Long‐term benefit of <scp>SGLT2</scp> inhibitors to prevent heart failure hospitalization in patients with diabetes, with potential time‐varying benefit
SGLT2 inhibitors show promise in reducing hospitalization for heart failure in diabetics, but their long-term effects and time-dependency remain unclear. We conducted a retrospective nested case-control study within a large type 2 diabetic cohort (n = 11,209) using electronic health records. Cases (heart failure hospitalization, n = 352) were matched to controls (n = 1372) based on age, sex, cohort entry date, and diabetes duration. Matched-set conditional logistic regression was used to estimate hazard ratios (HRs) for antidiabetic drug class and heart failure hospitalization risk. SGLT2 inhibitors were associated with a significant reduction in heart failure hospitalization risk (adjusted HR 0.56, 95% CI 0.38-0.82, p = 0.028). This protective effect appeared more pronounced with a longer duration of treatment, suggesting a potential cumulative benefit. Time-varying analysis within propensity score-matched cohorts revealed a progressive decrease in hospitalization risk with continued SGLT2 inhibitor use, indicating a strengthening effect over time (greedy nearest neighbor: HR 0.52, CI 0.31-0.87, p = 0.015; optimal matching: HR 0.54, CI 0.34-0.85, p = 0.008). While promising, further investigation with larger datasets is warranted to definitively confirm these findings.
Authors
- Hayato Akimoto (ORCID: https://orcid.org/0000-0002-5397-0137)
- Takuya Nagashima (ORCID: https://orcid.org/0000-0003-1299-2644)
- Yasuo Takahashi (ORCID: https://orcid.org/0000-0003-2543-7543)
- Kimino Minagawa (ORCID: https://orcid.org/0000-0001-9052-0568)
- Satoshi Asai
- T. Hayakawa (ORCID: https://orcid.org/0000-0002-8565-3486)
Institutions
- Nihon University (JP)
Publication Details
- Journal
- Clinical and Translational Science
- Published
- 2024-12-01
- DOI
- https://doi.org/10.1111/cts.70088
- Citations
- 2
- Primary Topic
- Diabetes Treatment and Management
- Type
- article
- Field-Weighted Citation Impact
- 0.72