This is a single center, prospective randomized double blind, parallel and placebo controlled study to evaluate oxidative stress and inflammation before and after treatment with linagliptin for 12 weeks. We will also, testing whether Linagliptin is an insulin sensitizer.
This is a single center, prospective randomized double blind, parallel and placebo-controlled study to evaluate oxidative stress and inflammation before and after treatment with linagliptin for 12 weeks. The study enrolls type 2 patients with diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
40
5 mg daily oral tablets of linagliptin
matching placebo giving orally daily
ECMC Ambulatory Center, 3rd Floor
Buffalo, New York, United States
JNK-1 Protein in MNC
JNK-1 protein in MNC before and after linagliptin use as compared to placebo.
Time frame: Week 0, Week 2, Week 4, Week 12
IL-1β mRNA Levels
Comparing IL-1B between Linagliptin group and placebo group based on the PCR test, between week 0 and week 12.
Time frame: Week 0, Week 2, Week 4, Week 12
Oxidative Stress (as ROS Generation Level)
oxidative stress (ROS generation level) following linagliptin. ROS generation measurement by chemiluminescence of PMN cells
Time frame: Week 0, Week 2, Week 4, Week 12
Insulin Sensitivity by Hyperinsulinemic-euglycemic Clamp
Insulin sensitivity is measured with HE clamp. Glucose Infusion Rate was titrated to maintain blood glucose concentration at the fasting glucose level. Plasma samples for glucose was obtained at 10-minute intervals starting 30 minutes before the clamp, to quantitate rates of whole-body glucose disposal. Difference from baseline at 12 weeks is calculated and compared to placebo arm
Time frame: At baseline and week 12
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