COX2 inhibitor use and type 2 diabetes treatment intensification: A registry-based cohort study

被引:4
|
作者
Tan, George S. Q. [1 ,2 ,6 ]
Morton, Jedidiah I. [1 ,2 ]
Wood, Stephen [1 ]
Trevaskis, Natalie L. [3 ]
Magliano, Dianna J. [2 ,4 ]
Windsor, John [5 ]
Shaw, Jonathan E. [2 ,4 ]
Ilomaki, Jenni [1 ,6 ]
机构
[1] Monash Univ, Fac Pharm & Pharmaceut Sci, Ctr Med Use & Safety, Melbourne, Vic, Australia
[2] Baker Heart & Diabet Inst, Melbourne, Vic, Australia
[3] Monash Univ, Fac Pharm & Pharmaceut Sci, Monash Inst Pharmaceut Sci, Drug Delivery Disposit & Dynam, Melbourne, Vic, Australia
[4] Monash Univ, Fac Med Nursing & Hlth Sci, Sch Publ Hlth & Prevent Med, Melbourne, Vic, Australia
[5] Univ Auckland, Fac Med & Hlth Sci, Surg & Translat Res Ctr, Auckland, New Zealand
[6] Monash Univ, Ctr Med Use & Safety, 381 Royal Parade, Parkville, Vic 3052, Australia
关键词
COX2; inhibitor; NSAID; Type; 2; diabetes; Treatment intensification; Retrospective cohort study; Diabetes registry; PROPENSITY SCORE METHODS; GUIDELINE; MEDICINE; BALANCE; PAIN;
D O I
10.1016/j.diabres.2023.111082
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: This study examined the association between cyclooxygenase-2 inhibitor (COX2i) use and diabetes progression in people with type 2 diabetes. Methods: 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. Results: 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). Conclusions: 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.
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页数:8
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