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Article: Association between glucagon-like peptidase 1 receptor agonist and obesity-related cancer in overweight or obese patients with type 2 diabetes: a nationwide cohort study
| Title | Association between glucagon-like peptidase 1 receptor agonist and obesity-related cancer in overweight or obese patients with type 2 diabetes: a nationwide cohort study |
|---|---|
| Authors | |
| Issue Date | 9-Jul-2025 |
| Publisher | Oxford University Press |
| Citation | Journal of the National Cancer Institute, 2025 How to Cite? |
| Abstract | Background Evidence regarding the effect of glucagon-like peptide 1 receptor (GLP-1) agonist, when compared with other glucose-lowering drugs, on obesity-related cancer in overweight or obese patients with type 2 diabetes is limited. Methods Using Merative Marketscan research databases, we identified all overweight or obese patients with type 2 diabetes aged 20-79 years who received GLP-1 agonist or other glucose-lowering drugs in the United States between January 2016 and June 2021. The primary outcome was obesity-related cancer, defined as a component of 13 cancer types. Results Among 919 609 overweight or obese individuals with type 2 diabetes (mean [SD] age = 52.3 [10.9] years; female, 53.5%), 16 653 newly diagnosed with obesity-related cancer were recorded during the 2 086 526 person-years of follow-up. GLP-1 agonist users (vs other glucose-lowering drugs users) were associated with lower incidence (7.5 vs 8.1 per 1000 person-years) and risk of obesity-related cancer (adjusted hazard ratio [HR] = 0.87, 95% confidence interval [CI] = 0.83 to 0.91). This statistically significant association was consistent when comparing GLP-1 agonist with metformin (adjusted HR = 0.90, 95% CI = 0.86 to 0.95), dipeptidyl peptidase-4 inhibitor (adjusted HR = 0.88, 95% CI = 0.84 to 0.93), thiazolidinediones (adjusted HR = 0.84, 95% CI = 0.71 to 0.99), sulfonylureas (adjusted HR = 0.81, 95% CI = 0.74 to 0.88), sodium-glucose transport protein 2 inhibitor (adjusted HR = 0.73, 95% CI = 0.66 to 0.80), and insulin (adjusted HR = 0.70, 95% CI = 0.65 to 0.76; all P < .05) and was strengthened with increasing weight (overweight, mild to moderate, and severe obesity: HR = 0.95, 95% CI = 0.81 to 1.10, vs HR = 0.90, 95% CI = 0.84 to 0.97, vs HR = 0.82, 95% CI = 0.77 to 0.88, respectively; Pinteraction = .032). Conclusions In a nationwide US cohort of overweight or obese patients with type 2 diabetes, GLP-1 agonist, when compared with other glucose-lowering drugs, was associated with a lower risk of obesity-related cancer, with more pronounced risk reduction with increasing body weight. |
| Persistent Identifier | http://hdl.handle.net/10722/362470 |
| ISSN | 2023 Impact Factor: 9.9 2023 SCImago Journal Rankings: 4.986 |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mao, Xianhua | - |
| dc.contributor.author | Zhang, Xinrong | - |
| dc.contributor.author | Henry, Linda | - |
| dc.contributor.author | Cheung, Ka Shing | - |
| dc.contributor.author | Yuen, Man-Fung | - |
| dc.contributor.author | Cheung, Ramsey | - |
| dc.contributor.author | Seto, Wai-Kay | - |
| dc.contributor.author | Nguyen, Mindie H | - |
| dc.date.accessioned | 2025-09-24T00:51:47Z | - |
| dc.date.available | 2025-09-24T00:51:47Z | - |
| dc.date.issued | 2025-07-09 | - |
| dc.identifier.citation | Journal of the National Cancer Institute, 2025 | - |
| dc.identifier.issn | 0027-8874 | - |
| dc.identifier.uri | http://hdl.handle.net/10722/362470 | - |
| dc.description.abstract | <p>Background</p><p>Evidence regarding the effect of glucagon-like peptide 1 receptor (GLP-1) agonist, when compared with other glucose-lowering drugs, on obesity-related cancer in overweight or obese patients with type 2 diabetes is limited.</p><p>Methods</p><p>Using Merative Marketscan research databases, we identified all overweight or obese patients with type 2 diabetes aged 20-79 years who received GLP-1 agonist or other glucose-lowering drugs in the United States between January 2016 and June 2021. The primary outcome was obesity-related cancer, defined as a component of 13 cancer types.</p><p>Results</p><p>Among 919 609 overweight or obese individuals with type 2 diabetes (mean [SD] age = 52.3 [10.9] years; female, 53.5%), 16 653 newly diagnosed with obesity-related cancer were recorded during the 2 086 526 person-years of follow-up. GLP-1 agonist users (vs other glucose-lowering drugs users) were associated with lower incidence (7.5 vs 8.1 per 1000 person-years) and risk of obesity-related cancer (adjusted hazard ratio [HR] = 0.87, 95% confidence interval [CI] = 0.83 to 0.91). This statistically significant association was consistent when comparing GLP-1 agonist with metformin (adjusted HR = 0.90, 95% CI = 0.86 to 0.95), dipeptidyl peptidase-4 inhibitor (adjusted HR = 0.88, 95% CI = 0.84 to 0.93), thiazolidinediones (adjusted HR = 0.84, 95% CI = 0.71 to 0.99), sulfonylureas (adjusted HR = 0.81, 95% CI = 0.74 to 0.88), sodium-glucose transport protein 2 inhibitor (adjusted HR = 0.73, 95% CI = 0.66 to 0.80), and insulin (adjusted HR = 0.70, 95% CI = 0.65 to 0.76; all <em>P</em> < .05) and was strengthened with increasing weight (overweight, mild to moderate, and severe obesity: HR = 0.95, 95% CI = 0.81 to 1.10, vs HR = 0.90, 95% CI = 0.84 to 0.97, vs HR = 0.82, 95% CI = 0.77 to 0.88, respectively; <em>P</em><sub>interaction</sub> = .032).</p><p>Conclusions</p><p>In a nationwide US cohort of overweight or obese patients with type 2 diabetes, GLP-1 agonist, when compared with other glucose-lowering drugs, was associated with a lower risk of obesity-related cancer, with more pronounced risk reduction with increasing body weight.</p> | - |
| dc.language | eng | - |
| dc.publisher | Oxford University Press | - |
| dc.relation.ispartof | Journal of the National Cancer Institute | - |
| dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
| dc.title | Association between glucagon-like peptidase 1 receptor agonist and obesity-related cancer in overweight or obese patients with type 2 diabetes: a nationwide cohort study | - |
| dc.type | Article | - |
| dc.identifier.doi | 10.1093/jnci/djaf163 | - |
| dc.identifier.eissn | 1460-2105 | - |
| dc.identifier.issnl | 0027-8874 | - |

