Nawaz Haq, Ali Asma, Rehman Tanzila, Aslam Amna
Department of Biochemistry, Bahauddin Zakariya University, Multan, 60800, Pakistan.
Department of Chemistry, The Women University Multan, Multan, 60800, Pakistan.
Clin Rheumatol. 2021 May;40(5):1767-1778. doi: 10.1007/s10067-020-05438-0. Epub 2020 Oct 3.
INTRODUCTION/OBJECTIVES: Non-steroidal anti-inflammatory drugs (NSAIDs) are effective in reducing pain and inflammation in rheumatoid arthritis and other joint- and muscle-associated diseases. However, the extensive, long-term, and over the counter administration of NSAIDs may cause various side effects in the patients. In the present study, the chronological effect of NSAIDs on oxidative stress and antioxidant status in patients with rheumatoid arthritis was studied.
The study included 100 female individuals categorized in four major groups: (1) control group consisting of age- and gender-matched healthy individuals, (2) NRA-NSAID individuals taking NSAIDs without any history of RA, (3) RA individuals with a history of RA but not taking NSAIDs, and (4) RA-NSAID individuals with chronic RA and taking NSAIDs for a long period. The sera of the participants were analyzed for the oxidative stress and antioxidant status.
The RA-NSAID group showed the significantly highest oxidative stress, in terms of malondialdehyde content and lipid-reducing ability as determined in thiocyanate and hemoglobin-induced linoleic acid systems. However, the free radical scavenging ability of the RA-NSAID group, against 2,2-diphenyl-1-picrylhydrazyl, hydroxyl, superoxide, and 2,2-azino-bis-tetrazolium sulfate radicals, was found to be lower than those of the other study groups. The regression analysis of the experimental data showed a significant positive relationship between duration of NSAID intake and malondialdehyde production, lipid-reducing ability, and metal chelating ability in the RA-NSAID patients. The free radical scavenging abilities of the RA-NSAID group were negatively correlated with the duration of NSAID intake.
The prolonged use of NSAIDs significantly increased the oxidative stress and decrease the antioxidant potential of both the RA patients and NRA individuals. The study provides awareness to the public particularly the RA patients regarding the risk of oxidative stress-associated abnormalities caused by the frequent and prolonged use of NSAIDs for temporary relief from pain. Key Points • The study presents the effects of long-term use of non-steroidal anti-inflammatory drugs (NSAIDs) on antioxidant status of patients with rheumatoid arthritis. • The continuous administration of NSAIDs has been found to significantly increase the oxidative stress of the patients with rheumatoid arthritis as well as the individuals with no signs of rheumatoid arthritis. • The prolonged NSAID therapy also decreased the antioxidant potential of the patients with rheumatoid arthritis as well as the individuals with no signs of rheumatoid arthritis. • The study would be a significant and valuable contribution to the literature for the awareness regarding the use of NSAIDs.
引言/目的:非甾体抗炎药(NSAIDs)在减轻类风湿关节炎及其他关节和肌肉相关疾病的疼痛和炎症方面有效。然而,NSAIDs的广泛、长期及非处方使用可能会给患者带来各种副作用。在本研究中,我们研究了NSAIDs对类风湿关节炎患者氧化应激和抗氧化状态的时间效应。
该研究纳入了100名女性个体,分为四个主要组:(1)对照组,由年龄和性别匹配的健康个体组成;(2)NRA-NSAID组,服用NSAIDs但无类风湿关节炎病史;(3)RA组,有类风湿关节炎病史但未服用NSAIDs;(4)RA-NSAID组,患有慢性类风湿关节炎且长期服用NSAIDs。分析参与者血清的氧化应激和抗氧化状态。
就硫氰酸盐和血红蛋白诱导的亚油酸系统中测定的丙二醛含量和脂质还原能力而言,RA-NSAID组显示出显著最高的氧化应激。然而,发现RA-NSAID组对2,2-二苯基-1-苦基肼、羟基、超氧阴离子和2,2-联氮-双-(3-乙基苯并噻唑啉-6-磺酸)自由基的自由基清除能力低于其他研究组。实验数据的回归分析表明,RA-NSAID患者中NSAID摄入持续时间与丙二醛生成、脂质还原能力和金属螯合能力之间存在显著正相关。RA-NSAID组的自由基清除能力与NSAID摄入持续时间呈负相关。
长期使用NSAIDs显著增加了类风湿关节炎患者和NRA个体的氧化应激并降低了其抗氧化潜力。该研究使公众尤其是类风湿关节炎患者意识到频繁和长期使用NSAIDs以暂时缓解疼痛会导致氧化应激相关异常的风险。要点 • 该研究展示了长期使用非甾体抗炎药(NSAIDs)对类风湿关节炎患者抗氧化状态的影响。 • 已发现持续使用NSAIDs会显著增加类风湿关节炎患者以及无类风湿关节炎迹象个体的氧化应激。 • 长期NSAID治疗也降低了类风湿关节炎患者以及无类风湿关节炎迹象个体的抗氧化潜力。 • 该研究将为有关NSAIDs使用的认识方面的文献做出重大且有价值的贡献。