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Nonsteroidal anti-inflammatory drugs may protect against Parkinson disease.非甾体抗炎药可能预防帕金森病。
Neurology. 2007 Nov 6;69(19):1836-42. doi: 10.1212/01.wnl.0000279519.99344.ad.
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Anti-inflammatory drugs in the 21st century.21世纪的抗炎药物。
Subcell Biochem. 2007;42:3-27. doi: 10.1007/1-4020-5688-5_1.
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Int J Clin Pract. 2007 Aug;61(8):1270-7. doi: 10.1111/j.1742-1241.2007.01453.x. Epub 2007 Jun 22.
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Long term NSAID treatment inhibits COX-2 synthesis in the knee synovial membrane of patients with osteoarthritis: differential proinflammatory cytokine profile between celecoxib and aceclofenac.长期使用非甾体抗炎药治疗可抑制骨关节炎患者膝关节滑膜中COX-2的合成:塞来昔布与醋氯芬酸之间促炎细胞因子谱的差异
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Brain Res Brain Res Rev. 2005 Apr;48(2):352-9. doi: 10.1016/j.brainresrev.2004.12.024.
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塞来昔布和依托考昔治疗期间炎症性关节炎患者血清和滑液中促炎细胞因子变化的体内研究及其与视觉模拟评分法(VAS)疼痛变化和滑膜渗透指数的相关性

In vivo study of pro-inflammatory cytokine changes in serum and synovial fluid during treatment with celecoxib and etoricoxib and correlation with VAS pain change and synovial membrane penetration index in patients with inflammatory arthritis.

作者信息

Theodoridou Athina, Gika Helen, Diza Eudoxia, Garyfallos Alexandros, Settas Loucas

机构信息

4 Department of Internal Medicine Hippokrateion University Hospital, Aristotle University of Thessaloniki Medical School, Thessaloniki, Greece.

Rheumatology Division, 1 Department of Internal Medicine, Aristotle University of Thessaloniki Medical School, Thessaloniki, Greece.

出版信息

Mediterr J Rheumatol. 2017 Mar 28;28(1):33-40. doi: 10.31138/mjr.28.1.33. eCollection 2017 Mar.

DOI:10.31138/mjr.28.1.33
PMID:32185252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7045925/
Abstract

OBJECTIVES

To determine the impact of celecoxib and etoricoxib therapy on serum and synovial fluid levels of IL-1β, IL-6, TNF-α, sTNFR1, sTNFR2 and IL-1Ra in patients with inflammatory arthritis. To determine the correlation between cytokine changes and synovial membrane penetration index of the study drugs, and pain VAS change.

METHODS

Fifty-one patients with inflammatory synovial fluid accumulation in a knee joint (33 women), randomized on 3 groups of 17 each: 100 mg b.i.d. celecoxib treated group, 90 mg o.d. etoricoxib treated group, and the control group with no NSAID treatment. Cytokines serum and synovial fluid levels as well as membrane penetration index were assessed prior and after treatment.

RESULTS

Celecoxib led to decrease of both synovial fluid and serum levels of IL-6 (p=0.017 and p=0.003, respectively). In the etoricoxib treated group synovial fluid IL-6 concentration was significantly decreased after treatment (p=0.019). Correlating the study drugs penetration index with the change of cytokines and their receptors levels, positive correlation was found with the reduction of synovial fluid IL-1β for the celecoxib (p=0.032) and with the increase of synovial fluid sTNFR1 for the etoricoxib group (p=0.028). Pain VAS reduction was positively correlated with decrease of synovial fluid IL-1β (p=0.041) and IL-6 levels (p<0.005) and negative with synovial fluid sTNFR1 changes (p=0.045) in celecoxib group, and negative with serum TNF-α decrease (p=0.044) in the etoricoxib group.

CONCLUSION

Our results suggest that celecoxib and etoricoxib inhibit the inflammatory cytokines, mostly in synovial fluid but also in serum, causing through this mechanism, decrease of inflammation, irrespective to COX-2 inhibition.

摘要

目的

确定塞来昔布和依托考昔治疗对炎性关节炎患者血清及滑液中白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)、可溶性肿瘤坏死因子受体1(sTNFR1)、可溶性肿瘤坏死因子受体2(sTNFR2)和白细胞介素-1受体拮抗剂(IL-1Ra)水平的影响。确定细胞因子变化与研究药物滑膜穿透指数以及疼痛视觉模拟评分(VAS)变化之间的相关性。

方法

51例膝关节有炎性滑液积聚的患者(33例女性),随机分为3组,每组17例:100mg每日两次塞来昔布治疗组、90mg每日一次依托考昔治疗组和未接受非甾体抗炎药(NSAID)治疗的对照组。在治疗前后评估细胞因子的血清和滑液水平以及滑膜穿透指数。

结果

塞来昔布导致滑液和血清中IL-6水平均降低(分别为p=0.017和p=0.003)。在依托考昔治疗组中,治疗后滑液IL-6浓度显著降低(p=0.019)。将研究药物的穿透指数与细胞因子及其受体水平的变化相关联,发现塞来昔布与滑液IL-1β的降低呈正相关(p=0.032),依托考昔组与滑液sTNFR1的增加呈正相关(p=0.028)。在塞来昔布组中,疼痛VAS降低与滑液IL-1β降低(p=0.041)和IL-6水平降低(p<0.005)呈正相关,与滑液sTNFR1变化呈负相关(p=0.045),在依托考昔组中与血清TNF-α降低呈负相关(p=0.044)。

结论

我们的结果表明,塞来昔布和依托考昔抑制炎性细胞因子,主要是在滑液中,但也在血清中,通过这种机制导致炎症减轻,与COX-2抑制无关。