 5904 名受试者的大型和独立的德国病例对照样本中,对两个 STAT3 多态性(rs744166 和 rs2293152)进行了遗传关联研究。我们观察到 rs744166 与 MS 易感性之间存在显著但较弱的关联(比值比=1.09,P=0.012)。本研究支持 STAT3 与 MS 风险增加之间的关联。考虑到 STAT3 的功能作用,我们的结果支持 T(h)17 淋巴细胞在 MS 中的参与。