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Zhibitai and low-dose atorvastatin reduce blood lipids and inflammation in patients with coronary artery disease

BACKGROUND: Atorvastatin decreases blood lipids but is associated with side effects. Zhibitai is a traditional Chinese medicine used to treat blood lipid disorders. The objective of this study is to evaluate the lipid-lowering effect, antiinflammatory effect, and adverse events of zhibitai combined...

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Autores principales: Zhao, Yuhong, Peng, Ran, Zhao, Wang, Liu, Qiong, Guo, Yuan, Zhao, Shuiping, Xu, Danyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319516/
https://www.ncbi.nlm.nih.gov/pubmed/28207527
http://dx.doi.org/10.1097/MD.0000000000006104
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author Zhao, Yuhong
Peng, Ran
Zhao, Wang
Liu, Qiong
Guo, Yuan
Zhao, Shuiping
Xu, Danyan
author_facet Zhao, Yuhong
Peng, Ran
Zhao, Wang
Liu, Qiong
Guo, Yuan
Zhao, Shuiping
Xu, Danyan
author_sort Zhao, Yuhong
collection PubMed
description BACKGROUND: Atorvastatin decreases blood lipids but is associated with side effects. Zhibitai is a traditional Chinese medicine used to treat blood lipid disorders. The objective of this study is to evaluate the lipid-lowering effect, antiinflammatory effect, and adverse events of zhibitai combined to atorvastatin in patients with coronary heart diseases (CHDs). METHODS: Patients with CHD (n = 150) were randomized to: zhibitai 480 mg + atorvastatin 10 mg (ZA10 group), atorvastatin 20 mg (A20 group), and atorvastatin 40 mg (A40 group). Lipid profile, cardiotrophin-1 (CT-1), and C-reactive protein (CRP) were measured after 4 and 8 weeks of treatment. Self-reported side effects, liver function, kidney function, and creatine kinase levels were monitored. RESULTS: After 8 weeks, triglycerides, total cholesterol (TC), LDL-cholesterol (LDL-C), and apolipoprotein B(100) (ApoB(100)) levels were decreased in the ZA10 group (−64%, −37%, −46%, and −54%, respectively, compared with baseline), and these changes were similar to those of the A40 group (P > 0.05). CT-1 and high sensitivity-C reactive protein (hs-CRP) levels were significantly decreased in the ZA10 group after 4 and 8 weeks (4 weeks: −73% and 96%; 8 weeks: −89% and −98%; all P < 0.01), without differences among the 3 groups (P > 0.05). After 8 weeks of treatment, adverse events (abdominal distention, nausea, vomiting, and hunger) were found in 4, 5, and 7 patients in the ZA10, A20, and A40 groups, respectively. CONCLUSION: ZA10 significantly reduced triglycerides, TC, LDL-C, ApoB, CT-1, and hs-CRP levels in patients with CHD, similar to the effects of A40 and A20, but ZA10 lead to fewer adverse events.
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spelling pubmed-53195162017-03-02 Zhibitai and low-dose atorvastatin reduce blood lipids and inflammation in patients with coronary artery disease Zhao, Yuhong Peng, Ran Zhao, Wang Liu, Qiong Guo, Yuan Zhao, Shuiping Xu, Danyan Medicine (Baltimore) 3700 BACKGROUND: Atorvastatin decreases blood lipids but is associated with side effects. Zhibitai is a traditional Chinese medicine used to treat blood lipid disorders. The objective of this study is to evaluate the lipid-lowering effect, antiinflammatory effect, and adverse events of zhibitai combined to atorvastatin in patients with coronary heart diseases (CHDs). METHODS: Patients with CHD (n = 150) were randomized to: zhibitai 480 mg + atorvastatin 10 mg (ZA10 group), atorvastatin 20 mg (A20 group), and atorvastatin 40 mg (A40 group). Lipid profile, cardiotrophin-1 (CT-1), and C-reactive protein (CRP) were measured after 4 and 8 weeks of treatment. Self-reported side effects, liver function, kidney function, and creatine kinase levels were monitored. RESULTS: After 8 weeks, triglycerides, total cholesterol (TC), LDL-cholesterol (LDL-C), and apolipoprotein B(100) (ApoB(100)) levels were decreased in the ZA10 group (−64%, −37%, −46%, and −54%, respectively, compared with baseline), and these changes were similar to those of the A40 group (P > 0.05). CT-1 and high sensitivity-C reactive protein (hs-CRP) levels were significantly decreased in the ZA10 group after 4 and 8 weeks (4 weeks: −73% and 96%; 8 weeks: −89% and −98%; all P < 0.01), without differences among the 3 groups (P > 0.05). After 8 weeks of treatment, adverse events (abdominal distention, nausea, vomiting, and hunger) were found in 4, 5, and 7 patients in the ZA10, A20, and A40 groups, respectively. CONCLUSION: ZA10 significantly reduced triglycerides, TC, LDL-C, ApoB, CT-1, and hs-CRP levels in patients with CHD, similar to the effects of A40 and A20, but ZA10 lead to fewer adverse events. Wolters Kluwer Health 2017-02-17 /pmc/articles/PMC5319516/ /pubmed/28207527 http://dx.doi.org/10.1097/MD.0000000000006104 Text en Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 3700
Zhao, Yuhong
Peng, Ran
Zhao, Wang
Liu, Qiong
Guo, Yuan
Zhao, Shuiping
Xu, Danyan
Zhibitai and low-dose atorvastatin reduce blood lipids and inflammation in patients with coronary artery disease
title Zhibitai and low-dose atorvastatin reduce blood lipids and inflammation in patients with coronary artery disease
title_full Zhibitai and low-dose atorvastatin reduce blood lipids and inflammation in patients with coronary artery disease
title_fullStr Zhibitai and low-dose atorvastatin reduce blood lipids and inflammation in patients with coronary artery disease
title_full_unstemmed Zhibitai and low-dose atorvastatin reduce blood lipids and inflammation in patients with coronary artery disease
title_short Zhibitai and low-dose atorvastatin reduce blood lipids and inflammation in patients with coronary artery disease
title_sort zhibitai and low-dose atorvastatin reduce blood lipids and inflammation in patients with coronary artery disease
topic 3700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319516/
https://www.ncbi.nlm.nih.gov/pubmed/28207527
http://dx.doi.org/10.1097/MD.0000000000006104
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