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SGLT2 inhibitors and geriatric syndromes in older adults with type 2 diabetes: A real-world cohort study
Chun-Ying Lee1, Tzu-Jung Fang2, Chun-Hao Jen3
1Department of Family Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan; Center for Metabolic Disorder and Obesity, Kaohsiung Medical University, Kaohsiung, Taiwan; Precision Sports Medicine and Health Promotion Center, Kaohsiung Medical University, Kaohsiung, Taiwan; Research Center for Precision Environmental Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.
Background:
Sodium-glucose cotransporter-2 (SGLT2) inhibitors provide cardiorenal benefits in type 2 diabetes mellitus (T2DM), but concerns persist regarding potential exacerbation of geriatric syndromes through osmotic diuresis, volume depletion, and catabolic weight loss in older adults. This study evaluated the association between SGLT2 inhibitors and geriatric syndromes, all-cause hospitalization, and all-cause mortality.
Methods:
A cohort study was conducted using data from TriNetX global health research network between January 1, 2014 to December 31, 2020. Adults aged ≥65 years with T2DM newly initiated on SGLT2 inhibitors or dipeptidyl peptidase-4 (DPP-4) inhibitors were included. Propensity score matching (1:1) was performed to minimize confounding and reduce bias from unequal distribution of baseline characteristics and treatment effects. Primary outcomes were incident geriatric syndromes; secondary outcomes were all-cause hospitalization and mortality at 6 months, 1 year, and 5 years.
Results:
After matching, 42,440 individuals were included in each group (mean age 71.4 years, 60% male). SGLT2 inhibitor initiation was associated with lower risks of multiple geriatric syndromes, including delirium, cognitive impairment, and pressure injuries. Five-year hazard ratios were 0.81 (95% CI: 0.78-0.83) for all-cause hospitalization and 0.65 (95% CI: 0.62-0.69) for all-cause mortality. Findings remained consistent across subgroups stratified by age, sex, glycated hemoglobin (HbA1c) control, heart disease, and renal function.
Conclusion:
In older adults with T2DM, SGLT2 inhibitor use was not associated with increased geriatric syndromes but rather with lower risks of geriatric outcomes, all-cause hospitalization, and all-cause mortality, supporting their use within comprehensive geriatric assessment frameworks.
Insights
Sodium-glucose cotransporter-2 (SGLT2) inhibitors are safe for older adults with type 2 diabetes mellitus (T2DM). These medications reduce risks of geriatric syndromes, hospitalization, and mortality in this population.
Area of Science:
- Geriatric Medicine
- Endocrinology
- Cardiology
Background:
- Concerns exist regarding SGLT2 inhibitors exacerbating geriatric syndromes in older adults with T2DM.
- This study investigated the association between SGLT2 inhibitors and geriatric syndromes, hospitalization, and mortality.
Purpose of the Study:
- To evaluate the safety and efficacy of SGLT2 inhibitors in older adults with T2DM.
- To assess the impact of SGLT2 inhibitors on geriatric syndromes, all-cause hospitalization, and all-cause mortality.
Main Methods:
- A 1:1 propensity score-matched cohort study using TriNetX data (2014-2020).
- Included adults aged ≥65 years with T2DM, comparing SGLT2 inhibitors to DPP-4 inhibitors.
- Primary outcomes: incident geriatric syndromes; secondary outcomes: hospitalization and mortality at 6 months, 1 year, and 5 years.
Main Results:
- SGLT2 inhibitor use was linked to reduced risks of delirium, cognitive impairment, and pressure injuries.
- Five-year hazard ratios showed decreased all-cause hospitalization (0.81) and mortality (0.65).
- Consistent findings across subgroups based on age, sex, HbA1c, heart disease, and renal function.
Conclusions:
- SGLT2 inhibitors are not associated with increased geriatric syndromes in older adults with T2DM.
- SGLT2 inhibitors demonstrate reduced risks of geriatric outcomes, hospitalization, and mortality.
- Supports SGLT2 inhibitor use within geriatric assessment frameworks for T2DM patients.
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