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Efficacy and safety of Ginkgo biloba extract as an “add-on” treatment to metformin for patients with metabolic syndrome: a pilot clinical study

BACKGROUND AND AIM: Ginkgo biloba (GKB) extract has shown to be beneficial in experimental models of metabolic and inflammatory disorders such as diabetes and metabolic syndrome (MTS). The objective of this pilot clinical study was to evaluate the effects of GKB extract as an “add-on” treatment with...

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Autores principales: Aziz, Tavga Ahmed, Hussain, Saad Abdulrahman, Mahwi, Taha Othman, Ahmed, Zheen Aorahman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047609/
https://www.ncbi.nlm.nih.gov/pubmed/30034238
http://dx.doi.org/10.2147/TCRM.S169503
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author Aziz, Tavga Ahmed
Hussain, Saad Abdulrahman
Mahwi, Taha Othman
Ahmed, Zheen Aorahman
author_facet Aziz, Tavga Ahmed
Hussain, Saad Abdulrahman
Mahwi, Taha Othman
Ahmed, Zheen Aorahman
author_sort Aziz, Tavga Ahmed
collection PubMed
description BACKGROUND AND AIM: Ginkgo biloba (GKB) extract has shown to be beneficial in experimental models of metabolic and inflammatory disorders such as diabetes and metabolic syndrome (MTS). The objective of this pilot clinical study was to evaluate the effects of GKB extract as an “add-on” treatment with metformin (Met) in MTS patients. PATIENTS AND METHODS: We performed a randomized, placebo-controlled, double-blinded clinical study in subjects with MTS. Forty patients completed the 90-day clinical trial and were randomly allocated to administer either GKB extract (120 mg capsule/day) or placebo (120 mg starch/day) as an add-on treatment with their currently used doses of Met for 90 days. During the study, body mass index (BMI), waist circumference (WC), serum leptin, glycated hemoglobin (HbA1c), fasting serum glucose (FSG), insulin, insulin resistance (IR), visceral adiposity index (VAI), lipid profile, and the inflammatory markers high sensitive C-reactive protein (hsCRP), tumor necrosis factor-α (TNF-α), and interleukin-6 (IL-6) were evaluated. RESULTS: GKB extract significantly decreases HbA1c, FSG and insulin levels, IR, BMI, WC, VAI, serum leptin, and the inflammatory markers compared to baseline values. Simultaneously, GKB did not negatively affect the functions of the liver, kidney, and hematopoietic system. CONCLUSION: The use of GKB extract as an adjuvant with Met was effective in improving the outcome of patients with MTS.
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spelling pubmed-60476092018-07-20 Efficacy and safety of Ginkgo biloba extract as an “add-on” treatment to metformin for patients with metabolic syndrome: a pilot clinical study Aziz, Tavga Ahmed Hussain, Saad Abdulrahman Mahwi, Taha Othman Ahmed, Zheen Aorahman Ther Clin Risk Manag Original Research BACKGROUND AND AIM: Ginkgo biloba (GKB) extract has shown to be beneficial in experimental models of metabolic and inflammatory disorders such as diabetes and metabolic syndrome (MTS). The objective of this pilot clinical study was to evaluate the effects of GKB extract as an “add-on” treatment with metformin (Met) in MTS patients. PATIENTS AND METHODS: We performed a randomized, placebo-controlled, double-blinded clinical study in subjects with MTS. Forty patients completed the 90-day clinical trial and were randomly allocated to administer either GKB extract (120 mg capsule/day) or placebo (120 mg starch/day) as an add-on treatment with their currently used doses of Met for 90 days. During the study, body mass index (BMI), waist circumference (WC), serum leptin, glycated hemoglobin (HbA1c), fasting serum glucose (FSG), insulin, insulin resistance (IR), visceral adiposity index (VAI), lipid profile, and the inflammatory markers high sensitive C-reactive protein (hsCRP), tumor necrosis factor-α (TNF-α), and interleukin-6 (IL-6) were evaluated. RESULTS: GKB extract significantly decreases HbA1c, FSG and insulin levels, IR, BMI, WC, VAI, serum leptin, and the inflammatory markers compared to baseline values. Simultaneously, GKB did not negatively affect the functions of the liver, kidney, and hematopoietic system. CONCLUSION: The use of GKB extract as an adjuvant with Met was effective in improving the outcome of patients with MTS. Dove Medical Press 2018-07-11 /pmc/articles/PMC6047609/ /pubmed/30034238 http://dx.doi.org/10.2147/TCRM.S169503 Text en © 2018 Aziz et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Aziz, Tavga Ahmed
Hussain, Saad Abdulrahman
Mahwi, Taha Othman
Ahmed, Zheen Aorahman
Efficacy and safety of Ginkgo biloba extract as an “add-on” treatment to metformin for patients with metabolic syndrome: a pilot clinical study
title Efficacy and safety of Ginkgo biloba extract as an “add-on” treatment to metformin for patients with metabolic syndrome: a pilot clinical study
title_full Efficacy and safety of Ginkgo biloba extract as an “add-on” treatment to metformin for patients with metabolic syndrome: a pilot clinical study
title_fullStr Efficacy and safety of Ginkgo biloba extract as an “add-on” treatment to metformin for patients with metabolic syndrome: a pilot clinical study
title_full_unstemmed Efficacy and safety of Ginkgo biloba extract as an “add-on” treatment to metformin for patients with metabolic syndrome: a pilot clinical study
title_short Efficacy and safety of Ginkgo biloba extract as an “add-on” treatment to metformin for patients with metabolic syndrome: a pilot clinical study
title_sort efficacy and safety of ginkgo biloba extract as an “add-on” treatment to metformin for patients with metabolic syndrome: a pilot clinical study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047609/
https://www.ncbi.nlm.nih.gov/pubmed/30034238
http://dx.doi.org/10.2147/TCRM.S169503
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