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验证现有的基因表达谱在类风湿关节炎患者抗 TNF 治疗中的应用。

Validation study of existing gene expression signatures for anti-TNF treatment in patients with rheumatoid arthritis.

机构信息

Department of Medicine, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

出版信息

PLoS One. 2012;7(3):e33199. doi: 10.1371/journal.pone.0033199. Epub 2012 Mar 21.

DOI:10.1371/journal.pone.0033199
PMID:22457743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3310059/
Abstract

So far, there are no means of identifying rheumatoid arthritis (RA) patients who will fail to respond to tumour necrosis factor blocking agents (anti-TNF), prior to treatment. We set out to validate eight previously reported gene expression signatures predicting therapy outcome. Genome-wide expression profiling using Affymetrix GeneChip Exon 1.0 ST arrays was performed on RNA isolated from whole blood of 42 RA patients starting treatment with infliximab or adalimumab. Clinical response according to EULAR criteria was determined at week 14 of therapy. Genes that have been reported to be associated with anti-TNF treatment were extracted from our dataset. K-means partition clustering was performed to assess the predictive value of the gene-sets. We performed a hypothesis-driven analysis of the dataset using eight existing gene sets predictive of anti-TNF treatment outcome. The set that performed best reached a sensitivity of 71% and a specificity of 61%, for classifying the patients in the current study. We successfully validated one of eight previously reported predictive expression profile. This replicated expression signature is a good starting point for developing a prediction model for anti-TNF treatment outcome that can be used in a daily clinical setting. Our results confirm that gene expression profiling prior to treatment is a useful tool to predict anti-TNF (non) response.

摘要

迄今为止,尚无手段可在使用肿瘤坏死因子阻断剂(anti-TNF)治疗前,确定哪些类风湿关节炎(RA)患者对其治疗反应不佳。我们旨在验证之前报道的八个预测治疗效果的基因表达特征。对 42 名开始接受英夫利昔单抗或阿达木单抗治疗的 RA 患者的全血 RNA 进行 Affymetrix GeneChip Exon 1.0 ST 芯片的全基因组表达谱分析。根据 EULAR 标准,在治疗的第 14 周确定临床反应。从我们的数据集中提取了与抗 TNF 治疗相关的基因。通过 K-均值分区聚类来评估基因集的预测价值。我们使用八种先前报道的预测抗 TNF 治疗结果的基因集对数据集进行了假设驱动分析。表现最佳的集合达到了 71%的敏感性和 61%的特异性,用于对当前研究中的患者进行分类。我们成功验证了之前报道的八个预测表达谱中的一个。这个复制的表达特征是开发可在日常临床环境中使用的抗 TNF 治疗效果预测模型的良好起点。我们的结果证实,治疗前的基因表达谱分析是预测抗 TNF(非)反应的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6de4/3310059/e462bcd675f0/pone.0033199.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6de4/3310059/e462bcd675f0/pone.0033199.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6de4/3310059/e462bcd675f0/pone.0033199.g001.jpg

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