Effects of lipid-modulation and antiplatelet treatment on the endothelial lipase expression

OBJECTIVE: To investigate the effects of lipid-modulation and antiplatelet treatment on the expression of endothelial lipase (EL) of patients with coronary artery disease (CAD), and investigate the role of EL in the development of CAD

Bibliographische Detailangaben
Veröffentlicht in:Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue. - 1998. - 22(2010), 11 vom: 30. Nov., Seite 663-5
1. Verfasser: Fang, Yu-qiang (VerfasserIn)
Weitere Verfasser: He, Duo-fen, Yang, Cheng-ming, Wang, Xu-kai, Zeng, Chun-yu, Wang, Hong-yong, Fu, Chun-jiang, Shi, Wei-bin, Zhang, Ye
Format: Aufsatz
Sprache:Chinese
Veröffentlicht: 2010
Zugriff auf das übergeordnete Werk:Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue
Schlagworte:Controlled Clinical Trial Journal Article Research Support, Non-U.S. Gov't Hypolipidemic Agents Lipids Simvastatin AGG2FN16EV LIPG protein, human EC 3.1.1.3 Lipase
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500 |a Date Revised 25.11.2016 
500 |a published: Print 
500 |a Citation Status MEDLINE 
520 |a OBJECTIVE: To investigate the effects of lipid-modulation and antiplatelet treatment on the expression of endothelial lipase (EL) of patients with coronary artery disease (CAD), and investigate the role of EL in the development of CAD 
520 |a METHODS: One hundred and fifty-seven cases were divided into three groups according to clinical manifestations and the results of coronary artery angiography: control group (n=41) with more than one risk factors of CAD and the vessel lesions was <30%; stable angina pectoris (SAP) group (n=55); acute coronary syndrome (ACS) group (n=61). The EL positive cell rate was measured 2 weeks after cessation of lipid-modulation and aspirin treatment, and 6 months after treatment with simvastatin and/or aspirin. The drug was ceased for the complications or not tolerance for the treatment 
520 |a RESULTS: Except the patients in control group with aspirin treatment, the EL positive cell rate was significantly decreased among other groups [control group with simvastatin: (3.93±0.87)% vs. (5.28±1.05)%, SAP group: (8.16±2.11)% vs. (15.12±2.53)%, ACS group: (13.93±3.22)% vs. (38.44±4.36)%; SAP group with aspirin: (10.57±4.07)% vs. (14.66±2.29)%, ACS group: (18.28±5.14)% vs. (40.27±3.96)%; control group with aspirin and simvastatin: (3.13±0.87)% vs. (5.33±1.25)%, SAP group: (5.68±2.20)% vs. (14.89±2.15)%, ACS group: (7.81±3.96)% vs. (39.27±5.17)%, P<0.05 or P<0.01] 
520 |a CONCLUSION: The treatment with lipid-modulation and/or antiplatelet drug may significantly decrease the expression of EL, implying that EL participates in the progression of CAD 
650 4 |a Controlled Clinical Trial 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Lipids  |2 NLM 
650 7 |a Simvastatin  |2 NLM 
650 7 |a AGG2FN16EV  |2 NLM 
650 7 |a LIPG protein, human  |2 NLM 
650 7 |a EC 3.1.1.3  |2 NLM 
650 7 |a Lipase  |2 NLM 
650 7 |a EC 3.1.1.3  |2 NLM 
700 1 |a He, Duo-fen  |e verfasserin  |4 aut 
700 1 |a Yang, Cheng-ming  |e verfasserin  |4 aut 
700 1 |a Wang, Xu-kai  |e verfasserin  |4 aut 
700 1 |a Zeng, Chun-yu  |e verfasserin  |4 aut 
700 1 |a Wang, Hong-yong  |e verfasserin  |4 aut 
700 1 |a Fu, Chun-jiang  |e verfasserin  |4 aut 
700 1 |a Shi, Wei-bin  |e verfasserin  |4 aut 
700 1 |a Zhang, Ye  |e verfasserin  |4 aut 
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773 1 8 |g volume:22  |g year:2010  |g number:11  |g day:30  |g month:11  |g pages:663-5 
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