Ferulic Acid Supplementation Improves Lipid Profiles, Oxidative Stress, and Inflammatory Status in Hyperlipidemic Subjects: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial
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作者:
Bumrungpert, Akkarach
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Mahidol Univ, Fac Publ Hlth, Dept Nutr, Bangkok 10400, ThailandMahidol Univ, Fac Publ Hlth, Dept Nutr, Bangkok 10400, Thailand
Bumrungpert, Akkarach
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Lilitchan, Supathra
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Mahidol Univ, Fac Publ Hlth, Dept Nutr, Bangkok 10400, ThailandMahidol Univ, Fac Publ Hlth, Dept Nutr, Bangkok 10400, Thailand
Ferulic acid is the most abundant phenolic compound found in vegetables and cereal grains. In vitro and animal studies have shown ferulic acid has anti-hyperlipidemic, anti-oxidative, and anti-inflammatory effects. The objective of this study is to investigate the effects of ferulic acid supplementation on lipid profiles, oxidative stress, and inflammatory status in hyperlipidemia. The study design is a randomized, double-blind, placebo-controlled trial. Subjects with hyperlipidemia were randomly divided into two groups. The treatment group (n = 24) was given ferulic acid (1000 mg daily) and the control group (n = 24) was provided with a placebo for six weeks. Lipid profiles, biomarkers of oxidative stress and inflammation were assessed before and after the intervention. Ferulic acid supplementation demonstrated a statistically significant decrease in total cholesterol (8.1%; p = 0.001), LDL-C (9.3%; p < 0.001), triglyceride (12.1%; p = 0.049), and increased HDL-C (4.3%; p = 0.045) compared with the placebo. Ferulic acid also significantly decreased the oxidative stress biomarker, MDA (24.5%; p < 0.001). Moreover, oxidized LDL-C was significantly decreased in the ferulic acid group (7.1%; p = 0.002) compared with the placebo group. In addition, ferulic acid supplementation demonstrated a statistically significant reduction in the inflammatory markers hs-CRP (32.66%; p < 0.001) and TNF- (13.06%; p < 0.001). These data indicate ferulic acid supplementation can improve lipid profiles and oxidative stress, oxidized LDL-C, and inflammation in hyperlipidemic subjects. Therefore, ferulic acid has the potential to reduce cardiovascular disease risk factors.
机构:
Vanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USAVanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USA
Jagasia, M. H.
Abonour, R.
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Indiana Univ, Div Hematol Oncol, Indianapolis, IN 46204 USAVanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USA
Abonour, R.
Long, G. D.
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Duke Univ, Med Ctr, Div Cellular Therapy, Durham, NC USAVanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USA
Long, G. D.
Bolwell, B. J.
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Cleveland Clin, Cleveland, OH 44106 USAVanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USA
Bolwell, B. J.
Laport, G. G.
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Stanford Univ, Med Ctr, Stanford, CA 94305 USAVanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USA
Laport, G. G.
Shore, T. B.
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New York Presbyterian Hosp, Weill Cornell Med Coll, Div Hematol Oncol, New York, NY USAVanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USA
Shore, T. B.
Durrant, S.
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Royal Brisbane & Womens Hosp, Div Oncol, Brisbane, Qld, AustraliaVanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USA
Durrant, S.
Szer, J.
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Royal Melbourne Hosp, Melbourne, Vic, AustraliaVanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USA
Szer, J.
Chen, M-G
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Amgen Inc, Thousand Oaks, CA 91320 USAVanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USA
Chen, M-G
Lizambri, R.
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Amgen Inc, Thousand Oaks, CA 91320 USAVanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USA
Lizambri, R.
Waller, E. K.
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机构:
Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USAVanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37203 USA