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Are sulphonylureas all the same? A cohort study on cardiovascular and cancer-related mortality
1Geriatric Unit, Department of Critical Care, University of Florence Medical School, Florence, Italy.
Insights
Glibenclamide treatment in type 2 diabetes patients showed higher all-cause mortality and malignancy rates compared to gliclazide. Glibenclamide may also increase cardiovascular event risk in patients with pre-existing ischemic heart disease.
Area of Science:
- Endocrinology
- Cardiology
- Pharmacology
Background:
- Type 2 diabetes management involves various oral hypoglycemic agents.
- Glibenclamide and gliclazide are commonly prescribed sulfonylureas.
- Comparative safety and efficacy data are crucial for clinical decision-making.
Purpose of the Study:
- To compare all-cause, cardiovascular, and non-cardiovascular mortality.
- To assess cardiac morbidity between glibenclamide and gliclazide treated patients.
- To evaluate the long-term safety profiles of these two antidiabetic drugs.
Main Methods:
- Retrospective observational cohort study.
- Involved 568 type 2 diabetes outpatients.
- Utilized registry data for mortality and hospital discharge data for cardiac events.
Main Results:
- Glibenclamide group had significantly higher all-cause mortality (4.3% vs 2.2% yearly).
- Adjusted analysis revealed increased all-cause mortality (OR 2.1) and malignancy mortality (OR 3.6) with glibenclamide.
- Glibenclamide was associated with cardiac events only in patients with prior ischemic heart disease.
Conclusions:
- Glibenclamide use may be linked to elevated mortality from cardiovascular diseases and malignancies compared to gliclazide.
- These findings suggest a potential differential risk profile between the two sulfonylureas.
- Further prospective studies are warranted to confirm these safety concerns.
Background:
Aim of the present study is the comparison of all-cause, cardiovascular and non-cardiovascular mortality, and cardiac morbidity, between patients treated with glibenclamide and gliclazide.
Methods:
A retrospective observational cohort study was performed on a consecutive series of 568 outpatients (282 women, 286 men) with type 2 diabetes treated with either glibenclamide (n = 378) or gliclazide (n = 190). Information on all-cause mortality and on causes of death up to 31 December 2004 was obtained by the City of Florence Registry Office. Non-fatal cases requiring hospitalization were identified through the regional hospital discharge system using International Classification of Diseases.
Results:
Mean follow-up was 5.0 +/- 1.6 and 4.4 +/- 2.0 years for death and cardiac events, respectively; during follow-up, 33 and 11 deaths were observed in the glibenclamide and gliclazide groups, with a yearly mortality rate of 4.3 and 2.2%, respectively (p < 0.05). At Cox regression, after adjustment for potential confounders, including comorbidity, glibenclamide treatment was associated with a significant increase in all-cause mortality [OR 2.1(1.2;2.7), p < 0.05], while the difference in cardiovascular mortality was not statistically significant after adjustment for age and sex. Mortality for malignancies was significantly higher in patients treated with glibenclamide after adjustment for age, sex, BMI, and insulin and metformin treatment, [OR 3.6(1.1;11.9); p < 0.05]. A higher incidence of cardiac events was associated with glibenclamide treatment only in patients with previously known ischaemic heart disease.
Conclusions:
Treatment with glibenclamide could be associated with higher mortality for cardiovascular diseases and malignancies, in comparison with gliclazide.
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