This randomized, prospective, double-blind, placebo-controlled, parallel-group study determined the impact of administering 20 mg Teneligliptin (oral antidiabetic agent) twice daily in conjunction with a low carbohydrate diet and regular physical exercise in obese individuals without diabetes.
In non-diabetic obese individuals, using 20 mg twice daily Teneligliptin is well-tolerated and remarkably improves GLP-1 levels, and reduces insulin resistance, body weight, triglyceride, appetite, and metabolic syndrome.
This randomized, prospective, double-blind, placebo-controlled, parallel-group study determined the impact of administering 20 mg Teneligliptin (oral antidiabetic agent) twice daily in conjunction with a low carbohydrate diet and regular physical exercise in obese individuals without diabetes.
At an outpatient department of an endocrinology hospital, the study was carried out over a period of forty-eight weeks. Overall, 150 nondiabetic obese volunteers were randomly allocated into:
At the end of forty-eight weeks, remarkable improvements were observed in body weight, glucagon-like peptide-1 (GLP-1) levels, simplified nutrition assessment questionnaire (SNAQ) scores, homeostasis model assessment of insulin resistance (HOMA-IR), and triglyceride levels. The mean differences and 95% confidence intervals for GLP-1 (pg/mL) were 76.42 (44.42-148.41) (P = 0.37); SNAQ score, -1.64 (-2.48 to -0.81) (P = 0.000); HOMA-IR, -0.9 (-0.59 to -0.38) (P = 0.000); triglycerides (mg/dL), -29.37 (-44.46 to -14.07) (P = 0.000); and reduction in body weight (kilograms), -3.09 (-6.11 to -0.07) (P = 0.043).
Treatment with Teneligliptin resulted in vital improvements in GLP-1 levels, decreased insulin resistance, body weight, metabolic syndrome markers, triglyceride levels, and appetite. It was generally well-tolerated, except for instances of upper respiratory tract infections.
Metabolic Syndrome and Related Disorders
Effect of Teneligliptin 20 mg Twice Daily on Glucagon-Like Peptide-1 Levels and Its Influence on Non-Glycemic Components in Non-Diabetic Obese Individuals
Ranakishor Pelluri et al.
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