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Effect of SGLT2 Inhibitors on Diabetes Progression in Statin-Treated Patients: A Population-Based Cohort Study
Jack Ssu-Chi Cheng1,2, Fang-Ju Lin1,3,4, Chih-Min Fu3
1Graduate Institute of Clinical Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan.
Background:
Statins, though widely used, may accelerate diabetes progression, necessitating interventions to counteract this effect.
Purpose:
To compare the effect of sodium-glucose co-transporter 2 inhibitors (SGLT2is) and sulfonylureas or meglitinides on diabetes progression in individuals receiving statins.
Patients And Methods:
This retrospective cohort study utilized data from the National Health Insurance Research Database of Taiwan. We included patients with diabetes receiving statins and newly initiated SGLT2is or sulfonylureas/meglitinides between July 1, 2016 and December 31, 2020. Diabetes progression was defined as insulin initiation, increase in antidiabetic medication class, or occurrence of new acute hyperglycemic complications. Propensity score matching was used to adjust baseline characteristics. Cox proportional hazards regression was used to calculate the hazard ratios for diabetes progression between users of SGLT2is and those of sulfonylureas or meglitinides. The statistical significance level was set at 0.05 for all analyses.
Results:
SGLT2i users had a significantly lower risk of diabetes progression compared to sulfonylurea/meglitinide users (HR: 0.53, 95% CI: 0.50-0.57, p-value < 0.001). Similar results were found in insulin initiation (HR: 0.48, 95% CI: 0.38-0.61, p-value < 0.001) and increase in antidiabetic medication class (HR: 0.53, 95% CI: 0.50-0.57, p-value < 0.17). However, the risk of new acute glycemic complications did not significantly differ between groups (HR: 2.47, 95% CI: 0.67-9.08, p-value = 0.17).
Conclusion:
SGLT2is may be an effective second-line therapy for statin-treated patients by slowing diabetes progression and potentially mitigating statin-induced metabolic disturbances. Further research, including randomized controlled trials or observational studies with comprehensive laboratory data, is needed to confirm these findings and evaluate their broader applicability.
Insights
Sodium-glucose co-transporter 2 inhibitors (SGLT2is) significantly reduced diabetes progression in patients taking statins compared to sulfonylureas/meglitinides. This suggests SGLT2is may mitigate statin-related metabolic effects and slow disease advancement.
Area of Science:
- Endocrinology
- Pharmacology
- Metabolic Diseases
Background:
- Statins, commonly prescribed medications, are associated with accelerated diabetes progression.
- There is a clinical need for interventions to counteract the adverse metabolic effects of statins in diabetic patients.
Purpose of the Study:
- To compare the efficacy of sodium-glucose co-transporter 2 inhibitors (SGLT2is) versus sulfonylureas or meglitinides in managing diabetes progression among patients concurrently using statins.
- To evaluate the impact of different second-line antidiabetic agents on key markers of diabetes advancement.
Main Methods:
- A retrospective cohort study using Taiwan's National Health Insurance Research Database (2016-2020).
- Inclusion criteria: patients with diabetes on statins, newly initiated on SGLT2is or sulfonylureas/meglitinides.
- Diabetes progression defined by insulin initiation, medication class escalation, or acute hyperglycemic events; propensity score matching and Cox regression were employed.
Main Results:
- SGLT2i users demonstrated a significantly lower risk of overall diabetes progression (HR: 0.53) compared to sulfonylurea/meglitinide users.
- SGLT2is were associated with reduced insulin initiation (HR: 0.48) and medication class escalation (HR: 0.53).
- No significant difference was observed in the risk of acute glycemic complications between the two groups (HR: 2.47).
Conclusions:
- Sodium-glucose co-transporter 2 inhibitors (SGLT2is) show promise as an effective second-line therapy for diabetic patients on statins, potentially slowing disease progression.
- SGLT2is may help mitigate statin-induced metabolic disturbances, warranting further investigation.
- Randomized controlled trials and studies with detailed laboratory data are recommended to validate these findings.
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