Amany Abd Elaal Aiad, Sahar Mohamed El-Haggar, Amal Mohamed El-Barbary, Dalia Refat El-Afify
{"title":"二甲双胍作为肥胖膝关节骨关节炎患者的辅助疗法。","authors":"Amany Abd Elaal Aiad, Sahar Mohamed El-Haggar, Amal Mohamed El-Barbary, Dalia Refat El-Afify","doi":"10.1007/s10787-024-01495-y","DOIUrl":null,"url":null,"abstract":"<p><strong>Aims: </strong>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.</p><p><strong>Patients and methods: </strong>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.</p><p><strong>Results: </strong>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).</p><p><strong>Conclusion: </strong>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.</p><p><strong>Clinicaltrials: </strong></p><p><strong>Gov id: </strong>NCT05638893/Registered December 6, 2022 - Retrospectively.</p>","PeriodicalId":13551,"journal":{"name":"Inflammopharmacology","volume":" ","pages":"2349-2359"},"PeriodicalIF":4.6000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11300470/pdf/","citationCount":"0","resultStr":"{\"title\":\"Metformin as adjuvant therapy in obese knee osteoarthritis patients.\",\"authors\":\"Amany Abd Elaal Aiad, Sahar Mohamed El-Haggar, Amal Mohamed El-Barbary, Dalia Refat El-Afify\",\"doi\":\"10.1007/s10787-024-01495-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aims: </strong>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.</p><p><strong>Patients and methods: </strong>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.</p><p><strong>Results: </strong>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).</p><p><strong>Conclusion: </strong>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. 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引用次数: 0
摘要
目的:考虑到二甲双胍的抗炎和软骨保护作用,本研究旨在探讨二甲双胍作为肥胖膝骨关节炎(OA)患者辅助疗法的疗效:在这项随机、双盲、安慰剂对照研究中,50名肥胖膝关节OA患者被随机分配到两组,二甲双胍组(25人)每天口服二甲双胍500毫克,同时口服塞来昔布200毫克,每天一次;安慰剂组(25人)每天口服安慰剂片剂,同时口服塞来昔布200毫克,每天一次,连续治疗12周。对软骨低聚基质蛋白(COMP)、I型胶原C端交联端肽(CTX-1)和白细胞介素1-β(IL-1β)的血清水平进行了测定,同时对基线和12周后的西安大略和麦克马斯特大学关节炎指数(WOMAC)进行了评分,以评估膝关节疼痛、僵硬和身体功能:治疗 12 周后,与安慰剂组相比,二甲双胍组血清中 COMP、CTX-1 和 IL-1β 的水平明显降低(分别为 p = 0.0081、p = 0.0106 和 p = 0.0223)。此外,二甲双胍组的 WOMAC 总评分也有明显改善(p 结论:二甲双胍作为一种辅助治疗药物,能显著改善 WOMAC 总评分:二甲双胍作为肥胖膝关节 OA 患者的辅助治疗药物,可能对软骨退化和炎症产生有益影响,血清 COMP、CTX-1 和 IL-1β 水平的显著下降就证明了这一点。此外,二甲双胍还能改善临床疗效,WOMAC评分的显著改善就证明了这一点:Gov id:NCT05638893/Registered December 6, 2022 - Retrospectively.
Metformin as adjuvant therapy in obese knee osteoarthritis patients.
Aims: 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.
Patients and methods: 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.
Results: 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).
Conclusion: 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.
Clinicaltrials:
Gov id: NCT05638893/Registered December 6, 2022 - Retrospectively.
期刊介绍:
Inflammopharmacology is the official publication of the Gastrointestinal Section of the International Union of Basic and Clinical Pharmacology (IUPHAR) and the Hungarian Experimental and Clinical Pharmacology Society (HECPS). Inflammopharmacology publishes papers on all aspects of inflammation and its pharmacological control emphasizing comparisons of (a) different inflammatory states, and (b) the actions, therapeutic efficacy and safety of drugs employed in the treatment of inflammatory conditions. The comparative aspects of the types of inflammatory conditions include gastrointestinal disease (e.g. ulcerative colitis, Crohn''s disease), parasitic diseases, toxicological manifestations of the effects of drugs and environmental agents, arthritic conditions, and inflammatory effects of injury or aging on skeletal muscle. The journal has seven main interest areas:
-Drug-Disease Interactions - Conditional Pharmacology - i.e. where the condition (disease or stress state) influences the therapeutic response and side (adverse) effects from anti-inflammatory drugs. Mechanisms of drug-disease and drug disease interactions and the role of different stress states
-Rheumatology - particular emphasis on methods of measurement of clinical response effects of new agents, adverse effects from anti-rheumatic drugs
-Gastroenterology - with particular emphasis on animal and human models, mechanisms of mucosal inflammation and ulceration and effects of novel and established anti-ulcer, anti-inflammatory agents, or antiparasitic agents
-Neuro-Inflammation and Pain - model systems, pharmacology of new analgesic agents and mechanisms of neuro-inflammation and pain
-Novel drugs, natural products and nutraceuticals - and their effects on inflammatory processes, especially where there are indications of novel modes action compared with conventional drugs e.g. NSAIDs
-Muscle-immune interactions during inflammation [...]