Metformin for Knee Osteoarthritis in Patients With Overweight or Obesity

JAMA Pub Date : 2025-04-25 DOI:10.1001/jama.2025.3471
Feng Pan, Yuanyuan Wang, Yuan Z. Lim, Donna M. Urquhart, Mahnuma Mahfuz Estee, Anita E. Wluka, Rory Wolfe, Flavia M. Cicuttini
{"title":"Metformin for Knee Osteoarthritis in Patients With Overweight or Obesity","authors":"Feng Pan, Yuanyuan Wang, Yuan Z. Lim, Donna M. Urquhart, Mahnuma Mahfuz Estee, Anita E. Wluka, Rory Wolfe, Flavia M. Cicuttini","doi":"10.1001/jama.2025.3471","DOIUrl":null,"url":null,"abstract":"ImportancePreclinical and preliminary human evidence suggests that metformin, a first-line treatment for type 2 diabetes, reduces inflammation, preserves cartilage, and improves knee pain in knee osteoarthritis.ObjectiveTo evaluate the effects of metformin on knee pain at 6 months in participants with symptomatic knee osteoarthritis and overweight or obesity.Design, Setting, and ParticipantsCommunity-based randomized, parallel-group, double-blind, placebo-controlled clinical trial that used telemedicine to recruit and follow up participants remotely. Individuals with knee pain for 6 months or longer, a pain score greater than 40 mm on a 100-mm visual analog scale (VAS), and body mass index of 25 or higher were recruited from the community through local and social media advertisements in Victoria, Australia, between June 16, 2021, and August 1, 2023. Final follow-up occurred on February 8, 2024.InterventionsParticipants were randomly assigned to receive either oral metformin, 2000 mg/d (n = 54), or identical placebo (n = 53) for 6 months.Main Outcomes and MeasuresThe primary outcome was change in knee pain, measured using a 100-mm VAS (score range, 0-100; 100 = worst; minimum clinically important difference = 15) at 6 months.ResultsOf 225 participants assessed for eligibility, 107 (48%) were randomized (mean age, 58.8 [SD, 9.5] years; 68% female) and assigned to receive metformin or placebo. Eighty-eight participants (82%) completed the trial. At 6 months, the mean change in VAS pain was −31.3 mm in the metformin group and −18.9 mm in the placebo group (between-group difference, −11.4 mm; 95% CI, −20.1 to −2.6 mm; <jats:italic>P</jats:italic> = .01), corresponding to an effect size (standardized mean difference) of 0.43 (95% CI, 0.02-0.83). The most common adverse events were diarrhea (8 [15%] in the metformin group and 4 [8%] in the placebo group) and abdominal discomfort (7 [13%] in the metformin group and 5 [9%] in the placebo group).Conclusions and RelevanceThese results support use of metformin for treatment of symptomatic knee osteoarthritis in people with overweight or obesity. Because of the modest sample size, confirmation in a larger clinical trial is warranted.Trial RegistrationANZCTR Identifier: <jats:ext-link xmlns:xlink=\"http://www.w3.org/1999/xlink\" ext-link-type=\"uri\" xlink:href=\"https://anzctr.org.au/Trial/Registration/TrialReview.aspx?id=381914&amp;amp;amp;isReview=true\">ACTRN12621000710820</jats:ext-link>","PeriodicalId":518009,"journal":{"name":"JAMA","volume":"7 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JAMA","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1001/jama.2025.3471","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

ImportancePreclinical and preliminary human evidence suggests that metformin, a first-line treatment for type 2 diabetes, reduces inflammation, preserves cartilage, and improves knee pain in knee osteoarthritis.ObjectiveTo evaluate the effects of metformin on knee pain at 6 months in participants with symptomatic knee osteoarthritis and overweight or obesity.Design, Setting, and ParticipantsCommunity-based randomized, parallel-group, double-blind, placebo-controlled clinical trial that used telemedicine to recruit and follow up participants remotely. Individuals with knee pain for 6 months or longer, a pain score greater than 40 mm on a 100-mm visual analog scale (VAS), and body mass index of 25 or higher were recruited from the community through local and social media advertisements in Victoria, Australia, between June 16, 2021, and August 1, 2023. Final follow-up occurred on February 8, 2024.InterventionsParticipants were randomly assigned to receive either oral metformin, 2000 mg/d (n = 54), or identical placebo (n = 53) for 6 months.Main Outcomes and MeasuresThe primary outcome was change in knee pain, measured using a 100-mm VAS (score range, 0-100; 100 = worst; minimum clinically important difference = 15) at 6 months.ResultsOf 225 participants assessed for eligibility, 107 (48%) were randomized (mean age, 58.8 [SD, 9.5] years; 68% female) and assigned to receive metformin or placebo. Eighty-eight participants (82%) completed the trial. At 6 months, the mean change in VAS pain was −31.3 mm in the metformin group and −18.9 mm in the placebo group (between-group difference, −11.4 mm; 95% CI, −20.1 to −2.6 mm; P = .01), corresponding to an effect size (standardized mean difference) of 0.43 (95% CI, 0.02-0.83). The most common adverse events were diarrhea (8 [15%] in the metformin group and 4 [8%] in the placebo group) and abdominal discomfort (7 [13%] in the metformin group and 5 [9%] in the placebo group).Conclusions and RelevanceThese results support use of metformin for treatment of symptomatic knee osteoarthritis in people with overweight or obesity. Because of the modest sample size, confirmation in a larger clinical trial is warranted.Trial RegistrationANZCTR Identifier: ACTRN12621000710820
二甲双胍治疗超重或肥胖患者的膝骨性关节炎
重要性临床和初步人体证据表明,二甲双胍是治疗 2 型糖尿病的一线药物,它能减轻炎症、保护软骨并改善膝骨关节炎患者的膝关节疼痛。目的评估二甲双胍在 6 个月时对有症状的膝骨关节炎患者膝关节疼痛的影响。设计、环境和参与者基于社区的随机、平行组、双盲、安慰剂对照临床试验,采用远程医疗招募和远程随访参与者。2021 年 6 月 16 日至 2023 年 8 月 1 日期间,澳大利亚维多利亚州通过当地和社交媒体广告从社区招募了膝关节疼痛 6 个月或更长时间、100 毫米视觉模拟量表(VAS)疼痛评分大于 40 毫米、体重指数大于等于 25 的患者。干预措施参与者被随机分配接受口服二甲双胍(2000 mg/d,n = 54)或相同的安慰剂(n = 53),为期 6 个月。主要结果和测量方法主要结果是膝关节疼痛的变化,使用 100 毫米 VAS 测量(评分范围为 0-100;100 = 最差;最小临床重要差异 = 15),时间为 6 个月。结果在 225 名通过资格评估的参与者中,107 人(48%)被随机分配(平均年龄为 58.8 [SD, 9.5] 岁;68% 为女性),并被分配接受二甲双胍或安慰剂治疗。88名参与者(82%)完成了试验。6个月后,二甲双胍组的VAS疼痛平均变化为-31.3毫米,安慰剂组为-18.9毫米(组间差异为-11.4毫米;95% CI为-20.1至-2.6毫米;P = .01),效应大小(标准化平均差异)为0.43(95% CI为0.02至0.83)。最常见的不良反应是腹泻(二甲双胍组8例[15%],安慰剂组4例[8%])和腹部不适(二甲双胍组7例[13%],安慰剂组5例[9%])。由于样本量不大,因此需要在更大规模的临床试验中进行确认:ACTRN12621000710820
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信