Association of lipoprotein(a) with long‐term mortality following coronary angiography or percutaneous coronary intervention
Background There is no consistent evidence to suggest the association of plasma lipoprotein(a) (Lp[a]) with long‐term mortality in patients undergoing coronary angiography (CAG) or percutaneous coronary intervention (PCI). Hypothesis Level of Lp(a) is associated with long‐term mortality following CA...
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Published in | Clinical cardiology (Mahwah, N.J.) Vol. 40; no. 9; pp. 674 - 678 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Wiley Periodicals, Inc
01.09.2017
John Wiley & Sons, Inc |
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Abstract | Background
There is no consistent evidence to suggest the association of plasma lipoprotein(a) (Lp[a]) with long‐term mortality in patients undergoing coronary angiography (CAG) or percutaneous coronary intervention (PCI).
Hypothesis
Level of Lp(a) is associated with long‐term mortality following CAG or PCI.
Methods
We enrolled 1684 patients with plasma Lp(a) data undergoing CAG or PCI between April 2009 and December 2013. The patients were divided into 2 groups: a low‐Lp(a) group (Lp[a] <16.0 mg/dL; n = 842) and a high‐Lp(a) group (Lp[a] ≥16.0 mg/dL; n = 842).
Results
In‐hospital mortality was not significantly different between the high and low Lp(a) groups (0.8% vs 0.5%, respectively; P = 0.364). During the median follow‐up period of 1.95 years, the high‐Lp(a) group had a higher long‐term mortality than did the low‐Lp(a) group (5.8% vs 2.5%, respectively; P = 0.003). After adjustment of confounders, multivariate Cox regression analysis revealed that a higher Lp(a) level was an independent predictor of long‐term mortality (hazard ratio: 1.96, 95% confidence interval: 1.07‐3.59, P = 0.029).
Conclusions
Our data suggested that an elevated Lp(a) level was significantly associated with long‐term mortality following CAG or PCI. However, additional larger multicenter studies will be required to investigate the predictive value of Lp(a) levels and evaluate the benefit of controlling Lp(a) levels for patients undergoing CAG or PCI. |
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AbstractList | BackgroundThere is no consistent evidence to suggest the association of plasma lipoprotein(a) (Lp[a]) with long‐term mortality in patients undergoing coronary angiography (CAG) or percutaneous coronary intervention (PCI).HypothesisLevel of Lp(a) is associated with long‐term mortality following CAG or PCI.MethodsWe enrolled 1684 patients with plasma Lp(a) data undergoing CAG or PCI between April 2009 and December 2013. The patients were divided into 2 groups: a low‐Lp(a) group (Lp[a] <16.0 mg/dL; n = 842) and a high‐Lp(a) group (Lp[a] ≥16.0 mg/dL; n = 842).ResultsIn‐hospital mortality was not significantly different between the high and low Lp(a) groups (0.8% vs 0.5%, respectively; P = 0.364). During the median follow‐up period of 1.95 years, the high‐Lp(a) group had a higher long‐term mortality than did the low‐Lp(a) group (5.8% vs 2.5%, respectively; P = 0.003). After adjustment of confounders, multivariate Cox regression analysis revealed that a higher Lp(a) level was an independent predictor of long‐term mortality (hazard ratio: 1.96, 95% confidence interval: 1.07‐3.59, P = 0.029).ConclusionsOur data suggested that an elevated Lp(a) level was significantly associated with long‐term mortality following CAG or PCI. However, additional larger multicenter studies will be required to investigate the predictive value of Lp(a) levels and evaluate the benefit of controlling Lp(a) levels for patients undergoing CAG or PCI. Background There is no consistent evidence to suggest the association of plasma lipoprotein(a) (Lp[a]) with long‐term mortality in patients undergoing coronary angiography (CAG) or percutaneous coronary intervention (PCI). Hypothesis Level of Lp(a) is associated with long‐term mortality following CAG or PCI. Methods We enrolled 1684 patients with plasma Lp(a) data undergoing CAG or PCI between April 2009 and December 2013. The patients were divided into 2 groups: a low‐Lp(a) group (Lp[a] <16.0 mg/dL; n = 842) and a high‐Lp(a) group (Lp[a] ≥16.0 mg/dL; n = 842). Results In‐hospital mortality was not significantly different between the high and low Lp(a) groups (0.8% vs 0.5%, respectively; P = 0.364). During the median follow‐up period of 1.95 years, the high‐Lp(a) group had a higher long‐term mortality than did the low‐Lp(a) group (5.8% vs 2.5%, respectively; P = 0.003). After adjustment of confounders, multivariate Cox regression analysis revealed that a higher Lp(a) level was an independent predictor of long‐term mortality (hazard ratio: 1.96, 95% confidence interval: 1.07‐3.59, P = 0.029). Conclusions Our data suggested that an elevated Lp(a) level was significantly associated with long‐term mortality following CAG or PCI. However, additional larger multicenter studies will be required to investigate the