4.2 Article

Effects of green tea extract on overweight and obese women with high levels of low density-lipoprotein-cholesterol (LDL-C): a randomised, double-blind, and cross-over placebo-controlled clinical trial

期刊

出版社

BMC
DOI: 10.1186/s12906-018-2355-x

关键词

Obesity; Green tea extract; Epigallocatechin gallant; EGCG; Hyperlipidemia; LDL-C; Low density lipoprotein; Leptin

资金

  1. National Science Council, Taiwan [NSC 101-2320-B-010-075]

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BackgroundThis study aims to examine the effects of green tea extract (GTE) supplement on overweight and obese women with high levels of low density lipoprotein-cholesterol (LDL-C).MethodsThe randomized, double-blind, crossover and placebo-controlled clinical trial was conducted from August 2012 to December 2013. Seventy-three out of 90 subjects aged between 18 and 65years, with body mass index (BMI)27kg/m(2) and LDL-C130mg/dl were included in the analysis. The subjects were randomly divided into Groups A and B. Group A received GTE supplement treatment for the first 6 weeks, while Group B received placebo daily. After 6 weeks of treatment and 14days of washout period, Group A switched to placebo and Group B switched to GTE treatment for 6 weeks. The reduction of LDL-C level between treatments was assessed as the outcome. Additionally, anthropometric measurements, plasma lipoproteins and hormone peptides of both groups were measure at the beginning of weeks 6, 8, and 14 after treatment.ResultsSubjects treated with GTE (n=73) for 6weeks showed significant differences, with 4.8% (p=0.048) reduction in LDL-C and 25.7% (p=0.046) increase in leptin. However, there was no statistical difference in the levels of total cholesterol, triglyceride and high density lipoprotein between the GTE and placebo groups after treatments.ConclusionsThis study shows that green tea extract effectively increases leptin and reduces LDL in overweight and obese women after 6weeks of treatment even though there were no significant changes in other biochemical markers related to overweight.Trial registrationThis clinical trial is registered with ClinicalTrials.gov: NCT02116517 on 17 April 2014. Retrospectively registered. The first patient enrolled in October 2012 and the study was completed December 2013.

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