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Associations of SGLT2i with Cardiorenal Outcomes Among Diabetics with Prostate Cancer on Hormone Therapy
Efstratios Koutroumpakis1, Rushin Patel2, Sumanth Khadke3
1Department of Cardiology, Division of Internal Medicine, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 1451, Houston, TX, 77030, USA. EKoutroumpakis@mdanderson.org.
Purpose:
Studies have reported associations between prostate cancer, type II diabetes mellitus (T2DM), and cardiovascular disease in the context of treatment with hormone therapy (HT). This study aimed to assess the role of Sodium-Glucose Cotransporter-2 Inhibitors (SGLT2i) in preventing adverse cardiovascular and renal outcomes in diabetics with prostate cancer.
Methods:
Patients ≥ 18 years of age with T2DM and prostate cancer who received HT between August 1, 2013, and August 31, 2021, were identified using the TriNetX research network. Patients were divided into two cohorts based on treatment with SGLT2i or alternative antidiabetic therapies. The primary outcome was the composite of all-cause mortality, new-onset heart failure (HF), acute myocardial infarction (MI), and peripheral artery disease over 2 years from HT initiation.
Results:
After propensity score matching, 2155 patients remained in each cohort. The primary composite outcome occurred in 218 patients (16.1%) in the SGLT2i cohort versus 355 patients (26.3%) in the non-SGLT2i cohort (OR 0.539, 95% CI 0.446-0.651; p < 0.001). Furthermore, SGLT2i were associated with significantly lower odds of HF, HF exacerbation, peripheral artery disease, atrial fibrillation/flutter, cardiac arrest, need for renal replacement therapy, overall emergency room visits/hospitalizations, and all-cause mortality.
Conclusions:
Use of SGLT2i for the treatment of T2DM among patients with prostate cancer on HT is associated with favorable cardiovascular, renal, and all-cause mortality outcomes. This observation supports the hypothesis that a therapeutically relevant link exists between HT and cardiovascular disease in the context of prostate cancer.
Insights
Sodium-Glucose Cotransporter-2 Inhibitors (SGLT2i) significantly reduced adverse cardiovascular and renal outcomes in diabetic prostate cancer patients on hormone therapy (HT). This suggests SGLT2i can mitigate risks associated with HT in this population.
Area of Science:
- Cardiology
- Endocrinology
- Oncology
Background:
- Hormone therapy (HT) for prostate cancer is linked to cardiovascular disease (CVD) and type II diabetes mellitus (T2DM).
- Previous studies indicate associations between prostate cancer, T2DM, and CVD in patients undergoing HT.
Purpose of the Study:
- To evaluate the role of Sodium-Glucose Cotransporter-2 Inhibitors (SGLT2i) in preventing adverse cardiovascular and renal outcomes.
- To assess the impact of SGLT2i on T2DM patients with prostate cancer receiving HT.
Main Methods:
- Retrospective cohort study using the TriNetX research network (August 2013-August 2021).
- Included patients aged ≥18 with T2DM and prostate cancer on HT.
- Compared outcomes between patients treated with SGLT2i versus alternative antidiabetic therapies after propensity score matching.
Main Results:
- SGLT2i use was associated with a significantly lower incidence of the primary composite outcome (all-cause mortality, heart failure, myocardial infarction, peripheral artery disease) (16.1% vs 26.3%).
- SGLT2i demonstrated significant reductions in heart failure, renal replacement therapy, and all-cause mortality.
- Reduced odds of atrial fibrillation/flutter, cardiac arrest, and hospitalizations were observed with SGLT2i.
Conclusions:
- SGLT2 inhibitors are associated with improved cardiovascular, renal, and mortality outcomes in diabetic prostate cancer patients on hormone therapy.
- Findings support a therapeutic link between HT and CVD in prostate cancer patients.
- SGLT2i may offer a protective benefit against adverse events in this high-risk population.
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