Department of Clinical Pharmacy, Faculty of Pharmacy, Tanta University, Tanta, 31527, Egypt.
Department of Physical Medicine, Rheumatology and Rehabilitation, Faculty of Medicine, Tanta University, Tanta, 31527, Egypt.
Inflammopharmacology. 2024 Aug;32(4):2349-2359. doi: 10.1007/s10787-024-01495-y. Epub 2024 Jun 13.
This study aimed at investigating the efficacy of metformin as adjuvant therapy for obese knee osteoarthritis (OA) patients, considering its anti-inflammatory and cartilage-protective effects.
In this randomized, double-blind, placebo-controlled study, 50 obese knee OA patients were assigned randomly to two groups, the metformin group (n = 25) which was treated with metformin 500 mg orally BID plus celecoxib 200 mg orally once daily, and the placebo group (n = 25) which was treated with placebo tablets BID plus celecoxib 200 mg orally once daily for 12 weeks. Cartilage Oligomeric Matrix Protein (COMP), C-terminal cross-linked telopeptide of type I collagen (CTX-1), and Interleukin 1-beta (IL-1β) serum levels were measured, while Western Ontario and McMaster Universities Arthritis Index (WOMAC) score assessed knee pain, stiffness, and physical function at baseline and after 12 weeks.
Following a 12-week treatment, the metformin group exhibited significantly reduced levels of COMP, CTX-1, and IL-1β in the serum compared to the placebo group (p = 0.0081, p = 0.0106, and p = 0.0223, respectively). Furthermore, metformin group produced significant improvements in WOMAC total scale (p < 0.0001), specifically in knee pain, stiffness, and physical function compared to placebo group (p < 0.0001, p < 0.0001, and p < 0.0001, respectively).
Metformin as an adjuvant therapy in obese knee OA patients may have beneficial effects on cartilage degradation and inflammation, as evidenced by the significant decreases in serum COMP, CTX-1, and IL-1β levels. Additionally, metformin may improve clinical outcomes, as shown by the significant improvements in WOMAC scores.
NCT05638893/Registered December 6, 2022 - Retrospectively.
本研究旨在探讨二甲双胍作为肥胖膝骨关节炎(OA)患者辅助治疗的疗效,考虑其抗炎和软骨保护作用。
在这项随机、双盲、安慰剂对照研究中,50 名肥胖膝 OA 患者被随机分为两组,二甲双胍组(n=25)接受二甲双胍 500mg 口服,每日 2 次,塞来昔布 200mg 口服,每日 1 次,安慰剂组(n=25)接受安慰剂片剂,每日 2 次,塞来昔布 200mg 口服,每日 1 次,共 12 周。测量软骨寡聚基质蛋白(COMP)、I 型胶原 C 端交联肽(CTX-1)和白细胞介素 1-β(IL-1β)血清水平,同时在基线和 12 周后使用西安大略和麦克马斯特大学骨关节炎指数(WOMAC)评分评估膝关节疼痛、僵硬和身体功能。
经过 12 周的治疗,与安慰剂组相比,二甲双胍组血清中 COMP、CTX-1 和 IL-1β 的水平显著降低(p=0.0081,p=0.0106 和 p=0.0223,分别)。此外,与安慰剂组相比,二甲双胍组 WOMAC 总分(p<0.0001),特别是膝关节疼痛、僵硬和身体功能(p<0.0001,p<0.0001 和 p<0.0001,分别)有显著改善。
二甲双胍作为肥胖膝骨关节炎患者的辅助治疗可能对软骨降解和炎症有有益的影响,这表现在血清 COMP、CTX-1 和 IL-1β 水平的显著降低。此外,二甲双胍可能改善临床结局,因为 WOMAC 评分的显著改善表明了这一点。
NCT05638893/于 2022 年 12 月 6 日注册-回顾性。