Too good to be true: Are GLP-1 receptor agonists the new metformin?

被引:0
|
作者
Kowall, Bernd [1 ]
Maier, Gregor [2 ]
Rathmann, Wolfgang [2 ]
机构
[1] Univ Hosp Essen, Inst Med Informat Biometry & Epidemiol, Essen, Germany
[2] Heinrich Heine Univ Dusseldorf, German Diabet Ctr, Leibniz Ctr Diabet Res, Inst Biometr & Epidemiol, Dusseldorf, Germany
关键词
Diabetes mellitus; Cancer; Glucagon-like peptide-1 receptor agonist; Metformin; Time-lag bias; Immortal time bias; CANCER; RISK;
D O I
10.1016/j.jdiacomp.2024.108851
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Recently, a health-care database study showed that persons with type 2 diabetes taking GLP-1 receptor agonists (GLP-1 RA) had a significantly lower risk of 10 out of 13 obesity-related cancers than patients taking insulin (Wang L, et al. JAMA Netw Open. 2024 7: e2421305). For some cancers, hazard ratios <0.5 were reported. This is reminiscent of studies published >10 years ago showing that people with type 2 diabetes taking metformin had a lower risk of many types of cancer than those not taking metformin. In some studies, also risk reductions of >50 % were reported. The strong effects observed in the metformin studies were explained by time-related biases, in particular, immortal time bias. In the current GLP-1 RA study, it was striking that the curves for the cumulative incidence of several cancers in GLP-1 RA and insulin users diverged immediately after therapy onset. This indicates that there is most likely a time-related bias: insulin is given at much later stages of type 2 diabetes than GLP-1 RA. The current study suggests that one should be sceptical about database results when spectacular risk reductions are reported. Time-related bias should always be considered as an alternative explanation.
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页数:2
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