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  4. 利用等距毛細管電泳法來研究富含三酸甘油酯之脂蛋白與臨床粥狀硬化性疾病發生之關連(3/3)
 
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利用等距毛細管電泳法來研究富含三酸甘油酯之脂蛋白與臨床粥狀硬化性疾病發生之關連(3/3)

Other Title
Study on the Clinical Implication of Triglyceride-rich Lipoprotein of
Hypertriglyceridemic Patients by Capillary Isotachophoresis (3/3)
Date Issued
2005
Date
2005
Author(s)
許秀卿
DOI
932314B002017
URI
http://ntur.lib.ntu.edu.tw//handle/246246/23681
Abstract
Increasing experimental and clinical evidences suggest that tiglyceride-rich lipoprotein (TGRL) play a significant role in the pathogenesis of atherosclerosis. The TGRL is composed of a number of different lipoprotein and can be identified, separated and/or quantified in plasma according to their density, charge, size, specific lipid component, apoprotein composition. This study is nevertheless under way for more accurate and clinical applicable TGRL assays that will be better define coronary artery disease risk in patients with hypertriglyceridemia. Isotachophoresis , a high resoluble technique of capillary electrophoresis, was used to separate plasma lipoproteins according their net charge and without molecular sieve effects. In the present study, plasma lipoproteins were separated into four subclasses of low density lipoprotein (LDL1~ LDL4), five subclasses of TGRL (TGRL1~ TGRL5) and two subclasses of high density lipoprotein (HDL1~ HDL2). The TGRL1 levels was higher in hypertriglyceridemic patients with coronary artery diseases (CAD) as compared with subjects without CAD (. 8.2±1.6 VS. 4.5±1.6). Interesting, the statistical analysis showed that high levels of HDL2, TGRL1 and LDL4 subclasses were associated to atherogenesis. Although other plasma lipoprotein subclass distributions were individually different, they were not associated with other atherogenic risk factors or related to atherogenesis. Some clinical cases showed the level of HDL2, TGRL1 and/or LDL4 subclasses distribution was predictive for CAD, however, the characteristics and biological effects of these lipoprotein subclasses will be further exploed.
Publisher
臺北市:國立臺灣大學醫學院內科
Type
report
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932314B002017.pdf

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