Disease response in rheumatoid arthritis across four biologic therapies associates with improvement in paraoxonase-1 activity and oxylipins.

IF 5.1 2区 医学 Q1 RHEUMATOLOGY RMD Open Pub Date : 2024-10-26 DOI:10.1136/rmdopen-2024-004829
Amir A Razmjou, Joel M Kremer, Dimitrios A Pappas, Jeffrey R Curtis, Jennifer Wang, Ani Shahbazian, David A Elashoff, Rong Guo, David Meriwether, Dawoud Sulaiman, Ellen O'Connor, Srinivasa T Reddy, Christina Charles-Schoeman
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Abstract

Objective: Paraoxonase-1 (PON1) is a high-density lipoprotein (HDL)-associated enzyme, that has been implicated as a biomarker of cardiovascular risk in patients with rheumatoid arthritis (RA). We aimed to investigate how different biologic therapies affect levels of PON1 and oxylipins.

Methods: 1213 adult patients with RA in the Comparative Effectiveness Registry to study Therapies for Arthritis and Inflammatory CoNditions cohort study with moderate-to-high disease activity (Clinical Disease Activity Index (CDAI) >10) who initiated a new biologic (tocilizumab (TCZ), n=296; abatacept, n=374; tumour necrosis factor inhibitors, n=427; rituximab, n=116) were followed prospectively with serum specimens analysed for PON1 activity by arylesterase (ARYL), lactonase (LAC) and PON assays at baseline and after 6 months of biologic therapy. A targeted panel of oxylipins was evaluated by liquid chromatography-mass spectrometry/mass spectrometry in a subset of patients with the lowest and highest 6-month Disease Activity Score 28 (DAS28)-C reactive protein (CRP) responses in each treatment group.

Results: PON1 activity generally increased in the entire cohort after 6 months of new biologic therapy, showing the greatest, most consistent increases in the TCZ group. Increases in all three PON1 domains associated with significant decreases in disease activity in DAS28-CRP/CDAI (p<0.05), and increases in LAC/ARYL were significantly associated with the American College of Rheumatology 20/50/70 responses (OR (95% CI) of 1.12 (1.04, 1.22) and 1.13 (1.04, 1.23), p<0.01, respectively), after controlling for other RA disease characteristics. Some oxylipins, including 12-hydroxyeicosatetraenoic acid correlated with RA disease activity measures.

Conclusion: Improvement in disease activity across four classes of biologics is associated with enhanced PON1 activity, which has significant implications for cardiovascular safety.

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四种生物疗法对类风湿性关节炎的疾病反应与副氧合酶-1活性和氧化脂的改善有关。
研究目的副氧合酶-1(PON1)是一种与高密度脂蛋白(HDL)相关的酶,被认为是类风湿性关节炎(RA)患者心血管风险的生物标志物。我们旨在研究不同的生物疗法如何影响 PON1 和氧化脂蛋白的水平。研究方法在关节炎和炎症性关节炎治疗方法比较疗效登记研究队列研究中,1213 名患有中度至高度疾病活动(临床疾病活动指数 (CDAI) >10)的成年 RA 患者开始使用一种新的生物制剂(托西珠单抗 (TCZ),n=296;阿巴他赛,374 人;肿瘤坏死因子抑制剂,427 人;利妥昔单抗,116 人)的患者进行了前瞻性随访,并在基线和生物制剂治疗 6 个月后通过丙烯酯酶 (ARYL)、内酯酶 (LAC) 和 PON 检测法对血清标本进行了 PON1 活性分析。通过液相色谱-质谱法/质谱法,对每个治疗组中6个月疾病活动评分28(DAS28)-C反应蛋白(CRP)反应最低和最高的一组患者的样本进行了有针对性的氧化脂素评估:结果:在接受新的生物疗法6个月后,整个组群的PON1活性普遍升高,其中TCZ组的升高幅度最大、最稳定。所有三个PON1域的增加都与DAS28-CRP/CDAI中疾病活动性的显著下降有关(p结论:四种生物制剂的疾病活动性均有所改善:四类生物制剂的疾病活动性改善与 PON1 活性增强有关,这对心血管安全性具有重要意义。
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来源期刊
RMD Open
RMD Open RHEUMATOLOGY-
CiteScore
7.30
自引率
6.50%
发文量
205
审稿时长
14 weeks
期刊介绍: RMD Open publishes high quality peer-reviewed original research covering the full spectrum of musculoskeletal disorders, rheumatism and connective tissue diseases, including osteoporosis, spine and rehabilitation. Clinical and epidemiological research, basic and translational medicine, interesting clinical cases, and smaller studies that add to the literature are all considered.
期刊最新文献
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