期刊文献+

Relationship between Platelet Activation Related Factors and Polymorphism of Related Genes in Patients with Coronary Heart Disease of Blood-stasis Syndrome 被引量:11

Relationship between Platelet Activation Related Factors and Polymorphism of Related Genes in Patients with Coronary Heart Disease of Blood-stasis Syndrome
原文传递
导出
摘要 Objective: To comparatively study the expressive conditions of platelet activation related factors (GPⅠb, GPⅡb-Ⅲa and GMP-140) in healthy subjects and patients with coronary heart disease (CHD) of blood-stasis (BS) or non-blood-stasis (non-BS) syndrome, and to analyze the relationship between the activities of various glycoproteins and the polymorphism of genes. Methods: With case control design adopted, patients with the CHD (40 of BS, 37 of non-BS) and 39 healthy subjects for control, all fitting to the inclusion criteria, were selected in this study. The number of affected coronary branches was recorded by the contrast examination. The mean fluorescence intensity (MFI) of GPⅠb, GPⅡb-Ⅲa, and GMP-140 (CD42b, CD61, CD62p) in patients and healthy persons was measured with flow cytometry, the polymorphism of HPA-3 gene was detected by Taqman probe technique and that of HPA-2 gene was determined by gene sequencing. Results: MFI of CD61 and CD62p was higher in the CHD patients than in the healthy control, which was also higher in patients of BS syndrome than in patients of non-BS syndrome (P〈0.05); MFI of CD42b was lower in the CHD patients than in the healthy control (P〈0.05), but showing insignificant difference between BS and non-BS syndrome (P〉0.05); at the same time, no significant difference of all the above-mentioned three MFI could be found in patients with various numbers of affected coronary branches, neither in patients with different genotypes at GPⅡb HPA-3 and GPⅠb HPA-2 polymorphism loci (P〉0.05). Conclusion: (1) The activities of GP Ⅱ b-Ⅲa and GMP-140 were obviously increased in the genesis and developing process of CHD and CHD of BS syndrome, and so they could be taken as one of the objective indexes for microscopic diagnosis of BS syndrome. (2) The level of GPⅠb was lower in CHD patients than in healthy persons, but it was not a sensitive indicator for BS syndrome of CHD. (3) Levels of GP Ⅱb-Ⅲa, GPⅠb and GMP-140 were not related with the number of affected coronary branches in CHD patients. (4) The changes in amino-acids expression induced by the two loci brought no significant influence on GPⅠb and GP Ⅱb-Ⅲa activities. Objective: To comparatively study the expressive conditions of platelet activation related factors (GPⅠb, GPⅡb-Ⅲa and GMP-140) in healthy subjects and patients with coronary heart disease (CHD) of blood-stasis (BS) or non-blood-stasis (non-BS) syndrome, and to analyze the relationship between the activities of various glycoproteins and the polymorphism of genes. Methods: With case control design adopted, patients with the CHD (40 of BS, 37 of non-BS) and 39 healthy subjects for control, all fitting to the inclusion criteria, were selected in this study. The number of affected coronary branches was recorded by the contrast examination. The mean fluorescence intensity (MFI) of GPⅠb, GPⅡb-Ⅲa, and GMP-140 (CD42b, CD61, CD62p) in patients and healthy persons was measured with flow cytometry, the polymorphism of HPA-3 gene was detected by Taqman probe technique and that of HPA-2 gene was determined by gene sequencing. Results: MFI of CD61 and CD62p was higher in the CHD patients than in the healthy control, which was also higher in patients of BS syndrome than in patients of non-BS syndrome (P〈0.05); MFI of CD42b was lower in the CHD patients than in the healthy control (P〈0.05), but showing insignificant difference between BS and non-BS syndrome (P〉0.05); at the same time, no significant difference of all the above-mentioned three MFI could be found in patients with various numbers of affected coronary branches, neither in patients with different genotypes at GPⅡb HPA-3 and GPⅠb HPA-2 polymorphism loci (P〉0.05). Conclusion: (1) The activities of GP Ⅱ b-Ⅲa and GMP-140 were obviously increased in the genesis and developing process of CHD and CHD of BS syndrome, and so they could be taken as one of the objective indexes for microscopic diagnosis of BS syndrome. (2) The level of GPⅠb was lower in CHD patients than in healthy persons, but it was not a sensitive indicator for BS syndrome of CHD. (3) Levels of GP Ⅱb-Ⅲa, GPⅠb and GMP-140 were not related with the number of affected coronary branches in CHD patients. (4) The changes in amino-acids expression induced by the two loci brought no significant influence on GPⅠb and GP Ⅱb-Ⅲa activities.
机构地区 Xiyuan Hospital
出处 《Chinese Journal of Integrative Medicine》 SCIE CAS 2008年第4期267-273,共7页 中国结合医学杂志(英文版)
基金 Supported by the Major Program Project of National Natural Science Foundation of China(No.90409021)
关键词 coronary heart disease blood-stasis syndrome GPⅡb-Ⅲa GPⅠb GMP-140 platelet activation gene polymorphism coronary heart disease blood-stasis syndrome GPⅡb-Ⅲa, GPⅠb GMP-140 platelet activation gene polymorphism
  • 相关文献

参考文献8

  • 1Society of Cardiology,Chinese Association of the Integration of Traditional and Western Medicine.The diagnostic criteria of TCM in coronary heart disease[].Chinese Journal of Integrated Traditional and Western Medicine.1991
  • 2.Applications of flow cytometry in clinical researches[]..2005
  • 3.Practice of Internal Medicine[]..2005
  • 4Jackson,SP,Schoenwaelder,SM.Antiplatelet therapy: In search of the ‘magic bullet’[].Nature Reviews Drug Discovery.2003
  • 5Rauch U,Osende JI,Fuster V, et al.Thrombus formation on athero- sclerotic plaques: pathogenesis and clinical consequences[].Annals of Internal Medicine.2001
  • 6Michelson AD,Barnard MR,Krueger LA,et al.Circulating monocyte-platelet aggregates are a more sensitive marker of in vivo platelet activation than platelet surface P-selectin: studies in baboons, human coronary intervention, and human acute myocardial infarction[].Circulation.2001
  • 7Tian XY,Liu ZZ,Zhang JL.Relationship between different coronary lesions of unstable angina pectoris and platelet GP Ⅱ b-Ⅲ a receptor expression[].Journal of Cardiovascular & Pul- monary Diseases.2002
  • 8Williams Ms,Ngalla LS,Vaidya Det al.Plateht functional implications of glycoprotein I balpha polymorphisms in Afri- can Americans[].American Journal of Hematology.2007

同被引文献124

引证文献11

二级引证文献116

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部