ß-Cell Function and Glycemic Control of Basal Insulin, Metformin or Sitagliptin in Newly Diagnosed Type 2 Diabetic Patients With Moderate Hyperglycemia
Overview
- Phase
- Phase 4
- Intervention
- Metformin
- Conditions
- Type 2 Diabetes
- Sponsor
- Taipei Veterans General Hospital, Taiwan
- Enrollment
- 160
- Locations
- 1
- Primary Endpoint
- The primary outcome was the comparison of A1C change.
- Last Updated
- 13 years ago
Overview
Brief Summary
We have found that a 6-month course of insulin therapy after a short-term intensive insulin therapy could shorten the period of hyperglycemia to preserve ß-cell function and further improve long-term glycemic control in recently diagnosed type 2 diabetes with severe hyperglycemia (>300 mg/dl, with HBA1C level around 9-11%) in our previous study. We thus hypothesized that a 6-month course of basal insulin therapy could also help to preserve ß-cell function in newly diagnosed type 2 diabetes with moderate hyperglycemia (200-300 mg/dl). This prospective study is outpatient-based to evaluate whether 6-month basal insulin therapy versus oral anti-diabetic treatment (Metformin and sitagliptin) soon after the diagnosis of type 2 diabetes with moderate hyperglycemia (200-300 mg/dl) is associated with better ß-cell function reservation. We skip a short-term intensive admission course of insulin therapy as our previous study in newly diagnosed type 2 diabetes with severe hyperglycemia.
Detailed Description
ß-Cell dysfunction and decreased insulin sensitivity are the main pathophysiological defects responsible for the development of hyperglycemia. There is a progressive deterioration in ß-cell function and mass in type 2 diabetics. Optimal metabolic control, especially early intensive glycemic control, plays a role in the prevention of progressive ß-cell dysfunction and possibly destruction of the ß-cells with worsening of diabetes. We have found that a 6-month course of insulin therapy after a short-term intensive insulin therapy could shorten the period of hyperglycemia to preserve ß-cell function and further improve long-term glycemic control in recently diagnosed type 2 diabetes with severe hyperglycemia (\>300 mg/dl, with HBA1C level around 9-11%) in our previous study. We thus hypothesized that a 6-month course of basal insulin therapy could also help to preserve ß-cell function in newly diagnosed type 2 diabetes with moderate hyperglycemia (200-300 mg/dl). This prospective study is outpatient-based to evaluate whether 6-month basal insulin therapy versus oral anti-diabetic treatment (Metformin and sitagliptin) soon after the diagnosis of type 2 diabetes with moderate hyperglycemia (200-300 mg/dl) is associated with better ß-cell function reservation. We skip a short-term intensive admission course of insulin therapy as our previous study in newly diagnosed type 2 diabetes with severe hyperglycemia. This study also can assess what readily available parameter would predict which patients will achieve long-term successful glycemic control after correction of glucose toxicity. Our results will provide evidence that a 6-month course of basal insulin therapy could shorten the exposure to moderate hyperglycemia and further improve beta-cell function to achieve long-term glycemic control.
Investigators
vghtpe user
Division of Endocrinology and Metabolism
Taipei Veterans General Hospital, Taiwan
Eligibility Criteria
Inclusion Criteria
- •Recently diagnosed type 2 diabetic patients.
- •Fasting plasma glucose between 200-300 mg/dl (A1C level between 7% and 10%).
- •Those who age between 30 and 80 years old and can inject insulin by themselves.
Exclusion Criteria
- •Previous treated with anti-diabetic medication
- •Pregnant or nursing women.
- •Impaired liver function (ALT \> 120 U/L)
- •Impaired renal function (Serum creatinine \>1.5 mg/dL in male, \>1.4 mg/dL in female )
- •Recently suffered from MI or CVA.
- •Patients are acute intercurrent illness.
- •2-hour C-peptide level \< 1.8 ng/mL.
Arms & Interventions
Metformin
The titration of metformin was used 500 mg for an adjust unit in splitting dose with the same target to the maximum daily dose of 2550 mg (1000 mg twice daily and then 850 mg tid).
Intervention: Metformin
Sitagliptin
The subjects treated with sitagliptin started with 100 mg before breakfast once daily. The dosage was fixed as 100mg per day. Decreased by 50mg if fasting blood glucose was \<70mg /dl, discontinued the study if blood glucose was still \<70mg/dl under sitagliptin 50mg per day.
Intervention: Sitagliptin
Insulin
In the insulin therapy group (Insulin glargine), subjects were instructed in the techniques for insulin injection and home capillary glucose monitoring. Daily dose was administrated before breakfast.
Intervention: Insulin
Outcomes
Primary Outcomes
The primary outcome was the comparison of A1C change.
Time Frame: Dec. 2013
The primary outcome was the comparison of A1C change.
Secondary Outcomes
- Beta-cell function and insulin sensitivity and the proportion of subjects who reached the treatment target (A1C <7.0% or <6.5% at 6 months).(Dec 2013)