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Completed

NCT Number: NCT02964572

Effect of Sodium Glucose Co-transporter 2 Inhibitor on Inflammatory Cytokine in Type 2 Diabetes

* 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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Key information

Age range

19 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Yonsei University College of Medicine, Department of Internal Medicine, Division of Endocrinology, Severance Hospital, Diabetes center

Seoul, 03722, South Korea

About this study

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.

  • 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
  • Healthy volunteers : effect of 3 day-ketogenic diet on changes in cytokines, metabolites (IL-1beta, beta-hydroxybutyrate , etc) and inflammasome activity in macrophages

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥19 years
  • inadequate glycaemic control : HbA1c ≥6.5% or fasting glucose >120 mg/dl or random glucose >180 mg/dl
  • High risk of cardiovascular events defined as the presence of ≥1 of the following:
  • History of myocardial infarction
  • Evidence of multi-vessel coronary artery disease
  • Evidence of single-vessel coronary artery disease with a positive non-invasive stress test for ischemia or history of hospitalization for unstable angina
  • History of stroke
  • Evidence of occlusive peripheral artery disease
  • Evidence of carotid atherosclerosis
  • Metabolic syndrome
  • Healthy volunteers

Exclusion criteria

  • Type 1 diabetes
  • Organ transplantation
  • Pregnant women
  • eGFR <45
  • Cortisol or growth hormone deficiency, pituitary diseases
  • Gastric surgery
  • Hematologic disorders
  • Active cancers

Treatment and study plan

Glimepiride

Drug

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

Drug

Empagliflozin as a drug of experimental will be administered to improve blood sugar in patients with poorly controlled blood sugar.

Other names: Jardiance

Primary outcomes

  1. changes in the secretion of IL-1 beta from peripheral blood mononuclear cells

    Time frame: Day 60

    The effect of empagliflozin on the secretion of IL-1beta from peripheral blood mononuclear cells

Secondary outcomes

  1. Changes in the secretion of TNF-alpha from peripheral blood mononuclear cells, before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  2. Changes in serum concentrations of beta-hydroxybutyrate, before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  3. Changes in body weight (kg), before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  4. Changes in serum concentrations of insulin (µU/mL), before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  5. Changes in serum concentrations of glucagon (pg/mL), before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  6. Changes in serum concentrations of free fatty acid (μEq/L), before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  7. Changes in serum glycated albumin (%), before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  8. Changes in serum concentrations of glucose (mg/dL), before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  9. Changes in serum concentrations of uric acid (mg/dL), before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  10. Changes in serum concentrations of liver enzymes (aspartate aminotransferase and alanine aminotransferase (IU/L)), before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  11. Changes in serum lipids (total cholesterol, triglyceride, HDL cholesterol, and LDL cholesterol (mg/dL)), before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  12. Changes in serum concentrations of creatinine (mg/dL), before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  13. Changes in spot urine concentrations of glucose (mg/dL) and creatinine (mg/dL) (those will be combined to report spot urine glucose-to-creatinine ratio in mg/mg), before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  14. Changes in mRNA expression level (PCR, fold) of IL-1beta, TNF-alpha, and NLRP3 in peripheral blood mononuclear cells, before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

  15. Changes in protein expression pattern (western blot, relative to control) of IL-1beta, TNF-alpha, and NLRP3 in peripheral blood mononuclear cells, before and after the administration of empagliflozin or glimepiride

    Time frame: Day 60 plus or minus 32 days

Sponsors and collaborators

Lead sponsor

Yonsei University

Other

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Nov 16, 2016
Registry last updated
Aug 27, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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