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DOI: 10.1055/s-0030-1248298
© Georg Thieme Verlag KG Stuttgart · New York
Antidiabetic Effect of Gynostemma pentaphyllum Tea in Randomly Assigned Type 2 Diabetic Patients[*]
Publication History
received 17.08.2009
accepted after second revision 28.01.2010
Publication Date:
08 March 2010 (online)

Abstract
The aim of the study was to investigate the antidiabetic effect of the traditional Vietnamese herb Gynostemma pentaphyllum in 24 drug-naïve type 2 diabetic patients. All patients were randomized to authenticated Gynostemma pentaphyllum tea or placebo tea, 6 g daily, during twelve weeks and received information regarding diet and exercise. Fasting plasma glucose, insulin levels, and glycosylated hemoglobin (HbA1C) were measured before, during, and after the treatment. Oral glucose tolerance tests were performed every four weeks. After 12-week treatment, fasting plasma glucose levels totally decreased to an extent of 3.0±1.8 mmol/l in the Gynostemma pentaphyllum tea group as compared to a decrease of 0.6±2.2 mmol/l in the control group (p<0.01). HbA1C levels after 12 weeks decreased approximately 2% units in the Gynostemma pentaphyllum group compared to 0.2% unit in the controls (p<0.001). Change in Homeostasis Model Assessment-Insulin Resistance between baseline and twelfth week indicated that insulin resistance decreased significantly in the Gynostemma pentaphyllum group (−2.1±3.0) compared with that (+1.1±3.3) in the control group (p<0.05). There were no hypoglycemias, or adverse effects regarding kidney and liver parameters or gastrointestinal function. In addition, lipid profiles, glucagon, cortisol levels, body measurements, and blood pressure were not different between the groups. This study shows a prompt improvement of glycemia and insulin sensitivity, and thereby provides a basis for a novel, effective, and safe approach, using Gynostemma pentaphyllum tea, to treat type 2 diabetic patients.
Key words
herbal medicine - type 2 diabetes - Gynostemma pentaphyllum tea - insulin sensitivity
1 This study is registered at ClinicalTrial.gov with ID: NCT00786500.*
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1 This study is registered at ClinicalTrial.gov with ID: NCT00786500.*
Correspondence
V. T. T. Huyen
Claes-Göran Östenson
Department of Molecular Medicine & Surgery
Endocrine & Diabetes Unit
Karolinska Institute
Karolinska University Hospital
17176 Stockholm
Sweden
Phone: +46/8/51776200
Fax: +46/8/51773096
Email: huyen.vu@ki.se
Email: claes.ostensson@karolinska.se