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Insights into the prognosis of lipidomic dysregulation for death risk in patients with coronary artery disease

BACKGROUND: Dyslipidaemia contributes to the progression of coronary artery disease (CAD) toward adverse outcomes. Plasma lipidomic measure may improve the prognostic performances of clinical endpoints of CAD. Our research is designed to identify the correlations between plasma lipid species and the...

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Autores principales: Qin, Min, Zhu, Qian, Lai, Weihua, Ma, Qilin, Liu, Chen, Chen, Xiaoping, Zhang, Yuelin, Wang, Zixian, Chen, Hui, Yan, Hong, Lei, Heping, Zhang, Shuyao, Dong, Xuekui, Wang, Hong, Huang, Min, Lian, Qizhou, Zhong, Shilong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522592/
https://www.ncbi.nlm.nih.gov/pubmed/32997403
http://dx.doi.org/10.1002/ctm2.189
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author Qin, Min
Zhu, Qian
Lai, Weihua
Ma, Qilin
Liu, Chen
Chen, Xiaoping
Zhang, Yuelin
Wang, Zixian
Chen, Hui
Yan, Hong
Lei, Heping
Zhang, Shuyao
Dong, Xuekui
Wang, Hong
Huang, Min
Lian, Qizhou
Zhong, Shilong
author_facet Qin, Min
Zhu, Qian
Lai, Weihua
Ma, Qilin
Liu, Chen
Chen, Xiaoping
Zhang, Yuelin
Wang, Zixian
Chen, Hui
Yan, Hong
Lei, Heping
Zhang, Shuyao
Dong, Xuekui
Wang, Hong
Huang, Min
Lian, Qizhou
Zhong, Shilong
author_sort Qin, Min
collection PubMed
description BACKGROUND: Dyslipidaemia contributes to the progression of coronary artery disease (CAD) toward adverse outcomes. Plasma lipidomic measure may improve the prognostic performances of clinical endpoints of CAD. Our research is designed to identify the correlations between plasma lipid species and the risks of death, major adverse cardiovascular event (MACE) and left ventricular (LV) remodeling in patients with CAD. METHODS: A total of 1569 Chinese patients with CAD, 1011 single‐centre patients as internal training cohort, and 558 multicentre patients as external validation cohort, were enrolled. The concentration of plasma lipids in both cohorts was determined through widely targeted lipidomic profiling. Least absolute shrinkage and selection operator Cox and multivariate Cox regressions were used to develop prognostic models for death and MACE, respectively. RESULTS: Ten (Cer(d18:1/20:1), Cer(d18:1/24:1), PE(30:2), PE(32:0), PE(32:2), PC(O‐38:2), PC(O‐36:4), PC(16:1/22:2), LPC(18:2/0:0) and LPE(0:0/24:6)) and two (Cer(d18:1/20:1) and LPC(20:0/0:0)) lipid species were independently related to death and MACE, respectively. Cer(d18:1/20:1) and Cer(d18:1/24:1) were correlated with LV remodeling (P < .05). The lipidic panel incorporating 10 lipid species and two traditional biomarkers for predicting 5‐year death risk represented a remarkable higher discrimination than traditional model with increased area under the curve from 76.56 to 83.65%, continuous NRI of 0.634 and IDI of 0.131. Furthermore, the panel was successfully used in differentiating multicentre patients with low, middle, or high risks (P < .0001). Further analysis indicated that the number of double bonds of phosphatidyl choline and the content of carbon atoms of phosphatidyl ethanolamines were negatively associated with death risk. CONCLUSIONS: Improvement in the prediction of death confirms the effectiveness of plasma lipids as predictors to risk classification in patients with CAD. The association between the structural characteristics of long‐chain polyunsaturated fatty acids and death risk highlights the need for mechanistic research that characterizes the role of individual lipid species in disease pathogenesis.
