Key result
SGLT2i use in older diabetics receiving anthracyclines is linked to ~100% lower HF hospitalization risk.
Why the study?
SGLT2is are hypothesized to reduce anthracycline-associated cardiotoxicity, but their association with cardiovascular disease after anthracycline-containing chemotherapy required evaluation.
Do SGLT2 inhibitors reduce the risk of heart failure hospitalization, incident heart failure, or cardiovascular disease in older patients with diabetes receiving anthracycline chemotherapy?
Population
933 patients >65 years of age with treated diabetes and no prior HF receiving anthracyclines
Comparison
SGLT2i-treated vs unexposed controls
Design
Population-based cohort study using administrative data sets with propensity score weighting
Follow-up
Median 1.6 years
Authors
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Supports potential SGLT2i cardioprotection in anthracycline-treated diabetes; leaves open confirmation by randomized trials before practice change.
Cohort (n=933)
Do SGLT2 inhibitors reduce the risk of heart failure hospitalization, incident heart failure, or cardiovascular disease in older patients with diabetes receiving anthracycline chemotherapy?
Effect estimate: HR 0
Absolute Event Rate: 0% vs 3.7%
p-value: p=<0.001
In older patients with diabetes receiving anthracycline chemotherapy, SGLT2 inhibitor use was associated with a significantly lower risk of heart failure hospitalization, suggesting a potential cardioprotective role in cardio-oncology.
Abdel‐Qadir et al. (2023) conducted a cohort in Treated diabetes and no prior heart failure receiving anthracyclines (n=933). Sodium-glucose cotransporter-2 inhibitors (SGLT2is) vs. Unexposed controls was evaluated on Hospitalization for HF (HR 0, p=<0.001). SGLT2i exposure in older patients with diabetes receiving anthracyclines was associated with a lower risk of heart failure hospitalization (HR 0; P<0.001) compared to unexposed controls.
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