Department of Biomedicine and Prevention, Section of Genetics, University of Rome "Tor Vergata", 00133 Rome, Italy.
Rheumatology, Allergology and Clinical Immunology, Department of System Medicine, University of Rome "Tor Vergata", 00133 Rome, Italy.
Int Immunopharmacol. 2024 Jun 15;134:112239. doi: 10.1016/j.intimp.2024.112239. Epub 2024 May 17.
We aimed to identify an expression profile of lncRNAs potentially related to treatment response in Psoriatic arthritis (PsA) patients, to be used as potential genomic biomarkers predictors of drug treatment effectiveness. In addition, we evaluated a possible association between lncRNAs genetic variants and the response to therapy using the clinical parameter of Disease Activity Index. For the expression study, we collected 48 treated PsA patients, monitoring the treatment response for 12 months. We initially used PCR Array and, then, we validated the results with qRT-PCR. We also retrospectively genotyped 163 treated PsA patients. Firstly, we observed a significant difference in the expression level between Responder and non-Responder patients, of 4 lncRNAs in the group of PsA patients treated with TNFi and of 3 lncRNAs in the group of patients treated with IL17i. Then, we confirmed a significant decrease of MEG3 expression in non-Responder patients compared to Responders, also considering separately the single groups of patients treated with TNFi and IL17i. In addition, our results seem to highlight a potential dose-dependent effect of rs941576 (MEG3) variant allele on Disease Activity Index. Our study suggests a possible role of the lncRNA MEG3 in the treatment response to biological drugs.
我们旨在确定与银屑病关节炎 (PsA) 患者治疗反应相关的 lncRNA 表达谱,将其用作药物治疗效果的潜在基因组生物标志物预测因子。此外,我们使用疾病活动指数的临床参数评估了 lncRNA 遗传变异与治疗反应之间的可能关联。在表达研究中,我们收集了 48 名接受治疗的 PsA 患者,监测治疗反应 12 个月。我们最初使用 PCR 阵列,然后使用 qRT-PCR 验证结果。我们还回顾性地对 163 名接受治疗的 PsA 患者进行了基因分型。首先,我们观察到在接受 TNFi 治疗的 PsA 患者组中,有 4 个 lncRNA 和在接受 IL17i 治疗的患者组中,有 3 个 lncRNA 的表达水平在应答者和非应答者之间存在显著差异。然后,我们确认与应答者相比,非应答者的 MEG3 表达明显下降,同时也分别考虑了接受 TNFi 和 IL17i 单一治疗的患者群体。此外,我们的结果似乎突出了 rs941576(MEG3)变异等位基因对疾病活动指数的潜在剂量依赖性影响。我们的研究表明,lncRNA MEG3 可能在生物药物治疗反应中发挥作用。