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      Association between proprotein convertase subtilisin/kexin type 9 and late saphenous vein graft disease after coronary artery bypass grafting: a cross-sectional study

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          Abstract

          Objective

          The study aims to explore the association between serum proprotein convertase subtilisin/kexin type 9 (PCSK9) level and saphenous vein grafts disease (SVGD) after coronary artery bypass grafting (CABG).

          Design

          A cross-sectional study.

          Setting

          A secondary hospital in Tianjin City, China.

          Participants

          A total of 231 participants were included in the study. Inclusion criteria were as follows: age ≥18 years, previous CABG surgery at least 12 months ago, at least one SVG for bypass during CABG, abnormal non-invasive test results or recurrent stable angina pectoris by coronary angiography indications, and willing to participate and sign informed consent. Participants with any of the following were excluded from the study: congenital valvular disease, decompensated heart failure, anaemia defined as a haemoglobin level of <12 g/dL in women or <13 g/dL in men, malignant neoplasms, renal failure, severe hepatic disease, thyroid disease, acute or chronic inflammatory disease and chronic obstructive lung disease.

          Primary outcome measure

          SVGD was defined as at least one SVG with significant stenosis (≥50%). Circulating PCSK9 levels were measured using commercial ELISA kits according to the manufacturer’s instructions.

          Results

          The mean PCSK9 level in the SVGD group was significantly higher than that in the patent group (275.2±38.6 vs 249.3±37.7, p<0.01). The multivariate logistic regression model revealed a significant association between serum PCSK9 and SVGD (OR 2.08, 95% CI 1.46–2.95) per 1 SD increase in serum PCSK9.

          Conclusions

          The present study is the first to identify an independent association between PCSK9 and late SVGD after adjustment for established cardiovascular risk factors. A multicentre prospective cohort study with large sample size should be conducted in the future to further research this relationship.

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          Most cited references32

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          Cross-talk between LOX-1 and PCSK9 in vascular tissues.

          Lectin-like ox-LDL receptor-1 (LOX-1) plays an important role in inflammatory diseases, such as atherosclerosis. Proprotein convertase subtilisin/kexin type 9 (PCSK9) modulates LDL receptor degradation and influences serum LDL levels. The present study was designed to investigate the possible interaction between PCSK9 and LOX-1.
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            Effects of PCSK9 Inhibition With Alirocumab on Lipoprotein Metabolism in Healthy Humans

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              Circulating Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Predicts Future Risk of Cardiovascular Events Independently of Established Risk Factors.

              The secreted protein proprotein convertase subtilisin/kexin type 9 (PCSK9) is a promising new target for lowering plasma low-density lipoprotein cholesterol and preventing cardiovascular disease (CVD). The relationship between circulating PCSK9 and incident CVD in the general population is unknown. We investigated whether serum PCSK9 concentration is associated with incident CVD in a prospective cohort study of 4232 men and women 60 years of age at the time of recruitment.
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                Author and article information

                Journal
                BMJ Open
                BMJ Open
                bmjopen
                bmjopen
                BMJ Open
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                2044-6055
                2018
                10 July 2018
                : 8
                : 7
                : e021951
                Affiliations
                [1 ] Logistics University of Chinese People’s Armed Police Forces , Tianjin, China
                [2 ] Cardiovascular Institute, Tianjin Chest Hospital , Tianjin, China
                [3 ] Peking University Clinical Research Institute , Beijing, China
                [4 ] departmentDepartment of Cardiology , Tianjin Chest Hospital , Tianjin, China
                [5 ] Independent Consultant , New York, USA
                Author notes
                [Correspondence to ] Professor Yu-Ming Li; cardiolab@ 123456live.com and Professor Yin Liu; liuyin2088@ 123456163.com
                Article
                bmjopen-2018-021951
                10.1136/bmjopen-2018-021951
                6089317
                29991632
                e853a451-18cd-4f21-9132-fb0989a39968
                © Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 30 January 2018
                : 07 May 2018
                : 08 June 2018
                Funding
                Funded by: the Key Project of Scientific and Technological Support Plan of Tianjin;
                Funded by: the Key Project of Healthcare Industry of Tianjin;
                Categories
                Cardiovascular Medicine
                Research
                1506
                1683
                Custom metadata
                unlocked

                Medicine
                coronary artery bypass grafting,saphenous vein grafts disease,proprotein convertase subtilisin/kexin type 9 (pcsk9),low-density lipoprotein cholesterol,atherosclerosis

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