Tan George S Q, Morton Jedidiah I, Wood Stephen, Trevaskis Natalie L, Magliano Dianna J, Windsor John, Shaw Jonathan E, Ilomäki Jenni
Centre for Medicine Use and Safety, Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, Melbourne, Victoria, Australia; Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Centre for Medicine Use and Safety, Faculty of Pharmacy and Pharmaceutical Sciences, Monash University, Melbourne, Victoria, Australia; Baker Heart and Diabetes Institute, Melbourne, Victoria, Australia.
Diabetes Res Clin Pract. 2024 Jan;207:111082. doi: 10.1016/j.diabres.2023.111082. Epub 2023 Dec 29.
This study examined the association between cyclooxygenase-2 inhibitor (COX2i) use and diabetes progression in people with type 2 diabetes.
We conducted a nation-wide cohort study using an Australian diabetes registry linked to medication dispensing data. We assessed time to diabetes treatment intensification among new users of COX2i compared to mild opioids. Inverse probability of treatment-weighted Cox regression models were used to adjust for age, sex, time since diabetes diagnosis, comorbidities, and socio-economic disadvantage. We conducted several sensitivity analyses, including per-protocol analyses and comparing use of any NSAID to mild opioids.
There were 8,071 new users of COX2i and 7,623 of mild opioids with 4,168 diabetes treatment intensifications over a median follow-up of 1.6 years. Use of COX2i was associated with decreased risk of treatment intensification when compared to mild opioids (HR 0.91, 95 %CI 0.85-0.96). The results were not significant in the per-protocol analyses. Use of any NSAID was associated with a lower risk of treatment intensification compared to mild opioids (HR 0.90, 95 %CI 0.85-0.96).
Treatment with COX2i may be associated with a modest decreased risk of diabetes treatment intensification compared to mild opioids. Future clinical studies are required to confirm whether COX2 inhibition has clinically significant benefits for glycaemic control.
本研究探讨了2型糖尿病患者使用环氧化酶-2抑制剂(COX2i)与糖尿病进展之间的关联。
我们利用澳大利亚糖尿病登记系统与药物配给数据进行了一项全国性队列研究。我们评估了与轻度阿片类药物相比,COX2i新使用者达到糖尿病治疗强化的时间。采用治疗加权逆概率Cox回归模型对年龄、性别、糖尿病诊断后的时间、合并症和社会经济劣势进行调整。我们进行了多项敏感性分析,包括符合方案分析以及比较使用任何非甾体抗炎药与轻度阿片类药物的情况。
在中位随访1.6年期间,有8071名COX2i新使用者和7623名轻度阿片类药物使用者,其中4168例出现糖尿病治疗强化。与轻度阿片类药物相比,使用COX2i与治疗强化风险降低相关(风险比0.91,95%置信区间0.85 - 0.96)。在符合方案分析中,结果不显著。与轻度阿片类药物相比,使用任何非甾体抗炎药与治疗强化风险较低相关(风险比0.90,95%置信区间0.85 - 0.96)。
与轻度阿片类药物相比,使用COX2i治疗可能与糖尿病治疗强化风险适度降低相关。未来需要进行临床研究以确认COX2抑制对血糖控制是否具有临床显著益处。