predictive value of Lp(a) levels and evaluate the benefit of controlling Lp(a) levels for patients undergoing CAG or PCI. There is no consistent evidence to suggest the association of plasma lipoprotein(a) (Lp[a]) with long-term mortality in patients undergoing coronary angiography (CAG) or percutaneous coronary intervention (PCI). Level of Lp(a) is associated with long-term mortality following CAG or PCI. We enrolled 1684 patients with plasma Lp(a) data undergoing CAG or PCI between April 2009 and December 2013. The patients were divided into 2 groups: a low-Lp(a) group (Lp[a] <16.0 mg/dL; n = 842) and a high-Lp(a) group (Lp[a] ≥16.0 mg/dL; n = 842). In-hospital mortality was not significantly different between the high and low Lp(a) groups (0.8% vs 0.5%, respectively; P = 0.364). During the median follow-up period of 1.95 years, the high-Lp(a) group had a higher long-term mortality than did the low-Lp(a) group (5.8% vs 2.5%, respectively; P = 0.003). After adjustment of confounders, multivariate Cox regression analysis revealed that a higher Lp(a) level was an independent predictor of long-term mortality (hazard ratio: 1.96, 95% confidence interval: 1.07-3.59, P = 0.029). Our data suggested that an elevated Lp(a) level was significantly associated with long-term mortality following CAG or PCI. However, additional larger multicenter studies will be required to investigate the predictive value of Lp(a) levels and evaluate the benefit of controlling Lp(a) levels for patients undergoing CAG or PCI. There is no consistent evidence to suggest the association of plasma lipoprotein(a) (Lp[a]) with long-term mortality in patients undergoing coronary angiography (CAG) or percutaneous coronary intervention (PCI).BACKGROUNDThere is no consistent evidence to suggest the association of plasma lipoprotein(a) (Lp[a]) with long-term mortality in patients undergoing coronary angiography (CAG) or percutaneous coronary intervention (PCI).Level of Lp(a) is associated with long-term mortality following CAG or PCI.HYPOTHESISLevel of Lp(a) is associated with long-term mortality following CAG or PCI.We enrolled 1684 patients with plasma Lp(a) data undergoing CAG or PCI between April 2009 and December 2013. The patients were divided into 2 groups: a low-Lp(a) group (Lp[a] <16.0 mg/dL; n = 842) and a high-Lp(a) group (Lp[a] ≥16.0 mg/dL; n = 842).METHODSWe enrolled 1684 patients with plasma Lp(a) data undergoing CAG or PCI between April 2009 and December 2013. The patients were divided into 2 groups: a low-Lp(a) group (Lp[a] <16.0 mg/dL; n = 842) and a high-Lp(a) group (Lp[a] ≥16.0 mg/dL; n = 842).In-hospital mortality was not significantly different between the high and low Lp(a) groups (0.8% vs 0.5%, respectively; P = 0.364). During the median follow-up period of 1.95 years, the high-Lp(a) group had a higher long-term mortality than did the low-Lp(a) group (5.8% vs 2.5%, respectively; P = 0.003). After adjustment of confounders, multivariate Cox regression analysis revealed that a higher Lp(a) level was an independent predictor of long-term mortality (hazard ratio: 1.96, 95% confidence interval: 1.07-3.59, P = 0.029).RESULTSIn-hospital mortality was not significantly different between the high and low Lp(a) groups (0.8% vs 0.5%, respectively; P = 0.364). During the median follow-up period of 1.95 years, the high-Lp(a) group had a higher long-term mortality than did the low-Lp(a) group (5.8% vs 2.5%, respectively; P = 0.003). After adjustment of confounders, multivariate Cox regression analysis revealed that a higher Lp(a) level was an independent predictor of long-term mortality (hazard ratio: 1.96, 95% confidence interval: 1.07-3.59, P = 0.029).Our data suggested that an elevated Lp(a) level was significantly associated with long-term mortality following CAG or PCI. However, additional larger multicenter studies will be required to investigate the predictive value of Lp(a) levels and evaluate the benefit of controlling Lp(a) levels for patients undergoing CAG or PCI.CONCLUSIONSOur data suggested that an elevated Lp(a) level was significantly associated with long-term mortality following CAG or PCI. However, additional larger multicenter studies will be required to investigate the predictive value of Lp(a) levels and evaluate the benefit of controlling Lp(a) levels for patients undergoing CAG or PCI. |
Author | Zhou, Ying‐ling Li, Hua‐long Ran, Peng Islam, Sheikh Mohammed Shariful Wang, Kun Chen, Shi‐qun Guo, Xiao‐sheng Chen, Ji‐yan Feng, Zhe Li, Xi‐da Bei, Wei‐jie Luo, De‐mou Chen, Peng‐yuan Yi, Shi‐xin Liu, Yong |
AuthorAffiliation | 1 Department of Cardiology, Guangdong Cardiovascular Institute, Guangdong Key Laboratory of Coronary Disease, Guangdong General Hospital Guangdong Academy of Medical Sciences Guangzhou Guangdong China 2 School of Medicine South China University of Technology Guangzhou Guangdong China 4 The George Institute for Global Health (Islam) University of Sydney Camperdown New South Wales Australia 3 Department of Graduate School (Wang) Southern Medical University Guangzhou Guangdong China |
