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  4. The autoantibody expression against different source of oxidized low density lipoprotein in patients with acute myocardial infarction
 
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The autoantibody expression against different source of oxidized low density lipoprotein in patients with acute myocardial infarction

Type
article
Resource
Thrombosis Research.():175-179.
Date Issued
2002
Author(s)
秦一平
Tze-Che wang; Chung-Chi; Yi-Ping Chin; Yuh-Ling Lin.
Subjects
學科:復健學科
期刊論文
Abstract
The aim of this study was to examine the expression of antibodies against two different sources of low density lipoprotein (LDL) that were oxidized by CuSO(4), in patients with early stage of acute myocardial infarction (AMI). When LDL purified from sera with high level of LDL was used as a modified antigen, the results indicated that the titers of antibodies against the oxidized LDL in 30 patients were increased by 135% compared to those in normal subjects; however, the titers of antibody against modified LDL purified from normal-range LDL in the same patients were only slightly increased by 52%. Comparing the levels of autoantibody expressed in the high LDL sera group, high triglyceride sera group, and AMI patients sera group (total of 41; in addition to 30 AMI patients, 11 more sera of AMI patients were collected), the amount of autoantibody against the oxLDL purified from high LDL sera in AMI patients sera group was significantly increased up to 195%. In contrast to AMI patients, the sera titers against the same antigen in two subject groups with either high LDL or high triglyceride are only 50% higher than normal subjects. Moreover, the ratio of thromboxane B(2) over 6-keto-prostaglandin F(1alpha) (6-keto-PG F(1alpha)) in the acute myocardial infarction patients was 1.79, which is much lower than the normal subjects, 4.19. Concluding from the above observations, we suggest that the expression level of anti-oxidized LDL antibody may play a role on the pathogenesis of acute myocardial infarction disease, but is independent with the levels of thromboxane A(2) and prostacyclin in the examined sera.

Copyright 2002 Elsevier Science Ltd.
URI
https://203.71.86.71/handle/123456789/19879
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