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Effect of Rubus Occidentalis Extract on Metabolic Parameters in Subjects with Prediabetes: A Proof-of-concept, Randomized, Double-blind, Placebo-controlled Clinical Trial

Authors
An, Jee HyunKim, Dong-LimLee, Tae-BumKim, Kyeong JinKim, Sun HwaKim, Nam HoonKim, Hee YoungChoi, Dong SeopKim, Sin Gon
Issue Date
10월-2016
Publisher
WILEY
Keywords
Rubus occidentalis; black raspberry; metabolic syndrome; prediabetes; atherosclerosis
Citation
PHYTOTHERAPY RESEARCH, v.30, no.10, pp.1634 - 1640
Indexed
SCIE
SCOPUS
Journal Title
PHYTOTHERAPY RESEARCH
Volume
30
Number
10
Start Page
1634
End Page
1640
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/87471
DOI
10.1002/ptr.5664
ISSN
0951-418X
Abstract
Rubus occidentalis (RO) has beneficial effects on glucose and lipid profiles in vitro. The aim of the study was to investigate RO extract effect on metabolic parameters in prediabetic patients, adopting a 12-week, randomized, double-blind, placebo-controlled trial. Forty-four patients (age 59.0 +/- 8.2years, 70.5% females, HbA1c 5.8 +/- 0.4%) were divided into placebo (n=13), low-dose RO extract (LRE; n=14), or high-dose RO extract (HRE; n=17) groups. Either 900 or 1800mg per day of RO extract was administered orally. Area under the curve for glucose obtained 2h after a 75-g oral glucose tolerance test was significantly decreased in the HRE group, compared with the placebo group (-28.1 +/- 42.4 vs. +13.4 +/- 52.6mg/dL, p<0.05). Homoeostasis model assessment-B was increased (+17.11 +/- 10.69, +5.24 +/- 4.10, and +0.86 +/- 6.01 in HRE, LRE, and placebo, respectively, p<0.05). Serum levels of monocyte chemoattractant protein-1 and oxidized low-density lipoprotein were significantly decreased by treatment in a dose-dependent manner (monocyte chemoattractant protein-1: -35.0 +/- 21.2, +8.4 +/- 18.1, and +24.2 +/- 14.5; oxidized low-density lipoprotein: -19.7 +/- 8.5, -13.1 +/- 7.2, and -2.2 +/- 11.0 in the HRE, LRE, and placebo, respectively, p<0.05). The results support the beneficial effects of RO extract on the control of glycemia and vascular inflammation in prediabetic patients. (ClinicalTrials.gov: NCT01964703). Copyright (c) 2016 John Wiley & Sons, Ltd.
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