Yonsei University College of Medicine, Department of Internal Medicine, Division of Endocrinology, Severance Hospital, Diabetes center
Seoul, 03722, South Korea
NCT Number: NCT02964572
* Single-center, prospective, active-controlled, open, randomized, 2 arm parallel, interventional, exploratory pilot * Type 2 diabetic patients with high cardiovascular risks who have inadequate glycaemic control with metformin-based oral hypoglycemic agents will be prescribed glimepiride (comparison group) or empagliflozin (study group) for 60 days (plus or minus 32 days) as add-on therapy * Changes in IL-1beta secretion, serum beta-hydroxybutyrate concentration, and NLRP3 inflammasome activity from baseline to final timepoint will be assessed.
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Notify Me19 year–85 year
All sexes
Interventional
Not applicable
Seoul, 03722, South Korea
First among cardiovascular (CV) end point trials of glucose-lowering agents, the EMPA-REG OUTCOME trial-using 10 or 25 mg/day SGLT2 inhibitor empagliflozin against placebo in 7,020 patients with T2DM who were at increased CV risk-reported a 14% reduction in major CV events and marked relative risk reductions in CV mortality (38%), hospitalization for heart failure (35%), and death from any cause (32%) over a median time period of 2.6 years. Though these results have raised the possibility that mechanisms other than those observed in the trial-modest improvement in glycemic control, small decrease in body weight, and persistent reductions in blood pressure and uric acid level-may be at play, it's not clearly known yet.
The inflammatory nature of atherosclerosis is well established. We hypothesized that empagliflozin might have an inhibitory effect on inflammasome activity in macrophages, thus contribute to cardioprotective effects in diabetes.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
In accordance with the standard treatment guidelines of diabetes, glimepiride as a drug of active comparator will be administered to improve blood sugar in patients with poorly controlled blood sugar.
Other names: Amaryl
Empagliflozin as a drug of experimental will be administered to improve blood sugar in patients with poorly controlled blood sugar.
Other names: Jardiance
Time frame: Day 60
The effect of empagliflozin on the secretion of IL-1beta from peripheral blood mononuclear cells
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Time frame: Day 60 plus or minus 32 days
Yonsei University
Other
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