Effect of early application of PCSK9 inhibitor on inflammation level and microcirculation function after PCI in patients with non-ST-segment elevation acute coronary syndrome
Author:
Affiliation:

The Fifth Clinical Medical College of Henan University of Chinese Medicine & People's Hospital of Henan University of Chinese Medicine, Zhengzhou, Henan 450000, China)

Clc Number:

R5

  • Article
  • | |
  • Metrics
  • |
  • Reference [15]
  • | | | |
  • Comments
    Abstract:

    Aim To investigate the effect of early application of proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor on inflammation level and microcirculation function after PCI in patients with non-ST-segment elevation acute coronary syndrome (NSTE-ACS). Methods From December 2019 to December 1,0 patients with NSTE-ACS who underwent PCI in the People's Hospital of Henan University of Chinese Medicine were selected and randomly divided into control group (55 cases) and PCSK9 inhibitor group (55 cases) according to the random number table method. Patients in control group was treated with atorvastatin calcium tablets, and patients in PCSK9 inhibitor group was treated with evolumab on the basis of the control group. After 6 months of treatment, the blood lipids, inflammation levels, coronary microcirculation resistance index and differences in coronary TIMI myocardial perfusion grade (TMPG) were compared. Results Compared with control group, the levels of triglyceride (TG), total cholesterol (TC), low density lipoprotein cholesterol (LDLC) and lipoprotein(a) in PCSK9 inhibitor group were significantly decreased after treatment, and the differences were statistically significant (P<0.05). The levels of high sensitivity C-reactive protein (hs-CRP), tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) were significantly decreased after treatment, and the differences were statistically significant (P<0.05). After treatment, the index of microcirculatory resistance (IMR) of PCSK9 inhibitor group was lower than that of control group, and the difference was statistically significant (P<0.05). Six months after surgery, TMPG level 3 in PCSK9 inhibitor group was higher than that in control group, the difference was statistically significant (P<0.05). Conclusion Early application of PCSK9 inhibitor on the basis of statins can improve inflammation level and microcirculation function after PCI in patients with NSTE-ACS, which is worthy of clinical promotion.

    Reference
    [1] 中国心血管健康与疾病报告编写组.中国心血管健康与疾病报告2020概要.中国循环杂志, 1,6(6):521-545.THE WRITING COMMITTEE OF THE REPORT ON CARDIOVASCULAR HEALTH AND DISEASES IN CHINA.Summary of China cardiovascular health and disease report 2020.Chin Circ J, 1,6 (6):521-545.
    [2] EISEN A, GIUGLIANO R P, BRAUNWALD E.Updates on acute coronary syndrome.JAMA Cardiol, 6,1(6):718-730.
    [3] ALI A, TOMAS J, EMIL H, et al.Application of the 2019 ESC/EAS dyslipidaemia guidelines to nationwide data of patients with a recent myocardial infarction:a simulation study.Eur Heart J, 0,1(40):3900-3909.
    [4] 李建军.血脂异常与动脉粥样硬化关系的现代观念.中国循环杂志, 2,7:212-214.LI J J.The modern concept of the relationship between dyslipidemia and atherosclerosis.Chin Circ J, 2,7:212-214.
    [5] FRANOIS M, COLIN B, CATAPANO A L, et al.2019 ESC/EAS guidelines for the management of dyslipidaemias:lipid modification to reduce cardiovascular risk.Eur Heart l, 9,1(1):111-188.
    [6] 颜红兵, 唐熠达, 杨艳敏, 等.急性冠状动脉综合征治疗指南:欧洲心脏病学会:2012年.北京:中国环境科学出版社, 2012:1-2.YAN H B, TANG Y D, YANG Y M, et al.Guidelines for the management of acute coronary syndromes:European Society of Cardiology:2012.Beijing:China Environmental Science Press, 2012:1-2.
    [7] RUPARELIA N, CHAI J, FISHER E, et al.Inflammatory processes in cardiovascular disease:a route to targeted therapies.Nat Rev Cardiol, 7,4(3):133-144.
    [8] MULHOLLAND M, JAKOBSSON G, YU L, et al.IL-2Rβγ signalling in lymphocytes promotes systemic inflammation and reduces plasma cholesterol in atherosclerotic mice.Atherosclerosis, 1,6:1-10.
    [9] SABATINE M S, GIUGLIANO R P, KEECH A C, et al.Evolocumab and clinical outcomes in patients with cardiovascular disease.N Engl J Med, 7,6(18):1713-1722.
    [10] ABBAS M, SARVENAZ S R, GOTTO A M, et al.PCSK9 and inflammation:a review of experimental and clinical evidence.Eur Heart J Cardiovasc Pharmacother, 9,5(4):237-245.
    [11] 罗星, 贾海波.斑块侵蚀导致ACS的深层机制及高效抗血小板策略.中华医学信息导报, 1,6(11):21.LUO X, JIA H B.Plaque erosion leads to the deep mechanism of ACS and efficient antiplatelet strategy.Chin Med News, 1,6 (11):21.
    [12] NAVARESE E P, KOLODZIEJCZAK M, KEREIAKES D J, et al.Proprotein convertase subtilisin/kexin type 9 monoclonal antibodies for acute coronary syndrome:a narrative review.Ann Inter Med, 6,4(9):600-607.
    [13] TANG Z H, PENG J, REN Z, et al.New role of PCSK9 in atherosclerotic inflammation promotion involving the TLR4/NF-κB pathway.Atherosclerosis, 7,2:113-122.
    [14] FRANSSEN C, CHEN S, UNGER A, et al.Myocardial microvascular inflammatory endothelial activation in heart failure with preserved ejection fraction.JACC Heart Fail, 6,4(4):312-324.
    [15] 徐慧慧, 谢艳辉, 宋恒良, 等.PCSK9抑制剂对急性ST段抬高型心肌梗死PCI术后的微循环功能及左心室重构的影响.临床心血管病杂志, 2,8(1):22-28.XU H H, XIE Y H, SONG H L, et al.Effect of PCSK9 inhibitors on microcirculation function and left ventricular remodeling after PCI in acute ST-segment elevation myocardial infarction.J Clin Cardiol, 2,8(1):22-28.
    Related
    Cited by
    Comments
    Comments
    分享到微博
    Submit
Get Citation

CHEN Wenshan, JI Jingrui, WEI Xiaoyun, Gen guo ying, LIU Yang, LIU Hengliang. Effect of early application of PCSK9 inhibitor on inflammation level and microcirculation function after PCI in patients with non-ST-segment elevation acute coronary syndrome[J]. Editorial Office of Chinese Journal of Arteriosclerosis,2022,30(7):601-605.

Copy
Share
Article Metrics
  • Abstract:237
  • PDF: 532
  • HTML: 0
  • Cited by: 0
History
  • Received:April 05,2022
  • Revised:May 19,2022
  • Online: July 11,2022
Article QR Code