AuthorAffiliation_xml | – name: 4 The George Institute for Global Health (Islam) University of Sydney Camperdown New South Wales Australia – name: 3 Department of Graduate School (Wang) Southern Medical University Guangzhou Guangdong China – name: 1 Department of Cardiology, Guangdong Cardiovascular Institute, Guangdong Key Laboratory of Coronary Disease, Guangdong General Hospital Guangdong Academy of Medical Sciences Guangzhou Guangdong China – name: 2 School of Medicine South China University of Technology Guangzhou Guangdong China |
Author_xml | – sequence: 1 givenname: Zhe surname: Feng fullname: Feng, Zhe organization: South China University of Technology – sequence: 2 givenname: Hua‐long surname: Li fullname: Li, Hua‐long organization: South China University of Technology – sequence: 3 givenname: Wei‐jie surname: Bei fullname: Bei, Wei‐jie organization: South China University of Technology – sequence: 4 givenname: Xiao‐sheng surname: Guo fullname: Guo, Xiao‐sheng organization: South China University of Technology – sequence: 5 givenname: Kun surname: Wang fullname: Wang, Kun organization: Southern Medical University – sequence: 6 givenname: Shi‐xin surname: Yi fullname: Yi, Shi‐xin organization: Guangdong Academy of Medical Sciences – sequence: 7 givenname: De‐mou surname: Luo fullname: Luo, De‐mou organization: Guangdong Academy of Medical Sciences – sequence: 8 givenname: Xi‐da surname: Li fullname: Li, Xi‐da organization: Guangdong Academy of Medical Sciences – sequence: 9 givenname: Shi‐qun surname: Chen fullname: Chen, Shi‐qun organization: South China University of Technology – sequence: 10 givenname: Peng surname: Ran fullname: Ran, Peng organization: Guangdong Academy of Medical Sciences – sequence: 11 givenname: Peng‐yuan surname: Chen fullname: Chen, Peng‐yuan organization: South China University of Technology – sequence: 12 givenname: Sheikh Mohammed Shariful surname: Islam fullname: Islam, Sheikh Mohammed Shariful organization: University of Sydney – sequence: 13 givenname: Ji‐yan surname: Chen fullname: Chen, Ji‐yan organization: South China University of Technology – sequence: 14 givenname: Yong surname: Liu fullname: Liu, Yong email: liuyongmd@126.com organization: South China University of Technology – sequence: 15 givenname: Ying‐ling orcidid: 0000-0002-8960-8076 surname: Zhou fullname: Zhou, Ying‐ling email: gdh_zyl@126.com organization: South China University of Technology |
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Keywords | Coronary Angiography Lipoprotein(a) Mortality Percutaneous Coronary Intervention |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 ObjectType-Undefined-3 Author contributions: Zhe Feng, MD, Hua‐long Li, MD, Wei‐jie Bei, MD, Xiao‐sheng Guo, MD, and Kun Wang, MD, contributed equally to this work. Funding information Guangdong Provincial Cardiovascular Clinical Medicine Research Fund, Grant/Award number: (Grant no. 2009X41by Yong Liu and Ning Tan); Science and Technology Planning Project of Guangdong Province, Grant/Awardnumber: (PRECOMIN study by Yong Liu in 2011 and study grant no. 2008A030201002 by Ji‐yan Chen); Guangdong Cardiovascular Institute. This study was also supported by Progress of Science and Technology project in Guangdong province, Grant/Award numbers: 2013b031800025, 2016b020215130; Cardiovascular Research Foundation Project of Chinese Medical Doctor Association, Grant/Award number: (SCRFCMDA201216). |
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There is no consistent evidence to suggest the association of plasma lipoprotein(a) (Lp[a]) with long‐term mortality in patients undergoing coronary... There is no consistent evidence to suggest the association of plasma lipoprotein(a) (Lp[a]) with long-term mortality in patients undergoing coronary... BackgroundThere is no consistent evidence to suggest the association of plasma lipoprotein(a) (Lp[a]) with long‐term mortality in patients undergoing coronary... |
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SubjectTerms | Aged Angioplasty Biomarkers - blood Chi-Square Distribution Clinical Investigations Coronary Angiography Coronary Angiography - adverse effects Coronary Angiography - mortality Coronary Artery Disease - blood Coronary Artery Disease - diagnostic imaging Coronary Artery Disease - mortality Coronary Artery Disease - therapy Female Hospital Mortality Humans Kaplan-Meier Estimate Lipoprotein(a) Lipoprotein(a) - blood Male Medical imaging Middle Aged Mortality Multivariate Analysis Percutaneous Coronary Intervention Percutaneous Coronary Intervention - adverse effects Percutaneous Coronary Intervention - mortality Predictive Value of Tests Proportional Hazards Models Retrospective Studies Risk Factors Time Factors Treatment Outcome Up-Regulation |
Title | Association of lipoprotein(a) with long‐term mortality following coronary angiography or percutaneous coronary intervention |
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