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Myocardial infarction in type 2 diabetes using sodium–glucose co-transporter-2 inhibitors, dipeptidyl peptidase-4 inhibitors or glucagon-like peptide-1 receptor agonists: proportional hazards analysis by deep neural network based machine learning
Heart attack risk in type 2 diabetes linked to three diabetes drug types analyzed by deep learning
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Abstract
Analysis of 199,116 patients showed a 37% lower risk of myocardial infarction for those using GLP-1 receptor agonists compared to dipeptidyl peptidase-4 inhibitors.
- Sodium-glucose co-transporter-2 inhibitors and glucagon-like peptide-1 receptor agonists are associated with a significantly lower risk of myocardial infarction compared to dipeptidyl peptidase-4 inhibitors.
- The hazard ratio for myocardial infarction with SGLT-2 inhibitors was 0.81 and for GLP-1 receptor agonists was 0.63, indicating a reduced risk.
- GLP-1 receptor agonists also demonstrated a significantly lower risk of myocardial infarction compared to SGLT-2 inhibitors, with a hazard ratio of 0.77.
- Receiver operating characteristics analysis indicated that machine learning provided higher precision in predicting myocardial infarction than logistic regression.
- The study's population primarily consisted of patients with commercial health plans, which may limit the generalizability of the findings.
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