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spelling pubmed-75225922020-10-02 Insights into the prognosis of lipidomic dysregulation for death risk in patients with coronary artery disease Qin, Min Zhu, Qian Lai, Weihua Ma, Qilin Liu, Chen Chen, Xiaoping Zhang, Yuelin Wang, Zixian Chen, Hui Yan, Hong Lei, Heping Zhang, Shuyao Dong, Xuekui Wang, Hong Huang, Min Lian, Qizhou Zhong, Shilong Clin Transl Med Research Articles BACKGROUND: Dyslipidaemia contributes to the progression of coronary artery disease (CAD) toward adverse outcomes. Plasma lipidomic measure may improve the prognostic performances of clinical endpoints of CAD. Our research is designed to identify the correlations between plasma lipid species and the risks of death, major adverse cardiovascular event (MACE) and left ventricular (LV) remodeling in patients with CAD. METHODS: A total of 1569 Chinese patients with CAD, 1011 single‐centre patients as internal training cohort, and 558 multicentre patients as external validation cohort, were enrolled. The concentration of plasma lipids in both cohorts was determined through widely targeted lipidomic profiling. Least absolute shrinkage and selection operator Cox and multivariate Cox regressions were used to develop prognostic models for death and MACE, respectively. RESULTS: Ten (Cer(d18:1/20:1), Cer(d18:1/24:1), PE(30:2), PE(32:0), PE(32:2), PC(O‐38:2), PC(O‐36:4), PC(16:1/22:2), LPC(18:2/0:0) and LPE(0:0/24:6)) and two (Cer(d18:1/20:1) and LPC(20:0/0:0)) lipid species were independently related to death and MACE, respectively. Cer(d18:1/20:1) and Cer(d18:1/24:1) were correlated with LV remodeling (P < .05). The lipidic panel incorporating 10 lipid species and two traditional biomarkers for predicting 5‐year death risk represented a remarkable higher discrimination than traditional model with increased area under the curve from 76.56 to 83.65%, continuous NRI of 0.634 and IDI of 0.131. Furthermore, the panel was successfully used in differentiating multicentre patients with low, middle, or high risks (P < .0001). Further analysis indicated that the number of double bonds of phosphatidyl choline and the content of carbon atoms of phosphatidyl ethanolamines were negatively associated with death risk. CONCLUSIONS: Improvement in the prediction of death confirms the effectiveness of plasma lipids as predictors to risk classification in patients with CAD. The association between the structural characteristics of long‐chain polyunsaturated fatty acids and death risk highlights the need for mechanistic research that characterizes the role of individual lipid species in disease pathogenesis. John Wiley and Sons Inc. 2020-09-28 /pmc/articles/PMC7522592/ /pubmed/32997403 http://dx.doi.org/10.1002/ctm2.189 Text en © 2020 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Qin, Min
Zhu, Qian
Lai, Weihua
Ma, Qilin
Liu, Chen
Chen, Xiaoping
Zhang, Yuelin
Wang, Zixian
Chen, Hui
Yan, Hong
Lei, Heping
Zhang, Shuyao
Dong, Xuekui
Wang, Hong
Huang, Min
Lian, Qizhou
Zhong, Shilong
Insights into the prognosis of lipidomic dysregulation for death risk in patients with coronary artery disease
title Insights into the prognosis of lipidomic dysregulation for death risk in patients with coronary artery disease
title_full Insights into the prognosis of lipidomic dysregulation for death risk in patients with coronary artery disease
title_fullStr Insights into the prognosis of lipidomic dysregulation for death risk in patients with coronary artery disease
title_full_unstemmed Insights into the prognosis of lipidomic dysregulation for death risk in patients with coronary artery disease
title_short Insights into the prognosis of lipidomic dysregulation for death risk in patients with coronary artery disease
title_sort insights into the prognosis of lipidomic dysregulation for death risk in patients with coronary artery disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522592/
https://www.ncbi.nlm.nih.gov/pubmed/32997403
http://dx.doi.org/10.1002/ctm2.189
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