Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, 1530 3rd Avenue South, SHEL 178, Birmingham, AL 35294-2182, USA.
Rheumatol Int. 2013 Jan;33(1):129-37. doi: 10.1007/s00296-011-2355-3. Epub 2012 Jan 12.
Gene expression profiling may be used to stratify patients by disease severity to test the hypothesis that variable disease outcome has a genetic component. In order to define unique expression signatures in African American rheumatoid arthritis (RA) patients with severe erosive disease, we undertook a gene expression study using samples of RNA from peripheral blood mononuclear cells (PBMCs). RNA from baseline PBMC samples of 96 African American RA patients with early RA (<2 years disease duration) was hybridized to cDNA probes of the Illumina Human HT-V3 expression array. Expression analyses were performed using the ca. 25,000 cDNA probes, and then expression levels were compared to the total number of erosions in radiographs of the hands and feet at baseline and 36 months. Using a false discovery rate cutoff of Q = 0.30, 1,138 genes at baseline and 680 genes at 36 months significantly correlated with total erosions. No evidence of a signal differentiating disease progression, or change in erosion scores between baseline and 36 months, was found. Further analyses demonstrated that the differential gene expression signature was localized to the patients with the most erosive disease (>10 erosions). Ingenuity Pathway Analysis demonstrated that genes with fold change greater than 1.5 implicated immune pathways such as CTLA signaling in cytotoxic T lymphocytes. These results demonstrate that CLEAR patients with early RA having the most severe erosive disease, as compared to more mild cases (<10 erosions), may be characterized by a set of differentially expressed genes that represent biological pathways with relevance to autoimmune disease.
基因表达谱分析可用于根据疾病严重程度对患者进行分层,以检验这样一种假设,即不同的疾病结局具有遗传成分。为了确定严重侵蚀性疾病的非裔美国类风湿关节炎(RA)患者中独特的表达特征,我们进行了一项基因表达研究,使用来自外周血单核细胞(PBMC)的 RNA 样本。96 名早期 RA(<2 年病程)非裔美国 RA 患者基线 PBMC 的 RNA 与 Illumina Human HT-V3 表达阵列的 cDNA 探针杂交。使用大约 25000 个 cDNA 探针进行表达分析,然后将表达水平与基线和 36 个月时手部和足部 X 光片的总侵蚀数进行比较。使用错误发现率截止值 Q = 0.30,基线时有 1138 个基因,36 个月时有 680 个基因与总侵蚀数显著相关。在基线和 36 个月之间,没有发现区分疾病进展或侵蚀评分变化的信号。进一步的分析表明,差异表达基因特征定位于侵蚀性疾病最严重的患者(>10 处侵蚀)。通路分析表明, fold change 大于 1.5 的基因涉及 CTLA 信号转导等免疫途径在细胞毒性 T 淋巴细胞中。这些结果表明,与更轻度病例(<10 处侵蚀)相比,早期 RA 的 CLEAR 患者中具有最严重侵蚀性疾病的患者可能具有一组差异表达的基因,这些基因代表与自身免疫性疾病相关的生物学途径。