ITIH4: A New Potential Biomarker of “Toxin Syndrome” in Coronary Heart Disease Patient Identified with Proteomic Method
Objective. This trial aims to look for the protein biomarker of “toxin syndrome” of CHD patients. Methods. We have performed two trials in this paper. The first trial was a randomized controlled trial (RCT) of the plasma proteome in unstable angina (UA) patients by Maldi-Tof Mass. The second trial w...
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doaj-15f8e381e657488391bc8ba90a607a8c2020-11-25T00:24:56ZengHindawi LimitedEvidence-Based Complementary and Alternative Medicine1741-427X1741-42882013-01-01201310.1155/2013/360149360149ITIH4: A New Potential Biomarker of “Toxin Syndrome” in Coronary Heart Disease Patient Identified with Proteomic MethodHao Xu0Qinghua Shang1Hao Chen2Jianpeng Du3Jianyan Wen4Geng Li5Dazhuo Shi6Keji Chen7Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, ChinaWuxi Hospital of Traditional Chinese Medicine, Wuxi 214001, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, ChinaChina-Japan Friendship Hospital, Beijing 100029, ChinaChina-Japan Friendship Hospital, Beijing 100029, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, ChinaXiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, ChinaObjective. This trial aims to look for the protein biomarker of “toxin syndrome” of CHD patients. Methods. We have performed two trials in this paper. The first trial was a randomized controlled trial (RCT) of the plasma proteome in unstable angina (UA) patients by Maldi-Tof Mass. The second trial was a nested case-control study in 1503 stable CHD patients with one-year followup for acute cardiovascular events (ACEs). Results. In the RCT study, 12 protein spots were found to be the differential protein for the significant differences between the difference of before and after treatment in group A and group B; 2 of them (3207.37 Da and 4279.95 Da) was considered to be unique to “toxin syndrome” for being differential proteins of group B but not group A. These 2 spots were identified as Isoform 1 of Fibrinogen alpha chain precursor (FGA, 3207.37 Da) and Isoform 2 of inter-alpha-trypsin inhibitor heavy chain H4 (ITIH4, 4279.95 Da), respectively. In the nested case-control study, the result of Western blot demonstrated that protein expression of ITIH4 in the group with followup ACEs was significantly lower than the matched group without followup ACEs (P=0.027). Conclusion. ITIH4 might be a new potential biomarker of CHD “toxin syndrome” in TCM, indicating the potential role in early identifying high-risk CHD patients in stable period.http://dx.doi.org/10.1155/2013/360149 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hao Xu Qinghua Shang Hao Chen Jianpeng Du Jianyan Wen Geng Li Dazhuo Shi Keji Chen |
spellingShingle |
Hao Xu Qinghua Shang Hao Chen Jianpeng Du Jianyan Wen Geng Li Dazhuo Shi Keji Chen ITIH4: A New Potential Biomarker of “Toxin Syndrome” in Coronary Heart Disease Patient Identified with Proteomic Method Evidence-Based Complementary and Alternative Medicine |
author_facet |
Hao Xu Qinghua Shang Hao Chen Jianpeng Du Jianyan Wen Geng Li Dazhuo Shi Keji Chen |
author_sort |
Hao Xu |
title |
ITIH4: A New Potential Biomarker of “Toxin Syndrome” in Coronary Heart Disease Patient Identified with Proteomic Method |
title_short |
ITIH4: A New Potential Biomarker of “Toxin Syndrome” in Coronary Heart Disease Patient Identified with Proteomic Method |
title_full |
ITIH4: A New Potential Biomarker of “Toxin Syndrome” in Coronary Heart Disease Patient Identified with Proteomic Method |
title_fullStr |
ITIH4: A New Potential Biomarker of “Toxin Syndrome” in Coronary Heart Disease Patient Identified with Proteomic Method |
title_full_unstemmed |
ITIH4: A New Potential Biomarker of “Toxin Syndrome” in Coronary Heart Disease Patient Identified with Proteomic Method |
title_sort |
itih4: a new potential biomarker of “toxin syndrome” in coronary heart disease patient identified with proteomic method |
publisher |
Hindawi Limited |
series |
Evidence-Based Complementary and Alternative Medicine |
issn |
1741-427X 1741-4288 |
publishDate |
2013-01-01 |
description |
Objective. This trial aims to look for the protein biomarker of “toxin syndrome” of CHD patients. Methods. We have performed two trials in this paper. The first trial was a randomized controlled trial (RCT) of the plasma proteome in unstable angina (UA) patients by Maldi-Tof Mass. The second trial was a nested case-control study in 1503 stable CHD patients with one-year followup for acute cardiovascular events (ACEs). Results. In the RCT study, 12 protein spots were found to be the differential protein for the significant differences between the difference of before and after treatment in group A and group B; 2 of them (3207.37 Da and 4279.95 Da) was considered to be unique to “toxin syndrome” for being differential proteins of group B but not group A. These 2 spots were identified as Isoform 1 of Fibrinogen alpha chain precursor (FGA, 3207.37 Da) and Isoform 2 of inter-alpha-trypsin inhibitor heavy chain H4 (ITIH4, 4279.95 Da), respectively. In the nested case-control study, the result of Western blot demonstrated that protein expression of ITIH4 in the group with followup ACEs was significantly lower than the matched group without followup ACEs (P=0.027). Conclusion. ITIH4 might be a new potential biomarker of CHD “toxin syndrome” in TCM, indicating the potential role in early identifying high-risk CHD patients in stable period. |
url |
http://dx.doi.org/10.1155/2013/360149 |
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