Abstract: SA-OR031
Extending Benefit to the Oldest Old: Efficacy of SGLT2 Inhibitors in Older Adults with CKD
Session Information
- CKD in Overlooked Populations
October 24, 2026 | Location: Mile High Ballroom 1A, Convention Center
Abstract Time: 05:00 PM - 05:10 PM
Category: Geriatric Nephrology
- 1300 Geriatric Nephrology
Authors
- Doricic, Julian, Medizinische Hochschule Hannover, Hanover, NDS, Germany
- Willerding, Jonas Michael, Medizinische Hochschule Hannover, Hanover, NDS, Germany
- Melk, Anette, Medizinische Hochschule Hannover, Hanover, NDS, Germany
- Schmidt-Ott, Kai M., Medizinische Hochschule Hannover, Hanover, NDS, Germany
- Greite, Robert, Medizinische Hochschule Hannover, Hanover, NDS, Germany
- Gwinner, Wilfried, Medizinische Hochschule Hannover, Hanover, NDS, Germany
- Schmidt, Bernhard M.W., Medizinische Hochschule Hannover, Hanover, NDS, Germany
Background
Prevalence of chronic kidney disease (CKD) is growing and aging has been identified as a major factor. Sodium-glucose cotransporter-2 inhibitors (SGLT2i) have become well established as a treatment for patients with CKD. Elderly patients over 80 years of age with CKD have been rarely studied and were underrepresented in previous large-scale trials. The effects of SGLT2i therapy in this specific cohort are understudied.
Methods
In a retrospective cohort study utilizing the TriNetX database, we investigated in a first-use design the implementation of SGLT2i in patients over 80 years of age with CKD. As the primary endpoint, all-cause mortality was investigated. Secondary endpoints focused on major adverse cardiovascular events (MACE) and major adverse kidney events (MAKE). Cox proportional hazards models were used to estimate hazard ratios with 95% confidence intervals and results were considered as adjusted hazard ratios (aHR), as previous propensity score matching had been performed. The Kaplan-Meier curves represented time-to-event analyses with censoring at the time of the last documented patient visit.
Results
After propensity score matching for comorbidities, laboratory parameters, and frailty-associated factors, the group of SGLT2i users and the group of non-users both consisted of 23,765 patients. After a two-year follow-up, a significant reduction in mortality was observed among patients treated with SGLT2i (aHR 0.734; 95% CI 0.705 – 0.765, p<0 .0001). In addition, the SGLT2i cohort demonstrated benefits regarding MACE (aHR 0.884; 95%CI 0.857-0.913, p<0.0001) and MAKE (aHR 0.775; 95%CI 0.745-0.806, p<0.0001). Across all predefined subgroups, SGLT2i treatment was consistently associated with a lower risk of mortality.
Conclusion
Even the oldest CKD patients benefit from SGLT2i treatment, which was associated with a reduced risk of mortality as well as improved cardiovascular and renal outcomes.